Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
TCGACTGC |
T |
4: 53,041,570 (GRCm39) |
|
probably null |
Het |
Abca15 |
T |
C |
7: 119,945,319 (GRCm39) |
I465T |
probably damaging |
Het |
Abca3 |
C |
T |
17: 24,593,274 (GRCm39) |
R224C |
probably damaging |
Het |
Abcb4 |
T |
A |
5: 8,959,054 (GRCm39) |
|
probably null |
Het |
Acan |
T |
C |
7: 78,742,556 (GRCm39) |
|
probably null |
Het |
Aebp2 |
G |
A |
6: 140,583,456 (GRCm39) |
R109Q |
possibly damaging |
Het |
Agfg2 |
A |
T |
5: 137,658,422 (GRCm39) |
|
probably null |
Het |
Ankib1 |
T |
A |
5: 3,784,011 (GRCm39) |
I322F |
possibly damaging |
Het |
AW551984 |
A |
T |
9: 39,509,261 (GRCm39) |
N293K |
probably benign |
Het |
BC028528 |
T |
A |
3: 95,796,135 (GRCm39) |
|
probably benign |
Het |
Bicc1 |
A |
G |
10: 70,783,713 (GRCm39) |
S393P |
possibly damaging |
Het |
Birc6 |
A |
G |
17: 74,999,327 (GRCm39) |
Y4656C |
probably damaging |
Het |
Bmp3 |
A |
G |
5: 99,020,683 (GRCm39) |
R369G |
probably damaging |
Het |
C1d |
T |
A |
11: 17,216,674 (GRCm39) |
N135K |
probably benign |
Het |
Ccdc148 |
G |
A |
2: 58,717,644 (GRCm39) |
A453V |
probably damaging |
Het |
Cd163 |
C |
T |
6: 124,302,247 (GRCm39) |
T937I |
probably damaging |
Het |
Celf2 |
C |
T |
2: 6,612,658 (GRCm39) |
|
probably benign |
Het |
Chga |
T |
C |
12: 102,529,096 (GRCm39) |
W358R |
probably damaging |
Het |
Clec4b2 |
A |
T |
6: 123,177,915 (GRCm39) |
S77C |
probably null |
Het |
Crim1 |
T |
C |
17: 78,587,558 (GRCm39) |
V221A |
possibly damaging |
Het |
D630003M21Rik |
A |
T |
2: 158,059,553 (GRCm39) |
S116T |
probably damaging |
Het |
Dlg5 |
T |
C |
14: 24,186,690 (GRCm39) |
E1847G |
probably damaging |
Het |
Dmxl1 |
T |
A |
18: 50,028,194 (GRCm39) |
I2206K |
probably damaging |
Het |
Dusp7 |
T |
A |
9: 106,250,940 (GRCm39) |
L355Q |
probably damaging |
Het |
Eif1ad15 |
T |
C |
12: 88,288,071 (GRCm39) |
I61V |
probably benign |
Het |
Eif1ad16 |
A |
T |
12: 87,985,481 (GRCm39) |
S21T |
unknown |
Het |
Exd2 |
T |
A |
12: 80,543,564 (GRCm39) |
N582K |
probably damaging |
Het |
Fbln1 |
G |
A |
15: 85,121,827 (GRCm39) |
S316N |
probably damaging |
Het |
Fchsd1 |
A |
G |
18: 38,097,863 (GRCm39) |
I340T |
possibly damaging |
Het |
Fn1 |
T |
C |
1: 71,663,338 (GRCm39) |
Y1050C |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,809,773 (GRCm39) |
I2031V |
probably benign |
Het |
Gm10803 |
A |
C |
2: 93,394,517 (GRCm39) |
L96F |
probably damaging |
Het |
Gm14569 |
T |
C |
X: 35,694,470 (GRCm39) |
D1413G |
probably benign |
Het |
Gm15455 |
T |
C |
1: 33,876,432 (GRCm39) |
|
noncoding transcript |
Het |
Gm1818 |
G |
C |
12: 48,602,318 (GRCm39) |
|
noncoding transcript |
Het |
Gm5420 |
A |
T |
10: 21,567,626 (GRCm39) |
|
noncoding transcript |
Het |
Gm7104 |
A |
T |
12: 88,252,529 (GRCm39) |
|
noncoding transcript |
Het |
Gp2 |
A |
G |
7: 119,048,337 (GRCm39) |
I427T |
probably damaging |
Het |
Gpc4 |
G |
A |
X: 51,163,440 (GRCm39) |
R148C |
probably damaging |
Het |
Gpr142 |
A |
C |
11: 114,695,214 (GRCm39) |
S60R |
probably benign |
Het |
Helz2 |
T |
C |
2: 180,882,362 (GRCm39) |
R144G |
probably benign |
Het |
Herc1 |
A |
T |
9: 66,377,608 (GRCm39) |
K3458M |
possibly damaging |
Het |
Hnf4g |
G |
T |
3: 3,709,647 (GRCm39) |
A144S |
probably damaging |
Het |
Irs2 |
A |
C |
8: 11,037,012 (GRCm39) |
*1322G |
probably null |
Het |
Keg1 |
A |
G |
19: 12,696,521 (GRCm39) |
N288S |
probably damaging |
Het |
Kif19a |
G |
A |
11: 114,658,053 (GRCm39) |
M37I |
probably benign |
Het |
Klhl1 |
G |
A |
14: 96,374,142 (GRCm39) |
P635S |
probably benign |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Lsm11 |
T |
C |
11: 45,835,666 (GRCm39) |
D25G |
probably damaging |
Het |
Manea |
A |
T |
4: 26,336,630 (GRCm39) |
Y215* |
probably null |
Het |
Mdga2 |
C |
T |
12: 66,517,534 (GRCm39) |
C100Y |
possibly damaging |
Het |
Mthfd1 |
T |
A |
12: 76,348,102 (GRCm39) |
M582K |
probably damaging |
Het |
Mthfd1 |
T |
G |
12: 76,341,148 (GRCm39) |
V480G |
probably damaging |
Het |
Myh7b |
G |
C |
2: 155,474,293 (GRCm39) |
R1669S |
possibly damaging |
Het |
Nanos1 |
T |
C |
19: 60,745,418 (GRCm39) |
Y239H |
probably damaging |
Het |
Nat8 |
G |
A |
6: 85,807,839 (GRCm39) |
T98I |
possibly damaging |
Het |
Ndufs3 |
C |
A |
2: 90,729,004 (GRCm39) |
A161S |
probably benign |
Het |
Nexmif |
A |
T |
X: 103,130,956 (GRCm39) |
N320K |
probably damaging |
Het |
Or10h1 |
T |
C |
17: 33,418,751 (GRCm39) |
F239S |
probably damaging |
Het |
Or2m12 |
A |
T |
16: 19,104,809 (GRCm39) |
V228D |
probably damaging |
Het |
Or2r3 |
A |
T |
6: 42,448,221 (GRCm39) |
V297E |
possibly damaging |
Het |
Or4c111 |
A |
G |
2: 88,844,387 (GRCm39) |
V7A |
probably damaging |
Het |
Or4c122 |
C |
T |
2: 89,079,761 (GRCm39) |
M92I |
probably benign |
Het |
Or4k15 |
T |
C |
14: 50,364,469 (GRCm39) |
V145A |
possibly damaging |
Het |
Or52e2 |
G |
A |
7: 102,804,942 (GRCm39) |
P4L |
probably benign |
Het |
Or6c69c |
T |
C |
10: 129,910,462 (GRCm39) |
L61P |
probably damaging |
Het |
Pcdhb14 |
T |
A |
18: 37,583,223 (GRCm39) |
N776K |
probably benign |
Het |
Pip5k1c |
G |
A |
10: 81,146,723 (GRCm39) |
|
probably null |
Het |
Plk4 |
G |
A |
3: 40,756,512 (GRCm39) |
|
probably null |
Het |
Prmt8 |
A |
G |
6: 127,688,126 (GRCm39) |
Y231H |
possibly damaging |
Het |
Prpf4b |
T |
C |
13: 35,067,582 (GRCm39) |
|
probably benign |
Het |
Ptpn21 |
G |
A |
12: 98,645,666 (GRCm39) |
R1091C |
probably damaging |
Het |
Pwwp2b |
C |
T |
7: 138,835,494 (GRCm39) |
P312S |
possibly damaging |
Het |
Rad21 |
A |
T |
15: 51,830,102 (GRCm39) |
I503K |
probably benign |
Het |
Rai14 |
A |
G |
15: 10,574,592 (GRCm39) |
S789P |
probably damaging |
Het |
Rbm26 |
C |
T |
14: 105,381,688 (GRCm39) |
D486N |
probably damaging |
Het |
Rnf20 |
A |
G |
4: 49,642,016 (GRCm39) |
|
probably benign |
Het |
Ros1 |
A |
G |
10: 52,000,171 (GRCm39) |
V1118A |
possibly damaging |
Het |
Sema3d |
A |
C |
5: 12,634,923 (GRCm39) |
Y663S |
probably damaging |
Het |
Serpina6 |
A |
G |
12: 103,617,971 (GRCm39) |
W281R |
probably damaging |
Het |
Slc8a3 |
A |
G |
12: 81,246,332 (GRCm39) |
V900A |
probably damaging |
Het |
Spats2l |
G |
T |
1: 57,918,715 (GRCm39) |
V30L |
probably damaging |
Het |
Spg21 |
A |
G |
9: 65,383,231 (GRCm39) |
D139G |
probably damaging |
Het |
Sun3 |
T |
C |
11: 8,988,314 (GRCm39) |
T3A |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,066,456 (GRCm39) |
Y2335H |
probably benign |
Het |
Tesl1 |
G |
A |
X: 23,773,480 (GRCm39) |
G327E |
probably damaging |
Het |
Timd5 |
T |
A |
11: 46,419,359 (GRCm39) |
D58E |
probably damaging |
Het |
Timm21 |
C |
A |
18: 84,967,539 (GRCm39) |
V112L |
possibly damaging |
Het |
Tlk1 |
A |
T |
2: 70,572,409 (GRCm39) |
N386K |
probably benign |
Het |
Trappc10 |
G |
T |
10: 78,052,994 (GRCm39) |
F260L |
possibly damaging |
Het |
Trgv1 |
T |
A |
13: 19,524,401 (GRCm39) |
S42T |
probably benign |
Het |
Trmt112 |
T |
C |
19: 6,888,121 (GRCm39) |
V91A |
probably benign |
Het |
Ucp2 |
A |
T |
7: 100,147,579 (GRCm39) |
N186I |
possibly damaging |
Het |
Vmn1r119 |
A |
G |
7: 20,746,245 (GRCm39) |
S46P |
probably benign |
Het |
Vmn2r101 |
A |
T |
17: 19,831,649 (GRCm39) |
|
probably null |
Het |
Vmn2r69 |
T |
C |
7: 85,060,367 (GRCm39) |
M406V |
possibly damaging |
Het |
Vmn2r84 |
A |
G |
10: 130,222,417 (GRCm39) |
L601P |
probably damaging |
Het |
Vps16 |
A |
G |
2: 130,281,372 (GRCm39) |
S235G |
probably benign |
Het |
Wap |
T |
C |
11: 6,587,339 (GRCm39) |
|
probably benign |
Het |
Wdr11 |
A |
G |
7: 129,226,435 (GRCm39) |
I744M |
probably benign |
Het |
Xiap |
T |
C |
X: 41,183,342 (GRCm39) |
F23L |
probably benign |
Het |
Xkr7 |
A |
G |
2: 152,896,300 (GRCm39) |
T385A |
probably benign |
Het |
Zfp524 |
A |
T |
7: 5,021,416 (GRCm39) |
I315F |
probably benign |
Het |
Zfp62 |
T |
A |
11: 49,106,556 (GRCm39) |
S216T |
probably damaging |
Het |
Znfx1 |
T |
C |
2: 166,881,746 (GRCm39) |
Y217C |
probably damaging |
Het |
|
Other mutations in Vmn2r105 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01433:Vmn2r105
|
APN |
17 |
20,448,817 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01909:Vmn2r105
|
APN |
17 |
20,444,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01925:Vmn2r105
|
APN |
17 |
20,428,973 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02021:Vmn2r105
|
APN |
17 |
20,448,157 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02828:Vmn2r105
|
APN |
17 |
20,429,345 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02838:Vmn2r105
|
APN |
17 |
20,447,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03343:Vmn2r105
|
APN |
17 |
20,446,631 (GRCm39) |
nonsense |
probably null |
|
R0096:Vmn2r105
|
UTSW |
17 |
20,447,741 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0096:Vmn2r105
|
UTSW |
17 |
20,447,741 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0212:Vmn2r105
|
UTSW |
17 |
20,428,827 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0268:Vmn2r105
|
UTSW |
17 |
20,428,938 (GRCm39) |
missense |
probably benign |
0.18 |
R0271:Vmn2r105
|
UTSW |
17 |
20,454,965 (GRCm39) |
missense |
probably damaging |
0.96 |
R0613:Vmn2r105
|
UTSW |
17 |
20,428,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R0765:Vmn2r105
|
UTSW |
17 |
20,448,119 (GRCm39) |
missense |
probably damaging |
0.98 |
R0765:Vmn2r105
|
UTSW |
17 |
20,447,973 (GRCm39) |
missense |
probably benign |
0.20 |
R1162:Vmn2r105
|
UTSW |
17 |
20,447,973 (GRCm39) |
missense |
probably benign |
0.20 |
R1263:Vmn2r105
|
UTSW |
17 |
20,428,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R1363:Vmn2r105
|
UTSW |
17 |
20,428,932 (GRCm39) |
missense |
probably benign |
0.00 |
R1464:Vmn2r105
|
UTSW |
17 |
20,449,004 (GRCm39) |
splice site |
probably benign |
|
R2029:Vmn2r105
|
UTSW |
17 |
20,444,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R2420:Vmn2r105
|
UTSW |
17 |
20,448,097 (GRCm39) |
missense |
probably benign |
0.15 |
R2421:Vmn2r105
|
UTSW |
17 |
20,448,097 (GRCm39) |
missense |
probably benign |
0.15 |
R2422:Vmn2r105
|
UTSW |
17 |
20,448,097 (GRCm39) |
missense |
probably benign |
0.15 |
R2570:Vmn2r105
|
UTSW |
17 |
20,447,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R3847:Vmn2r105
|
UTSW |
17 |
20,428,952 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3848:Vmn2r105
|
UTSW |
17 |
20,428,952 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4030:Vmn2r105
|
UTSW |
17 |
20,429,016 (GRCm39) |
missense |
probably damaging |
0.99 |
R4275:Vmn2r105
|
UTSW |
17 |
20,448,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R4551:Vmn2r105
|
UTSW |
17 |
20,446,613 (GRCm39) |
missense |
probably benign |
|
R4801:Vmn2r105
|
UTSW |
17 |
20,447,556 (GRCm39) |
missense |
probably benign |
0.00 |
R4802:Vmn2r105
|
UTSW |
17 |
20,447,556 (GRCm39) |
missense |
probably benign |
0.00 |
R4816:Vmn2r105
|
UTSW |
17 |
20,428,953 (GRCm39) |
missense |
probably benign |
0.27 |
R4929:Vmn2r105
|
UTSW |
17 |
20,448,280 (GRCm39) |
missense |
probably benign |
0.44 |
R5475:Vmn2r105
|
UTSW |
17 |
20,455,044 (GRCm39) |
missense |
probably benign |
|
R5576:Vmn2r105
|
UTSW |
17 |
20,444,836 (GRCm39) |
critical splice donor site |
probably null |
|
R5795:Vmn2r105
|
UTSW |
17 |
20,448,998 (GRCm39) |
missense |
probably benign |
0.00 |
R5895:Vmn2r105
|
UTSW |
17 |
20,448,929 (GRCm39) |
missense |
probably benign |
0.10 |
R6017:Vmn2r105
|
UTSW |
17 |
20,428,889 (GRCm39) |
missense |
probably damaging |
0.97 |
R6210:Vmn2r105
|
UTSW |
17 |
20,448,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R6491:Vmn2r105
|
UTSW |
17 |
20,447,992 (GRCm39) |
nonsense |
probably null |
|
R6542:Vmn2r105
|
UTSW |
17 |
20,448,803 (GRCm39) |
missense |
probably benign |
0.03 |
R6729:Vmn2r105
|
UTSW |
17 |
20,428,605 (GRCm39) |
missense |
probably damaging |
0.99 |
R7020:Vmn2r105
|
UTSW |
17 |
20,429,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Vmn2r105
|
UTSW |
17 |
20,428,874 (GRCm39) |
missense |
probably damaging |
0.97 |
R7488:Vmn2r105
|
UTSW |
17 |
20,429,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7491:Vmn2r105
|
UTSW |
17 |
20,448,827 (GRCm39) |
missense |
probably benign |
0.02 |
R7555:Vmn2r105
|
UTSW |
17 |
20,447,937 (GRCm39) |
missense |
probably damaging |
0.98 |
R7863:Vmn2r105
|
UTSW |
17 |
20,428,937 (GRCm39) |
missense |
probably benign |
0.18 |
R8137:Vmn2r105
|
UTSW |
17 |
20,454,966 (GRCm39) |
missense |
probably benign |
0.02 |
R8166:Vmn2r105
|
UTSW |
17 |
20,428,904 (GRCm39) |
missense |
probably benign |
0.07 |
R8186:Vmn2r105
|
UTSW |
17 |
20,444,880 (GRCm39) |
nonsense |
probably null |
|
R8214:Vmn2r105
|
UTSW |
17 |
20,448,775 (GRCm39) |
missense |
probably benign |
0.02 |
R8497:Vmn2r105
|
UTSW |
17 |
20,455,134 (GRCm39) |
start codon destroyed |
probably null |
0.75 |
R8850:Vmn2r105
|
UTSW |
17 |
20,428,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R8880:Vmn2r105
|
UTSW |
17 |
20,429,229 (GRCm39) |
missense |
probably damaging |
0.99 |
R9272:Vmn2r105
|
UTSW |
17 |
20,447,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R9506:Vmn2r105
|
UTSW |
17 |
20,429,404 (GRCm39) |
missense |
probably benign |
0.00 |
R9549:Vmn2r105
|
UTSW |
17 |
20,448,023 (GRCm39) |
missense |
probably benign |
0.12 |
|