Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alkal2 |
G |
T |
12: 30,934,850 (GRCm39) |
G23V |
probably damaging |
Het |
Atl2 |
C |
T |
17: 80,160,033 (GRCm39) |
W518* |
probably null |
Het |
Atp13a2 |
G |
A |
4: 140,730,046 (GRCm39) |
V646I |
probably benign |
Het |
Bcar1 |
A |
T |
8: 112,440,270 (GRCm39) |
F575I |
probably benign |
Het |
Bpifa6 |
T |
A |
2: 153,831,178 (GRCm39) |
L248* |
probably null |
Het |
Ccdc38 |
T |
C |
10: 93,399,111 (GRCm39) |
L193P |
probably damaging |
Het |
Ch25h |
A |
C |
19: 34,452,138 (GRCm39) |
I130S |
probably benign |
Het |
Chaf1a |
C |
A |
17: 56,351,109 (GRCm39) |
Q30K |
unknown |
Het |
Dab2ip |
T |
C |
2: 35,617,440 (GRCm39) |
L1106S |
probably damaging |
Het |
Dnah3 |
A |
G |
7: 119,550,375 (GRCm39) |
Y3315H |
probably benign |
Het |
Dnah7b |
G |
A |
1: 46,214,456 (GRCm39) |
V1074I |
possibly damaging |
Het |
Efemp1 |
A |
G |
11: 28,860,691 (GRCm39) |
Q200R |
probably benign |
Het |
Eif1ad3 |
A |
T |
12: 87,843,764 (GRCm39) |
D137V |
unknown |
Het |
Epx |
C |
T |
11: 87,763,557 (GRCm39) |
R221Q |
possibly damaging |
Het |
Exosc7 |
T |
C |
9: 122,956,942 (GRCm39) |
L109P |
probably damaging |
Het |
Fbxo22 |
T |
A |
9: 55,128,344 (GRCm39) |
F222I |
probably damaging |
Het |
Fcgbp |
A |
G |
7: 27,785,769 (GRCm39) |
D402G |
probably benign |
Het |
Foxr1 |
A |
G |
9: 44,347,351 (GRCm39) |
V62A |
probably damaging |
Het |
Gm8267 |
A |
T |
14: 44,961,515 (GRCm39) |
H59Q |
probably damaging |
Het |
Gnptab |
T |
A |
10: 88,275,071 (GRCm39) |
Y1090N |
probably damaging |
Het |
Gpr20 |
A |
G |
15: 73,568,161 (GRCm39) |
F76S |
probably damaging |
Het |
Gpr33 |
A |
G |
12: 52,070,907 (GRCm39) |
V44A |
probably benign |
Het |
Grin3a |
G |
A |
4: 49,665,599 (GRCm39) |
T1012I |
probably benign |
Het |
Itga1 |
T |
A |
13: 115,103,120 (GRCm39) |
T1104S |
probably benign |
Het |
Kidins220 |
T |
A |
12: 25,054,110 (GRCm39) |
Y537N |
probably damaging |
Het |
Lama1 |
A |
G |
17: 68,057,515 (GRCm39) |
T530A |
|
Het |
Lysmd2 |
A |
T |
9: 75,533,040 (GRCm39) |
|
probably benign |
Het |
Mdk |
T |
C |
2: 91,761,178 (GRCm39) |
K128E |
unknown |
Het |
Mphosph8 |
AC |
A |
14: 56,916,062 (GRCm39) |
|
probably null |
Het |
Muc16 |
A |
C |
9: 18,436,443 (GRCm39) |
L7915W |
possibly damaging |
Het |
Muc4 |
A |
T |
16: 32,753,423 (GRCm38) |
T1100S |
probably benign |
Het |
Mxra7 |
T |
C |
11: 116,695,376 (GRCm39) |
Y176C |
probably damaging |
Het |
Myh15 |
C |
A |
16: 48,940,381 (GRCm39) |
T777N |
probably damaging |
Het |
Myo18b |
A |
G |
5: 113,023,045 (GRCm39) |
S116P |
unknown |
Het |
Noc3l |
A |
G |
19: 38,784,254 (GRCm39) |
L543P |
probably damaging |
Het |
Or5h24 |
C |
T |
16: 58,919,004 (GRCm39) |
G117D |
unknown |
Het |
Or7a39 |
C |
T |
10: 78,715,170 (GRCm39) |
P55S |
probably benign |
Het |
Or8c10 |
T |
A |
9: 38,279,346 (GRCm39) |
V168E |
probably damaging |
Het |
Pkm |
G |
T |
9: 59,575,902 (GRCm39) |
R106L |
probably benign |
Het |
Prkab2 |
G |
T |
3: 97,570,911 (GRCm39) |
V112F |
probably benign |
Het |
Prkaca |
A |
T |
8: 84,717,151 (GRCm39) |
N172Y |
probably damaging |
Het |
Prmt8 |
A |
G |
6: 127,666,813 (GRCm39) |
V387A |
probably benign |
Het |
Rad17 |
T |
C |
13: 100,761,074 (GRCm39) |
T485A |
probably benign |
Het |
Rita1 |
G |
T |
5: 120,747,716 (GRCm39) |
T194K |
possibly damaging |
Het |
Rogdi |
C |
A |
16: 4,831,313 (GRCm39) |
|
probably benign |
Het |
Senp5 |
T |
C |
16: 31,808,117 (GRCm39) |
D379G |
probably benign |
Het |
Slc9a4 |
C |
T |
1: 40,619,520 (GRCm39) |
|
probably benign |
Het |
Tmem175 |
T |
A |
5: 108,791,075 (GRCm39) |
S208R |
probably benign |
Het |
Tmem237 |
A |
T |
1: 59,147,237 (GRCm39) |
Y299N |
probably damaging |
Het |
Tnrc6a |
T |
A |
7: 122,769,936 (GRCm39) |
N575K |
possibly damaging |
Het |
Trak2 |
A |
T |
1: 58,960,306 (GRCm39) |
C232* |
probably null |
Het |
Ubr3 |
A |
G |
2: 69,775,478 (GRCm39) |
H589R |
probably damaging |
Het |
Vcp |
T |
C |
4: 42,988,728 (GRCm39) |
T249A |
possibly damaging |
Het |
Vmn1r208 |
G |
C |
13: 22,956,947 (GRCm39) |
I183M |
probably benign |
Het |
Vmn1r231 |
C |
T |
17: 21,110,289 (GRCm39) |
V209I |
probably benign |
Het |
Vmn1r80 |
T |
C |
7: 11,926,994 (GRCm39) |
F35L |
probably benign |
Het |
Vmn2r58 |
A |
T |
7: 41,521,952 (GRCm39) |
I48N |
probably benign |
Het |
Vstm2a |
T |
A |
11: 16,231,898 (GRCm39) |
V231E |
probably damaging |
Het |
Zfp108 |
A |
C |
7: 23,960,087 (GRCm39) |
Y226S |
possibly damaging |
Het |
Zfp445 |
A |
T |
9: 122,682,695 (GRCm39) |
N415K |
possibly damaging |
Het |
Zfp938 |
T |
G |
10: 82,061,422 (GRCm39) |
R399S |
possibly damaging |
Het |
Zmym4 |
G |
A |
4: 126,804,762 (GRCm39) |
H464Y |
probably benign |
Het |
|
Other mutations in Slc4a4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00827:Slc4a4
|
APN |
5 |
89,327,545 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00976:Slc4a4
|
APN |
5 |
89,102,657 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01074:Slc4a4
|
APN |
5 |
89,327,633 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01120:Slc4a4
|
APN |
5 |
89,280,238 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01284:Slc4a4
|
APN |
5 |
89,277,532 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01375:Slc4a4
|
APN |
5 |
89,327,593 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01399:Slc4a4
|
APN |
5 |
89,376,794 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01487:Slc4a4
|
APN |
5 |
89,376,715 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02501:Slc4a4
|
APN |
5 |
89,277,508 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03104:Slc4a4
|
APN |
5 |
89,297,231 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03157:Slc4a4
|
APN |
5 |
89,304,372 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03205:Slc4a4
|
APN |
5 |
89,297,189 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03356:Slc4a4
|
APN |
5 |
89,270,342 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03372:Slc4a4
|
APN |
5 |
89,304,285 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03382:Slc4a4
|
APN |
5 |
89,376,695 (GRCm39) |
missense |
probably damaging |
1.00 |
camera
|
UTSW |
5 |
89,280,366 (GRCm39) |
missense |
probably damaging |
1.00 |
pixels
|
UTSW |
5 |
89,270,262 (GRCm39) |
missense |
probably damaging |
0.99 |
Shutter
|
UTSW |
5 |
89,373,807 (GRCm39) |
missense |
probably damaging |
1.00 |
Tetrapod
|
UTSW |
5 |
89,376,831 (GRCm39) |
missense |
probably damaging |
1.00 |
Therapod
|
UTSW |
5 |
89,283,581 (GRCm39) |
missense |
probably damaging |
1.00 |
tripod
|
UTSW |
5 |
89,297,192 (GRCm39) |
missense |
possibly damaging |
0.52 |
BB008:Slc4a4
|
UTSW |
5 |
89,318,640 (GRCm39) |
missense |
probably benign |
0.00 |
BB018:Slc4a4
|
UTSW |
5 |
89,318,640 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4515001:Slc4a4
|
UTSW |
5 |
89,281,112 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4544001:Slc4a4
|
UTSW |
5 |
89,186,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R0007:Slc4a4
|
UTSW |
5 |
89,186,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Slc4a4
|
UTSW |
5 |
89,304,195 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0052:Slc4a4
|
UTSW |
5 |
89,304,195 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0054:Slc4a4
|
UTSW |
5 |
89,304,195 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0055:Slc4a4
|
UTSW |
5 |
89,304,195 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0230:Slc4a4
|
UTSW |
5 |
89,304,195 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0234:Slc4a4
|
UTSW |
5 |
89,304,195 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0234:Slc4a4
|
UTSW |
5 |
89,304,195 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0632:Slc4a4
|
UTSW |
5 |
89,277,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R1199:Slc4a4
|
UTSW |
5 |
89,363,653 (GRCm39) |
critical splice donor site |
probably null |
|
R1597:Slc4a4
|
UTSW |
5 |
89,283,587 (GRCm39) |
missense |
probably benign |
0.01 |
R1783:Slc4a4
|
UTSW |
5 |
89,280,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:Slc4a4
|
UTSW |
5 |
89,194,167 (GRCm39) |
missense |
probably damaging |
0.98 |
R1896:Slc4a4
|
UTSW |
5 |
89,194,167 (GRCm39) |
missense |
probably damaging |
0.98 |
R2000:Slc4a4
|
UTSW |
5 |
89,176,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R2139:Slc4a4
|
UTSW |
5 |
89,194,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R2163:Slc4a4
|
UTSW |
5 |
89,362,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R2513:Slc4a4
|
UTSW |
5 |
89,304,257 (GRCm39) |
missense |
probably benign |
0.00 |
R2873:Slc4a4
|
UTSW |
5 |
89,283,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R2995:Slc4a4
|
UTSW |
5 |
89,082,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R3054:Slc4a4
|
UTSW |
5 |
89,373,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R3055:Slc4a4
|
UTSW |
5 |
89,373,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R3055:Slc4a4
|
UTSW |
5 |
89,280,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R3056:Slc4a4
|
UTSW |
5 |
89,373,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R3617:Slc4a4
|
UTSW |
5 |
89,382,663 (GRCm39) |
missense |
probably benign |
0.00 |
R3856:Slc4a4
|
UTSW |
5 |
89,380,698 (GRCm39) |
missense |
probably benign |
0.00 |
R3863:Slc4a4
|
UTSW |
5 |
89,283,507 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3896:Slc4a4
|
UTSW |
5 |
89,345,625 (GRCm39) |
splice site |
probably benign |
|
R4007:Slc4a4
|
UTSW |
5 |
89,362,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R4616:Slc4a4
|
UTSW |
5 |
89,186,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R4740:Slc4a4
|
UTSW |
5 |
89,373,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R5009:Slc4a4
|
UTSW |
5 |
89,297,157 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5119:Slc4a4
|
UTSW |
5 |
89,102,721 (GRCm39) |
missense |
probably null |
0.97 |
R5228:Slc4a4
|
UTSW |
5 |
89,304,384 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5394:Slc4a4
|
UTSW |
5 |
89,345,623 (GRCm39) |
critical splice donor site |
probably null |
|
R5396:Slc4a4
|
UTSW |
5 |
89,194,076 (GRCm39) |
missense |
probably benign |
0.00 |
R5662:Slc4a4
|
UTSW |
5 |
89,176,103 (GRCm39) |
missense |
probably damaging |
0.96 |
R5664:Slc4a4
|
UTSW |
5 |
89,176,103 (GRCm39) |
missense |
probably damaging |
0.96 |
R6021:Slc4a4
|
UTSW |
5 |
89,188,261 (GRCm39) |
intron |
probably benign |
|
R6088:Slc4a4
|
UTSW |
5 |
89,345,563 (GRCm39) |
missense |
probably benign |
0.12 |
R6337:Slc4a4
|
UTSW |
5 |
89,194,231 (GRCm39) |
missense |
probably benign |
0.21 |
R6416:Slc4a4
|
UTSW |
5 |
89,327,588 (GRCm39) |
missense |
probably benign |
0.26 |
R6452:Slc4a4
|
UTSW |
5 |
89,376,839 (GRCm39) |
missense |
probably benign |
0.05 |
R6524:Slc4a4
|
UTSW |
5 |
89,380,623 (GRCm39) |
missense |
probably benign |
0.01 |
R6566:Slc4a4
|
UTSW |
5 |
89,297,192 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6727:Slc4a4
|
UTSW |
5 |
89,318,624 (GRCm39) |
missense |
probably benign |
0.00 |
R6844:Slc4a4
|
UTSW |
5 |
89,376,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R6970:Slc4a4
|
UTSW |
5 |
89,327,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R7021:Slc4a4
|
UTSW |
5 |
89,188,205 (GRCm39) |
splice site |
probably null |
|
R7180:Slc4a4
|
UTSW |
5 |
89,194,095 (GRCm39) |
missense |
probably damaging |
0.97 |
R7197:Slc4a4
|
UTSW |
5 |
89,082,433 (GRCm39) |
intron |
probably benign |
|
R7246:Slc4a4
|
UTSW |
5 |
89,270,262 (GRCm39) |
missense |
probably damaging |
0.99 |
R7309:Slc4a4
|
UTSW |
5 |
89,318,610 (GRCm39) |
missense |
probably benign |
|
R7412:Slc4a4
|
UTSW |
5 |
89,362,506 (GRCm39) |
splice site |
probably null |
|
R7492:Slc4a4
|
UTSW |
5 |
89,277,509 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7561:Slc4a4
|
UTSW |
5 |
89,347,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R7577:Slc4a4
|
UTSW |
5 |
89,373,726 (GRCm39) |
missense |
probably damaging |
0.97 |
R7609:Slc4a4
|
UTSW |
5 |
89,283,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R7781:Slc4a4
|
UTSW |
5 |
89,376,791 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7931:Slc4a4
|
UTSW |
5 |
89,318,640 (GRCm39) |
missense |
probably benign |
0.00 |
R7950:Slc4a4
|
UTSW |
5 |
89,206,137 (GRCm39) |
splice site |
probably null |
|
R8078:Slc4a4
|
UTSW |
5 |
89,327,566 (GRCm39) |
missense |
probably benign |
0.00 |
R8332:Slc4a4
|
UTSW |
5 |
89,327,680 (GRCm39) |
missense |
probably benign |
0.11 |
R8534:Slc4a4
|
UTSW |
5 |
89,283,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R8735:Slc4a4
|
UTSW |
5 |
89,280,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R8786:Slc4a4
|
UTSW |
5 |
89,232,549 (GRCm39) |
missense |
probably benign |
0.07 |
R8968:Slc4a4
|
UTSW |
5 |
89,232,512 (GRCm39) |
missense |
probably benign |
|
R9014:Slc4a4
|
UTSW |
5 |
89,280,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R9031:Slc4a4
|
UTSW |
5 |
89,205,568 (GRCm39) |
intron |
probably benign |
|
R9195:Slc4a4
|
UTSW |
5 |
89,281,055 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9236:Slc4a4
|
UTSW |
5 |
89,194,158 (GRCm39) |
nonsense |
probably null |
|
R9261:Slc4a4
|
UTSW |
5 |
89,347,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R9325:Slc4a4
|
UTSW |
5 |
89,376,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R9401:Slc4a4
|
UTSW |
5 |
89,327,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R9457:Slc4a4
|
UTSW |
5 |
89,362,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R9462:Slc4a4
|
UTSW |
5 |
89,194,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R9681:Slc4a4
|
UTSW |
5 |
89,102,723 (GRCm39) |
nonsense |
probably null |
|
R9709:Slc4a4
|
UTSW |
5 |
89,188,205 (GRCm39) |
splice site |
probably null |
|
Z1177:Slc4a4
|
UTSW |
5 |
89,280,318 (GRCm39) |
missense |
probably damaging |
1.00 |
|