Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam23 |
A |
G |
1: 63,591,014 (GRCm39) |
T494A |
possibly damaging |
Het |
Adamts16 |
C |
T |
13: 70,984,234 (GRCm39) |
C143Y |
probably damaging |
Het |
Cacna1i |
A |
G |
15: 80,232,581 (GRCm39) |
I195V |
probably damaging |
Het |
Casp7 |
T |
C |
19: 56,392,896 (GRCm39) |
S17P |
probably benign |
Het |
Cfap298 |
T |
C |
16: 90,722,936 (GRCm39) |
N266S |
possibly damaging |
Het |
Cox6a1 |
C |
A |
5: 115,483,898 (GRCm39) |
|
probably benign |
Het |
Cpvl |
T |
A |
6: 53,951,640 (GRCm39) |
S48C |
possibly damaging |
Het |
Cyp2b19 |
G |
T |
7: 26,458,842 (GRCm39) |
M138I |
probably benign |
Het |
Dennd5a |
T |
C |
7: 109,518,611 (GRCm39) |
Y510C |
possibly damaging |
Het |
Derl2 |
A |
G |
11: 70,901,181 (GRCm39) |
F229S |
possibly damaging |
Het |
Dlec1 |
A |
G |
9: 118,949,979 (GRCm39) |
E452G |
probably damaging |
Het |
Dsc2 |
T |
C |
18: 20,180,214 (GRCm39) |
K180E |
probably benign |
Het |
Dus1l |
G |
A |
11: 120,683,918 (GRCm39) |
R177C |
possibly damaging |
Het |
Egfr |
A |
G |
11: 16,813,020 (GRCm39) |
I167V |
probably damaging |
Het |
Fam219b |
A |
T |
9: 57,445,305 (GRCm39) |
|
probably null |
Het |
Fn1 |
T |
C |
1: 71,665,369 (GRCm39) |
E916G |
probably damaging |
Het |
Gm2058 |
C |
T |
7: 39,238,580 (GRCm39) |
|
noncoding transcript |
Het |
Gpd1 |
T |
A |
15: 99,616,056 (GRCm39) |
V22E |
probably damaging |
Het |
Hsf2 |
T |
C |
10: 57,377,475 (GRCm39) |
F124L |
probably damaging |
Het |
I0C0044D17Rik |
A |
G |
4: 98,708,336 (GRCm39) |
|
probably benign |
Het |
Igfbp3 |
A |
T |
11: 7,158,478 (GRCm39) |
F262I |
possibly damaging |
Het |
Klhl18 |
A |
G |
9: 110,284,501 (GRCm39) |
Y62H |
probably damaging |
Het |
Lama2 |
C |
T |
10: 27,064,268 (GRCm39) |
E1238K |
probably benign |
Het |
Man1b1 |
A |
G |
2: 25,228,239 (GRCm39) |
K170E |
probably benign |
Het |
Mcrs1 |
A |
T |
15: 99,147,382 (GRCm39) |
I39N |
probably damaging |
Het |
Mug2 |
T |
C |
6: 122,026,587 (GRCm39) |
|
probably benign |
Het |
Nipal3 |
A |
C |
4: 135,199,194 (GRCm39) |
|
probably null |
Het |
Nrxn3 |
A |
G |
12: 89,221,804 (GRCm39) |
I528V |
possibly damaging |
Het |
Or10al6 |
A |
T |
17: 38,082,730 (GRCm39) |
H71L |
possibly damaging |
Het |
Osbpl8 |
A |
G |
10: 111,103,608 (GRCm39) |
K204R |
probably damaging |
Het |
Pax8 |
A |
G |
2: 24,325,931 (GRCm39) |
S318P |
possibly damaging |
Het |
Pcdh18 |
T |
A |
3: 49,710,590 (GRCm39) |
N242Y |
probably damaging |
Het |
Pkd1l2 |
T |
A |
8: 117,786,259 (GRCm39) |
K649* |
probably null |
Het |
Ppm1n |
A |
T |
7: 19,013,179 (GRCm39) |
D257E |
probably benign |
Het |
Pxdn |
A |
G |
12: 30,052,796 (GRCm39) |
E811G |
probably damaging |
Het |
Relb |
T |
C |
7: 19,350,298 (GRCm39) |
I218V |
probably benign |
Het |
Rreb1 |
T |
C |
13: 38,115,010 (GRCm39) |
C790R |
probably damaging |
Het |
Rtkn2 |
G |
T |
10: 67,861,349 (GRCm39) |
C258F |
possibly damaging |
Het |
Scn11a |
G |
A |
9: 119,613,227 (GRCm39) |
|
probably benign |
Het |
Snx8 |
G |
A |
5: 140,343,851 (GRCm39) |
R96C |
probably damaging |
Het |
Syne2 |
A |
T |
12: 76,107,000 (GRCm39) |
T5649S |
possibly damaging |
Het |
Tm2d3 |
T |
A |
7: 65,344,970 (GRCm39) |
C82* |
probably null |
Het |
Tnpo2 |
T |
C |
8: 85,767,155 (GRCm39) |
L55P |
probably damaging |
Het |
Tsc22d2 |
T |
C |
3: 58,324,836 (GRCm39) |
|
probably benign |
Het |
Ttll3 |
T |
G |
6: 113,371,690 (GRCm39) |
V19G |
probably damaging |
Het |
Ube2r2 |
A |
G |
4: 41,174,119 (GRCm39) |
I86V |
probably benign |
Het |
Vps13d |
G |
A |
4: 144,814,892 (GRCm39) |
T3153I |
probably damaging |
Het |
Wwp1 |
A |
G |
4: 19,627,636 (GRCm39) |
I753T |
probably damaging |
Het |
|
Other mutations in Neu3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01149:Neu3
|
APN |
7 |
99,463,087 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01530:Neu3
|
APN |
7 |
99,462,953 (GRCm39) |
missense |
probably benign |
0.00 |
R0395:Neu3
|
UTSW |
7 |
99,462,985 (GRCm39) |
missense |
probably benign |
|
R0519:Neu3
|
UTSW |
7 |
99,472,524 (GRCm39) |
splice site |
probably benign |
|
R0555:Neu3
|
UTSW |
7 |
99,463,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R1659:Neu3
|
UTSW |
7 |
99,462,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R1706:Neu3
|
UTSW |
7 |
99,472,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R1893:Neu3
|
UTSW |
7 |
99,472,627 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2271:Neu3
|
UTSW |
7 |
99,462,650 (GRCm39) |
missense |
probably benign |
0.00 |
R2472:Neu3
|
UTSW |
7 |
99,462,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Neu3
|
UTSW |
7 |
99,472,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R5589:Neu3
|
UTSW |
7 |
99,472,636 (GRCm39) |
missense |
probably benign |
0.01 |
R5932:Neu3
|
UTSW |
7 |
99,462,525 (GRCm39) |
nonsense |
probably null |
|
R6307:Neu3
|
UTSW |
7 |
99,462,929 (GRCm39) |
missense |
probably benign |
|
R7072:Neu3
|
UTSW |
7 |
99,463,404 (GRCm39) |
nonsense |
probably null |
|
R7099:Neu3
|
UTSW |
7 |
99,463,027 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7582:Neu3
|
UTSW |
7 |
99,463,174 (GRCm39) |
missense |
probably benign |
0.02 |
R8057:Neu3
|
UTSW |
7 |
99,463,435 (GRCm39) |
missense |
probably benign |
0.08 |
R8497:Neu3
|
UTSW |
7 |
99,472,342 (GRCm39) |
splice site |
probably null |
|
X0023:Neu3
|
UTSW |
7 |
99,462,811 (GRCm39) |
missense |
probably benign |
0.00 |
|