Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd17 |
G |
T |
5: 90,412,576 (GRCm39) |
N1249K |
probably damaging |
Het |
Anks1b |
T |
C |
10: 89,885,958 (GRCm39) |
M218T |
probably damaging |
Het |
Arfgef2 |
G |
C |
2: 166,707,679 (GRCm39) |
G1025A |
probably benign |
Het |
Arhgap21 |
T |
C |
2: 20,868,037 (GRCm39) |
I829V |
possibly damaging |
Het |
Arhgap42 |
T |
C |
9: 9,035,512 (GRCm39) |
M277V |
probably benign |
Het |
Cabin1 |
T |
C |
10: 75,589,295 (GRCm39) |
I87M |
probably benign |
Het |
Cdc42bpa |
A |
G |
1: 179,864,484 (GRCm39) |
N149D |
probably damaging |
Het |
Cdh20 |
C |
A |
1: 104,875,139 (GRCm39) |
A307E |
probably damaging |
Het |
Cdk18 |
A |
T |
1: 132,043,690 (GRCm39) |
Y385N |
probably damaging |
Het |
Cfap410 |
T |
C |
10: 77,817,476 (GRCm39) |
Y68H |
probably damaging |
Het |
Cnga1 |
C |
T |
5: 72,776,404 (GRCm39) |
V20I |
possibly damaging |
Het |
Cptp |
A |
G |
4: 155,950,878 (GRCm39) |
I196T |
probably damaging |
Het |
Cyp4b1 |
T |
A |
4: 115,497,557 (GRCm39) |
Y147F |
probably benign |
Het |
Dbf4 |
T |
C |
5: 8,471,333 (GRCm39) |
N36S |
possibly damaging |
Het |
Dbr1 |
G |
T |
9: 99,462,200 (GRCm39) |
Q166H |
probably benign |
Het |
Ddx42 |
T |
A |
11: 106,133,765 (GRCm39) |
D580E |
probably damaging |
Het |
Dnah17 |
T |
C |
11: 117,987,387 (GRCm39) |
K1308E |
possibly damaging |
Het |
Dpep1 |
A |
T |
8: 123,920,883 (GRCm39) |
D21V |
probably benign |
Het |
Dspp |
G |
A |
5: 104,326,250 (GRCm39) |
S871N |
unknown |
Het |
En1 |
T |
A |
1: 120,534,916 (GRCm39) |
*402K |
probably null |
Het |
Eogt |
G |
T |
6: 97,111,262 (GRCm39) |
R200S |
probably benign |
Het |
Epb41l3 |
A |
G |
17: 69,577,645 (GRCm39) |
T542A |
possibly damaging |
Het |
Gask1a |
T |
C |
9: 121,794,668 (GRCm39) |
I274T |
probably benign |
Het |
Gh |
T |
C |
11: 106,191,613 (GRCm39) |
E143G |
probably damaging |
Het |
Hcn3 |
C |
A |
3: 89,055,168 (GRCm39) |
R693L |
probably benign |
Het |
Htra1 |
A |
T |
7: 130,563,752 (GRCm39) |
I208F |
probably damaging |
Het |
Ifna13 |
T |
A |
4: 88,562,156 (GRCm39) |
E156V |
probably benign |
Het |
Ints6 |
A |
G |
14: 62,942,131 (GRCm39) |
|
probably null |
Het |
Kifc5b |
A |
G |
17: 27,144,515 (GRCm39) |
I545V |
probably damaging |
Het |
Lrrc4c |
C |
T |
2: 97,460,850 (GRCm39) |
S492F |
possibly damaging |
Het |
Madd |
A |
T |
2: 90,974,028 (GRCm39) |
C1419S |
possibly damaging |
Het |
Map2k6 |
T |
C |
11: 110,390,290 (GRCm39) |
S275P |
probably damaging |
Het |
Mpp2 |
T |
C |
11: 101,955,127 (GRCm39) |
E166G |
probably damaging |
Het |
Mrpl48 |
G |
A |
7: 100,214,471 (GRCm39) |
T48I |
probably damaging |
Het |
Neu1 |
A |
G |
17: 35,153,350 (GRCm39) |
D291G |
probably damaging |
Het |
Nktr |
A |
G |
9: 121,560,603 (GRCm39) |
K116E |
possibly damaging |
Het |
Npc1 |
T |
C |
18: 12,330,236 (GRCm39) |
|
probably null |
Het |
Or6b9 |
A |
T |
7: 106,555,834 (GRCm39) |
M103K |
probably benign |
Het |
Or6c1b |
A |
T |
10: 129,273,526 (GRCm39) |
M282L |
probably benign |
Het |
Or8k1 |
T |
C |
2: 86,047,148 (GRCm39) |
E302G |
probably benign |
Het |
Pclo |
T |
A |
5: 14,764,287 (GRCm39) |
D4253E |
unknown |
Het |
Phactr1 |
A |
T |
13: 43,231,265 (GRCm39) |
S244C |
possibly damaging |
Het |
Prex1 |
A |
T |
2: 166,419,875 (GRCm39) |
I79N |
probably benign |
Het |
Rhebl1 |
A |
T |
15: 98,776,167 (GRCm39) |
D162E |
probably benign |
Het |
Rnf32 |
G |
T |
5: 29,430,278 (GRCm39) |
V366F |
probably benign |
Het |
Rpn2 |
A |
G |
2: 157,152,208 (GRCm39) |
T394A |
possibly damaging |
Het |
Ryr3 |
A |
T |
2: 112,479,664 (GRCm39) |
M4386K |
possibly damaging |
Het |
Sirt7 |
T |
C |
11: 120,515,321 (GRCm39) |
S112G |
probably damaging |
Het |
Slc1a6 |
A |
T |
10: 78,624,882 (GRCm39) |
M96L |
probably benign |
Het |
Slc25a29 |
T |
C |
12: 108,792,852 (GRCm39) |
E242G |
probably benign |
Het |
Slc30a2 |
G |
T |
4: 134,075,857 (GRCm39) |
Q210H |
probably benign |
Het |
Sorcs2 |
A |
T |
5: 36,199,430 (GRCm39) |
|
probably null |
Het |
Spink5 |
A |
G |
18: 44,119,396 (GRCm39) |
N236D |
probably benign |
Het |
Syne2 |
A |
G |
12: 75,974,240 (GRCm39) |
E1146G |
possibly damaging |
Het |
Sytl3 |
A |
G |
17: 6,976,273 (GRCm39) |
|
probably benign |
Het |
Tasor |
A |
C |
14: 27,164,452 (GRCm39) |
K253Q |
probably damaging |
Het |
Tgm7 |
A |
G |
2: 120,929,045 (GRCm39) |
S284P |
probably damaging |
Het |
Tmem45a |
A |
T |
16: 56,643,882 (GRCm39) |
L89Q |
probably damaging |
Het |
Ttc23l |
A |
G |
15: 10,523,678 (GRCm39) |
I347T |
possibly damaging |
Het |
Txlna |
T |
C |
4: 129,525,935 (GRCm39) |
E304G |
probably damaging |
Het |
Zfp709 |
T |
C |
8: 72,642,934 (GRCm39) |
V121A |
probably benign |
Het |
|
Other mutations in Fam50b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
G1citation:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0395:Fam50b
|
UTSW |
13 |
34,931,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R2276:Fam50b
|
UTSW |
13 |
34,930,823 (GRCm39) |
nonsense |
probably null |
|
R3726:Fam50b
|
UTSW |
13 |
34,930,869 (GRCm39) |
missense |
probably damaging |
0.96 |
R6330:Fam50b
|
UTSW |
13 |
34,930,652 (GRCm39) |
missense |
probably benign |
0.01 |
R6820:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6822:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6824:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7019:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7193:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7795:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7796:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7797:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7871:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7880:Fam50b
|
UTSW |
13 |
34,930,802 (GRCm39) |
missense |
probably benign |
0.01 |
R7920:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7921:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8081:Fam50b
|
UTSW |
13 |
34,931,084 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8175:Fam50b
|
UTSW |
13 |
34,930,847 (GRCm39) |
missense |
probably benign |
|
R8443:Fam50b
|
UTSW |
13 |
34,930,856 (GRCm39) |
nonsense |
probably null |
|
|