Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930523C07Rik |
T |
A |
1: 159,905,092 (GRCm39) |
|
probably benign |
Het |
Bak1 |
T |
A |
17: 27,240,244 (GRCm39) |
T148S |
possibly damaging |
Het |
Cdc25a |
C |
A |
9: 109,710,585 (GRCm39) |
H157Q |
possibly damaging |
Het |
Chst5 |
T |
C |
8: 112,616,816 (GRCm39) |
Y268C |
probably damaging |
Het |
Csnk1g2 |
T |
C |
10: 80,474,130 (GRCm39) |
I145T |
possibly damaging |
Het |
Ctsr |
T |
C |
13: 61,309,084 (GRCm39) |
T224A |
probably benign |
Het |
Cux1 |
T |
C |
5: 136,336,750 (GRCm39) |
K921E |
probably damaging |
Het |
Dcaf12l1 |
T |
C |
X: 43,878,330 (GRCm39) |
N156S |
probably damaging |
Het |
Dennd2d |
T |
A |
3: 106,389,977 (GRCm39) |
D2E |
probably benign |
Het |
Dock2 |
T |
C |
11: 34,605,328 (GRCm39) |
K264E |
possibly damaging |
Het |
Eif3c |
C |
G |
7: 126,165,471 (GRCm39) |
|
probably benign |
Het |
Gabrb3 |
G |
T |
7: 57,241,036 (GRCm39) |
A5S |
probably benign |
Het |
Gcnt2 |
T |
A |
13: 41,041,283 (GRCm39) |
N147K |
probably damaging |
Het |
Gm6987 |
T |
A |
X: 93,068,216 (GRCm39) |
|
noncoding transcript |
Het |
Hbp1 |
A |
T |
12: 31,984,421 (GRCm39) |
L262Q |
probably damaging |
Het |
Hsd11b2 |
T |
C |
8: 106,249,798 (GRCm39) |
V303A |
probably benign |
Het |
Htr5a |
A |
G |
5: 28,047,690 (GRCm39) |
M82V |
probably benign |
Het |
Mcc |
T |
C |
18: 44,857,707 (GRCm39) |
D136G |
probably benign |
Het |
Mrpl32 |
C |
T |
13: 14,787,564 (GRCm39) |
V14M |
probably damaging |
Het |
Msl1 |
A |
G |
11: 98,687,126 (GRCm39) |
D157G |
possibly damaging |
Het |
Mthfd1 |
G |
A |
12: 76,329,648 (GRCm39) |
|
probably null |
Het |
Nkx6-1 |
T |
A |
5: 101,807,371 (GRCm39) |
D337V |
probably damaging |
Het |
Nlrp5 |
T |
C |
7: 23,117,823 (GRCm39) |
W516R |
possibly damaging |
Het |
Or2ag1 |
A |
G |
7: 106,313,210 (GRCm39) |
L226P |
probably damaging |
Het |
Or2l13b |
T |
A |
16: 19,349,452 (GRCm39) |
I73F |
possibly damaging |
Het |
Or2y3 |
A |
G |
17: 38,393,248 (GRCm39) |
V207A |
possibly damaging |
Het |
Or4l1 |
T |
C |
14: 50,166,272 (GRCm39) |
H243R |
probably damaging |
Het |
Or5af1 |
C |
A |
11: 58,722,820 (GRCm39) |
T280K |
probably damaging |
Het |
Pate5 |
A |
G |
9: 35,750,724 (GRCm39) |
S33P |
possibly damaging |
Het |
Pold3 |
T |
A |
7: 99,749,854 (GRCm39) |
R104* |
probably null |
Het |
Rapsn |
A |
T |
2: 90,867,162 (GRCm39) |
N155Y |
probably damaging |
Het |
Rorc |
C |
A |
3: 94,296,826 (GRCm39) |
Q269K |
probably damaging |
Het |
Rreb1 |
A |
T |
13: 38,131,099 (GRCm39) |
N1418Y |
probably damaging |
Het |
Rusc2 |
G |
A |
4: 43,425,563 (GRCm39) |
D1223N |
possibly damaging |
Het |
Sema6d |
T |
C |
2: 124,506,040 (GRCm39) |
I616T |
probably damaging |
Het |
Ttc6 |
T |
A |
12: 57,679,581 (GRCm39) |
|
probably benign |
Het |
Ugt3a1 |
A |
T |
15: 9,338,810 (GRCm39) |
Y58F |
probably damaging |
Het |
Vmn2r129 |
T |
G |
4: 156,691,085 (GRCm39) |
|
noncoding transcript |
Het |
Vwa5b1 |
A |
T |
4: 138,321,641 (GRCm39) |
M384K |
possibly damaging |
Het |
Washc3 |
G |
A |
10: 88,055,142 (GRCm39) |
E111K |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,355,741 (GRCm39) |
S3501G |
probably benign |
Het |
Zfp352 |
C |
T |
4: 90,113,261 (GRCm39) |
T467M |
probably damaging |
Het |
Zfp729a |
C |
A |
13: 67,767,925 (GRCm39) |
C768F |
probably damaging |
Het |
Zfp810 |
T |
C |
9: 22,190,369 (GRCm39) |
K180E |
probably damaging |
Het |
|
Other mutations in Zfp1004 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0254:Zfp1004
|
UTSW |
2 |
150,033,784 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0505:Zfp1004
|
UTSW |
2 |
150,035,000 (GRCm39) |
nonsense |
probably null |
|
R0562:Zfp1004
|
UTSW |
2 |
150,034,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R1239:Zfp1004
|
UTSW |
2 |
150,033,891 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1878:Zfp1004
|
UTSW |
2 |
150,034,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R1966:Zfp1004
|
UTSW |
2 |
150,033,827 (GRCm39) |
missense |
probably benign |
0.00 |
R2001:Zfp1004
|
UTSW |
2 |
150,034,867 (GRCm39) |
missense |
probably benign |
0.00 |
R2208:Zfp1004
|
UTSW |
2 |
150,035,065 (GRCm39) |
missense |
probably benign |
0.40 |
R3110:Zfp1004
|
UTSW |
2 |
150,034,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R3112:Zfp1004
|
UTSW |
2 |
150,034,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R4299:Zfp1004
|
UTSW |
2 |
150,032,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R4579:Zfp1004
|
UTSW |
2 |
150,034,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R4818:Zfp1004
|
UTSW |
2 |
150,033,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R4894:Zfp1004
|
UTSW |
2 |
150,033,899 (GRCm39) |
nonsense |
probably null |
|
R5432:Zfp1004
|
UTSW |
2 |
150,033,901 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5669:Zfp1004
|
UTSW |
2 |
150,034,098 (GRCm39) |
missense |
probably benign |
0.09 |
R6106:Zfp1004
|
UTSW |
2 |
150,034,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R6857:Zfp1004
|
UTSW |
2 |
150,033,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R7450:Zfp1004
|
UTSW |
2 |
150,035,046 (GRCm39) |
missense |
probably benign |
0.04 |
R8011:Zfp1004
|
UTSW |
2 |
150,034,266 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8519:Zfp1004
|
UTSW |
2 |
150,034,700 (GRCm39) |
missense |
probably benign |
0.37 |
R9482:Zfp1004
|
UTSW |
2 |
150,034,711 (GRCm39) |
missense |
probably benign |
0.01 |
|