Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
T |
17: 24,546,642 (GRCm39) |
S320T |
probably benign |
Het |
Anp32b |
G |
A |
4: 46,469,930 (GRCm39) |
E202K |
unknown |
Het |
Apcdd1 |
A |
G |
18: 63,069,973 (GRCm39) |
|
probably null |
Het |
Apobec2 |
A |
G |
17: 48,730,444 (GRCm39) |
V74A |
possibly damaging |
Het |
Arid3c |
A |
T |
4: 41,729,959 (GRCm39) |
C79S |
probably benign |
Het |
Atp1a2 |
A |
T |
1: 172,118,994 (GRCm39) |
|
probably benign |
Het |
B2m |
A |
T |
2: 121,981,471 (GRCm39) |
N62I |
probably damaging |
Het |
Borcs5 |
T |
C |
6: 134,663,086 (GRCm39) |
|
probably null |
Het |
Ccn1 |
A |
G |
3: 145,355,075 (GRCm39) |
L60P |
probably damaging |
Het |
Cdk11b |
A |
G |
4: 155,714,674 (GRCm39) |
K127E |
probably damaging |
Het |
Cep170 |
T |
C |
1: 176,563,433 (GRCm39) |
H726R |
possibly damaging |
Het |
Col5a2 |
A |
C |
1: 45,466,219 (GRCm39) |
S190A |
probably benign |
Het |
Cryba4 |
T |
C |
5: 112,398,990 (GRCm39) |
D5G |
probably damaging |
Het |
Cyp2a5 |
T |
G |
7: 26,535,299 (GRCm39) |
V87G |
probably damaging |
Het |
Dcaf8 |
A |
G |
1: 172,013,965 (GRCm39) |
|
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,404,500 (GRCm39) |
S2681P |
probably benign |
Het |
Ddx20 |
A |
G |
3: 105,586,327 (GRCm39) |
S673P |
probably damaging |
Het |
Deptor |
T |
A |
15: 55,044,428 (GRCm39) |
I198N |
probably damaging |
Het |
Ebf2 |
T |
C |
14: 67,628,007 (GRCm39) |
I334T |
possibly damaging |
Het |
F5 |
A |
G |
1: 164,020,134 (GRCm39) |
R870G |
probably benign |
Het |
Flg2 |
A |
C |
3: 93,109,871 (GRCm39) |
H633P |
unknown |
Het |
Gm11938 |
T |
A |
11: 99,494,119 (GRCm39) |
|
probably null |
Het |
Gm6370 |
A |
G |
5: 146,430,708 (GRCm39) |
T298A |
probably benign |
Het |
H60b |
C |
A |
10: 22,159,441 (GRCm39) |
|
probably benign |
Het |
Hsbp1 |
A |
G |
8: 120,071,324 (GRCm39) |
T4A |
possibly damaging |
Het |
Hsd3b3 |
A |
T |
3: 98,649,524 (GRCm39) |
D266E |
possibly damaging |
Het |
Ift172 |
T |
C |
5: 31,440,426 (GRCm39) |
Y287C |
probably damaging |
Het |
Il20rb |
T |
A |
9: 100,368,371 (GRCm39) |
Q4L |
probably benign |
Het |
Krt5 |
T |
C |
15: 101,617,470 (GRCm39) |
D421G |
probably damaging |
Het |
Lonp1 |
G |
C |
17: 56,927,263 (GRCm39) |
A330G |
probably benign |
Het |
Me3 |
A |
G |
7: 89,445,871 (GRCm39) |
D196G |
probably damaging |
Het |
Mfsd12 |
T |
A |
10: 81,199,461 (GRCm39) |
V451E |
probably null |
Het |
Mib1 |
A |
G |
18: 10,794,503 (GRCm39) |
N663S |
possibly damaging |
Het |
Mtus2 |
A |
T |
5: 148,015,244 (GRCm39) |
N679I |
probably benign |
Het |
Myt1 |
A |
G |
2: 181,438,915 (GRCm39) |
T146A |
probably benign |
Het |
Neb |
T |
A |
2: 52,160,281 (GRCm39) |
H2244L |
probably damaging |
Het |
Or51l4 |
T |
C |
7: 103,404,376 (GRCm39) |
T139A |
probably damaging |
Het |
Or5b21 |
A |
C |
19: 12,839,663 (GRCm39) |
I175L |
probably benign |
Het |
Or5p81 |
C |
T |
7: 108,267,289 (GRCm39) |
T222I |
probably benign |
Het |
Pabpc4 |
A |
G |
4: 123,185,524 (GRCm39) |
|
probably null |
Het |
Padi1 |
C |
A |
4: 140,552,266 (GRCm39) |
V393L |
probably damaging |
Het |
Pax2 |
A |
T |
19: 44,806,905 (GRCm39) |
D300V |
probably damaging |
Het |
Pcgf2 |
T |
C |
11: 97,581,078 (GRCm39) |
E71G |
probably damaging |
Het |
Pi4kb |
A |
G |
3: 94,906,172 (GRCm39) |
Q573R |
possibly damaging |
Het |
Pitpna |
T |
A |
11: 75,511,153 (GRCm39) |
M242K |
possibly damaging |
Het |
Pkd1 |
A |
G |
17: 24,793,014 (GRCm39) |
E1567G |
possibly damaging |
Het |
Plcb2 |
A |
T |
2: 118,545,210 (GRCm39) |
S630R |
probably damaging |
Het |
Prrt2 |
A |
T |
7: 126,618,937 (GRCm39) |
V176D |
probably benign |
Het |
Prss1l |
A |
C |
6: 41,373,084 (GRCm39) |
N119H |
probably damaging |
Het |
Prss42 |
T |
C |
9: 110,628,490 (GRCm39) |
|
probably null |
Het |
Rhoq |
A |
G |
17: 87,304,459 (GRCm39) |
R197G |
probably benign |
Het |
Rin2 |
A |
T |
2: 145,702,299 (GRCm39) |
T332S |
probably benign |
Het |
Rnps1-ps |
C |
T |
6: 7,982,605 (GRCm39) |
|
noncoding transcript |
Het |
Rp1 |
A |
T |
1: 4,418,060 (GRCm39) |
N1017K |
possibly damaging |
Het |
Setbp1 |
T |
A |
18: 78,900,700 (GRCm39) |
Y989F |
probably damaging |
Het |
Slc11a1 |
G |
A |
1: 74,420,065 (GRCm39) |
G191D |
probably damaging |
Het |
Slc35f5 |
G |
A |
1: 125,517,693 (GRCm39) |
R497Q |
probably damaging |
Het |
Slf1 |
T |
C |
13: 77,198,090 (GRCm39) |
K728R |
probably benign |
Het |
Tiparp |
T |
G |
3: 65,454,946 (GRCm39) |
S364A |
probably benign |
Het |
Tph1 |
G |
A |
7: 46,296,969 (GRCm39) |
Q409* |
probably null |
Het |
Trp73 |
A |
T |
4: 154,145,049 (GRCm39) |
I526N |
possibly damaging |
Het |
Ttc9c |
G |
A |
19: 8,793,332 (GRCm39) |
R103* |
probably null |
Het |
Vmn2r75 |
T |
A |
7: 85,797,702 (GRCm39) |
I704F |
probably benign |
Het |
Wdr76 |
A |
G |
2: 121,348,216 (GRCm39) |
R63G |
probably damaging |
Het |
Zc3h3 |
T |
A |
15: 75,648,928 (GRCm39) |
S735C |
probably damaging |
Het |
Zfp383 |
G |
A |
7: 29,611,615 (GRCm39) |
V32M |
probably damaging |
Het |
Zfp810 |
T |
A |
9: 22,190,392 (GRCm39) |
Y172F |
probably benign |
Het |
|
Other mutations in Alg8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01395:Alg8
|
APN |
7 |
97,027,383 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02349:Alg8
|
APN |
7 |
97,029,101 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02441:Alg8
|
APN |
7 |
97,029,504 (GRCm39) |
missense |
probably benign |
0.04 |
R0238:Alg8
|
UTSW |
7 |
97,032,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0238:Alg8
|
UTSW |
7 |
97,032,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0239:Alg8
|
UTSW |
7 |
97,032,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0239:Alg8
|
UTSW |
7 |
97,032,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1109:Alg8
|
UTSW |
7 |
97,032,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1429:Alg8
|
UTSW |
7 |
97,039,499 (GRCm39) |
missense |
probably benign |
0.18 |
R3838:Alg8
|
UTSW |
7 |
97,037,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R5343:Alg8
|
UTSW |
7 |
97,036,126 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5910:Alg8
|
UTSW |
7 |
97,039,493 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5963:Alg8
|
UTSW |
7 |
97,029,037 (GRCm39) |
missense |
probably benign |
0.00 |
R6484:Alg8
|
UTSW |
7 |
97,032,135 (GRCm39) |
missense |
probably benign |
|
R6735:Alg8
|
UTSW |
7 |
97,032,189 (GRCm39) |
missense |
probably benign |
0.05 |
R7896:Alg8
|
UTSW |
7 |
97,040,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R7957:Alg8
|
UTSW |
7 |
97,040,131 (GRCm39) |
missense |
probably benign |
0.04 |
R7958:Alg8
|
UTSW |
7 |
97,036,128 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9226:Alg8
|
UTSW |
7 |
97,027,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R9701:Alg8
|
UTSW |
7 |
97,027,486 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9802:Alg8
|
UTSW |
7 |
97,027,486 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1176:Alg8
|
UTSW |
7 |
97,032,968 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Alg8
|
UTSW |
7 |
97,020,869 (GRCm39) |
missense |
probably benign |
|
|