Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl3 |
A |
G |
4: 144,183,644 (GRCm39) |
S140P |
probably damaging |
Het |
Atp5mc1 |
A |
C |
11: 95,964,854 (GRCm39) |
C17W |
probably damaging |
Het |
Brd4 |
A |
G |
17: 32,417,470 (GRCm39) |
S161P |
unknown |
Het |
Cntrob |
A |
G |
11: 69,202,248 (GRCm39) |
V448A |
possibly damaging |
Het |
Col22a1 |
T |
C |
15: 71,693,886 (GRCm39) |
|
probably null |
Het |
Col6a4 |
T |
C |
9: 105,877,830 (GRCm39) |
Y2049C |
probably damaging |
Het |
Cpn1 |
C |
T |
19: 43,948,472 (GRCm39) |
D395N |
probably benign |
Het |
Csmd2 |
A |
G |
4: 128,266,390 (GRCm39) |
T769A |
probably benign |
Het |
Cts6 |
T |
A |
13: 61,349,607 (GRCm39) |
H62L |
probably damaging |
Het |
Ddx42 |
G |
T |
11: 106,119,646 (GRCm39) |
V144F |
probably benign |
Het |
E130308A19Rik |
A |
G |
4: 59,720,561 (GRCm39) |
S698G |
possibly damaging |
Het |
Eif2b3 |
T |
C |
4: 116,927,954 (GRCm39) |
L391P |
probably damaging |
Het |
Gm1043 |
T |
C |
5: 37,330,895 (GRCm39) |
I525T |
probably benign |
Het |
Kifc1 |
C |
T |
17: 34,104,829 (GRCm39) |
G59S |
probably benign |
Het |
Lancl1 |
T |
C |
1: 67,043,542 (GRCm39) |
E360G |
probably benign |
Het |
Lrp4 |
T |
C |
2: 91,332,340 (GRCm39) |
L1679S |
probably benign |
Het |
Mroh9 |
T |
A |
1: 162,903,130 (GRCm39) |
D91V |
probably damaging |
Het |
Myo1c |
C |
T |
11: 75,562,461 (GRCm39) |
P918S |
probably benign |
Het |
Ntsr1 |
T |
C |
2: 180,142,719 (GRCm39) |
I170T |
probably damaging |
Het |
Or2ag15 |
T |
A |
7: 106,340,911 (GRCm39) |
I77F |
probably benign |
Het |
Or2ag16 |
A |
G |
7: 106,351,776 (GRCm39) |
I273T |
probably benign |
Het |
Or6n2 |
T |
C |
1: 173,897,611 (GRCm39) |
L249P |
probably damaging |
Het |
Or6z5 |
G |
A |
7: 6,477,720 (GRCm39) |
D204N |
probably benign |
Het |
Pcolce |
T |
A |
5: 137,607,165 (GRCm39) |
T109S |
probably damaging |
Het |
Reg3b |
C |
A |
6: 78,349,905 (GRCm39) |
S148R |
possibly damaging |
Het |
Rps6ka4 |
A |
G |
19: 6,809,731 (GRCm39) |
S365P |
probably damaging |
Het |
Slc27a4 |
A |
G |
2: 29,702,860 (GRCm39) |
E563G |
probably benign |
Het |
Slc5a7 |
G |
T |
17: 54,583,644 (GRCm39) |
Q549K |
probably benign |
Het |
Stxbp3 |
A |
G |
3: 108,701,150 (GRCm39) |
L573P |
probably damaging |
Het |
Suco |
A |
T |
1: 161,687,001 (GRCm39) |
S120T |
possibly damaging |
Het |
Tnni2 |
G |
T |
7: 141,998,016 (GRCm39) |
G163V |
probably damaging |
Het |
Ttl |
T |
C |
2: 128,923,262 (GRCm39) |
I201T |
possibly damaging |
Het |
Vmn1r28 |
A |
G |
6: 58,242,945 (GRCm39) |
T263A |
probably benign |
Het |
Wdr1 |
A |
T |
5: 38,697,521 (GRCm39) |
D262E |
probably damaging |
Het |
Xylb |
A |
G |
9: 119,196,559 (GRCm39) |
H114R |
probably damaging |
Het |
Ywhaz |
T |
C |
15: 36,791,166 (GRCm39) |
Y19C |
probably damaging |
Het |
Zdbf2 |
A |
G |
1: 63,343,667 (GRCm39) |
E682G |
possibly 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 |
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 |
|
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 |
|