Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
A |
G |
14: 118,771,484 (GRCm39) |
V869A |
probably benign |
Het |
Ablim1 |
C |
T |
19: 57,071,979 (GRCm39) |
M1I |
probably null |
Het |
Adamts13 |
A |
T |
2: 26,865,687 (GRCm39) |
I81F |
probably benign |
Het |
Akap11 |
A |
T |
14: 78,747,685 (GRCm39) |
N1567K |
possibly damaging |
Het |
Arrdc4 |
G |
A |
7: 68,391,484 (GRCm39) |
T261M |
possibly damaging |
Het |
C4b |
T |
C |
17: 34,959,999 (GRCm39) |
I326V |
probably benign |
Het |
Casp8ap2 |
G |
A |
4: 32,640,541 (GRCm39) |
A532T |
probably benign |
Het |
Ccdc134 |
A |
G |
15: 82,019,337 (GRCm39) |
T187A |
probably benign |
Het |
Cdh8 |
T |
C |
8: 99,917,039 (GRCm39) |
N359D |
probably damaging |
Het |
Cep97 |
A |
G |
16: 55,748,184 (GRCm39) |
L82P |
probably damaging |
Het |
Cfap53 |
A |
T |
18: 74,440,444 (GRCm39) |
R404S |
probably benign |
Het |
Chrng |
C |
A |
1: 87,135,229 (GRCm39) |
F179L |
probably damaging |
Het |
Ddi1 |
A |
T |
9: 6,265,391 (GRCm39) |
I326K |
probably damaging |
Het |
Decr2 |
T |
C |
17: 26,302,002 (GRCm39) |
T243A |
possibly damaging |
Het |
Dip2c |
T |
C |
13: 9,715,900 (GRCm39) |
V1502A |
probably damaging |
Het |
Edem1 |
T |
C |
6: 108,818,640 (GRCm39) |
V216A |
probably damaging |
Het |
Fat2 |
A |
C |
11: 55,174,230 (GRCm39) |
V2161G |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,161,034 (GRCm39) |
T2169A |
probably benign |
Het |
Fmn1 |
T |
C |
2: 113,196,043 (GRCm39) |
V581A |
unknown |
Het |
Hip1r |
A |
T |
5: 124,134,638 (GRCm39) |
D350V |
probably damaging |
Het |
Ift140 |
G |
A |
17: 25,306,959 (GRCm39) |
R898H |
probably damaging |
Het |
Il12a |
A |
G |
3: 68,602,896 (GRCm39) |
I159V |
probably benign |
Het |
Itprid1 |
A |
G |
6: 55,955,488 (GRCm39) |
E1032G |
possibly damaging |
Het |
Kl |
A |
G |
5: 150,906,097 (GRCm39) |
E489G |
probably benign |
Het |
Klhl3 |
T |
C |
13: 58,161,712 (GRCm39) |
E461G |
probably damaging |
Het |
Masp1 |
T |
C |
16: 23,313,404 (GRCm39) |
Y177C |
probably damaging |
Het |
Nop58 |
T |
A |
1: 59,742,031 (GRCm39) |
Y187N |
probably damaging |
Het |
Npc1l1 |
A |
G |
11: 6,167,785 (GRCm39) |
V1002A |
probably benign |
Het |
Ntaq1 |
T |
A |
15: 58,021,285 (GRCm39) |
|
probably null |
Het |
Ntrk1 |
A |
T |
3: 87,687,384 (GRCm39) |
Y683* |
probably null |
Het |
Or11g26 |
A |
G |
14: 50,753,584 (GRCm39) |
I308V |
probably benign |
Het |
Or13j1 |
C |
T |
4: 43,705,923 (GRCm39) |
C215Y |
probably damaging |
Het |
Or2w4 |
C |
T |
13: 21,796,083 (GRCm39) |
D19N |
probably benign |
Het |
Or8k21 |
T |
C |
2: 86,144,874 (GRCm39) |
Y252C |
probably damaging |
Het |
Osbpl6 |
T |
C |
2: 76,409,560 (GRCm39) |
V367A |
probably benign |
Het |
Phip |
A |
G |
9: 82,782,881 (GRCm39) |
W855R |
probably damaging |
Het |
Phlpp1 |
A |
G |
1: 106,308,115 (GRCm39) |
S1131G |
probably damaging |
Het |
Pkdrej |
A |
T |
15: 85,701,442 (GRCm39) |
V1498E |
probably benign |
Het |
Pramel22 |
G |
T |
4: 143,382,121 (GRCm39) |
L192M |
probably damaging |
Het |
Prkaa2 |
T |
C |
4: 104,908,420 (GRCm39) |
N152D |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Pxdn |
G |
A |
12: 30,052,558 (GRCm39) |
V732M |
probably damaging |
Het |
Rccd1 |
C |
T |
7: 79,969,859 (GRCm39) |
W223* |
probably null |
Het |
Riox2 |
T |
A |
16: 59,295,946 (GRCm39) |
S16T |
possibly damaging |
Het |
Scn5a |
C |
T |
9: 119,350,367 (GRCm39) |
V836I |
probably damaging |
Het |
Serpinf1 |
G |
A |
11: 75,301,076 (GRCm39) |
R380C |
probably damaging |
Het |
Sf3b1 |
A |
T |
1: 55,036,336 (GRCm39) |
N912K |
probably benign |
Het |
Shprh |
T |
A |
10: 11,040,488 (GRCm39) |
C134S |
probably damaging |
Het |
Skint8 |
T |
A |
4: 111,785,924 (GRCm39) |
C123* |
probably null |
Het |
Slc16a13 |
G |
T |
11: 70,109,421 (GRCm39) |
S360* |
probably null |
Het |
Srr |
A |
G |
11: 74,799,629 (GRCm39) |
I282T |
possibly damaging |
Het |
Trpm1 |
T |
C |
7: 63,873,565 (GRCm39) |
F607L |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,539,870 (GRCm39) |
D34372G |
probably benign |
Het |
Tub |
C |
T |
7: 108,628,888 (GRCm39) |
T401I |
probably damaging |
Het |
Wdhd1 |
T |
C |
14: 47,493,693 (GRCm39) |
E9G |
probably damaging |
Het |
Yipf3 |
T |
A |
17: 46,561,787 (GRCm39) |
F198Y |
possibly damaging |
Het |
|
Other mutations in Zfp955a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01115:Zfp955a
|
APN |
17 |
33,461,554 (GRCm39) |
nonsense |
probably null |
|
IGL01859:Zfp955a
|
APN |
17 |
33,462,693 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02612:Zfp955a
|
APN |
17 |
33,463,039 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02894:Zfp955a
|
APN |
17 |
33,461,426 (GRCm39) |
nonsense |
probably null |
|
IGL02933:Zfp955a
|
APN |
17 |
33,462,683 (GRCm39) |
splice site |
probably null |
|
R0145:Zfp955a
|
UTSW |
17 |
33,461,430 (GRCm39) |
missense |
probably damaging |
0.98 |
R0577:Zfp955a
|
UTSW |
17 |
33,461,068 (GRCm39) |
missense |
probably damaging |
0.99 |
R0963:Zfp955a
|
UTSW |
17 |
33,462,726 (GRCm39) |
missense |
probably benign |
0.00 |
R1614:Zfp955a
|
UTSW |
17 |
33,461,306 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1704:Zfp955a
|
UTSW |
17 |
33,460,699 (GRCm39) |
nonsense |
probably null |
|
R1994:Zfp955a
|
UTSW |
17 |
33,460,620 (GRCm39) |
missense |
probably damaging |
0.99 |
R2043:Zfp955a
|
UTSW |
17 |
33,461,527 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2091:Zfp955a
|
UTSW |
17 |
33,461,731 (GRCm39) |
nonsense |
probably null |
|
R2091:Zfp955a
|
UTSW |
17 |
33,461,731 (GRCm39) |
nonsense |
probably null |
|
R4077:Zfp955a
|
UTSW |
17 |
33,460,675 (GRCm39) |
missense |
probably benign |
0.15 |
R4078:Zfp955a
|
UTSW |
17 |
33,460,675 (GRCm39) |
missense |
probably benign |
0.15 |
R4689:Zfp955a
|
UTSW |
17 |
33,461,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R4735:Zfp955a
|
UTSW |
17 |
33,460,696 (GRCm39) |
missense |
probably benign |
0.09 |
R4870:Zfp955a
|
UTSW |
17 |
33,460,699 (GRCm39) |
nonsense |
probably null |
|
R4904:Zfp955a
|
UTSW |
17 |
33,461,162 (GRCm39) |
nonsense |
probably null |
|
R5180:Zfp955a
|
UTSW |
17 |
33,461,592 (GRCm39) |
missense |
probably benign |
0.15 |
R6006:Zfp955a
|
UTSW |
17 |
33,460,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R7132:Zfp955a
|
UTSW |
17 |
33,460,589 (GRCm39) |
nonsense |
probably null |
|
R7403:Zfp955a
|
UTSW |
17 |
33,462,720 (GRCm39) |
missense |
probably benign |
0.01 |
R7457:Zfp955a
|
UTSW |
17 |
33,463,025 (GRCm39) |
nonsense |
probably null |
|
R7547:Zfp955a
|
UTSW |
17 |
33,461,797 (GRCm39) |
missense |
probably benign |
0.05 |
R8263:Zfp955a
|
UTSW |
17 |
33,463,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R8265:Zfp955a
|
UTSW |
17 |
33,463,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R8330:Zfp955a
|
UTSW |
17 |
33,463,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R8947:Zfp955a
|
UTSW |
17 |
33,460,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R9052:Zfp955a
|
UTSW |
17 |
33,461,279 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9352:Zfp955a
|
UTSW |
17 |
33,461,335 (GRCm39) |
missense |
probably benign |
0.01 |
R9557:Zfp955a
|
UTSW |
17 |
33,461,107 (GRCm39) |
nonsense |
probably null |
|
R9683:Zfp955a
|
UTSW |
17 |
33,461,587 (GRCm39) |
missense |
probably benign |
0.01 |
R9784:Zfp955a
|
UTSW |
17 |
33,461,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R9797:Zfp955a
|
UTSW |
17 |
33,461,888 (GRCm39) |
missense |
possibly damaging |
0.59 |
X0062:Zfp955a
|
UTSW |
17 |
33,460,976 (GRCm39) |
missense |
probably benign |
0.37 |
|