Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl1 |
T |
C |
4: 86,344,115 (GRCm39) |
V1731A |
probably damaging |
Het |
Bcat2 |
A |
G |
7: 45,225,429 (GRCm39) |
|
probably null |
Het |
Bcl6 |
T |
G |
16: 23,788,798 (GRCm39) |
E523D |
possibly damaging |
Het |
Cdcp3 |
C |
T |
7: 130,881,212 (GRCm39) |
S1828F |
unknown |
Het |
Col4a2 |
T |
A |
8: 11,471,250 (GRCm39) |
N503K |
probably damaging |
Het |
Cyb5r1 |
G |
A |
1: 134,335,576 (GRCm39) |
C166Y |
probably benign |
Het |
Cyp2w1 |
T |
C |
5: 139,342,775 (GRCm39) |
V490A |
possibly damaging |
Het |
Erich6b |
A |
G |
14: 75,901,024 (GRCm39) |
I113V |
probably benign |
Het |
Fabp12 |
C |
T |
3: 10,312,738 (GRCm39) |
V95I |
probably benign |
Het |
Gask1b |
T |
A |
3: 79,848,669 (GRCm39) |
F472I |
probably damaging |
Het |
Gpr3 |
T |
C |
4: 132,938,448 (GRCm39) |
M75V |
probably benign |
Het |
Grm5 |
T |
G |
7: 87,779,682 (GRCm39) |
S1073A |
probably benign |
Het |
Hoxc9 |
A |
G |
15: 102,892,414 (GRCm39) |
K209R |
probably damaging |
Het |
Irgm2 |
T |
G |
11: 58,110,291 (GRCm39) |
V6G |
probably benign |
Het |
Jakmip2 |
A |
G |
18: 43,690,444 (GRCm39) |
V627A |
possibly damaging |
Het |
Kansl1l |
C |
G |
1: 66,801,262 (GRCm39) |
S568T |
probably damaging |
Het |
Lims1 |
A |
G |
10: 58,230,301 (GRCm39) |
T21A |
probably benign |
Het |
Lpar2 |
G |
T |
8: 70,279,165 (GRCm39) |
A320S |
probably benign |
Het |
Lpcat4 |
A |
G |
2: 112,073,400 (GRCm39) |
N235S |
probably damaging |
Het |
Ly6g2 |
T |
C |
15: 75,088,567 (GRCm39) |
F12L |
probably benign |
Het |
Meis1 |
A |
T |
11: 18,835,542 (GRCm39) |
S359T |
unknown |
Het |
Mtor |
C |
T |
4: 148,549,416 (GRCm39) |
T600I |
probably benign |
Het |
Ncbp1 |
T |
C |
4: 46,149,910 (GRCm39) |
S144P |
probably damaging |
Het |
Ncor1 |
T |
C |
11: 62,274,025 (GRCm39) |
E205G |
probably damaging |
Het |
Nid1 |
T |
C |
13: 13,643,049 (GRCm39) |
I329T |
probably benign |
Het |
Nos3 |
T |
C |
5: 24,587,633 (GRCm39) |
I1031T |
probably damaging |
Het |
Nyap1 |
A |
G |
5: 137,734,530 (GRCm39) |
S168P |
probably damaging |
Het |
Or56a4 |
A |
G |
7: 104,806,106 (GRCm39) |
V261A |
probably damaging |
Het |
Pam |
T |
A |
1: 97,903,515 (GRCm39) |
K73* |
probably null |
Het |
Pcdhga11 |
T |
C |
18: 37,891,005 (GRCm39) |
V671A |
probably benign |
Het |
Ptpn18 |
G |
A |
1: 34,512,445 (GRCm39) |
D417N |
possibly damaging |
Het |
Ric1 |
A |
G |
19: 29,552,180 (GRCm39) |
D317G |
probably damaging |
Het |
Scn1a |
T |
C |
2: 66,103,389 (GRCm39) |
E1957G |
probably benign |
Het |
Srcap |
T |
C |
7: 127,159,414 (GRCm39) |
S3097P |
unknown |
Het |
Tas2r113 |
C |
T |
6: 132,870,272 (GRCm39) |
T100I |
probably benign |
Het |
Tnni1 |
A |
G |
1: 135,735,260 (GRCm39) |
D57G |
|
Het |
Trim29 |
G |
A |
9: 43,246,428 (GRCm39) |
V575I |
probably damaging |
Het |
Trpv3 |
G |
A |
11: 73,179,087 (GRCm39) |
V499M |
probably damaging |
Het |
Ubr1 |
C |
T |
2: 120,693,161 (GRCm39) |
M1748I |
probably benign |
Het |
Upk1a |
A |
T |
7: 30,306,617 (GRCm39) |
M99K |
probably damaging |
Het |
Usp16 |
T |
A |
16: 87,276,207 (GRCm39) |
L515* |
probably null |
Het |
Vmn1r103 |
T |
C |
7: 20,244,435 (GRCm39) |
K9E |
probably damaging |
Het |
Vwde |
A |
G |
6: 13,187,639 (GRCm39) |
V616A |
probably benign |
Het |
|
Other mutations in Zfp101 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0189:Zfp101
|
UTSW |
17 |
33,601,213 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0254:Zfp101
|
UTSW |
17 |
33,599,952 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0448:Zfp101
|
UTSW |
17 |
33,601,295 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0696:Zfp101
|
UTSW |
17 |
33,600,401 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0834:Zfp101
|
UTSW |
17 |
33,601,418 (GRCm39) |
missense |
probably benign |
0.33 |
R2000:Zfp101
|
UTSW |
17 |
33,600,491 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2366:Zfp101
|
UTSW |
17 |
33,599,972 (GRCm39) |
missense |
probably benign |
0.06 |
R2471:Zfp101
|
UTSW |
17 |
33,599,950 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3713:Zfp101
|
UTSW |
17 |
33,600,880 (GRCm39) |
missense |
probably benign |
0.05 |
R3857:Zfp101
|
UTSW |
17 |
33,601,405 (GRCm39) |
nonsense |
probably null |
|
R4537:Zfp101
|
UTSW |
17 |
33,601,466 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4712:Zfp101
|
UTSW |
17 |
33,613,457 (GRCm39) |
splice site |
probably null |
|
R5049:Zfp101
|
UTSW |
17 |
33,600,872 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5241:Zfp101
|
UTSW |
17 |
33,601,210 (GRCm39) |
missense |
probably benign |
|
R5499:Zfp101
|
UTSW |
17 |
33,601,318 (GRCm39) |
missense |
probably benign |
0.20 |
R5587:Zfp101
|
UTSW |
17 |
33,600,295 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5694:Zfp101
|
UTSW |
17 |
33,599,919 (GRCm39) |
missense |
probably benign |
|
R5994:Zfp101
|
UTSW |
17 |
33,599,936 (GRCm39) |
missense |
probably benign |
|
R6193:Zfp101
|
UTSW |
17 |
33,600,720 (GRCm39) |
nonsense |
probably null |
|
R7331:Zfp101
|
UTSW |
17 |
33,601,559 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7393:Zfp101
|
UTSW |
17 |
33,605,674 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7922:Zfp101
|
UTSW |
17 |
33,600,511 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8087:Zfp101
|
UTSW |
17 |
33,599,977 (GRCm39) |
missense |
probably benign |
|
R8684:Zfp101
|
UTSW |
17 |
33,600,977 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9443:Zfp101
|
UTSW |
17 |
33,601,418 (GRCm39) |
missense |
probably benign |
0.33 |
R9581:Zfp101
|
UTSW |
17 |
33,605,730 (GRCm39) |
nonsense |
probably null |
|
|