Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
T |
17: 24,537,242 (GRCm39) |
V447E |
probably damaging |
Het |
Adcyap1 |
T |
C |
17: 93,509,696 (GRCm39) |
L49P |
probably benign |
Het |
B4galt4 |
T |
C |
16: 38,572,621 (GRCm39) |
I102T |
probably damaging |
Het |
Cc2d2a |
A |
G |
5: 43,840,476 (GRCm39) |
D110G |
probably benign |
Het |
Ccdc141 |
C |
T |
2: 77,000,776 (GRCm39) |
V19I |
probably damaging |
Het |
Ccdc39 |
A |
G |
3: 33,892,031 (GRCm39) |
L147P |
probably damaging |
Het |
Cdc5l |
A |
T |
17: 45,721,712 (GRCm39) |
D519E |
probably benign |
Het |
Cdh23 |
G |
T |
10: 60,220,838 (GRCm39) |
T1305K |
probably damaging |
Het |
Cfi |
T |
A |
3: 129,644,478 (GRCm39) |
V158D |
possibly damaging |
Het |
Clstn2 |
T |
G |
9: 97,345,581 (GRCm39) |
Y589S |
probably damaging |
Het |
Dsp |
A |
G |
13: 38,380,640 (GRCm39) |
K1863E |
possibly damaging |
Het |
Enpp3 |
A |
T |
10: 24,669,487 (GRCm39) |
M491K |
probably damaging |
Het |
Fhdc1 |
C |
A |
3: 84,352,133 (GRCm39) |
V1031F |
probably benign |
Het |
Fkbp15 |
G |
A |
4: 62,221,456 (GRCm39) |
A1170V |
possibly damaging |
Het |
Foxa2 |
T |
C |
2: 147,886,623 (GRCm39) |
N64S |
possibly damaging |
Het |
Foxm1 |
T |
C |
6: 128,342,930 (GRCm39) |
I88T |
probably damaging |
Het |
Gm3173 |
A |
T |
14: 15,728,364 (GRCm39) |
I8L |
possibly damaging |
Het |
Gpatch3 |
A |
G |
4: 133,309,792 (GRCm39) |
D375G |
probably damaging |
Het |
Herc2 |
T |
C |
7: 55,876,402 (GRCm39) |
F4436L |
probably damaging |
Het |
Htr3b |
G |
A |
9: 48,856,809 (GRCm39) |
A223V |
probably damaging |
Het |
Iars2 |
T |
A |
1: 185,035,591 (GRCm39) |
T550S |
probably benign |
Het |
Igsf9 |
A |
T |
1: 172,321,779 (GRCm39) |
K149* |
probably null |
Het |
Khnyn |
A |
G |
14: 56,131,499 (GRCm39) |
D536G |
probably damaging |
Het |
Kng1 |
T |
C |
16: 22,898,370 (GRCm39) |
V409A |
possibly damaging |
Het |
Madd |
C |
T |
2: 90,970,917 (GRCm39) |
V1508I |
probably benign |
Het |
Micall2 |
T |
C |
5: 139,699,105 (GRCm39) |
E527G |
probably damaging |
Het |
Myo7b |
A |
G |
18: 32,110,040 (GRCm39) |
S1141P |
probably damaging |
Het |
Ncoa2 |
G |
A |
1: 13,245,187 (GRCm39) |
P504S |
possibly damaging |
Het |
Notch1 |
G |
A |
2: 26,350,048 (GRCm39) |
T2364I |
probably benign |
Het |
Pde4c |
T |
A |
8: 71,202,475 (GRCm39) |
|
probably null |
Het |
Pik3cb |
A |
G |
9: 98,943,904 (GRCm39) |
L633P |
probably damaging |
Het |
Ranbp2 |
T |
A |
10: 58,299,816 (GRCm39) |
D483E |
probably damaging |
Het |
Sh3tc2 |
A |
G |
18: 62,123,392 (GRCm39) |
N718D |
probably damaging |
Het |
Spast |
G |
A |
17: 74,659,010 (GRCm39) |
A126T |
probably damaging |
Het |
Ssc5d |
T |
C |
7: 4,946,663 (GRCm39) |
S1006P |
probably benign |
Het |
Tmprss6 |
T |
A |
15: 78,343,627 (GRCm39) |
|
probably null |
Het |
Ulk1 |
C |
T |
5: 110,937,223 (GRCm39) |
R691Q |
probably benign |
Het |
Unc79 |
C |
T |
12: 103,045,233 (GRCm39) |
T803M |
probably benign |
Het |
Vmn2r118 |
A |
T |
17: 55,917,347 (GRCm39) |
F388L |
possibly damaging |
Het |
Vmn2r71 |
T |
C |
7: 85,269,042 (GRCm39) |
V415A |
probably benign |
Het |
Wdr4 |
A |
T |
17: 31,718,126 (GRCm39) |
F316Y |
possibly damaging |
Het |
Zfp810 |
T |
C |
9: 22,190,080 (GRCm39) |
Y276C |
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 |
|
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 |
R6517:Krt1
|
UTSW |
15 |
101,758,702 (GRCm39) |
missense |
possibly damaging |
0.92 |
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 |
|
|