AutismKB 2.0

Evidence Details for OR6P1


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:OR6P1 ( - )
Gene Full Name: olfactory receptor, family 6, subfamily P, member 1
Band: 1q23.1
Quick LinksEntrez ID:128366; OMIM: NA; Uniprot ID:OR6P1_HUMAN; ENSEMBL ID: ENSG00000186440; HGNC ID: 15036
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>OR6P1|128366|nucleotide
ATGAGAAATTTGAGTGGAGGCCATGTCGAGGAGTTTGTCTTGGTGGGTTTCCCTACCACGCCTCCCCTCCAGCTGCTCCTCTTTGTCCTTTTTTTTGCAATTTAC
CTTCTGACATTGTTGGAGAATGCACTTATTGTCTTCACAATATGGCTTGCTCCAAGCCTTCATCGTCCCATGTACTTTTTCCTTGGCCATCTCTCTTTCCTGGAG
CTATGGTACATCAATGTCACCATTCCTCGGCTCTTGGCAGCCTTTCTTACCCAGGATGGTAGAGTCTCCTACGTAGGTTGCATGACCCAACTGTACTTCTTTATT
GCCTTAGCCTGTACTGAATGTGTGCTGTTGGCAGTTATGGCCTATGATCGCTACCTGGCCATCTGTGGACCCCTCCTTTACCCTAGTCTCATGCCTTCCAGTCTG
GCCACTCGCCTTGCTGCTGCCTCTTGGGGCAGTGGCTTCTTCAGCTCCATGATGAAGCTTCTTTTTATTTCCCAATTGTCCTACTGTGGACCCAACATTATCAAC
CACTTTTTCTGTGATATTTCCCCACTACTCAACCTCACCTGCTCTGACAAGGAGCAAGCAGAGCTAGTAGACTTCCTTCTGGCCCTGGTGATGATTCTACTCCCT
CTATTGGCTGTGGTTTCATCATACACTGCCATCATTGCAGCCATCCTGAGGATCCCTACGTCCAGGGGACGCCACAAAGCCTTTTCCACTTGTGCCGCTCATCTG
GCAGTGGTTGTTATCTACTACTCCTCCACTCTCTTCACCTATGCACGGCCCCGGGCCATGTACACCTTCAACCACAACAAGATTATCTCTGTGCTCTACACTATC
ATTGTACCATTCTTCAACCCAGCCATCTACTGCCTGAGGAACAAGGAGGTGAAGGAGGCCTTCAGGAAGACAGTGATGGGCAGATGTCACTATCCTAGGGATGTT
CAGGACTGA

Show »

>OR6P1|128366|protein
MRNLSGGHVEEFVLVGFPTTPPLQLLLFVLFFAIYLLTLLENALIVFTIWLAPSLHRPMYFFLGHLSFLELWYINVTIPRLLAAFLTQDGRVSYVGCMTQLYFFI
ALACTECVLLAVMAYDRYLAICGPLLYPSLMPSSLATRLAAASWGSGFFSSMMKLLFISQLSYCGPNIINHFFCDISPLLNLTCSDKEQAELVDFLLALVMILLP
LLAVVSSYTAIIAAILRIPTSRGRHKAFSTCAAHLAVVVIYYSSTLFTYARPRAMYTFNHNKIISVLYTIIVPFFNPAIYCLRNKEVKEAFRKTVMGRCHYPRDV
QD

Show »

Evidence summary Top

Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
Evidences Syndromic Gene GWAS CNV Linkage Association Expression NGS de novo NGS Mosaic NGS Other Low-Scale Gene Studies Total
Score (No. of Studies) No 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 0 (1)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference Case Number Family Number de novo Number Title
Hashimoto R, 2016 30 - 38 Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder.
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top

Contact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.

Simple Query:


  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018