Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
C |
12: 71,213,849 (GRCm39) |
V692A |
possibly damaging |
Het |
Aco2 |
C |
G |
15: 81,756,620 (GRCm39) |
|
probably benign |
Het |
Adcy10 |
T |
C |
1: 165,345,914 (GRCm39) |
I321T |
probably damaging |
Het |
Agbl2 |
C |
T |
2: 90,645,730 (GRCm39) |
T821I |
probably benign |
Het |
Alpk1 |
A |
G |
3: 127,473,192 (GRCm39) |
L937P |
probably damaging |
Het |
Atp5f1b |
A |
G |
10: 127,919,767 (GRCm39) |
D45G |
probably benign |
Het |
C8a |
C |
T |
4: 104,679,200 (GRCm39) |
R530H |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,016,057 (GRCm39) |
S694P |
probably benign |
Het |
Cdca7 |
T |
A |
2: 72,312,856 (GRCm39) |
D162E |
probably benign |
Het |
Cert1 |
C |
T |
13: 96,679,717 (GRCm39) |
P16S |
probably benign |
Het |
Coq8b |
A |
C |
7: 26,950,011 (GRCm39) |
R363S |
probably benign |
Het |
Cpne3 |
A |
T |
4: 19,540,770 (GRCm39) |
C202S |
probably damaging |
Het |
Csmd3 |
G |
T |
15: 47,483,308 (GRCm39) |
|
probably benign |
Het |
Cyp4a14 |
A |
T |
4: 115,344,461 (GRCm39) |
V468E |
probably damaging |
Het |
Dchs1 |
A |
T |
7: 105,405,215 (GRCm39) |
D2442E |
probably benign |
Het |
Dip2a |
T |
C |
10: 76,163,553 (GRCm39) |
Y49C |
probably benign |
Het |
Dop1a |
A |
G |
9: 86,382,870 (GRCm39) |
R268G |
probably damaging |
Het |
Eid3 |
C |
T |
10: 82,703,565 (GRCm39) |
S342L |
possibly damaging |
Het |
Ezh2 |
A |
G |
6: 47,528,671 (GRCm39) |
L296P |
possibly damaging |
Het |
Fgfrl1 |
G |
C |
5: 108,853,439 (GRCm39) |
|
probably null |
Het |
Flg2 |
A |
G |
3: 93,110,899 (GRCm39) |
R976G |
unknown |
Het |
Fsip2 |
C |
A |
2: 82,828,545 (GRCm39) |
Q6781K |
probably benign |
Het |
Golga3 |
C |
T |
5: 110,352,799 (GRCm39) |
H857Y |
probably benign |
Het |
Hmcn2 |
T |
A |
2: 31,244,646 (GRCm39) |
V701E |
probably damaging |
Het |
Il21 |
A |
T |
3: 37,286,602 (GRCm39) |
I38N |
probably benign |
Het |
Ip6k2 |
G |
T |
9: 108,681,807 (GRCm39) |
G246V |
probably damaging |
Het |
Ipo13 |
T |
C |
4: 117,758,185 (GRCm39) |
Q726R |
probably damaging |
Het |
Itsn1 |
A |
T |
16: 91,703,658 (GRCm39) |
N1521Y |
unknown |
Het |
Kif2b |
A |
G |
11: 91,467,131 (GRCm39) |
V384A |
possibly damaging |
Het |
L3mbtl1 |
G |
T |
2: 162,807,988 (GRCm39) |
R541L |
probably damaging |
Het |
Lama3 |
T |
A |
18: 12,614,120 (GRCm39) |
C1296* |
probably null |
Het |
Lars1 |
T |
C |
18: 42,390,234 (GRCm39) |
D11G |
probably damaging |
Het |
Ly6c1 |
C |
A |
15: 74,917,300 (GRCm39) |
G116V |
probably damaging |
Het |
Mmp27 |
C |
A |
9: 7,581,250 (GRCm39) |
F478L |
probably benign |
Het |
Moxd1 |
T |
A |
10: 24,155,251 (GRCm39) |
|
probably benign |
Het |
Naaa |
T |
A |
5: 92,420,300 (GRCm39) |
|
probably benign |
Het |
Nav1 |
T |
A |
1: 135,371,487 (GRCm39) |
Q1746L |
unknown |
Het |
Nedd9 |
T |
C |
13: 41,471,984 (GRCm39) |
Y165C |
probably damaging |
Het |
Neurod1 |
T |
C |
2: 79,284,720 (GRCm39) |
Y221C |
probably damaging |
Het |
Or2q1 |
A |
T |
6: 42,794,545 (GRCm39) |
I47F |
probably damaging |
Het |
Or4c122 |
G |
T |
2: 89,079,545 (GRCm39) |
F152L |
probably benign |
Het |
Or5al6 |
T |
C |
2: 85,976,625 (GRCm39) |
Y151C |
probably damaging |
Het |
Or9m1 |
T |
C |
2: 87,733,907 (GRCm39) |
T38A |
probably damaging |
Het |
Orm3 |
A |
G |
4: 63,274,533 (GRCm39) |
N33D |
possibly damaging |
Het |
Ppp1r3a |
G |
A |
6: 14,754,525 (GRCm39) |
P241S |
probably damaging |
Het |
Ppp1r9a |
A |
G |
6: 5,134,657 (GRCm39) |
T949A |
probably benign |
Het |
Prdx6 |
A |
T |
1: 161,078,619 (GRCm39) |
I23N |
probably damaging |
Het |
Prkd3 |
A |
T |
17: 79,280,003 (GRCm39) |
V334E |
probably benign |
Het |
Prr12 |
A |
T |
7: 44,684,146 (GRCm39) |
D1631E |
probably damaging |
Het |
Ptpn22 |
A |
G |
3: 103,819,551 (GRCm39) |
|
probably benign |
Het |
Pum2 |
T |
G |
12: 8,794,430 (GRCm39) |
D773E |
probably damaging |
Het |
Sidt2 |
A |
G |
9: 45,856,648 (GRCm39) |
C451R |
probably benign |
Het |
Slc37a2 |
A |
G |
9: 37,148,658 (GRCm39) |
S275P |
probably benign |
Het |
Slmap |
G |
T |
14: 26,254,519 (GRCm39) |
N54K |
probably benign |
Het |
Susd4 |
A |
G |
1: 182,681,597 (GRCm39) |
D146G |
probably benign |
Het |
Tekt3 |
G |
A |
11: 62,972,169 (GRCm39) |
R275H |
possibly damaging |
Het |
Tkfc |
A |
G |
19: 10,573,612 (GRCm39) |
L242P |
probably damaging |
Het |
Tm9sf2 |
T |
A |
14: 122,363,576 (GRCm39) |
L99I |
probably benign |
Het |
Triqk |
A |
T |
4: 12,980,490 (GRCm39) |
D78V |
probably damaging |
Het |
Trmo |
T |
C |
4: 46,382,322 (GRCm39) |
D258G |
probably benign |
Het |
Tsc2 |
A |
G |
17: 24,826,489 (GRCm39) |
V920A |
probably benign |
Het |
Tspan17 |
C |
T |
13: 54,943,991 (GRCm39) |
Q257* |
probably null |
Het |
Tube1 |
T |
A |
10: 39,011,017 (GRCm39) |
F45I |
probably damaging |
Het |
Vmn1r4 |
A |
G |
6: 56,933,822 (GRCm39) |
T109A |
possibly damaging |
Het |
Vmn2r14 |
A |
T |
5: 109,367,902 (GRCm39) |
Y363* |
probably null |
Het |
Zfp324 |
G |
T |
7: 12,705,455 (GRCm39) |
G548V |
probably benign |
Het |
Zpld2 |
C |
A |
4: 133,922,858 (GRCm39) |
V492F |
probably damaging |
Het |
|
Other mutations in Cep78 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Cep78
|
APN |
19 |
15,946,504 (GRCm39) |
missense |
probably benign |
|
IGL00920:Cep78
|
APN |
19 |
15,958,850 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01548:Cep78
|
APN |
19 |
15,958,564 (GRCm39) |
splice site |
probably benign |
|
IGL01662:Cep78
|
APN |
19 |
15,938,359 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01933:Cep78
|
APN |
19 |
15,933,304 (GRCm39) |
missense |
probably benign |
|
IGL02014:Cep78
|
APN |
19 |
15,962,102 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02198:Cep78
|
APN |
19 |
15,933,733 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02331:Cep78
|
APN |
19 |
15,951,779 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02431:Cep78
|
APN |
19 |
15,936,943 (GRCm39) |
missense |
probably benign |
|
IGL02731:Cep78
|
APN |
19 |
15,933,670 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03268:Cep78
|
APN |
19 |
15,951,806 (GRCm39) |
nonsense |
probably null |
|
IGL03338:Cep78
|
APN |
19 |
15,936,987 (GRCm39) |
missense |
probably damaging |
0.97 |
himalayas
|
UTSW |
19 |
15,946,492 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0426:Cep78
|
UTSW |
19 |
15,948,334 (GRCm39) |
nonsense |
probably null |
|
R0619:Cep78
|
UTSW |
19 |
15,956,226 (GRCm39) |
missense |
probably damaging |
0.99 |
R0659:Cep78
|
UTSW |
19 |
15,933,554 (GRCm39) |
missense |
probably damaging |
0.97 |
R1517:Cep78
|
UTSW |
19 |
15,937,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R1758:Cep78
|
UTSW |
19 |
15,936,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Cep78
|
UTSW |
19 |
15,946,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Cep78
|
UTSW |
19 |
15,933,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1920:Cep78
|
UTSW |
19 |
15,951,715 (GRCm39) |
splice site |
probably benign |
|
R2483:Cep78
|
UTSW |
19 |
15,938,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R2958:Cep78
|
UTSW |
19 |
15,956,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R3814:Cep78
|
UTSW |
19 |
15,959,166 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4133:Cep78
|
UTSW |
19 |
15,946,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R4214:Cep78
|
UTSW |
19 |
15,936,943 (GRCm39) |
missense |
probably benign |
|
R5783:Cep78
|
UTSW |
19 |
15,933,723 (GRCm39) |
missense |
probably benign |
0.02 |
R5791:Cep78
|
UTSW |
19 |
15,938,436 (GRCm39) |
missense |
probably benign |
0.19 |
R5910:Cep78
|
UTSW |
19 |
15,946,492 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5924:Cep78
|
UTSW |
19 |
15,938,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R6148:Cep78
|
UTSW |
19 |
15,959,150 (GRCm39) |
nonsense |
probably null |
|
R6162:Cep78
|
UTSW |
19 |
15,952,304 (GRCm39) |
missense |
probably benign |
0.28 |
R6235:Cep78
|
UTSW |
19 |
15,953,850 (GRCm39) |
splice site |
probably null |
|
R6968:Cep78
|
UTSW |
19 |
15,959,102 (GRCm39) |
missense |
probably benign |
0.38 |
R7228:Cep78
|
UTSW |
19 |
15,946,561 (GRCm39) |
missense |
probably benign |
0.01 |
R7913:Cep78
|
UTSW |
19 |
15,947,941 (GRCm39) |
missense |
probably benign |
|
R7914:Cep78
|
UTSW |
19 |
15,953,672 (GRCm39) |
missense |
probably benign |
0.30 |
R7934:Cep78
|
UTSW |
19 |
15,933,754 (GRCm39) |
missense |
probably damaging |
0.96 |
R8059:Cep78
|
UTSW |
19 |
15,958,876 (GRCm39) |
missense |
probably benign |
0.02 |
R8146:Cep78
|
UTSW |
19 |
15,933,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R8532:Cep78
|
UTSW |
19 |
15,936,948 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9062:Cep78
|
UTSW |
19 |
15,956,318 (GRCm39) |
missense |
probably benign |
0.23 |
R9264:Cep78
|
UTSW |
19 |
15,951,830 (GRCm39) |
missense |
probably damaging |
1.00 |
|