Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy1 |
G |
A |
11: 7,029,012 (GRCm39) |
R254Q |
probably benign |
Het |
Adgrv1 |
T |
C |
13: 81,727,833 (GRCm39) |
Y269C |
probably damaging |
Het |
Apol7a |
C |
A |
15: 77,277,650 (GRCm39) |
E33* |
probably null |
Het |
Arhgap29 |
T |
C |
3: 121,786,509 (GRCm39) |
V358A |
probably benign |
Het |
B3galt1 |
T |
C |
2: 67,948,728 (GRCm39) |
S148P |
probably damaging |
Het |
BC061237 |
A |
G |
14: 44,740,779 (GRCm39) |
N60D |
possibly damaging |
Het |
Bcl9l |
C |
T |
9: 44,412,047 (GRCm39) |
P11L |
probably damaging |
Het |
Ccdc89 |
A |
C |
7: 90,076,110 (GRCm39) |
K107Q |
probably benign |
Het |
Col27a1 |
T |
C |
4: 63,249,663 (GRCm39) |
|
probably benign |
Het |
Col5a2 |
T |
C |
1: 45,424,225 (GRCm39) |
D1067G |
probably damaging |
Het |
Col9a2 |
A |
T |
4: 120,910,389 (GRCm39) |
R511S |
probably benign |
Het |
Disp3 |
G |
A |
4: 148,333,658 (GRCm39) |
S1060F |
possibly damaging |
Het |
Dusp8 |
T |
C |
7: 141,636,667 (GRCm39) |
T308A |
probably benign |
Het |
Ern1 |
T |
C |
11: 106,314,266 (GRCm39) |
N178S |
probably damaging |
Het |
Gas6 |
C |
A |
8: 13,527,136 (GRCm39) |
C204F |
probably damaging |
Het |
Gga1 |
T |
C |
15: 78,777,522 (GRCm39) |
S558P |
possibly damaging |
Het |
Gli1 |
T |
C |
10: 127,168,279 (GRCm39) |
T525A |
probably benign |
Het |
Gse1 |
A |
G |
8: 121,304,808 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
G |
A |
1: 150,532,958 (GRCm39) |
S3075L |
probably benign |
Het |
Hnf4a |
G |
A |
2: 163,408,037 (GRCm39) |
|
probably benign |
Het |
Htt |
A |
T |
5: 35,034,097 (GRCm39) |
E1894D |
probably damaging |
Het |
Kcnh8 |
G |
A |
17: 53,263,650 (GRCm39) |
E716K |
probably benign |
Het |
Kntc1 |
A |
G |
5: 123,937,874 (GRCm39) |
Y1524C |
probably damaging |
Het |
Krtap9-5 |
A |
G |
11: 99,839,931 (GRCm39) |
T211A |
unknown |
Het |
Lin54 |
T |
C |
5: 100,628,180 (GRCm39) |
I8V |
possibly damaging |
Het |
Lipe |
A |
G |
7: 25,082,760 (GRCm39) |
|
probably benign |
Het |
Lpin2 |
T |
A |
17: 71,545,678 (GRCm39) |
V508E |
probably damaging |
Het |
Lrrc9 |
C |
A |
12: 72,500,923 (GRCm39) |
H216Q |
probably damaging |
Het |
Lrrn1 |
T |
C |
6: 107,544,709 (GRCm39) |
L169P |
probably damaging |
Het |
Map9 |
C |
A |
3: 82,284,428 (GRCm39) |
T334K |
possibly damaging |
Het |
Msantd5f1 |
G |
A |
4: 73,605,602 (GRCm39) |
A338T |
probably damaging |
Het |
Mst1 |
A |
T |
9: 107,961,841 (GRCm39) |
|
probably null |
Het |
Mtor |
T |
A |
4: 148,549,421 (GRCm39) |
F602I |
probably benign |
Het |
Mylpf |
T |
A |
7: 126,812,798 (GRCm39) |
D98E |
probably benign |
Het |
Naca |
C |
A |
10: 127,883,551 (GRCm39) |
Q2059K |
probably damaging |
Het |
Nefh |
G |
A |
11: 4,891,356 (GRCm39) |
T421I |
possibly damaging |
Het |
Nlrp4g |
T |
A |
9: 124,348,940 (GRCm38) |
|
noncoding transcript |
Het |
Npat |
C |
T |
9: 53,482,341 (GRCm39) |
Q1350* |
probably null |
Het |
Oaz3 |
T |
C |
3: 94,342,287 (GRCm39) |
N123S |
probably benign |
Het |
Patj |
A |
G |
4: 98,299,410 (GRCm39) |
|
probably benign |
Het |
Pgap6 |
T |
A |
17: 26,336,923 (GRCm39) |
F280L |
probably benign |
Het |
Piezo1 |
A |
C |
8: 123,210,258 (GRCm39) |
D2224E |
probably damaging |
Het |
Pnpla7 |
A |
T |
2: 24,905,241 (GRCm39) |
I610F |
possibly damaging |
Het |
Psapl1 |
A |
T |
5: 36,362,233 (GRCm39) |
D275V |
probably damaging |
Het |
Ptpdc1 |
T |
A |
13: 48,744,095 (GRCm39) |
|
probably benign |
Het |
Rac2 |
T |
C |
15: 78,454,947 (GRCm39) |
E31G |
possibly damaging |
Het |
Sdhc |
T |
C |
1: 170,971,124 (GRCm39) |
|
probably benign |
Het |
Smim23 |
G |
T |
11: 32,770,667 (GRCm39) |
P80T |
probably damaging |
Het |
Tjp2 |
A |
G |
19: 24,073,996 (GRCm39) |
V1097A |
probably benign |
Het |
Ttc16 |
A |
G |
2: 32,661,939 (GRCm39) |
Y164H |
probably damaging |
Het |
Txlnb |
A |
G |
10: 17,703,730 (GRCm39) |
E296G |
probably damaging |
Het |
Ube2l6 |
G |
A |
2: 84,633,195 (GRCm39) |
V34M |
probably damaging |
Het |
Vwf |
A |
C |
6: 125,592,931 (GRCm39) |
S764R |
possibly damaging |
Het |
Zfand3 |
A |
G |
17: 30,411,611 (GRCm39) |
S146G |
probably benign |
Het |
Zfp280d |
T |
G |
9: 72,203,307 (GRCm39) |
F18L |
probably benign |
Het |
|
Other mutations in Snupn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02820:Snupn
|
APN |
9 |
56,870,332 (GRCm39) |
missense |
probably benign |
|
R1160:Snupn
|
UTSW |
9 |
56,864,389 (GRCm39) |
missense |
probably benign |
0.28 |
R4569:Snupn
|
UTSW |
9 |
56,885,346 (GRCm39) |
missense |
probably benign |
0.22 |
R4570:Snupn
|
UTSW |
9 |
56,885,346 (GRCm39) |
missense |
probably benign |
0.22 |
R5318:Snupn
|
UTSW |
9 |
56,864,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R6139:Snupn
|
UTSW |
9 |
56,890,108 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6140:Snupn
|
UTSW |
9 |
56,890,108 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6141:Snupn
|
UTSW |
9 |
56,890,108 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6208:Snupn
|
UTSW |
9 |
56,890,247 (GRCm39) |
missense |
probably damaging |
0.99 |
R6625:Snupn
|
UTSW |
9 |
56,890,054 (GRCm39) |
missense |
probably benign |
0.01 |
R7278:Snupn
|
UTSW |
9 |
56,890,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R8251:Snupn
|
UTSW |
9 |
56,888,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R9290:Snupn
|
UTSW |
9 |
56,882,547 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9458:Snupn
|
UTSW |
9 |
56,890,039 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9729:Snupn
|
UTSW |
9 |
56,877,915 (GRCm39) |
missense |
possibly damaging |
0.57 |
X0025:Snupn
|
UTSW |
9 |
56,877,632 (GRCm39) |
missense |
possibly damaging |
0.85 |
|