Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503L19Rik |
A |
T |
18: 70,602,687 (GRCm39) |
V42E |
probably benign |
Het |
Abca12 |
T |
C |
1: 71,390,916 (GRCm39) |
E153G |
probably benign |
Het |
Adamts20 |
A |
C |
15: 94,189,533 (GRCm39) |
I1440S |
probably benign |
Het |
Aspm |
T |
A |
1: 139,385,042 (GRCm39) |
S229T |
probably benign |
Het |
Atp2b2 |
A |
T |
6: 113,742,680 (GRCm39) |
|
probably null |
Het |
Cd101 |
G |
T |
3: 100,900,989 (GRCm39) |
H1032N |
unknown |
Het |
Col6a2 |
A |
G |
10: 76,444,540 (GRCm39) |
|
probably null |
Het |
Crot |
A |
T |
5: 9,026,027 (GRCm39) |
I320K |
possibly damaging |
Het |
D5Ertd579e |
A |
T |
5: 36,772,588 (GRCm39) |
D602E |
probably damaging |
Het |
Degs1 |
A |
G |
1: 182,107,160 (GRCm39) |
V69A |
probably benign |
Het |
Dgkz |
A |
G |
2: 91,769,994 (GRCm39) |
S557P |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,405,055 (GRCm39) |
L602Q |
|
Het |
Gli2 |
A |
T |
1: 118,772,167 (GRCm39) |
Y513N |
probably damaging |
Het |
H2-Q10 |
A |
G |
17: 35,781,983 (GRCm39) |
T202A |
probably benign |
Het |
Hnrnpa3 |
A |
G |
2: 75,492,860 (GRCm39) |
N195D |
probably benign |
Het |
Ifna1 |
C |
T |
4: 88,768,628 (GRCm39) |
T102I |
possibly damaging |
Het |
Igfbp3 |
T |
A |
11: 7,160,152 (GRCm39) |
H167L |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,895,782 (GRCm39) |
T1595A |
probably benign |
Het |
Krt14 |
A |
G |
11: 100,094,178 (GRCm39) |
V472A |
probably damaging |
Het |
Lrrc74b |
T |
A |
16: 17,376,089 (GRCm39) |
H187L |
probably benign |
Het |
Magoh |
T |
G |
4: 107,738,132 (GRCm39) |
V44G |
possibly damaging |
Het |
Mbnl1 |
A |
T |
3: 60,532,551 (GRCm39) |
I274L |
probably benign |
Het |
Or13a27 |
T |
G |
7: 139,925,411 (GRCm39) |
M164L |
probably benign |
Het |
Or4c108 |
C |
T |
2: 88,804,082 (GRCm39) |
R51H |
probably benign |
Het |
Pdcd1 |
A |
G |
1: 93,967,142 (GRCm39) |
V252A |
probably damaging |
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Plcxd3 |
A |
G |
15: 4,546,317 (GRCm39) |
D107G |
possibly damaging |
Het |
Polr2m |
T |
A |
9: 71,390,866 (GRCm39) |
D112V |
probably benign |
Het |
Ptprn |
A |
T |
1: 75,229,796 (GRCm39) |
M701K |
probably damaging |
Het |
Rxrb |
A |
G |
17: 34,255,879 (GRCm39) |
D421G |
possibly damaging |
Het |
Slfn4 |
A |
G |
11: 83,078,355 (GRCm39) |
E381G |
probably damaging |
Het |
Son |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,457,222 (GRCm39) |
|
probably benign |
Het |
Srgap1 |
A |
G |
10: 121,661,341 (GRCm39) |
I530T |
probably damaging |
Het |
Stmn4 |
A |
G |
14: 66,595,341 (GRCm39) |
H122R |
probably damaging |
Het |
Sycp2 |
T |
C |
2: 177,998,427 (GRCm39) |
E1031G |
probably damaging |
Het |
Tle1 |
T |
C |
4: 72,043,181 (GRCm39) |
T553A |
probably benign |
Het |
Tnik |
T |
A |
3: 28,609,086 (GRCm39) |
W217R |
unknown |
Het |
Tyrp1 |
T |
C |
4: 80,769,190 (GRCm39) |
V161A |
unknown |
Het |
Usp29 |
T |
A |
7: 6,965,406 (GRCm39) |
F416L |
probably benign |
Het |
Usp45 |
T |
C |
4: 21,781,736 (GRCm39) |
V34A |
probably benign |
Het |
|
Other mutations in Vmn1r119 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01363:Vmn1r119
|
APN |
7 |
20,746,056 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02218:Vmn1r119
|
APN |
7 |
20,745,561 (GRCm39) |
missense |
probably benign |
0.11 |
R0639:Vmn1r119
|
UTSW |
7 |
20,745,593 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1844:Vmn1r119
|
UTSW |
7 |
20,746,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R2250:Vmn1r119
|
UTSW |
7 |
20,746,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R2927:Vmn1r119
|
UTSW |
7 |
20,746,056 (GRCm39) |
missense |
probably benign |
0.41 |
R4279:Vmn1r119
|
UTSW |
7 |
20,745,786 (GRCm39) |
missense |
probably benign |
0.00 |
R5022:Vmn1r119
|
UTSW |
7 |
20,746,245 (GRCm39) |
missense |
probably benign |
0.08 |
R6160:Vmn1r119
|
UTSW |
7 |
20,745,740 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6523:Vmn1r119
|
UTSW |
7 |
20,745,777 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7013:Vmn1r119
|
UTSW |
7 |
20,745,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R7218:Vmn1r119
|
UTSW |
7 |
20,745,572 (GRCm39) |
missense |
probably benign |
0.00 |
R7320:Vmn1r119
|
UTSW |
7 |
20,746,271 (GRCm39) |
missense |
probably damaging |
0.99 |
R8550:Vmn1r119
|
UTSW |
7 |
20,745,980 (GRCm39) |
missense |
probably benign |
0.00 |
R9151:Vmn1r119
|
UTSW |
7 |
20,745,593 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9300:Vmn1r119
|
UTSW |
7 |
20,745,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R9343:Vmn1r119
|
UTSW |
7 |
20,746,358 (GRCm39) |
missense |
probably benign |
0.03 |
R9345:Vmn1r119
|
UTSW |
7 |
20,746,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R9661:Vmn1r119
|
UTSW |
7 |
20,746,224 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0060:Vmn1r119
|
UTSW |
7 |
20,746,208 (GRCm39) |
missense |
possibly damaging |
0.79 |
Z1177:Vmn1r119
|
UTSW |
7 |
20,745,705 (GRCm39) |
missense |
probably benign |
0.02 |
|