Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26b |
G |
A |
8: 43,974,472 (GRCm39) |
R177C |
possibly damaging |
Het |
Adgrb2 |
CG |
C |
4: 129,908,155 (GRCm39) |
|
probably null |
Het |
Bahcc1 |
G |
A |
11: 120,173,985 (GRCm39) |
V1582M |
probably damaging |
Het |
Baiap2 |
A |
T |
11: 119,897,231 (GRCm39) |
R529* |
probably null |
Het |
Bcl9l |
C |
T |
9: 44,420,685 (GRCm39) |
Q1327* |
probably null |
Het |
Brsk2 |
T |
A |
7: 141,538,270 (GRCm39) |
C139S |
possibly damaging |
Het |
Catsper3 |
T |
A |
13: 55,946,672 (GRCm39) |
I123N |
probably damaging |
Het |
Cd84 |
A |
G |
1: 171,713,976 (GRCm39) |
N325D |
possibly damaging |
Het |
Chid1 |
T |
A |
7: 141,076,297 (GRCm39) |
Y357F |
possibly damaging |
Het |
Clstn2 |
A |
T |
9: 97,408,459 (GRCm39) |
Y416* |
probably null |
Het |
Cnot1 |
A |
T |
8: 96,451,160 (GRCm39) |
L2189Q |
probably damaging |
Het |
Csnk2b |
T |
A |
17: 35,336,758 (GRCm39) |
I170L |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,631,977 (GRCm39) |
Q1326R |
probably damaging |
Het |
Drd1 |
T |
C |
13: 54,207,564 (GRCm39) |
I210V |
probably damaging |
Het |
Eef1d |
G |
T |
15: 75,775,558 (GRCm39) |
Q34K |
probably benign |
Het |
Fam184a |
T |
C |
10: 53,531,095 (GRCm39) |
T760A |
probably benign |
Het |
Fnip1 |
G |
T |
11: 54,373,385 (GRCm39) |
V199F |
probably benign |
Het |
Glyatl3 |
T |
C |
17: 41,215,829 (GRCm39) |
K226E |
probably damaging |
Het |
Gm19410 |
C |
T |
8: 36,285,127 (GRCm39) |
T2093I |
possibly damaging |
Het |
Herc1 |
A |
T |
9: 66,318,347 (GRCm39) |
E1206D |
probably benign |
Het |
Hs6st1 |
G |
A |
1: 36,143,299 (GRCm39) |
W411* |
probably null |
Het |
Hsf2 |
C |
A |
10: 57,372,080 (GRCm39) |
S60R |
probably damaging |
Het |
Hyal5 |
C |
A |
6: 24,891,291 (GRCm39) |
N368K |
probably damaging |
Het |
Itgb2l |
A |
T |
16: 96,231,843 (GRCm39) |
F308I |
probably benign |
Het |
Kdm7a |
G |
A |
6: 39,129,773 (GRCm39) |
L468F |
probably damaging |
Het |
Lamp3 |
A |
T |
16: 19,518,403 (GRCm39) |
L278* |
probably null |
Het |
Ly6c1 |
A |
T |
15: 74,917,289 (GRCm39) |
|
probably benign |
Het |
Mark3 |
A |
G |
12: 111,606,458 (GRCm39) |
N524D |
probably damaging |
Het |
Mical1 |
A |
T |
10: 41,355,750 (GRCm39) |
Q198L |
probably damaging |
Het |
Nacad |
T |
A |
11: 6,552,634 (GRCm39) |
I186F |
possibly damaging |
Het |
Nt5c3b |
A |
T |
11: 100,320,750 (GRCm39) |
M257K |
probably benign |
Het |
Nuak2 |
T |
C |
1: 132,252,770 (GRCm39) |
M108T |
possibly damaging |
Het |
Nub1 |
T |
A |
5: 24,894,470 (GRCm39) |
Y51N |
probably damaging |
Het |
Nxpe5 |
T |
C |
5: 138,237,679 (GRCm39) |
S68P |
probably damaging |
Het |
Or10ag58 |
C |
T |
2: 87,265,623 (GRCm39) |
T264I |
probably damaging |
Het |
Or5d44 |
A |
G |
2: 88,141,835 (GRCm39) |
S102P |
probably benign |
Het |
Or6c66 |
A |
G |
10: 129,461,633 (GRCm39) |
V99A |
probably benign |
Het |
Pias3 |
A |
G |
3: 96,609,511 (GRCm39) |
D276G |
probably damaging |
Het |
Setd7 |
A |
G |
3: 51,437,605 (GRCm39) |
Y217H |
probably damaging |
Het |
Slc23a1 |
A |
T |
18: 35,758,114 (GRCm39) |
I142N |
probably damaging |
Het |
Slx4ip |
T |
C |
2: 136,910,144 (GRCm39) |
S310P |
probably damaging |
Het |
Tcp11l2 |
G |
A |
10: 84,427,133 (GRCm39) |
R199Q |
possibly damaging |
Het |
Tgm4 |
T |
A |
9: 122,880,207 (GRCm39) |
D226E |
possibly damaging |
Het |
Tspyl4 |
C |
A |
10: 34,173,673 (GRCm39) |
A55E |
probably benign |
Het |
Uap1l1 |
A |
G |
2: 25,254,950 (GRCm39) |
I146T |
probably damaging |
Het |
Ush2a |
G |
A |
1: 188,308,441 (GRCm39) |
G2030D |
probably damaging |
Het |
Uts2r |
G |
A |
11: 121,052,213 (GRCm39) |
G359D |
possibly damaging |
Het |
Vwa7 |
T |
C |
17: 35,236,072 (GRCm39) |
S9P |
probably benign |
Het |
Zbtb16 |
A |
G |
9: 48,568,654 (GRCm39) |
C604R |
probably damaging |
Het |
Zfp804b |
A |
G |
5: 6,821,615 (GRCm39) |
S483P |
probably damaging |
Het |
Zfpm1 |
G |
A |
8: 123,058,904 (GRCm39) |
A175T |
probably damaging |
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 |
IGL01843:Met
|
APN |
6 |
17,491,700 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|