Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110009E18Rik |
C |
T |
1: 120,099,192 (GRCm39) |
T95I |
probably damaging |
Het |
Acte1 |
A |
G |
7: 143,450,127 (GRCm39) |
Y291C |
probably damaging |
Het |
Alyref |
C |
G |
11: 120,486,758 (GRCm39) |
V168L |
probably damaging |
Het |
Ap1g1 |
G |
A |
8: 110,545,571 (GRCm39) |
A75T |
probably benign |
Het |
Atp8a2 |
T |
C |
14: 60,097,719 (GRCm39) |
K770E |
probably benign |
Het |
Baz2b |
T |
C |
2: 59,792,826 (GRCm39) |
N434S |
probably benign |
Het |
Cebpzos |
A |
G |
17: 79,225,817 (GRCm39) |
K11E |
probably damaging |
Het |
Cers1 |
A |
T |
8: 70,774,186 (GRCm39) |
I148F |
probably benign |
Het |
Cpne4 |
A |
T |
9: 104,871,057 (GRCm39) |
I300F |
possibly damaging |
Het |
Fsip2 |
C |
A |
2: 82,819,780 (GRCm39) |
S5171* |
probably null |
Het |
Gabra2 |
T |
C |
5: 71,130,938 (GRCm39) |
S297G |
probably damaging |
Het |
Irak3 |
A |
T |
10: 120,012,251 (GRCm39) |
I171N |
probably damaging |
Het |
Lama1 |
A |
G |
17: 68,059,893 (GRCm39) |
I661V |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,367,609 (GRCm39) |
D2384G |
probably damaging |
Het |
Or14a260 |
T |
C |
7: 85,985,113 (GRCm39) |
M164V |
probably benign |
Het |
Or6b2b |
T |
A |
1: 92,419,445 (GRCm39) |
T11S |
probably benign |
Het |
Pdcd6ip |
G |
A |
9: 113,491,354 (GRCm39) |
L630F |
probably damaging |
Het |
Pkn2 |
A |
G |
3: 142,527,326 (GRCm39) |
|
probably null |
Het |
Slc26a4 |
T |
G |
12: 31,578,736 (GRCm39) |
D639A |
probably damaging |
Het |
Svep1 |
C |
T |
4: 58,087,817 (GRCm39) |
C1754Y |
possibly damaging |
Het |
Trpa1 |
C |
A |
1: 14,974,407 (GRCm39) |
M258I |
probably benign |
Het |
Vmn1r17 |
A |
T |
6: 57,338,240 (GRCm39) |
S42T |
probably benign |
Het |
Vmn2r57 |
A |
G |
7: 41,077,228 (GRCm39) |
F313L |
probably benign |
Het |
Zfp811 |
A |
G |
17: 33,017,618 (GRCm39) |
Y140H |
probably benign |
Het |
|
Other mutations in 1700067P10Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00546:1700067P10Rik
|
APN |
17 |
48,401,096 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02792:1700067P10Rik
|
APN |
17 |
48,401,107 (GRCm39) |
missense |
probably benign |
0.11 |
R0445:1700067P10Rik
|
UTSW |
17 |
48,400,542 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1494:1700067P10Rik
|
UTSW |
17 |
48,400,991 (GRCm39) |
missense |
probably benign |
|
R2133:1700067P10Rik
|
UTSW |
17 |
48,400,972 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6059:1700067P10Rik
|
UTSW |
17 |
48,400,847 (GRCm39) |
missense |
probably benign |
|
R8460:1700067P10Rik
|
UTSW |
17 |
48,400,849 (GRCm39) |
nonsense |
probably null |
|
R8461:1700067P10Rik
|
UTSW |
17 |
48,400,849 (GRCm39) |
nonsense |
probably null |
|
R8558:1700067P10Rik
|
UTSW |
17 |
48,400,849 (GRCm39) |
nonsense |
probably null |
|
R8672:1700067P10Rik
|
UTSW |
17 |
48,400,849 (GRCm39) |
nonsense |
probably null |
|
R8673:1700067P10Rik
|
UTSW |
17 |
48,400,849 (GRCm39) |
nonsense |
probably null |
|
R8675:1700067P10Rik
|
UTSW |
17 |
48,400,849 (GRCm39) |
nonsense |
probably null |
|
R8872:1700067P10Rik
|
UTSW |
17 |
48,401,164 (GRCm39) |
missense |
possibly damaging |
0.62 |
|