Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Camk2b |
A |
G |
11: 5,978,932 (GRCm39) |
V32A |
probably damaging |
Het |
Cbr2 |
A |
T |
11: 120,621,278 (GRCm39) |
H140Q |
probably benign |
Het |
Cdk19 |
T |
C |
10: 40,351,609 (GRCm39) |
V258A |
probably damaging |
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 |
Commd9 |
C |
A |
2: 101,727,486 (GRCm39) |
N93K |
probably benign |
Het |
Cplane2 |
C |
T |
4: 140,945,900 (GRCm39) |
R148C |
probably damaging |
Het |
Cx3cl1 |
A |
T |
8: 95,503,934 (GRCm39) |
|
probably benign |
Het |
Cxcr6 |
A |
T |
9: 123,639,934 (GRCm39) |
M319L |
probably benign |
Het |
Dlg5 |
T |
A |
14: 24,196,226 (GRCm39) |
K1308I |
probably damaging |
Het |
Dnah17 |
G |
A |
11: 117,931,984 (GRCm39) |
|
probably benign |
Het |
Ffar2 |
A |
T |
7: 30,519,510 (GRCm39) |
I10N |
possibly damaging |
Het |
Gm17521 |
C |
A |
X: 121,938,922 (GRCm39) |
G149C |
unknown |
Het |
Gm5862 |
T |
G |
5: 26,224,345 (GRCm39) |
H208P |
probably benign |
Het |
Gpat4 |
G |
A |
8: 23,670,171 (GRCm39) |
P286L |
probably damaging |
Het |
Ino80d |
A |
T |
1: 63,101,237 (GRCm39) |
M463K |
possibly damaging |
Het |
Lrp2 |
G |
A |
2: 69,256,356 (GRCm39) |
P4595S |
probably benign |
Het |
Mark4 |
A |
G |
7: 19,177,112 (GRCm39) |
I239T |
possibly damaging |
Het |
Mcoln1 |
C |
T |
8: 3,550,601 (GRCm39) |
A2V |
possibly damaging |
Het |
Mcts1 |
T |
C |
X: 37,691,445 (GRCm39) |
|
probably benign |
Het |
Mrgprb5 |
T |
A |
7: 47,817,839 (GRCm39) |
M299L |
probably benign |
Het |
Ncapg2 |
A |
T |
12: 116,370,938 (GRCm39) |
|
probably benign |
Het |
Or56a3 |
A |
G |
7: 104,735,504 (GRCm39) |
N194D |
probably benign |
Het |
Pcdhga4 |
G |
T |
18: 37,820,654 (GRCm39) |
L734F |
possibly damaging |
Het |
Rrm2 |
G |
T |
12: 24,758,598 (GRCm39) |
A47S |
probably benign |
Het |
Rsph6a |
T |
C |
7: 18,791,539 (GRCm39) |
L236P |
probably damaging |
Het |
Rtkn2 |
A |
T |
10: 67,833,456 (GRCm39) |
|
probably null |
Het |
Stk11 |
T |
C |
10: 79,963,782 (GRCm39) |
|
probably null |
Het |
Syt14 |
T |
C |
1: 192,584,083 (GRCm39) |
N444S |
probably damaging |
Het |
Tmem59l |
A |
G |
8: 70,939,951 (GRCm39) |
L6S |
unknown |
Het |
Tnks |
A |
G |
8: 35,340,332 (GRCm39) |
F429L |
probably damaging |
Het |
Usp15 |
T |
A |
10: 123,032,775 (GRCm39) |
I16F |
possibly damaging |
Het |
Vps50 |
T |
C |
6: 3,533,500 (GRCm39) |
I244T |
probably benign |
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 |
R3829:Col4a1
|
UTSW |
8 |
11,259,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R3830: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 |
|
|