Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agpat5 |
A |
G |
8: 18,929,621 (GRCm39) |
E250G |
probably benign |
Het |
Aox4 |
A |
T |
1: 58,294,670 (GRCm39) |
T960S |
probably damaging |
Het |
Bach2 |
T |
A |
4: 32,563,150 (GRCm39) |
L539H |
probably damaging |
Het |
Capn1 |
A |
T |
19: 6,044,877 (GRCm39) |
L465Q |
probably damaging |
Het |
Cd300c |
A |
G |
11: 114,850,453 (GRCm39) |
F117L |
probably benign |
Het |
Cep104 |
T |
G |
4: 154,069,400 (GRCm39) |
M207R |
probably damaging |
Het |
Chd2 |
A |
G |
7: 73,141,163 (GRCm39) |
Y577H |
possibly damaging |
Het |
Cplane2 |
C |
T |
4: 140,945,900 (GRCm39) |
R148C |
probably damaging |
Het |
Cspg4 |
T |
G |
9: 56,804,905 (GRCm39) |
D1905E |
probably damaging |
Het |
Dhx37 |
T |
C |
5: 125,508,677 (GRCm39) |
K86R |
probably benign |
Het |
Drd2 |
T |
A |
9: 49,313,443 (GRCm39) |
V204D |
probably damaging |
Het |
Gclc |
A |
T |
9: 77,699,242 (GRCm39) |
I520L |
probably benign |
Het |
Gpat3 |
A |
G |
5: 101,032,252 (GRCm39) |
D183G |
probably benign |
Het |
Gpat4 |
G |
A |
8: 23,670,171 (GRCm39) |
P286L |
probably damaging |
Het |
Gprin3 |
T |
C |
6: 59,330,618 (GRCm39) |
E563G |
probably benign |
Het |
Grm8 |
A |
T |
6: 27,761,228 (GRCm39) |
L332* |
probably null |
Het |
Grpel1 |
T |
A |
5: 36,626,827 (GRCm39) |
N36K |
probably benign |
Het |
Hecw1 |
C |
T |
13: 14,520,643 (GRCm39) |
S198N |
probably benign |
Het |
Kcna2 |
T |
C |
3: 107,012,112 (GRCm39) |
I231T |
probably benign |
Het |
Lpcat1 |
T |
C |
13: 73,637,212 (GRCm39) |
I114T |
possibly damaging |
Het |
Mast4 |
G |
T |
13: 102,875,319 (GRCm39) |
H1350N |
probably damaging |
Het |
Ncor2 |
T |
C |
5: 125,195,756 (GRCm39) |
|
probably benign |
Het |
Ntn1 |
C |
G |
11: 68,276,619 (GRCm39) |
D110H |
probably damaging |
Het |
Or2b11 |
G |
T |
11: 59,462,427 (GRCm39) |
N46K |
probably damaging |
Het |
Pigb |
T |
C |
9: 72,924,755 (GRCm39) |
N468S |
probably benign |
Het |
Pik3r2 |
G |
A |
8: 71,223,065 (GRCm39) |
R452C |
probably benign |
Het |
Plekhg1 |
A |
G |
10: 3,823,400 (GRCm39) |
T123A |
probably damaging |
Het |
Ptges3l |
T |
C |
11: 101,312,443 (GRCm39) |
*67W |
probably null |
Het |
Rgs12 |
G |
A |
5: 35,123,359 (GRCm39) |
V381M |
possibly damaging |
Het |
Rrm2 |
G |
T |
12: 24,758,598 (GRCm39) |
A47S |
probably benign |
Het |
Six2 |
G |
T |
17: 85,992,615 (GRCm39) |
S296Y |
probably damaging |
Het |
Slc5a12 |
T |
A |
2: 110,463,081 (GRCm39) |
C392* |
probably null |
Het |
Snx5 |
A |
T |
2: 144,096,821 (GRCm39) |
|
probably null |
Het |
Svep1 |
A |
G |
4: 58,096,177 (GRCm39) |
L1481P |
probably damaging |
Het |
Tspan18 |
T |
C |
2: 93,050,453 (GRCm39) |
I57V |
probably benign |
Het |
Ube3b |
C |
A |
5: 114,538,012 (GRCm39) |
Q368K |
probably damaging |
Het |
Zfhx4 |
A |
T |
3: 5,466,269 (GRCm39) |
K2142N |
probably damaging |
Het |
Zfp729a |
A |
T |
13: 67,767,997 (GRCm39) |
F744Y |
probably damaging |
Het |
|
Other mutations in Col4a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Col4a1
|
APN |
8 |
11,290,077 (GRCm39) |
splice site |
probably benign |
|
IGL00503:Col4a1
|
APN |
8 |
11,290,076 (GRCm39) |
splice site |
probably benign |
|
IGL00938:Col4a1
|
APN |
8 |
11,286,456 (GRCm39) |
intron |
probably benign |
|
IGL01295:Col4a1
|
APN |
8 |
11,286,075 (GRCm39) |
intron |
probably benign |
|
IGL01406:Col4a1
|
APN |
8 |
11,268,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01807:Col4a1
|
APN |
8 |
11,297,056 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL01865:Col4a1
|
APN |
8 |
11,251,790 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02166:Col4a1
|
APN |
8 |
11,294,509 (GRCm39) |
unclassified |
probably benign |
|
IGL02234:Col4a1
|
APN |
8 |
11,266,713 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02445:Col4a1
|
APN |
8 |
11,283,911 (GRCm39) |
intron |
probably benign |
|
IGL02719:Col4a1
|
APN |
8 |
11,281,950 (GRCm39) |
intron |
probably benign |
|
IGL02817:Col4a1
|
APN |
8 |
11,270,259 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02821:Col4a1
|
APN |
8 |
11,271,375 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02870:Col4a1
|
APN |
8 |
11,271,375 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02935:Col4a1
|
APN |
8 |
11,269,166 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03085:Col4a1
|
APN |
8 |
11,272,198 (GRCm39) |
nonsense |
probably null |
|
Wayne
|
UTSW |
8 |
11,259,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03134:Col4a1
|
UTSW |
8 |
11,290,069 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0076:Col4a1
|
UTSW |
8 |
11,268,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R0076:Col4a1
|
UTSW |
8 |
11,268,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Col4a1
|
UTSW |
8 |
11,268,780 (GRCm39) |
splice site |
probably benign |
|
R0239:Col4a1
|
UTSW |
8 |
11,268,780 (GRCm39) |
splice site |
probably benign |
|
R0268:Col4a1
|
UTSW |
8 |
11,317,588 (GRCm39) |
splice site |
probably benign |
|
R0320:Col4a1
|
UTSW |
8 |
11,292,782 (GRCm39) |
splice site |
probably null |
|
R0402:Col4a1
|
UTSW |
8 |
11,249,838 (GRCm39) |
utr 3 prime |
probably benign |
|
R0483:Col4a1
|
UTSW |
8 |
11,286,423 (GRCm39) |
splice site |
probably benign |
|
R0511:Col4a1
|
UTSW |
8 |
11,258,333 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0544:Col4a1
|
UTSW |
8 |
11,276,487 (GRCm39) |
intron |
probably benign |
|
R0630:Col4a1
|
UTSW |
8 |
11,249,889 (GRCm39) |
splice site |
probably benign |
|
R0648:Col4a1
|
UTSW |
8 |
11,296,892 (GRCm39) |
missense |
unknown |
|
R0733:Col4a1
|
UTSW |
8 |
11,268,934 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0839:Col4a1
|
UTSW |
8 |
11,271,015 (GRCm39) |
missense |
probably damaging |
0.96 |
R0900:Col4a1
|
UTSW |
8 |
11,268,014 (GRCm39) |
small deletion |
probably benign |
|
R0941:Col4a1
|
UTSW |
8 |
11,258,296 (GRCm39) |
missense |
unknown |
|
R1456:Col4a1
|
UTSW |
8 |
11,292,829 (GRCm39) |
splice site |
probably benign |
|
R1728:Col4a1
|
UTSW |
8 |
11,262,712 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1832:Col4a1
|
UTSW |
8 |
11,264,644 (GRCm39) |
splice site |
probably benign |
|
R1862:Col4a1
|
UTSW |
8 |
11,276,439 (GRCm39) |
intron |
probably benign |
|
R1955:Col4a1
|
UTSW |
8 |
11,258,228 (GRCm39) |
splice site |
probably null |
|
R2058:Col4a1
|
UTSW |
8 |
11,260,792 (GRCm39) |
missense |
probably damaging |
0.96 |
R2263:Col4a1
|
UTSW |
8 |
11,362,586 (GRCm39) |
unclassified |
probably benign |
|
R2696:Col4a1
|
UTSW |
8 |
11,285,092 (GRCm39) |
splice site |
probably null |
|
R3826:Col4a1
|
UTSW |
8 |
11,259,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R3828:Col4a1
|
UTSW |
8 |
11,259,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R3829:Col4a1
|
UTSW |
8 |
11,259,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Col4a1
|
UTSW |
8 |
11,251,665 (GRCm39) |
utr 3 prime |
probably benign |
|
R3980:Col4a1
|
UTSW |
8 |
11,289,155 (GRCm39) |
intron |
probably benign |
|
R4120:Col4a1
|
UTSW |
8 |
11,256,263 (GRCm39) |
missense |
unknown |
|
R4152:Col4a1
|
UTSW |
8 |
11,267,227 (GRCm39) |
splice site |
probably null |
|
R4437:Col4a1
|
UTSW |
8 |
11,256,387 (GRCm39) |
nonsense |
probably null |
|
R5237:Col4a1
|
UTSW |
8 |
11,295,068 (GRCm39) |
unclassified |
probably benign |
|
R5362:Col4a1
|
UTSW |
8 |
11,295,760 (GRCm39) |
unclassified |
probably benign |
|
R5488:Col4a1
|
UTSW |
8 |
11,362,550 (GRCm39) |
unclassified |
probably benign |
|
R5489:Col4a1
|
UTSW |
8 |
11,362,550 (GRCm39) |
unclassified |
probably benign |
|
R5864:Col4a1
|
UTSW |
8 |
11,252,973 (GRCm39) |
utr 3 prime |
probably benign |
|
R5929:Col4a1
|
UTSW |
8 |
11,266,788 (GRCm39) |
missense |
probably benign |
0.17 |
R6159:Col4a1
|
UTSW |
8 |
11,270,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R6261:Col4a1
|
UTSW |
8 |
11,257,409 (GRCm39) |
splice site |
probably null |
|
R6404:Col4a1
|
UTSW |
8 |
11,257,409 (GRCm39) |
splice site |
probably null |
|
R6520:Col4a1
|
UTSW |
8 |
11,269,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R6862:Col4a1
|
UTSW |
8 |
11,252,926 (GRCm39) |
utr 3 prime |
probably benign |
|
R6974:Col4a1
|
UTSW |
8 |
11,362,538 (GRCm39) |
unclassified |
probably benign |
|
R7329:Col4a1
|
UTSW |
8 |
11,276,494 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7893:Col4a1
|
UTSW |
8 |
11,270,243 (GRCm39) |
missense |
unknown |
|
R8392:Col4a1
|
UTSW |
8 |
11,258,333 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8809:Col4a1
|
UTSW |
8 |
11,295,916 (GRCm39) |
missense |
unknown |
|
R8957:Col4a1
|
UTSW |
8 |
11,295,906 (GRCm39) |
unclassified |
probably benign |
|
R9013:Col4a1
|
UTSW |
8 |
11,272,270 (GRCm39) |
missense |
probably benign |
0.02 |
R9048:Col4a1
|
UTSW |
8 |
11,281,944 (GRCm39) |
splice site |
probably benign |
|
R9102:Col4a1
|
UTSW |
8 |
11,253,007 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9154:Col4a1
|
UTSW |
8 |
11,267,446 (GRCm39) |
missense |
probably damaging |
0.99 |
R9379:Col4a1
|
UTSW |
8 |
11,249,838 (GRCm39) |
missense |
unknown |
|
Z1088:Col4a1
|
UTSW |
8 |
11,296,859 (GRCm39) |
splice site |
probably benign |
|
Z1177:Col4a1
|
UTSW |
8 |
11,289,024 (GRCm39) |
missense |
unknown |
|
Z1177:Col4a1
|
UTSW |
8 |
11,285,218 (GRCm39) |
missense |
unknown |
|
|