Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26b |
G |
A |
8: 43,973,832 (GRCm39) |
T390I |
probably benign |
Het |
Adgb |
A |
G |
10: 10,287,456 (GRCm39) |
|
probably null |
Het |
Ado |
G |
T |
10: 67,384,265 (GRCm39) |
Y113* |
probably null |
Het |
Angptl1 |
A |
G |
1: 156,672,885 (GRCm39) |
E237G |
probably damaging |
Het |
Arid2 |
T |
A |
15: 96,254,578 (GRCm39) |
Y141* |
probably null |
Het |
Dnah1 |
T |
C |
14: 31,014,295 (GRCm39) |
K1817E |
probably benign |
Het |
Eif3e |
C |
A |
15: 43,126,642 (GRCm39) |
R271L |
probably damaging |
Het |
Eml6 |
A |
G |
11: 29,703,085 (GRCm39) |
V1611A |
probably damaging |
Het |
Enpp3 |
G |
T |
10: 24,660,739 (GRCm39) |
Y634* |
probably null |
Het |
Evi5l |
C |
T |
8: 4,250,886 (GRCm39) |
R394W |
probably damaging |
Het |
Fcgr3 |
A |
C |
1: 170,881,661 (GRCm39) |
F156V |
probably damaging |
Het |
Fmo1 |
T |
A |
1: 162,661,402 (GRCm39) |
T294S |
probably benign |
Het |
Gabrb3 |
A |
G |
7: 57,466,203 (GRCm39) |
Q339R |
probably damaging |
Het |
Gen1 |
T |
A |
12: 11,292,167 (GRCm39) |
T606S |
probably benign |
Het |
Gfod1 |
T |
C |
13: 43,354,528 (GRCm39) |
Q149R |
probably benign |
Het |
Golm1 |
A |
G |
13: 59,788,071 (GRCm39) |
V276A |
probably benign |
Het |
Hc |
C |
A |
2: 34,914,161 (GRCm39) |
V849F |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,459,627 (GRCm39) |
I832T |
possibly damaging |
Het |
Hspa14 |
T |
C |
2: 3,497,643 (GRCm39) |
D283G |
probably damaging |
Het |
Lztfl1 |
C |
T |
9: 123,541,536 (GRCm39) |
W94* |
probably null |
Het |
Lzts3 |
T |
C |
2: 130,477,306 (GRCm39) |
S381G |
probably benign |
Het |
Mgat2 |
A |
G |
12: 69,231,444 (GRCm39) |
Y6C |
probably damaging |
Het |
Mrpl30 |
T |
C |
1: 37,934,439 (GRCm39) |
I27T |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,406,966 (GRCm39) |
T1045S |
unknown |
Het |
Nlrp4a |
G |
A |
7: 26,148,690 (GRCm39) |
R99Q |
probably benign |
Het |
Or10g1 |
T |
C |
14: 52,647,945 (GRCm39) |
Y128C |
probably damaging |
Het |
Or5b98 |
A |
G |
19: 12,931,006 (GRCm39) |
T18A |
possibly damaging |
Het |
Phlpp1 |
T |
C |
1: 106,209,132 (GRCm39) |
L495P |
probably damaging |
Het |
Pla2g4d |
T |
C |
2: 120,109,776 (GRCm39) |
D178G |
possibly damaging |
Het |
Prl5a1 |
C |
G |
13: 28,333,997 (GRCm39) |
L167V |
probably damaging |
Het |
Sardh |
A |
G |
2: 27,087,651 (GRCm39) |
V740A |
probably benign |
Het |
Sbno1 |
T |
G |
5: 124,543,709 (GRCm39) |
T277P |
probably benign |
Het |
Slc2a1 |
T |
C |
4: 118,993,462 (GRCm39) |
V433A |
probably damaging |
Het |
Slc4a10 |
T |
C |
2: 62,134,308 (GRCm39) |
V1008A |
possibly damaging |
Het |
Smarcal1 |
T |
G |
1: 72,625,179 (GRCm39) |
S109A |
probably benign |
Het |
Speg |
A |
G |
1: 75,377,834 (GRCm39) |
D864G |
probably benign |
Het |
Steap4 |
T |
C |
5: 8,026,976 (GRCm39) |
I313T |
probably benign |
Het |
Tab2 |
A |
T |
10: 7,786,869 (GRCm39) |
D614E |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,544,610 (GRCm39) |
K2246E |
probably damaging |
Het |
Timm23 |
A |
G |
14: 31,902,520 (GRCm39) |
S208P |
probably damaging |
Het |
Tmem229a |
C |
A |
6: 24,955,211 (GRCm39) |
C181F |
probably benign |
Het |
Ugdh |
T |
C |
5: 65,574,958 (GRCm39) |
Y356C |
probably damaging |
Het |
Ugt2a1 |
A |
G |
5: 87,634,586 (GRCm39) |
L7P |
probably damaging |
Het |
Uhrf1 |
A |
G |
17: 56,619,905 (GRCm39) |
D272G |
possibly damaging |
Het |
Vmn1r206 |
T |
A |
13: 22,804,827 (GRCm39) |
I127F |
probably damaging |
Het |
Vmn2r106 |
T |
C |
17: 20,505,490 (GRCm39) |
Y68C |
possibly damaging |
Het |
Zfand6 |
G |
A |
7: 84,283,141 (GRCm39) |
P72L |
not run |
Het |
|
Other mutations in Clvs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00233:Clvs1
|
APN |
4 |
9,281,939 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01293:Clvs1
|
APN |
4 |
9,281,559 (GRCm39) |
start codon destroyed |
probably null |
|
IGL01463:Clvs1
|
APN |
4 |
9,429,818 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03031:Clvs1
|
APN |
4 |
9,449,385 (GRCm39) |
splice site |
probably benign |
|
R0472:Clvs1
|
UTSW |
4 |
9,281,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R0496:Clvs1
|
UTSW |
4 |
9,424,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R0848:Clvs1
|
UTSW |
4 |
9,282,003 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1541:Clvs1
|
UTSW |
4 |
9,281,814 (GRCm39) |
missense |
probably benign |
0.00 |
R1992:Clvs1
|
UTSW |
4 |
9,281,899 (GRCm39) |
missense |
probably benign |
0.01 |
R2901:Clvs1
|
UTSW |
4 |
9,281,972 (GRCm39) |
missense |
probably damaging |
0.96 |
R2902:Clvs1
|
UTSW |
4 |
9,281,972 (GRCm39) |
missense |
probably damaging |
0.96 |
R4321:Clvs1
|
UTSW |
4 |
9,282,029 (GRCm39) |
intron |
probably benign |
|
R4934:Clvs1
|
UTSW |
4 |
9,424,216 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4946:Clvs1
|
UTSW |
4 |
9,281,831 (GRCm39) |
nonsense |
probably null |
|
R4970:Clvs1
|
UTSW |
4 |
9,350,857 (GRCm39) |
intron |
probably benign |
|
R5187:Clvs1
|
UTSW |
4 |
9,281,865 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5327:Clvs1
|
UTSW |
4 |
9,424,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5605:Clvs1
|
UTSW |
4 |
9,281,751 (GRCm39) |
missense |
probably damaging |
0.98 |
R5940:Clvs1
|
UTSW |
4 |
9,449,443 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6818:Clvs1
|
UTSW |
4 |
9,282,014 (GRCm39) |
critical splice donor site |
probably null |
|
R6857:Clvs1
|
UTSW |
4 |
9,449,433 (GRCm39) |
missense |
probably benign |
0.00 |
R8247:Clvs1
|
UTSW |
4 |
9,281,885 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8791:Clvs1
|
UTSW |
4 |
9,429,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R9500:Clvs1
|
UTSW |
4 |
9,429,834 (GRCm39) |
missense |
probably damaging |
0.98 |
|