Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco1 |
A |
T |
4: 40,177,848 (GRCm39) |
I290F |
probably damaging |
Het |
Cfap107 |
A |
T |
4: 144,150,372 (GRCm39) |
W70R |
probably damaging |
Het |
Cmip |
T |
A |
8: 118,149,629 (GRCm39) |
C155S |
probably damaging |
Het |
Cyba |
G |
T |
8: 123,153,718 (GRCm39) |
P82T |
possibly damaging |
Het |
Dgkb |
C |
T |
12: 38,177,299 (GRCm39) |
R202W |
possibly damaging |
Het |
Dnah6 |
T |
C |
6: 73,014,598 (GRCm39) |
E3611G |
probably damaging |
Het |
Dnah7b |
A |
T |
1: 46,256,351 (GRCm39) |
S1885C |
probably benign |
Het |
Dop1b |
A |
G |
16: 93,560,298 (GRCm39) |
E748G |
probably damaging |
Het |
Dusp18 |
C |
A |
11: 3,847,037 (GRCm39) |
P9Q |
probably damaging |
Het |
Fat4 |
T |
A |
3: 38,943,013 (GRCm39) |
D635E |
probably damaging |
Het |
Fbxo25 |
T |
A |
8: 13,971,886 (GRCm39) |
S79R |
probably benign |
Het |
Fgfr4 |
T |
A |
13: 55,315,230 (GRCm39) |
L675Q |
probably damaging |
Het |
Foxo1 |
T |
A |
3: 52,176,446 (GRCm39) |
L75Q |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,805,742 (GRCm39) |
V687A |
possibly damaging |
Het |
Gga3 |
G |
T |
11: 115,479,257 (GRCm39) |
P354Q |
probably damaging |
Het |
Gm11077 |
A |
T |
6: 140,675,048 (GRCm39) |
K13N |
unknown |
Het |
Haus4 |
T |
A |
14: 54,787,232 (GRCm39) |
K75M |
probably damaging |
Het |
Igfn1 |
G |
A |
1: 135,893,825 (GRCm39) |
T2085M |
probably damaging |
Het |
Igkv4-80 |
A |
C |
6: 68,993,649 (GRCm39) |
S81A |
probably benign |
Het |
Lims1 |
A |
T |
10: 58,252,492 (GRCm39) |
I321L |
probably damaging |
Het |
Ms4a6b |
A |
T |
19: 11,499,044 (GRCm39) |
I53F |
probably damaging |
Het |
Msl3l2 |
A |
G |
10: 55,991,668 (GRCm39) |
D131G |
probably damaging |
Het |
Nrap |
A |
G |
19: 56,370,035 (GRCm39) |
V189A |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pfkl |
T |
G |
10: 77,833,423 (GRCm39) |
I260L |
possibly damaging |
Het |
Pkd2l1 |
A |
G |
19: 44,146,171 (GRCm39) |
Y128H |
probably benign |
Het |
Prpf6 |
T |
A |
2: 181,250,059 (GRCm39) |
L73Q |
probably damaging |
Het |
R3hdm2 |
T |
C |
10: 127,321,316 (GRCm39) |
V658A |
probably damaging |
Het |
Rab27b |
T |
C |
18: 70,129,226 (GRCm39) |
T23A |
probably damaging |
Het |
Rabif |
A |
G |
1: 134,433,980 (GRCm39) |
E98G |
probably damaging |
Het |
Ror2 |
T |
C |
13: 53,271,185 (GRCm39) |
D378G |
possibly damaging |
Het |
Spata21 |
A |
G |
4: 140,834,496 (GRCm39) |
T494A |
probably damaging |
Het |
Ssh2 |
A |
G |
11: 77,344,771 (GRCm39) |
K919E |
probably benign |
Het |
Tnrc6b |
C |
G |
15: 80,763,766 (GRCm39) |
P423A |
possibly damaging |
Het |
Tomm40 |
A |
G |
7: 19,435,675 (GRCm39) |
F352L |
probably benign |
Het |
Tsg101 |
A |
T |
7: 46,540,868 (GRCm39) |
D158E |
probably damaging |
Het |
Tspo2 |
A |
G |
17: 48,755,780 (GRCm39) |
F93L |
probably benign |
Het |
V1ra8 |
T |
A |
6: 90,180,004 (GRCm39) |
I69K |
probably damaging |
Het |
Zan |
T |
C |
5: 137,456,102 (GRCm39) |
T1353A |
unknown |
Het |
Zfp281 |
A |
G |
1: 136,553,676 (GRCm39) |
K218R |
possibly damaging |
Het |
|
Other mutations in Zdhhc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01315:Zdhhc1
|
APN |
8 |
106,199,630 (GRCm39) |
missense |
probably benign |
|
hacked
|
UTSW |
8 |
106,210,376 (GRCm39) |
frame shift |
probably null |
|
middleman
|
UTSW |
8 |
106,210,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R0329:Zdhhc1
|
UTSW |
8 |
106,210,175 (GRCm39) |
missense |
probably benign |
0.04 |
R1898:Zdhhc1
|
UTSW |
8 |
106,205,378 (GRCm39) |
splice site |
probably null |
|
R2511:Zdhhc1
|
UTSW |
8 |
106,210,190 (GRCm39) |
missense |
probably benign |
0.16 |
R4734:Zdhhc1
|
UTSW |
8 |
106,210,376 (GRCm39) |
frame shift |
probably null |
|
R4741:Zdhhc1
|
UTSW |
8 |
106,210,376 (GRCm39) |
frame shift |
probably null |
|
R4795:Zdhhc1
|
UTSW |
8 |
106,210,376 (GRCm39) |
frame shift |
probably null |
|
R4818:Zdhhc1
|
UTSW |
8 |
106,210,376 (GRCm39) |
frame shift |
probably null |
|
R4819:Zdhhc1
|
UTSW |
8 |
106,210,376 (GRCm39) |
frame shift |
probably null |
|
R4822:Zdhhc1
|
UTSW |
8 |
106,210,376 (GRCm39) |
frame shift |
probably null |
|
R4871:Zdhhc1
|
UTSW |
8 |
106,210,376 (GRCm39) |
frame shift |
probably null |
|
R4891:Zdhhc1
|
UTSW |
8 |
106,199,649 (GRCm39) |
missense |
probably benign |
0.00 |
R4901:Zdhhc1
|
UTSW |
8 |
106,199,484 (GRCm39) |
missense |
probably benign |
|
R4905:Zdhhc1
|
UTSW |
8 |
106,210,326 (GRCm39) |
missense |
probably damaging |
0.98 |
R4953:Zdhhc1
|
UTSW |
8 |
106,210,376 (GRCm39) |
frame shift |
probably null |
|
R5128:Zdhhc1
|
UTSW |
8 |
106,210,268 (GRCm39) |
missense |
probably benign |
0.02 |
R5274:Zdhhc1
|
UTSW |
8 |
106,210,402 (GRCm39) |
missense |
probably benign |
0.30 |
R5381:Zdhhc1
|
UTSW |
8 |
106,210,376 (GRCm39) |
frame shift |
probably null |
|
R6852:Zdhhc1
|
UTSW |
8 |
106,203,704 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6962:Zdhhc1
|
UTSW |
8 |
106,210,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R7990:Zdhhc1
|
UTSW |
8 |
106,203,001 (GRCm39) |
critical splice donor site |
probably null |
|
R8836:Zdhhc1
|
UTSW |
8 |
106,200,173 (GRCm39) |
missense |
probably benign |
0.43 |
R9047:Zdhhc1
|
UTSW |
8 |
106,205,533 (GRCm39) |
missense |
probably damaging |
1.00 |
|