Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc3 |
A |
G |
11: 94,242,750 (GRCm39) |
S1326P |
probably damaging |
Het |
Alpk1 |
A |
T |
3: 127,466,970 (GRCm39) |
L1103Q |
probably damaging |
Het |
Arhgap11a |
A |
C |
2: 113,667,906 (GRCm39) |
|
probably benign |
Het |
Arl6ip6 |
A |
G |
2: 53,082,226 (GRCm39) |
Y31C |
possibly damaging |
Het |
Arpin |
G |
T |
7: 79,577,395 (GRCm39) |
D217E |
possibly damaging |
Het |
Atp13a4 |
C |
T |
16: 29,241,521 (GRCm39) |
V735I |
probably benign |
Het |
Ccdc146 |
A |
T |
5: 21,502,631 (GRCm39) |
F753L |
probably benign |
Het |
Cdh3 |
T |
A |
8: 107,270,880 (GRCm39) |
L511* |
probably null |
Het |
Chrna1 |
A |
T |
2: 73,397,206 (GRCm39) |
I361N |
possibly damaging |
Het |
Clk2 |
G |
A |
3: 89,083,020 (GRCm39) |
R432H |
probably damaging |
Het |
Col9a1 |
T |
C |
1: 24,261,018 (GRCm39) |
|
probably benign |
Het |
Cstf1 |
G |
T |
2: 172,219,774 (GRCm39) |
R295L |
probably benign |
Het |
Dsg2 |
A |
G |
18: 20,725,467 (GRCm39) |
D526G |
probably damaging |
Het |
Dsg4 |
T |
A |
18: 20,595,577 (GRCm39) |
H593Q |
probably benign |
Het |
Dysf |
T |
C |
6: 84,107,109 (GRCm39) |
Y1171H |
possibly damaging |
Het |
Erbb4 |
A |
G |
1: 68,345,023 (GRCm39) |
L566P |
probably benign |
Het |
Fam185a |
T |
A |
5: 21,660,829 (GRCm39) |
D281E |
probably damaging |
Het |
Fam185a |
T |
A |
5: 21,634,839 (GRCm39) |
|
probably benign |
Het |
Fam91a1 |
T |
A |
15: 58,304,831 (GRCm39) |
|
probably null |
Het |
Fat2 |
A |
G |
11: 55,202,109 (GRCm39) |
W322R |
probably damaging |
Het |
Fbxw8 |
T |
A |
5: 118,204,125 (GRCm39) |
|
probably benign |
Het |
Ganc |
A |
G |
2: 120,288,615 (GRCm39) |
T874A |
probably benign |
Het |
Gm3543 |
T |
C |
14: 41,802,048 (GRCm39) |
I145M |
probably benign |
Het |
Gtf2i |
G |
A |
5: 134,274,015 (GRCm39) |
T712I |
probably damaging |
Het |
Hk1 |
A |
G |
10: 62,131,552 (GRCm39) |
S268P |
possibly damaging |
Het |
Hmcn1 |
A |
G |
1: 150,868,774 (GRCm39) |
V10A |
probably benign |
Het |
Hsd17b4 |
C |
T |
18: 50,295,164 (GRCm39) |
|
probably benign |
Het |
Ighv1-75 |
A |
T |
12: 115,797,725 (GRCm39) |
W66R |
probably damaging |
Het |
Kif21b |
G |
T |
1: 136,081,859 (GRCm39) |
D636Y |
probably damaging |
Het |
Kif5b |
A |
T |
18: 6,220,914 (GRCm39) |
I398N |
probably benign |
Het |
Metap2 |
T |
C |
10: 93,701,311 (GRCm39) |
M165V |
probably damaging |
Het |
Mterf2 |
A |
C |
10: 84,956,331 (GRCm39) |
L98V |
probably damaging |
Het |
Muc16 |
A |
G |
9: 18,409,849 (GRCm39) |
|
probably null |
Het |
Myo3b |
A |
G |
2: 69,925,568 (GRCm39) |
M12V |
probably benign |
Het |
Nat10 |
C |
A |
2: 103,583,013 (GRCm39) |
R136I |
probably damaging |
Het |
Nsd2 |
T |
G |
5: 34,003,542 (GRCm39) |
S231A |
probably damaging |
Het |
Or4a71 |
T |
C |
2: 89,358,275 (GRCm39) |
T160A |
probably benign |
Het |
Or4k37 |
A |
T |
2: 111,159,333 (GRCm39) |
M190L |
probably benign |
Het |
Pcdhb14 |
T |
A |
18: 37,581,071 (GRCm39) |
L59* |
probably null |
Het |
Pias4 |
A |
G |
10: 80,999,621 (GRCm39) |
L144P |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,433,746 (GRCm39) |
N598K |
probably benign |
Het |
Polq |
A |
G |
16: 36,862,130 (GRCm39) |
Y550C |
probably damaging |
Het |
Pot1b |
T |
A |
17: 56,002,024 (GRCm39) |
|
probably benign |
Het |
Proz |
T |
C |
8: 13,115,260 (GRCm39) |
V92A |
probably benign |
Het |
Rab4a |
T |
C |
8: 124,550,561 (GRCm39) |
F14L |
probably benign |
Het |
Riok3 |
T |
A |
18: 12,276,073 (GRCm39) |
C256* |
probably null |
Het |
Slc6a1 |
T |
A |
6: 114,279,451 (GRCm39) |
|
probably benign |
Het |
Spata3 |
T |
C |
1: 85,952,211 (GRCm39) |
L135P |
probably damaging |
Het |
Spata46 |
A |
G |
1: 170,139,534 (GRCm39) |
K178E |
probably damaging |
Het |
Spr |
T |
C |
6: 85,114,430 (GRCm39) |
N100D |
probably damaging |
Het |
Srrm4 |
C |
T |
5: 116,582,624 (GRCm39) |
|
probably benign |
Het |
Stard3 |
T |
C |
11: 98,267,389 (GRCm39) |
F169S |
possibly damaging |
Het |
Tbx1 |
T |
A |
16: 18,402,847 (GRCm39) |
D222V |
probably damaging |
Het |
Trbv23 |
C |
T |
6: 41,193,279 (GRCm39) |
Q56* |
probably null |
Het |
Tsc22d1 |
A |
G |
14: 76,654,838 (GRCm39) |
N357S |
possibly damaging |
Het |
Ugt1a6a |
C |
T |
1: 88,066,811 (GRCm39) |
P206S |
probably benign |
Het |
Utp20 |
A |
G |
10: 88,600,657 (GRCm39) |
V19A |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,646,447 (GRCm39) |
N1517S |
probably benign |
Het |
Washc2 |
T |
C |
6: 116,218,571 (GRCm39) |
I672T |
probably damaging |
Het |
|
Other mutations in Socs5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02426:Socs5
|
APN |
17 |
87,442,320 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Socs5
|
UTSW |
17 |
87,441,044 (GRCm39) |
splice site |
probably benign |
|
R0909:Socs5
|
UTSW |
17 |
87,441,201 (GRCm39) |
missense |
probably benign |
0.11 |
R1595:Socs5
|
UTSW |
17 |
87,441,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R2397:Socs5
|
UTSW |
17 |
87,442,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R3160:Socs5
|
UTSW |
17 |
87,442,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Socs5
|
UTSW |
17 |
87,442,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R5264:Socs5
|
UTSW |
17 |
87,441,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R5483:Socs5
|
UTSW |
17 |
87,442,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R6604:Socs5
|
UTSW |
17 |
87,442,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R7790:Socs5
|
UTSW |
17 |
87,441,791 (GRCm39) |
missense |
probably benign |
0.03 |
R8205:Socs5
|
UTSW |
17 |
87,441,138 (GRCm39) |
missense |
probably benign |
0.01 |
R9411:Socs5
|
UTSW |
17 |
87,442,521 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9428:Socs5
|
UTSW |
17 |
87,441,067 (GRCm39) |
missense |
probably benign |
|
R9456:Socs5
|
UTSW |
17 |
87,442,266 (GRCm39) |
missense |
probably damaging |
1.00 |
X0011:Socs5
|
UTSW |
17 |
87,442,368 (GRCm39) |
missense |
probably damaging |
1.00 |
|