Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb2 |
A |
G |
2: 103,547,505 (GRCm39) |
I960V |
probably benign |
Het |
Alpk3 |
A |
G |
7: 80,742,079 (GRCm39) |
D632G |
probably benign |
Het |
Aplp2 |
A |
T |
9: 31,122,935 (GRCm39) |
L30Q |
unknown |
Het |
Axl |
A |
T |
7: 25,473,544 (GRCm39) |
Y361N |
probably damaging |
Het |
Brinp2 |
A |
T |
1: 158,077,090 (GRCm39) |
|
probably benign |
Het |
Bsn |
T |
C |
9: 107,992,701 (GRCm39) |
D1017G |
probably damaging |
Het |
Cc2d2a |
A |
T |
5: 43,875,999 (GRCm39) |
D1046V |
probably damaging |
Het |
Cdc42bpg |
G |
A |
19: 6,364,553 (GRCm39) |
G594S |
probably damaging |
Het |
Clcn6 |
A |
G |
4: 148,098,458 (GRCm39) |
S519P |
probably benign |
Het |
Cnot2 |
T |
G |
10: 116,346,326 (GRCm39) |
H92P |
|
Het |
Col2a1 |
T |
C |
15: 97,877,775 (GRCm39) |
D1049G |
probably damaging |
Het |
Creld1 |
C |
T |
6: 113,466,728 (GRCm39) |
A237V |
probably benign |
Het |
Csf2rb2 |
A |
T |
15: 78,171,287 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
G |
A |
15: 48,015,001 (GRCm39) |
T643I |
probably damaging |
Het |
Fam186b |
G |
A |
15: 99,177,616 (GRCm39) |
A570V |
probably damaging |
Het |
Fcmr |
A |
T |
1: 130,802,072 (GRCm39) |
T109S |
|
Het |
Grap |
C |
A |
11: 61,562,551 (GRCm39) |
P174Q |
possibly damaging |
Het |
Itgb5 |
T |
A |
16: 33,730,826 (GRCm39) |
|
probably benign |
Het |
Kidins220 |
A |
G |
12: 25,058,078 (GRCm39) |
N561S |
probably damaging |
Het |
Mri1 |
A |
T |
8: 84,983,796 (GRCm39) |
S32T |
probably benign |
Het |
Mrtfb |
T |
C |
16: 13,218,791 (GRCm39) |
V479A |
probably benign |
Het |
Muc4 |
A |
T |
16: 32,569,971 (GRCm39) |
T344S |
possibly damaging |
Het |
Npc1 |
A |
G |
18: 12,334,769 (GRCm39) |
I661T |
possibly damaging |
Het |
Npy1r |
A |
G |
8: 67,156,751 (GRCm39) |
N57S |
probably damaging |
Het |
Pds5b |
A |
G |
5: 150,704,186 (GRCm39) |
D863G |
probably damaging |
Het |
Phf14 |
T |
A |
6: 11,961,563 (GRCm39) |
V400D |
probably damaging |
Het |
Polr2l |
A |
G |
7: 141,053,246 (GRCm39) |
I56T |
probably benign |
Het |
Ppat |
A |
G |
5: 77,063,884 (GRCm39) |
I422T |
probably benign |
Het |
Prkcg |
T |
A |
7: 3,359,124 (GRCm39) |
S110R |
possibly damaging |
Het |
Rab7b |
A |
T |
1: 131,639,540 (GRCm39) |
|
probably benign |
Het |
Rnf152 |
A |
T |
1: 105,212,251 (GRCm39) |
L102Q |
|
Het |
Samd12 |
A |
G |
15: 53,583,088 (GRCm39) |
V82A |
probably damaging |
Het |
Serpina1e |
T |
A |
12: 103,917,299 (GRCm39) |
R123S |
probably benign |
Het |
Slit1 |
T |
A |
19: 41,615,737 (GRCm39) |
N794I |
probably damaging |
Het |
Surf6 |
T |
C |
2: 26,783,006 (GRCm39) |
K154R |
probably damaging |
Het |
Tln2 |
C |
T |
9: 67,230,353 (GRCm39) |
A71T |
probably benign |
Het |
Trim3 |
A |
G |
7: 105,260,673 (GRCm39) |
Y649H |
probably benign |
Het |
Ttll7 |
T |
A |
3: 146,667,497 (GRCm39) |
W808R |
probably damaging |
Het |
Tvp23a |
T |
C |
16: 10,245,287 (GRCm39) |
D104G |
probably damaging |
Het |
Upp2 |
A |
G |
2: 58,645,339 (GRCm39) |
|
probably benign |
Het |
Vipr1 |
G |
A |
9: 121,471,993 (GRCm39) |
|
probably null |
Het |
Vmn1r209 |
T |
A |
13: 22,990,546 (GRCm39) |
H48L |
probably damaging |
Het |
Wdr11 |
T |
C |
7: 129,232,523 (GRCm39) |
|
probably null |
Het |
Zcchc17 |
T |
C |
4: 130,210,546 (GRCm39) |
D207G |
probably damaging |
Het |
Zfp78 |
T |
C |
7: 6,381,942 (GRCm39) |
S331P |
probably damaging |
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 |
R8233:Vmn1r119
|
UTSW |
7 |
20,745,932 (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 |
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 |
|