Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810055G02Rik |
C |
A |
19: 3,766,972 (GRCm39) |
S186R |
possibly damaging |
Het |
Acap2 |
A |
G |
16: 30,915,163 (GRCm39) |
|
probably benign |
Het |
Cacna1h |
G |
T |
17: 25,599,506 (GRCm39) |
R1726S |
probably damaging |
Het |
Cdca2 |
T |
C |
14: 67,944,946 (GRCm39) |
S133G |
probably damaging |
Het |
Cep295nl |
A |
T |
11: 118,224,735 (GRCm39) |
S36R |
probably benign |
Het |
Crispld1 |
A |
G |
1: 17,817,013 (GRCm39) |
N190S |
possibly damaging |
Het |
Crtam |
A |
G |
9: 40,905,797 (GRCm39) |
V44A |
probably benign |
Het |
Crtc1 |
C |
T |
8: 70,858,775 (GRCm39) |
G112S |
probably benign |
Het |
Cyp17a1 |
T |
C |
19: 46,657,790 (GRCm39) |
N254S |
probably benign |
Het |
Dmrta1 |
T |
C |
4: 89,577,011 (GRCm39) |
S156P |
probably benign |
Het |
Eno2 |
A |
C |
6: 124,743,172 (GRCm39) |
V188G |
probably damaging |
Het |
Fam20a |
A |
T |
11: 109,565,953 (GRCm39) |
I427N |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,147,444 (GRCm39) |
K3933E |
probably benign |
Het |
Igkv8-30 |
T |
C |
6: 70,094,601 (GRCm39) |
M1V |
probably null |
Het |
Ist1 |
G |
A |
8: 110,410,300 (GRCm39) |
|
probably benign |
Het |
Kank4 |
T |
C |
4: 98,661,690 (GRCm39) |
E765G |
possibly damaging |
Het |
Kat14 |
T |
C |
2: 144,235,449 (GRCm39) |
L92S |
probably damaging |
Het |
Kcnu1 |
G |
A |
8: 26,339,855 (GRCm39) |
V58I |
probably benign |
Het |
Lrba |
T |
A |
3: 86,261,513 (GRCm39) |
V1489E |
probably damaging |
Het |
Lrba |
T |
A |
3: 86,352,720 (GRCm39) |
I1956N |
probably damaging |
Het |
Mdn1 |
G |
A |
4: 32,763,199 (GRCm39) |
V5100I |
probably benign |
Het |
Mkrn2os |
C |
A |
6: 115,563,670 (GRCm39) |
G122* |
probably null |
Het |
Nme3 |
T |
C |
17: 25,115,880 (GRCm39) |
Y78H |
probably benign |
Het |
Pira13 |
A |
G |
7: 3,825,179 (GRCm39) |
S488P |
possibly damaging |
Het |
Pkd1l2 |
G |
A |
8: 117,792,484 (GRCm39) |
T436I |
probably benign |
Het |
Ppp2r5c |
T |
G |
12: 110,488,997 (GRCm39) |
V56G |
possibly damaging |
Het |
Pramel16 |
T |
C |
4: 143,676,418 (GRCm39) |
T229A |
possibly damaging |
Het |
Prdm10 |
G |
A |
9: 31,238,644 (GRCm39) |
V179M |
probably damaging |
Het |
Rab11fip2 |
A |
G |
19: 59,895,430 (GRCm39) |
V344A |
probably damaging |
Het |
Selp |
G |
A |
1: 163,957,671 (GRCm39) |
A267T |
probably benign |
Het |
Sf3a1 |
T |
A |
11: 4,129,192 (GRCm39) |
W718R |
probably damaging |
Het |
Taar9 |
T |
C |
10: 23,985,378 (GRCm39) |
N19D |
probably benign |
Het |
Tas2r113 |
T |
G |
6: 132,870,382 (GRCm39) |
S137A |
probably damaging |
Het |
Traf4 |
A |
T |
11: 78,052,447 (GRCm39) |
I66N |
possibly damaging |
Het |
Ucp3 |
A |
T |
7: 100,129,849 (GRCm39) |
T164S |
probably benign |
Het |
Uggt1 |
A |
T |
1: 36,216,696 (GRCm39) |
N96K |
probably benign |
Het |
Uqcc1 |
T |
A |
2: 155,753,749 (GRCm39) |
Q42L |
possibly damaging |
Het |
|
Other mutations in Vmn1r128 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00972:Vmn1r128
|
APN |
7 |
21,084,001 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02169:Vmn1r128
|
APN |
7 |
21,084,163 (GRCm39) |
missense |
probably damaging |
0.99 |
R1740:Vmn1r128
|
UTSW |
7 |
21,083,869 (GRCm39) |
missense |
probably benign |
0.00 |
R2969:Vmn1r128
|
UTSW |
7 |
21,084,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R4583:Vmn1r128
|
UTSW |
7 |
21,083,644 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4867:Vmn1r128
|
UTSW |
7 |
21,083,939 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5266:Vmn1r128
|
UTSW |
7 |
21,083,328 (GRCm39) |
missense |
probably benign |
0.14 |
R5631:Vmn1r128
|
UTSW |
7 |
21,083,300 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R6267:Vmn1r128
|
UTSW |
7 |
21,084,221 (GRCm39) |
makesense |
probably null |
|
R7376:Vmn1r128
|
UTSW |
7 |
21,083,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R8351:Vmn1r128
|
UTSW |
7 |
21,083,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R8440:Vmn1r128
|
UTSW |
7 |
21,083,745 (GRCm39) |
missense |
probably benign |
0.22 |
R8773:Vmn1r128
|
UTSW |
7 |
21,083,922 (GRCm39) |
missense |
probably benign |
0.41 |
R8889:Vmn1r128
|
UTSW |
7 |
21,083,740 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9182:Vmn1r128
|
UTSW |
7 |
21,083,683 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9200:Vmn1r128
|
UTSW |
7 |
21,083,316 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9665:Vmn1r128
|
UTSW |
7 |
21,083,362 (GRCm39) |
missense |
probably damaging |
1.00 |
|