Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam39 |
A |
T |
8: 41,278,190 (GRCm39) |
I194L |
probably benign |
Het |
Akirin1 |
A |
G |
4: 123,631,855 (GRCm39) |
V171A |
probably damaging |
Het |
Camk2b |
A |
T |
11: 5,951,340 (GRCm39) |
D91E |
possibly damaging |
Het |
Ccser1 |
A |
G |
6: 62,356,815 (GRCm39) |
D751G |
probably damaging |
Het |
D6Wsu163e |
G |
A |
6: 126,951,450 (GRCm39) |
G500D |
probably damaging |
Het |
Dchs1 |
G |
T |
7: 105,405,698 (GRCm39) |
D2395E |
probably damaging |
Het |
Entrep3 |
A |
T |
3: 89,094,089 (GRCm39) |
T223S |
possibly damaging |
Het |
Fat3 |
T |
C |
9: 15,826,636 (GRCm39) |
T4439A |
probably benign |
Het |
Fn1 |
A |
G |
1: 71,637,531 (GRCm39) |
|
probably null |
Het |
Galnt14 |
A |
C |
17: 73,816,519 (GRCm39) |
|
probably null |
Het |
Gemin4 |
A |
C |
11: 76,102,090 (GRCm39) |
S890R |
probably damaging |
Het |
Glrp1 |
T |
A |
1: 88,437,510 (GRCm39) |
|
probably null |
Het |
Grik1 |
A |
G |
16: 87,693,690 (GRCm39) |
|
probably benign |
Het |
H2bc14 |
G |
T |
13: 21,906,356 (GRCm39) |
R30L |
probably benign |
Het |
Hspa12a |
C |
T |
19: 58,809,431 (GRCm39) |
|
probably null |
Het |
Hykk |
C |
T |
9: 54,827,995 (GRCm39) |
P78L |
probably benign |
Het |
Kctd13 |
G |
A |
7: 126,529,903 (GRCm39) |
G115R |
probably benign |
Het |
Kctd16 |
A |
G |
18: 40,390,080 (GRCm39) |
|
probably benign |
Het |
Ltn1 |
C |
T |
16: 87,206,185 (GRCm39) |
|
probably null |
Het |
Mat2a |
A |
G |
6: 72,413,229 (GRCm39) |
L167P |
probably damaging |
Het |
Myo6 |
A |
G |
9: 80,173,456 (GRCm39) |
E532G |
probably damaging |
Het |
Nrbp2 |
G |
T |
15: 75,961,306 (GRCm39) |
L272M |
probably damaging |
Het |
Nrdc |
A |
G |
4: 108,911,116 (GRCm39) |
D790G |
possibly damaging |
Het |
Or4e5 |
T |
A |
14: 52,728,368 (GRCm39) |
T18S |
probably benign |
Het |
Or5k16 |
T |
C |
16: 58,736,737 (GRCm39) |
D89G |
probably benign |
Het |
Or8g26 |
T |
C |
9: 39,095,564 (GRCm39) |
L27P |
probably damaging |
Het |
Pcdh10 |
A |
T |
3: 45,347,052 (GRCm39) |
H949L |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,269,956 (GRCm39) |
Y547C |
probably benign |
Het |
Pkhd1 |
A |
T |
1: 20,431,235 (GRCm39) |
V2392D |
probably damaging |
Het |
Ppp1r3g |
A |
T |
13: 36,153,314 (GRCm39) |
T245S |
probably damaging |
Het |
Prkaa1 |
A |
G |
15: 5,206,567 (GRCm39) |
N439S |
possibly damaging |
Het |
Radil |
A |
G |
5: 142,529,463 (GRCm39) |
Y78H |
probably damaging |
Het |
Ric8b |
A |
T |
10: 84,837,731 (GRCm39) |
M513L |
possibly damaging |
Het |
Slc5a12 |
T |
C |
2: 110,454,478 (GRCm39) |
|
probably benign |
Het |
Smg1 |
G |
A |
7: 117,784,724 (GRCm39) |
|
probably benign |
Het |
Spef2 |
C |
T |
15: 9,748,853 (GRCm39) |
M1I |
probably null |
Het |
Tmc5 |
A |
T |
7: 118,244,653 (GRCm39) |
|
probably benign |
Het |
Tpp2 |
C |
T |
1: 44,038,850 (GRCm39) |
A1132V |
probably damaging |
Het |
Ttll4 |
A |
T |
1: 74,726,498 (GRCm39) |
K699* |
probably null |
Het |
|
Other mutations in Slc4a10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00676:Slc4a10
|
APN |
2 |
62,120,345 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00990:Slc4a10
|
APN |
2 |
62,117,284 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01294:Slc4a10
|
APN |
2 |
62,083,653 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01628:Slc4a10
|
APN |
2 |
62,099,010 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01773:Slc4a10
|
APN |
2 |
62,021,101 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02119:Slc4a10
|
APN |
2 |
62,059,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02125:Slc4a10
|
APN |
2 |
62,098,515 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02406:Slc4a10
|
APN |
2 |
62,021,113 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02959:Slc4a10
|
APN |
2 |
62,098,487 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02979:Slc4a10
|
APN |
2 |
62,119,091 (GRCm39) |
missense |
probably null |
1.00 |
IGL03144:Slc4a10
|
APN |
2 |
62,080,810 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03175:Slc4a10
|
APN |
2 |
62,127,304 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03383:Slc4a10
|
APN |
2 |
62,097,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03412:Slc4a10
|
APN |
2 |
62,080,887 (GRCm39) |
splice site |
probably benign |
|
R0085:Slc4a10
|
UTSW |
2 |
62,074,690 (GRCm39) |
splice site |
probably benign |
|
R0401:Slc4a10
|
UTSW |
2 |
62,021,192 (GRCm39) |
missense |
probably benign |
0.27 |
R0433:Slc4a10
|
UTSW |
2 |
62,120,327 (GRCm39) |
missense |
probably benign |
0.01 |
R0482:Slc4a10
|
UTSW |
2 |
62,127,361 (GRCm39) |
splice site |
probably benign |
|
R0506:Slc4a10
|
UTSW |
2 |
62,080,877 (GRCm39) |
missense |
probably benign |
0.13 |
R0511:Slc4a10
|
UTSW |
2 |
62,117,206 (GRCm39) |
missense |
probably damaging |
0.97 |
R0590:Slc4a10
|
UTSW |
2 |
62,021,237 (GRCm39) |
splice site |
probably benign |
|
R0883:Slc4a10
|
UTSW |
2 |
62,073,742 (GRCm39) |
missense |
probably benign |
0.11 |
R1167:Slc4a10
|
UTSW |
2 |
62,058,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R1276:Slc4a10
|
UTSW |
2 |
62,080,787 (GRCm39) |
missense |
probably damaging |
0.99 |
R1395:Slc4a10
|
UTSW |
2 |
62,143,630 (GRCm39) |
missense |
probably benign |
0.00 |
R1455:Slc4a10
|
UTSW |
2 |
62,117,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R1589:Slc4a10
|
UTSW |
2 |
62,087,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R1677:Slc4a10
|
UTSW |
2 |
62,155,071 (GRCm39) |
missense |
probably benign |
|
R1848:Slc4a10
|
UTSW |
2 |
62,146,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R1987:Slc4a10
|
UTSW |
2 |
62,098,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Slc4a10
|
UTSW |
2 |
62,098,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R2018:Slc4a10
|
UTSW |
2 |
62,064,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Slc4a10
|
UTSW |
2 |
62,064,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R2407:Slc4a10
|
UTSW |
2 |
62,143,687 (GRCm39) |
missense |
probably benign |
|
R4067:Slc4a10
|
UTSW |
2 |
61,876,989 (GRCm39) |
start codon destroyed |
probably benign |
0.00 |
R4184:Slc4a10
|
UTSW |
2 |
62,147,786 (GRCm39) |
intron |
probably benign |
|
R4255:Slc4a10
|
UTSW |
2 |
62,112,280 (GRCm39) |
missense |
probably benign |
0.10 |
R4282:Slc4a10
|
UTSW |
2 |
62,074,687 (GRCm39) |
splice site |
probably null |
|
R4296:Slc4a10
|
UTSW |
2 |
62,064,772 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4361:Slc4a10
|
UTSW |
2 |
62,073,729 (GRCm39) |
missense |
probably benign |
0.00 |
R4596:Slc4a10
|
UTSW |
2 |
62,127,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R4709:Slc4a10
|
UTSW |
2 |
62,087,861 (GRCm39) |
missense |
probably null |
1.00 |
R4755:Slc4a10
|
UTSW |
2 |
62,127,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4836:Slc4a10
|
UTSW |
2 |
62,098,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R4841:Slc4a10
|
UTSW |
2 |
62,087,939 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4998:Slc4a10
|
UTSW |
2 |
62,074,783 (GRCm39) |
missense |
probably benign |
0.00 |
R5069:Slc4a10
|
UTSW |
2 |
62,097,915 (GRCm39) |
missense |
probably benign |
0.06 |
R5223:Slc4a10
|
UTSW |
2 |
62,083,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R5244:Slc4a10
|
UTSW |
2 |
62,119,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Slc4a10
|
UTSW |
2 |
62,120,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R5808:Slc4a10
|
UTSW |
2 |
62,080,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R5999:Slc4a10
|
UTSW |
2 |
62,073,775 (GRCm39) |
missense |
probably benign |
0.10 |
R6007:Slc4a10
|
UTSW |
2 |
62,099,216 (GRCm39) |
missense |
probably benign |
0.44 |
R6009:Slc4a10
|
UTSW |
2 |
61,877,034 (GRCm39) |
missense |
probably benign |
0.00 |
R6015:Slc4a10
|
UTSW |
2 |
62,059,046 (GRCm39) |
missense |
probably benign |
0.05 |
R6103:Slc4a10
|
UTSW |
2 |
62,064,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R6141:Slc4a10
|
UTSW |
2 |
62,041,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R6193:Slc4a10
|
UTSW |
2 |
62,073,701 (GRCm39) |
splice site |
probably null |
|
R6217:Slc4a10
|
UTSW |
2 |
62,134,295 (GRCm39) |
missense |
probably benign |
0.27 |
R6280:Slc4a10
|
UTSW |
2 |
62,112,310 (GRCm39) |
missense |
probably benign |
0.05 |
R6523:Slc4a10
|
UTSW |
2 |
62,117,305 (GRCm39) |
nonsense |
probably null |
|
R6643:Slc4a10
|
UTSW |
2 |
62,059,054 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6660:Slc4a10
|
UTSW |
2 |
62,080,747 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7008:Slc4a10
|
UTSW |
2 |
62,117,266 (GRCm39) |
missense |
probably benign |
0.00 |
R7083:Slc4a10
|
UTSW |
2 |
62,064,839 (GRCm39) |
missense |
probably benign |
0.03 |
R7223:Slc4a10
|
UTSW |
2 |
62,099,009 (GRCm39) |
missense |
probably damaging |
0.99 |
R7243:Slc4a10
|
UTSW |
2 |
62,134,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R7449:Slc4a10
|
UTSW |
2 |
62,134,290 (GRCm39) |
missense |
probably benign |
|
R7621:Slc4a10
|
UTSW |
2 |
62,080,823 (GRCm39) |
missense |
probably damaging |
0.98 |
R7692:Slc4a10
|
UTSW |
2 |
62,134,308 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7742:Slc4a10
|
UTSW |
2 |
62,127,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7905:Slc4a10
|
UTSW |
2 |
62,098,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8179:Slc4a10
|
UTSW |
2 |
62,073,792 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8528:Slc4a10
|
UTSW |
2 |
62,127,140 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8531:Slc4a10
|
UTSW |
2 |
62,097,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R8772:Slc4a10
|
UTSW |
2 |
62,134,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R9307:Slc4a10
|
UTSW |
2 |
62,083,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R9531:Slc4a10
|
UTSW |
2 |
62,099,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R9732:Slc4a10
|
UTSW |
2 |
62,135,086 (GRCm39) |
missense |
probably damaging |
0.97 |
U24488:Slc4a10
|
UTSW |
2 |
61,877,002 (GRCm39) |
missense |
probably benign |
0.05 |
X0019:Slc4a10
|
UTSW |
2 |
62,058,943 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Slc4a10
|
UTSW |
2 |
62,058,915 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Slc4a10
|
UTSW |
2 |
62,074,760 (GRCm39) |
missense |
probably benign |
|
Z1176:Slc4a10
|
UTSW |
2 |
62,041,723 (GRCm39) |
missense |
probably damaging |
1.00 |
|