Incidental Mutation 'R5001:Lgr6'
ID |
389876 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Lgr6
|
Ensembl Gene |
ENSMUSG00000042793 |
Gene Name |
leucine-rich repeat-containing G protein-coupled receptor 6 |
Synonyms |
A530037C04Rik |
MMRRC Submission |
042595-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R5001 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
134911039-135033014 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 134918370 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Threonine
at position 264
(P264T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000122334
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044828]
[ENSMUST00000137968]
|
AlphaFold |
Q3UVD5 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000044828
AA Change: P541T
PolyPhen 2
Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
|
SMART Domains |
Protein: ENSMUSP00000035444 Gene: ENSMUSG00000042793 AA Change: P541T
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
LRRNT
|
34 |
70 |
5.19e-3 |
SMART |
LRR
|
64 |
88 |
1.03e1 |
SMART |
LRR_TYP
|
89 |
112 |
6.52e-5 |
SMART |
LRR_TYP
|
113 |
136 |
2.71e-2 |
SMART |
LRR_TYP
|
137 |
160 |
4.79e-3 |
SMART |
LRR_TYP
|
161 |
184 |
1.58e-3 |
SMART |
LRR_TYP
|
185 |
208 |
2.36e-2 |
SMART |
LRR_TYP
|
209 |
232 |
3.39e-3 |
SMART |
LRR
|
233 |
255 |
8.97e0 |
SMART |
LRR_TYP
|
256 |
279 |
1.36e-2 |
SMART |
Blast:LRR
|
281 |
303 |
6e-7 |
BLAST |
LRR
|
327 |
350 |
9.24e1 |
SMART |
LRR
|
351 |
373 |
1.41e0 |
SMART |
LRR
|
374 |
396 |
4.84e1 |
SMART |
LRR_TYP
|
397 |
420 |
4.54e-4 |
SMART |
LRR_TYP
|
421 |
444 |
7.15e-2 |
SMART |
transmembrane domain
|
568 |
590 |
N/A |
INTRINSIC |
transmembrane domain
|
599 |
621 |
N/A |
INTRINSIC |
transmembrane domain
|
643 |
665 |
N/A |
INTRINSIC |
transmembrane domain
|
686 |
708 |
N/A |
INTRINSIC |
transmembrane domain
|
728 |
750 |
N/A |
INTRINSIC |
transmembrane domain
|
776 |
798 |
N/A |
INTRINSIC |
transmembrane domain
|
808 |
830 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000137968
AA Change: P264T
PolyPhen 2
Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
|
SMART Domains |
Protein: ENSMUSP00000122334 Gene: ENSMUSG00000042793 AA Change: P264T
Domain | Start | End | E-Value | Type |
Blast:LRR
|
4 |
26 |
2e-7 |
BLAST |
LRR
|
50 |
73 |
9.24e1 |
SMART |
LRR
|
74 |
96 |
1.41e0 |
SMART |
LRR
|
97 |
119 |
4.84e1 |
SMART |
LRR_TYP
|
120 |
143 |
4.54e-4 |
SMART |
LRR_TYP
|
144 |
167 |
7.15e-2 |
SMART |
Pfam:7tm_1
|
301 |
550 |
3.6e-9 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.4%
- 20x: 92.7%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the leucine-rich repeat-containing subgroup of the G protein-coupled 7-transmembrane protein superfamily. The encoded protein is a glycoprotein hormone receptor with a large N-terminal extracellular domain that contains leucine-rich repeats important for the formation of a horseshoe-shaped interaction motif for ligand binding. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008] PHENOTYPE: Mice homozygous for a reporter/null allele are viable and fertile with no apparent abnormal phenotype. Similarly, mice homozygous for a knock-in allele are healthy and fertile. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy3 |
G |
A |
12: 4,248,434 (GRCm39) |
V499M |
possibly damaging |
Het |
Aff4 |
T |
C |
11: 53,295,184 (GRCm39) |
S795P |
probably damaging |
Het |
Ank |
G |
A |
15: 27,562,819 (GRCm39) |
V176I |
probably damaging |
Het |
Ankfn1 |
A |
G |
11: 89,332,268 (GRCm39) |
I446T |
possibly damaging |
Het |
Arhgap33 |
C |
A |
7: 30,232,441 (GRCm39) |
S32I |
possibly damaging |
Het |
Ascc3 |
T |
A |
10: 50,699,744 (GRCm39) |
Y1856N |
probably damaging |
Het |
Atf3 |
T |
C |
1: 190,909,472 (GRCm39) |
T66A |
probably benign |
Het |
Atf7ip |
T |
C |
6: 136,538,386 (GRCm39) |
C548R |
probably damaging |
Het |
Bag6 |
A |
G |
17: 35,364,152 (GRCm39) |
T841A |
probably damaging |
Het |
Bbof1 |
A |
T |
12: 84,473,630 (GRCm39) |
Q320L |
possibly damaging |
Het |
Bmp2k |
A |
T |
5: 97,201,001 (GRCm39) |
Q307L |
probably damaging |
Het |
Btaf1 |
T |
A |
19: 36,964,052 (GRCm39) |
N874K |
possibly damaging |
Het |
Calr4 |
G |
A |
4: 109,096,179 (GRCm39) |
|
probably null |
Het |
Camk1d |
T |
C |
2: 5,317,912 (GRCm39) |
I248V |
possibly damaging |
Het |
Ccdc177 |
G |
A |
12: 80,804,160 (GRCm39) |
R705C |
unknown |
Het |
Cdk18 |
C |
T |
1: 132,046,587 (GRCm39) |
|
probably null |
Het |
Cers4 |
A |
G |
8: 4,565,565 (GRCm39) |
S4G |
probably benign |
Het |
Cfap54 |
A |
G |
10: 92,800,396 (GRCm39) |
V1604A |
probably benign |
Het |
Chd8 |
C |
T |
14: 52,441,372 (GRCm39) |
G907S |
probably benign |
Het |
Cilk1 |
T |
C |
9: 78,038,801 (GRCm39) |
S17P |
probably damaging |
Het |
Cnksr3 |
G |
A |
10: 7,076,746 (GRCm39) |
Q149* |
probably null |
Het |
Cntd1 |
T |
C |
11: 101,176,557 (GRCm39) |
V218A |
possibly damaging |
Het |
Cog7 |
A |
T |
7: 121,549,109 (GRCm39) |
V384E |
probably damaging |
Het |
Col5a2 |
A |
G |
1: 45,542,058 (GRCm39) |
V6A |
unknown |
Het |
Col7a1 |
T |
C |
9: 108,794,146 (GRCm39) |
|
probably null |
Het |
Cpsf6 |
T |
A |
10: 117,203,866 (GRCm39) |
I29L |
possibly damaging |
Het |
Cyp3a13 |
T |
C |
5: 137,897,178 (GRCm39) |
T379A |
probably benign |
Het |
Ddx46 |
T |
C |
13: 55,800,732 (GRCm39) |
S296P |
probably damaging |
Het |
Dmbt1 |
A |
G |
7: 130,651,742 (GRCm39) |
D328G |
probably damaging |
Het |
Dnah8 |
T |
G |
17: 31,006,159 (GRCm39) |
L3692W |
probably damaging |
Het |
Dnmt3l |
A |
C |
10: 77,895,565 (GRCm39) |
S368R |
probably null |
Het |
Egfr |
A |
G |
11: 16,854,434 (GRCm39) |
K869E |
probably damaging |
Het |
Ehd1 |
G |
A |
19: 6,347,724 (GRCm39) |
M359I |
probably benign |
Het |
F5 |
A |
T |
1: 164,023,139 (GRCm39) |
T1566S |
probably benign |
Het |
Flrt2 |
T |
C |
12: 95,745,725 (GRCm39) |
I21T |
probably benign |
Het |
Galnt1 |
T |
A |
18: 24,404,812 (GRCm39) |
I383K |
probably benign |
Het |
Ghdc |
G |
T |
11: 100,657,660 (GRCm39) |
A523D |
probably damaging |
Het |
Gm24022 |
A |
G |
12: 113,393,399 (GRCm39) |
|
probably benign |
Het |
Golga3 |
T |
C |
5: 110,353,643 (GRCm39) |
S934P |
probably damaging |
Het |
Gpr135 |
T |
A |
12: 72,117,282 (GRCm39) |
T162S |
probably benign |
Het |
Gucd1 |
G |
A |
10: 75,353,036 (GRCm39) |
|
probably null |
Het |
Hcrtr2 |
T |
A |
9: 76,137,886 (GRCm39) |
I410F |
probably benign |
Het |
Igkv6-15 |
T |
C |
6: 70,383,633 (GRCm39) |
Y56C |
probably damaging |
Het |
Il22ra1 |
A |
T |
4: 135,460,415 (GRCm39) |
Y57F |
probably damaging |
Het |
Irak4 |
A |
G |
15: 94,456,154 (GRCm39) |
E247G |
possibly damaging |
Het |
Kank3 |
T |
C |
17: 34,040,746 (GRCm39) |
V13A |
possibly damaging |
Het |
Klhl1 |
A |
T |
14: 96,374,046 (GRCm39) |
S667T |
probably damaging |
Het |
Klhl6 |
T |
G |
16: 19,765,741 (GRCm39) |
*620C |
probably null |
Het |
Lct |
A |
G |
1: 128,235,978 (GRCm39) |
L343P |
probably damaging |
Het |
Lilrb4a |
T |
A |
10: 51,367,516 (GRCm39) |
|
probably null |
Het |
Lin7a |
G |
T |
10: 107,218,530 (GRCm39) |
G25* |
probably null |
Het |
Lmnb2 |
G |
A |
10: 80,753,946 (GRCm39) |
T36M |
probably damaging |
Het |
Manba |
T |
C |
3: 135,273,391 (GRCm39) |
F775S |
probably benign |
Het |
Marchf6 |
A |
G |
15: 31,465,468 (GRCm39) |
V812A |
probably damaging |
Het |
Megf6 |
T |
A |
4: 154,352,517 (GRCm39) |
L1292H |
probably damaging |
Het |
Myo18b |
T |
G |
5: 112,909,206 (GRCm39) |
Q1979P |
probably damaging |
Het |
Myoz1 |
T |
C |
14: 20,703,769 (GRCm39) |
M59V |
probably damaging |
Het |
Naa35 |
T |
C |
13: 59,773,345 (GRCm39) |
I100T |
possibly damaging |
Het |
Nox4 |
A |
T |
7: 87,010,011 (GRCm39) |
Y404F |
probably damaging |
Het |
Ntn1 |
T |
C |
11: 68,151,358 (GRCm39) |
Y441C |
probably damaging |
Het |
Onecut3 |
A |
G |
10: 80,331,154 (GRCm39) |
T105A |
unknown |
Het |
Or10ak8 |
C |
A |
4: 118,774,440 (GRCm39) |
V75F |
probably damaging |
Het |
Or1n1 |
T |
C |
2: 36,750,082 (GRCm39) |
T93A |
probably benign |
Het |
Or4d5 |
G |
A |
9: 40,012,523 (GRCm39) |
H88Y |
probably benign |
Het |
Pabpc1l |
A |
G |
2: 163,884,438 (GRCm39) |
S392G |
probably benign |
Het |
Pan3 |
T |
A |
5: 147,463,492 (GRCm39) |
|
probably null |
Het |
Pcdha4 |
G |
A |
18: 37,088,001 (GRCm39) |
S728N |
probably benign |
Het |
Pds5a |
T |
C |
5: 65,854,128 (GRCm39) |
D38G |
probably damaging |
Het |
Pgm2l1 |
A |
G |
7: 99,921,583 (GRCm39) |
I605V |
probably benign |
Het |
Phip |
T |
C |
9: 82,778,072 (GRCm39) |
|
probably null |
Het |
Pilra |
T |
C |
5: 137,833,777 (GRCm39) |
I96M |
probably damaging |
Het |
Ppig |
T |
A |
2: 69,571,830 (GRCm39) |
V183D |
unknown |
Het |
Ppp2r2a |
A |
T |
14: 67,259,757 (GRCm39) |
L313* |
probably null |
Het |
Ppp4c |
A |
G |
7: 126,386,709 (GRCm39) |
F126S |
probably damaging |
Het |
Ptger2 |
C |
A |
14: 45,226,824 (GRCm39) |
R135S |
probably damaging |
Het |
Rab11fip5 |
T |
A |
6: 85,324,788 (GRCm39) |
E506D |
probably damaging |
Het |
Rdh12 |
G |
A |
12: 79,259,516 (GRCm39) |
G133R |
probably damaging |
Het |
Rims2 |
A |
T |
15: 39,315,824 (GRCm39) |
D610V |
probably benign |
Het |
Saa1 |
T |
A |
7: 46,390,132 (GRCm39) |
Y122F |
probably damaging |
Het |
Septin10 |
A |
T |
10: 59,012,811 (GRCm39) |
V269E |
probably damaging |
Het |
Serpina3n |
T |
A |
12: 104,374,998 (GRCm39) |
D23E |
probably benign |
Het |
Serpinb11 |
A |
G |
1: 107,304,598 (GRCm39) |
K188E |
possibly damaging |
Het |
Slc18a3 |
C |
T |
14: 32,185,736 (GRCm39) |
V216M |
possibly damaging |
Het |
Slc19a3 |
G |
T |
1: 83,000,341 (GRCm39) |
N225K |
probably benign |
Het |
Slc4a1 |
T |
A |
11: 102,242,329 (GRCm39) |
I797F |
probably benign |
Het |
Slx9 |
A |
G |
10: 77,325,850 (GRCm39) |
V154A |
probably benign |
Het |
Spic |
A |
G |
10: 88,511,761 (GRCm39) |
M165T |
possibly damaging |
Het |
Timm44 |
A |
T |
8: 4,325,886 (GRCm39) |
M1K |
probably null |
Het |
Tmc6 |
A |
G |
11: 117,661,610 (GRCm39) |
L572P |
probably benign |
Het |
Tnc |
G |
A |
4: 63,918,299 (GRCm39) |
T1204M |
probably benign |
Het |
Tnc |
G |
A |
4: 63,902,726 (GRCm39) |
T1517I |
probably damaging |
Het |
Trip11 |
A |
T |
12: 101,851,169 (GRCm39) |
L680* |
probably null |
Het |
Trps1 |
T |
A |
15: 50,524,703 (GRCm39) |
M887L |
possibly damaging |
Het |
Tulp3 |
A |
C |
6: 128,302,031 (GRCm39) |
V330G |
probably damaging |
Het |
Upf1 |
A |
G |
8: 70,787,350 (GRCm39) |
S835P |
probably damaging |
Het |
Wdr64 |
A |
G |
1: 175,620,525 (GRCm39) |
|
probably null |
Het |
Yju2b |
G |
A |
8: 84,985,304 (GRCm39) |
P322S |
probably benign |
Het |
Zbtb40 |
A |
G |
4: 136,723,461 (GRCm39) |
L643P |
probably damaging |
Het |
Zc3h18 |
A |
T |
8: 123,110,259 (GRCm39) |
D36V |
probably damaging |
Het |
|
Other mutations in Lgr6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02481:Lgr6
|
APN |
1 |
134,929,429 (GRCm39) |
splice site |
probably benign |
|
IGL02483:Lgr6
|
APN |
1 |
134,929,429 (GRCm39) |
splice site |
probably benign |
|
IGL03270:Lgr6
|
APN |
1 |
134,925,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R0002:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0294:Lgr6
|
UTSW |
1 |
135,032,799 (GRCm39) |
missense |
unknown |
|
R0294:Lgr6
|
UTSW |
1 |
134,915,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R0361:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0731:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0734:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0741:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0742:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0765:Lgr6
|
UTSW |
1 |
134,921,624 (GRCm39) |
missense |
probably benign |
0.04 |
R0903:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0904:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0905:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0906:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0907:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0908:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0967:Lgr6
|
UTSW |
1 |
134,921,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R1079:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R1131:Lgr6
|
UTSW |
1 |
134,915,042 (GRCm39) |
missense |
probably damaging |
0.98 |
R1440:Lgr6
|
UTSW |
1 |
134,915,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:Lgr6
|
UTSW |
1 |
135,032,670 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1728:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1728:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1728:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1729:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1729:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1730:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1730:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1730:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1739:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1739:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1739:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1762:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1762:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1762:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1782:Lgr6
|
UTSW |
1 |
134,915,717 (GRCm39) |
missense |
probably damaging |
0.98 |
R1783:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1783:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1783:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1783:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1784:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1784:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R1785:Lgr6
|
UTSW |
1 |
134,915,747 (GRCm39) |
missense |
probably benign |
|
R1785:Lgr6
|
UTSW |
1 |
134,914,826 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Lgr6
|
UTSW |
1 |
134,931,214 (GRCm39) |
missense |
probably benign |
|
R1785:Lgr6
|
UTSW |
1 |
134,918,373 (GRCm39) |
missense |
probably benign |
0.18 |
R2020:Lgr6
|
UTSW |
1 |
135,003,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R3104:Lgr6
|
UTSW |
1 |
134,928,210 (GRCm39) |
splice site |
probably null |
|
R4629:Lgr6
|
UTSW |
1 |
135,032,670 (GRCm39) |
missense |
probably damaging |
0.99 |
R4792:Lgr6
|
UTSW |
1 |
134,949,544 (GRCm39) |
missense |
probably benign |
0.03 |
R5191:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5194:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5195:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5196:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5197:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5228:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5230:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5243:Lgr6
|
UTSW |
1 |
135,037,010 (GRCm39) |
unclassified |
probably benign |
|
R5299:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5300:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5417:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5419:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5601:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5603:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5636:Lgr6
|
UTSW |
1 |
134,914,816 (GRCm39) |
missense |
probably benign |
0.28 |
R5699:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5748:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5767:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5825:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5971:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6078:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6079:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6138:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6258:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6259:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6740:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6871:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6984:Lgr6
|
UTSW |
1 |
134,915,740 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6986:Lgr6
|
UTSW |
1 |
134,921,694 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7233:Lgr6
|
UTSW |
1 |
134,928,214 (GRCm39) |
critical splice donor site |
probably null |
|
R7699:Lgr6
|
UTSW |
1 |
134,923,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Lgr6
|
UTSW |
1 |
134,923,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R7734:Lgr6
|
UTSW |
1 |
134,930,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R7849:Lgr6
|
UTSW |
1 |
134,915,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R7970:Lgr6
|
UTSW |
1 |
134,921,723 (GRCm39) |
missense |
probably benign |
|
R8068:Lgr6
|
UTSW |
1 |
134,991,402 (GRCm39) |
missense |
probably benign |
0.00 |
R8252:Lgr6
|
UTSW |
1 |
134,931,215 (GRCm39) |
missense |
probably null |
0.78 |
R8516:Lgr6
|
UTSW |
1 |
135,003,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R8771:Lgr6
|
UTSW |
1 |
134,933,429 (GRCm39) |
nonsense |
probably null |
|
R8858:Lgr6
|
UTSW |
1 |
134,923,849 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8885:Lgr6
|
UTSW |
1 |
134,915,342 (GRCm39) |
missense |
probably benign |
0.00 |
R9014:Lgr6
|
UTSW |
1 |
134,931,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R9277:Lgr6
|
UTSW |
1 |
134,915,217 (GRCm39) |
nonsense |
probably null |
|
R9660:Lgr6
|
UTSW |
1 |
134,915,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R9728:Lgr6
|
UTSW |
1 |
134,915,245 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Lgr6
|
UTSW |
1 |
134,915,809 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1191:Lgr6
|
UTSW |
1 |
134,921,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GCTTCCCCTGTATAGACACCAAG -3'
(R):5'- AGCAGGGCTGTTGAATAAGC -3'
Sequencing Primer
(F):5'- TTCCAACCCCTCCTGACAGG -3'
(R):5'- GCTGTTGAATAAGCAGTGTTGAAC -3'
|
Posted On |
2016-06-06 |