Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930544G11Rik |
A |
T |
6: 65,930,212 (GRCm39) |
N149I |
probably benign |
Het |
Agxt |
G |
T |
1: 93,063,502 (GRCm39) |
A135S |
probably benign |
Het |
Aldh1a2 |
A |
T |
9: 71,159,880 (GRCm39) |
I40F |
probably damaging |
Het |
Ang |
T |
A |
14: 51,339,103 (GRCm39) |
C81* |
probably null |
Het |
Apc |
G |
T |
18: 34,447,315 (GRCm39) |
V1370F |
possibly damaging |
Het |
Arfgef3 |
T |
C |
10: 18,553,614 (GRCm39) |
T127A |
possibly damaging |
Het |
Cd1d1 |
A |
G |
3: 86,905,489 (GRCm39) |
L168P |
probably damaging |
Het |
Cfap251 |
A |
T |
5: 123,428,032 (GRCm39) |
M510L |
probably benign |
Het |
Epb42 |
C |
A |
2: 120,855,233 (GRCm39) |
V451F |
probably damaging |
Het |
F5 |
T |
A |
1: 164,039,441 (GRCm39) |
L2017Q |
probably damaging |
Het |
Hmcn2 |
A |
T |
2: 31,225,424 (GRCm39) |
|
probably null |
Het |
Kif13a |
G |
A |
13: 46,930,573 (GRCm39) |
P164S |
probably damaging |
Het |
Kirrel1 |
T |
A |
3: 86,992,150 (GRCm39) |
I593F |
probably benign |
Het |
Lin28b |
A |
T |
10: 45,257,183 (GRCm39) |
I265N |
possibly damaging |
Het |
Mctp2 |
A |
T |
7: 71,850,155 (GRCm39) |
D507E |
probably benign |
Het |
Morc3 |
G |
A |
16: 93,641,215 (GRCm39) |
|
probably null |
Het |
Myo3b |
T |
C |
2: 70,085,597 (GRCm39) |
Y750H |
probably damaging |
Het |
Nrp1 |
T |
C |
8: 129,158,426 (GRCm39) |
S238P |
probably damaging |
Het |
Nsf |
C |
T |
11: 103,821,578 (GRCm39) |
E26K |
possibly damaging |
Het |
Otog |
A |
G |
7: 45,890,964 (GRCm39) |
E41G |
probably benign |
Het |
Pclo |
G |
T |
5: 14,728,946 (GRCm39) |
|
probably benign |
Het |
Pdzd2 |
T |
C |
15: 12,373,247 (GRCm39) |
D2296G |
probably damaging |
Het |
Peak1 |
A |
G |
9: 56,166,510 (GRCm39) |
C473R |
probably damaging |
Het |
Rad51ap2 |
T |
A |
12: 11,508,502 (GRCm39) |
M808K |
probably damaging |
Het |
Sec24b |
A |
C |
3: 129,795,965 (GRCm39) |
S651A |
probably benign |
Het |
Slc17a3 |
G |
A |
13: 24,036,418 (GRCm39) |
|
probably null |
Het |
Spata31d1b |
A |
G |
13: 59,864,660 (GRCm39) |
K603E |
possibly damaging |
Het |
Spata31e2 |
A |
T |
1: 26,721,919 (GRCm39) |
M1087K |
possibly damaging |
Het |
Sptbn4 |
T |
A |
7: 27,117,523 (GRCm39) |
K409* |
probably null |
Het |
Tacc2 |
G |
A |
7: 130,223,770 (GRCm39) |
V152I |
possibly damaging |
Het |
Tiam2 |
A |
G |
17: 3,527,536 (GRCm39) |
M65V |
probably benign |
Het |
Tmem131l |
G |
T |
3: 83,829,355 (GRCm39) |
Q1100K |
probably benign |
Het |
Togaram1 |
T |
C |
12: 65,014,444 (GRCm39) |
M565T |
probably damaging |
Het |
Trib1 |
T |
C |
15: 59,526,449 (GRCm39) |
Y340H |
probably benign |
Het |
Wdr7 |
A |
T |
18: 63,893,794 (GRCm39) |
M643L |
probably benign |
Het |
Zfp51 |
A |
T |
17: 21,684,093 (GRCm39) |
H236L |
probably damaging |
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 |
IGL02890:Slc4a10
|
APN |
2 |
62,117,260 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|