Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
C |
A |
5: 125,592,041 (GRCm39) |
N576K |
probably benign |
Het |
Abca5 |
G |
T |
11: 110,190,804 (GRCm39) |
L769M |
probably damaging |
Het |
Abca5 |
T |
A |
11: 110,190,812 (GRCm39) |
H766L |
possibly damaging |
Het |
Acvr1c |
A |
G |
2: 58,177,896 (GRCm39) |
I191T |
probably damaging |
Het |
Agps |
A |
T |
2: 75,697,123 (GRCm39) |
E314D |
probably damaging |
Het |
Agxt |
G |
A |
1: 93,063,490 (GRCm39) |
G131R |
probably damaging |
Het |
Ak8 |
A |
G |
2: 28,632,758 (GRCm39) |
T326A |
probably benign |
Het |
Aldoart2 |
T |
A |
12: 55,613,062 (GRCm39) |
I329N |
probably benign |
Het |
Apaf1 |
T |
C |
10: 90,896,047 (GRCm39) |
I342V |
possibly damaging |
Het |
Arhgap40 |
T |
C |
2: 158,369,081 (GRCm39) |
S68P |
probably benign |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
AU022252 |
C |
T |
4: 119,085,294 (GRCm39) |
R71Q |
possibly damaging |
Het |
Baz1b |
T |
C |
5: 135,246,636 (GRCm39) |
L695P |
probably damaging |
Het |
Baz2b |
A |
T |
2: 59,792,368 (GRCm39) |
S587T |
probably benign |
Het |
Cep76 |
T |
C |
18: 67,758,028 (GRCm39) |
M421V |
probably benign |
Het |
Clk2 |
A |
G |
3: 89,076,010 (GRCm39) |
D60G |
probably damaging |
Het |
Clstn3 |
G |
T |
6: 124,439,128 (GRCm39) |
T6K |
probably damaging |
Het |
Cluap1 |
T |
A |
16: 3,737,422 (GRCm39) |
D180E |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,606,834 (GRCm39) |
I530V |
probably benign |
Het |
Cpt1a |
T |
C |
19: 3,415,788 (GRCm39) |
|
probably benign |
Het |
Cr2 |
T |
G |
1: 194,837,580 (GRCm39) |
K797Q |
possibly damaging |
Het |
Crybg3 |
C |
A |
16: 59,374,475 (GRCm39) |
V2260L |
probably benign |
Het |
Csnk1a1 |
T |
A |
18: 61,718,321 (GRCm39) |
|
probably benign |
Het |
Cxcr1 |
T |
C |
1: 74,231,929 (GRCm39) |
D31G |
probably benign |
Het |
Cyp2a5 |
G |
T |
7: 26,535,361 (GRCm39) |
D108Y |
probably damaging |
Het |
Dnajc1 |
A |
G |
2: 18,227,538 (GRCm39) |
V376A |
possibly damaging |
Het |
Eif4enif1 |
T |
C |
11: 3,186,278 (GRCm39) |
V462A |
probably benign |
Het |
Elmo1 |
A |
G |
13: 20,474,647 (GRCm39) |
K357R |
possibly damaging |
Het |
Eml6 |
T |
A |
11: 29,768,374 (GRCm39) |
H771L |
probably damaging |
Het |
Epb41l4a |
A |
G |
18: 33,965,717 (GRCm39) |
I370T |
probably benign |
Het |
Esp36 |
A |
T |
17: 38,728,172 (GRCm39) |
N79K |
possibly damaging |
Het |
Fam229b |
A |
G |
10: 38,994,915 (GRCm39) |
*81Q |
probably null |
Het |
Fat4 |
T |
C |
3: 39,037,225 (GRCm39) |
Y3626H |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,148,205 (GRCm39) |
F2681Y |
probably benign |
Het |
Gad1-ps |
A |
G |
10: 99,281,331 (GRCm39) |
|
noncoding transcript |
Het |
Galm |
C |
A |
17: 80,490,696 (GRCm39) |
N284K |
probably damaging |
Het |
Gtf3c2 |
A |
T |
5: 31,316,446 (GRCm39) |
S735T |
probably benign |
Het |
Hsph1 |
A |
T |
5: 149,553,848 (GRCm39) |
S207T |
probably benign |
Het |
Il33 |
C |
T |
19: 29,932,615 (GRCm39) |
R159C |
probably damaging |
Het |
Invs |
A |
G |
4: 48,382,148 (GRCm39) |
N106S |
possibly damaging |
Het |
Kif21b |
G |
T |
1: 136,097,062 (GRCm39) |
|
probably null |
Het |
Kirrel2 |
A |
G |
7: 30,155,923 (GRCm39) |
C42R |
probably damaging |
Het |
Letm1 |
A |
C |
5: 33,909,899 (GRCm39) |
C378W |
probably damaging |
Het |
Lrrc71 |
T |
A |
3: 87,652,791 (GRCm39) |
K160N |
probably benign |
Het |
Lrrtm3 |
A |
G |
10: 63,924,804 (GRCm39) |
I121T |
probably damaging |
Het |
Lztr1 |
T |
A |
16: 17,327,534 (GRCm39) |
V79E |
probably damaging |
Het |
Mmp8 |
T |
G |
9: 7,566,279 (GRCm39) |
D378E |
probably damaging |
Het |
Mpzl3 |
A |
G |
9: 44,977,827 (GRCm39) |
E145G |
probably damaging |
Het |
Mrps2 |
C |
T |
2: 28,359,676 (GRCm39) |
L178F |
probably damaging |
Het |
Mzb1 |
A |
G |
18: 35,780,875 (GRCm39) |
|
probably null |
Het |
Nckap1 |
T |
C |
2: 80,383,759 (GRCm39) |
D135G |
probably damaging |
Het |
Ndst1 |
A |
G |
18: 60,830,242 (GRCm39) |
F623L |
possibly damaging |
Het |
Nlrp5 |
A |
T |
7: 23,112,772 (GRCm39) |
D143V |
probably damaging |
Het |
Or14a260 |
T |
C |
7: 85,985,553 (GRCm39) |
D17G |
possibly damaging |
Het |
Or4a69 |
T |
C |
2: 89,312,592 (GRCm39) |
M296V |
probably null |
Het |
Or4b1d |
A |
G |
2: 89,968,748 (GRCm39) |
V245A |
probably benign |
Het |
Or4c120 |
A |
G |
2: 89,001,281 (GRCm39) |
S92P |
probably damaging |
Het |
Or4f58 |
A |
G |
2: 111,851,749 (GRCm39) |
V150A |
probably benign |
Het |
Or52b4i |
T |
C |
7: 102,191,332 (GRCm39) |
L63P |
probably damaging |
Het |
Or8b44 |
A |
G |
9: 38,410,114 (GRCm39) |
I50V |
probably benign |
Het |
Or8g17 |
T |
C |
9: 38,930,321 (GRCm39) |
D172G |
probably benign |
Het |
Parp14 |
T |
G |
16: 35,677,594 (GRCm39) |
E791D |
probably benign |
Het |
Pcdh8 |
C |
T |
14: 80,006,829 (GRCm39) |
R578H |
possibly damaging |
Het |
Phrf1 |
T |
A |
7: 140,839,714 (GRCm39) |
|
probably benign |
Het |
Polr3b |
C |
A |
10: 84,516,249 (GRCm39) |
H626N |
probably benign |
Het |
Ppp1r12a |
A |
G |
10: 108,087,720 (GRCm39) |
T58A |
probably benign |
Het |
Ppp4r3b |
T |
A |
11: 29,132,460 (GRCm39) |
V33D |
probably damaging |
Het |
Ppp5c |
A |
G |
7: 16,743,907 (GRCm39) |
Y176H |
probably damaging |
Het |
R3hdm1 |
A |
G |
1: 128,124,742 (GRCm39) |
Y343C |
probably damaging |
Het |
Rabac1 |
C |
T |
7: 24,671,555 (GRCm39) |
V122M |
probably damaging |
Het |
Rasef |
G |
T |
4: 73,653,985 (GRCm39) |
Q561K |
probably damaging |
Het |
Rbl1 |
A |
G |
2: 157,037,554 (GRCm39) |
S198P |
probably damaging |
Het |
Rbm12 |
A |
T |
2: 155,939,456 (GRCm39) |
M272K |
probably damaging |
Het |
Rexo1 |
T |
G |
10: 80,385,884 (GRCm39) |
K391N |
possibly damaging |
Het |
Rnf43 |
T |
C |
11: 87,622,173 (GRCm39) |
S384P |
probably benign |
Het |
Rpsa |
A |
T |
9: 119,960,066 (GRCm39) |
I210F |
possibly damaging |
Het |
Rslcan18 |
A |
G |
13: 67,247,016 (GRCm39) |
Y75H |
possibly damaging |
Het |
Scn9a |
T |
A |
2: 66,357,157 (GRCm39) |
D1048V |
probably benign |
Het |
Sec11a |
T |
C |
7: 80,577,482 (GRCm39) |
|
probably null |
Het |
Sidt2 |
A |
G |
9: 45,861,387 (GRCm39) |
V19A |
probably damaging |
Het |
Snx14 |
G |
A |
9: 88,280,417 (GRCm39) |
Q522* |
probably null |
Het |
Stx1b |
A |
G |
7: 127,414,144 (GRCm39) |
L74S |
probably damaging |
Het |
Tm7sf3 |
A |
T |
6: 146,511,376 (GRCm39) |
M371K |
probably benign |
Het |
Tmem115 |
T |
C |
9: 107,412,174 (GRCm39) |
V166A |
probably benign |
Het |
Traf5 |
T |
A |
1: 191,731,912 (GRCm39) |
T310S |
probably benign |
Het |
Trdn |
A |
G |
10: 33,342,448 (GRCm39) |
K619E |
probably benign |
Het |
Trmt10a |
T |
A |
3: 137,857,945 (GRCm39) |
|
probably null |
Het |
Txk |
A |
C |
5: 72,865,014 (GRCm39) |
I287R |
probably damaging |
Het |
Txndc16 |
T |
C |
14: 45,389,344 (GRCm39) |
D452G |
probably damaging |
Het |
Ube2f |
G |
A |
1: 91,190,023 (GRCm39) |
|
probably null |
Het |
Ubtfl1 |
T |
G |
9: 18,321,489 (GRCm39) |
I339R |
probably benign |
Het |
Upf1 |
A |
G |
8: 70,791,155 (GRCm39) |
I529T |
probably damaging |
Het |
Vmn1r197 |
A |
G |
13: 22,512,823 (GRCm39) |
D248G |
possibly damaging |
Het |
Vmn1r5 |
A |
T |
6: 56,962,771 (GRCm39) |
T149S |
probably benign |
Het |
Vmn1r83 |
C |
T |
7: 12,055,197 (GRCm39) |
V287I |
possibly damaging |
Het |
Vmn2r130 |
A |
G |
17: 23,282,775 (GRCm39) |
T152A |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,840,121 (GRCm39) |
F2448L |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,841,719 (GRCm39) |
N2583S |
probably benign |
Het |
Wscd1 |
C |
T |
11: 71,679,501 (GRCm39) |
P458L |
probably damaging |
Het |
Xylt2 |
T |
A |
11: 94,561,259 (GRCm39) |
D168V |
probably damaging |
Het |
Zdhhc2 |
A |
G |
8: 40,921,013 (GRCm39) |
T306A |
probably benign |
Het |
Zfp804b |
A |
T |
5: 6,819,771 (GRCm39) |
D1097E |
possibly damaging |
Het |
Zfp93 |
T |
A |
7: 23,975,156 (GRCm39) |
C380* |
probably null |
Het |
Zfp960 |
T |
A |
17: 17,308,518 (GRCm39) |
C411S |
probably damaging |
Het |
Zmynd15 |
T |
A |
11: 70,355,619 (GRCm39) |
V430E |
probably damaging |
Het |
|
Other mutations in Vmn2r118 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Vmn2r118
|
APN |
17 |
55,899,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00976:Vmn2r118
|
APN |
17 |
55,900,204 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01419:Vmn2r118
|
APN |
17 |
55,900,000 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01796:Vmn2r118
|
APN |
17 |
55,915,585 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01799:Vmn2r118
|
APN |
17 |
55,899,990 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02002:Vmn2r118
|
APN |
17 |
55,899,619 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02075:Vmn2r118
|
APN |
17 |
55,917,517 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02172:Vmn2r118
|
APN |
17 |
55,931,598 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02529:Vmn2r118
|
APN |
17 |
55,917,870 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02712:Vmn2r118
|
APN |
17 |
55,899,655 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03096:Vmn2r118
|
APN |
17 |
55,914,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R0306:Vmn2r118
|
UTSW |
17 |
55,915,616 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0329:Vmn2r118
|
UTSW |
17 |
55,917,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R0330:Vmn2r118
|
UTSW |
17 |
55,917,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Vmn2r118
|
UTSW |
17 |
55,915,643 (GRCm39) |
missense |
probably benign |
0.00 |
R0411:Vmn2r118
|
UTSW |
17 |
55,918,021 (GRCm39) |
splice site |
probably benign |
|
R0513:Vmn2r118
|
UTSW |
17 |
55,917,970 (GRCm39) |
nonsense |
probably null |
|
R0627:Vmn2r118
|
UTSW |
17 |
55,917,772 (GRCm39) |
missense |
probably benign |
0.01 |
R0638:Vmn2r118
|
UTSW |
17 |
55,915,466 (GRCm39) |
missense |
probably benign |
0.03 |
R1328:Vmn2r118
|
UTSW |
17 |
55,915,620 (GRCm39) |
missense |
probably benign |
0.01 |
R1366:Vmn2r118
|
UTSW |
17 |
55,900,237 (GRCm39) |
nonsense |
probably null |
|
R1465:Vmn2r118
|
UTSW |
17 |
55,917,935 (GRCm39) |
missense |
probably benign |
0.33 |
R1465:Vmn2r118
|
UTSW |
17 |
55,917,935 (GRCm39) |
missense |
probably benign |
0.33 |
R1515:Vmn2r118
|
UTSW |
17 |
55,917,643 (GRCm39) |
missense |
probably benign |
0.25 |
R1550:Vmn2r118
|
UTSW |
17 |
55,915,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Vmn2r118
|
UTSW |
17 |
55,918,530 (GRCm39) |
missense |
probably benign |
0.03 |
R1834:Vmn2r118
|
UTSW |
17 |
55,899,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Vmn2r118
|
UTSW |
17 |
55,917,406 (GRCm39) |
nonsense |
probably null |
|
R1854:Vmn2r118
|
UTSW |
17 |
55,918,556 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1967:Vmn2r118
|
UTSW |
17 |
55,899,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R1976:Vmn2r118
|
UTSW |
17 |
55,899,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R2308:Vmn2r118
|
UTSW |
17 |
55,931,650 (GRCm39) |
missense |
probably benign |
0.33 |
R3700:Vmn2r118
|
UTSW |
17 |
55,915,421 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4334:Vmn2r118
|
UTSW |
17 |
55,917,347 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4647:Vmn2r118
|
UTSW |
17 |
55,917,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R4709:Vmn2r118
|
UTSW |
17 |
55,917,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R4805:Vmn2r118
|
UTSW |
17 |
55,899,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R4858:Vmn2r118
|
UTSW |
17 |
55,899,894 (GRCm39) |
missense |
probably damaging |
0.98 |
R5384:Vmn2r118
|
UTSW |
17 |
55,918,565 (GRCm39) |
missense |
probably benign |
0.00 |
R5385:Vmn2r118
|
UTSW |
17 |
55,918,565 (GRCm39) |
missense |
probably benign |
0.00 |
R5664:Vmn2r118
|
UTSW |
17 |
55,899,765 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5740:Vmn2r118
|
UTSW |
17 |
55,900,103 (GRCm39) |
missense |
probably benign |
0.00 |
R5927:Vmn2r118
|
UTSW |
17 |
55,931,494 (GRCm39) |
missense |
probably benign |
0.04 |
R6143:Vmn2r118
|
UTSW |
17 |
55,899,871 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6513:Vmn2r118
|
UTSW |
17 |
55,915,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Vmn2r118
|
UTSW |
17 |
55,899,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R6760:Vmn2r118
|
UTSW |
17 |
55,899,714 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6794:Vmn2r118
|
UTSW |
17 |
55,899,348 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6929:Vmn2r118
|
UTSW |
17 |
55,917,440 (GRCm39) |
missense |
probably benign |
0.01 |
R7201:Vmn2r118
|
UTSW |
17 |
55,915,496 (GRCm39) |
nonsense |
probably null |
|
R7539:Vmn2r118
|
UTSW |
17 |
55,899,853 (GRCm39) |
missense |
probably damaging |
0.98 |
R7836:Vmn2r118
|
UTSW |
17 |
55,900,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R8179:Vmn2r118
|
UTSW |
17 |
55,915,484 (GRCm39) |
missense |
probably benign |
0.36 |
R8248:Vmn2r118
|
UTSW |
17 |
55,917,936 (GRCm39) |
missense |
probably benign |
0.18 |
R8347:Vmn2r118
|
UTSW |
17 |
55,917,423 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8415:Vmn2r118
|
UTSW |
17 |
55,915,057 (GRCm39) |
missense |
probably benign |
0.08 |
R8428:Vmn2r118
|
UTSW |
17 |
55,915,642 (GRCm39) |
missense |
probably benign |
0.33 |
R8917:Vmn2r118
|
UTSW |
17 |
55,917,216 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8993:Vmn2r118
|
UTSW |
17 |
55,917,835 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9038:Vmn2r118
|
UTSW |
17 |
55,918,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R9155:Vmn2r118
|
UTSW |
17 |
55,917,207 (GRCm39) |
missense |
probably null |
0.83 |
R9603:Vmn2r118
|
UTSW |
17 |
55,899,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R9742:Vmn2r118
|
UTSW |
17 |
55,918,009 (GRCm39) |
missense |
probably damaging |
0.98 |
R9749:Vmn2r118
|
UTSW |
17 |
55,915,415 (GRCm39) |
critical splice donor site |
probably null |
|
R9792:Vmn2r118
|
UTSW |
17 |
55,899,496 (GRCm39) |
missense |
probably damaging |
0.99 |
R9793:Vmn2r118
|
UTSW |
17 |
55,899,496 (GRCm39) |
missense |
probably damaging |
0.99 |
R9795:Vmn2r118
|
UTSW |
17 |
55,899,496 (GRCm39) |
missense |
probably damaging |
0.99 |
X0022:Vmn2r118
|
UTSW |
17 |
55,900,218 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Vmn2r118
|
UTSW |
17 |
55,917,655 (GRCm39) |
nonsense |
probably null |
|
|