Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A3galt2 |
T |
C |
4: 128,660,779 (GRCm39) |
Y143H |
possibly damaging |
Het |
Aco1 |
G |
A |
4: 40,186,367 (GRCm39) |
R593Q |
probably benign |
Het |
Adamts2 |
T |
C |
11: 50,679,567 (GRCm39) |
V849A |
possibly damaging |
Het |
Ash1l |
A |
T |
3: 88,892,368 (GRCm39) |
T1416S |
probably damaging |
Het |
Cdc5l |
A |
G |
17: 45,737,570 (GRCm39) |
W63R |
probably damaging |
Het |
Cep95 |
T |
A |
11: 106,692,328 (GRCm39) |
D169E |
probably damaging |
Het |
Col14a1 |
A |
C |
15: 55,235,977 (GRCm39) |
N297T |
unknown |
Het |
Fbxl19 |
G |
T |
7: 127,347,525 (GRCm39) |
|
probably benign |
Het |
Flnc |
T |
C |
6: 29,446,376 (GRCm39) |
V931A |
possibly damaging |
Het |
Foxj2 |
A |
G |
6: 122,810,202 (GRCm39) |
H187R |
probably benign |
Het |
Hectd4 |
G |
A |
5: 121,441,634 (GRCm39) |
V1199I |
probably benign |
Het |
Ighv7-4 |
A |
G |
12: 114,186,470 (GRCm39) |
Y101H |
possibly damaging |
Het |
Igkv10-94 |
T |
A |
6: 68,681,507 (GRCm39) |
Y111F |
probably benign |
Het |
Lin28a |
C |
T |
4: 133,745,372 (GRCm39) |
V74M |
possibly damaging |
Het |
Lrrc49 |
T |
C |
9: 60,592,335 (GRCm39) |
N53S |
possibly damaging |
Het |
Mroh9 |
T |
G |
1: 162,866,541 (GRCm39) |
T701P |
possibly damaging |
Het |
Ndst4 |
A |
T |
3: 125,515,801 (GRCm39) |
K309* |
probably null |
Het |
Nlrp9a |
T |
C |
7: 26,256,817 (GRCm39) |
V145A |
possibly damaging |
Het |
Or2l5 |
T |
C |
16: 19,333,571 (GRCm39) |
I272V |
probably benign |
Het |
Ovgp1 |
A |
T |
3: 105,893,897 (GRCm39) |
K557* |
probably null |
Het |
Pde4b |
T |
C |
4: 102,459,073 (GRCm39) |
L546P |
probably damaging |
Het |
Pkd1 |
G |
A |
17: 24,794,951 (GRCm39) |
V2213M |
probably damaging |
Het |
Plekhh1 |
A |
G |
12: 79,111,263 (GRCm39) |
I542V |
probably benign |
Het |
Ppan |
A |
G |
9: 20,802,506 (GRCm39) |
|
probably null |
Het |
Prdm15 |
A |
T |
16: 97,637,005 (GRCm39) |
V104E |
probably benign |
Het |
Semp2l2a |
A |
C |
8: 13,887,573 (GRCm39) |
S173A |
probably benign |
Het |
Sik3 |
A |
G |
9: 46,123,351 (GRCm39) |
H1050R |
probably benign |
Het |
Slc35d3 |
A |
G |
10: 19,725,086 (GRCm39) |
F257L |
possibly damaging |
Het |
Tfip11 |
A |
G |
5: 112,482,263 (GRCm39) |
|
probably null |
Het |
Tmem132d |
A |
G |
5: 128,345,596 (GRCm39) |
S309P |
possibly damaging |
Het |
Tmem87a |
T |
C |
2: 120,234,400 (GRCm39) |
I48V |
probably benign |
Het |
V1rd19 |
T |
A |
7: 23,703,056 (GRCm39) |
L174* |
probably null |
Het |
Zfp729a |
A |
G |
13: 67,767,767 (GRCm39) |
C821R |
possibly damaging |
Het |
Zfp970 |
C |
A |
2: 177,167,388 (GRCm39) |
H321N |
probably damaging |
Het |
Zzef1 |
T |
C |
11: 72,804,055 (GRCm39) |
L2599P |
probably damaging |
Het |
|
Other mutations in Cp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00423:Cp
|
APN |
3 |
20,039,826 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00923:Cp
|
APN |
3 |
20,024,165 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01302:Cp
|
APN |
3 |
20,020,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01407:Cp
|
APN |
3 |
20,031,369 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01505:Cp
|
APN |
3 |
20,031,356 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01677:Cp
|
APN |
3 |
20,020,598 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02013:Cp
|
APN |
3 |
20,042,213 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02114:Cp
|
APN |
3 |
20,020,511 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02950:Cp
|
APN |
3 |
20,042,165 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03330:Cp
|
APN |
3 |
20,020,599 (GRCm39) |
missense |
probably damaging |
1.00 |
iron10
|
UTSW |
3 |
20,043,311 (GRCm39) |
unclassified |
probably benign |
|
R0008:Cp
|
UTSW |
3 |
20,022,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R0008:Cp
|
UTSW |
3 |
20,022,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R0320:Cp
|
UTSW |
3 |
20,029,012 (GRCm39) |
splice site |
probably benign |
|
R0632:Cp
|
UTSW |
3 |
20,025,246 (GRCm39) |
missense |
probably null |
0.98 |
R1103:Cp
|
UTSW |
3 |
20,036,149 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1137:Cp
|
UTSW |
3 |
20,033,116 (GRCm39) |
missense |
probably benign |
0.04 |
R1199:Cp
|
UTSW |
3 |
20,031,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R1523:Cp
|
UTSW |
3 |
20,043,229 (GRCm39) |
missense |
probably benign |
0.00 |
R1629:Cp
|
UTSW |
3 |
20,020,614 (GRCm39) |
critical splice donor site |
probably null |
|
R1678:Cp
|
UTSW |
3 |
20,026,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R1733:Cp
|
UTSW |
3 |
20,022,383 (GRCm39) |
splice site |
probably benign |
|
R1779:Cp
|
UTSW |
3 |
20,011,549 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1816:Cp
|
UTSW |
3 |
20,022,384 (GRCm39) |
splice site |
probably benign |
|
R1990:Cp
|
UTSW |
3 |
20,033,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Cp
|
UTSW |
3 |
20,041,598 (GRCm39) |
missense |
probably benign |
0.00 |
R2179:Cp
|
UTSW |
3 |
20,042,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R2249:Cp
|
UTSW |
3 |
20,041,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R3440:Cp
|
UTSW |
3 |
20,029,121 (GRCm39) |
missense |
probably benign |
0.02 |
R3441:Cp
|
UTSW |
3 |
20,029,121 (GRCm39) |
missense |
probably benign |
0.02 |
R3886:Cp
|
UTSW |
3 |
20,043,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3937:Cp
|
UTSW |
3 |
20,025,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R4387:Cp
|
UTSW |
3 |
20,031,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R4412:Cp
|
UTSW |
3 |
20,020,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R4413:Cp
|
UTSW |
3 |
20,020,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R4514:Cp
|
UTSW |
3 |
20,042,177 (GRCm39) |
missense |
probably damaging |
0.99 |
R4578:Cp
|
UTSW |
3 |
20,028,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R4579:Cp
|
UTSW |
3 |
20,011,599 (GRCm39) |
splice site |
probably null |
|
R4694:Cp
|
UTSW |
3 |
20,029,049 (GRCm39) |
missense |
probably benign |
0.07 |
R4724:Cp
|
UTSW |
3 |
20,026,811 (GRCm39) |
missense |
probably benign |
0.02 |
R4910:Cp
|
UTSW |
3 |
20,043,388 (GRCm39) |
unclassified |
probably benign |
|
R4960:Cp
|
UTSW |
3 |
20,027,961 (GRCm39) |
missense |
probably damaging |
0.96 |
R5043:Cp
|
UTSW |
3 |
20,028,081 (GRCm39) |
missense |
probably benign |
0.00 |
R5063:Cp
|
UTSW |
3 |
20,043,379 (GRCm39) |
missense |
probably benign |
0.27 |
R5294:Cp
|
UTSW |
3 |
20,020,480 (GRCm39) |
missense |
probably benign |
0.00 |
R5382:Cp
|
UTSW |
3 |
20,033,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R5404:Cp
|
UTSW |
3 |
20,043,292 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5569:Cp
|
UTSW |
3 |
20,033,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R5789:Cp
|
UTSW |
3 |
20,011,454 (GRCm39) |
missense |
probably benign |
|
R5943:Cp
|
UTSW |
3 |
20,018,470 (GRCm39) |
missense |
probably benign |
0.11 |
R6492:Cp
|
UTSW |
3 |
20,036,186 (GRCm39) |
missense |
probably benign |
0.20 |
R7007:Cp
|
UTSW |
3 |
20,024,137 (GRCm39) |
missense |
probably damaging |
0.97 |
R7126:Cp
|
UTSW |
3 |
20,034,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R7136:Cp
|
UTSW |
3 |
20,039,822 (GRCm39) |
nonsense |
probably null |
|
R7212:Cp
|
UTSW |
3 |
20,029,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R7269:Cp
|
UTSW |
3 |
20,037,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R7316:Cp
|
UTSW |
3 |
20,026,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R7336:Cp
|
UTSW |
3 |
20,018,696 (GRCm39) |
splice site |
probably null |
|
R7361:Cp
|
UTSW |
3 |
20,018,470 (GRCm39) |
missense |
probably benign |
0.11 |
R7578:Cp
|
UTSW |
3 |
20,043,262 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7593:Cp
|
UTSW |
3 |
20,020,494 (GRCm39) |
missense |
probably benign |
0.00 |
R7782:Cp
|
UTSW |
3 |
20,029,223 (GRCm39) |
critical splice donor site |
probably null |
|
R7858:Cp
|
UTSW |
3 |
20,025,219 (GRCm39) |
missense |
probably benign |
0.05 |
R8246:Cp
|
UTSW |
3 |
20,029,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Cp
|
UTSW |
3 |
20,020,570 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8300:Cp
|
UTSW |
3 |
20,011,385 (GRCm39) |
start gained |
probably benign |
|
R8507:Cp
|
UTSW |
3 |
20,025,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R8756:Cp
|
UTSW |
3 |
20,059,736 (GRCm39) |
critical splice donor site |
probably null |
|
R8826:Cp
|
UTSW |
3 |
20,039,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R8875:Cp
|
UTSW |
3 |
20,027,994 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9018:Cp
|
UTSW |
3 |
20,043,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R9072:Cp
|
UTSW |
3 |
20,033,158 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9111:Cp
|
UTSW |
3 |
20,027,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R9439:Cp
|
UTSW |
3 |
20,046,671 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9443:Cp
|
UTSW |
3 |
20,033,083 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9460:Cp
|
UTSW |
3 |
20,018,566 (GRCm39) |
missense |
|
|
R9733:Cp
|
UTSW |
3 |
20,033,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R9748:Cp
|
UTSW |
3 |
20,043,335 (GRCm39) |
missense |
possibly damaging |
0.71 |
|