Incidental Mutation 'R7286:Dscaml1'
ID |
566011 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dscaml1
|
Ensembl Gene |
ENSMUSG00000032087 |
Gene Name |
DS cell adhesion molecule like 1 |
Synonyms |
4921507G06Rik, 4930435C18Rik |
MMRRC Submission |
045394-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.416)
|
Stock # |
R7286 (G1)
|
Quality Score |
152.008 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
45338735-45665011 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
T to C
at 45654044 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000034592
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034592]
|
AlphaFold |
Q4VA61 |
Predicted Effect |
probably null
Transcript: ENSMUST00000034592
|
SMART Domains |
Protein: ENSMUSP00000034592 Gene: ENSMUSG00000032087
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
17 |
N/A |
INTRINSIC |
low complexity region
|
28 |
55 |
N/A |
INTRINSIC |
IG_like
|
96 |
168 |
1.22e0 |
SMART |
IG
|
189 |
277 |
1.15e-3 |
SMART |
IGc2
|
296 |
359 |
2.54e-14 |
SMART |
IGc2
|
385 |
451 |
8.12e-13 |
SMART |
IGc2
|
478 |
550 |
9.55e-10 |
SMART |
IGc2
|
575 |
640 |
9.78e-7 |
SMART |
IGc2
|
666 |
734 |
5.93e-6 |
SMART |
IGc2
|
760 |
832 |
6.75e-10 |
SMART |
IG
|
853 |
943 |
1e-3 |
SMART |
FN3
|
945 |
1029 |
6.64e-7 |
SMART |
FN3
|
1045 |
1133 |
9.46e-12 |
SMART |
FN3
|
1148 |
1234 |
3.2e-9 |
SMART |
FN3
|
1249 |
1332 |
3.48e-10 |
SMART |
IGc2
|
1363 |
1428 |
1.49e-11 |
SMART |
FN3
|
1442 |
1522 |
3.42e-9 |
SMART |
FN3
|
1537 |
1618 |
2.14e-1 |
SMART |
low complexity region
|
1671 |
1683 |
N/A |
INTRINSIC |
low complexity region
|
2018 |
2026 |
N/A |
INTRINSIC |
low complexity region
|
2035 |
2069 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000216685
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.6%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the Ig superfamily of cell adhesion molecules and is involved in neuronal differentiation. The encoded membrane-bound protein localizes to the cell surface, where it forms aggregates that repel neuronal processes of the same cell type. [provided by RefSeq, Sep 2016] PHENOTYPE: Mice homozygous for a gene trapped allele exhibit impaired self-avoidance in multiple cell types in the retina. [provided by MGI curators]
|
Allele List at MGI |
All alleles(4) : Gene trapped(4) |
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
A |
T |
9: 53,334,317 (GRCm39) |
M187L |
possibly damaging |
Het |
9930012K11Rik |
T |
C |
14: 70,394,686 (GRCm39) |
E156G |
possibly damaging |
Het |
Acad9 |
C |
T |
3: 36,130,139 (GRCm39) |
A194V |
probably damaging |
Het |
Agps |
T |
A |
2: 75,683,128 (GRCm39) |
V151E |
probably benign |
Het |
Ak9 |
A |
T |
10: 41,283,367 (GRCm39) |
I1273L |
|
Het |
Akr1c19 |
T |
A |
13: 4,296,818 (GRCm39) |
L288Q |
probably damaging |
Het |
Carmil1 |
T |
G |
13: 24,197,377 (GRCm39) |
D1353A |
probably damaging |
Het |
Ccz1 |
T |
A |
5: 143,949,897 (GRCm39) |
I43F |
probably damaging |
Het |
Cep70 |
G |
A |
9: 99,157,638 (GRCm39) |
C179Y |
probably damaging |
Het |
Comt |
A |
T |
16: 18,229,440 (GRCm39) |
L196H |
probably damaging |
Het |
Cspg5 |
A |
T |
9: 110,076,023 (GRCm39) |
D253V |
probably damaging |
Het |
Dars2 |
A |
G |
1: 160,874,378 (GRCm39) |
V437A |
possibly damaging |
Het |
Dcaf5 |
A |
G |
12: 80,395,164 (GRCm39) |
I335T |
probably damaging |
Het |
Ddn |
T |
C |
15: 98,703,906 (GRCm39) |
K462R |
possibly damaging |
Het |
Eef1ece2 |
T |
C |
16: 20,451,341 (GRCm39) |
S325P |
probably benign |
Het |
Ethe1 |
A |
G |
7: 24,307,377 (GRCm39) |
Y197C |
probably damaging |
Het |
Evc |
A |
T |
5: 37,479,527 (GRCm39) |
L269* |
probably null |
Het |
Fam161a |
T |
C |
11: 22,970,001 (GRCm39) |
S60P |
possibly damaging |
Het |
Fam20b |
A |
G |
1: 156,509,012 (GRCm39) |
V400A |
probably benign |
Het |
Fam53b |
T |
A |
7: 132,361,390 (GRCm39) |
S213C |
possibly damaging |
Het |
Flot2 |
A |
G |
11: 77,945,612 (GRCm39) |
I45V |
probably benign |
Het |
Gemin4 |
A |
C |
11: 76,103,579 (GRCm39) |
L394R |
probably damaging |
Het |
Glis2 |
T |
G |
16: 4,429,182 (GRCm39) |
S128R |
possibly damaging |
Het |
Gm3696 |
A |
G |
14: 18,435,009 (GRCm39) |
Y92H |
probably damaging |
Het |
Gpbp1l1 |
T |
C |
4: 116,447,442 (GRCm39) |
V374A |
probably benign |
Het |
Grm1 |
T |
C |
10: 10,565,440 (GRCm39) |
N956S |
probably benign |
Het |
Hbb-bh1 |
T |
C |
7: 103,492,238 (GRCm39) |
E27G |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,458,088 (GRCm39) |
C5233S |
probably damaging |
Het |
Hmgcr |
C |
T |
13: 96,803,105 (GRCm39) |
C30Y |
probably damaging |
Het |
Hoxb6 |
A |
G |
11: 96,183,651 (GRCm39) |
|
probably benign |
Het |
Igf2 |
T |
C |
7: 142,209,555 (GRCm39) |
Q35R |
possibly damaging |
Het |
Ighv1-4 |
C |
T |
12: 114,450,941 (GRCm39) |
V56I |
probably benign |
Het |
Kif13a |
C |
T |
13: 46,905,931 (GRCm39) |
V671M |
possibly damaging |
Het |
Lmtk2 |
C |
T |
5: 144,111,178 (GRCm39) |
Q633* |
probably null |
Het |
Mesd |
T |
C |
7: 83,544,957 (GRCm39) |
Y136H |
probably damaging |
Het |
Mga |
T |
A |
2: 119,795,269 (GRCm39) |
S2984R |
possibly damaging |
Het |
Mkrn3 |
T |
C |
7: 62,068,675 (GRCm39) |
N372S |
probably benign |
Het |
Mtpap |
A |
G |
18: 4,387,068 (GRCm39) |
I373V |
probably benign |
Het |
Mycbp2 |
G |
A |
14: 103,358,027 (GRCm39) |
T4589M |
probably damaging |
Het |
Myh2 |
A |
G |
11: 67,079,195 (GRCm39) |
Q921R |
probably benign |
Het |
Myom1 |
A |
G |
17: 71,352,544 (GRCm39) |
D324G |
possibly damaging |
Het |
Nat10 |
T |
C |
2: 103,584,514 (GRCm39) |
K88E |
probably benign |
Het |
Ncapd3 |
A |
G |
9: 26,981,254 (GRCm39) |
R915G |
probably damaging |
Het |
Nek4 |
T |
C |
14: 30,679,249 (GRCm39) |
Y190H |
probably damaging |
Het |
Nfasc |
A |
C |
1: 132,529,790 (GRCm39) |
Y797D |
probably damaging |
Het |
Ngp |
A |
G |
9: 110,249,978 (GRCm39) |
D92G |
probably benign |
Het |
Nos2 |
A |
C |
11: 78,820,680 (GRCm39) |
H95P |
probably damaging |
Het |
Nr3c1 |
ACGTC |
ACGTCGTC |
18: 39,619,513 (GRCm39) |
|
probably benign |
Het |
Or10ag59 |
C |
T |
2: 87,405,863 (GRCm39) |
T145I |
probably benign |
Het |
Or5bw2 |
C |
A |
7: 6,573,715 (GRCm39) |
H242N |
probably damaging |
Het |
Or5p73 |
T |
C |
7: 108,064,642 (GRCm39) |
I37T |
possibly damaging |
Het |
Or5t18 |
A |
T |
2: 86,636,967 (GRCm39) |
H125Q |
possibly damaging |
Het |
Otogl |
T |
A |
10: 107,606,471 (GRCm39) |
D2154V |
probably benign |
Het |
Pdss1 |
T |
A |
2: 22,825,653 (GRCm39) |
|
probably null |
Het |
Pex5 |
A |
T |
6: 124,375,022 (GRCm39) |
L609* |
probably null |
Het |
Pglyrp4 |
C |
A |
3: 90,640,281 (GRCm39) |
A177D |
probably damaging |
Het |
Phactr4 |
A |
G |
4: 132,104,489 (GRCm39) |
|
probably null |
Het |
Phf8-ps |
T |
C |
17: 33,284,501 (GRCm39) |
D767G |
probably benign |
Het |
Pik3cd |
G |
C |
4: 149,744,171 (GRCm39) |
N193K |
probably benign |
Het |
Prr36 |
TACCTCTTC |
T |
8: 4,265,163 (GRCm39) |
|
probably benign |
Het |
Prss38 |
A |
T |
11: 59,266,384 (GRCm39) |
W25R |
probably benign |
Het |
Prss8 |
T |
A |
7: 127,526,056 (GRCm39) |
Q189L |
probably damaging |
Het |
Psd |
T |
A |
19: 46,303,240 (GRCm39) |
D713V |
probably damaging |
Het |
Rad51ap2 |
C |
T |
12: 11,507,692 (GRCm39) |
T538I |
probably benign |
Het |
Rarres1 |
T |
C |
3: 67,422,517 (GRCm39) |
T78A |
probably benign |
Het |
Rbl2 |
G |
T |
8: 91,828,922 (GRCm39) |
G651* |
probably null |
Het |
Rev3l |
A |
T |
10: 39,699,601 (GRCm39) |
Q1366L |
probably damaging |
Het |
Rundc1 |
T |
C |
11: 101,320,413 (GRCm39) |
S215P |
probably benign |
Het |
Sanbr |
A |
T |
11: 23,572,479 (GRCm39) |
C130S |
probably benign |
Het |
Scarf2 |
G |
A |
16: 17,620,837 (GRCm39) |
W168* |
probably null |
Het |
Sh2d7 |
A |
G |
9: 54,448,186 (GRCm39) |
D69G |
possibly damaging |
Het |
Slc26a4 |
A |
T |
12: 31,579,527 (GRCm39) |
Y578* |
probably null |
Het |
Slc2a9 |
A |
T |
5: 38,610,538 (GRCm39) |
L87Q |
probably damaging |
Het |
Slc39a10 |
A |
T |
1: 46,849,230 (GRCm39) |
H795Q |
probably damaging |
Het |
Spata13 |
C |
T |
14: 60,993,871 (GRCm39) |
R1108W |
probably damaging |
Het |
Sqle |
T |
C |
15: 59,187,901 (GRCm39) |
S70P |
probably benign |
Het |
Syncrip |
A |
T |
9: 88,346,716 (GRCm39) |
F263I |
probably damaging |
Het |
Synj2 |
T |
C |
17: 6,088,220 (GRCm39) |
S1424P |
possibly damaging |
Het |
Tax1bp3 |
A |
T |
11: 73,071,941 (GRCm39) |
T89S |
possibly damaging |
Het |
Tcaim |
G |
A |
9: 122,648,092 (GRCm39) |
|
probably null |
Het |
Tcp10c |
T |
C |
17: 13,582,438 (GRCm39) |
I240T |
possibly damaging |
Het |
Ttll8 |
G |
T |
15: 88,801,442 (GRCm39) |
N415K |
probably benign |
Het |
Tut7 |
T |
C |
13: 59,969,463 (GRCm39) |
E144G |
probably benign |
Het |
Ugcg |
T |
C |
4: 59,217,111 (GRCm39) |
S212P |
possibly damaging |
Het |
Vmn2r32 |
T |
C |
7: 7,482,807 (GRCm39) |
K56E |
probably benign |
Het |
Vmn2r55 |
T |
C |
7: 12,386,000 (GRCm39) |
E660G |
probably damaging |
Het |
Vmn2r7 |
T |
C |
3: 64,598,301 (GRCm39) |
N752S |
probably benign |
Het |
Vps54 |
T |
A |
11: 21,225,005 (GRCm39) |
M167K |
probably benign |
Het |
Vwa2 |
A |
C |
19: 56,897,791 (GRCm39) |
M699L |
probably benign |
Het |
Wdr59 |
A |
G |
8: 112,192,494 (GRCm39) |
V689A |
|
Het |
Whamm |
T |
G |
7: 81,235,995 (GRCm39) |
N399K |
probably damaging |
Het |
Zfp760 |
A |
G |
17: 21,941,760 (GRCm39) |
K312E |
probably benign |
Het |
Zkscan3 |
C |
A |
13: 21,578,983 (GRCm39) |
V171L |
probably benign |
Het |
|
Other mutations in Dscaml1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00418:Dscaml1
|
APN |
9 |
45,581,498 (GRCm39) |
nonsense |
probably null |
|
IGL00497:Dscaml1
|
APN |
9 |
45,663,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00895:Dscaml1
|
APN |
9 |
45,662,551 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01011:Dscaml1
|
APN |
9 |
45,594,970 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01086:Dscaml1
|
APN |
9 |
45,613,960 (GRCm39) |
splice site |
probably benign |
|
IGL01125:Dscaml1
|
APN |
9 |
45,660,930 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01132:Dscaml1
|
APN |
9 |
45,663,626 (GRCm39) |
nonsense |
probably null |
|
IGL01356:Dscaml1
|
APN |
9 |
45,658,155 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01459:Dscaml1
|
APN |
9 |
45,653,981 (GRCm39) |
nonsense |
probably null |
|
IGL01552:Dscaml1
|
APN |
9 |
45,359,206 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02033:Dscaml1
|
APN |
9 |
45,595,080 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02044:Dscaml1
|
APN |
9 |
45,658,241 (GRCm39) |
nonsense |
probably null |
|
IGL02095:Dscaml1
|
APN |
9 |
45,359,001 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02166:Dscaml1
|
APN |
9 |
45,594,999 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02262:Dscaml1
|
APN |
9 |
45,643,378 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02262:Dscaml1
|
APN |
9 |
45,656,414 (GRCm39) |
missense |
probably benign |
|
IGL02340:Dscaml1
|
APN |
9 |
45,581,474 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02604:Dscaml1
|
APN |
9 |
45,655,626 (GRCm39) |
unclassified |
probably benign |
|
IGL02619:Dscaml1
|
APN |
9 |
45,359,094 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02805:Dscaml1
|
APN |
9 |
45,359,195 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03409:Dscaml1
|
APN |
9 |
45,581,401 (GRCm39) |
missense |
probably damaging |
1.00 |
D3080:Dscaml1
|
UTSW |
9 |
45,595,623 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03050:Dscaml1
|
UTSW |
9 |
45,654,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R0149:Dscaml1
|
UTSW |
9 |
45,653,978 (GRCm39) |
nonsense |
probably null |
|
R0582:Dscaml1
|
UTSW |
9 |
45,579,562 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0629:Dscaml1
|
UTSW |
9 |
45,632,716 (GRCm39) |
missense |
probably damaging |
0.98 |
R0632:Dscaml1
|
UTSW |
9 |
45,643,432 (GRCm39) |
missense |
probably benign |
0.06 |
R0815:Dscaml1
|
UTSW |
9 |
45,656,372 (GRCm39) |
missense |
probably benign |
0.00 |
R1162:Dscaml1
|
UTSW |
9 |
45,663,647 (GRCm39) |
splice site |
probably benign |
|
R1449:Dscaml1
|
UTSW |
9 |
45,653,521 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1474:Dscaml1
|
UTSW |
9 |
45,596,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R1481:Dscaml1
|
UTSW |
9 |
45,583,941 (GRCm39) |
missense |
probably benign |
0.01 |
R1533:Dscaml1
|
UTSW |
9 |
45,361,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R1542:Dscaml1
|
UTSW |
9 |
45,660,738 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1572:Dscaml1
|
UTSW |
9 |
45,632,631 (GRCm39) |
missense |
probably benign |
0.00 |
R1627:Dscaml1
|
UTSW |
9 |
45,664,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:Dscaml1
|
UTSW |
9 |
45,584,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Dscaml1
|
UTSW |
9 |
45,663,988 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1777:Dscaml1
|
UTSW |
9 |
45,595,054 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1812:Dscaml1
|
UTSW |
9 |
45,662,584 (GRCm39) |
critical splice donor site |
probably null |
|
R1834:Dscaml1
|
UTSW |
9 |
45,594,930 (GRCm39) |
missense |
probably benign |
0.00 |
R1907:Dscaml1
|
UTSW |
9 |
45,651,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R1953:Dscaml1
|
UTSW |
9 |
45,581,522 (GRCm39) |
missense |
probably benign |
0.01 |
R2056:Dscaml1
|
UTSW |
9 |
45,661,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R2193:Dscaml1
|
UTSW |
9 |
45,596,532 (GRCm39) |
missense |
probably benign |
0.21 |
R2497:Dscaml1
|
UTSW |
9 |
45,656,376 (GRCm39) |
missense |
probably benign |
0.00 |
R3768:Dscaml1
|
UTSW |
9 |
45,643,435 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3891:Dscaml1
|
UTSW |
9 |
45,628,782 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4110:Dscaml1
|
UTSW |
9 |
45,643,366 (GRCm39) |
missense |
probably benign |
0.07 |
R4706:Dscaml1
|
UTSW |
9 |
45,361,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Dscaml1
|
UTSW |
9 |
45,361,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Dscaml1
|
UTSW |
9 |
45,583,993 (GRCm39) |
missense |
probably benign |
0.13 |
R4770:Dscaml1
|
UTSW |
9 |
45,581,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R4924:Dscaml1
|
UTSW |
9 |
45,656,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R5167:Dscaml1
|
UTSW |
9 |
45,628,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R5346:Dscaml1
|
UTSW |
9 |
45,361,857 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5737:Dscaml1
|
UTSW |
9 |
45,656,483 (GRCm39) |
missense |
probably damaging |
0.99 |
R5977:Dscaml1
|
UTSW |
9 |
45,632,596 (GRCm39) |
missense |
probably benign |
0.19 |
R6073:Dscaml1
|
UTSW |
9 |
45,361,881 (GRCm39) |
missense |
probably benign |
0.22 |
R6276:Dscaml1
|
UTSW |
9 |
45,579,458 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6415:Dscaml1
|
UTSW |
9 |
45,594,975 (GRCm39) |
nonsense |
probably null |
|
R6527:Dscaml1
|
UTSW |
9 |
45,623,482 (GRCm39) |
nonsense |
probably null |
|
R6582:Dscaml1
|
UTSW |
9 |
45,664,104 (GRCm39) |
missense |
probably benign |
0.00 |
R6655:Dscaml1
|
UTSW |
9 |
45,658,235 (GRCm39) |
missense |
probably benign |
0.00 |
R6772:Dscaml1
|
UTSW |
9 |
45,621,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R6799:Dscaml1
|
UTSW |
9 |
45,361,881 (GRCm39) |
missense |
probably benign |
0.22 |
R6892:Dscaml1
|
UTSW |
9 |
45,595,128 (GRCm39) |
missense |
probably damaging |
0.99 |
R6918:Dscaml1
|
UTSW |
9 |
45,341,805 (GRCm39) |
missense |
probably benign |
|
R6967:Dscaml1
|
UTSW |
9 |
45,585,821 (GRCm39) |
missense |
probably damaging |
0.97 |
R7214:Dscaml1
|
UTSW |
9 |
45,581,437 (GRCm39) |
missense |
probably benign |
0.01 |
R7315:Dscaml1
|
UTSW |
9 |
45,656,423 (GRCm39) |
missense |
probably benign |
0.00 |
R7338:Dscaml1
|
UTSW |
9 |
45,585,802 (GRCm39) |
missense |
probably benign |
0.12 |
R7343:Dscaml1
|
UTSW |
9 |
45,664,214 (GRCm39) |
missense |
probably benign |
|
R7395:Dscaml1
|
UTSW |
9 |
45,613,703 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7439:Dscaml1
|
UTSW |
9 |
45,621,624 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7484:Dscaml1
|
UTSW |
9 |
45,660,744 (GRCm39) |
splice site |
probably null |
|
R7545:Dscaml1
|
UTSW |
9 |
45,596,681 (GRCm39) |
missense |
probably benign |
0.11 |
R7979:Dscaml1
|
UTSW |
9 |
45,595,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8005:Dscaml1
|
UTSW |
9 |
45,628,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R8181:Dscaml1
|
UTSW |
9 |
45,658,140 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8262:Dscaml1
|
UTSW |
9 |
45,658,438 (GRCm39) |
intron |
probably benign |
|
R8428:Dscaml1
|
UTSW |
9 |
45,653,884 (GRCm39) |
missense |
probably benign |
0.00 |
R8725:Dscaml1
|
UTSW |
9 |
45,341,759 (GRCm39) |
missense |
probably benign |
0.00 |
R8727:Dscaml1
|
UTSW |
9 |
45,341,759 (GRCm39) |
missense |
probably benign |
0.00 |
R8796:Dscaml1
|
UTSW |
9 |
45,359,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R8840:Dscaml1
|
UTSW |
9 |
45,634,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R9291:Dscaml1
|
UTSW |
9 |
45,359,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9394:Dscaml1
|
UTSW |
9 |
45,661,354 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9610:Dscaml1
|
UTSW |
9 |
45,579,522 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9611:Dscaml1
|
UTSW |
9 |
45,579,522 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9653:Dscaml1
|
UTSW |
9 |
45,643,466 (GRCm39) |
critical splice donor site |
probably null |
|
R9699:Dscaml1
|
UTSW |
9 |
45,654,315 (GRCm39) |
missense |
probably damaging |
0.97 |
X0058:Dscaml1
|
UTSW |
9 |
45,663,426 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Dscaml1
|
UTSW |
9 |
45,584,089 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
PCR Primer
(F):5'- TGGTCTGGCAGTGAAGACTC -3'
(R):5'- GCTCTCAGTGCAAAAGGTCTGG -3'
Sequencing Primer
(F):5'- TCTGGCAGTGAAGACTCAGCAATC -3'
(R):5'- TGCAAAAGGTCTGGAGTGTCCC -3'
|
Posted On |
2019-06-26 |