Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427D14Rik |
A |
G |
11: 72,086,628 (GRCm39) |
L261P |
probably damaging |
Het |
A4gnt |
A |
G |
9: 99,502,598 (GRCm39) |
I253V |
probably benign |
Het |
AAdacl4fm3 |
A |
T |
4: 144,429,798 (GRCm39) |
V397D |
possibly damaging |
Het |
Acap2 |
A |
T |
16: 30,973,385 (GRCm39) |
|
probably null |
Het |
Adora2b |
G |
T |
11: 62,156,146 (GRCm39) |
M198I |
probably damaging |
Het |
Akap5 |
C |
A |
12: 76,375,303 (GRCm39) |
T245K |
probably benign |
Het |
Aldh1a2 |
T |
C |
9: 71,192,245 (GRCm39) |
I399T |
probably damaging |
Het |
Ank2 |
G |
A |
3: 126,819,252 (GRCm39) |
S473L |
probably benign |
Het |
Anln |
A |
T |
9: 22,272,153 (GRCm39) |
D655E |
probably damaging |
Het |
Arhgef10 |
T |
C |
8: 15,025,956 (GRCm39) |
V820A |
probably benign |
Het |
Arid1b |
A |
G |
17: 5,391,989 (GRCm39) |
K1787E |
probably benign |
Het |
Art4 |
T |
C |
6: 136,831,739 (GRCm39) |
H134R |
probably benign |
Het |
Borcs6 |
G |
A |
11: 68,951,410 (GRCm39) |
V263M |
probably damaging |
Het |
C8a |
A |
T |
4: 104,703,247 (GRCm39) |
M314K |
possibly damaging |
Het |
Cbfa2t3 |
T |
G |
8: 123,361,865 (GRCm39) |
M386L |
probably damaging |
Het |
Ccdc170 |
T |
A |
10: 4,496,839 (GRCm39) |
V459E |
probably benign |
Het |
Cdh4 |
T |
A |
2: 179,532,636 (GRCm39) |
N699K |
possibly damaging |
Het |
Cdk12 |
T |
C |
11: 98,113,484 (GRCm39) |
L756P |
unknown |
Het |
Chsy1 |
A |
G |
7: 65,821,868 (GRCm39) |
D701G |
probably damaging |
Het |
Cnot9 |
A |
G |
1: 74,567,921 (GRCm39) |
T270A |
probably benign |
Het |
Crat |
C |
T |
2: 30,294,577 (GRCm39) |
R497Q |
probably benign |
Het |
Csnk2a1-ps3 |
A |
G |
1: 156,352,324 (GRCm39) |
D175G |
probably benign |
Het |
Cyb5r1 |
A |
G |
1: 134,338,268 (GRCm39) |
E228G |
probably damaging |
Het |
D630003M21Rik |
A |
G |
2: 158,059,273 (GRCm39) |
L209P |
probably damaging |
Het |
Dennd2c |
T |
A |
3: 103,070,378 (GRCm39) |
D791E |
probably benign |
Het |
Dnah14 |
T |
C |
1: 181,455,632 (GRCm39) |
I919T |
probably damaging |
Het |
Dpp8 |
T |
C |
9: 64,986,036 (GRCm39) |
L842S |
probably damaging |
Het |
Ern1 |
A |
G |
11: 106,300,719 (GRCm39) |
|
probably null |
Het |
Exo1 |
T |
C |
1: 175,734,232 (GRCm39) |
|
probably null |
Het |
Fam161b |
T |
G |
12: 84,404,512 (GRCm39) |
E56A |
possibly damaging |
Het |
Fbrsl1 |
T |
C |
5: 110,580,799 (GRCm39) |
T153A |
probably benign |
Het |
Fcgr3 |
T |
G |
1: 170,886,912 (GRCm39) |
D4A |
probably benign |
Het |
Gltp |
C |
T |
5: 114,808,521 (GRCm39) |
A193T |
probably benign |
Het |
Gm3159 |
A |
T |
14: 4,399,690 (GRCm38) |
S142C |
probably damaging |
Het |
Gphn |
T |
C |
12: 78,672,939 (GRCm39) |
V485A |
probably damaging |
Het |
Grik2 |
A |
T |
10: 49,399,904 (GRCm39) |
N275K |
probably damaging |
Het |
Gstt3 |
G |
T |
10: 75,612,625 (GRCm39) |
Q102K |
probably damaging |
Het |
Hivep3 |
T |
A |
4: 119,954,052 (GRCm39) |
F789L |
possibly damaging |
Het |
Ing5 |
A |
G |
1: 93,744,164 (GRCm39) |
N157D |
possibly damaging |
Het |
Itga3 |
C |
T |
11: 94,956,722 (GRCm39) |
W177* |
probably null |
Het |
Jag2 |
T |
C |
12: 112,892,672 (GRCm39) |
T83A |
probably benign |
Het |
Lcn2 |
A |
G |
2: 32,277,861 (GRCm39) |
|
probably null |
Het |
Lrig2 |
A |
G |
3: 104,373,076 (GRCm39) |
S602P |
probably damaging |
Het |
Lsm1 |
A |
C |
8: 26,282,237 (GRCm39) |
R33S |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,923,934 (GRCm39) |
Y492* |
probably null |
Het |
Mcm3 |
A |
T |
1: 20,876,120 (GRCm39) |
L658Q |
probably benign |
Het |
Myh4 |
G |
A |
11: 67,134,148 (GRCm39) |
|
probably null |
Het |
Nck2 |
T |
C |
1: 43,608,381 (GRCm39) |
V341A |
probably benign |
Het |
Nucb1 |
T |
C |
7: 45,151,142 (GRCm39) |
|
probably null |
Het |
Nup210l |
G |
C |
3: 90,117,766 (GRCm39) |
|
probably null |
Het |
Or1j1 |
A |
G |
2: 36,702,651 (GRCm39) |
I151T |
probably benign |
Het |
Or5al5 |
A |
T |
2: 85,961,972 (GRCm39) |
F12I |
probably damaging |
Het |
Or7g22 |
A |
T |
9: 19,049,161 (GRCm39) |
S291C |
possibly damaging |
Het |
Or8b48 |
T |
A |
9: 38,493,347 (GRCm39) |
M258K |
probably damaging |
Het |
Or8b54 |
G |
A |
9: 38,686,974 (GRCm39) |
C141Y |
probably damaging |
Het |
Pla2g4a |
G |
A |
1: 149,727,113 (GRCm39) |
P556S |
probably damaging |
Het |
Plat |
T |
C |
8: 23,265,658 (GRCm39) |
C234R |
probably damaging |
Het |
Ppfia1 |
T |
C |
7: 144,071,450 (GRCm39) |
I321V |
probably benign |
Het |
Prrc1 |
T |
A |
18: 57,496,325 (GRCm39) |
V92E |
probably benign |
Het |
Prss3 |
A |
G |
6: 41,350,848 (GRCm39) |
V214A |
probably damaging |
Het |
Ptprg |
G |
T |
14: 12,179,342 (GRCm38) |
K786N |
possibly damaging |
Het |
Rabgap1 |
G |
T |
2: 37,427,354 (GRCm39) |
G645V |
probably damaging |
Het |
Rfx4 |
T |
C |
10: 84,716,090 (GRCm39) |
S470P |
probably damaging |
Het |
Rin3 |
C |
T |
12: 102,335,909 (GRCm39) |
Q607* |
probably null |
Het |
Sema3a |
A |
G |
5: 13,573,093 (GRCm39) |
H207R |
probably benign |
Het |
Serpinb12 |
G |
A |
1: 106,878,534 (GRCm39) |
E181K |
probably damaging |
Het |
Serpinb6c |
G |
A |
13: 34,081,386 (GRCm39) |
Q88* |
probably null |
Het |
Shmt1 |
A |
C |
11: 60,692,812 (GRCm39) |
C90W |
probably damaging |
Het |
Slc16a13 |
C |
T |
11: 70,109,710 (GRCm39) |
V264M |
probably damaging |
Het |
Slc17a8 |
G |
T |
10: 89,427,969 (GRCm39) |
P286Q |
probably damaging |
Het |
Slc27a6 |
C |
T |
18: 58,745,293 (GRCm39) |
Q576* |
probably null |
Het |
Slc30a9 |
T |
C |
5: 67,505,421 (GRCm39) |
S470P |
possibly damaging |
Het |
Slc44a2 |
G |
T |
9: 21,253,768 (GRCm39) |
K136N |
possibly damaging |
Het |
Smarca5 |
A |
T |
8: 81,444,163 (GRCm39) |
H534Q |
probably damaging |
Het |
Son |
T |
G |
16: 91,451,748 (GRCm39) |
L165R |
probably damaging |
Het |
Sox10 |
G |
A |
15: 79,040,421 (GRCm39) |
P373L |
probably benign |
Het |
Sp100 |
C |
T |
1: 85,608,860 (GRCm39) |
R330* |
probably null |
Het |
Srrm4 |
A |
G |
5: 116,584,570 (GRCm39) |
L500P |
probably damaging |
Het |
Tap1 |
T |
C |
17: 34,415,639 (GRCm39) |
L689P |
probably damaging |
Het |
Tfg |
A |
G |
16: 56,525,972 (GRCm39) |
|
probably null |
Het |
Tjp2 |
C |
T |
19: 24,088,886 (GRCm39) |
V677I |
probably benign |
Het |
Tmprss11g |
T |
G |
5: 86,645,176 (GRCm39) |
D85A |
probably damaging |
Het |
Tnfsf9 |
T |
C |
17: 57,414,238 (GRCm39) |
S222P |
probably damaging |
Het |
Trank1 |
A |
G |
9: 111,193,824 (GRCm39) |
N616S |
probably damaging |
Het |
Tubgcp6 |
C |
A |
15: 89,004,728 (GRCm39) |
W297L |
probably damaging |
Het |
Twist1 |
T |
C |
12: 34,008,355 (GRCm39) |
S127P |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,179,966 (GRCm39) |
I247T |
unknown |
Het |
Ubr5 |
G |
A |
15: 37,988,481 (GRCm39) |
T2153M |
|
Het |
Utrn |
A |
G |
10: 12,573,833 (GRCm39) |
V1079A |
probably benign |
Het |
Vcan |
T |
C |
13: 89,852,237 (GRCm39) |
T908A |
probably damaging |
Het |
Vmn2r104 |
A |
G |
17: 20,249,791 (GRCm39) |
F827L |
probably damaging |
Het |
Vmn2r111 |
T |
A |
17: 22,767,380 (GRCm39) |
T706S |
probably benign |
Het |
Vmn2r114 |
T |
C |
17: 23,527,035 (GRCm39) |
D499G |
probably null |
Het |
Vmn2r92 |
T |
C |
17: 18,391,533 (GRCm39) |
S512P |
probably damaging |
Het |
Vps4b |
A |
T |
1: 106,708,232 (GRCm39) |
|
probably null |
Het |
Vwa8 |
A |
C |
14: 79,219,674 (GRCm39) |
|
probably null |
Het |
Wnt10b |
T |
C |
15: 98,672,045 (GRCm39) |
Q224R |
probably benign |
Het |
Ylpm1 |
C |
T |
12: 85,077,268 (GRCm39) |
P1331L |
possibly damaging |
Het |
Zfhx4 |
G |
A |
3: 5,307,267 (GRCm39) |
M164I |
possibly damaging |
Het |
Zfp51 |
A |
G |
17: 21,683,762 (GRCm39) |
T126A |
probably benign |
Het |
Zfp609 |
A |
G |
9: 65,613,418 (GRCm39) |
V339A |
probably benign |
Het |
Zfp687 |
C |
T |
3: 94,914,841 (GRCm39) |
R1220H |
probably damaging |
Het |
Zfyve21 |
C |
T |
12: 111,790,249 (GRCm39) |
L84F |
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 |
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 |
R9355:Krt90
|
UTSW |
15 |
101,461,714 (GRCm39) |
missense |
unknown |
|
|