Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Asf1b |
A |
G |
8: 84,694,611 (GRCm39) |
N125S |
probably benign |
Het |
BC048671 |
T |
A |
6: 90,282,145 (GRCm39) |
L101I |
probably damaging |
Het |
Camta1 |
A |
G |
4: 151,216,043 (GRCm39) |
L959P |
probably benign |
Het |
Cfap91 |
T |
C |
16: 38,148,720 (GRCm39) |
E236G |
probably damaging |
Het |
Cfh |
C |
A |
1: 140,040,303 (GRCm39) |
V598F |
probably damaging |
Het |
Cyp2j7 |
G |
T |
4: 96,103,575 (GRCm39) |
T320K |
probably damaging |
Het |
Ddr1 |
A |
G |
17: 35,998,141 (GRCm39) |
I468T |
possibly damaging |
Het |
Dhx15 |
A |
G |
5: 52,318,300 (GRCm39) |
V510A |
probably damaging |
Het |
Dpp4 |
T |
A |
2: 62,186,988 (GRCm39) |
K507N |
probably benign |
Het |
Evpl |
G |
A |
11: 116,124,225 (GRCm39) |
T198M |
possibly damaging |
Het |
Gabbr1 |
G |
A |
17: 37,367,242 (GRCm39) |
V373I |
probably damaging |
Het |
Gak |
A |
T |
5: 108,728,791 (GRCm39) |
S1049T |
probably benign |
Het |
Gipr |
C |
T |
7: 18,894,543 (GRCm39) |
R253H |
probably benign |
Het |
Gm3685 |
T |
A |
14: 7,043,960 (GRCm38) |
M73L |
probably benign |
Het |
Gm5168 |
C |
T |
X: 25,994,840 (GRCm39) |
R129Q |
probably null |
Het |
Kcnh1 |
T |
A |
1: 192,100,992 (GRCm39) |
V555D |
probably damaging |
Het |
Kif26b |
T |
C |
1: 178,745,651 (GRCm39) |
S1916P |
probably damaging |
Het |
Lingo4 |
T |
C |
3: 94,309,239 (GRCm39) |
V59A |
probably benign |
Het |
Mroh8 |
T |
A |
2: 157,067,454 (GRCm39) |
Q635L |
probably damaging |
Het |
Msh6 |
T |
A |
17: 88,293,616 (GRCm39) |
D790E |
probably damaging |
Het |
Nrxn1 |
A |
T |
17: 90,905,007 (GRCm39) |
W809R |
probably damaging |
Het |
Or5ac19 |
C |
A |
16: 59,089,493 (GRCm39) |
C179F |
probably damaging |
Het |
Polr3d |
T |
C |
14: 70,676,903 (GRCm39) |
H397R |
probably benign |
Het |
Pwp2 |
G |
A |
10: 78,014,304 (GRCm39) |
T432I |
probably benign |
Het |
Rad21 |
G |
C |
15: 51,836,639 (GRCm39) |
F177L |
probably benign |
Het |
Rnf182 |
G |
A |
13: 43,822,153 (GRCm39) |
V235I |
probably benign |
Het |
Scn11a |
C |
T |
9: 119,599,014 (GRCm39) |
C1172Y |
probably damaging |
Het |
Sh2b3 |
A |
G |
5: 121,966,742 (GRCm39) |
L124P |
possibly damaging |
Het |
Six2 |
T |
C |
17: 85,992,906 (GRCm39) |
N199S |
probably benign |
Het |
Slc5a3 |
A |
G |
16: 91,874,702 (GRCm39) |
D253G |
probably benign |
Het |
Synm |
A |
G |
7: 67,385,025 (GRCm39) |
M879T |
probably benign |
Het |
Tasp1 |
A |
G |
2: 139,752,455 (GRCm39) |
I328T |
possibly damaging |
Het |
Tbrg4 |
T |
C |
11: 6,569,689 (GRCm39) |
Q309R |
probably damaging |
Het |
Tmtc2 |
A |
G |
10: 105,139,465 (GRCm39) |
L687P |
probably damaging |
Het |
Trgc3 |
A |
T |
13: 19,447,532 (GRCm39) |
R162* |
probably null |
Het |
Tufm |
T |
C |
7: 126,086,621 (GRCm39) |
M1T |
probably null |
Het |
Vmn2r116 |
A |
C |
17: 23,607,921 (GRCm39) |
L496F |
probably benign |
Het |
Vmn2r75 |
C |
T |
7: 85,814,791 (GRCm39) |
C234Y |
probably damaging |
Het |
Wars2 |
G |
T |
3: 99,112,595 (GRCm39) |
V162L |
possibly damaging |
Het |
Zc3h11a |
A |
T |
1: 133,552,349 (GRCm39) |
V586D |
probably benign |
Het |
Zfp52 |
T |
C |
17: 21,777,478 (GRCm39) |
Y38H |
probably damaging |
Het |
Zfp729b |
T |
C |
13: 67,739,542 (GRCm39) |
M908V |
probably benign |
Het |
Zfp772 |
T |
C |
7: 7,207,350 (GRCm39) |
I114V |
probably benign |
Het |
|
Other mutations in Zdhhc5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01669:Zdhhc5
|
APN |
2 |
84,521,538 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01795:Zdhhc5
|
APN |
2 |
84,520,390 (GRCm39) |
missense |
probably benign |
|
IGL01862:Zdhhc5
|
APN |
2 |
84,520,836 (GRCm39) |
missense |
probably benign |
0.01 |
R0270:Zdhhc5
|
UTSW |
2 |
84,520,459 (GRCm39) |
missense |
probably benign |
0.06 |
R0419:Zdhhc5
|
UTSW |
2 |
84,521,587 (GRCm39) |
splice site |
probably null |
|
R0543:Zdhhc5
|
UTSW |
2 |
84,522,824 (GRCm39) |
unclassified |
probably benign |
|
R1171:Zdhhc5
|
UTSW |
2 |
84,522,685 (GRCm39) |
missense |
probably benign |
0.00 |
R1450:Zdhhc5
|
UTSW |
2 |
84,532,733 (GRCm39) |
missense |
probably damaging |
0.99 |
R1922:Zdhhc5
|
UTSW |
2 |
84,523,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R2229:Zdhhc5
|
UTSW |
2 |
84,520,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Zdhhc5
|
UTSW |
2 |
84,523,775 (GRCm39) |
missense |
probably damaging |
0.97 |
R5473:Zdhhc5
|
UTSW |
2 |
84,520,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R5968:Zdhhc5
|
UTSW |
2 |
84,524,719 (GRCm39) |
splice site |
probably null |
|
R6299:Zdhhc5
|
UTSW |
2 |
84,520,825 (GRCm39) |
missense |
probably benign |
0.06 |
R6550:Zdhhc5
|
UTSW |
2 |
84,526,685 (GRCm39) |
missense |
probably benign |
0.03 |
R7069:Zdhhc5
|
UTSW |
2 |
84,545,355 (GRCm39) |
start gained |
probably benign |
|
R7169:Zdhhc5
|
UTSW |
2 |
84,532,675 (GRCm39) |
critical splice donor site |
probably null |
|
R7383:Zdhhc5
|
UTSW |
2 |
84,524,748 (GRCm39) |
missense |
probably benign |
0.44 |
R8703:Zdhhc5
|
UTSW |
2 |
84,520,596 (GRCm39) |
missense |
probably benign |
0.06 |
R9647:Zdhhc5
|
UTSW |
2 |
84,524,750 (GRCm39) |
missense |
probably benign |
0.01 |
R9789:Zdhhc5
|
UTSW |
2 |
84,524,662 (GRCm39) |
missense |
probably damaging |
1.00 |
|