Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700062C07Rik |
A |
G |
18: 24,608,580 (GRCm39) |
|
probably null |
Het |
Alms1 |
T |
C |
6: 85,604,986 (GRCm39) |
F2212S |
possibly damaging |
Het |
Anpep |
T |
C |
7: 79,475,098 (GRCm39) |
I155V |
possibly damaging |
Het |
Aoc1 |
G |
A |
6: 48,885,223 (GRCm39) |
V653M |
probably damaging |
Het |
Arl8b |
T |
C |
6: 108,798,518 (GRCm39) |
|
probably benign |
Het |
Bax |
A |
C |
7: 45,115,552 (GRCm39) |
|
probably null |
Het |
Cpne7 |
G |
A |
8: 123,852,382 (GRCm39) |
E195K |
probably damaging |
Het |
Csmd3 |
A |
G |
15: 47,539,168 (GRCm39) |
I2330T |
possibly damaging |
Het |
Dnajc16 |
A |
G |
4: 141,501,940 (GRCm39) |
S297P |
probably benign |
Het |
Farp2 |
A |
G |
1: 93,504,155 (GRCm39) |
K311E |
probably damaging |
Het |
Fhad1 |
A |
G |
4: 141,691,906 (GRCm39) |
L410P |
probably damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,798,886 (GRCm39) |
T536A |
possibly damaging |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
Hydin |
C |
T |
8: 111,245,806 (GRCm39) |
T2173I |
possibly damaging |
Het |
Kpnb1 |
A |
G |
11: 97,055,556 (GRCm39) |
V783A |
probably benign |
Het |
Lrwd1 |
A |
T |
5: 136,164,729 (GRCm39) |
L26* |
probably null |
Het |
Mal2 |
T |
A |
15: 54,451,728 (GRCm39) |
W50R |
probably damaging |
Het |
Map3k21 |
A |
T |
8: 126,668,871 (GRCm39) |
E819V |
probably damaging |
Het |
Mrgprx3-ps |
T |
C |
7: 46,959,959 (GRCm39) |
T11A |
probably benign |
Het |
Mroh2b |
T |
C |
15: 4,953,170 (GRCm39) |
F635L |
probably benign |
Het |
Mylip |
G |
A |
13: 45,562,178 (GRCm39) |
E327K |
probably damaging |
Het |
Nfix |
T |
C |
8: 85,453,103 (GRCm39) |
D308G |
probably damaging |
Het |
Or1l8 |
G |
A |
2: 36,817,824 (GRCm39) |
Q101* |
probably null |
Het |
Or7e166 |
G |
A |
9: 19,624,638 (GRCm39) |
V172I |
probably benign |
Het |
Psma6 |
A |
G |
12: 55,454,254 (GRCm39) |
E26G |
probably damaging |
Het |
Rgs16 |
T |
A |
1: 153,617,804 (GRCm39) |
S105T |
probably damaging |
Het |
Slc25a23 |
T |
A |
17: 57,354,291 (GRCm39) |
N372Y |
possibly damaging |
Het |
Slc35e2 |
A |
G |
4: 155,697,187 (GRCm39) |
M234V |
probably benign |
Het |
Tbc1d8 |
A |
G |
1: 39,431,334 (GRCm39) |
V346A |
probably damaging |
Het |
Tgfb1i1 |
C |
T |
7: 127,847,654 (GRCm39) |
|
probably benign |
Het |
Triml2 |
A |
C |
8: 43,643,349 (GRCm39) |
T177P |
probably damaging |
Het |
Uba6 |
T |
C |
5: 86,267,245 (GRCm39) |
T959A |
probably benign |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
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 |
|
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 |
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 |
|
|