Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adck2 |
G |
T |
6: 39,551,678 (GRCm39) |
L148F |
probably damaging |
Het |
Arhgef10 |
G |
A |
8: 15,047,551 (GRCm39) |
R1138H |
probably damaging |
Het |
Arpp21 |
T |
C |
9: 111,948,266 (GRCm39) |
T668A |
probably benign |
Het |
Atp6v0b |
T |
A |
4: 117,742,850 (GRCm39) |
I79F |
possibly damaging |
Het |
Atp8b5 |
A |
T |
4: 43,334,205 (GRCm39) |
N324Y |
probably benign |
Het |
Bach2 |
A |
G |
4: 32,579,975 (GRCm39) |
I610M |
possibly damaging |
Het |
Casr |
G |
T |
16: 36,315,051 (GRCm39) |
D929E |
probably benign |
Het |
Cbln2 |
T |
C |
18: 86,731,479 (GRCm39) |
S96P |
probably damaging |
Het |
Cpxm1 |
T |
C |
2: 130,238,344 (GRCm39) |
K73E |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,814,645 (GRCm39) |
Y457C |
probably benign |
Het |
Etl4 |
T |
C |
2: 20,535,000 (GRCm39) |
Y152H |
probably damaging |
Het |
Fbh1 |
A |
T |
2: 11,751,969 (GRCm39) |
S910T |
possibly damaging |
Het |
Gm10142 |
T |
C |
10: 77,551,947 (GRCm39) |
S103P |
probably benign |
Het |
Gm12886 |
A |
G |
4: 121,280,229 (GRCm39) |
S16P |
unknown |
Het |
Gpr146 |
T |
C |
5: 139,378,443 (GRCm39) |
Y82H |
probably benign |
Het |
Herc1 |
C |
T |
9: 66,399,293 (GRCm39) |
Q4282* |
probably null |
Het |
Htr2a |
A |
T |
14: 74,943,722 (GRCm39) |
E434V |
probably benign |
Het |
Iqsec3 |
T |
C |
6: 121,389,893 (GRCm39) |
|
probably benign |
Het |
Islr |
A |
C |
9: 58,064,907 (GRCm39) |
V200G |
probably damaging |
Het |
Katnal1 |
T |
C |
5: 148,815,737 (GRCm39) |
D400G |
probably benign |
Het |
Lonrf2 |
A |
G |
1: 38,850,913 (GRCm39) |
|
probably benign |
Het |
Lrp2 |
A |
T |
2: 69,294,980 (GRCm39) |
L3446Q |
probably damaging |
Het |
Med12l |
G |
A |
3: 59,164,794 (GRCm39) |
V1425I |
probably benign |
Het |
Myh13 |
T |
C |
11: 67,251,100 (GRCm39) |
|
probably benign |
Het |
Nutm2 |
T |
G |
13: 50,623,944 (GRCm39) |
S214A |
probably benign |
Het |
Or10aa1 |
T |
A |
1: 173,869,539 (GRCm39) |
W8R |
possibly damaging |
Het |
Or2h1b |
A |
G |
17: 37,462,665 (GRCm39) |
F66S |
probably damaging |
Het |
Or5b99 |
T |
C |
19: 12,977,072 (GRCm39) |
S241P |
probably damaging |
Het |
Or6c33 |
C |
A |
10: 129,853,425 (GRCm39) |
A65E |
possibly damaging |
Het |
Pax5 |
A |
T |
4: 44,691,919 (GRCm39) |
M109K |
probably damaging |
Het |
Pfkfb2 |
G |
A |
1: 130,628,572 (GRCm39) |
R345W |
probably damaging |
Het |
Pkd1l3 |
A |
G |
8: 110,342,977 (GRCm39) |
D105G |
unknown |
Het |
Prdm11 |
A |
G |
2: 92,805,864 (GRCm39) |
V362A |
probably benign |
Het |
Prex2 |
T |
C |
1: 11,171,393 (GRCm39) |
|
probably null |
Het |
Prl8a1 |
T |
C |
13: 27,760,924 (GRCm39) |
T103A |
possibly damaging |
Het |
Rgl1 |
T |
C |
1: 152,409,357 (GRCm39) |
I493V |
probably damaging |
Het |
Rimkla |
A |
G |
4: 119,335,146 (GRCm39) |
V79A |
possibly damaging |
Het |
Ryr2 |
A |
T |
13: 11,634,382 (GRCm39) |
S3791R |
possibly damaging |
Het |
Sh3rf2 |
C |
A |
18: 42,289,222 (GRCm39) |
S681* |
probably null |
Het |
Tspan8 |
C |
A |
10: 115,675,782 (GRCm39) |
F149L |
probably benign |
Het |
Tspan8 |
A |
C |
10: 115,675,783 (GRCm39) |
K150Q |
probably benign |
Het |
Ttn |
T |
C |
2: 76,772,720 (GRCm39) |
E2425G |
probably damaging |
Het |
|
Other mutations in Stmnd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01413:Stmnd1
|
APN |
13 |
46,453,157 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01871:Stmnd1
|
APN |
13 |
46,443,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Stmnd1
|
UTSW |
13 |
46,438,962 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1674:Stmnd1
|
UTSW |
13 |
46,453,097 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5127:Stmnd1
|
UTSW |
13 |
46,453,071 (GRCm39) |
missense |
probably benign |
0.04 |
R5290:Stmnd1
|
UTSW |
13 |
46,453,074 (GRCm39) |
missense |
probably benign |
0.44 |
R6924:Stmnd1
|
UTSW |
13 |
46,452,969 (GRCm39) |
missense |
probably benign |
|
R6957:Stmnd1
|
UTSW |
13 |
46,427,375 (GRCm39) |
missense |
probably benign |
0.09 |
R7745:Stmnd1
|
UTSW |
13 |
46,453,077 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8346:Stmnd1
|
UTSW |
13 |
46,452,936 (GRCm39) |
missense |
probably benign |
0.00 |
R9026:Stmnd1
|
UTSW |
13 |
46,452,983 (GRCm39) |
missense |
probably benign |
|
R9339:Stmnd1
|
UTSW |
13 |
46,453,079 (GRCm39) |
missense |
probably benign |
0.00 |
R9696:Stmnd1
|
UTSW |
13 |
46,443,224 (GRCm39) |
missense |
probably damaging |
1.00 |
|