Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl2 |
T |
C |
1: 156,461,349 (GRCm39) |
V417A |
probably damaging |
Het |
Adgrb2 |
T |
C |
4: 129,906,121 (GRCm39) |
V881A |
possibly damaging |
Het |
Arl5c |
G |
A |
11: 97,886,662 (GRCm39) |
R10* |
probably null |
Het |
Atad1 |
A |
G |
19: 32,673,197 (GRCm39) |
C229R |
probably benign |
Het |
Atp6v0a2 |
T |
C |
5: 124,784,674 (GRCm39) |
V319A |
probably damaging |
Het |
Cage1 |
A |
G |
13: 38,207,393 (GRCm39) |
S257P |
possibly damaging |
Het |
Ccndbp1 |
A |
G |
2: 120,842,876 (GRCm39) |
D179G |
probably damaging |
Het |
Cngb3 |
T |
C |
4: 19,415,684 (GRCm39) |
I398T |
probably benign |
Het |
Crmp1 |
A |
G |
5: 37,433,675 (GRCm39) |
D178G |
probably damaging |
Het |
Csmd3 |
C |
T |
15: 48,177,429 (GRCm39) |
V370I |
possibly damaging |
Het |
Dapk1 |
A |
G |
13: 60,865,942 (GRCm39) |
T180A |
probably benign |
Het |
Dmtf1 |
A |
G |
5: 9,190,379 (GRCm39) |
|
probably benign |
Het |
Dnah12 |
T |
C |
14: 26,455,758 (GRCm39) |
L827S |
possibly damaging |
Het |
F5 |
T |
C |
1: 164,044,964 (GRCm39) |
V2084A |
probably benign |
Het |
Fan1 |
A |
T |
7: 64,018,928 (GRCm39) |
S476T |
possibly damaging |
Het |
Far2 |
T |
C |
6: 148,074,907 (GRCm39) |
L380P |
possibly damaging |
Het |
Gbp2 |
A |
G |
3: 142,329,525 (GRCm39) |
N24S |
probably benign |
Het |
Gm14325 |
T |
C |
2: 177,474,776 (GRCm39) |
H101R |
possibly damaging |
Het |
Gpr55 |
C |
T |
1: 85,869,540 (GRCm39) |
V14M |
probably damaging |
Het |
Herc6 |
A |
T |
6: 57,631,480 (GRCm39) |
Y724F |
probably damaging |
Het |
Impg1 |
T |
A |
9: 80,301,341 (GRCm39) |
Q195L |
probably damaging |
Het |
Inf2 |
T |
C |
12: 112,566,638 (GRCm39) |
F68L |
probably damaging |
Het |
Kcnh8 |
T |
C |
17: 53,268,905 (GRCm39) |
|
probably null |
Het |
Klb |
A |
G |
5: 65,533,137 (GRCm39) |
N482S |
probably benign |
Het |
Kpnb1 |
A |
G |
11: 97,062,424 (GRCm39) |
V447A |
probably benign |
Het |
Nckap5l |
G |
A |
15: 99,324,011 (GRCm39) |
P831S |
probably benign |
Het |
Ncor2 |
A |
G |
5: 125,113,879 (GRCm39) |
|
probably null |
Het |
Or4b1d |
A |
T |
2: 89,969,261 (GRCm39) |
V74D |
probably damaging |
Het |
Pgm3 |
T |
C |
9: 86,443,893 (GRCm39) |
Y337C |
probably damaging |
Het |
Prdm1 |
G |
T |
10: 44,322,903 (GRCm39) |
Y197* |
probably null |
Het |
Prdm4 |
A |
T |
10: 85,736,763 (GRCm39) |
C626S |
probably damaging |
Het |
Prex2 |
T |
A |
1: 11,232,487 (GRCm39) |
S851R |
probably benign |
Het |
Ranbp6 |
A |
G |
19: 29,787,733 (GRCm39) |
L873P |
probably damaging |
Het |
Rin2 |
A |
G |
2: 145,664,194 (GRCm39) |
T23A |
possibly damaging |
Het |
Rxra |
G |
T |
2: 27,631,207 (GRCm39) |
R118L |
probably damaging |
Het |
Spice1 |
T |
C |
16: 44,202,476 (GRCm39) |
L750P |
probably damaging |
Het |
Trpm1 |
C |
T |
7: 63,858,660 (GRCm39) |
Q228* |
probably null |
Het |
Tsc1 |
A |
G |
2: 28,560,937 (GRCm39) |
D265G |
probably damaging |
Het |
Usp29 |
T |
C |
7: 6,964,949 (GRCm39) |
I264T |
possibly damaging |
Het |
Vmn2r26 |
T |
C |
6: 124,027,697 (GRCm39) |
L479P |
possibly damaging |
Het |
|
Other mutations in Zfp9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Zfp9
|
APN |
6 |
118,441,436 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01093:Zfp9
|
APN |
6 |
118,442,800 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01512:Zfp9
|
APN |
6 |
118,444,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R0491:Zfp9
|
UTSW |
6 |
118,442,163 (GRCm39) |
missense |
probably damaging |
0.96 |
R1716:Zfp9
|
UTSW |
6 |
118,441,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Zfp9
|
UTSW |
6 |
118,442,021 (GRCm39) |
missense |
probably benign |
0.15 |
R4088:Zfp9
|
UTSW |
6 |
118,441,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R4627:Zfp9
|
UTSW |
6 |
118,441,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R4951:Zfp9
|
UTSW |
6 |
118,441,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R5344:Zfp9
|
UTSW |
6 |
118,442,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R5594:Zfp9
|
UTSW |
6 |
118,442,000 (GRCm39) |
missense |
probably damaging |
0.98 |
R6198:Zfp9
|
UTSW |
6 |
118,454,282 (GRCm39) |
start codon destroyed |
probably null |
|
R6682:Zfp9
|
UTSW |
6 |
118,444,202 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6986:Zfp9
|
UTSW |
6 |
118,441,426 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7147:Zfp9
|
UTSW |
6 |
118,441,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R7799:Zfp9
|
UTSW |
6 |
118,441,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R7921:Zfp9
|
UTSW |
6 |
118,442,032 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7934:Zfp9
|
UTSW |
6 |
118,441,847 (GRCm39) |
missense |
probably damaging |
0.99 |
R8111:Zfp9
|
UTSW |
6 |
118,441,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R8369:Zfp9
|
UTSW |
6 |
118,441,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R8916:Zfp9
|
UTSW |
6 |
118,442,223 (GRCm39) |
nonsense |
probably null |
|
R9660:Zfp9
|
UTSW |
6 |
118,443,851 (GRCm39) |
missense |
probably benign |
|
R9728:Zfp9
|
UTSW |
6 |
118,443,851 (GRCm39) |
missense |
probably benign |
|
|