Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
A |
T |
16: 4,682,200 (GRCm39) |
H1010L |
probably benign |
Het |
A2ml1 |
C |
A |
6: 128,545,706 (GRCm39) |
E474* |
probably null |
Het |
Agtr1b |
T |
C |
3: 20,369,838 (GRCm39) |
H256R |
probably damaging |
Het |
Amacr |
C |
T |
15: 10,982,032 (GRCm39) |
A46V |
possibly damaging |
Het |
Atosb |
A |
T |
4: 43,034,647 (GRCm39) |
|
probably benign |
Het |
Cabp5 |
A |
T |
7: 13,135,260 (GRCm39) |
M67L |
probably damaging |
Het |
Caskin2 |
T |
C |
11: 115,691,842 (GRCm39) |
E981G |
probably damaging |
Het |
Ccdc88a |
A |
G |
11: 29,411,042 (GRCm39) |
|
probably benign |
Het |
Cd180 |
A |
G |
13: 102,839,382 (GRCm39) |
|
probably benign |
Het |
Cd200l1 |
T |
A |
16: 45,264,536 (GRCm39) |
|
probably benign |
Het |
Cemip |
G |
A |
7: 83,613,318 (GRCm39) |
H627Y |
probably damaging |
Het |
Cep131 |
G |
T |
11: 119,964,588 (GRCm39) |
H289Q |
probably damaging |
Het |
Cep350 |
G |
A |
1: 155,836,941 (GRCm39) |
|
probably benign |
Het |
Cfap52 |
A |
T |
11: 67,840,425 (GRCm39) |
C169S |
probably benign |
Het |
Cps1 |
A |
T |
1: 67,205,608 (GRCm39) |
T544S |
possibly damaging |
Het |
Cul7 |
T |
C |
17: 46,962,929 (GRCm39) |
S187P |
probably damaging |
Het |
Dhx40 |
C |
A |
11: 86,661,993 (GRCm39) |
R688L |
probably damaging |
Het |
E330034G19Rik |
C |
A |
14: 24,356,985 (GRCm39) |
Q174K |
probably benign |
Het |
Efna5 |
T |
C |
17: 63,188,031 (GRCm39) |
Y32C |
probably damaging |
Het |
Ethe1 |
A |
G |
7: 24,307,314 (GRCm39) |
H176R |
probably benign |
Het |
Exoc3 |
A |
G |
13: 74,330,394 (GRCm39) |
|
probably null |
Het |
Fam135b |
T |
A |
15: 71,362,686 (GRCm39) |
N232Y |
possibly damaging |
Het |
Fndc9 |
C |
T |
11: 46,128,984 (GRCm39) |
L168F |
probably damaging |
Het |
Fpr-rs3 |
G |
A |
17: 20,844,283 (GRCm39) |
A286V |
probably damaging |
Het |
Immt |
T |
A |
6: 71,823,467 (GRCm39) |
|
probably benign |
Het |
Ipo7 |
T |
C |
7: 109,648,800 (GRCm39) |
|
probably benign |
Het |
Ipo8 |
A |
T |
6: 148,688,221 (GRCm39) |
L747H |
probably damaging |
Het |
Ireb2 |
A |
T |
9: 54,807,267 (GRCm39) |
N610Y |
probably damaging |
Het |
Irs2 |
A |
G |
8: 11,054,592 (GRCm39) |
V1280A |
probably damaging |
Het |
Kcnj3 |
T |
A |
2: 55,485,276 (GRCm39) |
M458K |
probably benign |
Het |
Kl |
A |
G |
5: 150,904,409 (GRCm39) |
K387R |
possibly damaging |
Het |
L3mbtl2 |
C |
A |
15: 81,568,487 (GRCm39) |
|
probably benign |
Het |
Lamb1 |
A |
C |
12: 31,348,914 (GRCm39) |
I649L |
probably benign |
Het |
Lipm |
A |
C |
19: 34,093,906 (GRCm39) |
L274F |
probably benign |
Het |
Lrfn3 |
A |
G |
7: 30,060,216 (GRCm39) |
V3A |
probably benign |
Het |
Lrrc8c |
A |
C |
5: 105,754,894 (GRCm39) |
D223A |
probably damaging |
Het |
Ltn1 |
C |
A |
16: 87,212,898 (GRCm39) |
K554N |
probably benign |
Het |
Mertk |
T |
C |
2: 128,613,403 (GRCm39) |
I473T |
probably benign |
Het |
Mfsd12 |
C |
A |
10: 81,197,243 (GRCm39) |
N245K |
probably benign |
Het |
Mmp16 |
A |
G |
4: 17,987,705 (GRCm39) |
D89G |
probably damaging |
Het |
Myo5a |
T |
A |
9: 75,087,394 (GRCm39) |
N1083K |
probably benign |
Het |
Ncapd3 |
C |
T |
9: 26,999,294 (GRCm39) |
A1290V |
probably benign |
Het |
Nefm |
A |
G |
14: 68,362,070 (GRCm39) |
S65P |
probably damaging |
Het |
Nt5c2 |
C |
T |
19: 46,886,064 (GRCm39) |
R220H |
probably damaging |
Het |
Or4c102 |
T |
A |
2: 88,422,353 (GRCm39) |
D68E |
probably benign |
Het |
Osbpl1a |
A |
T |
18: 12,892,501 (GRCm39) |
S438R |
probably damaging |
Het |
Pcdhb5 |
T |
C |
18: 37,453,820 (GRCm39) |
S67P |
possibly damaging |
Het |
Per3 |
A |
T |
4: 151,118,409 (GRCm39) |
I228N |
probably damaging |
Het |
Pnpla7 |
T |
G |
2: 24,870,129 (GRCm39) |
|
probably benign |
Het |
Ppp1r15b |
G |
T |
1: 133,064,391 (GRCm39) |
|
probably benign |
Het |
Psmd2 |
G |
T |
16: 20,479,176 (GRCm39) |
L678F |
probably null |
Het |
Ptch2 |
A |
G |
4: 116,963,340 (GRCm39) |
|
probably benign |
Het |
Ranbp2 |
T |
A |
10: 58,312,158 (GRCm39) |
D959E |
probably benign |
Het |
Rph3al |
C |
T |
11: 75,724,227 (GRCm39) |
|
probably null |
Het |
Sec31b |
T |
A |
19: 44,512,992 (GRCm39) |
E499V |
probably damaging |
Het |
Sel1l |
T |
C |
12: 91,778,663 (GRCm39) |
I667M |
probably benign |
Het |
Sel1l |
C |
A |
12: 91,780,719 (GRCm39) |
V641L |
possibly damaging |
Het |
Slc7a1 |
T |
A |
5: 148,288,879 (GRCm39) |
I123F |
probably damaging |
Het |
Smarca2 |
G |
A |
19: 26,659,275 (GRCm39) |
R855Q |
possibly damaging |
Het |
Sphk1 |
G |
T |
11: 116,427,184 (GRCm39) |
|
probably benign |
Het |
Spink12 |
C |
A |
18: 44,237,755 (GRCm39) |
S11* |
probably null |
Het |
Sstr2 |
A |
T |
11: 113,516,445 (GRCm39) |
I342F |
probably benign |
Het |
Stxbp1 |
T |
C |
2: 32,709,860 (GRCm39) |
T78A |
probably benign |
Het |
Trim11 |
T |
A |
11: 58,881,410 (GRCm39) |
S434R |
probably damaging |
Het |
Ubr2 |
T |
C |
17: 47,266,812 (GRCm39) |
E1113G |
probably damaging |
Het |
Upb1 |
T |
A |
10: 75,264,188 (GRCm39) |
|
probably benign |
Het |
Vit |
T |
A |
17: 78,932,266 (GRCm39) |
C458S |
probably damaging |
Het |
Vps25 |
T |
C |
11: 101,149,731 (GRCm39) |
|
probably benign |
Het |
Wbp2 |
G |
T |
11: 115,973,211 (GRCm39) |
D65E |
possibly damaging |
Het |
Wdr72 |
A |
G |
9: 74,124,588 (GRCm39) |
D980G |
probably benign |
Het |
Xkr8 |
A |
C |
4: 132,458,228 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Vmn1r58 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01287:Vmn1r58
|
APN |
7 |
5,414,054 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02792:Vmn1r58
|
APN |
7 |
5,414,228 (GRCm39) |
start codon destroyed |
probably null |
0.04 |
IGL03215:Vmn1r58
|
APN |
7 |
5,413,835 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03259:Vmn1r58
|
APN |
7 |
5,414,086 (GRCm39) |
nonsense |
probably null |
|
K7894:Vmn1r58
|
UTSW |
7 |
5,413,702 (GRCm39) |
missense |
probably benign |
0.01 |
R0033:Vmn1r58
|
UTSW |
7 |
5,413,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R0225:Vmn1r58
|
UTSW |
7 |
5,413,865 (GRCm39) |
missense |
probably benign |
0.02 |
R0304:Vmn1r58
|
UTSW |
7 |
5,413,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Vmn1r58
|
UTSW |
7 |
5,413,329 (GRCm39) |
missense |
probably benign |
0.25 |
R0363:Vmn1r58
|
UTSW |
7 |
5,413,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Vmn1r58
|
UTSW |
7 |
5,413,997 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0612:Vmn1r58
|
UTSW |
7 |
5,413,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Vmn1r58
|
UTSW |
7 |
5,413,676 (GRCm39) |
missense |
probably benign |
0.00 |
R0853:Vmn1r58
|
UTSW |
7 |
5,413,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R0920:Vmn1r58
|
UTSW |
7 |
5,413,788 (GRCm39) |
missense |
probably benign |
0.00 |
R1696:Vmn1r58
|
UTSW |
7 |
5,413,727 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1823:Vmn1r58
|
UTSW |
7 |
5,413,405 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2326:Vmn1r58
|
UTSW |
7 |
5,413,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Vmn1r58
|
UTSW |
7 |
5,413,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5065:Vmn1r58
|
UTSW |
7 |
5,413,834 (GRCm39) |
missense |
probably benign |
0.00 |
R5087:Vmn1r58
|
UTSW |
7 |
5,413,666 (GRCm39) |
missense |
probably benign |
0.04 |
R5407:Vmn1r58
|
UTSW |
7 |
5,413,872 (GRCm39) |
missense |
probably benign |
0.01 |
R6855:Vmn1r58
|
UTSW |
7 |
5,413,451 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7052:Vmn1r58
|
UTSW |
7 |
5,414,134 (GRCm39) |
missense |
probably benign |
0.04 |
R7334:Vmn1r58
|
UTSW |
7 |
5,414,066 (GRCm39) |
missense |
probably benign |
0.04 |
R7763:Vmn1r58
|
UTSW |
7 |
5,413,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R7840:Vmn1r58
|
UTSW |
7 |
5,414,242 (GRCm39) |
start gained |
probably benign |
|
R7875:Vmn1r58
|
UTSW |
7 |
5,413,753 (GRCm39) |
missense |
probably damaging |
0.98 |
R8004:Vmn1r58
|
UTSW |
7 |
5,413,506 (GRCm39) |
nonsense |
probably null |
|
R8115:Vmn1r58
|
UTSW |
7 |
5,413,341 (GRCm39) |
missense |
probably benign |
0.00 |
R8781:Vmn1r58
|
UTSW |
7 |
5,413,482 (GRCm39) |
missense |
probably benign |
0.00 |
R8802:Vmn1r58
|
UTSW |
7 |
5,414,080 (GRCm39) |
missense |
probably damaging |
1.00 |
X0058:Vmn1r58
|
UTSW |
7 |
5,413,394 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1176:Vmn1r58
|
UTSW |
7 |
5,413,903 (GRCm39) |
missense |
probably damaging |
0.99 |
|