Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ano9 |
A |
G |
7: 140,681,817 (GRCm39) |
V747A |
probably benign |
Het |
Arfgef1 |
G |
A |
1: 10,270,000 (GRCm39) |
P383L |
probably benign |
Het |
Arhgef4 |
A |
G |
1: 34,849,630 (GRCm39) |
E407G |
probably benign |
Het |
Astn1 |
C |
T |
1: 158,511,721 (GRCm39) |
L1188F |
probably damaging |
Het |
Atg2b |
G |
A |
12: 105,636,980 (GRCm39) |
P179S |
possibly damaging |
Het |
Bcl9l |
G |
A |
9: 44,419,000 (GRCm39) |
R983H |
probably benign |
Het |
Bmp2k |
T |
A |
5: 97,211,366 (GRCm39) |
Y511* |
probably null |
Het |
C1galt1 |
G |
T |
6: 7,866,474 (GRCm39) |
V107F |
probably damaging |
Het |
Car3 |
T |
A |
3: 14,928,664 (GRCm39) |
N11K |
|
Het |
Ccdc170 |
A |
G |
10: 4,508,695 (GRCm39) |
R640G |
probably benign |
Het |
Cep126 |
A |
G |
9: 8,100,038 (GRCm39) |
V832A |
possibly damaging |
Het |
Ces1h |
C |
T |
8: 94,101,149 (GRCm39) |
V49I |
|
Het |
Clasp2 |
T |
A |
9: 113,664,309 (GRCm39) |
V310D |
probably damaging |
Het |
Comp |
C |
T |
8: 70,828,699 (GRCm39) |
T177M |
probably benign |
Het |
Coro1c |
T |
C |
5: 114,003,726 (GRCm39) |
S98G |
probably damaging |
Het |
Cpa6 |
C |
T |
1: 10,479,520 (GRCm39) |
V238I |
probably benign |
Het |
Crebrf |
T |
C |
17: 26,962,094 (GRCm39) |
F397S |
probably damaging |
Het |
Dcpp1 |
C |
A |
17: 24,099,987 (GRCm39) |
Q3K |
possibly damaging |
Het |
Dzip1l |
A |
G |
9: 99,543,144 (GRCm39) |
D533G |
possibly damaging |
Het |
Ecpas |
A |
T |
4: 58,844,114 (GRCm39) |
S551T |
probably benign |
Het |
Epha5 |
T |
C |
5: 84,253,890 (GRCm39) |
E524G |
probably damaging |
Het |
Epha7 |
A |
G |
4: 28,935,806 (GRCm39) |
Y476C |
probably damaging |
Het |
Erich5 |
G |
T |
15: 34,471,001 (GRCm39) |
V77F |
probably damaging |
Het |
Fat4 |
A |
G |
3: 39,036,047 (GRCm39) |
Y3233C |
probably damaging |
Het |
Ggt1 |
T |
A |
10: 75,421,716 (GRCm39) |
V521E |
probably benign |
Het |
Gm5431 |
A |
G |
11: 48,785,275 (GRCm39) |
Y89H |
probably damaging |
Het |
Gm5624 |
A |
T |
14: 44,799,272 (GRCm39) |
L95* |
probably null |
Het |
Gphn |
A |
G |
12: 78,538,968 (GRCm39) |
T205A |
probably damaging |
Het |
Grik5 |
C |
A |
7: 24,767,597 (GRCm39) |
A28S |
possibly damaging |
Het |
H2-K2 |
A |
G |
17: 34,216,120 (GRCm39) |
S300P |
probably benign |
Het |
H2-Oa |
T |
C |
17: 34,313,723 (GRCm39) |
L227P |
possibly damaging |
Het |
Hhip |
T |
C |
8: 80,778,233 (GRCm39) |
N99S |
probably damaging |
Het |
Hmcn2 |
A |
T |
2: 31,328,302 (GRCm39) |
M4328L |
probably benign |
Het |
Htt |
A |
T |
5: 35,053,247 (GRCm39) |
M2527L |
probably benign |
Het |
Impdh2 |
A |
T |
9: 108,442,402 (GRCm39) |
H466L |
probably benign |
Het |
Itgae |
G |
A |
11: 73,006,906 (GRCm39) |
G384D |
probably damaging |
Het |
Krtap5-5 |
A |
G |
7: 141,783,114 (GRCm39) |
S179P |
unknown |
Het |
Lif |
C |
T |
11: 4,219,044 (GRCm39) |
R63W |
probably damaging |
Het |
Lrrc10 |
T |
C |
10: 116,881,881 (GRCm39) |
V185A |
probably damaging |
Het |
Lrrc27 |
A |
C |
7: 138,822,648 (GRCm39) |
Q513P |
probably damaging |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Map2k3 |
T |
C |
11: 60,823,055 (GRCm39) |
S3P |
possibly damaging |
Het |
Mc2r |
T |
C |
18: 68,541,195 (GRCm39) |
T33A |
probably benign |
Het |
Mefv |
T |
A |
16: 3,525,882 (GRCm39) |
D795V |
probably damaging |
Het |
Megf6 |
A |
T |
4: 154,338,282 (GRCm39) |
R451W |
probably damaging |
Het |
Mrpl21 |
G |
A |
19: 3,336,937 (GRCm39) |
V103M |
probably damaging |
Het |
Mtmr14 |
GCCGCCGCCTCGGCGGGTTCCACCGCCTCGTCGGGCAGCCCGCCGCCTC |
GCCGCCGCCTC |
6: 113,214,948 (GRCm39) |
|
probably null |
Het |
Myom1 |
T |
C |
17: 71,384,888 (GRCm39) |
S760P |
probably damaging |
Het |
Ndst4 |
A |
G |
3: 125,403,246 (GRCm39) |
Y451C |
probably damaging |
Het |
Nkain4 |
T |
C |
2: 180,577,775 (GRCm39) |
N193S |
possibly damaging |
Het |
Opa1 |
T |
A |
16: 29,432,807 (GRCm39) |
L490H |
probably damaging |
Het |
Opcml |
A |
C |
9: 28,814,650 (GRCm39) |
I301L |
probably benign |
Het |
Or10ak16 |
G |
A |
4: 118,750,784 (GRCm39) |
S168N |
probably benign |
Het |
Or1e33 |
A |
G |
11: 73,738,643 (GRCm39) |
F103L |
probably damaging |
Het |
Or4p23 |
A |
T |
2: 88,576,749 (GRCm39) |
I161N |
probably damaging |
Het |
Or52s19 |
T |
C |
7: 103,008,125 (GRCm39) |
H92R |
probably benign |
Het |
Pabpc1l |
T |
C |
2: 163,884,469 (GRCm39) |
L402P |
probably benign |
Het |
Palld |
C |
T |
8: 61,969,691 (GRCm39) |
R1211H |
unknown |
Het |
Peak1 |
G |
T |
9: 56,167,454 (GRCm39) |
A158E |
probably damaging |
Het |
Ppfibp2 |
C |
T |
7: 107,322,169 (GRCm39) |
P406L |
probably benign |
Het |
Qpctl |
T |
C |
7: 18,875,146 (GRCm39) |
H362R |
probably damaging |
Het |
Ripor2 |
A |
G |
13: 24,885,694 (GRCm39) |
H643R |
probably benign |
Het |
Scn11a |
A |
T |
9: 119,584,160 (GRCm39) |
L1485Q |
probably damaging |
Het |
Scn2a |
A |
T |
2: 65,594,433 (GRCm39) |
I1761F |
probably damaging |
Het |
Scrn3 |
A |
G |
2: 73,166,077 (GRCm39) |
D370G |
probably benign |
Het |
Sec24b |
A |
T |
3: 129,787,489 (GRCm39) |
F877Y |
possibly damaging |
Het |
Slc35f3 |
T |
C |
8: 127,108,967 (GRCm39) |
I172T |
probably damaging |
Het |
Smc3 |
T |
C |
19: 53,622,544 (GRCm39) |
|
probably null |
Het |
Smpd3 |
C |
T |
8: 106,991,825 (GRCm39) |
V243M |
probably damaging |
Het |
Sos1 |
T |
A |
17: 80,722,479 (GRCm39) |
I856F |
possibly damaging |
Het |
Sp2 |
A |
T |
11: 96,852,231 (GRCm39) |
L231H |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 5,318,255 (GRCm39) |
Y457C |
probably damaging |
Het |
Tdpoz6 |
T |
C |
3: 93,600,307 (GRCm39) |
T21A |
possibly damaging |
Het |
Tekt5 |
T |
C |
16: 10,213,268 (GRCm39) |
T6A |
possibly damaging |
Het |
Tln2 |
G |
T |
9: 67,262,529 (GRCm39) |
T574K |
possibly damaging |
Het |
Tmem161a |
T |
C |
8: 70,633,821 (GRCm39) |
S313P |
probably damaging |
Het |
Trmt12 |
G |
A |
15: 58,744,824 (GRCm39) |
C74Y |
probably damaging |
Het |
Trpc6 |
A |
G |
9: 8,649,473 (GRCm39) |
D561G |
probably benign |
Het |
Ttn |
A |
G |
2: 76,700,769 (GRCm39) |
V62A |
|
Het |
Tubgcp5 |
T |
C |
7: 55,467,177 (GRCm39) |
|
probably null |
Het |
Unc13a |
C |
T |
8: 72,098,375 (GRCm39) |
V1137M |
possibly damaging |
Het |
Zfp729a |
A |
G |
13: 67,767,515 (GRCm39) |
C905R |
probably damaging |
Het |
Zfp735 |
A |
G |
11: 73,602,362 (GRCm39) |
I435M |
probably benign |
Het |
Zswim4 |
C |
A |
8: 84,955,687 (GRCm39) |
G271W |
probably damaging |
Het |
|
Other mutations in Krt90 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01608:Krt90
|
APN |
15 |
101,471,064 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01656:Krt90
|
APN |
15 |
101,463,878 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02064:Krt90
|
APN |
15 |
101,471,088 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0243:Krt90
|
UTSW |
15 |
101,471,110 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0732:Krt90
|
UTSW |
15 |
101,468,860 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1036:Krt90
|
UTSW |
15 |
101,471,151 (GRCm39) |
missense |
probably benign |
0.05 |
R1616:Krt90
|
UTSW |
15 |
101,469,026 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1750:Krt90
|
UTSW |
15 |
101,461,800 (GRCm39) |
unclassified |
probably benign |
|
R1919:Krt90
|
UTSW |
15 |
101,465,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R2063:Krt90
|
UTSW |
15 |
101,466,794 (GRCm39) |
missense |
probably benign |
0.07 |
R2107:Krt90
|
UTSW |
15 |
101,471,064 (GRCm39) |
missense |
probably benign |
0.06 |
R2155:Krt90
|
UTSW |
15 |
101,471,046 (GRCm39) |
missense |
probably benign |
0.00 |
R2404:Krt90
|
UTSW |
15 |
101,463,105 (GRCm39) |
critical splice donor site |
probably null |
|
R3412:Krt90
|
UTSW |
15 |
101,469,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R3910:Krt90
|
UTSW |
15 |
101,471,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R3911:Krt90
|
UTSW |
15 |
101,471,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R3913:Krt90
|
UTSW |
15 |
101,471,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R4476:Krt90
|
UTSW |
15 |
101,465,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R4748:Krt90
|
UTSW |
15 |
101,463,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R4918:Krt90
|
UTSW |
15 |
101,470,914 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5883:Krt90
|
UTSW |
15 |
101,461,654 (GRCm39) |
unclassified |
probably benign |
|
R6416:Krt90
|
UTSW |
15 |
101,467,679 (GRCm39) |
missense |
probably benign |
0.12 |
R6674:Krt90
|
UTSW |
15 |
101,465,761 (GRCm39) |
missense |
probably damaging |
0.99 |
R7025:Krt90
|
UTSW |
15 |
101,465,610 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7514:Krt90
|
UTSW |
15 |
101,461,605 (GRCm39) |
missense |
unknown |
|
R7915:Krt90
|
UTSW |
15 |
101,466,838 (GRCm39) |
splice site |
probably null |
|
R8307:Krt90
|
UTSW |
15 |
101,467,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R8756:Krt90
|
UTSW |
15 |
101,470,779 (GRCm39) |
critical splice donor site |
probably null |
|
R9011:Krt90
|
UTSW |
15 |
101,471,235 (GRCm39) |
missense |
probably benign |
0.17 |
|