Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap31 |
A |
G |
16: 38,423,190 (GRCm39) |
S959P |
probably damaging |
Het |
Arrb2 |
G |
A |
11: 70,327,005 (GRCm39) |
G24D |
probably damaging |
Het |
Catsper4 |
A |
G |
4: 133,945,519 (GRCm39) |
I180T |
probably damaging |
Het |
Chst15 |
G |
A |
7: 131,872,186 (GRCm39) |
Q32* |
probably null |
Het |
Cntnap5c |
A |
T |
17: 58,469,200 (GRCm39) |
Y594F |
possibly damaging |
Het |
Cse1l |
T |
A |
2: 166,784,977 (GRCm39) |
|
probably benign |
Het |
Dab1 |
A |
T |
4: 104,538,798 (GRCm39) |
I201F |
possibly damaging |
Het |
Eif2ak4 |
T |
C |
2: 118,252,799 (GRCm39) |
V457A |
probably benign |
Het |
Fkbp1b |
T |
C |
12: 4,888,220 (GRCm39) |
|
probably benign |
Het |
Fryl |
C |
A |
5: 73,245,792 (GRCm39) |
V1122F |
possibly damaging |
Het |
Gas2l2 |
A |
G |
11: 83,317,036 (GRCm39) |
|
probably benign |
Het |
Gstt2 |
A |
T |
10: 75,668,655 (GRCm39) |
|
probably null |
Het |
H4c14 |
T |
C |
3: 96,170,458 (GRCm39) |
T55A |
possibly damaging |
Het |
Hcst |
T |
G |
7: 30,118,036 (GRCm39) |
|
probably benign |
Het |
Hectd4 |
A |
G |
5: 121,466,445 (GRCm39) |
E2420G |
possibly damaging |
Het |
Ifi206 |
A |
T |
1: 173,308,344 (GRCm39) |
S551T |
probably benign |
Het |
Itgb3bp |
A |
G |
4: 99,657,724 (GRCm39) |
|
probably benign |
Het |
Krtap6-5 |
T |
G |
16: 88,844,740 (GRCm39) |
|
probably benign |
Het |
Muc5b |
A |
G |
7: 141,415,699 (GRCm39) |
T2882A |
possibly damaging |
Het |
Nup214 |
C |
T |
2: 31,900,233 (GRCm39) |
T854M |
probably damaging |
Het |
Olfml2b |
A |
G |
1: 170,477,401 (GRCm39) |
K179E |
probably benign |
Het |
Or10d1b |
A |
G |
9: 39,613,871 (GRCm39) |
S65P |
probably damaging |
Het |
Or4k37 |
A |
T |
2: 111,159,229 (GRCm39) |
H155L |
probably damaging |
Het |
Per2 |
A |
T |
1: 91,351,950 (GRCm39) |
I852K |
possibly damaging |
Het |
Pkhd1 |
A |
T |
1: 20,187,247 (GRCm39) |
I3687N |
probably damaging |
Het |
Slc7a2 |
A |
T |
8: 41,369,410 (GRCm39) |
S622C |
probably damaging |
Het |
Smarcc2 |
G |
A |
10: 128,318,781 (GRCm39) |
V719I |
probably damaging |
Het |
Syne2 |
T |
C |
12: 75,972,209 (GRCm39) |
I1033T |
possibly damaging |
Het |
Tmod1 |
T |
C |
4: 46,096,999 (GRCm39) |
I264T |
probably damaging |
Het |
Tmtc3 |
G |
A |
10: 100,283,581 (GRCm39) |
A658V |
possibly damaging |
Het |
Top6bl |
T |
C |
19: 4,748,206 (GRCm39) |
E164G |
probably benign |
Het |
Tpm3 |
A |
G |
3: 89,981,079 (GRCm39) |
E56G |
possibly damaging |
Het |
Tra2b |
T |
C |
16: 22,065,993 (GRCm39) |
|
probably benign |
Het |
Trmu |
T |
A |
15: 85,779,138 (GRCm39) |
Y262N |
possibly damaging |
Het |
Uox |
C |
T |
3: 146,331,590 (GRCm39) |
T213I |
probably damaging |
Het |
Vps13d |
A |
G |
4: 144,818,517 (GRCm39) |
W2R |
probably damaging |
Het |
|
Other mutations in Krtap6-2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1566:Krtap6-2
|
UTSW |
16 |
89,216,626 (GRCm39) |
missense |
unknown |
|
R4896:Krtap6-2
|
UTSW |
16 |
89,216,806 (GRCm39) |
missense |
unknown |
|
R5857:Krtap6-2
|
UTSW |
16 |
89,216,530 (GRCm39) |
missense |
unknown |
|
R6390:Krtap6-2
|
UTSW |
16 |
89,216,834 (GRCm39) |
nonsense |
probably null |
|
R6958:Krtap6-2
|
UTSW |
16 |
89,216,698 (GRCm39) |
missense |
unknown |
|
R7432:Krtap6-2
|
UTSW |
16 |
89,216,761 (GRCm39) |
missense |
unknown |
|
R7454:Krtap6-2
|
UTSW |
16 |
89,216,800 (GRCm39) |
missense |
unknown |
|
R7780:Krtap6-2
|
UTSW |
16 |
89,216,510 (GRCm39) |
nonsense |
probably null |
|
R7981:Krtap6-2
|
UTSW |
16 |
89,216,562 (GRCm39) |
missense |
unknown |
|
R8949:Krtap6-2
|
UTSW |
16 |
89,216,703 (GRCm39) |
missense |
unknown |
|
R9113:Krtap6-2
|
UTSW |
16 |
89,216,613 (GRCm39) |
small deletion |
probably benign |
|
R9562:Krtap6-2
|
UTSW |
16 |
89,216,722 (GRCm39) |
missense |
unknown |
|
R9565:Krtap6-2
|
UTSW |
16 |
89,216,722 (GRCm39) |
missense |
unknown |
|
R9747:Krtap6-2
|
UTSW |
16 |
89,216,776 (GRCm39) |
missense |
unknown |
|
R9757:Krtap6-2
|
UTSW |
16 |
89,216,958 (GRCm39) |
missense |
unknown |
|
R9762:Krtap6-2
|
UTSW |
16 |
89,216,763 (GRCm39) |
missense |
unknown |
|
|