Incidental Mutation 'IGL01010:Gpr6'
ID |
53795 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Gpr6
|
Ensembl Gene |
ENSMUSG00000046922 |
Gene Name |
G protein-coupled receptor 6 |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL01010
|
Quality Score |
|
Status
|
|
Chromosome |
10 |
Chromosomal Location |
40945973-40948281 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 40947147 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Threonine
at position 145
(M145T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000057323
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061796]
|
AlphaFold |
Q6YNI2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000061796
AA Change: M145T
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000057323 Gene: ENSMUSG00000046922 AA Change: M145T
Domain | Start | End | E-Value | Type |
low complexity region
|
13 |
30 |
N/A |
INTRINSIC |
low complexity region
|
37 |
59 |
N/A |
INTRINSIC |
Pfam:7tm_1
|
90 |
330 |
2.5e-32 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000213704
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Homozygous mutation of this gene does not appear to result in a phenotype. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
C |
A |
8: 73,199,059 (GRCm39) |
S155R |
probably damaging |
Het |
Acss3 |
G |
T |
10: 106,859,710 (GRCm39) |
|
probably benign |
Het |
Ano4 |
G |
A |
10: 88,796,462 (GRCm39) |
T680I |
probably benign |
Het |
Drosha |
C |
T |
15: 12,827,375 (GRCm39) |
|
probably benign |
Het |
Ehd3 |
A |
G |
17: 74,134,484 (GRCm39) |
D281G |
probably damaging |
Het |
Exoc5 |
A |
G |
14: 49,275,212 (GRCm39) |
L196P |
probably damaging |
Het |
Gal3st1 |
T |
C |
11: 3,946,914 (GRCm39) |
|
probably benign |
Het |
Gart |
G |
A |
16: 91,439,980 (GRCm39) |
R4* |
probably null |
Het |
Gm21738 |
T |
A |
14: 19,417,361 (GRCm38) |
T56S |
probably benign |
Het |
Gm3573 |
T |
A |
14: 42,009,523 (GRCm39) |
I141L |
probably benign |
Het |
Kcns3 |
T |
C |
12: 11,142,427 (GRCm39) |
M91V |
probably benign |
Het |
Mtarc2 |
T |
G |
1: 184,551,513 (GRCm39) |
I308L |
probably benign |
Het |
Mto1 |
A |
G |
9: 78,368,925 (GRCm39) |
K529R |
probably benign |
Het |
Naip2 |
A |
T |
13: 100,291,446 (GRCm39) |
V1164D |
probably damaging |
Het |
Or2ag13 |
T |
C |
7: 106,473,460 (GRCm39) |
|
probably benign |
Het |
Or8k21 |
A |
T |
2: 86,145,288 (GRCm39) |
I114N |
probably damaging |
Het |
Plekha1 |
T |
C |
7: 130,503,984 (GRCm39) |
|
probably benign |
Het |
Psg26 |
T |
C |
7: 18,212,255 (GRCm39) |
S367G |
possibly damaging |
Het |
Rps6kb1 |
T |
C |
11: 86,393,592 (GRCm39) |
M513V |
probably benign |
Het |
Slitrk3 |
C |
T |
3: 72,956,606 (GRCm39) |
G722D |
probably benign |
Het |
Stag1 |
A |
G |
9: 100,827,986 (GRCm39) |
E1005G |
probably benign |
Het |
Tgfbr2 |
A |
T |
9: 115,959,048 (GRCm39) |
L122Q |
possibly damaging |
Het |
Traf2 |
G |
A |
2: 25,410,450 (GRCm39) |
R400* |
probably null |
Het |
Trim33 |
C |
T |
3: 103,254,031 (GRCm39) |
Q153* |
probably null |
Het |
Zmynd15 |
T |
C |
11: 70,356,742 (GRCm39) |
Y551H |
probably damaging |
Het |
Znrd2 |
A |
G |
19: 5,781,293 (GRCm39) |
S78P |
probably damaging |
Het |
|
Other mutations in Gpr6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00309:Gpr6
|
APN |
10 |
40,946,812 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01098:Gpr6
|
APN |
10 |
40,946,739 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01323:Gpr6
|
APN |
10 |
40,947,555 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1153:Gpr6
|
UTSW |
10 |
40,946,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R1154:Gpr6
|
UTSW |
10 |
40,946,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R1622:Gpr6
|
UTSW |
10 |
40,947,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R1628:Gpr6
|
UTSW |
10 |
40,947,544 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1638:Gpr6
|
UTSW |
10 |
40,946,530 (GRCm39) |
missense |
probably benign |
0.02 |
R1935:Gpr6
|
UTSW |
10 |
40,947,477 (GRCm39) |
missense |
probably benign |
0.02 |
R1936:Gpr6
|
UTSW |
10 |
40,947,477 (GRCm39) |
missense |
probably benign |
0.02 |
R2108:Gpr6
|
UTSW |
10 |
40,946,649 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2129:Gpr6
|
UTSW |
10 |
40,947,168 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4024:Gpr6
|
UTSW |
10 |
40,947,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R4237:Gpr6
|
UTSW |
10 |
40,946,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R4418:Gpr6
|
UTSW |
10 |
40,946,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R4703:Gpr6
|
UTSW |
10 |
40,947,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R4814:Gpr6
|
UTSW |
10 |
40,947,258 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6821:Gpr6
|
UTSW |
10 |
40,947,004 (GRCm39) |
missense |
probably benign |
0.04 |
R7190:Gpr6
|
UTSW |
10 |
40,946,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R7573:Gpr6
|
UTSW |
10 |
40,946,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R7574:Gpr6
|
UTSW |
10 |
40,946,652 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7611:Gpr6
|
UTSW |
10 |
40,946,875 (GRCm39) |
missense |
probably benign |
0.02 |
R8011:Gpr6
|
UTSW |
10 |
40,946,911 (GRCm39) |
missense |
probably benign |
0.01 |
R9416:Gpr6
|
UTSW |
10 |
40,946,944 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
Posted On |
2013-06-28 |