Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam17 |
T |
C |
12: 21,390,520 (GRCm39) |
S382G |
probably damaging |
Het |
Agr2 |
G |
A |
12: 36,046,090 (GRCm39) |
V74I |
probably benign |
Het |
Aldh3a1 |
T |
C |
11: 61,108,867 (GRCm39) |
S423P |
probably damaging |
Het |
Ampd1 |
C |
T |
3: 102,986,488 (GRCm39) |
H56Y |
possibly damaging |
Het |
Arhgef2 |
C |
A |
3: 88,550,304 (GRCm39) |
P670T |
probably benign |
Het |
Bmi1 |
T |
C |
2: 18,686,714 (GRCm39) |
I31T |
probably damaging |
Het |
Cacna1d |
G |
A |
14: 30,072,790 (GRCm39) |
Q62* |
probably null |
Het |
Ccdc88c |
A |
G |
12: 100,879,698 (GRCm39) |
S1801P |
probably damaging |
Het |
Cdkal1 |
C |
T |
13: 29,961,270 (GRCm39) |
A100T |
probably damaging |
Het |
Cfap251 |
G |
T |
5: 123,425,829 (GRCm39) |
|
probably null |
Het |
Chst4 |
G |
T |
8: 110,756,606 (GRCm39) |
S419Y |
probably damaging |
Het |
Cntn4 |
T |
C |
6: 106,649,844 (GRCm39) |
I680T |
probably damaging |
Het |
Ddx55 |
T |
C |
5: 124,694,875 (GRCm39) |
V101A |
probably damaging |
Het |
Ddx60 |
A |
T |
8: 62,411,091 (GRCm39) |
E451V |
probably damaging |
Het |
Dffa |
T |
A |
4: 149,190,772 (GRCm39) |
|
probably null |
Het |
Dgkd |
A |
G |
1: 87,861,832 (GRCm39) |
R796G |
probably damaging |
Het |
Dzank1 |
T |
A |
2: 144,323,605 (GRCm39) |
M614L |
probably benign |
Het |
Elf2 |
G |
T |
3: 51,215,555 (GRCm39) |
Q52K |
probably damaging |
Het |
Fcamr |
T |
A |
1: 130,741,793 (GRCm39) |
L522Q |
probably damaging |
Het |
Fscn2 |
T |
C |
11: 120,258,858 (GRCm39) |
Y468H |
probably damaging |
Het |
Gm12689 |
T |
C |
4: 99,184,402 (GRCm39) |
I85T |
unknown |
Het |
Gm4787 |
A |
G |
12: 81,425,102 (GRCm39) |
V352A |
possibly damaging |
Het |
Gtsf1 |
T |
C |
15: 103,336,802 (GRCm39) |
Q13R |
probably benign |
Het |
Itpkb |
G |
A |
1: 180,241,474 (GRCm39) |
V715M |
probably damaging |
Het |
Jmjd1c |
T |
A |
10: 67,053,928 (GRCm39) |
S263T |
probably damaging |
Het |
Krba1 |
T |
G |
6: 48,390,429 (GRCm39) |
L736R |
probably damaging |
Het |
Lrrc8d |
C |
G |
5: 105,960,650 (GRCm39) |
F353L |
probably damaging |
Het |
Lrrc8d |
G |
A |
5: 105,960,651 (GRCm39) |
E354K |
probably benign |
Het |
Mtor |
T |
A |
4: 148,630,901 (GRCm39) |
V2286E |
probably damaging |
Het |
Mybbp1a |
T |
A |
11: 72,341,462 (GRCm39) |
V1100E |
possibly damaging |
Het |
Myo5a |
G |
A |
9: 75,061,048 (GRCm39) |
G518D |
probably damaging |
Het |
Nalcn |
A |
T |
14: 123,521,123 (GRCm39) |
I1594N |
probably benign |
Het |
Nav1 |
C |
G |
1: 135,398,299 (GRCm39) |
G761A |
probably benign |
Het |
Ncoa2 |
A |
T |
1: 13,251,445 (GRCm39) |
L276H |
probably damaging |
Het |
Ndufaf7 |
T |
C |
17: 79,245,051 (GRCm39) |
Y57H |
probably damaging |
Het |
Nfkb2 |
A |
G |
19: 46,299,847 (GRCm39) |
Y807C |
probably damaging |
Het |
Nid2 |
A |
T |
14: 19,852,535 (GRCm39) |
Q1081L |
probably damaging |
Het |
Nkain2 |
T |
A |
10: 31,827,189 (GRCm39) |
I134F |
probably damaging |
Het |
Nmu |
A |
C |
5: 76,497,979 (GRCm39) |
S69A |
probably damaging |
Het |
Or4c15b |
A |
T |
2: 89,112,817 (GRCm39) |
I220N |
probably damaging |
Het |
Or5t7 |
T |
C |
2: 86,507,225 (GRCm39) |
I151V |
probably benign |
Het |
Pard3 |
A |
G |
8: 128,153,086 (GRCm39) |
R886G |
probably damaging |
Het |
Pde6b |
G |
T |
5: 108,571,317 (GRCm39) |
Q423H |
probably benign |
Het |
Pip5k1b |
A |
T |
19: 24,327,505 (GRCm39) |
D450E |
probably damaging |
Het |
Plcg1 |
T |
C |
2: 160,595,275 (GRCm39) |
|
probably null |
Het |
Pnpt1 |
T |
C |
11: 29,103,246 (GRCm39) |
S504P |
possibly damaging |
Het |
Pomt2 |
A |
T |
12: 87,175,797 (GRCm39) |
D312E |
probably damaging |
Het |
Ppp1r1b |
T |
C |
11: 98,246,228 (GRCm39) |
L70P |
probably damaging |
Het |
Prr5 |
C |
A |
15: 84,587,096 (GRCm39) |
P282Q |
probably benign |
Het |
Reln |
A |
T |
5: 22,176,883 (GRCm39) |
W1928R |
possibly damaging |
Het |
Sacm1l |
A |
T |
9: 123,415,419 (GRCm39) |
R465* |
probably null |
Het |
Sema7a |
A |
G |
9: 57,863,046 (GRCm39) |
Y239C |
probably damaging |
Het |
Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
Svep1 |
T |
C |
4: 58,044,054 (GRCm39) |
T3531A |
possibly damaging |
Het |
Tjp1 |
A |
T |
7: 65,004,609 (GRCm39) |
W19R |
probably damaging |
Het |
Tmc2 |
T |
A |
2: 130,083,564 (GRCm39) |
M507K |
possibly damaging |
Het |
Unc13a |
A |
G |
8: 72,095,795 (GRCm39) |
Y1241H |
probably damaging |
Het |
Upp1 |
C |
T |
11: 9,081,771 (GRCm39) |
P103S |
probably damaging |
Het |
Vldlr |
A |
G |
19: 27,221,624 (GRCm39) |
E663G |
probably damaging |
Het |
Vmn2r68 |
G |
A |
7: 84,886,767 (GRCm39) |
T49I |
possibly damaging |
Het |
Xirp2 |
A |
T |
2: 67,335,465 (GRCm39) |
M95L |
probably benign |
Het |
|
Other mutations in Blk |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00499:Blk
|
APN |
14 |
63,618,169 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02146:Blk
|
APN |
14 |
63,611,648 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02684:Blk
|
APN |
14 |
63,617,143 (GRCm39) |
missense |
probably benign |
0.17 |
blaenka
|
UTSW |
14 |
63,621,451 (GRCm39) |
missense |
probably damaging |
1.00 |
BB009:Blk
|
UTSW |
14 |
63,611,008 (GRCm39) |
missense |
possibly damaging |
0.67 |
BB019:Blk
|
UTSW |
14 |
63,611,008 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0254:Blk
|
UTSW |
14 |
63,618,253 (GRCm39) |
missense |
probably benign |
0.08 |
R0318:Blk
|
UTSW |
14 |
63,611,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R1567:Blk
|
UTSW |
14 |
63,618,178 (GRCm39) |
missense |
probably damaging |
0.99 |
R1871:Blk
|
UTSW |
14 |
63,613,364 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3719:Blk
|
UTSW |
14 |
63,621,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R4606:Blk
|
UTSW |
14 |
63,611,652 (GRCm39) |
missense |
probably benign |
0.00 |
R4879:Blk
|
UTSW |
14 |
63,613,414 (GRCm39) |
missense |
probably benign |
|
R4935:Blk
|
UTSW |
14 |
63,618,711 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5014:Blk
|
UTSW |
14 |
63,617,236 (GRCm39) |
missense |
probably benign |
0.00 |
R5352:Blk
|
UTSW |
14 |
63,613,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R5406:Blk
|
UTSW |
14 |
63,618,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R5518:Blk
|
UTSW |
14 |
63,615,956 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6289:Blk
|
UTSW |
14 |
63,613,341 (GRCm39) |
splice site |
probably null |
|
R6743:Blk
|
UTSW |
14 |
63,622,375 (GRCm39) |
missense |
probably benign |
|
R7932:Blk
|
UTSW |
14 |
63,611,008 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8696:Blk
|
UTSW |
14 |
63,618,149 (GRCm39) |
critical splice donor site |
probably benign |
|
R9169:Blk
|
UTSW |
14 |
63,620,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R9215:Blk
|
UTSW |
14 |
63,610,999 (GRCm39) |
missense |
probably damaging |
1.00 |
|