Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp7 |
T |
A |
7: 28,316,085 (GRCm39) |
Y167F |
probably damaging |
Het |
Acsl1 |
A |
T |
8: 46,966,602 (GRCm39) |
|
probably benign |
Het |
Bcr |
T |
C |
10: 74,971,772 (GRCm39) |
V599A |
probably benign |
Het |
Brd1 |
C |
T |
15: 88,573,821 (GRCm39) |
V1093I |
possibly damaging |
Het |
Cep152 |
A |
G |
2: 125,466,972 (GRCm39) |
|
probably benign |
Het |
Cstf2t |
T |
G |
19: 31,060,695 (GRCm39) |
L77R |
probably damaging |
Het |
Drd3 |
C |
T |
16: 43,637,466 (GRCm39) |
R254W |
probably damaging |
Het |
E2f1 |
C |
G |
2: 154,405,942 (GRCm39) |
G144R |
probably damaging |
Het |
Fam187a |
C |
T |
11: 102,776,675 (GRCm39) |
P160S |
probably benign |
Het |
Fat1 |
G |
A |
8: 45,478,516 (GRCm39) |
E2521K |
probably damaging |
Het |
Fbln1 |
T |
A |
15: 85,111,279 (GRCm39) |
C144* |
probably null |
Het |
Flii |
T |
C |
11: 60,606,306 (GRCm39) |
D1128G |
probably benign |
Het |
Gask1a |
A |
T |
9: 121,794,899 (GRCm39) |
D351V |
probably damaging |
Het |
Gata3 |
T |
A |
2: 9,873,651 (GRCm39) |
H281L |
probably benign |
Het |
Iqsec3 |
C |
T |
6: 121,353,214 (GRCm39) |
A1135T |
probably benign |
Het |
Irak4 |
T |
C |
15: 94,459,476 (GRCm39) |
I364T |
probably damaging |
Het |
Mib2 |
A |
G |
4: 155,739,741 (GRCm39) |
F810S |
probably damaging |
Het |
Nbn |
G |
A |
4: 15,964,269 (GRCm39) |
V115I |
probably damaging |
Het |
Nfyc |
G |
T |
4: 120,622,527 (GRCm39) |
|
probably benign |
Het |
Nup210 |
A |
T |
6: 90,998,377 (GRCm39) |
|
probably null |
Het |
Or2g1 |
T |
C |
17: 38,107,123 (GRCm39) |
S263P |
possibly damaging |
Het |
Or2t48 |
C |
T |
11: 58,420,516 (GRCm39) |
A99T |
probably benign |
Het |
Or8j3b |
C |
T |
2: 86,205,259 (GRCm39) |
V166I |
possibly damaging |
Het |
Paqr8 |
A |
G |
1: 21,005,856 (GRCm39) |
T337A |
probably benign |
Het |
Plce1 |
T |
C |
19: 38,640,278 (GRCm39) |
V508A |
probably benign |
Het |
Prmt2 |
G |
T |
10: 76,061,137 (GRCm39) |
D116E |
probably benign |
Het |
Prss51 |
T |
A |
14: 64,333,624 (GRCm39) |
|
probably benign |
Het |
Prune2 |
T |
A |
19: 17,102,818 (GRCm39) |
V2659D |
probably benign |
Het |
Ptpn3 |
C |
T |
4: 57,270,144 (GRCm39) |
R6H |
probably damaging |
Het |
Ramac |
C |
T |
7: 81,417,395 (GRCm39) |
R32C |
probably damaging |
Het |
Rdh12 |
C |
T |
12: 79,260,446 (GRCm39) |
R181* |
probably null |
Het |
Rsf1 |
T |
A |
7: 97,311,359 (GRCm39) |
D696E |
probably benign |
Het |
Sh3rf2 |
C |
T |
18: 42,244,373 (GRCm39) |
R280C |
probably damaging |
Het |
Slco6d1 |
T |
A |
1: 98,427,502 (GRCm39) |
I611K |
probably damaging |
Het |
Snph |
G |
A |
2: 151,435,374 (GRCm39) |
P449L |
probably benign |
Het |
Spg7 |
G |
C |
8: 123,814,112 (GRCm39) |
R457P |
probably damaging |
Het |
Swap70 |
T |
A |
7: 109,867,088 (GRCm39) |
W297R |
probably damaging |
Het |
Tcaf3 |
T |
A |
6: 42,566,738 (GRCm39) |
I784F |
probably damaging |
Het |
Tcstv2c |
A |
T |
13: 120,616,167 (GRCm39) |
D2V |
possibly damaging |
Het |
Tox2 |
T |
A |
2: 163,156,243 (GRCm39) |
I138N |
probably damaging |
Het |
Trim54 |
A |
C |
5: 31,291,488 (GRCm39) |
E203A |
probably damaging |
Het |
Vmn2r19 |
A |
T |
6: 123,292,548 (GRCm39) |
T197S |
possibly damaging |
Het |
Vmn2r28 |
T |
A |
7: 5,491,026 (GRCm39) |
H407L |
probably damaging |
Het |
Wdr19 |
G |
A |
5: 65,382,069 (GRCm39) |
V430M |
probably damaging |
Het |
|
Other mutations in 1700001J03Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02022:1700001J03Rik
|
APN |
5 |
146,120,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02141:1700001J03Rik
|
APN |
5 |
146,120,275 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02475:1700001J03Rik
|
APN |
5 |
146,119,343 (GRCm39) |
utr 3 prime |
probably benign |
|
R0682:1700001J03Rik
|
UTSW |
5 |
146,121,650 (GRCm39) |
missense |
probably benign |
0.05 |
R1808:1700001J03Rik
|
UTSW |
5 |
146,121,691 (GRCm39) |
nonsense |
probably null |
|
R2083:1700001J03Rik
|
UTSW |
5 |
146,121,681 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2919:1700001J03Rik
|
UTSW |
5 |
146,122,001 (GRCm39) |
missense |
probably benign |
0.00 |
R4764:1700001J03Rik
|
UTSW |
5 |
146,122,029 (GRCm39) |
missense |
probably benign |
0.00 |
R7242:1700001J03Rik
|
UTSW |
5 |
146,121,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R7578:1700001J03Rik
|
UTSW |
5 |
146,120,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7784:1700001J03Rik
|
UTSW |
5 |
146,119,638 (GRCm39) |
splice site |
probably null |
|
R9176:1700001J03Rik
|
UTSW |
5 |
146,121,004 (GRCm39) |
missense |
probably damaging |
1.00 |
|