Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afap1 |
C |
T |
5: 36,102,553 (GRCm39) |
P82S |
probably damaging |
Het |
Ankrd28 |
A |
G |
14: 31,449,698 (GRCm39) |
Y481H |
probably damaging |
Het |
Arid1b |
C |
T |
17: 5,389,605 (GRCm39) |
T1717I |
probably damaging |
Het |
Atad2b |
A |
G |
12: 5,002,676 (GRCm39) |
K348R |
probably benign |
Het |
Bcl3 |
C |
T |
7: 19,543,576 (GRCm39) |
V5M |
probably damaging |
Het |
C2cd3 |
A |
G |
7: 100,118,725 (GRCm39) |
E2321G |
probably benign |
Het |
Casq1 |
C |
T |
1: 172,037,992 (GRCm39) |
V380M |
probably damaging |
Het |
Cd209e |
T |
A |
8: 3,901,274 (GRCm39) |
T127S |
probably benign |
Het |
Cdh23 |
G |
T |
10: 60,143,835 (GRCm39) |
Y2921* |
probably null |
Het |
Cdh6 |
A |
G |
15: 13,034,410 (GRCm39) |
L750P |
probably damaging |
Het |
Cdk12 |
T |
C |
11: 98,102,073 (GRCm39) |
|
probably benign |
Het |
Ces5a |
T |
C |
8: 94,255,183 (GRCm39) |
E170G |
probably damaging |
Het |
Clec4f |
A |
G |
6: 83,629,335 (GRCm39) |
|
probably null |
Het |
Col19a1 |
T |
C |
1: 24,565,539 (GRCm39) |
N264S |
unknown |
Het |
Col2a1 |
T |
A |
15: 97,896,743 (GRCm39) |
I43F |
unknown |
Het |
Col4a2 |
A |
G |
8: 11,458,871 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
T |
A |
15: 47,454,112 (GRCm39) |
D3578V |
probably damaging |
Het |
Cyp2c37 |
T |
C |
19: 39,982,546 (GRCm39) |
L128P |
probably damaging |
Het |
Dennd2b |
A |
G |
7: 109,141,718 (GRCm39) |
S132P |
possibly damaging |
Het |
Dysf |
A |
G |
6: 84,042,084 (GRCm39) |
|
probably benign |
Het |
Eml1 |
T |
C |
12: 108,472,867 (GRCm39) |
V225A |
probably benign |
Het |
Eml1 |
A |
G |
12: 108,475,437 (GRCm39) |
Y256C |
probably damaging |
Het |
Epb41l5 |
T |
A |
1: 119,561,370 (GRCm39) |
K64* |
probably null |
Het |
Fat2 |
A |
G |
11: 55,174,504 (GRCm39) |
F2070L |
probably damaging |
Het |
Fbxw18 |
G |
T |
9: 109,520,583 (GRCm39) |
H259N |
probably benign |
Het |
Gm10764 |
A |
T |
10: 87,126,610 (GRCm39) |
T6S |
unknown |
Het |
Gm14412 |
A |
G |
2: 177,007,705 (GRCm39) |
|
probably benign |
Het |
Heatr5b |
A |
T |
17: 79,133,646 (GRCm39) |
|
probably benign |
Het |
Hid1 |
T |
C |
11: 115,247,649 (GRCm39) |
T250A |
probably damaging |
Het |
Hnf4g |
A |
G |
3: 3,708,142 (GRCm39) |
|
probably benign |
Het |
Ifnar1 |
C |
T |
16: 91,296,425 (GRCm39) |
Q309* |
probably null |
Het |
Lrriq1 |
C |
T |
10: 103,006,281 (GRCm39) |
|
probably null |
Het |
Map3k13 |
A |
G |
16: 21,722,506 (GRCm39) |
T223A |
possibly damaging |
Het |
Matn2 |
C |
T |
15: 34,426,297 (GRCm39) |
|
probably benign |
Het |
Myo6 |
A |
G |
9: 80,215,056 (GRCm39) |
E1253G |
probably damaging |
Het |
Nomo1 |
G |
T |
7: 45,732,652 (GRCm39) |
|
probably benign |
Het |
Or1ak2 |
A |
T |
2: 36,827,268 (GRCm39) |
I46F |
possibly damaging |
Het |
Or4c116 |
A |
T |
2: 88,942,088 (GRCm39) |
I256K |
possibly damaging |
Het |
Or8a1b |
A |
G |
9: 37,622,759 (GRCm39) |
V272A |
possibly damaging |
Het |
Papolg |
C |
T |
11: 23,817,535 (GRCm39) |
A582T |
probably benign |
Het |
Plekhm3 |
C |
T |
1: 64,960,910 (GRCm39) |
E449K |
probably damaging |
Het |
Pole |
T |
G |
5: 110,451,858 (GRCm39) |
M900R |
probably damaging |
Het |
Ppp1cb |
T |
A |
5: 32,640,822 (GRCm39) |
|
probably benign |
Het |
Pramel17 |
A |
G |
4: 101,692,570 (GRCm39) |
*477Q |
probably null |
Het |
Pros1 |
A |
G |
16: 62,734,309 (GRCm39) |
T372A |
possibly damaging |
Het |
Scara3 |
A |
T |
14: 66,168,670 (GRCm39) |
S316T |
probably benign |
Het |
Stau2 |
C |
T |
1: 16,533,352 (GRCm39) |
A61T |
probably damaging |
Het |
Stx3 |
T |
C |
19: 11,769,163 (GRCm39) |
E54G |
possibly damaging |
Het |
Sun1 |
T |
C |
5: 139,232,434 (GRCm39) |
|
probably benign |
Het |
Swt1 |
A |
T |
1: 151,267,280 (GRCm39) |
C634S |
probably damaging |
Het |
Syt6 |
A |
G |
3: 103,494,842 (GRCm39) |
Y269C |
probably damaging |
Het |
Tfap2a |
G |
A |
13: 40,870,887 (GRCm39) |
|
probably benign |
Het |
Tmx4 |
A |
T |
2: 134,481,640 (GRCm39) |
|
probably null |
Het |
Ttc39d |
T |
C |
17: 80,524,375 (GRCm39) |
C345R |
probably damaging |
Het |
Vmn1r27 |
T |
C |
6: 58,192,233 (GRCm39) |
Y257C |
probably damaging |
Het |
Vmn2r27 |
T |
A |
6: 124,208,578 (GRCm39) |
T56S |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,576,674 (GRCm39) |
|
probably null |
Het |
Wdr17 |
A |
G |
8: 55,088,526 (GRCm39) |
S1175P |
probably damaging |
Het |
Wsb2 |
T |
C |
5: 117,501,823 (GRCm39) |
F63L |
probably benign |
Het |
Zfp142 |
A |
G |
1: 74,607,782 (GRCm39) |
Y1561H |
probably damaging |
Het |
|
Other mutations in 1700003E16Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01087:1700003E16Rik
|
APN |
6 |
83,139,770 (GRCm39) |
splice site |
probably null |
|
IGL02616:1700003E16Rik
|
APN |
6 |
83,138,644 (GRCm39) |
missense |
probably benign |
|
IGL03171:1700003E16Rik
|
APN |
6 |
83,139,377 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03196:1700003E16Rik
|
APN |
6 |
83,138,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1081:1700003E16Rik
|
UTSW |
6 |
83,139,002 (GRCm39) |
missense |
probably benign |
|
R1184:1700003E16Rik
|
UTSW |
6 |
83,137,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:1700003E16Rik
|
UTSW |
6 |
83,139,568 (GRCm39) |
missense |
probably damaging |
0.96 |
R4361:1700003E16Rik
|
UTSW |
6 |
83,139,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R4688:1700003E16Rik
|
UTSW |
6 |
83,139,680 (GRCm39) |
missense |
probably damaging |
0.99 |
R5326:1700003E16Rik
|
UTSW |
6 |
83,138,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R6007:1700003E16Rik
|
UTSW |
6 |
83,137,900 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7212:1700003E16Rik
|
UTSW |
6 |
83,138,654 (GRCm39) |
missense |
probably benign |
0.00 |
R7343:1700003E16Rik
|
UTSW |
6 |
83,139,353 (GRCm39) |
missense |
probably benign |
0.12 |
R8081:1700003E16Rik
|
UTSW |
6 |
83,138,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R8121:1700003E16Rik
|
UTSW |
6 |
83,138,893 (GRCm39) |
missense |
probably benign |
|
R9188:1700003E16Rik
|
UTSW |
6 |
83,139,230 (GRCm39) |
missense |
probably benign |
0.12 |
R9329:1700003E16Rik
|
UTSW |
6 |
83,133,556 (GRCm39) |
start codon destroyed |
probably null |
0.55 |
Z1176:1700003E16Rik
|
UTSW |
6 |
83,138,097 (GRCm39) |
missense |
probably damaging |
1.00 |
|