Other mutations in this stock |
Total: 109 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd4 |
G |
A |
12: 84,662,156 (GRCm39) |
S30F |
probably benign |
Het |
Abtb1 |
T |
C |
6: 88,813,601 (GRCm39) |
D379G |
possibly damaging |
Het |
Adgre1 |
A |
G |
17: 57,748,350 (GRCm39) |
I517V |
probably benign |
Het |
Ajm1 |
C |
T |
2: 25,468,000 (GRCm39) |
G637D |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
Angpt4 |
G |
A |
2: 151,780,909 (GRCm39) |
V386M |
probably damaging |
Het |
Asic1 |
A |
G |
15: 99,594,535 (GRCm39) |
H360R |
probably null |
Het |
Asxl1 |
G |
A |
2: 153,243,526 (GRCm39) |
A1359T |
probably benign |
Het |
Atp8a2 |
C |
T |
14: 60,258,207 (GRCm39) |
|
probably null |
Het |
Bltp3a |
T |
C |
17: 28,109,045 (GRCm39) |
F1088S |
possibly damaging |
Het |
C1qtnf2 |
T |
A |
11: 43,382,114 (GRCm39) |
F279I |
probably damaging |
Het |
Car8 |
A |
T |
4: 8,221,671 (GRCm39) |
L100* |
probably null |
Het |
Cd52 |
T |
C |
4: 133,822,295 (GRCm39) |
M1V |
probably null |
Het |
Celf5 |
T |
C |
10: 81,303,053 (GRCm39) |
I163V |
possibly damaging |
Het |
Cep250 |
A |
T |
2: 155,834,107 (GRCm39) |
T2010S |
possibly damaging |
Het |
Cfap65 |
C |
T |
1: 74,958,107 (GRCm39) |
V934M |
probably damaging |
Het |
Colec11 |
A |
T |
12: 28,644,858 (GRCm39) |
I212N |
probably damaging |
Het |
Cpa3 |
C |
T |
3: 20,277,391 (GRCm39) |
|
probably null |
Het |
Ctnnd1 |
G |
T |
2: 84,445,553 (GRCm39) |
H495N |
probably damaging |
Het |
Cyb5a |
T |
C |
18: 84,869,686 (GRCm39) |
V28A |
probably benign |
Het |
Ddo |
A |
T |
10: 40,523,625 (GRCm39) |
Q205L |
probably benign |
Het |
Dnah1 |
T |
A |
14: 30,983,050 (GRCm39) |
N4195I |
probably benign |
Het |
E2f1 |
A |
T |
2: 154,402,849 (GRCm39) |
V306E |
probably benign |
Het |
Ece1 |
C |
T |
4: 137,685,312 (GRCm39) |
R601W |
probably damaging |
Het |
Eef1d |
A |
C |
15: 75,773,024 (GRCm39) |
F25C |
probably damaging |
Het |
Ehd3 |
A |
T |
17: 74,137,354 (GRCm39) |
I508F |
probably damaging |
Het |
Eml6 |
T |
A |
11: 29,831,975 (GRCm39) |
I232F |
probably benign |
Het |
Enc1 |
T |
A |
13: 97,382,991 (GRCm39) |
D500E |
probably benign |
Het |
Enc1 |
C |
A |
13: 97,382,993 (GRCm39) |
T501K |
possibly damaging |
Het |
Fam83f |
C |
T |
15: 80,574,283 (GRCm39) |
R213W |
possibly damaging |
Het |
Fbxo31 |
A |
T |
8: 122,287,177 (GRCm39) |
L158* |
probably null |
Het |
Fcgbpl1 |
C |
T |
7: 27,854,797 (GRCm39) |
P1808S |
probably damaging |
Het |
Foxi3 |
C |
A |
6: 70,937,794 (GRCm39) |
T342N |
possibly damaging |
Het |
Gpr179 |
T |
A |
11: 97,227,382 (GRCm39) |
D1591V |
possibly damaging |
Het |
Gpsm2 |
A |
G |
3: 108,609,166 (GRCm39) |
V151A |
probably damaging |
Het |
Grk2 |
T |
G |
19: 4,337,968 (GRCm39) |
I513L |
probably benign |
Het |
H2-Ab1 |
A |
G |
17: 34,486,346 (GRCm39) |
E135G |
probably damaging |
Het |
Herc1 |
A |
T |
9: 66,296,138 (GRCm39) |
K578* |
probably null |
Het |
Hycc1 |
T |
G |
5: 24,191,149 (GRCm39) |
T173P |
probably damaging |
Het |
Itpr2 |
T |
C |
6: 146,198,171 (GRCm39) |
N1533S |
probably benign |
Het |
Kif3c |
A |
G |
12: 3,417,299 (GRCm39) |
N440S |
probably benign |
Het |
Klhdc2 |
T |
C |
12: 69,347,071 (GRCm39) |
|
probably null |
Het |
Kmo |
G |
T |
1: 175,465,461 (GRCm39) |
V72L |
probably benign |
Het |
Krt71 |
A |
G |
15: 101,651,315 (GRCm39) |
I56T |
possibly damaging |
Het |
Krt72 |
T |
C |
15: 101,689,987 (GRCm39) |
|
probably null |
Het |
Loxhd1 |
C |
T |
18: 77,493,603 (GRCm39) |
R1521C |
probably damaging |
Het |
Loxhd1 |
G |
A |
18: 77,513,335 (GRCm39) |
E1774K |
possibly damaging |
Het |
Ly6g6f |
T |
C |
17: 35,302,478 (GRCm39) |
S20G |
probably benign |
Het |
Mecr |
T |
A |
4: 131,592,382 (GRCm39) |
M282K |
probably damaging |
Het |
Mfsd14a |
G |
T |
3: 116,428,596 (GRCm39) |
A353D |
probably damaging |
Het |
Mroh9 |
A |
T |
1: 162,873,279 (GRCm39) |
N564K |
probably damaging |
Het |
Mrs2 |
T |
A |
13: 25,181,111 (GRCm39) |
T237S |
possibly damaging |
Het |
Mycbpap |
A |
G |
11: 94,398,377 (GRCm39) |
L534S |
probably damaging |
Het |
Myh1 |
T |
C |
11: 67,115,183 (GRCm39) |
I1906T |
probably benign |
Het |
Myh4 |
T |
A |
11: 67,151,150 (GRCm39) |
V1935D |
probably benign |
Het |
Myo18a |
T |
C |
11: 77,720,170 (GRCm39) |
I684T |
possibly damaging |
Het |
Myo7b |
C |
T |
18: 32,119,728 (GRCm39) |
R788H |
possibly damaging |
Het |
Nbea |
A |
T |
3: 55,551,129 (GRCm39) |
D2678E |
possibly damaging |
Het |
Ndufs3 |
A |
C |
2: 90,729,050 (GRCm39) |
Y145* |
probably null |
Het |
Nrros |
A |
G |
16: 31,962,329 (GRCm39) |
F563L |
probably damaging |
Het |
Ntn4 |
T |
C |
10: 93,581,633 (GRCm39) |
V602A |
probably damaging |
Het |
Obscn |
C |
A |
11: 58,920,163 (GRCm39) |
R6736L |
possibly damaging |
Het |
Odr4 |
T |
C |
1: 150,251,305 (GRCm39) |
N283S |
probably benign |
Het |
Or13c7d |
T |
A |
4: 43,770,495 (GRCm39) |
D172V |
possibly damaging |
Het |
Or2ag16 |
T |
C |
7: 106,351,756 (GRCm39) |
I280V |
probably benign |
Het |
Or7g22 |
C |
A |
9: 19,049,213 (GRCm39) |
T308K |
probably benign |
Het |
Or8d1 |
T |
A |
9: 38,766,820 (GRCm39) |
V154D |
probably benign |
Het |
Or8g54 |
C |
T |
9: 39,707,301 (GRCm39) |
P210L |
possibly damaging |
Het |
Or8g55 |
A |
G |
9: 39,785,267 (GRCm39) |
E232G |
probably benign |
Het |
Pik3cd |
A |
G |
4: 149,738,576 (GRCm39) |
F751L |
possibly damaging |
Het |
Plekhh2 |
A |
G |
17: 84,906,561 (GRCm39) |
|
probably null |
Het |
Postn |
A |
G |
3: 54,281,177 (GRCm39) |
H434R |
probably damaging |
Het |
Prss39 |
A |
G |
1: 34,539,114 (GRCm39) |
D118G |
possibly damaging |
Het |
Ralyl |
G |
T |
3: 14,208,493 (GRCm39) |
G211V |
possibly damaging |
Het |
Rbak |
T |
A |
5: 143,159,202 (GRCm39) |
E617V |
probably damaging |
Het |
Rbms3 |
A |
T |
9: 116,548,401 (GRCm39) |
W80R |
probably damaging |
Het |
Retnlg |
A |
T |
16: 48,694,610 (GRCm39) |
Y86F |
probably benign |
Het |
Rtel1 |
T |
A |
2: 180,993,896 (GRCm39) |
S643T |
probably benign |
Het |
Semp2l2a |
A |
T |
8: 13,886,816 (GRCm39) |
L425* |
probably null |
Het |
Serpina11 |
A |
T |
12: 103,950,954 (GRCm39) |
F256I |
probably damaging |
Het |
Setd2 |
A |
T |
9: 110,446,884 (GRCm39) |
|
probably null |
Het |
Setd2 |
A |
T |
9: 110,379,413 (GRCm39) |
Y1076F |
probably benign |
Het |
Sgsm1 |
T |
C |
5: 113,421,483 (GRCm39) |
T248A |
possibly damaging |
Het |
Slc6a21 |
T |
C |
7: 44,930,179 (GRCm39) |
Y193H |
probably damaging |
Het |
Slfn9 |
T |
C |
11: 82,872,781 (GRCm39) |
K652E |
probably benign |
Het |
Stt3b |
A |
T |
9: 115,077,675 (GRCm39) |
Y692* |
probably null |
Het |
Sval3 |
A |
G |
6: 41,945,096 (GRCm39) |
Q8R |
probably benign |
Het |
Synm |
T |
A |
7: 67,383,748 (GRCm39) |
I1305F |
possibly damaging |
Het |
Tdrd1 |
T |
C |
19: 56,826,215 (GRCm39) |
F169L |
probably damaging |
Het |
Tecta |
T |
A |
9: 42,295,493 (GRCm39) |
D334V |
probably damaging |
Het |
Tle2 |
G |
A |
10: 81,425,331 (GRCm39) |
|
probably null |
Het |
Tmem243 |
A |
G |
5: 9,166,489 (GRCm39) |
I30V |
probably benign |
Het |
Treml2 |
T |
C |
17: 48,616,530 (GRCm39) |
*330R |
probably null |
Het |
Trpm6 |
A |
G |
19: 18,804,931 (GRCm39) |
D961G |
possibly damaging |
Het |
Ubr4 |
T |
C |
4: 139,155,907 (GRCm39) |
V2244A |
probably benign |
Het |
Unc79 |
G |
T |
12: 103,109,005 (GRCm39) |
V2148F |
probably damaging |
Het |
Ush2a |
A |
C |
1: 188,643,024 (GRCm39) |
T4129P |
probably benign |
Het |
Vgll2 |
G |
A |
10: 51,901,324 (GRCm39) |
V85I |
probably damaging |
Het |
Vmn1r16 |
T |
C |
6: 57,300,256 (GRCm39) |
Y122C |
probably benign |
Het |
Vmn1r22 |
A |
T |
6: 57,877,134 (GRCm39) |
I91N |
probably damaging |
Het |
Vmn2r70 |
A |
T |
7: 85,213,011 (GRCm39) |
Y465* |
probably null |
Het |
Wdr64 |
A |
T |
1: 175,544,897 (GRCm39) |
E110V |
probably damaging |
Het |
Wfdc6a |
A |
T |
2: 164,422,231 (GRCm39) |
C123S |
probably damaging |
Het |
Xrcc1 |
A |
G |
7: 24,247,252 (GRCm39) |
Y30C |
probably damaging |
Het |
Zdhhc7 |
T |
C |
8: 120,812,157 (GRCm39) |
K155R |
probably benign |
Het |
Zfp560 |
A |
G |
9: 20,263,226 (GRCm39) |
F50S |
possibly damaging |
Het |
Zfp616 |
C |
T |
11: 73,976,671 (GRCm39) |
T980I |
probably damaging |
Het |
Zfp808 |
C |
T |
13: 62,319,670 (GRCm39) |
P300S |
probably damaging |
Het |
Zfp979 |
G |
A |
4: 147,697,740 (GRCm39) |
T323I |
probably damaging |
Het |
|
Other mutations in Krt78 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Krt78
|
APN |
15 |
101,855,945 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01358:Krt78
|
APN |
15 |
101,854,698 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01723:Krt78
|
APN |
15 |
101,860,233 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01743:Krt78
|
APN |
15 |
101,859,333 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01778:Krt78
|
APN |
15 |
101,859,402 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01792:Krt78
|
APN |
15 |
101,855,085 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02271:Krt78
|
APN |
15 |
101,857,028 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02481:Krt78
|
APN |
15 |
101,856,853 (GRCm39) |
splice site |
probably benign |
|
IGL02494:Krt78
|
APN |
15 |
101,862,486 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02708:Krt78
|
APN |
15 |
101,861,842 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02747:Krt78
|
APN |
15 |
101,858,819 (GRCm39) |
splice site |
probably benign |
|
IGL02997:Krt78
|
APN |
15 |
101,855,598 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03350:Krt78
|
APN |
15 |
101,854,952 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03410:Krt78
|
APN |
15 |
101,862,421 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4812001:Krt78
|
UTSW |
15 |
101,856,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R0090:Krt78
|
UTSW |
15 |
101,856,272 (GRCm39) |
missense |
probably benign |
0.35 |
R0513:Krt78
|
UTSW |
15 |
101,859,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R0908:Krt78
|
UTSW |
15 |
101,859,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R1067:Krt78
|
UTSW |
15 |
101,854,896 (GRCm39) |
nonsense |
probably null |
|
R1070:Krt78
|
UTSW |
15 |
101,854,728 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1194:Krt78
|
UTSW |
15 |
101,860,221 (GRCm39) |
missense |
probably damaging |
0.99 |
R1213:Krt78
|
UTSW |
15 |
101,860,245 (GRCm39) |
missense |
probably benign |
0.10 |
R1467:Krt78
|
UTSW |
15 |
101,854,728 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1467:Krt78
|
UTSW |
15 |
101,854,728 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1612:Krt78
|
UTSW |
15 |
101,860,279 (GRCm39) |
splice site |
probably null |
|
R1750:Krt78
|
UTSW |
15 |
101,854,812 (GRCm39) |
missense |
probably benign |
0.33 |
R1863:Krt78
|
UTSW |
15 |
101,855,004 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1901:Krt78
|
UTSW |
15 |
101,855,398 (GRCm39) |
nonsense |
probably null |
|
R1902:Krt78
|
UTSW |
15 |
101,855,398 (GRCm39) |
nonsense |
probably null |
|
R1975:Krt78
|
UTSW |
15 |
101,854,603 (GRCm39) |
makesense |
probably null |
|
R2105:Krt78
|
UTSW |
15 |
101,855,849 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2418:Krt78
|
UTSW |
15 |
101,855,069 (GRCm39) |
missense |
probably benign |
|
R2421:Krt78
|
UTSW |
15 |
101,855,699 (GRCm39) |
missense |
probably damaging |
0.96 |
R2422:Krt78
|
UTSW |
15 |
101,855,699 (GRCm39) |
missense |
probably damaging |
0.96 |
R2443:Krt78
|
UTSW |
15 |
101,855,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R2897:Krt78
|
UTSW |
15 |
101,855,541 (GRCm39) |
missense |
probably benign |
|
R4422:Krt78
|
UTSW |
15 |
101,856,375 (GRCm39) |
missense |
probably benign |
0.13 |
R4424:Krt78
|
UTSW |
15 |
101,856,375 (GRCm39) |
missense |
probably benign |
0.13 |
R4425:Krt78
|
UTSW |
15 |
101,856,375 (GRCm39) |
missense |
probably benign |
0.13 |
R4583:Krt78
|
UTSW |
15 |
101,855,055 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4752:Krt78
|
UTSW |
15 |
101,856,637 (GRCm39) |
missense |
probably benign |
0.05 |
R4927:Krt78
|
UTSW |
15 |
101,855,334 (GRCm39) |
missense |
probably benign |
0.02 |
R5129:Krt78
|
UTSW |
15 |
101,856,015 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5391:Krt78
|
UTSW |
15 |
101,860,263 (GRCm39) |
nonsense |
probably null |
|
R5575:Krt78
|
UTSW |
15 |
101,855,787 (GRCm39) |
nonsense |
probably null |
|
R5617:Krt78
|
UTSW |
15 |
101,856,044 (GRCm39) |
missense |
probably damaging |
0.99 |
R5806:Krt78
|
UTSW |
15 |
101,858,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R5906:Krt78
|
UTSW |
15 |
101,857,030 (GRCm39) |
missense |
probably damaging |
0.98 |
R5993:Krt78
|
UTSW |
15 |
101,858,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R6520:Krt78
|
UTSW |
15 |
101,860,206 (GRCm39) |
missense |
probably benign |
0.26 |
R6531:Krt78
|
UTSW |
15 |
101,860,708 (GRCm39) |
missense |
probably benign |
0.03 |
R6587:Krt78
|
UTSW |
15 |
101,860,704 (GRCm39) |
missense |
probably benign |
0.10 |
R6749:Krt78
|
UTSW |
15 |
101,859,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R7126:Krt78
|
UTSW |
15 |
101,856,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R7158:Krt78
|
UTSW |
15 |
101,860,241 (GRCm39) |
missense |
probably benign |
0.17 |
R7229:Krt78
|
UTSW |
15 |
101,855,829 (GRCm39) |
missense |
probably benign |
0.01 |
R7523:Krt78
|
UTSW |
15 |
101,855,036 (GRCm39) |
missense |
not run |
|
R7638:Krt78
|
UTSW |
15 |
101,859,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R7879:Krt78
|
UTSW |
15 |
101,856,624 (GRCm39) |
missense |
probably benign |
0.22 |
R8013:Krt78
|
UTSW |
15 |
101,856,977 (GRCm39) |
missense |
probably damaging |
0.99 |
R8085:Krt78
|
UTSW |
15 |
101,855,715 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8209:Krt78
|
UTSW |
15 |
101,855,480 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8226:Krt78
|
UTSW |
15 |
101,855,480 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8309:Krt78
|
UTSW |
15 |
101,854,922 (GRCm39) |
missense |
probably benign |
0.00 |
R8728:Krt78
|
UTSW |
15 |
101,856,225 (GRCm39) |
missense |
probably benign |
0.11 |
R8729:Krt78
|
UTSW |
15 |
101,855,455 (GRCm39) |
missense |
probably damaging |
0.98 |
R8887:Krt78
|
UTSW |
15 |
101,861,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R9008:Krt78
|
UTSW |
15 |
101,855,211 (GRCm39) |
small deletion |
probably benign |
|
X0018:Krt78
|
UTSW |
15 |
101,860,235 (GRCm39) |
missense |
possibly damaging |
0.96 |
Z1088:Krt78
|
UTSW |
15 |
101,855,766 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Krt78
|
UTSW |
15 |
101,856,095 (GRCm39) |
missense |
probably benign |
|
|