Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ang6 |
A |
G |
14: 44,239,285 (GRCm39) |
*148Q |
probably null |
Het |
Ankrd28 |
A |
T |
14: 31,457,048 (GRCm39) |
|
probably null |
Het |
Ark2c |
G |
A |
18: 77,556,034 (GRCm39) |
A174V |
probably benign |
Het |
Aurkc |
T |
A |
7: 6,999,664 (GRCm39) |
L57* |
probably null |
Het |
Brca1 |
T |
C |
11: 101,416,802 (GRCm39) |
D444G |
probably damaging |
Het |
Cd200l1 |
T |
A |
16: 45,240,235 (GRCm39) |
I134F |
possibly damaging |
Het |
Cdhr4 |
T |
C |
9: 107,872,198 (GRCm39) |
V204A |
probably damaging |
Het |
Chd7 |
A |
G |
4: 8,822,412 (GRCm39) |
D835G |
possibly damaging |
Het |
Cux1 |
C |
A |
5: 136,303,944 (GRCm39) |
A1328S |
possibly damaging |
Het |
Cwc27 |
G |
T |
13: 104,940,772 (GRCm39) |
P196T |
probably benign |
Het |
Cwc27 |
C |
A |
13: 104,940,776 (GRCm39) |
L194F |
possibly damaging |
Het |
Cyp39a1 |
A |
G |
17: 43,993,898 (GRCm39) |
D186G |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,536,253 (GRCm39) |
I3677V |
probably benign |
Het |
Dnmt3b |
A |
G |
2: 153,516,306 (GRCm39) |
D477G |
probably damaging |
Het |
Drc1 |
A |
T |
5: 30,507,785 (GRCm39) |
Y269F |
probably benign |
Het |
Esco2 |
T |
C |
14: 66,069,118 (GRCm39) |
H64R |
probably benign |
Het |
Gcnt3 |
A |
T |
9: 69,941,959 (GRCm39) |
V203E |
probably damaging |
Het |
Gpam |
A |
C |
19: 55,077,374 (GRCm39) |
V139G |
probably damaging |
Het |
Gsta3 |
G |
A |
1: 21,333,063 (GRCm39) |
S104N |
probably damaging |
Het |
Hsd17b13 |
C |
T |
5: 104,125,049 (GRCm39) |
G45R |
probably damaging |
Het |
Ipo5 |
A |
G |
14: 121,183,560 (GRCm39) |
E1046G |
probably benign |
Het |
Kank4 |
T |
A |
4: 98,659,615 (GRCm39) |
Q821L |
probably damaging |
Het |
Kat6b |
G |
T |
14: 21,719,461 (GRCm39) |
S1271I |
probably damaging |
Het |
Klhl1 |
A |
G |
14: 96,619,370 (GRCm39) |
S176P |
probably benign |
Het |
Lbhd2 |
G |
A |
12: 111,378,190 (GRCm39) |
D86N |
probably damaging |
Het |
Lrp1 |
G |
A |
10: 127,394,519 (GRCm39) |
R2565C |
probably damaging |
Het |
Lrrc55 |
A |
T |
2: 85,022,295 (GRCm39) |
C299S |
probably benign |
Het |
Mtres1 |
T |
C |
10: 43,408,915 (GRCm39) |
Y76C |
probably benign |
Het |
Nprl3 |
T |
A |
11: 32,213,083 (GRCm39) |
S44C |
probably damaging |
Het |
Nucks1 |
A |
G |
1: 131,855,829 (GRCm39) |
H86R |
possibly damaging |
Het |
Or14j3 |
A |
G |
17: 37,900,866 (GRCm39) |
V126A |
possibly damaging |
Het |
Or4s2 |
A |
G |
2: 88,473,678 (GRCm39) |
D189G |
probably benign |
Het |
Or6c219 |
T |
A |
10: 129,780,998 (GRCm39) |
H311L |
probably benign |
Het |
Ovgp1 |
T |
A |
3: 105,894,311 (GRCm39) |
|
probably benign |
Het |
Oxa1l |
G |
A |
14: 54,606,001 (GRCm39) |
|
probably null |
Het |
Patj |
C |
A |
4: 98,312,539 (GRCm39) |
H292Q |
probably damaging |
Het |
Pcdha9 |
A |
G |
18: 37,131,636 (GRCm39) |
N235S |
probably benign |
Het |
Pcdhb12 |
A |
T |
18: 37,570,590 (GRCm39) |
T579S |
possibly damaging |
Het |
Pde3b |
A |
G |
7: 114,118,803 (GRCm39) |
I647M |
probably benign |
Het |
Pdp1 |
T |
C |
4: 11,961,982 (GRCm39) |
R110G |
probably benign |
Het |
Prb1a |
T |
G |
6: 132,185,398 (GRCm39) |
R78S |
unknown |
Het |
Prmt8 |
A |
C |
6: 127,680,976 (GRCm39) |
|
probably null |
Het |
Semp2l2a |
T |
A |
8: 13,888,229 (GRCm39) |
|
probably benign |
Het |
Slc35f2 |
T |
A |
9: 53,716,985 (GRCm39) |
Y249* |
probably null |
Het |
Smok2b |
A |
C |
17: 13,453,908 (GRCm39) |
M23L |
probably benign |
Het |
Sra1 |
A |
G |
18: 36,800,879 (GRCm39) |
I153T |
probably benign |
Het |
Stk38l |
T |
A |
6: 146,660,017 (GRCm39) |
H16Q |
possibly damaging |
Het |
Tent5c |
T |
A |
3: 100,379,784 (GRCm39) |
H324L |
probably damaging |
Het |
Unc80 |
T |
C |
1: 66,732,869 (GRCm39) |
S3073P |
possibly damaging |
Het |
Usp24 |
T |
C |
4: 106,230,953 (GRCm39) |
I844T |
probably damaging |
Het |
V1ra8 |
A |
T |
6: 90,179,916 (GRCm39) |
I40F |
probably benign |
Het |
Vmn2r88 |
T |
A |
14: 51,650,530 (GRCm39) |
M81K |
possibly damaging |
Het |
Vps8 |
T |
C |
16: 21,393,763 (GRCm39) |
I1182T |
probably damaging |
Het |
Wdr54 |
A |
G |
6: 83,130,591 (GRCm39) |
V181A |
probably benign |
Het |
Zbed4 |
A |
G |
15: 88,665,990 (GRCm39) |
Y686C |
probably damaging |
Het |
Zfyve28 |
T |
C |
5: 34,393,480 (GRCm39) |
N62S |
possibly damaging |
Het |
Zic1 |
T |
C |
9: 91,246,424 (GRCm39) |
Y216C |
probably damaging |
Het |
|
Other mutations in Ighe |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00235:Ighe
|
APN |
12 |
113,235,135 (GRCm39) |
missense |
unknown |
|
IGL01315:Ighe
|
APN |
12 |
113,234,972 (GRCm39) |
missense |
unknown |
|
IGL01415:Ighe
|
APN |
12 |
113,235,011 (GRCm39) |
missense |
unknown |
|
Allegra
|
UTSW |
12 |
113,234,994 (GRCm39) |
nonsense |
probably null |
|
R0610:Ighe
|
UTSW |
12 |
113,235,363 (GRCm39) |
missense |
unknown |
|
R1540:Ighe
|
UTSW |
12 |
113,235,066 (GRCm39) |
missense |
unknown |
|
R1838:Ighe
|
UTSW |
12 |
113,235,470 (GRCm39) |
missense |
unknown |
|
R2010:Ighe
|
UTSW |
12 |
113,235,108 (GRCm39) |
missense |
unknown |
|
R3498:Ighe
|
UTSW |
12 |
113,234,994 (GRCm39) |
nonsense |
probably null |
|
R5230:Ighe
|
UTSW |
12 |
113,235,006 (GRCm39) |
missense |
unknown |
|
R5288:Ighe
|
UTSW |
12 |
113,235,092 (GRCm39) |
missense |
probably benign |
0.00 |
R6713:Ighe
|
UTSW |
12 |
113,232,908 (GRCm39) |
unclassified |
probably benign |
|
R7010:Ighe
|
UTSW |
12 |
113,236,761 (GRCm39) |
missense |
|
|
R7146:Ighe
|
UTSW |
12 |
113,235,975 (GRCm39) |
missense |
|
|
R7324:Ighe
|
UTSW |
12 |
113,235,954 (GRCm39) |
missense |
|
|
R7443:Ighe
|
UTSW |
12 |
113,235,785 (GRCm39) |
nonsense |
probably null |
|
R7473:Ighe
|
UTSW |
12 |
113,234,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R7493:Ighe
|
UTSW |
12 |
113,235,023 (GRCm39) |
missense |
|
|
R7862:Ighe
|
UTSW |
12 |
113,235,428 (GRCm39) |
missense |
|
|
R7873:Ighe
|
UTSW |
12 |
113,234,942 (GRCm39) |
missense |
|
|
R7973:Ighe
|
UTSW |
12 |
113,236,677 (GRCm39) |
missense |
|
|
R8038:Ighe
|
UTSW |
12 |
113,233,053 (GRCm39) |
missense |
|
|
R8355:Ighe
|
UTSW |
12 |
113,235,167 (GRCm39) |
nonsense |
probably null |
|
R8508:Ighe
|
UTSW |
12 |
113,235,413 (GRCm39) |
nonsense |
probably null |
|
R8844:Ighe
|
UTSW |
12 |
113,235,006 (GRCm39) |
missense |
|
|
R9401:Ighe
|
UTSW |
12 |
113,233,107 (GRCm39) |
missense |
|
|
R9635:Ighe
|
UTSW |
12 |
113,235,899 (GRCm39) |
missense |
|
|
R9786:Ighe
|
UTSW |
12 |
113,236,851 (GRCm39) |
missense |
|
|
|