Incidental Mutation 'IGL02288:Gpr152'
ID |
290013 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Gpr152
|
Ensembl Gene |
ENSMUSG00000044724 |
Gene Name |
G protein-coupled receptor 152 |
Synonyms |
LOC269053, A930009H15Rik |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL02288
|
Quality Score |
|
Status
|
|
Chromosome |
19 |
Chromosomal Location |
4189798-4195740 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 4193694 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Valine
at position 412
(M412V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000094062
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000008893]
[ENSMUST00000025761]
[ENSMUST00000096338]
[ENSMUST00000123874]
|
AlphaFold |
Q8BXS7 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000008893
|
SMART Domains |
Protein: ENSMUSP00000008893 Gene: ENSMUSG00000024835
Domain | Start | End | E-Value | Type |
DUF1899
|
5 |
69 |
1.48e-37 |
SMART |
WD40
|
68 |
111 |
2.1e-7 |
SMART |
WD40
|
121 |
161 |
1.44e-5 |
SMART |
WD40
|
164 |
204 |
4.08e-5 |
SMART |
DUF1900
|
258 |
392 |
6.41e-88 |
SMART |
coiled coil region
|
445 |
482 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000025761
|
SMART Domains |
Protein: ENSMUSP00000025761 Gene: ENSMUSG00000024842
Domain | Start | End | E-Value | Type |
low complexity region
|
45 |
67 |
N/A |
INTRINSIC |
low complexity region
|
79 |
97 |
N/A |
INTRINSIC |
EFh
|
129 |
157 |
1.08e-6 |
SMART |
Blast:EFh
|
165 |
193 |
2e-7 |
BLAST |
EFh
|
206 |
234 |
1.05e-4 |
SMART |
EFh
|
243 |
271 |
1.55e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000096338
AA Change: M412V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000094062 Gene: ENSMUSG00000044724 AA Change: M412V
Domain | Start | End | E-Value | Type |
Pfam:7tm_1
|
47 |
295 |
7e-19 |
PFAM |
low complexity region
|
347 |
361 |
N/A |
INTRINSIC |
low complexity region
|
419 |
433 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000123874
|
SMART Domains |
Protein: ENSMUSP00000118450 Gene: ENSMUSG00000024835
Domain | Start | End | E-Value | Type |
DUF1899
|
5 |
69 |
1.48e-37 |
SMART |
WD40
|
68 |
111 |
2.1e-7 |
SMART |
WD40
|
121 |
161 |
1.44e-5 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134194
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142878
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000143613
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148733
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 20 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arid1b |
A |
G |
17: 5,314,315 (GRCm39) |
M706V |
possibly damaging |
Het |
Clec1b |
T |
A |
6: 129,374,586 (GRCm39) |
D3E |
probably damaging |
Het |
Dqx1 |
A |
G |
6: 83,037,309 (GRCm39) |
H324R |
probably damaging |
Het |
Ep400 |
A |
G |
5: 110,831,702 (GRCm39) |
|
probably benign |
Het |
Ewsr1 |
T |
C |
11: 5,043,689 (GRCm39) |
T32A |
possibly damaging |
Het |
Exoc1 |
C |
A |
5: 76,693,160 (GRCm39) |
H349N |
probably benign |
Het |
Fgg |
T |
C |
3: 82,915,460 (GRCm39) |
Y26H |
probably benign |
Het |
Gpld1 |
T |
A |
13: 25,163,666 (GRCm39) |
Y41* |
probably null |
Het |
Matn2 |
T |
A |
15: 34,422,532 (GRCm39) |
C540S |
probably damaging |
Het |
Nars1 |
T |
C |
18: 64,643,606 (GRCm39) |
|
probably benign |
Het |
Ncor1 |
A |
G |
11: 62,240,229 (GRCm39) |
I914T |
probably benign |
Het |
Or1e33 |
A |
G |
11: 73,738,207 (GRCm39) |
V248A |
possibly damaging |
Het |
Or4k42 |
A |
T |
2: 111,320,065 (GRCm39) |
F146Y |
probably benign |
Het |
Rev3l |
T |
C |
10: 39,704,212 (GRCm39) |
L2086P |
probably benign |
Het |
Snrnp200 |
T |
A |
2: 127,071,815 (GRCm39) |
I1165N |
probably damaging |
Het |
Spindoc |
G |
A |
19: 7,335,667 (GRCm39) |
Q374* |
probably null |
Het |
Thsd1 |
A |
C |
8: 22,749,565 (GRCm39) |
D751A |
probably damaging |
Het |
Ttll4 |
G |
A |
1: 74,718,560 (GRCm39) |
R137H |
probably benign |
Het |
Vmn2r70 |
T |
A |
7: 85,214,342 (GRCm39) |
Y270F |
probably benign |
Het |
Zscan20 |
A |
G |
4: 128,480,436 (GRCm39) |
I685T |
probably damaging |
Het |
|
Other mutations in Gpr152 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Gpr152
|
APN |
19 |
4,193,506 (GRCm39) |
missense |
probably benign |
|
IGL01400:Gpr152
|
APN |
19 |
4,193,626 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01538:Gpr152
|
APN |
19 |
4,192,951 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02513:Gpr152
|
APN |
19 |
4,192,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03335:Gpr152
|
APN |
19 |
4,193,770 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0318:Gpr152
|
UTSW |
19 |
4,193,541 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1216:Gpr152
|
UTSW |
19 |
4,193,554 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1936:Gpr152
|
UTSW |
19 |
4,192,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R2248:Gpr152
|
UTSW |
19 |
4,193,805 (GRCm39) |
missense |
probably benign |
0.00 |
R3161:Gpr152
|
UTSW |
19 |
4,192,713 (GRCm39) |
missense |
probably benign |
0.00 |
R4193:Gpr152
|
UTSW |
19 |
4,192,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Gpr152
|
UTSW |
19 |
4,193,223 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4852:Gpr152
|
UTSW |
19 |
4,193,790 (GRCm39) |
missense |
probably benign |
0.00 |
R5014:Gpr152
|
UTSW |
19 |
4,193,506 (GRCm39) |
missense |
probably benign |
0.00 |
R5381:Gpr152
|
UTSW |
19 |
4,192,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R5431:Gpr152
|
UTSW |
19 |
4,193,746 (GRCm39) |
missense |
probably benign |
0.21 |
R5470:Gpr152
|
UTSW |
19 |
4,193,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R7331:Gpr152
|
UTSW |
19 |
4,192,608 (GRCm39) |
missense |
probably damaging |
0.99 |
R7350:Gpr152
|
UTSW |
19 |
4,192,963 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7806:Gpr152
|
UTSW |
19 |
4,193,487 (GRCm39) |
missense |
probably benign |
|
R8315:Gpr152
|
UTSW |
19 |
4,193,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R8889:Gpr152
|
UTSW |
19 |
4,192,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R9455:Gpr152
|
UTSW |
19 |
4,193,844 (GRCm39) |
missense |
probably benign |
0.01 |
R9651:Gpr152
|
UTSW |
19 |
4,192,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R9709:Gpr152
|
UTSW |
19 |
4,192,640 (GRCm39) |
missense |
probably benign |
0.00 |
R9761:Gpr152
|
UTSW |
19 |
4,193,227 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2015-04-16 |