Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A4galt |
G |
T |
15: 83,111,810 (GRCm39) |
N324K |
probably damaging |
Het |
Ahcyl1 |
A |
G |
3: 107,574,547 (GRCm39) |
|
probably benign |
Het |
Atrnl1 |
T |
A |
19: 57,641,382 (GRCm39) |
N343K |
probably benign |
Het |
Batf2 |
C |
A |
19: 6,221,357 (GRCm39) |
Q56K |
probably benign |
Het |
Cfh |
A |
T |
1: 140,036,274 (GRCm39) |
V691D |
probably damaging |
Het |
Chst10 |
T |
C |
1: 38,904,922 (GRCm39) |
Y257C |
probably damaging |
Het |
Dlg5 |
A |
T |
14: 24,228,051 (GRCm39) |
L290Q |
possibly damaging |
Het |
Dnah2 |
T |
A |
11: 69,407,416 (GRCm39) |
T456S |
possibly damaging |
Het |
Dnah6 |
T |
C |
6: 73,001,995 (GRCm39) |
|
probably null |
Het |
Efhb |
T |
C |
17: 53,758,697 (GRCm39) |
K313R |
probably damaging |
Het |
Eprs1 |
T |
A |
1: 185,160,305 (GRCm39) |
N1500K |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,183,236 (GRCm39) |
T1748A |
probably benign |
Het |
Gfra2 |
T |
A |
14: 71,163,377 (GRCm39) |
L87H |
probably damaging |
Het |
Gfral |
T |
A |
9: 76,100,727 (GRCm39) |
Y237F |
possibly damaging |
Het |
Gsdmc |
G |
T |
15: 63,651,386 (GRCm39) |
T272N |
probably benign |
Het |
Hspe1 |
T |
A |
1: 55,128,269 (GRCm39) |
S21R |
probably benign |
Het |
Kctd16 |
G |
T |
18: 40,390,233 (GRCm39) |
|
probably benign |
Het |
Kif21a |
A |
T |
15: 90,868,958 (GRCm39) |
I483N |
probably damaging |
Het |
Kif4-ps |
T |
C |
12: 101,112,534 (GRCm39) |
|
noncoding transcript |
Het |
Lpp |
T |
C |
16: 24,580,407 (GRCm39) |
V166A |
possibly damaging |
Het |
Lrp2 |
A |
C |
2: 69,336,895 (GRCm39) |
D1292E |
probably damaging |
Het |
Manba |
T |
C |
3: 135,250,575 (GRCm39) |
Y401H |
probably damaging |
Het |
Msh2 |
T |
G |
17: 87,985,813 (GRCm39) |
|
probably benign |
Het |
Myef2 |
A |
T |
2: 124,930,757 (GRCm39) |
|
probably benign |
Het |
Ncor1 |
T |
A |
11: 62,235,660 (GRCm39) |
Q598L |
probably damaging |
Het |
Obox3 |
A |
G |
7: 15,360,764 (GRCm39) |
V125A |
probably benign |
Het |
Or1n1 |
A |
T |
2: 36,750,381 (GRCm39) |
|
probably null |
Het |
Or2b4 |
T |
A |
17: 38,116,591 (GRCm39) |
L185* |
probably null |
Het |
Or9k7 |
G |
A |
10: 130,046,291 (GRCm39) |
T236I |
possibly damaging |
Het |
Pcdh9 |
C |
A |
14: 94,126,067 (GRCm39) |
L34F |
probably damaging |
Het |
Pcdha3 |
A |
T |
18: 37,079,560 (GRCm39) |
I101F |
probably damaging |
Het |
Pced1b |
A |
G |
15: 97,282,675 (GRCm39) |
E238G |
probably benign |
Het |
Pla2r1 |
A |
T |
2: 60,258,994 (GRCm39) |
N1131K |
probably damaging |
Het |
Prmt1 |
A |
T |
7: 44,631,060 (GRCm39) |
S99R |
probably damaging |
Het |
Qng1 |
G |
A |
13: 58,529,617 (GRCm39) |
R332C |
probably benign |
Het |
Rbp3 |
T |
C |
14: 33,682,615 (GRCm39) |
S1116P |
probably damaging |
Het |
Rhobtb2 |
T |
C |
14: 70,037,160 (GRCm39) |
D88G |
probably damaging |
Het |
Rngtt |
A |
G |
4: 33,379,394 (GRCm39) |
E432G |
probably benign |
Het |
Sh3rf1 |
A |
G |
8: 61,814,793 (GRCm39) |
T451A |
probably benign |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Siva1 |
T |
A |
12: 112,613,336 (GRCm39) |
D61E |
probably benign |
Het |
Skor1 |
A |
C |
9: 63,046,855 (GRCm39) |
|
probably null |
Het |
Slc20a1 |
A |
G |
2: 129,041,611 (GRCm39) |
|
probably benign |
Het |
Slc2a7 |
A |
G |
4: 150,252,926 (GRCm39) |
E522G |
probably benign |
Het |
Tmprss7 |
A |
T |
16: 45,511,123 (GRCm39) |
I85N |
probably damaging |
Het |
Tpx2 |
T |
A |
2: 152,726,958 (GRCm39) |
D408E |
probably damaging |
Het |
Ulk4 |
A |
T |
9: 121,073,436 (GRCm39) |
I551N |
probably benign |
Het |
Zfat |
A |
T |
15: 67,982,324 (GRCm39) |
|
probably null |
Het |
Zfp101 |
C |
A |
17: 33,613,457 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Gpr137b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Gpr137b
|
APN |
13 |
13,549,000 (GRCm39) |
splice site |
probably benign |
|
IGL00969:Gpr137b
|
APN |
13 |
13,539,650 (GRCm39) |
nonsense |
probably null |
|
R0276:Gpr137b
|
UTSW |
13 |
13,542,160 (GRCm39) |
splice site |
probably benign |
|
R1102:Gpr137b
|
UTSW |
13 |
13,539,616 (GRCm39) |
splice site |
probably benign |
|
R4012:Gpr137b
|
UTSW |
13 |
13,533,947 (GRCm39) |
missense |
probably benign |
|
R5892:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R6269:Gpr137b
|
UTSW |
13 |
13,538,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R6841:Gpr137b
|
UTSW |
13 |
13,538,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R7165:Gpr137b
|
UTSW |
13 |
13,542,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R7772:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R7996:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R7997:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R7998:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R7999:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8049:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8093:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8108:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8109:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8111:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8153:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8154:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8156:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8358:Gpr137b
|
UTSW |
13 |
13,533,929 (GRCm39) |
missense |
probably benign |
|
R8686:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8687:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8688:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
R8921:Gpr137b
|
UTSW |
13 |
13,533,991 (GRCm39) |
missense |
|
|
|