Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
A |
T |
1: 130,670,573 (GRCm39) |
Q265L |
possibly damaging |
Het |
Akr1c18 |
T |
A |
13: 4,187,232 (GRCm39) |
H168L |
probably damaging |
Het |
Arid3b |
A |
G |
9: 57,741,207 (GRCm39) |
S80P |
possibly damaging |
Het |
Barhl2 |
C |
T |
5: 106,603,365 (GRCm39) |
A265T |
possibly damaging |
Het |
Brd1 |
A |
C |
15: 88,614,361 (GRCm39) |
V178G |
probably benign |
Het |
Brd2 |
C |
T |
17: 34,333,397 (GRCm39) |
R26Q |
probably damaging |
Het |
Ddr2 |
T |
C |
1: 169,825,527 (GRCm39) |
M358V |
probably benign |
Het |
Dnajc14 |
A |
G |
10: 128,642,201 (GRCm39) |
D41G |
probably damaging |
Het |
Gchfr |
A |
G |
2: 119,000,229 (GRCm39) |
R37G |
probably damaging |
Het |
Gm20518 |
T |
A |
16: 17,676,362 (GRCm39) |
N136I |
probably damaging |
Het |
Grm6 |
A |
T |
11: 50,754,124 (GRCm39) |
|
probably benign |
Het |
Hydin |
T |
A |
8: 111,327,884 (GRCm39) |
V4797E |
probably damaging |
Het |
Iws1 |
C |
A |
18: 32,217,741 (GRCm39) |
N448K |
probably benign |
Het |
Lin7c |
T |
C |
2: 109,726,798 (GRCm39) |
|
probably benign |
Het |
Lrrc40 |
T |
A |
3: 157,754,087 (GRCm39) |
L196Q |
probably damaging |
Het |
Lrrtm2 |
C |
T |
18: 35,346,321 (GRCm39) |
G327D |
probably benign |
Het |
Masp1 |
C |
T |
16: 23,332,601 (GRCm39) |
C78Y |
probably damaging |
Het |
Mmd |
C |
T |
11: 90,155,360 (GRCm39) |
R101W |
probably damaging |
Het |
Myo1d |
A |
G |
11: 80,492,566 (GRCm39) |
Y730H |
probably benign |
Het |
Pcdh15 |
A |
G |
10: 74,126,914 (GRCm39) |
|
probably benign |
Het |
Pglyrp4 |
G |
A |
3: 90,646,335 (GRCm39) |
V290M |
probably damaging |
Het |
Plxna2 |
G |
A |
1: 194,326,404 (GRCm39) |
V113I |
probably benign |
Het |
Prkch |
T |
A |
12: 73,749,363 (GRCm39) |
|
probably benign |
Het |
Rabgef1 |
G |
T |
5: 130,237,565 (GRCm39) |
E213* |
probably null |
Het |
Rdh16f2 |
T |
A |
10: 127,702,533 (GRCm39) |
C37S |
probably damaging |
Het |
Reln |
A |
G |
5: 22,215,125 (GRCm39) |
Y1109H |
probably damaging |
Het |
Scn7a |
A |
T |
2: 66,572,326 (GRCm39) |
L215* |
probably null |
Het |
Slc25a33 |
A |
T |
4: 149,829,376 (GRCm39) |
L261H |
probably damaging |
Het |
Slc28a3 |
A |
T |
13: 58,717,225 (GRCm39) |
|
probably null |
Het |
Slc38a6 |
T |
C |
12: 73,398,577 (GRCm39) |
I369T |
probably benign |
Het |
Tgm4 |
A |
T |
9: 122,891,447 (GRCm39) |
|
probably benign |
Het |
Tnr |
A |
G |
1: 159,688,815 (GRCm39) |
I426V |
probably benign |
Het |
Vmn1r216 |
A |
G |
13: 23,283,574 (GRCm39) |
I86V |
probably benign |
Het |
Wwc1 |
G |
A |
11: 35,735,029 (GRCm39) |
P949S |
possibly damaging |
Het |
Zfp326 |
A |
T |
5: 106,044,399 (GRCm39) |
I286F |
probably damaging |
Het |
|
Other mutations in Erap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00661:Erap1
|
APN |
13 |
74,822,908 (GRCm39) |
unclassified |
probably benign |
|
IGL00903:Erap1
|
APN |
13 |
74,821,826 (GRCm39) |
missense |
probably benign |
|
IGL01095:Erap1
|
APN |
13 |
74,816,213 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01536:Erap1
|
APN |
13 |
74,810,542 (GRCm39) |
nonsense |
probably null |
|
IGL01646:Erap1
|
APN |
13 |
74,814,291 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01674:Erap1
|
APN |
13 |
74,812,350 (GRCm39) |
unclassified |
probably benign |
|
IGL01795:Erap1
|
APN |
13 |
74,814,209 (GRCm39) |
splice site |
probably null |
|
IGL01922:Erap1
|
APN |
13 |
74,810,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01951:Erap1
|
APN |
13 |
74,823,414 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02106:Erap1
|
APN |
13 |
74,794,758 (GRCm39) |
missense |
probably benign |
|
IGL02369:Erap1
|
APN |
13 |
74,814,645 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02669:Erap1
|
APN |
13 |
74,823,987 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02866:Erap1
|
APN |
13 |
74,816,118 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03093:Erap1
|
APN |
13 |
74,823,399 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03265:Erap1
|
APN |
13 |
74,812,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R0091:Erap1
|
UTSW |
13 |
74,816,171 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0456:Erap1
|
UTSW |
13 |
74,812,339 (GRCm39) |
missense |
probably benign |
0.24 |
R0556:Erap1
|
UTSW |
13 |
74,808,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R0627:Erap1
|
UTSW |
13 |
74,823,933 (GRCm39) |
unclassified |
probably benign |
|
R0825:Erap1
|
UTSW |
13 |
74,822,733 (GRCm39) |
unclassified |
probably benign |
|
R1123:Erap1
|
UTSW |
13 |
74,821,762 (GRCm39) |
missense |
probably benign |
|
R1530:Erap1
|
UTSW |
13 |
74,794,662 (GRCm39) |
missense |
probably benign |
0.06 |
R1619:Erap1
|
UTSW |
13 |
74,819,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R1731:Erap1
|
UTSW |
13 |
74,814,241 (GRCm39) |
nonsense |
probably null |
|
R1944:Erap1
|
UTSW |
13 |
74,794,758 (GRCm39) |
missense |
probably benign |
|
R2016:Erap1
|
UTSW |
13 |
74,812,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R2022:Erap1
|
UTSW |
13 |
74,814,627 (GRCm39) |
missense |
probably benign |
0.08 |
R2023:Erap1
|
UTSW |
13 |
74,814,627 (GRCm39) |
missense |
probably benign |
0.08 |
R2045:Erap1
|
UTSW |
13 |
74,817,569 (GRCm39) |
missense |
probably benign |
0.01 |
R2081:Erap1
|
UTSW |
13 |
74,823,426 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2187:Erap1
|
UTSW |
13 |
74,810,524 (GRCm39) |
missense |
probably damaging |
0.98 |
R2198:Erap1
|
UTSW |
13 |
74,794,806 (GRCm39) |
missense |
probably damaging |
0.97 |
R3938:Erap1
|
UTSW |
13 |
74,816,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R4052:Erap1
|
UTSW |
13 |
74,823,459 (GRCm39) |
missense |
probably benign |
0.13 |
R4062:Erap1
|
UTSW |
13 |
74,811,655 (GRCm39) |
missense |
probably benign |
0.02 |
R4128:Erap1
|
UTSW |
13 |
74,814,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R4247:Erap1
|
UTSW |
13 |
74,823,414 (GRCm39) |
missense |
probably damaging |
0.99 |
R4562:Erap1
|
UTSW |
13 |
74,821,778 (GRCm39) |
missense |
probably benign |
0.21 |
R4691:Erap1
|
UTSW |
13 |
74,821,811 (GRCm39) |
missense |
probably damaging |
0.99 |
R4831:Erap1
|
UTSW |
13 |
74,838,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R4916:Erap1
|
UTSW |
13 |
74,794,647 (GRCm39) |
missense |
probably benign |
|
R4983:Erap1
|
UTSW |
13 |
74,838,829 (GRCm39) |
missense |
probably benign |
0.01 |
R5213:Erap1
|
UTSW |
13 |
74,819,614 (GRCm39) |
splice site |
probably null |
|
R5229:Erap1
|
UTSW |
13 |
74,808,494 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5367:Erap1
|
UTSW |
13 |
74,794,680 (GRCm39) |
missense |
probably damaging |
0.99 |
R5463:Erap1
|
UTSW |
13 |
74,794,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R5566:Erap1
|
UTSW |
13 |
74,810,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R5972:Erap1
|
UTSW |
13 |
74,810,423 (GRCm39) |
splice site |
probably null |
|
R6112:Erap1
|
UTSW |
13 |
74,794,398 (GRCm39) |
missense |
probably benign |
0.44 |
R6132:Erap1
|
UTSW |
13 |
74,808,401 (GRCm39) |
missense |
probably benign |
0.00 |
R6180:Erap1
|
UTSW |
13 |
74,814,345 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6314:Erap1
|
UTSW |
13 |
74,822,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R6479:Erap1
|
UTSW |
13 |
74,811,612 (GRCm39) |
splice site |
probably null |
|
R6919:Erap1
|
UTSW |
13 |
74,819,552 (GRCm39) |
missense |
probably benign |
0.20 |
R7199:Erap1
|
UTSW |
13 |
74,814,258 (GRCm39) |
missense |
probably benign |
0.10 |
R7283:Erap1
|
UTSW |
13 |
74,821,903 (GRCm39) |
splice site |
probably null |
|
R7543:Erap1
|
UTSW |
13 |
74,822,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R8174:Erap1
|
UTSW |
13 |
74,794,683 (GRCm39) |
missense |
probably benign |
0.09 |
R8217:Erap1
|
UTSW |
13 |
74,820,937 (GRCm39) |
missense |
probably benign |
0.33 |
R8320:Erap1
|
UTSW |
13 |
74,814,668 (GRCm39) |
missense |
probably benign |
0.02 |
R8799:Erap1
|
UTSW |
13 |
74,805,755 (GRCm39) |
missense |
probably benign |
0.02 |
R9041:Erap1
|
UTSW |
13 |
74,822,818 (GRCm39) |
missense |
probably benign |
0.02 |
R9232:Erap1
|
UTSW |
13 |
74,811,637 (GRCm39) |
missense |
probably benign |
0.36 |
R9244:Erap1
|
UTSW |
13 |
74,821,903 (GRCm39) |
splice site |
probably null |
|
X0067:Erap1
|
UTSW |
13 |
74,808,491 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Erap1
|
UTSW |
13 |
74,805,757 (GRCm39) |
missense |
probably damaging |
1.00 |
|