AutismKB 2.0

Evidence Details for OR4M2


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Basic Information Top
Gene Symbol:OR4M2 ( OR15-3 )
Gene Full Name: olfactory receptor, family 4, subfamily M, member 2
Band: 15q11.2
Quick LinksEntrez ID:390538; OMIM: NA; Uniprot ID:OR4M2_HUMAN; ENSEMBL ID: ENSG00000182974; HGNC ID: 15373
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>OR4M2|390538|nucleotide
ATGGAAACTGCAAATTACACCAAGGTGACAGAATTTGTTCTCACTGGCCTATCCCAGACTCCAGAGGTCCAACTAGTCCTATTTGTTATATTTCTATCCTTCTAT
TTGTTCATCCTACCAGGAAATATCCTTATCATTTGCACCATCAGTCTAGACCCTCATCTGACCTCTCCTATGTATTTCCTGTTGGCTAATCTGGCCTTCCTTGAT
ATTTGGTACTCTTCCATTACAGCCCCTGAAATGCTCATAGACTTCTTTGTGGAGAGGAAGATAATTTCTTTTGATGGATGCATTGCACAGCTCTTCTTCTTACAC
TTTGCTGGGGCTTCGGAGATGTTCTTGCTCACAGTGATGGCCTTTGACCTCTACACTGCTATCTGCCGACCCCTCCACTATGCTACCATCATGAATCAACGTCTC
TGCTGTATCCTGGTGGCTCTCTCCTGGAGGGGGGGCTTCATTCATTCTATCATACAGGTGGCTCTCATTGTTCGACTTCCTTTCTGTGGGCCCAATGAGTTAGAC
AGTTACTTCTGTGACATCACACAGGTTGTCCGGATTGCCTGTGCCAACACCTTCCCAGAGGAGTTAGTGATGATCTGTAGTAGTGGTCTGATCTCTGTGGTGTGT
TTGATTGCTCTGTTAATGTCCTATGCCTTCCTTCTGGCCTTGTTCAAGAAACTTTCAGGCTCAGGTGAGAATACCAACAGGGCCATGTCCACCTGCTATTCCCAC
ATTACCATTGTGGTGCTAATGTTTGGGCCATCCATCTACATTTATGCTCGCCCATTTGACTCGTTTTCCCTAGATAAAGTGGTGTCTGTGTTCAATACTTTAATA
TTCCCTTTACGTAATCCCATTATTTACACATTGAGAAACAAGGAAGTAAAGGCAGCCATGAGGAAGTTGGTCACCAAATATATTTTGTGTAAAGAGAAGTGA


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>OR4M2|390538|protein
METANYTKVTEFVLTGLSQTPEVQLVLFVIFLSFYLFILPGNILIICTISLDPHLTSPMYFLLANLAFLDIWYSSITAPEMLIDFFVERKIISFDGCIAQLFFLH
FAGASEMFLLTVMAFDLYTAICRPLHYATIMNQRLCCILVALSWRGGFIHSIIQVALIVRLPFCGPNELDSYFCDITQVVRIACANTFPEELVMICSSGLISVVC
LIALLMSYAFLLALFKKLSGSGENTNRAMSTCYSHITIVVLMFGPSIYIYARPFDSFSLDKVVSVFNTLIFPLRNPIIYTLRNKEVKAAMRKLVTKYILCKEK


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Evidence summary Top

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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) 3 (14) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 6 (15)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Wolpert, 2000 - STS mappingautism 3 - 3 - 3 - 3
Wassink, 2001 USA Chromosomal analysis of G-bandautism - - - - 278 - 278
Silva, 2002 - FISHautism - - - - 1 - 1
Keller, 2003 USA FISHASD - - - - 2 - 2
Sahoo, 2005 USA aCGHautism - - - - 9 - 9
Sebat, 2007 USA aCGHautism 165 118 47 99 195 196 391
Wassink, 2007 USA FISHPDD - - - - 104 - 104
Weiss, 2008 USA, Ireland aCGH, SNP microarrayASD 751 - - - 2252 23502 25754
Marshall, 2008 - SNP microarrayASD 427 238 189 - 427 500 927
Gregory, 2009 USA aCGHASD - - - - 119 54 173
Bremer, 2009 - aCGHASD - - - - 148 - 148
Bucan, 2009 USA SNP microarrayautism, ASD 912 - 912 - - 1488 1488
Sanders, 2011 Simons Simplex Collection SNP microarray--ASD 1127 1127 - - - - -
Laplana M, 2014 - aCGHASD 1 - - - 1 5 6
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Reference Source Platform ADI-R ADOS Diagnosis Family Affected Validation Method
Total Simplex Multiplex
Cukier HN, 2014 - Illumina HiSeq 2000ASD 40 - - 100 HumanExome BeadChip or Sanger sequencing
Low Scale Gene Studies Top

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  (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