Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
A |
T |
6: 142,546,673 (GRCm39) |
I1353N |
probably damaging |
Het |
Actr1a |
C |
A |
19: 46,384,157 (GRCm39) |
|
probably benign |
Het |
Adamts14 |
A |
T |
10: 61,065,431 (GRCm39) |
M356K |
probably benign |
Het |
Adamtsl2 |
A |
G |
2: 26,971,736 (GRCm39) |
H7R |
probably benign |
Het |
Angptl2 |
T |
C |
2: 33,118,628 (GRCm39) |
V134A |
probably damaging |
Het |
Armc8 |
A |
G |
9: 99,378,202 (GRCm39) |
|
probably null |
Het |
Astn2 |
T |
C |
4: 65,868,375 (GRCm39) |
D488G |
probably damaging |
Het |
Cat |
A |
T |
2: 103,303,339 (GRCm39) |
V146E |
probably damaging |
Het |
Dmxl1 |
T |
C |
18: 50,027,324 (GRCm39) |
V2144A |
probably damaging |
Het |
Efcab5 |
T |
G |
11: 77,079,701 (GRCm39) |
D15A |
probably benign |
Het |
Epha10 |
C |
T |
4: 124,796,446 (GRCm39) |
A385V |
unknown |
Het |
Erg |
C |
A |
16: 95,161,890 (GRCm39) |
E388D |
probably benign |
Het |
Fbxo10 |
T |
A |
4: 45,035,970 (GRCm39) |
I931F |
probably damaging |
Het |
Frem1 |
A |
G |
4: 82,912,353 (GRCm39) |
L673P |
probably damaging |
Het |
Gm4922 |
A |
C |
10: 18,660,035 (GRCm39) |
I229S |
possibly damaging |
Het |
Gnptab |
T |
A |
10: 88,250,348 (GRCm39) |
D153E |
probably benign |
Het |
Htr7 |
T |
C |
19: 36,034,521 (GRCm39) |
M45V |
probably benign |
Het |
Hycc1 |
C |
A |
5: 24,196,794 (GRCm39) |
L31F |
probably damaging |
Het |
Igkv4-51 |
C |
T |
6: 69,658,911 (GRCm39) |
V5M |
probably damaging |
Het |
Ints7 |
G |
A |
1: 191,318,730 (GRCm39) |
E156K |
probably damaging |
Het |
Map3k21 |
A |
G |
8: 126,671,507 (GRCm39) |
T932A |
probably benign |
Het |
Mapk1 |
T |
G |
16: 16,836,333 (GRCm39) |
D160E |
probably benign |
Het |
Mast4 |
A |
T |
13: 102,910,701 (GRCm39) |
Y479* |
probably null |
Het |
Meig1 |
T |
A |
2: 3,412,999 (GRCm39) |
K7N |
probably damaging |
Het |
Mthfd1l |
T |
A |
10: 3,985,239 (GRCm39) |
D548E |
possibly damaging |
Het |
Myo16 |
A |
G |
8: 10,619,606 (GRCm39) |
R1386G |
probably benign |
Het |
Nphs2 |
T |
C |
1: 156,153,607 (GRCm39) |
S353P |
probably benign |
Het |
Or12j4 |
T |
C |
7: 140,046,644 (GRCm39) |
F177L |
probably benign |
Het |
Or8b1 |
T |
A |
9: 38,399,532 (GRCm39) |
I69K |
probably damaging |
Het |
Pcdha9 |
G |
T |
18: 37,131,425 (GRCm39) |
V165L |
probably benign |
Het |
Pde3a |
T |
A |
6: 141,196,228 (GRCm39) |
S305T |
possibly damaging |
Het |
Phf14 |
C |
A |
6: 11,990,124 (GRCm39) |
L718I |
possibly damaging |
Het |
Plscr5 |
A |
T |
9: 92,087,564 (GRCm39) |
K178* |
probably null |
Het |
Rab44 |
T |
A |
17: 29,364,940 (GRCm39) |
M645K |
unknown |
Het |
Rab44 |
T |
C |
17: 29,359,474 (GRCm39) |
L554P |
probably damaging |
Het |
Rnf222 |
A |
G |
11: 68,783,723 (GRCm39) |
T97A |
probably benign |
Het |
Rnpepl1 |
T |
C |
1: 92,846,663 (GRCm39) |
S522P |
probably benign |
Het |
Serpinb10 |
A |
T |
1: 107,463,187 (GRCm39) |
|
probably null |
Het |
Siglech |
T |
A |
7: 55,418,404 (GRCm39) |
F124Y |
probably damaging |
Het |
Smarcc2 |
A |
T |
10: 128,319,996 (GRCm39) |
I790L |
probably benign |
Het |
Sos2 |
C |
A |
12: 69,637,689 (GRCm39) |
R1007S |
probably damaging |
Het |
Stk4 |
C |
T |
2: 163,942,484 (GRCm39) |
T372M |
possibly damaging |
Het |
Tbc1d10c |
A |
T |
19: 4,234,963 (GRCm39) |
L366H |
probably damaging |
Het |
Tor4a |
T |
C |
2: 25,084,932 (GRCm39) |
T324A |
probably benign |
Het |
Trim12a |
C |
A |
7: 103,956,450 (GRCm39) |
C30F |
probably damaging |
Het |
Ttll3 |
G |
A |
6: 113,376,669 (GRCm39) |
V350M |
probably damaging |
Het |
Uggt1 |
A |
T |
1: 36,218,737 (GRCm39) |
D63E |
probably damaging |
Het |
Unc5b |
G |
A |
10: 60,609,526 (GRCm39) |
T590I |
probably benign |
Het |
Wee1 |
TCCCC |
TCCC |
7: 109,723,776 (GRCm39) |
|
probably null |
Het |
Wls |
A |
C |
3: 159,545,624 (GRCm39) |
I16L |
probably benign |
Het |
Zfp101 |
T |
C |
17: 33,599,919 (GRCm39) |
I612M |
probably benign |
Het |
Zfp677 |
C |
A |
17: 21,618,021 (GRCm39) |
D359E |
probably damaging |
Het |
|
Other mutations in Serinc5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00985:Serinc5
|
APN |
13 |
92,842,779 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01954:Serinc5
|
APN |
13 |
92,819,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02248:Serinc5
|
APN |
13 |
92,842,648 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03259:Serinc5
|
APN |
13 |
92,827,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R0352:Serinc5
|
UTSW |
13 |
92,844,497 (GRCm39) |
splice site |
probably null |
|
R0600:Serinc5
|
UTSW |
13 |
92,844,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Serinc5
|
UTSW |
13 |
92,825,245 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0944:Serinc5
|
UTSW |
13 |
92,797,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R0972:Serinc5
|
UTSW |
13 |
92,825,128 (GRCm39) |
missense |
probably benign |
0.18 |
R1163:Serinc5
|
UTSW |
13 |
92,819,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R1459:Serinc5
|
UTSW |
13 |
92,797,695 (GRCm39) |
critical splice donor site |
probably null |
|
R1703:Serinc5
|
UTSW |
13 |
92,825,305 (GRCm39) |
missense |
probably damaging |
0.99 |
R1866:Serinc5
|
UTSW |
13 |
92,842,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R1887:Serinc5
|
UTSW |
13 |
92,838,214 (GRCm39) |
missense |
possibly damaging |
0.70 |
R3018:Serinc5
|
UTSW |
13 |
92,825,189 (GRCm39) |
missense |
probably benign |
0.01 |
R4863:Serinc5
|
UTSW |
13 |
92,827,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R5715:Serinc5
|
UTSW |
13 |
92,842,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Serinc5
|
UTSW |
13 |
92,797,644 (GRCm39) |
missense |
probably benign |
0.01 |
R6228:Serinc5
|
UTSW |
13 |
92,844,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R6270:Serinc5
|
UTSW |
13 |
92,825,170 (GRCm39) |
missense |
probably damaging |
0.97 |
R6592:Serinc5
|
UTSW |
13 |
92,844,634 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6622:Serinc5
|
UTSW |
13 |
92,825,194 (GRCm39) |
missense |
probably benign |
0.05 |
R6787:Serinc5
|
UTSW |
13 |
92,842,740 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7730:Serinc5
|
UTSW |
13 |
92,821,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R7773:Serinc5
|
UTSW |
13 |
92,797,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R7961:Serinc5
|
UTSW |
13 |
92,797,699 (GRCm39) |
splice site |
probably null |
|
R8009:Serinc5
|
UTSW |
13 |
92,797,699 (GRCm39) |
splice site |
probably null |
|
R8819:Serinc5
|
UTSW |
13 |
92,844,544 (GRCm39) |
missense |
probably benign |
0.02 |
R8820:Serinc5
|
UTSW |
13 |
92,844,544 (GRCm39) |
missense |
probably benign |
0.02 |
R9116:Serinc5
|
UTSW |
13 |
92,797,514 (GRCm39) |
splice site |
probably benign |
|
R9460:Serinc5
|
UTSW |
13 |
92,844,619 (GRCm39) |
missense |
probably benign |
0.03 |
R9460:Serinc5
|
UTSW |
13 |
92,844,607 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0018:Serinc5
|
UTSW |
13 |
92,797,583 (GRCm39) |
missense |
probably benign |
0.02 |
|