Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg6 |
A |
G |
10: 14,307,423 (GRCm39) |
V793A |
probably benign |
Het |
Als2 |
G |
T |
1: 59,231,109 (GRCm39) |
P834Q |
probably damaging |
Het |
Alx1 |
T |
C |
10: 102,864,335 (GRCm39) |
T45A |
probably benign |
Het |
Angptl7 |
T |
G |
4: 148,584,575 (GRCm39) |
S58R |
possibly damaging |
Het |
Atg3 |
A |
G |
16: 44,979,481 (GRCm39) |
T7A |
probably benign |
Het |
Bpifc |
A |
T |
10: 85,815,118 (GRCm39) |
S283T |
possibly damaging |
Het |
C2cd2l |
T |
A |
9: 44,227,914 (GRCm39) |
E231V |
probably damaging |
Het |
Cdk5r2 |
T |
C |
1: 74,894,504 (GRCm39) |
V83A |
probably damaging |
Het |
Chst10 |
T |
C |
1: 38,907,116 (GRCm39) |
E178G |
probably damaging |
Het |
Crocc2 |
T |
A |
1: 93,143,106 (GRCm39) |
L1236Q |
probably benign |
Het |
Dleu7 |
T |
C |
14: 62,514,351 (GRCm39) |
*210W |
probably null |
Het |
Emc1 |
T |
G |
4: 139,088,201 (GRCm39) |
V323G |
probably damaging |
Het |
Fcrla |
T |
C |
1: 170,745,949 (GRCm39) |
T278A |
probably benign |
Het |
Flrt3 |
T |
C |
2: 140,503,590 (GRCm39) |
T13A |
probably benign |
Het |
Galntl6 |
A |
T |
8: 58,310,549 (GRCm39) |
|
probably null |
Het |
Gen1 |
A |
G |
12: 11,305,186 (GRCm39) |
V203A |
possibly damaging |
Het |
Gm3149 |
T |
A |
14: 15,698,287 (GRCm39) |
V169E |
probably benign |
Het |
Hjurp |
CTCCTCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCA |
C |
1: 88,193,996 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,610,281 (GRCm39) |
S1463P |
probably benign |
Het |
Irag1 |
A |
T |
7: 110,545,259 (GRCm39) |
D12E |
probably benign |
Het |
Jsrp1 |
A |
T |
10: 80,644,734 (GRCm39) |
I224N |
possibly damaging |
Het |
Kcnk2 |
CAAA |
CAA |
1: 188,988,891 (GRCm39) |
|
probably null |
Het |
Kcnma1 |
A |
T |
14: 23,441,033 (GRCm39) |
M591K |
probably benign |
Het |
Kmt2d |
A |
C |
15: 98,763,046 (GRCm39) |
W268G |
probably damaging |
Het |
Knop1 |
A |
G |
7: 118,447,710 (GRCm39) |
S417P |
unknown |
Het |
Lpin3 |
T |
C |
2: 160,746,416 (GRCm39) |
F692L |
probably damaging |
Het |
Mycbp |
T |
C |
4: 123,803,880 (GRCm39) |
C130R |
unknown |
Het |
Myh1 |
T |
C |
11: 67,108,745 (GRCm39) |
I1387T |
probably damaging |
Het |
Nbeal2 |
T |
C |
9: 110,463,066 (GRCm39) |
D1333G |
probably benign |
Het |
Nedd4l |
G |
T |
18: 65,021,031 (GRCm39) |
|
probably benign |
Het |
Nucks1 |
A |
G |
1: 131,846,744 (GRCm39) |
N7D |
probably benign |
Het |
Nup210 |
A |
G |
6: 91,019,608 (GRCm39) |
I991T |
probably damaging |
Het |
Or4a72 |
C |
T |
2: 89,405,953 (GRCm39) |
G39D |
probably damaging |
Het |
Pcdhb3 |
A |
G |
18: 37,434,736 (GRCm39) |
D234G |
probably damaging |
Het |
Phyh |
C |
T |
2: 4,923,863 (GRCm39) |
|
probably benign |
Het |
Pik3c2a |
G |
A |
7: 115,961,289 (GRCm39) |
T1070I |
probably benign |
Het |
Prss52 |
C |
T |
14: 64,351,129 (GRCm39) |
L305F |
probably damaging |
Het |
Rasef |
T |
C |
4: 73,708,933 (GRCm39) |
D100G |
probably benign |
Het |
Rb1 |
A |
C |
14: 73,443,493 (GRCm39) |
M754R |
probably damaging |
Het |
Rbm6 |
T |
C |
9: 107,669,208 (GRCm39) |
Q568R |
possibly damaging |
Het |
Selplg |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
5: 113,957,756 (GRCm39) |
|
probably benign |
Het |
Serf2 |
T |
C |
2: 121,281,206 (GRCm39) |
S41P |
possibly damaging |
Het |
Serf2 |
C |
A |
2: 121,281,205 (GRCm39) |
D40E |
possibly damaging |
Het |
Sh2b1 |
AGCTC |
AGCTCAGCCACGGGGACCCGCTC |
7: 126,066,768 (GRCm39) |
|
probably benign |
Het |
Sympk |
G |
T |
7: 18,771,986 (GRCm39) |
R350L |
possibly damaging |
Het |
Tab2 |
C |
A |
10: 7,795,124 (GRCm39) |
V379L |
probably damaging |
Het |
Tnk1 |
T |
G |
11: 69,743,666 (GRCm39) |
T485P |
probably benign |
Het |
Trmt6 |
T |
C |
2: 132,648,699 (GRCm39) |
T412A |
probably benign |
Het |
Vgll3 |
A |
G |
16: 65,636,229 (GRCm39) |
T182A |
probably benign |
Het |
Zfat |
A |
G |
15: 68,084,652 (GRCm39) |
S80P |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,291,239 (GRCm39) |
L2122S |
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 |
R4135:Zfp1004
|
UTSW |
2 |
150,023,788 (GRCm39) |
splice site |
probably benign |
|
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 |
|