Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933412E24Rik |
T |
C |
15: 59,888,425 (GRCm39) |
E5G |
probably benign |
Het |
Adam23 |
T |
C |
1: 63,567,957 (GRCm39) |
V202A |
noncoding transcript |
Het |
Adamtsl1 |
A |
C |
4: 86,195,120 (GRCm39) |
E512D |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,982,817 (GRCm39) |
D1367V |
probably damaging |
Het |
Angpt4 |
A |
T |
2: 151,769,084 (GRCm39) |
Q198L |
probably benign |
Het |
Apcdd1 |
T |
A |
18: 63,066,974 (GRCm39) |
H29Q |
possibly damaging |
Het |
Cdh16 |
T |
A |
8: 105,341,811 (GRCm39) |
K755* |
probably null |
Het |
Cdk6 |
T |
G |
5: 3,440,685 (GRCm39) |
F80V |
probably benign |
Het |
Chd1 |
T |
C |
17: 17,607,804 (GRCm39) |
S451P |
probably benign |
Het |
Chd6 |
A |
G |
2: 160,799,002 (GRCm39) |
L2361P |
probably damaging |
Het |
Chst8 |
A |
G |
7: 34,447,579 (GRCm39) |
M13T |
possibly damaging |
Het |
Cntnap2 |
T |
C |
6: 47,072,627 (GRCm39) |
L1065P |
probably damaging |
Het |
Dctn4 |
T |
C |
18: 60,659,343 (GRCm39) |
V14A |
possibly damaging |
Het |
Dicer1 |
A |
T |
12: 104,657,865 (GRCm39) |
V1903D |
probably damaging |
Het |
E2f2 |
A |
G |
4: 135,911,791 (GRCm39) |
|
silent |
Het |
Eif4g3 |
T |
A |
4: 137,898,429 (GRCm39) |
S902T |
possibly damaging |
Het |
Emid1 |
G |
T |
11: 5,084,353 (GRCm39) |
A152D |
probably benign |
Het |
Fer1l6 |
T |
A |
15: 58,432,345 (GRCm39) |
N297K |
possibly damaging |
Het |
Fes |
T |
C |
7: 80,032,902 (GRCm39) |
D281G |
probably null |
Het |
Frmpd2 |
T |
C |
14: 33,224,934 (GRCm39) |
V133A |
probably benign |
Het |
Fry |
A |
G |
5: 150,369,372 (GRCm39) |
Y2282C |
probably damaging |
Het |
Gm10377 |
C |
T |
14: 42,616,664 (GRCm39) |
|
probably null |
Het |
Gm1527 |
A |
G |
3: 28,974,749 (GRCm39) |
T521A |
probably damaging |
Het |
Gpr141 |
T |
A |
13: 19,936,013 (GRCm39) |
H254L |
probably benign |
Het |
Gpr160 |
A |
G |
3: 30,950,096 (GRCm39) |
E56G |
probably benign |
Het |
Grid2ip |
T |
G |
5: 143,367,695 (GRCm39) |
|
probably null |
Het |
Grin2a |
A |
G |
16: 9,481,382 (GRCm39) |
F473S |
probably damaging |
Het |
Igkv1-131 |
T |
C |
6: 67,743,102 (GRCm39) |
T94A |
probably damaging |
Het |
Inava |
T |
A |
1: 136,153,215 (GRCm39) |
N226Y |
probably damaging |
Het |
Iqgap2 |
A |
G |
13: 95,772,078 (GRCm39) |
L1367P |
probably damaging |
Het |
Kirrel1 |
T |
C |
3: 86,995,309 (GRCm39) |
|
probably benign |
Het |
Lad1 |
T |
C |
1: 135,755,500 (GRCm39) |
S259P |
probably damaging |
Het |
Lalba |
A |
T |
15: 98,379,992 (GRCm39) |
F86Y |
possibly damaging |
Het |
Lrfn5 |
G |
A |
12: 61,886,323 (GRCm39) |
C37Y |
probably damaging |
Het |
Man2c1 |
A |
G |
9: 57,046,942 (GRCm39) |
T665A |
probably benign |
Het |
Ms4a20 |
T |
A |
19: 11,087,707 (GRCm39) |
S75C |
probably damaging |
Het |
Myh11 |
T |
C |
16: 14,041,867 (GRCm39) |
I719V |
|
Het |
Nbl1 |
A |
T |
4: 138,812,832 (GRCm39) |
C34S |
probably damaging |
Het |
Ncapg |
T |
A |
5: 45,844,730 (GRCm39) |
I575N |
possibly damaging |
Het |
Nlgn1 |
T |
C |
3: 25,487,816 (GRCm39) |
T840A |
possibly damaging |
Het |
Nrdc |
T |
C |
4: 108,873,876 (GRCm39) |
S231P |
possibly damaging |
Het |
Nrg2 |
T |
C |
18: 36,165,428 (GRCm39) |
K395E |
probably benign |
Het |
Nrip1 |
A |
T |
16: 76,088,949 (GRCm39) |
N869K |
possibly damaging |
Het |
Or2a14 |
T |
A |
6: 43,130,242 (GRCm39) |
M1K |
probably null |
Het |
Or4c12 |
A |
G |
2: 89,773,716 (GRCm39) |
F248L |
probably benign |
Het |
Or8s16 |
A |
T |
15: 98,210,546 (GRCm39) |
M295K |
probably benign |
Het |
Otub2 |
G |
T |
12: 103,369,161 (GRCm39) |
|
probably null |
Het |
Paxbp1 |
T |
C |
16: 90,834,303 (GRCm39) |
D161G |
probably benign |
Het |
Pcnx3 |
C |
T |
19: 5,715,412 (GRCm39) |
G1946E |
probably damaging |
Het |
Per2 |
T |
A |
1: 91,361,170 (GRCm39) |
Q495L |
possibly damaging |
Het |
Plxna2 |
T |
A |
1: 194,431,724 (GRCm39) |
V571E |
probably damaging |
Het |
Prr7 |
C |
A |
13: 55,620,735 (GRCm39) |
P248T |
possibly damaging |
Het |
Ptprr |
A |
T |
10: 116,073,169 (GRCm39) |
T464S |
possibly damaging |
Het |
Rapgef2 |
A |
G |
3: 78,993,325 (GRCm39) |
V721A |
probably benign |
Het |
Rfx1 |
A |
T |
8: 84,819,479 (GRCm39) |
Y625F |
probably benign |
Het |
Rps6kb2 |
G |
T |
19: 4,211,195 (GRCm39) |
A110D |
possibly damaging |
Het |
Setdb2 |
A |
T |
14: 59,651,141 (GRCm39) |
|
probably benign |
Het |
Slc25a31 |
T |
C |
3: 40,679,351 (GRCm39) |
I272T |
probably damaging |
Het |
Smpd1 |
T |
C |
7: 105,204,520 (GRCm39) |
V133A |
probably benign |
Het |
Sorl1 |
T |
C |
9: 41,925,777 (GRCm39) |
D1185G |
probably damaging |
Het |
Spag6 |
T |
A |
2: 18,750,301 (GRCm39) |
L449H |
probably benign |
Het |
Sptb |
C |
A |
12: 76,668,036 (GRCm39) |
R687L |
probably benign |
Het |
Sptbn5 |
A |
T |
2: 119,877,616 (GRCm39) |
V1012E |
noncoding transcript |
Het |
Tmem192 |
A |
G |
8: 65,416,972 (GRCm39) |
I188V |
probably benign |
Het |
Tmem253 |
G |
A |
14: 52,256,708 (GRCm39) |
V194M |
probably benign |
Het |
Tph1 |
A |
G |
7: 46,303,173 (GRCm39) |
|
silent |
Het |
Trak1 |
A |
G |
9: 121,280,733 (GRCm39) |
E374G |
probably damaging |
Het |
Trpv1 |
A |
T |
11: 73,145,593 (GRCm39) |
|
probably null |
Het |
Trub2 |
T |
C |
2: 29,667,725 (GRCm39) |
H305R |
probably benign |
Het |
Ttn |
A |
G |
2: 76,747,768 (GRCm39) |
V4427A |
probably benign |
Het |
Vasn |
A |
G |
16: 4,466,160 (GRCm39) |
T36A |
probably damaging |
Het |
Vmn1r8 |
A |
T |
6: 57,013,158 (GRCm39) |
I70F |
probably benign |
Het |
Vps13c |
A |
T |
9: 67,862,262 (GRCm39) |
I2960L |
probably damaging |
Het |
Zdhhc4 |
C |
A |
5: 143,307,588 (GRCm39) |
M144I |
probably benign |
Het |
Zfp273 |
T |
A |
13: 67,974,070 (GRCm39) |
N399K |
probably benign |
Het |
Zfp976 |
T |
A |
7: 42,262,125 (GRCm39) |
T572S |
unknown |
Het |
Zmym4 |
A |
G |
4: 126,798,360 (GRCm39) |
C756R |
probably damaging |
Het |
|
Other mutations in Kdm5d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0013:Kdm5d
|
UTSW |
Y |
941,715 (GRCm39) |
missense |
probably benign |
0.37 |
R0013:Kdm5d
|
UTSW |
Y |
941,715 (GRCm39) |
missense |
probably benign |
0.37 |
R0426:Kdm5d
|
UTSW |
Y |
942,437 (GRCm39) |
splice site |
probably benign |
|
R0486:Kdm5d
|
UTSW |
Y |
927,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R0620:Kdm5d
|
UTSW |
Y |
927,330 (GRCm39) |
missense |
probably damaging |
0.98 |
R0781:Kdm5d
|
UTSW |
Y |
910,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R1015:Kdm5d
|
UTSW |
Y |
941,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1110:Kdm5d
|
UTSW |
Y |
910,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R1163:Kdm5d
|
UTSW |
Y |
898,029 (GRCm39) |
missense |
probably benign |
0.18 |
R1203:Kdm5d
|
UTSW |
Y |
941,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R1238:Kdm5d
|
UTSW |
Y |
941,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R1723:Kdm5d
|
UTSW |
Y |
927,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R1842:Kdm5d
|
UTSW |
Y |
927,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R1885:Kdm5d
|
UTSW |
Y |
940,781 (GRCm39) |
splice site |
probably null |
|
R2131:Kdm5d
|
UTSW |
Y |
941,483 (GRCm39) |
missense |
probably benign |
0.02 |
R2571:Kdm5d
|
UTSW |
Y |
940,932 (GRCm39) |
missense |
probably benign |
0.11 |
R2931:Kdm5d
|
UTSW |
Y |
942,992 (GRCm39) |
missense |
probably benign |
0.18 |
R3123:Kdm5d
|
UTSW |
Y |
900,558 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3919:Kdm5d
|
UTSW |
Y |
939,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R4018:Kdm5d
|
UTSW |
Y |
910,441 (GRCm39) |
splice site |
probably benign |
|
R4031:Kdm5d
|
UTSW |
Y |
916,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R4403:Kdm5d
|
UTSW |
Y |
899,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R4571:Kdm5d
|
UTSW |
Y |
927,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R4583:Kdm5d
|
UTSW |
Y |
914,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Kdm5d
|
UTSW |
Y |
940,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R5105:Kdm5d
|
UTSW |
Y |
941,752 (GRCm39) |
missense |
probably benign |
0.00 |
R5249:Kdm5d
|
UTSW |
Y |
916,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R5367:Kdm5d
|
UTSW |
Y |
941,645 (GRCm39) |
missense |
probably benign |
0.05 |
R5373:Kdm5d
|
UTSW |
Y |
927,995 (GRCm39) |
missense |
probably benign |
0.09 |
R5374:Kdm5d
|
UTSW |
Y |
927,995 (GRCm39) |
missense |
probably benign |
0.09 |
R5876:Kdm5d
|
UTSW |
Y |
900,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R5909:Kdm5d
|
UTSW |
Y |
941,306 (GRCm39) |
missense |
probably benign |
0.01 |
R6014:Kdm5d
|
UTSW |
Y |
921,528 (GRCm39) |
missense |
probably benign |
0.45 |
R6109:Kdm5d
|
UTSW |
Y |
921,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Kdm5d
|
UTSW |
Y |
921,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R6349:Kdm5d
|
UTSW |
Y |
916,847 (GRCm39) |
missense |
probably damaging |
0.99 |
R6450:Kdm5d
|
UTSW |
Y |
927,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R6595:Kdm5d
|
UTSW |
Y |
939,829 (GRCm39) |
missense |
probably benign |
|
R6628:Kdm5d
|
UTSW |
Y |
900,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R6745:Kdm5d
|
UTSW |
Y |
927,112 (GRCm39) |
missense |
probably benign |
0.28 |
R6867:Kdm5d
|
UTSW |
Y |
927,425 (GRCm39) |
missense |
probably benign |
|
R6963:Kdm5d
|
UTSW |
Y |
937,975 (GRCm39) |
missense |
probably benign |
0.01 |
R7163:Kdm5d
|
UTSW |
Y |
899,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R7374:Kdm5d
|
UTSW |
Y |
941,491 (GRCm39) |
missense |
probably benign |
0.41 |
R7483:Kdm5d
|
UTSW |
Y |
914,044 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7501:Kdm5d
|
UTSW |
Y |
941,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R7815:Kdm5d
|
UTSW |
Y |
940,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R7835:Kdm5d
|
UTSW |
Y |
900,558 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8057:Kdm5d
|
UTSW |
Y |
927,355 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8080:Kdm5d
|
UTSW |
Y |
910,742 (GRCm39) |
missense |
probably benign |
0.01 |
R8130:Kdm5d
|
UTSW |
Y |
940,658 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8213:Kdm5d
|
UTSW |
Y |
941,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R8344:Kdm5d
|
UTSW |
Y |
942,477 (GRCm39) |
missense |
probably benign |
0.05 |
R8348:Kdm5d
|
UTSW |
Y |
914,056 (GRCm39) |
missense |
probably benign |
0.00 |
R8445:Kdm5d
|
UTSW |
Y |
916,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R8448:Kdm5d
|
UTSW |
Y |
914,056 (GRCm39) |
missense |
probably benign |
0.00 |
R8754:Kdm5d
|
UTSW |
Y |
941,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R9203:Kdm5d
|
UTSW |
Y |
940,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R9259:Kdm5d
|
UTSW |
Y |
942,640 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9541:Kdm5d
|
UTSW |
Y |
910,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R9668:Kdm5d
|
UTSW |
Y |
943,075 (GRCm39) |
missense |
possibly damaging |
0.73 |
|