Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AAdacl4fm3 |
A |
G |
4: 144,430,263 (GRCm39) |
V242A |
possibly damaging |
Het |
Antxr2 |
T |
C |
5: 98,152,155 (GRCm39) |
D152G |
probably benign |
Het |
Blmh |
A |
T |
11: 76,856,758 (GRCm39) |
K118* |
probably null |
Het |
Bnip3 |
G |
A |
7: 138,499,801 (GRCm39) |
P62L |
probably damaging |
Het |
Catsperb |
A |
T |
12: 101,554,357 (GRCm39) |
T684S |
probably damaging |
Het |
Chd3 |
C |
A |
11: 69,248,209 (GRCm39) |
K894N |
possibly damaging |
Het |
Chkb |
T |
A |
15: 89,311,794 (GRCm39) |
R133S |
probably benign |
Het |
Dennd5a |
T |
C |
7: 109,507,579 (GRCm39) |
N803S |
probably benign |
Het |
Dync2li1 |
A |
T |
17: 84,956,668 (GRCm39) |
D276V |
possibly damaging |
Het |
Hgsnat |
C |
T |
8: 26,462,965 (GRCm39) |
V70M |
probably benign |
Het |
Leprot |
T |
C |
4: 101,509,673 (GRCm39) |
|
probably null |
Het |
Lhcgr |
G |
A |
17: 89,057,546 (GRCm39) |
A315V |
probably benign |
Het |
Lrrn4 |
C |
T |
2: 132,712,588 (GRCm39) |
V412I |
probably benign |
Het |
Macrod2 |
G |
A |
2: 140,261,824 (GRCm39) |
|
probably null |
Het |
Mmaa |
G |
A |
8: 80,008,199 (GRCm39) |
R13C |
probably damaging |
Het |
Plpp4 |
T |
A |
7: 128,918,023 (GRCm39) |
I66N |
probably damaging |
Het |
Prl4a1 |
T |
C |
13: 28,205,359 (GRCm39) |
V108A |
probably benign |
Het |
Prss1 |
G |
T |
6: 41,439,553 (GRCm39) |
K95N |
possibly damaging |
Het |
Rasa2 |
C |
T |
9: 96,459,606 (GRCm39) |
|
probably benign |
Het |
Relb |
A |
G |
7: 19,350,336 (GRCm39) |
V208A |
possibly damaging |
Het |
Sema3d |
T |
C |
5: 12,555,806 (GRCm39) |
S178P |
probably damaging |
Het |
Slc18a1 |
A |
T |
8: 69,526,383 (GRCm39) |
W102R |
probably benign |
Het |
Slc39a8 |
A |
C |
3: 135,563,873 (GRCm39) |
K239N |
probably benign |
Het |
Stap1 |
A |
G |
5: 86,229,132 (GRCm39) |
H100R |
probably benign |
Het |
Suz12 |
T |
A |
11: 79,889,918 (GRCm39) |
V143E |
probably damaging |
Het |
Tmf1 |
A |
G |
6: 97,153,455 (GRCm39) |
V206A |
probably benign |
Het |
Trim16 |
T |
A |
11: 62,728,058 (GRCm39) |
|
probably benign |
Het |
Ube2b |
C |
T |
11: 51,891,119 (GRCm39) |
|
probably null |
Het |
Vmn1r223 |
T |
C |
13: 23,434,254 (GRCm39) |
S283P |
probably damaging |
Het |
Wrn |
T |
A |
8: 33,809,173 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Erap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00432:Erap1
|
APN |
13 |
74,821,778 (GRCm39) |
missense |
probably benign |
0.17 |
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 |
|