Incidental Mutation 'R0883:Celsr3'
ID |
80854 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Celsr3
|
Ensembl Gene |
ENSMUSG00000023473 |
Gene Name |
cadherin, EGF LAG seven-pass G-type receptor 3 |
Synonyms |
Fmi1, flamingo, Adgrc3 |
MMRRC Submission |
039050-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R0883 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
108703519-108730168 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 108719832 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Asparagine
at position 2470
(I2470N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000024238
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000024238]
[ENSMUST00000194079]
[ENSMUST00000213524]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000024238
AA Change: I2470N
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000024238 Gene: ENSMUSG00000023473 AA Change: I2470N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
31 |
N/A |
INTRINSIC |
low complexity region
|
264 |
293 |
N/A |
INTRINSIC |
CA
|
338 |
422 |
2.25e-27 |
SMART |
CA
|
446 |
534 |
5.05e-30 |
SMART |
CA
|
558 |
640 |
7.6e-25 |
SMART |
CA
|
664 |
745 |
7.36e-32 |
SMART |
CA
|
769 |
847 |
5.95e-18 |
SMART |
CA
|
871 |
950 |
5.25e-28 |
SMART |
CA
|
974 |
1056 |
2.67e-29 |
SMART |
CA
|
1080 |
1158 |
1.18e-21 |
SMART |
CA
|
1186 |
1262 |
3.2e-1 |
SMART |
low complexity region
|
1328 |
1335 |
N/A |
INTRINSIC |
low complexity region
|
1350 |
1360 |
N/A |
INTRINSIC |
EGF
|
1369 |
1424 |
1.02e-2 |
SMART |
EGF
|
1429 |
1464 |
3.23e0 |
SMART |
EGF
|
1467 |
1503 |
8.78e-2 |
SMART |
LamG
|
1524 |
1691 |
2.27e-35 |
SMART |
EGF
|
1714 |
1747 |
4.22e-4 |
SMART |
LamG
|
1774 |
1913 |
9.02e-21 |
SMART |
EGF
|
1938 |
1971 |
2.43e-4 |
SMART |
EGF
|
1973 |
2009 |
1.3e-4 |
SMART |
EGF_Lam
|
2066 |
2111 |
5.08e-7 |
SMART |
HormR
|
2114 |
2176 |
3.42e-21 |
SMART |
Pfam:GAIN
|
2188 |
2441 |
1.1e-57 |
PFAM |
GPS
|
2467 |
2520 |
7.92e-20 |
SMART |
Pfam:7tm_2
|
2527 |
2758 |
1.5e-56 |
PFAM |
low complexity region
|
2813 |
2829 |
N/A |
INTRINSIC |
low complexity region
|
2882 |
2906 |
N/A |
INTRINSIC |
low complexity region
|
3058 |
3072 |
N/A |
INTRINSIC |
low complexity region
|
3149 |
3189 |
N/A |
INTRINSIC |
low complexity region
|
3239 |
3261 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000175326
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000194079
|
SMART Domains |
Protein: ENSMUSP00000141789 Gene: ENSMUSG00000023473
Domain | Start | End | E-Value | Type |
Pfam:7tm_2
|
1 |
185 |
6.9e-45 |
PFAM |
low complexity region
|
240 |
256 |
N/A |
INTRINSIC |
low complexity region
|
309 |
333 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000195255
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000195857
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000213524
AA Change: I2477N
PolyPhen 2
Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)
|
Coding Region Coverage |
- 1x: 99.5%
- 3x: 99.0%
- 10x: 97.8%
- 20x: 96.1%
|
Validation Efficiency |
98% (148/151) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene belongs to the flamingo subfamily, which is included in the cadherin superfamily. The flamingo cadherins consist of nonclassic-type cadherins that do not interact with catenins. They are plasma membrane proteins containing seven epidermal growth factor-like repeats, nine cadherin domains and two laminin A G-type repeats in their ectodomain. They also have seven transmembrane domains, a characteristic feature of their subfamily. The encoded protein may be involved in the regulation of contact-dependent neurite growth and may play a role in tumor formation. [provided by RefSeq, Jun 2013] PHENOTYPE: Mice homozygous for a null allele exhibit neonatal lethality, abnormal neurvous system development, and abnormal respiratory system development. [provided by MGI curators]
|
Allele List at MGI |
All alleles(4) : Targeted, knock-out(2) Targeted, other(2) |
Other mutations in this stock |
Total: 150 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,775,632 (GRCm39) |
L1607P |
probably damaging |
Het |
1700016H13Rik |
T |
C |
5: 103,796,687 (GRCm39) |
*118W |
probably null |
Het |
4930595M18Rik |
G |
T |
X: 80,464,537 (GRCm39) |
T390N |
possibly damaging |
Het |
Abca13 |
C |
T |
11: 9,241,238 (GRCm39) |
Q1034* |
probably null |
Het |
Acsbg3 |
A |
T |
17: 57,190,835 (GRCm39) |
N468Y |
probably benign |
Het |
Adgra3 |
T |
C |
5: 50,118,065 (GRCm39) |
H1161R |
probably damaging |
Het |
Aff1 |
T |
C |
5: 103,974,004 (GRCm39) |
|
probably benign |
Het |
Agap2 |
A |
G |
10: 126,927,571 (GRCm39) |
T1131A |
possibly damaging |
Het |
Ankrd12 |
A |
G |
17: 66,292,127 (GRCm39) |
V1102A |
probably benign |
Het |
Ankrd54 |
A |
T |
15: 78,946,931 (GRCm39) |
C23S |
probably damaging |
Het |
Anxa10 |
C |
T |
8: 62,531,001 (GRCm39) |
V70I |
probably benign |
Het |
Asap3 |
T |
C |
4: 135,961,636 (GRCm39) |
|
probably benign |
Het |
Asb13 |
T |
C |
13: 3,695,052 (GRCm39) |
|
probably null |
Het |
Atp6v1a |
A |
T |
16: 43,922,055 (GRCm39) |
|
probably benign |
Het |
Atp8b1 |
T |
G |
18: 64,697,612 (GRCm39) |
I411L |
probably benign |
Het |
Baiap3 |
T |
A |
17: 25,468,075 (GRCm39) |
N313I |
probably damaging |
Het |
Bok |
T |
C |
1: 93,614,209 (GRCm39) |
I14T |
probably benign |
Het |
Bri3bp |
T |
A |
5: 125,518,808 (GRCm39) |
|
probably null |
Het |
C2cd2l |
A |
G |
9: 44,227,499 (GRCm39) |
L186P |
probably damaging |
Het |
Cadm2 |
A |
T |
16: 66,679,702 (GRCm39) |
C44S |
probably damaging |
Het |
Capn11 |
T |
C |
17: 45,949,807 (GRCm39) |
|
probably benign |
Het |
Carm1 |
T |
A |
9: 21,480,887 (GRCm39) |
|
probably benign |
Het |
Ccdc27 |
T |
C |
4: 154,120,941 (GRCm39) |
E285G |
unknown |
Het |
Cct3 |
T |
A |
3: 88,220,864 (GRCm39) |
D298E |
probably damaging |
Het |
Cd59b |
T |
A |
2: 103,911,331 (GRCm39) |
|
probably benign |
Het |
Cdh2 |
T |
C |
18: 16,762,633 (GRCm39) |
N437S |
probably benign |
Het |
Cfap100 |
G |
A |
6: 90,392,888 (GRCm39) |
|
probably benign |
Het |
Cfap119 |
T |
C |
7: 127,184,034 (GRCm39) |
E261G |
probably damaging |
Het |
Cfap45 |
A |
T |
1: 172,359,756 (GRCm39) |
R98S |
possibly damaging |
Het |
Cfap54 |
T |
A |
10: 92,706,531 (GRCm39) |
H2757L |
unknown |
Het |
Chd1 |
C |
A |
17: 15,945,693 (GRCm39) |
N72K |
probably benign |
Het |
Cntn4 |
A |
T |
6: 106,644,501 (GRCm39) |
|
probably benign |
Het |
Cstf2t |
A |
T |
19: 31,062,026 (GRCm39) |
M521L |
probably benign |
Het |
Daam2 |
A |
T |
17: 49,805,911 (GRCm39) |
|
probably benign |
Het |
Ddias |
A |
T |
7: 92,508,545 (GRCm39) |
W457R |
probably benign |
Het |
Ddr2 |
C |
T |
1: 169,822,198 (GRCm39) |
V417I |
probably benign |
Het |
Dhx57 |
T |
C |
17: 80,577,800 (GRCm39) |
T570A |
probably damaging |
Het |
Dmp1 |
A |
G |
5: 104,355,496 (GRCm39) |
E32G |
possibly damaging |
Het |
Dtymk |
C |
T |
1: 93,729,510 (GRCm39) |
V14M |
possibly damaging |
Het |
Dync2li1 |
G |
A |
17: 84,956,699 (GRCm39) |
M286I |
probably benign |
Het |
Eea1 |
G |
A |
10: 95,857,529 (GRCm39) |
D664N |
possibly damaging |
Het |
Esp6 |
G |
T |
17: 40,876,287 (GRCm39) |
V112L |
probably benign |
Het |
Fam83h |
G |
T |
15: 75,878,018 (GRCm39) |
Q127K |
probably damaging |
Het |
Gabbr2 |
G |
A |
4: 46,677,474 (GRCm39) |
T802I |
probably benign |
Het |
Gart |
C |
A |
16: 91,420,291 (GRCm39) |
D851Y |
possibly damaging |
Het |
Gemin6 |
T |
A |
17: 80,535,524 (GRCm39) |
H161Q |
probably damaging |
Het |
Gm10912 |
T |
C |
2: 103,896,875 (GRCm39) |
S5P |
probably benign |
Het |
Gm5941 |
G |
A |
X: 91,533,817 (GRCm39) |
A62T |
possibly damaging |
Het |
Gng2 |
G |
T |
14: 19,941,363 (GRCm39) |
D26E |
probably benign |
Het |
Gpr33 |
A |
G |
12: 52,070,418 (GRCm39) |
V207A |
probably benign |
Het |
Gstm3 |
T |
A |
3: 107,873,586 (GRCm39) |
|
probably benign |
Het |
Havcr1 |
T |
C |
11: 46,643,259 (GRCm39) |
C60R |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,268,751 (GRCm39) |
S2157P |
probably benign |
Het |
Ift140 |
A |
G |
17: 25,309,907 (GRCm39) |
T1105A |
probably benign |
Het |
Igsf8 |
C |
A |
1: 172,143,826 (GRCm39) |
A56D |
possibly damaging |
Het |
Kat6a |
G |
T |
8: 23,352,230 (GRCm39) |
A5S |
probably damaging |
Het |
Kctd16 |
A |
G |
18: 40,663,828 (GRCm39) |
E319G |
probably damaging |
Het |
Kmo |
T |
C |
1: 175,474,706 (GRCm39) |
V157A |
possibly damaging |
Het |
Lrp5 |
T |
A |
19: 3,655,308 (GRCm39) |
I1071F |
probably damaging |
Het |
Lrrc17 |
A |
G |
5: 21,766,276 (GRCm39) |
T253A |
probably benign |
Het |
Mast2 |
T |
A |
4: 116,168,964 (GRCm39) |
H769L |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,990,408 (GRCm39) |
K50E |
probably damaging |
Het |
Mbd5 |
A |
G |
2: 49,146,701 (GRCm39) |
T304A |
possibly damaging |
Het |
Mbp |
T |
C |
18: 82,590,995 (GRCm39) |
S73P |
probably damaging |
Het |
Mc5r |
T |
A |
18: 68,472,163 (GRCm39) |
V174E |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,197,864 (GRCm39) |
T736S |
probably benign |
Het |
Med13l |
T |
C |
5: 118,809,067 (GRCm39) |
|
probably benign |
Het |
Minar1 |
T |
C |
9: 89,484,470 (GRCm39) |
H309R |
probably benign |
Het |
Mlh3 |
C |
G |
12: 85,282,488 (GRCm39) |
A1382P |
possibly damaging |
Het |
Mpdz |
T |
C |
4: 81,278,228 (GRCm39) |
|
probably benign |
Het |
Muc5ac |
A |
G |
7: 141,350,002 (GRCm39) |
T582A |
possibly damaging |
Het |
Nalcn |
A |
G |
14: 123,702,152 (GRCm39) |
F453S |
probably damaging |
Het |
Nrap |
T |
A |
19: 56,333,906 (GRCm39) |
M902L |
probably damaging |
Het |
Nup85 |
C |
T |
11: 115,459,196 (GRCm39) |
R100* |
probably null |
Het |
Nxf1 |
T |
G |
19: 8,741,955 (GRCm39) |
N296K |
probably damaging |
Het |
Ogg1 |
A |
G |
6: 113,305,381 (GRCm39) |
T65A |
probably damaging |
Het |
Ogt |
A |
G |
X: 100,687,805 (GRCm39) |
|
probably benign |
Het |
Or4c10 |
A |
G |
2: 89,760,545 (GRCm39) |
T131A |
probably benign |
Het |
Or4k48 |
C |
T |
2: 111,476,136 (GRCm39) |
V69I |
probably benign |
Het |
Or51e1 |
T |
A |
7: 102,359,202 (GRCm39) |
H245Q |
probably damaging |
Het |
Or56b1b |
T |
A |
7: 108,164,483 (GRCm39) |
N173I |
probably benign |
Het |
Ovol2 |
T |
C |
2: 144,173,710 (GRCm39) |
D24G |
probably damaging |
Het |
Pabpc1 |
A |
G |
15: 36,599,298 (GRCm39) |
|
probably benign |
Het |
Pak6 |
T |
C |
2: 118,524,168 (GRCm39) |
L441P |
probably damaging |
Het |
Pappa |
T |
A |
4: 65,107,552 (GRCm39) |
C654* |
probably null |
Het |
Paqr6 |
T |
A |
3: 88,273,298 (GRCm39) |
S97T |
probably damaging |
Het |
Parp14 |
T |
C |
16: 35,678,888 (GRCm39) |
N360S |
probably benign |
Het |
Pclo |
G |
T |
5: 14,727,873 (GRCm39) |
G2244* |
probably null |
Het |
Pdzrn3 |
A |
T |
6: 101,132,903 (GRCm39) |
|
probably null |
Het |
Pes1 |
T |
C |
11: 3,925,557 (GRCm39) |
M220T |
probably damaging |
Het |
Phip |
A |
T |
9: 82,758,274 (GRCm39) |
V1473E |
probably benign |
Het |
Pkd2l2 |
T |
A |
18: 34,563,321 (GRCm39) |
|
probably null |
Het |
Plch1 |
T |
C |
3: 63,660,677 (GRCm39) |
D302G |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,925,459 (GRCm39) |
T1419A |
probably benign |
Het |
Ppara |
A |
T |
15: 85,682,372 (GRCm39) |
E356V |
probably damaging |
Het |
Ppp1r37 |
G |
A |
7: 19,266,102 (GRCm39) |
P555S |
probably benign |
Het |
Ppp6r1 |
T |
C |
7: 4,642,709 (GRCm39) |
E545G |
possibly damaging |
Het |
Proser3 |
G |
A |
7: 30,240,124 (GRCm39) |
H327Y |
probably damaging |
Het |
Prss43 |
T |
A |
9: 110,658,576 (GRCm39) |
I292N |
probably damaging |
Het |
Pwwp3b |
T |
A |
X: 138,136,444 (GRCm39) |
D327E |
probably damaging |
Het |
Pygl |
G |
C |
12: 70,253,178 (GRCm39) |
N271K |
probably damaging |
Het |
Rassf7 |
T |
A |
7: 140,796,903 (GRCm39) |
|
probably benign |
Het |
Rfx2 |
T |
C |
17: 57,110,722 (GRCm39) |
Y88C |
probably damaging |
Het |
Rpl6 |
T |
C |
5: 121,346,541 (GRCm39) |
V214A |
probably benign |
Het |
Rspo1 |
T |
A |
4: 124,885,225 (GRCm39) |
|
probably null |
Het |
Sav1 |
A |
C |
12: 70,012,979 (GRCm39) |
L366V |
probably benign |
Het |
Sema3b |
T |
G |
9: 107,481,355 (GRCm39) |
T52P |
possibly damaging |
Het |
Senp6 |
A |
G |
9: 80,023,841 (GRCm39) |
D40G |
probably damaging |
Het |
Sh3pxd2a |
A |
G |
19: 47,256,646 (GRCm39) |
S719P |
probably damaging |
Het |
Shank1 |
C |
T |
7: 44,001,718 (GRCm39) |
R1146W |
unknown |
Het |
Slc34a3 |
G |
T |
2: 25,121,245 (GRCm39) |
D307E |
probably benign |
Het |
Slc35b3 |
T |
C |
13: 39,121,251 (GRCm39) |
I330V |
probably benign |
Het |
Slc4a10 |
G |
A |
2: 62,073,742 (GRCm39) |
C268Y |
probably benign |
Het |
Slco6d1 |
A |
G |
1: 98,349,124 (GRCm39) |
E65G |
probably benign |
Het |
Slit2 |
A |
G |
5: 48,402,915 (GRCm39) |
|
probably benign |
Het |
Smcr8 |
T |
C |
11: 60,668,941 (GRCm39) |
Y30H |
probably damaging |
Het |
Snap47 |
A |
G |
11: 59,329,326 (GRCm39) |
|
probably benign |
Het |
Snrnp25 |
G |
A |
11: 32,156,960 (GRCm39) |
V15I |
probably damaging |
Het |
Spns2 |
T |
C |
11: 72,345,223 (GRCm39) |
Y449C |
probably damaging |
Het |
Stab2 |
T |
A |
10: 86,760,314 (GRCm39) |
|
probably benign |
Het |
Strip1 |
C |
A |
3: 107,521,929 (GRCm39) |
D750Y |
probably damaging |
Het |
Taf1c |
A |
T |
8: 120,326,722 (GRCm39) |
I438N |
probably damaging |
Het |
Tbc1d2 |
T |
A |
4: 46,609,003 (GRCm39) |
K745* |
probably null |
Het |
Tctn1 |
T |
C |
5: 122,402,207 (GRCm39) |
T76A |
probably damaging |
Het |
Tesl1 |
A |
T |
X: 23,773,290 (GRCm39) |
I264F |
probably benign |
Het |
Tfpi |
T |
C |
2: 84,273,664 (GRCm39) |
|
probably benign |
Het |
Timm44 |
A |
T |
8: 4,316,592 (GRCm39) |
H317Q |
probably benign |
Het |
Tnfaip1 |
A |
T |
11: 78,420,840 (GRCm39) |
|
probably benign |
Het |
Tnpo3 |
A |
T |
6: 29,554,992 (GRCm39) |
|
probably benign |
Het |
Top3b |
T |
C |
16: 16,697,301 (GRCm39) |
|
probably benign |
Het |
Trak1 |
T |
A |
9: 121,282,351 (GRCm39) |
M410K |
possibly damaging |
Het |
Trpm3 |
C |
A |
19: 22,956,018 (GRCm39) |
P1160Q |
probably damaging |
Het |
Tyk2 |
T |
A |
9: 21,022,433 (GRCm39) |
T799S |
possibly damaging |
Het |
Ubfd1 |
G |
A |
7: 121,666,714 (GRCm39) |
|
probably benign |
Het |
Unc13a |
G |
A |
8: 72,094,817 (GRCm39) |
R1272* |
probably null |
Het |
Unc45b |
T |
A |
11: 82,831,031 (GRCm39) |
L797Q |
possibly damaging |
Het |
Urb2 |
C |
T |
8: 124,757,709 (GRCm39) |
Q1139* |
probably null |
Het |
Vmn2r66 |
A |
T |
7: 84,657,070 (GRCm39) |
S112T |
probably benign |
Het |
Vmn2r71 |
A |
T |
7: 85,272,842 (GRCm39) |
D552V |
probably benign |
Het |
Vmn2r76 |
A |
G |
7: 85,877,904 (GRCm39) |
Y498H |
probably benign |
Het |
Vmn2r84 |
A |
C |
10: 130,226,984 (GRCm39) |
W285G |
probably damaging |
Het |
Vps72 |
G |
T |
3: 95,029,894 (GRCm39) |
L304F |
probably damaging |
Het |
Wiz |
A |
T |
17: 32,575,415 (GRCm39) |
I907N |
probably damaging |
Het |
Yaf2 |
T |
C |
15: 93,183,417 (GRCm39) |
K131R |
probably damaging |
Het |
Zfp141 |
A |
T |
7: 42,125,480 (GRCm39) |
Y331N |
possibly damaging |
Het |
Zfp324 |
G |
T |
7: 12,704,951 (GRCm39) |
C380F |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 13,978,119 (GRCm39) |
T765A |
probably benign |
Het |
Zfp616 |
A |
T |
11: 73,976,500 (GRCm39) |
H923L |
probably damaging |
Het |
Zfpm1 |
C |
T |
8: 123,062,585 (GRCm39) |
T548M |
probably damaging |
Het |
Zp2 |
A |
T |
7: 119,742,799 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Celsr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00233:Celsr3
|
APN |
9 |
108,726,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00536:Celsr3
|
APN |
9 |
108,706,391 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00552:Celsr3
|
APN |
9 |
108,718,462 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00801:Celsr3
|
APN |
9 |
108,719,775 (GRCm39) |
missense |
probably benign |
|
IGL01420:Celsr3
|
APN |
9 |
108,718,389 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01541:Celsr3
|
APN |
9 |
108,708,907 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01619:Celsr3
|
APN |
9 |
108,711,756 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01619:Celsr3
|
APN |
9 |
108,714,603 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01631:Celsr3
|
APN |
9 |
108,714,603 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01777:Celsr3
|
APN |
9 |
108,713,141 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01938:Celsr3
|
APN |
9 |
108,705,614 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02135:Celsr3
|
APN |
9 |
108,704,755 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02231:Celsr3
|
APN |
9 |
108,719,709 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02234:Celsr3
|
APN |
9 |
108,707,159 (GRCm39) |
missense |
probably benign |
|
IGL02392:Celsr3
|
APN |
9 |
108,711,920 (GRCm39) |
splice site |
probably benign |
|
IGL02416:Celsr3
|
APN |
9 |
108,709,318 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02421:Celsr3
|
APN |
9 |
108,717,662 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02455:Celsr3
|
APN |
9 |
108,720,092 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02798:Celsr3
|
APN |
9 |
108,720,774 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Celsr3
|
APN |
9 |
108,726,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02947:Celsr3
|
APN |
9 |
108,723,134 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02986:Celsr3
|
APN |
9 |
108,718,454 (GRCm39) |
splice site |
probably null |
|
IGL03089:Celsr3
|
APN |
9 |
108,703,806 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03162:Celsr3
|
APN |
9 |
108,719,757 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03267:Celsr3
|
APN |
9 |
108,713,724 (GRCm39) |
splice site |
probably benign |
|
Diminishment
|
UTSW |
9 |
108,719,907 (GRCm39) |
intron |
probably benign |
|
little_d
|
UTSW |
9 |
108,704,891 (GRCm39) |
missense |
probably damaging |
0.98 |
nogal
|
UTSW |
9 |
108,713,037 (GRCm39) |
missense |
probably benign |
|
F6893:Celsr3
|
UTSW |
9 |
108,712,266 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4243001:Celsr3
|
UTSW |
9 |
108,709,507 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4810001:Celsr3
|
UTSW |
9 |
108,722,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Celsr3
|
UTSW |
9 |
108,704,204 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0243:Celsr3
|
UTSW |
9 |
108,720,923 (GRCm39) |
splice site |
probably benign |
|
R0382:Celsr3
|
UTSW |
9 |
108,706,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0482:Celsr3
|
UTSW |
9 |
108,706,272 (GRCm39) |
nonsense |
probably null |
|
R0510:Celsr3
|
UTSW |
9 |
108,704,204 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0630:Celsr3
|
UTSW |
9 |
108,704,891 (GRCm39) |
missense |
probably damaging |
0.98 |
R0656:Celsr3
|
UTSW |
9 |
108,711,854 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0764:Celsr3
|
UTSW |
9 |
108,705,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R0924:Celsr3
|
UTSW |
9 |
108,723,224 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1015:Celsr3
|
UTSW |
9 |
108,710,375 (GRCm39) |
missense |
probably benign |
0.17 |
R1321:Celsr3
|
UTSW |
9 |
108,713,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R1423:Celsr3
|
UTSW |
9 |
108,704,104 (GRCm39) |
missense |
probably benign |
0.00 |
R1497:Celsr3
|
UTSW |
9 |
108,726,064 (GRCm39) |
missense |
probably benign |
0.14 |
R1520:Celsr3
|
UTSW |
9 |
108,725,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Celsr3
|
UTSW |
9 |
108,726,083 (GRCm39) |
missense |
probably damaging |
0.99 |
R1569:Celsr3
|
UTSW |
9 |
108,706,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R1657:Celsr3
|
UTSW |
9 |
108,720,151 (GRCm39) |
nonsense |
probably null |
|
R1753:Celsr3
|
UTSW |
9 |
108,709,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R1764:Celsr3
|
UTSW |
9 |
108,706,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R1801:Celsr3
|
UTSW |
9 |
108,711,825 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1838:Celsr3
|
UTSW |
9 |
108,707,105 (GRCm39) |
missense |
probably benign |
|
R1839:Celsr3
|
UTSW |
9 |
108,707,105 (GRCm39) |
missense |
probably benign |
|
R1874:Celsr3
|
UTSW |
9 |
108,713,037 (GRCm39) |
missense |
probably benign |
|
R1875:Celsr3
|
UTSW |
9 |
108,713,037 (GRCm39) |
missense |
probably benign |
|
R1953:Celsr3
|
UTSW |
9 |
108,720,381 (GRCm39) |
missense |
probably benign |
0.19 |
R1960:Celsr3
|
UTSW |
9 |
108,723,016 (GRCm39) |
missense |
probably benign |
|
R2113:Celsr3
|
UTSW |
9 |
108,715,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Celsr3
|
UTSW |
9 |
108,720,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R2369:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2373:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2374:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2375:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2844:Celsr3
|
UTSW |
9 |
108,706,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R2968:Celsr3
|
UTSW |
9 |
108,709,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R3103:Celsr3
|
UTSW |
9 |
108,714,338 (GRCm39) |
missense |
probably benign |
0.31 |
R3159:Celsr3
|
UTSW |
9 |
108,704,909 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3791:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R4194:Celsr3
|
UTSW |
9 |
108,720,501 (GRCm39) |
critical splice donor site |
probably null |
|
R4329:Celsr3
|
UTSW |
9 |
108,723,248 (GRCm39) |
missense |
probably benign |
0.00 |
R4365:Celsr3
|
UTSW |
9 |
108,707,046 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4419:Celsr3
|
UTSW |
9 |
108,720,443 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4484:Celsr3
|
UTSW |
9 |
108,723,262 (GRCm39) |
critical splice donor site |
probably null |
|
R4582:Celsr3
|
UTSW |
9 |
108,722,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R4681:Celsr3
|
UTSW |
9 |
108,704,953 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4729:Celsr3
|
UTSW |
9 |
108,724,851 (GRCm39) |
missense |
probably benign |
0.05 |
R4881:Celsr3
|
UTSW |
9 |
108,721,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R4893:Celsr3
|
UTSW |
9 |
108,726,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R5183:Celsr3
|
UTSW |
9 |
108,714,759 (GRCm39) |
missense |
probably damaging |
0.99 |
R5207:Celsr3
|
UTSW |
9 |
108,709,958 (GRCm39) |
missense |
probably benign |
0.01 |
R5290:Celsr3
|
UTSW |
9 |
108,720,357 (GRCm39) |
missense |
probably benign |
0.01 |
R5327:Celsr3
|
UTSW |
9 |
108,719,907 (GRCm39) |
intron |
probably benign |
|
R5345:Celsr3
|
UTSW |
9 |
108,709,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R5358:Celsr3
|
UTSW |
9 |
108,709,224 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5396:Celsr3
|
UTSW |
9 |
108,705,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R5414:Celsr3
|
UTSW |
9 |
108,717,241 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5452:Celsr3
|
UTSW |
9 |
108,721,233 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5467:Celsr3
|
UTSW |
9 |
108,705,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R5479:Celsr3
|
UTSW |
9 |
108,721,743 (GRCm39) |
critical splice donor site |
probably null |
|
R5629:Celsr3
|
UTSW |
9 |
108,726,266 (GRCm39) |
missense |
probably benign |
0.41 |
R5637:Celsr3
|
UTSW |
9 |
108,714,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Celsr3
|
UTSW |
9 |
108,715,671 (GRCm39) |
missense |
probably benign |
0.03 |
R5739:Celsr3
|
UTSW |
9 |
108,704,357 (GRCm39) |
missense |
probably benign |
|
R5785:Celsr3
|
UTSW |
9 |
108,704,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R5877:Celsr3
|
UTSW |
9 |
108,722,926 (GRCm39) |
missense |
probably damaging |
0.98 |
R5961:Celsr3
|
UTSW |
9 |
108,708,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R6046:Celsr3
|
UTSW |
9 |
108,714,350 (GRCm39) |
missense |
probably benign |
0.01 |
R6176:Celsr3
|
UTSW |
9 |
108,705,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R6291:Celsr3
|
UTSW |
9 |
108,706,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R6468:Celsr3
|
UTSW |
9 |
108,712,989 (GRCm39) |
missense |
probably benign |
0.08 |
R6481:Celsr3
|
UTSW |
9 |
108,714,283 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6547:Celsr3
|
UTSW |
9 |
108,706,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R6763:Celsr3
|
UTSW |
9 |
108,704,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R6870:Celsr3
|
UTSW |
9 |
108,706,390 (GRCm39) |
missense |
probably benign |
0.02 |
R6977:Celsr3
|
UTSW |
9 |
108,704,914 (GRCm39) |
missense |
probably benign |
|
R7061:Celsr3
|
UTSW |
9 |
108,724,793 (GRCm39) |
nonsense |
probably null |
|
R7122:Celsr3
|
UTSW |
9 |
108,705,766 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7156:Celsr3
|
UTSW |
9 |
108,715,203 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7166:Celsr3
|
UTSW |
9 |
108,720,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R7176:Celsr3
|
UTSW |
9 |
108,722,961 (GRCm39) |
missense |
probably benign |
|
R7213:Celsr3
|
UTSW |
9 |
108,726,239 (GRCm39) |
missense |
probably damaging |
0.98 |
R7314:Celsr3
|
UTSW |
9 |
108,706,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7478:Celsr3
|
UTSW |
9 |
108,720,777 (GRCm39) |
missense |
probably benign |
0.37 |
R7508:Celsr3
|
UTSW |
9 |
108,713,821 (GRCm39) |
missense |
probably benign |
|
R7554:Celsr3
|
UTSW |
9 |
108,718,408 (GRCm39) |
missense |
probably benign |
|
R7615:Celsr3
|
UTSW |
9 |
108,714,851 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7653:Celsr3
|
UTSW |
9 |
108,712,269 (GRCm39) |
nonsense |
probably null |
|
R7747:Celsr3
|
UTSW |
9 |
108,707,177 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7881:Celsr3
|
UTSW |
9 |
108,705,271 (GRCm39) |
missense |
probably benign |
0.28 |
R7935:Celsr3
|
UTSW |
9 |
108,706,840 (GRCm39) |
missense |
probably benign |
0.01 |
R7995:Celsr3
|
UTSW |
9 |
108,722,282 (GRCm39) |
missense |
probably damaging |
0.99 |
R8006:Celsr3
|
UTSW |
9 |
108,706,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R8077:Celsr3
|
UTSW |
9 |
108,705,530 (GRCm39) |
missense |
probably benign |
0.15 |
R8284:Celsr3
|
UTSW |
9 |
108,723,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R8291:Celsr3
|
UTSW |
9 |
108,715,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R8322:Celsr3
|
UTSW |
9 |
108,725,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Celsr3
|
UTSW |
9 |
108,718,471 (GRCm39) |
frame shift |
probably null |
|
R8337:Celsr3
|
UTSW |
9 |
108,718,471 (GRCm39) |
frame shift |
probably null |
|
R8338:Celsr3
|
UTSW |
9 |
108,704,539 (GRCm39) |
nonsense |
probably null |
|
R8353:Celsr3
|
UTSW |
9 |
108,703,734 (GRCm39) |
missense |
probably benign |
0.00 |
R8407:Celsr3
|
UTSW |
9 |
108,706,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R8408:Celsr3
|
UTSW |
9 |
108,708,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R8459:Celsr3
|
UTSW |
9 |
108,706,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R8510:Celsr3
|
UTSW |
9 |
108,715,319 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8713:Celsr3
|
UTSW |
9 |
108,707,062 (GRCm39) |
missense |
probably benign |
|
R8728:Celsr3
|
UTSW |
9 |
108,723,940 (GRCm39) |
missense |
probably benign |
0.24 |
R8829:Celsr3
|
UTSW |
9 |
108,717,582 (GRCm39) |
missense |
probably benign |
|
R8877:Celsr3
|
UTSW |
9 |
108,706,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:Celsr3
|
UTSW |
9 |
108,718,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R9008:Celsr3
|
UTSW |
9 |
108,706,151 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9072:Celsr3
|
UTSW |
9 |
108,704,293 (GRCm39) |
missense |
probably benign |
|
R9157:Celsr3
|
UTSW |
9 |
108,707,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R9183:Celsr3
|
UTSW |
9 |
108,706,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Celsr3
|
UTSW |
9 |
108,715,689 (GRCm39) |
missense |
probably benign |
0.27 |
R9361:Celsr3
|
UTSW |
9 |
108,726,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R9382:Celsr3
|
UTSW |
9 |
108,706,961 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9407:Celsr3
|
UTSW |
9 |
108,723,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R9432:Celsr3
|
UTSW |
9 |
108,726,032 (GRCm39) |
missense |
probably benign |
0.00 |
R9607:Celsr3
|
UTSW |
9 |
108,717,701 (GRCm39) |
critical splice donor site |
probably null |
|
R9626:Celsr3
|
UTSW |
9 |
108,726,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R9628:Celsr3
|
UTSW |
9 |
108,703,559 (GRCm39) |
nonsense |
probably null |
|
R9630:Celsr3
|
UTSW |
9 |
108,704,296 (GRCm39) |
missense |
probably benign |
|
R9645:Celsr3
|
UTSW |
9 |
108,704,691 (GRCm39) |
nonsense |
probably null |
|
R9683:Celsr3
|
UTSW |
9 |
108,704,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R9794:Celsr3
|
UTSW |
9 |
108,728,502 (GRCm39) |
missense |
probably benign |
0.00 |
R9798:Celsr3
|
UTSW |
9 |
108,705,794 (GRCm39) |
missense |
probably damaging |
1.00 |
RF020:Celsr3
|
UTSW |
9 |
108,726,256 (GRCm39) |
missense |
probably benign |
|
X0018:Celsr3
|
UTSW |
9 |
108,717,611 (GRCm39) |
missense |
probably benign |
0.01 |
X0018:Celsr3
|
UTSW |
9 |
108,704,977 (GRCm39) |
missense |
possibly damaging |
0.65 |
X0026:Celsr3
|
UTSW |
9 |
108,706,129 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Celsr3
|
UTSW |
9 |
108,703,676 (GRCm39) |
missense |
probably benign |
0.34 |
|
Predicted Primers |
PCR Primer
(F):5'- TCCAAGACCAGATGGGTGTCTTCTC -3'
(R):5'- CCCTCTAGCCGCTGTGAAGTTAAG -3'
Sequencing Primer
(F):5'- TCTCAGGCTCCCTCAGAAC -3'
(R):5'- CTGTCCTGTATCCAGAGGAGAG -3'
|
Posted On |
2013-11-07 |