Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110008E08Rik |
A |
T |
16: 90,351,098 (GRCm39) |
|
noncoding transcript |
Het |
2700049A03Rik |
C |
A |
12: 71,235,565 (GRCm39) |
P1172T |
probably benign |
Het |
Abi3bp |
T |
A |
16: 56,462,838 (GRCm39) |
|
probably null |
Het |
Apod |
T |
A |
16: 31,129,884 (GRCm39) |
H24L |
probably damaging |
Het |
Arfgef3 |
T |
C |
10: 18,476,208 (GRCm39) |
E1537G |
probably damaging |
Het |
B020004C17Rik |
T |
C |
14: 57,254,036 (GRCm39) |
V53A |
possibly damaging |
Het |
Ccdc113 |
C |
A |
8: 96,267,424 (GRCm39) |
|
probably null |
Het |
Cd7 |
T |
G |
11: 120,928,936 (GRCm39) |
D105A |
probably damaging |
Het |
Celsr3 |
C |
T |
9: 108,720,357 (GRCm39) |
T2550M |
probably benign |
Het |
Cibar1 |
T |
C |
4: 12,171,195 (GRCm39) |
Q86R |
probably benign |
Het |
Col6a5 |
C |
T |
9: 105,823,282 (GRCm39) |
G25D |
unknown |
Het |
Cps1 |
A |
G |
1: 67,211,868 (GRCm39) |
M679V |
probably benign |
Het |
Dnai4 |
A |
T |
4: 102,906,730 (GRCm39) |
D694E |
probably benign |
Het |
Dync1h1 |
A |
T |
12: 110,581,502 (GRCm39) |
T316S |
probably benign |
Het |
Edrf1 |
T |
C |
7: 133,252,295 (GRCm39) |
Y449H |
probably damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Flg2 |
A |
T |
3: 93,127,873 (GRCm39) |
I2262L |
unknown |
Het |
Flnc |
T |
C |
6: 29,457,553 (GRCm39) |
L2417P |
probably damaging |
Het |
Gabrp |
A |
T |
11: 33,517,310 (GRCm39) |
Y121N |
probably damaging |
Het |
Gdpd4 |
A |
G |
7: 97,615,543 (GRCm39) |
T123A |
possibly damaging |
Het |
Gpr162 |
C |
A |
6: 124,838,232 (GRCm39) |
M139I |
probably benign |
Het |
Greb1l |
G |
A |
18: 10,542,427 (GRCm39) |
E1341K |
probably damaging |
Het |
Gsn |
G |
A |
2: 35,186,484 (GRCm39) |
S410N |
probably benign |
Het |
Gtf2f2 |
T |
C |
14: 76,135,089 (GRCm39) |
Y212C |
probably damaging |
Het |
Hao2 |
C |
T |
3: 98,784,493 (GRCm39) |
A291T |
probably damaging |
Het |
Igkv1-133 |
A |
G |
6: 67,702,563 (GRCm39) |
T94A |
possibly damaging |
Het |
Irf2bp1 |
G |
A |
7: 18,738,923 (GRCm39) |
A188T |
possibly damaging |
Het |
Itpr1 |
T |
C |
6: 108,383,106 (GRCm39) |
V1478A |
possibly damaging |
Het |
Kdm5b |
T |
C |
1: 134,549,837 (GRCm39) |
|
probably null |
Het |
Kif5b |
A |
T |
18: 6,234,882 (GRCm39) |
D49E |
probably damaging |
Het |
Lmbr1l |
A |
G |
15: 98,810,123 (GRCm39) |
W113R |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,343,698 (GRCm39) |
D887G |
probably damaging |
Het |
Lrrc14 |
T |
A |
15: 76,598,143 (GRCm39) |
M291K |
probably benign |
Het |
Lypd11 |
T |
C |
7: 24,422,836 (GRCm39) |
E79G |
probably benign |
Het |
Mgarp |
G |
A |
3: 51,296,387 (GRCm39) |
A205V |
possibly damaging |
Het |
Msl2 |
T |
C |
9: 100,978,606 (GRCm39) |
|
probably null |
Het |
Nfix |
G |
A |
8: 85,440,406 (GRCm39) |
Q487* |
probably null |
Het |
Notch4 |
T |
C |
17: 34,784,263 (GRCm39) |
V22A |
probably benign |
Het |
Npc1l1 |
T |
A |
11: 6,172,221 (GRCm39) |
Q823L |
probably benign |
Het |
Obox3 |
T |
C |
7: 15,360,774 (GRCm39) |
K122E |
probably benign |
Het |
Or10ab5 |
C |
T |
7: 108,245,755 (GRCm39) |
M9I |
probably benign |
Het |
Or2a12 |
A |
G |
6: 42,904,972 (GRCm39) |
K269R |
probably damaging |
Het |
Or8s10 |
T |
C |
15: 98,336,213 (GRCm39) |
Y288H |
probably damaging |
Het |
Plekhh3 |
T |
A |
11: 101,057,397 (GRCm39) |
M287L |
possibly damaging |
Het |
Prpf3 |
A |
T |
3: 95,760,857 (GRCm39) |
I15K |
probably benign |
Het |
Rpl12-ps1 |
G |
T |
1: 36,997,423 (GRCm39) |
|
noncoding transcript |
Het |
Rps8 |
G |
C |
4: 117,012,352 (GRCm39) |
|
probably benign |
Het |
Setd2 |
T |
C |
9: 110,446,899 (GRCm39) |
V2489A |
probably damaging |
Het |
Slfn10-ps |
T |
A |
11: 82,919,851 (GRCm39) |
|
noncoding transcript |
Het |
Smad2 |
C |
T |
18: 76,395,795 (GRCm39) |
P78L |
probably damaging |
Het |
Spen |
G |
A |
4: 141,201,127 (GRCm39) |
T2500I |
probably damaging |
Het |
Tjp2 |
T |
G |
19: 24,108,568 (GRCm39) |
E181D |
probably benign |
Het |
Tmem131l |
T |
C |
3: 83,806,572 (GRCm39) |
D1478G |
probably benign |
Het |
Trim72 |
G |
T |
7: 127,609,176 (GRCm39) |
R326L |
probably benign |
Het |
Ttn |
A |
T |
2: 76,727,584 (GRCm39) |
|
probably benign |
Het |
Vmn1r177 |
A |
T |
7: 23,565,498 (GRCm39) |
M126K |
probably damaging |
Het |
Vmn1r57 |
A |
G |
7: 5,224,319 (GRCm39) |
I281M |
probably damaging |
Het |
Vmn2r108 |
C |
A |
17: 20,691,665 (GRCm39) |
R286L |
probably benign |
Het |
Wdr25 |
T |
C |
12: 108,863,968 (GRCm39) |
S38P |
probably benign |
Het |
Zfp937 |
T |
A |
2: 150,080,229 (GRCm39) |
Y86* |
probably null |
Het |
Zfr2 |
CTCAGACTGGTGTCAGAC |
CTCAGAC |
10: 81,082,544 (GRCm39) |
|
probably null |
Het |
Zswim1 |
C |
T |
2: 164,667,845 (GRCm39) |
H366Y |
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 |
IGL02369:Stmnd1
|
APN |
13 |
46,439,029 (GRCm39) |
missense |
probably benign |
0.25 |
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 |
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 |
|