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) question?
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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
GeneRefVarChr/LocMutationPredicted EffectZygosity
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
AlleleSourceChrCoordTypePredicted EffectPPH 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