Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
C |
T |
6: 128,530,301 (GRCm39) |
|
probably benign |
Het |
Ap1b1 |
T |
C |
11: 4,989,169 (GRCm39) |
L782P |
probably damaging |
Het |
Arid1a |
T |
C |
4: 133,408,765 (GRCm39) |
D1914G |
unknown |
Het |
C8a |
G |
A |
4: 104,719,808 (GRCm39) |
Q57* |
probably null |
Het |
Cachd1 |
T |
C |
4: 100,850,069 (GRCm39) |
S1144P |
probably damaging |
Het |
Cdh23 |
A |
T |
10: 60,255,598 (GRCm39) |
|
probably null |
Het |
Cenpe |
A |
G |
3: 134,924,268 (GRCm39) |
Q198R |
possibly damaging |
Het |
Cpne8 |
T |
C |
15: 90,453,700 (GRCm39) |
I228V |
probably benign |
Het |
Cr2 |
A |
T |
1: 194,833,222 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
T |
C |
15: 47,522,395 (GRCm39) |
|
probably benign |
Het |
Cyp2c23 |
A |
G |
19: 43,994,046 (GRCm39) |
V440A |
probably benign |
Het |
Dag1 |
T |
C |
9: 108,085,281 (GRCm39) |
D620G |
possibly damaging |
Het |
Dmxl1 |
T |
A |
18: 50,011,449 (GRCm39) |
L1202* |
probably null |
Het |
Dnah3 |
T |
G |
7: 119,542,798 (GRCm39) |
H3538P |
probably benign |
Het |
Dock8 |
A |
T |
19: 25,067,292 (GRCm39) |
Q312L |
probably benign |
Het |
E2f7 |
T |
G |
10: 110,610,596 (GRCm39) |
V407G |
probably benign |
Het |
F13b |
T |
C |
1: 139,444,165 (GRCm39) |
S500P |
probably damaging |
Het |
F5 |
A |
G |
1: 164,039,395 (GRCm39) |
I2002V |
probably benign |
Het |
Flywch1 |
T |
A |
17: 23,979,319 (GRCm39) |
M439L |
possibly damaging |
Het |
Gcn1 |
C |
A |
5: 115,757,759 (GRCm39) |
A2488E |
probably damaging |
Het |
Gria1 |
T |
C |
11: 57,208,600 (GRCm39) |
S832P |
probably damaging |
Het |
Hnrnpr |
T |
C |
4: 136,066,724 (GRCm39) |
|
probably benign |
Het |
Hps3 |
A |
G |
3: 20,083,165 (GRCm39) |
I177T |
probably benign |
Het |
Irgm2 |
G |
A |
11: 58,111,167 (GRCm39) |
G298D |
probably benign |
Het |
Kcnk7 |
G |
A |
19: 5,756,230 (GRCm39) |
G152D |
probably damaging |
Het |
Man2a2 |
T |
C |
7: 80,012,654 (GRCm39) |
T620A |
probably benign |
Het |
Mapk12 |
A |
G |
15: 89,021,669 (GRCm39) |
|
probably benign |
Het |
Mapk6 |
T |
C |
9: 75,297,572 (GRCm39) |
Y315C |
probably damaging |
Het |
Mdga2 |
T |
A |
12: 66,769,905 (GRCm39) |
|
probably null |
Het |
Mtrex |
T |
C |
13: 113,055,095 (GRCm39) |
|
probably benign |
Het |
Nap1l1 |
A |
G |
10: 111,328,772 (GRCm39) |
R234G |
possibly damaging |
Het |
Olfm5 |
C |
A |
7: 103,809,951 (GRCm39) |
V137F |
possibly damaging |
Het |
Or4d11 |
G |
T |
19: 12,014,041 (GRCm39) |
H22N |
probably benign |
Het |
Pcdha11 |
C |
T |
18: 37,145,886 (GRCm39) |
T659I |
probably benign |
Het |
Pfkm |
T |
C |
15: 98,027,187 (GRCm39) |
V620A |
possibly damaging |
Het |
Rbak |
A |
G |
5: 143,162,355 (GRCm39) |
|
probably benign |
Het |
Rbl2 |
A |
G |
8: 91,816,844 (GRCm39) |
I401M |
probably benign |
Het |
Rragc |
T |
C |
4: 123,814,852 (GRCm39) |
S183P |
probably damaging |
Het |
Septin3 |
A |
G |
15: 82,163,814 (GRCm39) |
|
probably benign |
Het |
Slc22a6 |
A |
T |
19: 8,603,578 (GRCm39) |
|
probably benign |
Het |
Spag4 |
A |
T |
2: 155,910,417 (GRCm39) |
T348S |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,054,623 (GRCm39) |
R2157G |
probably benign |
Het |
Tmem168 |
G |
A |
6: 13,582,940 (GRCm39) |
T263M |
probably damaging |
Het |
Tnik |
T |
A |
3: 28,625,007 (GRCm39) |
|
probably null |
Het |
Tnpo2 |
T |
A |
8: 85,777,137 (GRCm39) |
V549E |
probably damaging |
Het |
Ttll7 |
A |
C |
3: 146,645,776 (GRCm39) |
K545Q |
possibly damaging |
Het |
Tubgcp5 |
T |
G |
7: 55,449,221 (GRCm39) |
D139E |
probably benign |
Het |
Vmn1r233 |
T |
A |
17: 21,214,861 (GRCm39) |
N30Y |
probably damaging |
Het |
Vmn2r25 |
T |
G |
6: 123,829,962 (GRCm39) |
D63A |
possibly damaging |
Het |
Vmn2r79 |
T |
A |
7: 86,686,485 (GRCm39) |
L622Q |
probably damaging |
Het |
Vmn2r84 |
T |
C |
10: 130,222,148 (GRCm39) |
M691V |
probably benign |
Het |
Zc3hc1 |
A |
T |
6: 30,372,729 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Met |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00533:Met
|
APN |
6 |
17,534,936 (GRCm39) |
unclassified |
probably benign |
|
IGL01066:Met
|
APN |
6 |
17,535,104 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01344:Met
|
APN |
6 |
17,547,031 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01413:Met
|
APN |
6 |
17,558,895 (GRCm39) |
splice site |
probably benign |
|
IGL01608:Met
|
APN |
6 |
17,558,729 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01613:Met
|
APN |
6 |
17,540,576 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01820:Met
|
APN |
6 |
17,534,230 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02014:Met
|
APN |
6 |
17,527,256 (GRCm39) |
splice site |
probably benign |
|
IGL02027:Met
|
APN |
6 |
17,563,726 (GRCm39) |
splice site |
probably benign |
|
IGL02243:Met
|
APN |
6 |
17,549,093 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02373:Met
|
APN |
6 |
17,491,528 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02616:Met
|
APN |
6 |
17,553,346 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02702:Met
|
APN |
6 |
17,534,142 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02704:Met
|
APN |
6 |
17,491,256 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02714:Met
|
APN |
6 |
17,491,851 (GRCm39) |
nonsense |
probably null |
|
IGL02936:Met
|
APN |
6 |
17,553,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02943:Met
|
APN |
6 |
17,535,928 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03057:Met
|
APN |
6 |
17,558,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03124:Met
|
APN |
6 |
17,492,077 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03171:Met
|
APN |
6 |
17,562,272 (GRCm39) |
splice site |
probably benign |
|
IGL03266:Met
|
APN |
6 |
17,540,537 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03285:Met
|
APN |
6 |
17,553,336 (GRCm39) |
missense |
probably damaging |
0.98 |
R0453:Met
|
UTSW |
6 |
17,534,197 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0543:Met
|
UTSW |
6 |
17,491,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Met
|
UTSW |
6 |
17,555,631 (GRCm39) |
splice site |
probably null |
|
R0652:Met
|
UTSW |
6 |
17,491,709 (GRCm39) |
missense |
probably benign |
0.00 |
R0941:Met
|
UTSW |
6 |
17,491,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R1142:Met
|
UTSW |
6 |
17,527,182 (GRCm39) |
nonsense |
probably null |
|
R1553:Met
|
UTSW |
6 |
17,491,460 (GRCm39) |
missense |
probably benign |
0.01 |
R1569:Met
|
UTSW |
6 |
17,531,503 (GRCm39) |
nonsense |
probably null |
|
R1744:Met
|
UTSW |
6 |
17,540,645 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2224:Met
|
UTSW |
6 |
17,563,721 (GRCm39) |
splice site |
probably null |
|
R2308:Met
|
UTSW |
6 |
17,491,741 (GRCm39) |
missense |
probably benign |
0.00 |
R2369:Met
|
UTSW |
6 |
17,531,527 (GRCm39) |
missense |
probably benign |
0.04 |
R2393:Met
|
UTSW |
6 |
17,534,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R2419:Met
|
UTSW |
6 |
17,535,829 (GRCm39) |
splice site |
probably benign |
|
R2483:Met
|
UTSW |
6 |
17,549,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R2511:Met
|
UTSW |
6 |
17,491,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R3622:Met
|
UTSW |
6 |
17,549,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R3623:Met
|
UTSW |
6 |
17,549,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R3624:Met
|
UTSW |
6 |
17,549,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4050:Met
|
UTSW |
6 |
17,533,983 (GRCm39) |
missense |
probably benign |
|
R4051:Met
|
UTSW |
6 |
17,548,728 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4159:Met
|
UTSW |
6 |
17,562,271 (GRCm39) |
splice site |
probably null |
|
R4208:Met
|
UTSW |
6 |
17,548,728 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4622:Met
|
UTSW |
6 |
17,513,383 (GRCm39) |
missense |
probably benign |
0.19 |
R4672:Met
|
UTSW |
6 |
17,571,803 (GRCm39) |
missense |
probably benign |
0.33 |
R4737:Met
|
UTSW |
6 |
17,491,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R4738:Met
|
UTSW |
6 |
17,491,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Met
|
UTSW |
6 |
17,491,412 (GRCm39) |
missense |
probably damaging |
0.97 |
R4846:Met
|
UTSW |
6 |
17,491,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R4855:Met
|
UTSW |
6 |
17,558,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R4878:Met
|
UTSW |
6 |
17,549,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R4902:Met
|
UTSW |
6 |
17,546,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5208:Met
|
UTSW |
6 |
17,526,422 (GRCm39) |
nonsense |
probably null |
|
R5355:Met
|
UTSW |
6 |
17,491,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R5415:Met
|
UTSW |
6 |
17,527,084 (GRCm39) |
missense |
probably benign |
0.01 |
R5556:Met
|
UTSW |
6 |
17,534,175 (GRCm39) |
missense |
probably benign |
0.04 |
R5590:Met
|
UTSW |
6 |
17,548,781 (GRCm39) |
missense |
probably benign |
0.00 |
R5683:Met
|
UTSW |
6 |
17,571,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Met
|
UTSW |
6 |
17,562,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R5891:Met
|
UTSW |
6 |
17,491,538 (GRCm39) |
missense |
probably benign |
0.02 |
R5895:Met
|
UTSW |
6 |
17,531,581 (GRCm39) |
missense |
probably benign |
0.02 |
R6063:Met
|
UTSW |
6 |
17,491,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R6262:Met
|
UTSW |
6 |
17,553,403 (GRCm39) |
missense |
probably benign |
0.00 |
R6362:Met
|
UTSW |
6 |
17,558,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Met
|
UTSW |
6 |
17,571,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R6966:Met
|
UTSW |
6 |
17,531,531 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6989:Met
|
UTSW |
6 |
17,535,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R6989:Met
|
UTSW |
6 |
17,535,927 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7017:Met
|
UTSW |
6 |
17,491,286 (GRCm39) |
nonsense |
probably null |
|
R7037:Met
|
UTSW |
6 |
17,547,127 (GRCm39) |
intron |
probably benign |
|
R7141:Met
|
UTSW |
6 |
17,527,154 (GRCm39) |
missense |
probably benign |
0.01 |
R7242:Met
|
UTSW |
6 |
17,491,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R7282:Met
|
UTSW |
6 |
17,547,011 (GRCm39) |
nonsense |
probably null |
|
R7624:Met
|
UTSW |
6 |
17,558,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R7770:Met
|
UTSW |
6 |
17,491,406 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7797:Met
|
UTSW |
6 |
17,533,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8082:Met
|
UTSW |
6 |
17,492,312 (GRCm39) |
missense |
probably damaging |
0.98 |
R8109:Met
|
UTSW |
6 |
17,562,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R8162:Met
|
UTSW |
6 |
17,547,061 (GRCm39) |
missense |
probably damaging |
0.98 |
R8315:Met
|
UTSW |
6 |
17,533,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R8325:Met
|
UTSW |
6 |
17,571,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R8348:Met
|
UTSW |
6 |
17,571,799 (GRCm39) |
missense |
probably benign |
0.00 |
R8354:Met
|
UTSW |
6 |
17,491,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R8448:Met
|
UTSW |
6 |
17,571,799 (GRCm39) |
missense |
probably benign |
0.00 |
R8454:Met
|
UTSW |
6 |
17,491,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R8465:Met
|
UTSW |
6 |
17,571,809 (GRCm39) |
missense |
probably benign |
0.04 |
R8479:Met
|
UTSW |
6 |
17,491,746 (GRCm39) |
splice site |
probably null |
|
R8737:Met
|
UTSW |
6 |
17,540,510 (GRCm39) |
missense |
probably benign |
0.00 |
R8903:Met
|
UTSW |
6 |
17,549,137 (GRCm39) |
missense |
probably benign |
0.19 |
R8964:Met
|
UTSW |
6 |
17,527,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R8998:Met
|
UTSW |
6 |
17,491,534 (GRCm39) |
missense |
probably benign |
0.43 |
R9088:Met
|
UTSW |
6 |
17,548,715 (GRCm39) |
nonsense |
probably null |
|
R9369:Met
|
UTSW |
6 |
17,492,228 (GRCm39) |
missense |
probably benign |
|
R9394:Met
|
UTSW |
6 |
17,513,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R9530:Met
|
UTSW |
6 |
17,558,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Met
|
UTSW |
6 |
17,531,425 (GRCm39) |
missense |
probably benign |
|
R9759:Met
|
UTSW |
6 |
17,555,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|