Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atg9a |
G |
T |
1: 75,164,625 (GRCm39) |
P113Q |
probably damaging |
Het |
Ccdc150 |
A |
G |
1: 54,407,176 (GRCm39) |
D1073G |
probably benign |
Het |
Cd8a |
A |
G |
6: 71,350,913 (GRCm39) |
Y126C |
probably damaging |
Het |
Cdca8 |
A |
G |
4: 124,830,168 (GRCm39) |
M68T |
probably damaging |
Het |
Cyp2d26 |
G |
A |
15: 82,676,825 (GRCm39) |
P174S |
possibly damaging |
Het |
Dnai3 |
A |
G |
3: 145,801,143 (GRCm39) |
L105P |
probably damaging |
Het |
Esco1 |
T |
G |
18: 10,567,528 (GRCm39) |
N311H |
probably damaging |
Het |
Evx1 |
A |
G |
6: 52,292,842 (GRCm39) |
M183V |
probably benign |
Het |
Fam111a |
T |
G |
19: 12,565,524 (GRCm39) |
Y424* |
probably null |
Het |
Fat4 |
T |
C |
3: 39,034,529 (GRCm39) |
I2727T |
probably damaging |
Het |
Ggt6 |
T |
A |
11: 72,327,437 (GRCm39) |
Y107N |
possibly damaging |
Het |
Habp2 |
G |
C |
19: 56,295,255 (GRCm39) |
E49Q |
possibly damaging |
Het |
Hibadh |
A |
C |
6: 52,533,474 (GRCm39) |
L214R |
probably damaging |
Het |
Ift57 |
T |
G |
16: 49,582,836 (GRCm39) |
|
probably null |
Het |
Irak4 |
T |
C |
15: 94,459,367 (GRCm39) |
S328P |
probably damaging |
Het |
Lrrc46 |
T |
C |
11: 96,931,757 (GRCm39) |
T22A |
probably damaging |
Het |
Muc2 |
G |
T |
7: 141,305,883 (GRCm39) |
V230L |
probably damaging |
Het |
Ncan |
T |
C |
8: 70,567,899 (GRCm39) |
D71G |
probably benign |
Het |
Nsd2 |
T |
C |
5: 34,038,525 (GRCm39) |
S779P |
probably damaging |
Het |
Rps6ka5 |
G |
T |
12: 100,537,251 (GRCm39) |
T493K |
probably damaging |
Het |
Slc6a21 |
A |
T |
7: 44,936,426 (GRCm39) |
M135L |
probably benign |
Het |
Sprtn |
A |
G |
8: 125,629,958 (GRCm39) |
N417S |
probably benign |
Het |
Trim61 |
T |
A |
8: 65,466,842 (GRCm39) |
M140L |
probably benign |
Het |
Vars1 |
C |
A |
17: 35,234,615 (GRCm39) |
A1148E |
probably benign |
Het |
Vmn2r106 |
C |
T |
17: 20,488,725 (GRCm39) |
C558Y |
probably damaging |
Het |
Vmn2r112 |
T |
C |
17: 22,824,230 (GRCm39) |
V495A |
probably benign |
Het |
Vmn2r117 |
A |
T |
17: 23,679,088 (GRCm39) |
V712E |
possibly damaging |
Het |
Wdfy4 |
T |
C |
14: 32,826,051 (GRCm39) |
D1200G |
probably damaging |
Het |
Zbtb6 |
A |
T |
2: 37,318,690 (GRCm39) |
S413T |
probably benign |
Het |
Zp2 |
G |
T |
7: 119,740,453 (GRCm39) |
N170K |
probably benign |
Het |
|
Other mutations in Krtap6-2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03375:Krtap6-2
|
APN |
16 |
89,216,644 (GRCm39) |
missense |
unknown |
|
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 |
|
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 |
|
|