Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,353,874 (GRCm39) |
I3732T |
probably benign |
Het |
Ago1 |
C |
A |
4: 126,354,830 (GRCm39) |
K127N |
possibly damaging |
Het |
Akap8l |
T |
C |
17: 32,557,374 (GRCm39) |
N79S |
probably damaging |
Het |
AY358078 |
A |
G |
14: 52,042,065 (GRCm39) |
T147A |
unknown |
Het |
Cabp4 |
T |
C |
19: 4,189,251 (GRCm39) |
D102G |
probably benign |
Het |
Cdc34 |
C |
T |
10: 79,520,655 (GRCm39) |
R61C |
probably damaging |
Het |
Chac1 |
A |
G |
2: 119,181,887 (GRCm39) |
K2E |
unknown |
Het |
Cltc |
C |
T |
11: 86,621,093 (GRCm39) |
V305I |
probably damaging |
Het |
Cog7 |
T |
C |
7: 121,524,683 (GRCm39) |
T704A |
probably benign |
Het |
Cux1 |
A |
G |
5: 136,421,174 (GRCm39) |
V184A |
probably damaging |
Het |
Daglb |
A |
T |
5: 143,464,274 (GRCm39) |
T262S |
probably benign |
Het |
Dglucy |
A |
G |
12: 100,753,905 (GRCm39) |
I12V |
probably null |
Het |
Dnah7a |
A |
G |
1: 53,621,753 (GRCm39) |
V1124A |
probably benign |
Het |
Eef2 |
C |
CN |
10: 81,014,603 (GRCm39) |
|
probably null |
Het |
Eif3k |
C |
A |
7: 28,681,133 (GRCm39) |
A9S |
probably benign |
Het |
Elapor1 |
T |
A |
3: 108,378,731 (GRCm39) |
I408F |
probably damaging |
Het |
Gli3 |
A |
T |
13: 15,723,038 (GRCm39) |
M60L |
possibly damaging |
Het |
Hk1 |
C |
T |
10: 62,178,330 (GRCm39) |
E4K |
probably benign |
Het |
Kmt2b |
C |
A |
7: 30,276,570 (GRCm39) |
V1701L |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 41,231,807 (GRCm39) |
H1107R |
probably damaging |
Het |
Lypd10 |
A |
T |
7: 24,413,711 (GRCm39) |
R242S |
possibly damaging |
Het |
Ncor1 |
A |
G |
11: 62,249,679 (GRCm39) |
|
probably null |
Het |
Or5h23 |
T |
A |
16: 58,906,439 (GRCm39) |
M136L |
possibly damaging |
Het |
Or6c70 |
T |
G |
10: 129,710,607 (GRCm39) |
R6S |
probably benign |
Het |
Plekhg4 |
G |
A |
8: 106,106,134 (GRCm39) |
|
probably null |
Het |
Pmfbp1 |
G |
T |
8: 110,251,739 (GRCm39) |
E327D |
probably damaging |
Het |
Slc22a17 |
G |
A |
14: 55,146,427 (GRCm39) |
P63L |
probably damaging |
Het |
Slc37a1 |
G |
A |
17: 31,556,982 (GRCm39) |
V383M |
possibly damaging |
Het |
Slc9a9 |
T |
A |
9: 94,691,990 (GRCm39) |
Y182N |
probably damaging |
Het |
Slx4ip |
A |
G |
2: 136,842,162 (GRCm39) |
D29G |
probably damaging |
Het |
St3gal5 |
T |
C |
6: 72,130,446 (GRCm39) |
V319A |
possibly damaging |
Het |
Tbc1d10c |
C |
T |
19: 4,239,881 (GRCm39) |
M76I |
possibly damaging |
Het |
Thrb |
C |
A |
14: 18,033,526 (GRCm38) |
H416N |
probably benign |
Het |
Timp2 |
T |
A |
11: 118,210,987 (GRCm39) |
D60V |
probably damaging |
Het |
Ubxn6 |
C |
T |
17: 56,376,745 (GRCm39) |
E216K |
probably benign |
Het |
Unc79 |
T |
C |
12: 103,094,527 (GRCm39) |
M1977T |
probably benign |
Het |
Uri1 |
G |
A |
7: 37,662,954 (GRCm39) |
R347* |
probably null |
Het |
Vmn1r73 |
G |
A |
7: 11,490,591 (GRCm39) |
W136* |
probably null |
Het |
Vmn2r124 |
T |
C |
17: 18,294,102 (GRCm39) |
Y730H |
probably benign |
Het |
Wnk4 |
C |
T |
11: 101,166,462 (GRCm39) |
|
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,468,679 (GRCm39) |
N2971D |
probably damaging |
Het |
|
Other mutations in Ano5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00653:Ano5
|
APN |
7 |
51,216,261 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01328:Ano5
|
APN |
7 |
51,206,019 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01800:Ano5
|
APN |
7 |
51,222,823 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01888:Ano5
|
APN |
7 |
51,216,048 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02221:Ano5
|
APN |
7 |
51,220,071 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02538:Ano5
|
APN |
7 |
51,233,523 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Ano5
|
APN |
7 |
51,216,025 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03133:Ano5
|
APN |
7 |
51,226,260 (GRCm39) |
nonsense |
probably null |
|
IGL03167:Ano5
|
APN |
7 |
51,235,259 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03233:Ano5
|
APN |
7 |
51,220,116 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4466001:Ano5
|
UTSW |
7 |
51,194,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Ano5
|
UTSW |
7 |
51,185,218 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0233:Ano5
|
UTSW |
7 |
51,185,218 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0675:Ano5
|
UTSW |
7 |
51,224,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Ano5
|
UTSW |
7 |
51,237,506 (GRCm39) |
missense |
probably benign |
0.20 |
R0764:Ano5
|
UTSW |
7 |
51,187,590 (GRCm39) |
splice site |
probably benign |
|
R1159:Ano5
|
UTSW |
7 |
51,229,222 (GRCm39) |
splice site |
probably benign |
|
R1218:Ano5
|
UTSW |
7 |
51,220,169 (GRCm39) |
splice site |
probably null |
|
R1288:Ano5
|
UTSW |
7 |
51,196,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1329:Ano5
|
UTSW |
7 |
51,196,533 (GRCm39) |
missense |
probably benign |
|
R1484:Ano5
|
UTSW |
7 |
51,216,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Ano5
|
UTSW |
7 |
51,233,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Ano5
|
UTSW |
7 |
51,229,316 (GRCm39) |
missense |
probably benign |
0.00 |
R1691:Ano5
|
UTSW |
7 |
51,240,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R1859:Ano5
|
UTSW |
7 |
51,196,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Ano5
|
UTSW |
7 |
51,187,561 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2066:Ano5
|
UTSW |
7 |
51,235,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R2088:Ano5
|
UTSW |
7 |
51,237,454 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2103:Ano5
|
UTSW |
7 |
51,187,561 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2248:Ano5
|
UTSW |
7 |
51,243,537 (GRCm39) |
missense |
probably benign |
0.00 |
R3692:Ano5
|
UTSW |
7 |
51,240,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R3723:Ano5
|
UTSW |
7 |
51,226,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R3805:Ano5
|
UTSW |
7 |
51,226,398 (GRCm39) |
missense |
probably benign |
0.22 |
R3883:Ano5
|
UTSW |
7 |
51,216,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R3978:Ano5
|
UTSW |
7 |
51,237,554 (GRCm39) |
missense |
probably benign |
|
R4035:Ano5
|
UTSW |
7 |
51,216,233 (GRCm39) |
splice site |
probably benign |
|
R4239:Ano5
|
UTSW |
7 |
51,237,414 (GRCm39) |
missense |
probably damaging |
0.99 |
R4466:Ano5
|
UTSW |
7 |
51,220,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R4644:Ano5
|
UTSW |
7 |
51,237,433 (GRCm39) |
nonsense |
probably null |
|
R5021:Ano5
|
UTSW |
7 |
51,205,933 (GRCm39) |
missense |
probably benign |
|
R5028:Ano5
|
UTSW |
7 |
51,187,458 (GRCm39) |
splice site |
probably null |
|
R5659:Ano5
|
UTSW |
7 |
51,233,562 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5660:Ano5
|
UTSW |
7 |
51,233,562 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5680:Ano5
|
UTSW |
7 |
51,233,562 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5786:Ano5
|
UTSW |
7 |
51,216,066 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5787:Ano5
|
UTSW |
7 |
51,216,066 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5788:Ano5
|
UTSW |
7 |
51,216,066 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5856:Ano5
|
UTSW |
7 |
51,235,074 (GRCm39) |
missense |
probably benign |
0.01 |
R5930:Ano5
|
UTSW |
7 |
51,235,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R5984:Ano5
|
UTSW |
7 |
51,243,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R6015:Ano5
|
UTSW |
7 |
51,224,525 (GRCm39) |
missense |
probably benign |
0.00 |
R6030:Ano5
|
UTSW |
7 |
51,224,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R6030:Ano5
|
UTSW |
7 |
51,224,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Ano5
|
UTSW |
7 |
51,215,879 (GRCm39) |
splice site |
probably null |
|
R7552:Ano5
|
UTSW |
7 |
51,196,528 (GRCm39) |
missense |
probably benign |
0.31 |
R7559:Ano5
|
UTSW |
7 |
51,224,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R7712:Ano5
|
UTSW |
7 |
51,240,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R7712:Ano5
|
UTSW |
7 |
51,222,805 (GRCm39) |
missense |
probably benign |
0.00 |
R7805:Ano5
|
UTSW |
7 |
51,187,548 (GRCm39) |
missense |
probably damaging |
0.97 |
R7808:Ano5
|
UTSW |
7 |
51,237,543 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7840:Ano5
|
UTSW |
7 |
51,237,480 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7886:Ano5
|
UTSW |
7 |
51,220,141 (GRCm39) |
missense |
probably benign |
0.12 |
R7975:Ano5
|
UTSW |
7 |
51,216,286 (GRCm39) |
missense |
probably null |
0.98 |
R8006:Ano5
|
UTSW |
7 |
51,243,518 (GRCm39) |
missense |
probably benign |
0.05 |
R8060:Ano5
|
UTSW |
7 |
51,237,531 (GRCm39) |
missense |
probably benign |
0.01 |
R8084:Ano5
|
UTSW |
7 |
51,229,287 (GRCm39) |
missense |
probably benign |
0.01 |
R8351:Ano5
|
UTSW |
7 |
51,203,626 (GRCm39) |
missense |
probably benign |
0.10 |
R8504:Ano5
|
UTSW |
7 |
51,222,776 (GRCm39) |
missense |
probably benign |
0.01 |
R8699:Ano5
|
UTSW |
7 |
51,243,519 (GRCm39) |
missense |
probably benign |
|
R8710:Ano5
|
UTSW |
7 |
51,243,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R8752:Ano5
|
UTSW |
7 |
51,196,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R8771:Ano5
|
UTSW |
7 |
51,220,047 (GRCm39) |
nonsense |
probably null |
|
R8771:Ano5
|
UTSW |
7 |
51,216,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R8815:Ano5
|
UTSW |
7 |
51,194,548 (GRCm39) |
nonsense |
probably null |
|
R9057:Ano5
|
UTSW |
7 |
51,203,654 (GRCm39) |
missense |
probably benign |
0.05 |
R9118:Ano5
|
UTSW |
7 |
51,220,122 (GRCm39) |
missense |
probably damaging |
0.99 |
R9217:Ano5
|
UTSW |
7 |
51,243,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R9462:Ano5
|
UTSW |
7 |
51,235,200 (GRCm39) |
missense |
probably benign |
0.19 |
R9699:Ano5
|
UTSW |
7 |
51,229,309 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Ano5
|
UTSW |
7 |
51,243,399 (GRCm39) |
nonsense |
probably null |
|
X0065:Ano5
|
UTSW |
7 |
51,226,376 (GRCm39) |
nonsense |
probably null |
|
Z1176:Ano5
|
UTSW |
7 |
51,224,451 (GRCm39) |
missense |
probably damaging |
0.99 |
|