Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
G |
11: 110,204,187 (GRCm39) |
C363R |
probably damaging |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Anln |
A |
C |
9: 22,271,803 (GRCm39) |
I684R |
probably damaging |
Het |
Atoh7 |
A |
T |
10: 62,936,278 (GRCm39) |
D115V |
probably damaging |
Het |
Atp11a |
T |
A |
8: 12,896,100 (GRCm39) |
I223K |
probably damaging |
Het |
Cabs1 |
C |
T |
5: 88,127,613 (GRCm39) |
T88I |
possibly damaging |
Het |
Cblb |
T |
A |
16: 51,961,419 (GRCm39) |
C345S |
probably damaging |
Het |
Cep250 |
A |
G |
2: 155,823,358 (GRCm39) |
E1003G |
possibly damaging |
Het |
Chpf |
C |
T |
1: 75,452,287 (GRCm39) |
R389H |
possibly damaging |
Het |
Cntnap5c |
A |
G |
17: 58,593,881 (GRCm39) |
D740G |
possibly damaging |
Het |
Col19a1 |
T |
C |
1: 24,413,702 (GRCm39) |
T411A |
unknown |
Het |
Dgat2 |
T |
C |
7: 98,813,885 (GRCm39) |
N99S |
probably benign |
Het |
Fbxo7 |
A |
T |
10: 85,860,560 (GRCm39) |
T56S |
probably benign |
Het |
Gm15130 |
T |
A |
2: 110,974,950 (GRCm39) |
Q71L |
unknown |
Het |
Gpr161 |
T |
A |
1: 165,137,864 (GRCm39) |
V150E |
possibly damaging |
Het |
Hmcn1 |
T |
C |
1: 150,441,176 (GRCm39) |
E5360G |
probably damaging |
Het |
Hmg20a |
A |
G |
9: 56,388,892 (GRCm39) |
D153G |
probably damaging |
Het |
Hrct1 |
T |
A |
4: 43,727,498 (GRCm39) |
V46D |
possibly damaging |
Het |
Idh1 |
T |
C |
1: 65,198,689 (GRCm39) |
T394A |
probably damaging |
Het |
Kazn |
A |
G |
4: 141,836,598 (GRCm39) |
I547T |
unknown |
Het |
Klhdc3 |
A |
T |
17: 46,988,633 (GRCm39) |
I142N |
probably damaging |
Het |
Lrrc39 |
G |
T |
3: 116,364,624 (GRCm39) |
|
probably null |
Het |
Mamdc4 |
T |
C |
2: 25,457,451 (GRCm39) |
D510G |
probably damaging |
Het |
Mcm2 |
TTCTGATAGATGGTCTG |
TTCTG |
6: 88,866,891 (GRCm39) |
|
probably benign |
Het |
Ndfip2 |
A |
G |
14: 105,535,538 (GRCm39) |
I275V |
possibly damaging |
Het |
Or1i2 |
T |
C |
10: 78,448,409 (GRCm39) |
D22G |
probably benign |
Het |
Or5b24 |
A |
T |
19: 12,912,851 (GRCm39) |
I250L |
probably benign |
Het |
Pacsin2 |
A |
C |
15: 83,261,900 (GRCm39) |
D154E |
probably damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,455,886 (GRCm39) |
C755* |
probably null |
Het |
Pcnx2 |
T |
C |
8: 126,480,491 (GRCm39) |
S1939G |
probably damaging |
Het |
Pfkl |
A |
T |
10: 77,825,985 (GRCm39) |
H602Q |
probably benign |
Het |
Pon3 |
G |
A |
6: 5,221,716 (GRCm39) |
R305C |
probably damaging |
Het |
Prpf6 |
A |
G |
2: 181,263,580 (GRCm39) |
R147G |
probably damaging |
Het |
Sh3yl1 |
A |
G |
12: 30,992,034 (GRCm39) |
E201G |
probably benign |
Het |
Slc25a36 |
A |
G |
9: 96,982,210 (GRCm39) |
Y22H |
probably damaging |
Het |
Susd2 |
C |
T |
10: 75,473,853 (GRCm39) |
A581T |
probably damaging |
Het |
Tysnd1 |
A |
G |
10: 61,532,113 (GRCm39) |
D255G |
probably damaging |
Het |
Zbtb6 |
A |
C |
2: 37,319,255 (GRCm39) |
I224M |
probably benign |
Het |
Zdhhc8 |
G |
T |
16: 18,041,202 (GRCm39) |
N719K |
possibly damaging |
Het |
Zkscan16 |
A |
G |
4: 58,946,260 (GRCm39) |
E45G |
possibly damaging |
Het |
|
Other mutations in Sult6b2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00436:Sult6b2
|
APN |
6 |
142,743,563 (GRCm39) |
splice site |
probably benign |
|
IGL00694:Sult6b2
|
APN |
6 |
142,736,015 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01146:Sult6b2
|
APN |
6 |
142,750,034 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01886:Sult6b2
|
APN |
6 |
142,735,852 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02385:Sult6b2
|
APN |
6 |
142,747,498 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02477:Sult6b2
|
APN |
6 |
142,747,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R0088:Sult6b2
|
UTSW |
6 |
142,743,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2850:Sult6b2
|
UTSW |
6 |
142,743,613 (GRCm39) |
missense |
probably benign |
0.18 |
R4015:Sult6b2
|
UTSW |
6 |
142,735,988 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4667:Sult6b2
|
UTSW |
6 |
142,747,421 (GRCm39) |
nonsense |
probably null |
|
R5172:Sult6b2
|
UTSW |
6 |
142,743,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R5973:Sult6b2
|
UTSW |
6 |
142,736,021 (GRCm39) |
missense |
probably benign |
0.01 |
R6893:Sult6b2
|
UTSW |
6 |
142,750,025 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7667:Sult6b2
|
UTSW |
6 |
142,732,085 (GRCm39) |
missense |
probably benign |
0.10 |
R7853:Sult6b2
|
UTSW |
6 |
142,747,524 (GRCm39) |
missense |
not run |
|
R8071:Sult6b2
|
UTSW |
6 |
142,735,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R8225:Sult6b2
|
UTSW |
6 |
142,750,055 (GRCm39) |
missense |
probably benign |
0.00 |
R8344:Sult6b2
|
UTSW |
6 |
142,736,022 (GRCm39) |
missense |
probably benign |
0.13 |
|