Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr8 |
C |
T |
14: 29,704,673 (GRCm39) |
Q58* |
probably null |
Het |
Adamts20 |
A |
C |
15: 94,180,985 (GRCm39) |
|
probably null |
Het |
Alpk3 |
T |
A |
7: 80,728,327 (GRCm39) |
S486T |
possibly damaging |
Het |
Cep162 |
T |
A |
9: 87,104,227 (GRCm39) |
E553V |
probably damaging |
Het |
Epha5 |
T |
C |
5: 84,304,360 (GRCm39) |
I370V |
possibly damaging |
Het |
Ets1 |
A |
T |
9: 32,664,093 (GRCm39) |
|
probably null |
Het |
Fbxo38 |
C |
T |
18: 62,666,634 (GRCm39) |
E180K |
probably damaging |
Het |
Fscn1 |
A |
G |
5: 142,957,741 (GRCm39) |
D296G |
probably damaging |
Het |
Glul |
A |
G |
1: 153,783,779 (GRCm39) |
I325V |
probably benign |
Het |
Keg1 |
A |
G |
19: 12,693,274 (GRCm39) |
D99G |
probably benign |
Het |
Mdfic |
T |
A |
6: 15,770,324 (GRCm39) |
I110N |
probably damaging |
Het |
Myo1g |
T |
C |
11: 6,462,509 (GRCm39) |
N541D |
probably damaging |
Het |
Nos3 |
T |
A |
5: 24,588,622 (GRCm39) |
V1116D |
probably damaging |
Het |
Or8h8 |
A |
G |
2: 86,753,441 (GRCm39) |
I145T |
probably benign |
Het |
Piwil2 |
G |
T |
14: 70,611,785 (GRCm39) |
Q954K |
probably benign |
Het |
Ppm1l |
T |
C |
3: 69,224,916 (GRCm39) |
M6T |
probably damaging |
Het |
Scn3a |
T |
A |
2: 65,327,907 (GRCm39) |
E861V |
possibly damaging |
Het |
Senp2 |
C |
T |
16: 21,845,474 (GRCm39) |
T236M |
possibly damaging |
Het |
Sgo2b |
A |
T |
8: 64,384,528 (GRCm39) |
V156D |
probably damaging |
Het |
Sis |
T |
C |
3: 72,814,475 (GRCm39) |
Y1585C |
probably damaging |
Het |
Slc22a22 |
A |
G |
15: 57,114,365 (GRCm39) |
S321P |
probably benign |
Het |
Slu7 |
T |
A |
11: 43,328,975 (GRCm39) |
Y66N |
probably damaging |
Het |
Stra6l |
A |
G |
4: 45,879,473 (GRCm39) |
H365R |
probably benign |
Het |
Stt3b |
T |
C |
9: 115,096,410 (GRCm39) |
T246A |
probably benign |
Het |
Taf1c |
T |
G |
8: 120,330,986 (GRCm39) |
N44T |
possibly damaging |
Het |
Tcirg1 |
C |
T |
19: 3,951,933 (GRCm39) |
V376M |
probably damaging |
Het |
Tkt |
A |
G |
14: 30,271,280 (GRCm39) |
D17G |
probably damaging |
Het |
Tle6 |
G |
A |
10: 81,427,810 (GRCm39) |
H482Y |
probably damaging |
Het |
Tnks1bp1 |
T |
C |
2: 84,889,689 (GRCm39) |
V672A |
probably benign |
Het |
Zdbf2 |
T |
G |
1: 63,344,679 (GRCm39) |
D1019E |
possibly damaging |
Het |
Zfp608 |
A |
T |
18: 55,032,150 (GRCm39) |
C597S |
possibly damaging |
Het |
Zfp986 |
G |
C |
4: 145,625,870 (GRCm39) |
D177H |
probably benign |
Het |
|
Other mutations in Krt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01133:Krt1
|
APN |
15 |
101,756,628 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01478:Krt1
|
APN |
15 |
101,754,721 (GRCm39) |
splice site |
probably benign |
|
IGL01919:Krt1
|
APN |
15 |
101,754,811 (GRCm39) |
missense |
unknown |
|
IGL01970:Krt1
|
APN |
15 |
101,755,299 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02207:Krt1
|
APN |
15 |
101,757,051 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02643:Krt1
|
APN |
15 |
101,755,479 (GRCm39) |
missense |
probably benign |
0.26 |
R0445:Krt1
|
UTSW |
15 |
101,756,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R0683:Krt1
|
UTSW |
15 |
101,758,901 (GRCm39) |
missense |
unknown |
|
R1006:Krt1
|
UTSW |
15 |
101,756,326 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1163:Krt1
|
UTSW |
15 |
101,756,600 (GRCm39) |
nonsense |
probably null |
|
R1217:Krt1
|
UTSW |
15 |
101,757,416 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1325:Krt1
|
UTSW |
15 |
101,756,641 (GRCm39) |
splice site |
probably null |
|
R1965:Krt1
|
UTSW |
15 |
101,757,427 (GRCm39) |
missense |
probably benign |
0.13 |
R1966:Krt1
|
UTSW |
15 |
101,757,427 (GRCm39) |
missense |
probably benign |
0.13 |
R2101:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R2302:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R2697:Krt1
|
UTSW |
15 |
101,755,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R3034:Krt1
|
UTSW |
15 |
101,759,068 (GRCm39) |
missense |
unknown |
|
R3079:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R3080:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R3891:Krt1
|
UTSW |
15 |
101,758,847 (GRCm39) |
missense |
unknown |
|
R3892:Krt1
|
UTSW |
15 |
101,758,847 (GRCm39) |
missense |
unknown |
|
R4180:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R4305:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R4334:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R4597:Krt1
|
UTSW |
15 |
101,756,063 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4625:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R4626:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R4628:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R4629:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R4630:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R4631:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R4632:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R4633:Krt1
|
UTSW |
15 |
101,754,622 (GRCm39) |
missense |
unknown |
|
R4893:Krt1
|
UTSW |
15 |
101,758,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R4948:Krt1
|
UTSW |
15 |
101,754,376 (GRCm39) |
missense |
unknown |
|
R5193:Krt1
|
UTSW |
15 |
101,754,357 (GRCm39) |
missense |
unknown |
|
R5254:Krt1
|
UTSW |
15 |
101,754,803 (GRCm39) |
missense |
unknown |
|
R5448:Krt1
|
UTSW |
15 |
101,757,464 (GRCm39) |
nonsense |
probably null |
|
R5494:Krt1
|
UTSW |
15 |
101,759,149 (GRCm39) |
missense |
unknown |
|
R5567:Krt1
|
UTSW |
15 |
101,755,340 (GRCm39) |
missense |
probably benign |
0.12 |
R5570:Krt1
|
UTSW |
15 |
101,755,340 (GRCm39) |
missense |
probably benign |
0.12 |
R5869:Krt1
|
UTSW |
15 |
101,758,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R6200:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R6224:Krt1
|
UTSW |
15 |
101,758,702 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6326:Krt1
|
UTSW |
15 |
101,758,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R6525:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R6918:Krt1
|
UTSW |
15 |
101,758,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R7018:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R7040:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R7110:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R7296:Krt1
|
UTSW |
15 |
101,759,064 (GRCm39) |
missense |
unknown |
|
R7368:Krt1
|
UTSW |
15 |
101,755,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R7706:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R8416:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R8418:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R8842:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R8914:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R8964:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R8979:Krt1
|
UTSW |
15 |
101,755,340 (GRCm39) |
missense |
probably benign |
0.12 |
R8988:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R9134:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R9248:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R9380:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R9404:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R9430:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R9638:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
R9768:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
RF003:Krt1
|
UTSW |
15 |
101,758,813 (GRCm39) |
small deletion |
probably benign |
|
X0067:Krt1
|
UTSW |
15 |
101,756,190 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Krt1
|
UTSW |
15 |
101,758,970 (GRCm39) |
missense |
unknown |
|
Z1177:Krt1
|
UTSW |
15 |
101,754,451 (GRCm39) |
missense |
unknown |
|
|