Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
C |
A |
11: 109,847,924 (GRCm39) |
L852F |
possibly damaging |
Het |
Abcc6 |
T |
C |
7: 45,669,558 (GRCm39) |
|
probably null |
Het |
Alg11 |
T |
G |
8: 22,555,584 (GRCm39) |
C240G |
probably damaging |
Het |
Aox1 |
A |
G |
1: 58,141,783 (GRCm39) |
I1190V |
probably damaging |
Het |
Apc2 |
T |
G |
10: 80,150,678 (GRCm39) |
S1911A |
probably benign |
Het |
Arfgef3 |
T |
C |
10: 18,528,511 (GRCm39) |
D292G |
possibly damaging |
Het |
Arhgef4 |
C |
A |
1: 34,763,340 (GRCm39) |
S865R |
probably benign |
Het |
Ass1 |
T |
A |
2: 31,383,160 (GRCm39) |
Y190* |
probably null |
Het |
B4galnt3 |
A |
T |
6: 120,187,051 (GRCm39) |
|
probably null |
Het |
Btnl10 |
C |
A |
11: 58,811,367 (GRCm39) |
P230Q |
possibly damaging |
Het |
C3 |
A |
G |
17: 57,516,489 (GRCm39) |
Y1348H |
probably damaging |
Het |
Ccdc198 |
G |
T |
14: 49,464,032 (GRCm39) |
D292E |
probably damaging |
Het |
Cebpz |
A |
T |
17: 79,242,336 (GRCm39) |
Y439* |
probably null |
Het |
Cic |
C |
A |
7: 24,986,265 (GRCm39) |
T1229K |
probably damaging |
Het |
Clip4 |
T |
C |
17: 72,144,744 (GRCm39) |
S524P |
probably damaging |
Het |
Col6a3 |
A |
C |
1: 90,739,421 (GRCm39) |
I269R |
probably damaging |
Het |
Dbh |
C |
T |
2: 27,071,506 (GRCm39) |
T533I |
possibly damaging |
Het |
Dcaf17 |
A |
T |
2: 70,890,713 (GRCm39) |
R83* |
probably null |
Het |
Dennd2b |
G |
A |
7: 109,124,533 (GRCm39) |
Q686* |
probably null |
Het |
Dnah1 |
A |
G |
14: 30,984,515 (GRCm39) |
L3923P |
probably damaging |
Het |
Dnah7a |
A |
T |
1: 53,670,721 (GRCm39) |
D510E |
probably benign |
Het |
Dock6 |
A |
G |
9: 21,752,925 (GRCm39) |
F296S |
probably damaging |
Het |
Eif4enif1 |
T |
C |
11: 3,177,455 (GRCm39) |
S341P |
probably damaging |
Het |
Epb41l1 |
G |
T |
2: 156,352,737 (GRCm39) |
G461V |
possibly damaging |
Het |
Epg5 |
T |
A |
18: 78,002,247 (GRCm39) |
D555E |
probably benign |
Het |
Fes |
T |
C |
7: 80,036,609 (GRCm39) |
R113G |
probably damaging |
Het |
Garre1 |
T |
A |
7: 33,957,461 (GRCm39) |
I59L |
probably benign |
Het |
Gm10684 |
A |
G |
9: 45,021,511 (GRCm39) |
|
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,806,231 (GRCm39) |
E320G |
probably benign |
Het |
Gm14412 |
G |
T |
2: 177,007,269 (GRCm39) |
H209N |
probably damaging |
Het |
Gm14412 |
A |
C |
2: 177,007,630 (GRCm39) |
S88R |
probably benign |
Het |
Grhl1 |
T |
A |
12: 24,658,555 (GRCm39) |
L400Q |
probably damaging |
Het |
Hephl1 |
A |
C |
9: 14,985,420 (GRCm39) |
Y745* |
probably null |
Het |
Hmcn2 |
T |
G |
2: 31,301,922 (GRCm39) |
|
probably null |
Het |
Hs3st6 |
A |
G |
17: 24,977,110 (GRCm39) |
K197E |
possibly damaging |
Het |
Ifi214 |
C |
T |
1: 173,357,077 (GRCm39) |
V9I |
probably benign |
Het |
Jakmip2 |
T |
C |
18: 43,700,209 (GRCm39) |
T450A |
probably benign |
Het |
Lrp4 |
T |
A |
2: 91,328,753 (GRCm39) |
V1551D |
possibly damaging |
Het |
Macf1 |
A |
T |
4: 123,351,634 (GRCm39) |
H1634Q |
possibly damaging |
Het |
Mcpt8 |
T |
A |
14: 56,321,291 (GRCm39) |
I58F |
probably benign |
Het |
Mga |
T |
A |
2: 119,757,075 (GRCm39) |
H1018Q |
possibly damaging |
Het |
Myo10 |
T |
A |
15: 25,801,308 (GRCm39) |
V1499E |
probably damaging |
Het |
Myom2 |
G |
T |
8: 15,131,023 (GRCm39) |
D320Y |
probably damaging |
Het |
Or11g7 |
T |
A |
14: 50,691,295 (GRCm39) |
M262K |
probably damaging |
Het |
Or13a27 |
T |
C |
7: 139,925,378 (GRCm39) |
I175V |
probably benign |
Het |
Or2r11 |
C |
T |
6: 42,437,360 (GRCm39) |
V198M |
probably benign |
Het |
Or2t26 |
A |
C |
11: 49,039,101 (GRCm39) |
N6H |
possibly damaging |
Het |
Or4c115 |
G |
A |
2: 88,927,888 (GRCm39) |
P128S |
probably damaging |
Het |
Or5d47 |
A |
T |
2: 87,804,403 (GRCm39) |
V202D |
possibly damaging |
Het |
Pabpc4 |
G |
T |
4: 123,182,861 (GRCm39) |
R166L |
possibly damaging |
Het |
Pcdhb8 |
A |
G |
18: 37,489,015 (GRCm39) |
E231G |
possibly damaging |
Het |
Pomgnt2 |
A |
T |
9: 121,811,257 (GRCm39) |
I508N |
possibly damaging |
Het |
Ppp2r5e |
C |
G |
12: 75,516,341 (GRCm39) |
A239P |
probably damaging |
Het |
Prdm15 |
G |
T |
16: 97,638,885 (GRCm39) |
D58E |
probably benign |
Het |
Rgl2 |
A |
G |
17: 34,151,122 (GRCm39) |
T117A |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,418,943 (GRCm39) |
I723T |
probably damaging |
Het |
Serpina3g |
A |
G |
12: 104,207,536 (GRCm39) |
E233G |
probably damaging |
Het |
Skint6 |
T |
A |
4: 112,749,187 (GRCm39) |
S798C |
probably benign |
Het |
Slc35f1 |
T |
C |
10: 52,898,000 (GRCm39) |
L137P |
possibly damaging |
Het |
Slc6a20a |
T |
C |
9: 123,485,373 (GRCm39) |
N246S |
probably damaging |
Het |
Slc7a2 |
T |
C |
8: 41,369,534 (GRCm39) |
L663S |
probably benign |
Het |
Slco1a4 |
A |
G |
6: 141,761,173 (GRCm39) |
|
probably null |
Het |
Slit2 |
A |
G |
5: 48,439,330 (GRCm39) |
T41A |
probably damaging |
Het |
Smc2 |
T |
C |
4: 52,450,863 (GRCm39) |
I227T |
probably damaging |
Het |
Smg1 |
A |
G |
7: 117,753,422 (GRCm39) |
|
probably benign |
Het |
Ssu2 |
A |
T |
6: 112,361,388 (GRCm39) |
L23M |
probably benign |
Het |
Syne2 |
A |
G |
12: 76,141,053 (GRCm39) |
|
probably null |
Het |
Tekt1 |
T |
C |
11: 72,242,761 (GRCm39) |
T249A |
probably benign |
Het |
Tfr2 |
T |
C |
5: 137,569,954 (GRCm39) |
V120A |
probably benign |
Het |
Thsd7b |
C |
T |
1: 129,605,846 (GRCm39) |
P529L |
probably damaging |
Het |
Tll1 |
C |
T |
8: 64,478,141 (GRCm39) |
D871N |
probably damaging |
Het |
Tlr11 |
A |
C |
14: 50,598,664 (GRCm39) |
I217L |
probably benign |
Het |
Tmem87b |
T |
A |
2: 128,673,479 (GRCm39) |
V241D |
probably damaging |
Het |
Tshz2 |
T |
A |
2: 169,727,465 (GRCm39) |
I218N |
possibly damaging |
Het |
Vmn1r18 |
A |
T |
6: 57,367,026 (GRCm39) |
I176N |
possibly damaging |
Het |
Vmn2r68 |
T |
A |
7: 84,883,260 (GRCm39) |
H164L |
probably benign |
Het |
Vmn2r74 |
T |
C |
7: 85,601,650 (GRCm39) |
T663A |
probably benign |
Het |
Vmn2r8 |
T |
C |
5: 108,945,436 (GRCm39) |
T724A |
probably benign |
Het |
Wdr11 |
T |
C |
7: 129,206,954 (GRCm39) |
V289A |
possibly damaging |
Het |
Zfp62 |
T |
A |
11: 49,107,047 (GRCm39) |
D379E |
probably damaging |
Het |
Zfp78 |
C |
T |
7: 6,381,897 (GRCm39) |
P316S |
probably damaging |
Het |
Zfyve27 |
T |
G |
19: 42,159,987 (GRCm39) |
M1R |
probably null |
Het |
Zkscan8 |
G |
A |
13: 21,709,325 (GRCm39) |
P191L |
probably damaging |
Het |
|
Other mutations in Havcr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02119:Havcr1
|
APN |
11 |
46,666,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02207:Havcr1
|
APN |
11 |
46,669,403 (GRCm39) |
missense |
probably benign |
0.28 |
R0355:Havcr1
|
UTSW |
11 |
46,647,051 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0371:Havcr1
|
UTSW |
11 |
46,643,416 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0488:Havcr1
|
UTSW |
11 |
46,643,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Havcr1
|
UTSW |
11 |
46,643,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R1307:Havcr1
|
UTSW |
11 |
46,647,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R1308:Havcr1
|
UTSW |
11 |
46,647,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R1554:Havcr1
|
UTSW |
11 |
46,643,334 (GRCm39) |
missense |
probably benign |
|
R2165:Havcr1
|
UTSW |
11 |
46,669,379 (GRCm39) |
missense |
probably benign |
0.14 |
R3085:Havcr1
|
UTSW |
11 |
46,647,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R3757:Havcr1
|
UTSW |
11 |
46,643,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Havcr1
|
UTSW |
11 |
46,643,268 (GRCm39) |
missense |
probably benign |
0.02 |
R5191:Havcr1
|
UTSW |
11 |
46,647,024 (GRCm39) |
missense |
probably benign |
0.40 |
R5440:Havcr1
|
UTSW |
11 |
46,643,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R5710:Havcr1
|
UTSW |
11 |
46,643,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5988:Havcr1
|
UTSW |
11 |
46,646,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R7570:Havcr1
|
UTSW |
11 |
46,661,369 (GRCm39) |
critical splice donor site |
probably null |
|
R7962:Havcr1
|
UTSW |
11 |
46,643,402 (GRCm39) |
nonsense |
probably null |
|
R8953:Havcr1
|
UTSW |
11 |
46,647,006 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9259:Havcr1
|
UTSW |
11 |
46,661,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R9424:Havcr1
|
UTSW |
11 |
46,669,391 (GRCm39) |
missense |
probably benign |
|
R9576:Havcr1
|
UTSW |
11 |
46,669,391 (GRCm39) |
missense |
probably benign |
|
Z1177:Havcr1
|
UTSW |
11 |
46,666,325 (GRCm39) |
missense |
probably benign |
0.25 |
|