Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
T |
7: 119,847,190 (GRCm39) |
M685L |
possibly damaging |
Het |
Abi3bp |
A |
G |
16: 56,394,862 (GRCm39) |
Y190C |
probably damaging |
Het |
Adam26a |
C |
A |
8: 44,022,888 (GRCm39) |
V201L |
probably benign |
Het |
Adamts20 |
G |
T |
15: 94,229,277 (GRCm39) |
D947E |
probably benign |
Het |
Ankrd26 |
A |
G |
6: 118,517,410 (GRCm39) |
|
probably null |
Het |
Apol11a |
C |
A |
15: 77,397,766 (GRCm39) |
T39N |
possibly damaging |
Het |
Arhgef38 |
T |
A |
3: 132,839,501 (GRCm39) |
|
probably null |
Het |
Armh4 |
T |
C |
14: 49,919,815 (GRCm39) |
D772G |
probably damaging |
Het |
Atp11b |
T |
C |
3: 35,893,296 (GRCm39) |
L883P |
probably damaging |
Het |
Btnl10 |
T |
A |
11: 58,814,586 (GRCm39) |
I422N |
probably damaging |
Het |
C2cd3 |
A |
G |
7: 100,056,232 (GRCm39) |
K547E |
possibly damaging |
Het |
Cdh2 |
T |
A |
18: 16,757,934 (GRCm39) |
L549F |
probably benign |
Het |
Celsr3 |
T |
C |
9: 108,713,037 (GRCm39) |
V1825A |
probably benign |
Het |
Cfap221 |
T |
C |
1: 119,881,389 (GRCm39) |
I358V |
probably benign |
Het |
Cimap2 |
G |
A |
4: 106,470,453 (GRCm39) |
|
probably benign |
Het |
Csmd1 |
T |
C |
8: 15,979,101 (GRCm39) |
K2828E |
probably damaging |
Het |
Ddah2 |
T |
C |
17: 35,279,821 (GRCm39) |
F137S |
probably damaging |
Het |
Ddx21 |
A |
G |
10: 62,429,847 (GRCm39) |
I299T |
probably damaging |
Het |
Dnah7a |
A |
T |
1: 53,495,691 (GRCm39) |
|
probably benign |
Het |
Elmod1 |
A |
G |
9: 53,843,151 (GRCm39) |
I9T |
probably benign |
Het |
Epha2 |
A |
G |
4: 141,036,290 (GRCm39) |
E242G |
probably benign |
Het |
Erbb3 |
T |
C |
10: 128,410,335 (GRCm39) |
H641R |
possibly damaging |
Het |
Fbxl18 |
G |
A |
5: 142,871,978 (GRCm39) |
A419V |
probably damaging |
Het |
Fli1 |
T |
C |
9: 32,335,209 (GRCm39) |
M408V |
probably benign |
Het |
Fmo4 |
T |
C |
1: 162,631,187 (GRCm39) |
N260S |
possibly damaging |
Het |
Fry |
A |
G |
5: 150,249,597 (GRCm39) |
E136G |
probably damaging |
Het |
Gm10477 |
T |
A |
X: 55,570,127 (GRCm39) |
F9Y |
probably damaging |
Het |
Gm8258 |
A |
G |
5: 104,924,320 (GRCm39) |
|
noncoding transcript |
Het |
Gpr68 |
T |
A |
12: 100,845,049 (GRCm39) |
D165V |
probably damaging |
Het |
Htt |
T |
A |
5: 34,951,456 (GRCm39) |
M139K |
probably benign |
Het |
Jup |
A |
G |
11: 100,263,120 (GRCm39) |
|
probably null |
Het |
Kifc5b |
G |
A |
17: 27,136,264 (GRCm39) |
|
probably null |
Het |
Krba1 |
T |
A |
6: 48,390,983 (GRCm39) |
|
probably null |
Het |
Lamp1 |
G |
A |
8: 13,217,257 (GRCm39) |
G89R |
probably damaging |
Het |
Lrrc17 |
C |
T |
5: 21,765,650 (GRCm39) |
S44F |
possibly damaging |
Het |
Mdga1 |
T |
C |
17: 30,071,581 (GRCm39) |
T347A |
probably damaging |
Het |
Mical3 |
A |
T |
6: 121,019,025 (GRCm39) |
W66R |
probably damaging |
Het |
Mpl |
A |
G |
4: 118,314,026 (GRCm39) |
Y73H |
probably benign |
Het |
Mterf1b |
T |
A |
5: 4,247,364 (GRCm39) |
I335N |
possibly damaging |
Het |
Mylk3 |
A |
G |
8: 86,079,494 (GRCm39) |
I388T |
probably damaging |
Het |
Myo15a |
C |
T |
11: 60,398,354 (GRCm39) |
R2775W |
probably damaging |
Het |
Myoz2 |
A |
T |
3: 122,819,765 (GRCm39) |
S65T |
probably damaging |
Het |
Ndrg1 |
T |
C |
15: 66,802,940 (GRCm39) |
T137A |
possibly damaging |
Het |
Neil3 |
G |
T |
8: 54,052,454 (GRCm39) |
N381K |
probably damaging |
Het |
Obsl1 |
T |
C |
1: 75,474,877 (GRCm39) |
Y841C |
probably damaging |
Het |
Or2b4 |
A |
G |
17: 38,115,996 (GRCm39) |
|
probably benign |
Het |
Or6b6 |
G |
A |
7: 106,571,389 (GRCm39) |
S54F |
possibly damaging |
Het |
Otogl |
T |
C |
10: 107,735,451 (GRCm39) |
D111G |
probably damaging |
Het |
Parp10 |
T |
C |
15: 76,127,051 (GRCm39) |
E103G |
probably damaging |
Het |
Pars2 |
T |
C |
4: 106,510,913 (GRCm39) |
F232L |
possibly damaging |
Het |
Pcdh18 |
A |
T |
3: 49,709,154 (GRCm39) |
F720L |
probably damaging |
Het |
Phf3 |
T |
C |
1: 30,869,704 (GRCm39) |
E448G |
possibly damaging |
Het |
Pigc |
A |
G |
1: 161,798,516 (GRCm39) |
Y166C |
probably damaging |
Het |
Pik3c2a |
A |
T |
7: 116,017,206 (GRCm39) |
S184T |
probably benign |
Het |
Pkd1l1 |
A |
G |
11: 8,794,670 (GRCm39) |
|
probably benign |
Het |
Plch2 |
G |
A |
4: 155,082,965 (GRCm39) |
S485F |
probably damaging |
Het |
Plxnd1 |
G |
T |
6: 115,955,045 (GRCm39) |
|
probably null |
Het |
Pnliprp2 |
G |
T |
19: 58,751,821 (GRCm39) |
V189L |
probably benign |
Het |
Prl8a2 |
T |
C |
13: 27,535,037 (GRCm39) |
V103A |
probably benign |
Het |
Psg23 |
G |
A |
7: 18,344,375 (GRCm39) |
T360I |
probably benign |
Het |
Rad51c |
A |
T |
11: 87,279,469 (GRCm39) |
I323N |
probably damaging |
Het |
Rsbn1l |
C |
T |
5: 21,156,696 (GRCm39) |
E30K |
probably benign |
Het |
Serpina3c |
C |
A |
12: 104,118,145 (GRCm39) |
L64F |
probably damaging |
Het |
Shroom1 |
A |
G |
11: 53,356,502 (GRCm39) |
D392G |
probably damaging |
Het |
Slc37a4 |
A |
G |
9: 44,312,808 (GRCm39) |
T321A |
probably damaging |
Het |
Slc41a2 |
A |
G |
10: 83,091,949 (GRCm39) |
L438S |
probably damaging |
Het |
Spef2 |
C |
T |
15: 9,584,194 (GRCm39) |
E1624K |
probably damaging |
Het |
Spef2 |
C |
T |
15: 9,597,487 (GRCm39) |
G1390R |
possibly damaging |
Het |
Spmap2l |
A |
T |
5: 77,202,431 (GRCm39) |
K284M |
probably benign |
Het |
Synj2 |
G |
T |
17: 6,078,825 (GRCm39) |
A740S |
possibly damaging |
Het |
Tigd4 |
A |
C |
3: 84,502,394 (GRCm39) |
D437A |
probably benign |
Het |
Timm21 |
G |
C |
18: 84,967,387 (GRCm39) |
L130V |
probably damaging |
Het |
Tmem106a |
CAGCTCAACACGACGGTA |
CAGCTCAACACGACGGTAAGCTCAACACGACGGTA |
11: 101,477,204 (GRCm39) |
|
probably benign |
Het |
Tmem131l |
A |
T |
3: 83,812,383 (GRCm39) |
C1313* |
probably null |
Het |
Tmem86b |
A |
T |
7: 4,632,698 (GRCm39) |
I47N |
possibly damaging |
Het |
Tspan13 |
T |
C |
12: 36,070,550 (GRCm39) |
|
probably null |
Het |
Vps54 |
A |
G |
11: 21,250,251 (GRCm39) |
T396A |
probably benign |
Het |
Zfp106 |
A |
T |
2: 120,344,096 (GRCm39) |
|
probably null |
Het |
Zfp668 |
T |
C |
7: 127,465,654 (GRCm39) |
|
probably null |
Het |
Zfp809 |
A |
T |
9: 22,150,027 (GRCm39) |
R175* |
probably null |
Het |
|
Other mutations in Slc26a5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01412:Slc26a5
|
APN |
5 |
22,020,734 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02486:Slc26a5
|
APN |
5 |
22,051,323 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02639:Slc26a5
|
APN |
5 |
22,024,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02810:Slc26a5
|
APN |
5 |
22,018,381 (GRCm39) |
splice site |
probably benign |
|
R0002:Slc26a5
|
UTSW |
5 |
22,019,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R0002:Slc26a5
|
UTSW |
5 |
22,019,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Slc26a5
|
UTSW |
5 |
22,016,342 (GRCm39) |
splice site |
probably null |
|
R0136:Slc26a5
|
UTSW |
5 |
22,039,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R0212:Slc26a5
|
UTSW |
5 |
22,028,547 (GRCm39) |
nonsense |
probably null |
|
R0522:Slc26a5
|
UTSW |
5 |
22,051,343 (GRCm39) |
missense |
probably damaging |
0.96 |
R0557:Slc26a5
|
UTSW |
5 |
22,024,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0711:Slc26a5
|
UTSW |
5 |
22,052,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R0959:Slc26a5
|
UTSW |
5 |
22,021,959 (GRCm39) |
missense |
probably benign |
0.01 |
R1214:Slc26a5
|
UTSW |
5 |
22,019,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Slc26a5
|
UTSW |
5 |
22,021,962 (GRCm39) |
missense |
probably benign |
0.12 |
R1647:Slc26a5
|
UTSW |
5 |
22,018,974 (GRCm39) |
nonsense |
probably null |
|
R1648:Slc26a5
|
UTSW |
5 |
22,018,974 (GRCm39) |
nonsense |
probably null |
|
R1861:Slc26a5
|
UTSW |
5 |
22,021,956 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2106:Slc26a5
|
UTSW |
5 |
22,028,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R2169:Slc26a5
|
UTSW |
5 |
22,018,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R2219:Slc26a5
|
UTSW |
5 |
22,028,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R2276:Slc26a5
|
UTSW |
5 |
22,028,545 (GRCm39) |
missense |
probably benign |
0.39 |
R2281:Slc26a5
|
UTSW |
5 |
22,036,508 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2325:Slc26a5
|
UTSW |
5 |
22,024,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R4031:Slc26a5
|
UTSW |
5 |
22,052,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R4793:Slc26a5
|
UTSW |
5 |
22,042,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R4941:Slc26a5
|
UTSW |
5 |
22,025,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R5122:Slc26a5
|
UTSW |
5 |
22,052,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R5274:Slc26a5
|
UTSW |
5 |
22,018,899 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5312:Slc26a5
|
UTSW |
5 |
22,052,258 (GRCm39) |
missense |
probably damaging |
0.99 |
R5628:Slc26a5
|
UTSW |
5 |
22,021,974 (GRCm39) |
missense |
probably benign |
0.20 |
R5806:Slc26a5
|
UTSW |
5 |
22,028,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R6227:Slc26a5
|
UTSW |
5 |
22,026,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R6525:Slc26a5
|
UTSW |
5 |
22,025,348 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6609:Slc26a5
|
UTSW |
5 |
22,024,717 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6885:Slc26a5
|
UTSW |
5 |
22,039,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R6974:Slc26a5
|
UTSW |
5 |
22,045,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R7001:Slc26a5
|
UTSW |
5 |
22,016,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7027:Slc26a5
|
UTSW |
5 |
22,021,972 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7174:Slc26a5
|
UTSW |
5 |
22,018,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R7184:Slc26a5
|
UTSW |
5 |
22,042,244 (GRCm39) |
nonsense |
probably null |
|
R7650:Slc26a5
|
UTSW |
5 |
22,039,328 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8431:Slc26a5
|
UTSW |
5 |
22,018,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R8812:Slc26a5
|
UTSW |
5 |
22,018,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R9184:Slc26a5
|
UTSW |
5 |
22,018,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R9215:Slc26a5
|
UTSW |
5 |
22,042,285 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9281:Slc26a5
|
UTSW |
5 |
22,019,051 (GRCm39) |
missense |
probably benign |
0.39 |
R9324:Slc26a5
|
UTSW |
5 |
22,018,334 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9516:Slc26a5
|
UTSW |
5 |
22,016,337 (GRCm39) |
nonsense |
probably null |
|
|