Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
A |
C |
12: 118,838,379 (GRCm39) |
V1061G |
probably damaging |
Het |
Acap1 |
A |
G |
11: 69,781,413 (GRCm39) |
|
probably null |
Het |
Apbb1 |
A |
G |
7: 105,215,902 (GRCm39) |
F112L |
probably benign |
Het |
Atg9a |
A |
G |
1: 75,161,702 (GRCm39) |
S615P |
probably benign |
Het |
Atp8a2 |
G |
A |
14: 60,249,848 (GRCm39) |
R548* |
probably null |
Het |
Bbof1 |
A |
T |
12: 84,457,942 (GRCm39) |
N69I |
possibly damaging |
Het |
Bcl2l14 |
T |
A |
6: 134,404,370 (GRCm39) |
V186D |
probably benign |
Het |
Bmp1 |
T |
G |
14: 70,728,823 (GRCm39) |
Y583S |
possibly damaging |
Het |
Boc |
A |
C |
16: 44,312,711 (GRCm39) |
S586R |
probably benign |
Het |
Btbd9 |
A |
T |
17: 30,518,710 (GRCm39) |
|
probably null |
Het |
Cacna1e |
T |
C |
1: 154,317,919 (GRCm39) |
M1180V |
probably damaging |
Het |
Ciao1 |
T |
C |
2: 127,088,376 (GRCm39) |
H149R |
probably damaging |
Het |
Cops5 |
T |
C |
1: 10,100,920 (GRCm39) |
|
probably benign |
Het |
Doc2b |
C |
T |
11: 75,671,093 (GRCm39) |
R209Q |
probably damaging |
Het |
Doc2b |
T |
C |
11: 75,686,451 (GRCm39) |
Y90C |
probably benign |
Het |
Ep400 |
A |
G |
5: 110,901,675 (GRCm39) |
F481L |
probably benign |
Het |
Fat4 |
T |
A |
3: 39,061,229 (GRCm39) |
|
probably null |
Het |
Fbxw16 |
T |
A |
9: 109,277,837 (GRCm39) |
|
probably benign |
Het |
Fbxw27 |
T |
C |
9: 109,601,154 (GRCm39) |
E17G |
possibly damaging |
Het |
Gm29735 |
G |
A |
7: 141,710,367 (GRCm39) |
P162S |
unknown |
Het |
Gypa |
T |
G |
8: 81,222,969 (GRCm39) |
S24R |
unknown |
Het |
Hdhd5 |
T |
C |
6: 120,495,485 (GRCm39) |
N153D |
probably benign |
Het |
Ibsp |
C |
A |
5: 104,449,987 (GRCm39) |
|
probably null |
Het |
Klhdc3 |
C |
T |
17: 46,988,972 (GRCm39) |
V73I |
probably benign |
Het |
Lrrc37a |
T |
C |
11: 103,388,459 (GRCm39) |
E2322G |
unknown |
Het |
Lrrtm3 |
T |
C |
10: 63,765,913 (GRCm39) |
H558R |
probably benign |
Het |
Mbtd1 |
C |
T |
11: 93,823,058 (GRCm39) |
H493Y |
possibly damaging |
Het |
Mphosph9 |
A |
G |
5: 124,458,978 (GRCm39) |
V64A |
possibly damaging |
Het |
Nthl1 |
C |
T |
17: 24,857,475 (GRCm39) |
R251C |
probably damaging |
Het |
Numa1 |
G |
A |
7: 101,649,974 (GRCm39) |
R1235H |
probably benign |
Het |
Opn1sw |
T |
A |
6: 29,379,413 (GRCm39) |
Y197F |
possibly damaging |
Het |
Or10a3m |
T |
C |
7: 108,312,845 (GRCm39) |
V95A |
probably damaging |
Het |
Pcca |
A |
T |
14: 122,896,187 (GRCm39) |
I268F |
probably benign |
Het |
Per2 |
A |
T |
1: 91,377,594 (GRCm39) |
D76E |
unknown |
Het |
Pfas |
T |
C |
11: 68,888,825 (GRCm39) |
N374S |
probably benign |
Het |
Pomk |
C |
A |
8: 26,472,955 (GRCm39) |
V333F |
probably damaging |
Het |
Ptgfr |
T |
C |
3: 151,540,926 (GRCm39) |
E194G |
probably benign |
Het |
Ptpn14 |
C |
T |
1: 189,582,997 (GRCm39) |
P615S |
probably damaging |
Het |
Pyroxd1 |
T |
C |
6: 142,300,479 (GRCm39) |
I203T |
probably benign |
Het |
Rgs22 |
T |
C |
15: 36,087,520 (GRCm39) |
N466S |
probably benign |
Het |
Rpl3l |
G |
A |
17: 24,952,966 (GRCm39) |
V309I |
probably benign |
Het |
Rtkn2 |
C |
T |
10: 67,815,529 (GRCm39) |
|
probably benign |
Het |
Sec16a |
C |
T |
2: 26,318,253 (GRCm39) |
A1613T |
probably damaging |
Het |
Sis |
T |
A |
3: 72,874,103 (GRCm39) |
T33S |
probably damaging |
Het |
Slc22a4 |
C |
A |
11: 53,898,634 (GRCm39) |
V153F |
possibly damaging |
Het |
Stxbp1 |
C |
G |
2: 32,684,621 (GRCm39) |
E603Q |
probably damaging |
Het |
Tiam2 |
A |
G |
17: 3,559,831 (GRCm39) |
S1291G |
probably damaging |
Het |
Tmem94 |
T |
A |
11: 115,687,572 (GRCm39) |
L1144M |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,579,673 (GRCm39) |
T23740M |
probably damaging |
Het |
Wdr7 |
T |
A |
18: 63,888,182 (GRCm39) |
C552S |
probably damaging |
Het |
|
Other mutations in Vmn1r201 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02792:Vmn1r201
|
APN |
13 |
22,659,014 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03137:Vmn1r201
|
APN |
13 |
22,658,974 (GRCm39) |
missense |
probably benign |
0.01 |
R0278:Vmn1r201
|
UTSW |
13 |
22,659,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R0381:Vmn1r201
|
UTSW |
13 |
22,659,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R0544:Vmn1r201
|
UTSW |
13 |
22,659,316 (GRCm39) |
missense |
probably benign |
0.04 |
R1411:Vmn1r201
|
UTSW |
13 |
22,658,849 (GRCm39) |
missense |
probably benign |
0.01 |
R1544:Vmn1r201
|
UTSW |
13 |
22,658,968 (GRCm39) |
missense |
probably benign |
0.20 |
R1850:Vmn1r201
|
UTSW |
13 |
22,658,801 (GRCm39) |
missense |
probably benign |
0.08 |
R1891:Vmn1r201
|
UTSW |
13 |
22,659,425 (GRCm39) |
missense |
probably benign |
0.01 |
R2071:Vmn1r201
|
UTSW |
13 |
22,658,995 (GRCm39) |
missense |
probably benign |
0.34 |
R4183:Vmn1r201
|
UTSW |
13 |
22,659,022 (GRCm39) |
missense |
probably benign |
0.01 |
R4924:Vmn1r201
|
UTSW |
13 |
22,658,882 (GRCm39) |
missense |
probably benign |
0.00 |
R4989:Vmn1r201
|
UTSW |
13 |
22,659,622 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5028:Vmn1r201
|
UTSW |
13 |
22,659,530 (GRCm39) |
nonsense |
probably null |
|
R5318:Vmn1r201
|
UTSW |
13 |
22,659,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R5369:Vmn1r201
|
UTSW |
13 |
22,659,672 (GRCm39) |
missense |
probably benign |
0.00 |
R5682:Vmn1r201
|
UTSW |
13 |
22,659,355 (GRCm39) |
missense |
probably damaging |
0.99 |
R5699:Vmn1r201
|
UTSW |
13 |
22,659,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R6180:Vmn1r201
|
UTSW |
13 |
22,659,499 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6273:Vmn1r201
|
UTSW |
13 |
22,659,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R6331:Vmn1r201
|
UTSW |
13 |
22,659,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R7296:Vmn1r201
|
UTSW |
13 |
22,659,509 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7758:Vmn1r201
|
UTSW |
13 |
22,658,989 (GRCm39) |
missense |
not run |
|
R7832:Vmn1r201
|
UTSW |
13 |
22,659,538 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7887:Vmn1r201
|
UTSW |
13 |
22,658,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R7976:Vmn1r201
|
UTSW |
13 |
22,658,875 (GRCm39) |
missense |
probably benign |
0.32 |
R8676:Vmn1r201
|
UTSW |
13 |
22,659,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R9228:Vmn1r201
|
UTSW |
13 |
22,659,670 (GRCm39) |
missense |
probably benign |
0.21 |
R9570:Vmn1r201
|
UTSW |
13 |
22,659,236 (GRCm39) |
missense |
probably damaging |
1.00 |
|