Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
A |
11: 109,843,386 (GRCm39) |
Y946F |
probably benign |
Het |
Abcb4 |
T |
G |
5: 8,984,240 (GRCm39) |
W657G |
probably benign |
Het |
Adcy1 |
T |
C |
11: 7,088,279 (GRCm39) |
|
probably benign |
Het |
Arap3 |
A |
G |
18: 38,124,047 (GRCm39) |
V351A |
probably benign |
Het |
Carns1 |
C |
T |
19: 4,223,083 (GRCm39) |
C47Y |
probably benign |
Het |
Chd5 |
C |
T |
4: 152,445,050 (GRCm39) |
H344Y |
probably damaging |
Het |
Ctnna2 |
T |
C |
6: 76,957,807 (GRCm39) |
T481A |
probably benign |
Het |
Cyth1 |
T |
A |
11: 118,073,072 (GRCm39) |
D264V |
probably damaging |
Het |
Dph1 |
C |
A |
11: 75,071,461 (GRCm39) |
L311F |
probably benign |
Het |
Eif3l |
A |
G |
15: 78,961,142 (GRCm39) |
D65G |
probably damaging |
Het |
Gtf2a1l |
T |
A |
17: 88,976,146 (GRCm39) |
F3Y |
probably benign |
Het |
Hcn4 |
A |
T |
9: 58,766,748 (GRCm39) |
T770S |
unknown |
Het |
Hydin |
A |
T |
8: 111,139,908 (GRCm39) |
I726F |
possibly damaging |
Het |
Klf2 |
A |
G |
8: 73,072,940 (GRCm39) |
I7V |
probably benign |
Het |
Ltn1 |
A |
T |
16: 87,212,662 (GRCm39) |
L633H |
probably damaging |
Het |
Ncoa3 |
A |
G |
2: 165,893,313 (GRCm39) |
D206G |
probably benign |
Het |
Nlrp4a |
T |
G |
7: 26,149,138 (GRCm39) |
D248E |
probably benign |
Het |
Nyap1 |
A |
G |
5: 137,733,746 (GRCm39) |
I429T |
probably damaging |
Het |
Or1j10 |
T |
A |
2: 36,267,072 (GRCm39) |
C95S |
probably damaging |
Het |
Or2p2 |
G |
A |
13: 21,256,982 (GRCm39) |
T163I |
probably damaging |
Het |
Or2t6 |
T |
A |
14: 14,175,732 (GRCm38) |
M117L |
possibly damaging |
Het |
Or51g1 |
A |
G |
7: 102,633,537 (GRCm39) |
M278T |
probably benign |
Het |
Or8s16 |
A |
G |
15: 98,211,237 (GRCm39) |
S65P |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,296,254 (GRCm39) |
E1322G |
probably damaging |
Het |
Plcxd2 |
A |
T |
16: 45,792,689 (GRCm39) |
F217I |
probably benign |
Het |
Plxna4 |
A |
T |
6: 32,162,346 (GRCm39) |
I1389N |
probably damaging |
Het |
Ppp1r15a |
T |
C |
7: 45,174,091 (GRCm39) |
Y239C |
probably benign |
Het |
Psma6 |
A |
G |
12: 55,458,996 (GRCm39) |
E126G |
probably benign |
Het |
R3hcc1l |
T |
A |
19: 42,551,141 (GRCm39) |
V46E |
probably damaging |
Het |
Rap1gds1 |
G |
T |
3: 138,663,240 (GRCm39) |
H320N |
probably damaging |
Het |
Sdhaf3 |
A |
G |
6: 7,038,992 (GRCm39) |
M105V |
probably damaging |
Het |
Slc22a26 |
T |
A |
19: 7,765,613 (GRCm39) |
N345I |
probably benign |
Het |
Sncaip |
T |
C |
18: 53,028,027 (GRCm39) |
I412T |
possibly damaging |
Het |
Sorcs1 |
A |
T |
19: 50,178,530 (GRCm39) |
I864N |
probably damaging |
Het |
Spag5 |
C |
T |
11: 78,212,157 (GRCm39) |
Q1062* |
probably null |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Szrd1 |
A |
G |
4: 140,867,057 (GRCm39) |
|
probably benign |
Het |
Tns2 |
C |
A |
15: 102,016,231 (GRCm39) |
|
probably benign |
Het |
Trcg1 |
C |
A |
9: 57,149,511 (GRCm39) |
S361* |
probably null |
Het |
Tshz3 |
T |
C |
7: 36,468,583 (GRCm39) |
F191L |
probably damaging |
Het |
Ttc39a |
T |
C |
4: 109,280,090 (GRCm39) |
V124A |
probably damaging |
Het |
Ttf1 |
T |
C |
2: 28,964,023 (GRCm39) |
I633T |
probably damaging |
Het |
Zfp691 |
A |
G |
4: 119,027,704 (GRCm39) |
F176S |
probably damaging |
Het |
|
Other mutations in Bpifb9b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01621:Bpifb9b
|
APN |
2 |
154,158,871 (GRCm39) |
splice site |
probably null |
|
IGL02119:Bpifb9b
|
APN |
2 |
154,155,544 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0230:Bpifb9b
|
UTSW |
2 |
154,158,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R0269:Bpifb9b
|
UTSW |
2 |
154,161,545 (GRCm39) |
missense |
probably benign |
0.00 |
R0617:Bpifb9b
|
UTSW |
2 |
154,161,545 (GRCm39) |
missense |
probably benign |
0.00 |
R1953:Bpifb9b
|
UTSW |
2 |
154,153,234 (GRCm39) |
missense |
probably damaging |
0.99 |
R2050:Bpifb9b
|
UTSW |
2 |
154,151,524 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2160:Bpifb9b
|
UTSW |
2 |
154,161,595 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2200:Bpifb9b
|
UTSW |
2 |
154,155,574 (GRCm39) |
missense |
probably benign |
0.00 |
R2354:Bpifb9b
|
UTSW |
2 |
154,153,662 (GRCm39) |
missense |
probably benign |
|
R4755:Bpifb9b
|
UTSW |
2 |
154,161,614 (GRCm39) |
missense |
probably benign |
0.01 |
R4872:Bpifb9b
|
UTSW |
2 |
154,155,551 (GRCm39) |
missense |
probably damaging |
0.99 |
R4914:Bpifb9b
|
UTSW |
2 |
154,156,026 (GRCm39) |
splice site |
probably null |
|
R4915:Bpifb9b
|
UTSW |
2 |
154,156,026 (GRCm39) |
splice site |
probably null |
|
R4917:Bpifb9b
|
UTSW |
2 |
154,156,026 (GRCm39) |
splice site |
probably null |
|
R4918:Bpifb9b
|
UTSW |
2 |
154,156,026 (GRCm39) |
splice site |
probably null |
|
R4950:Bpifb9b
|
UTSW |
2 |
154,153,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R5438:Bpifb9b
|
UTSW |
2 |
154,151,288 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5507:Bpifb9b
|
UTSW |
2 |
154,158,947 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6255:Bpifb9b
|
UTSW |
2 |
154,151,284 (GRCm39) |
missense |
probably damaging |
0.98 |
R7130:Bpifb9b
|
UTSW |
2 |
154,153,592 (GRCm39) |
missense |
probably damaging |
0.98 |
R7161:Bpifb9b
|
UTSW |
2 |
154,155,535 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7736:Bpifb9b
|
UTSW |
2 |
154,154,025 (GRCm39) |
missense |
probably benign |
0.00 |
R8536:Bpifb9b
|
UTSW |
2 |
154,158,197 (GRCm39) |
missense |
probably benign |
0.00 |
R9134:Bpifb9b
|
UTSW |
2 |
154,151,441 (GRCm39) |
missense |
probably benign |
|
R9348:Bpifb9b
|
UTSW |
2 |
154,160,766 (GRCm39) |
missense |
probably benign |
0.28 |
R9528:Bpifb9b
|
UTSW |
2 |
154,153,297 (GRCm39) |
missense |
probably benign |
0.02 |
|