Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad11 |
A |
G |
9: 103,972,824 (GRCm39) |
T506A |
probably damaging |
Het |
Ankib1 |
A |
C |
5: 3,743,479 (GRCm39) |
D845E |
probably benign |
Het |
Atxn2 |
T |
C |
5: 121,919,399 (GRCm39) |
V369A |
possibly damaging |
Het |
Ccdc50 |
T |
A |
16: 27,225,534 (GRCm39) |
|
probably benign |
Het |
Clec2g |
A |
G |
6: 128,957,224 (GRCm39) |
I61V |
possibly damaging |
Het |
Col16a1 |
G |
A |
4: 129,955,172 (GRCm39) |
|
probably benign |
Het |
Dapk2 |
A |
G |
9: 66,139,096 (GRCm39) |
Y139C |
probably damaging |
Het |
Ecpas |
A |
G |
4: 58,840,757 (GRCm39) |
V667A |
probably damaging |
Het |
Fnip1 |
T |
C |
11: 54,384,177 (GRCm39) |
L334P |
probably damaging |
Het |
Igf1r |
A |
G |
7: 67,839,739 (GRCm39) |
E682G |
possibly damaging |
Het |
Ints8 |
T |
C |
4: 11,241,627 (GRCm39) |
E272G |
possibly damaging |
Het |
Jph2 |
G |
A |
2: 163,217,699 (GRCm39) |
P326S |
probably damaging |
Het |
Krtap1-4 |
T |
C |
11: 99,473,940 (GRCm39) |
|
probably benign |
Het |
Lrp5 |
A |
G |
19: 3,654,022 (GRCm39) |
I1135T |
probably damaging |
Het |
Lrrk1 |
A |
G |
7: 65,958,439 (GRCm39) |
V320A |
probably benign |
Het |
Myh6 |
A |
C |
14: 55,191,381 (GRCm39) |
I820S |
possibly damaging |
Het |
Napg |
A |
T |
18: 63,119,319 (GRCm39) |
T110S |
probably damaging |
Het |
Nova1 |
G |
A |
12: 46,767,475 (GRCm39) |
Q56* |
probably null |
Het |
Phyhip |
A |
G |
14: 70,699,367 (GRCm39) |
|
probably null |
Het |
Pkd2l2 |
C |
A |
18: 34,549,970 (GRCm39) |
S205* |
probably null |
Het |
Ppp2r1a |
G |
T |
17: 21,179,265 (GRCm39) |
C101F |
probably benign |
Het |
Serpinb3c |
G |
A |
1: 107,200,872 (GRCm39) |
R182* |
probably null |
Het |
St18 |
A |
C |
1: 6,872,540 (GRCm39) |
|
probably benign |
Het |
St6galnac4 |
C |
T |
2: 32,487,096 (GRCm39) |
R264C |
possibly damaging |
Het |
Tmem168 |
T |
C |
6: 13,603,261 (GRCm39) |
Y35C |
probably benign |
Het |
Tmem219 |
A |
G |
7: 126,496,220 (GRCm39) |
L74P |
probably damaging |
Het |
Trpc4 |
T |
A |
3: 54,206,667 (GRCm39) |
N622K |
probably damaging |
Het |
Trpm6 |
A |
C |
19: 18,807,376 (GRCm39) |
|
probably benign |
Het |
Ttl |
C |
A |
2: 128,908,213 (GRCm39) |
F49L |
possibly damaging |
Het |
Tut7 |
C |
T |
13: 59,964,156 (GRCm39) |
D250N |
probably damaging |
Het |
Vmn2r97 |
T |
G |
17: 19,149,432 (GRCm39) |
I273M |
probably damaging |
Het |
Wdr5 |
C |
A |
2: 27,410,437 (GRCm39) |
|
probably benign |
Het |
Zfp37 |
C |
A |
4: 62,110,548 (GRCm39) |
C172F |
possibly damaging |
Het |
|
Other mutations in Vmn1r123 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00927:Vmn1r123
|
APN |
7 |
20,896,216 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02330:Vmn1r123
|
APN |
7 |
20,896,969 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03240:Vmn1r123
|
APN |
7 |
20,896,282 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1173:Vmn1r123
|
UTSW |
7 |
20,896,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R6278:Vmn1r123
|
UTSW |
7 |
20,896,774 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6610:Vmn1r123
|
UTSW |
7 |
20,896,515 (GRCm39) |
missense |
probably benign |
0.00 |
R6679:Vmn1r123
|
UTSW |
7 |
20,896,868 (GRCm39) |
nonsense |
probably null |
|
R7241:Vmn1r123
|
UTSW |
7 |
20,896,537 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7642:Vmn1r123
|
UTSW |
7 |
20,896,795 (GRCm39) |
missense |
probably benign |
0.11 |
R7702:Vmn1r123
|
UTSW |
7 |
20,896,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R7870:Vmn1r123
|
UTSW |
7 |
20,896,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R7981:Vmn1r123
|
UTSW |
7 |
20,896,914 (GRCm39) |
missense |
probably damaging |
0.98 |
R8554:Vmn1r123
|
UTSW |
7 |
20,896,971 (GRCm39) |
missense |
probably benign |
|
R9079:Vmn1r123
|
UTSW |
7 |
20,896,979 (GRCm39) |
missense |
probably benign |
0.01 |
R9090:Vmn1r123
|
UTSW |
7 |
20,896,794 (GRCm39) |
missense |
probably benign |
|
R9271:Vmn1r123
|
UTSW |
7 |
20,896,794 (GRCm39) |
missense |
probably benign |
|
R9544:Vmn1r123
|
UTSW |
7 |
20,896,987 (GRCm39) |
missense |
probably benign |
0.30 |
R9779:Vmn1r123
|
UTSW |
7 |
20,896,111 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
|