Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700129C05Rik |
G |
A |
14: 59,380,061 (GRCm39) |
S79F |
probably damaging |
Het |
Acss3 |
G |
A |
10: 106,840,609 (GRCm39) |
A384V |
probably damaging |
Het |
Aff2 |
G |
A |
X: 68,878,409 (GRCm39) |
E732K |
possibly damaging |
Het |
Atp12a |
A |
G |
14: 56,613,715 (GRCm39) |
T496A |
probably benign |
Het |
B3gnt3 |
A |
T |
8: 72,145,462 (GRCm39) |
M302K |
probably damaging |
Het |
Bptf |
G |
T |
11: 107,002,148 (GRCm39) |
D321E |
probably damaging |
Het |
C1ql3 |
C |
T |
2: 13,015,130 (GRCm39) |
V177I |
possibly damaging |
Het |
C2cd5 |
A |
T |
6: 142,982,042 (GRCm39) |
Y607* |
probably null |
Het |
Casp3 |
G |
T |
8: 47,090,990 (GRCm39) |
W214L |
probably damaging |
Het |
Cd248 |
A |
G |
19: 5,118,154 (GRCm39) |
M1V |
probably null |
Het |
Cdh18 |
A |
G |
15: 23,410,891 (GRCm39) |
T405A |
probably benign |
Het |
Cldn24 |
G |
T |
8: 48,275,363 (GRCm39) |
R62S |
probably benign |
Het |
Cnot1 |
A |
G |
8: 96,489,814 (GRCm39) |
V463A |
probably benign |
Het |
Cul2 |
A |
T |
18: 3,399,876 (GRCm39) |
L3F |
probably damaging |
Het |
Ep400 |
A |
T |
5: 110,866,957 (GRCm39) |
N1062K |
unknown |
Het |
Gch1 |
T |
C |
14: 47,426,798 (GRCm39) |
|
probably benign |
Het |
Gzf1 |
T |
C |
2: 148,525,856 (GRCm39) |
M109T |
probably damaging |
Het |
Itch |
T |
A |
2: 155,054,259 (GRCm39) |
M701K |
probably benign |
Het |
Kank4 |
A |
T |
4: 98,667,463 (GRCm39) |
I328N |
probably damaging |
Het |
Krt9 |
A |
T |
11: 100,081,685 (GRCm39) |
N281K |
possibly damaging |
Het |
Lgals12 |
T |
A |
19: 7,584,130 (GRCm39) |
|
probably benign |
Het |
Lrrc37a |
T |
C |
11: 103,392,293 (GRCm39) |
Q1044R |
probably benign |
Het |
Mbtps2 |
A |
T |
X: 156,342,029 (GRCm39) |
F270L |
probably benign |
Het |
Nr3c1 |
G |
T |
18: 39,619,804 (GRCm39) |
T161K |
probably benign |
Het |
Or2w3b |
T |
C |
11: 58,623,821 (GRCm39) |
T57A |
probably benign |
Het |
Or4g16 |
A |
G |
2: 111,136,655 (GRCm39) |
Y35C |
probably damaging |
Het |
Or5ak20 |
A |
G |
2: 85,184,202 (GRCm39) |
S23P |
possibly damaging |
Het |
Or5b116 |
T |
C |
19: 13,422,549 (GRCm39) |
Y58H |
probably damaging |
Het |
Pla2g4d |
T |
C |
2: 120,101,622 (GRCm39) |
K453E |
probably damaging |
Het |
Plcb2 |
T |
C |
2: 118,554,246 (GRCm39) |
N69S |
probably benign |
Het |
Prl3d1 |
T |
C |
13: 27,278,981 (GRCm39) |
Y59H |
possibly damaging |
Het |
Rnf133 |
T |
C |
6: 23,649,174 (GRCm39) |
M252V |
probably benign |
Het |
Rnf181 |
G |
T |
6: 72,338,467 (GRCm39) |
H14N |
possibly damaging |
Het |
Sash1 |
A |
T |
10: 8,605,741 (GRCm39) |
M883K |
probably benign |
Het |
Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
Slc13a4 |
A |
G |
6: 35,257,418 (GRCm39) |
V240A |
probably benign |
Het |
Slc2a5 |
T |
C |
4: 150,224,447 (GRCm39) |
Y315H |
possibly damaging |
Het |
Slc7a2 |
T |
C |
8: 41,358,658 (GRCm39) |
Y334H |
probably benign |
Het |
Spib |
A |
G |
7: 44,179,392 (GRCm39) |
S23P |
probably benign |
Het |
Tbc1d1 |
A |
G |
5: 64,442,143 (GRCm39) |
N721S |
probably benign |
Het |
Tcf25 |
A |
G |
8: 124,100,772 (GRCm39) |
E54G |
probably benign |
Het |
Tesl2 |
G |
A |
X: 23,824,950 (GRCm39) |
A75V |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Uba7 |
A |
G |
9: 107,853,563 (GRCm39) |
H131R |
probably benign |
Het |
Vmn2r6 |
C |
T |
3: 64,467,139 (GRCm39) |
C120Y |
probably damaging |
Het |
Zfp970 |
T |
A |
2: 177,166,614 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Zdhhc18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01100:Zdhhc18
|
APN |
4 |
133,340,269 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01575:Zdhhc18
|
APN |
4 |
133,341,210 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02122:Zdhhc18
|
APN |
4 |
133,340,946 (GRCm39) |
splice site |
probably benign |
|
R0316:Zdhhc18
|
UTSW |
4 |
133,340,966 (GRCm39) |
nonsense |
probably null |
|
R1398:Zdhhc18
|
UTSW |
4 |
133,354,608 (GRCm39) |
missense |
probably benign |
0.00 |
R1764:Zdhhc18
|
UTSW |
4 |
133,335,987 (GRCm39) |
missense |
probably benign |
0.00 |
R1912:Zdhhc18
|
UTSW |
4 |
133,341,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R2921:Zdhhc18
|
UTSW |
4 |
133,360,455 (GRCm39) |
missense |
probably benign |
0.00 |
R2923:Zdhhc18
|
UTSW |
4 |
133,360,455 (GRCm39) |
missense |
probably benign |
0.00 |
R4735:Zdhhc18
|
UTSW |
4 |
133,341,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R4985:Zdhhc18
|
UTSW |
4 |
133,340,228 (GRCm39) |
splice site |
probably null |
|
R6551:Zdhhc18
|
UTSW |
4 |
133,340,960 (GRCm39) |
missense |
probably benign |
0.03 |
R7358:Zdhhc18
|
UTSW |
4 |
133,360,482 (GRCm39) |
nonsense |
probably null |
|
R7577:Zdhhc18
|
UTSW |
4 |
133,342,520 (GRCm39) |
nonsense |
probably null |
|
R8194:Zdhhc18
|
UTSW |
4 |
133,341,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R9532:Zdhhc18
|
UTSW |
4 |
133,342,541 (GRCm39) |
missense |
possibly damaging |
0.92 |
X0024:Zdhhc18
|
UTSW |
4 |
133,342,618 (GRCm39) |
nonsense |
probably null |
|
|