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TMEM269 transmembrane protein 269 [ Homo sapiens (human) ]

Gene ID: 100129924, updated on 23-Nov-2021

Summary

Official Symbol
TMEM269provided by HGNC
Official Full Name
transmembrane protein 269provided by HGNC
Primary source
HGNC:HGNC:52381
See related
Ensembl:ENSG00000274386
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Biased expression in testis (RPKM 1.1), fat (RPKM 0.1) and 2 other tissues See more
Orthologs
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Genomic context

See TMEM269 in Genome Data Viewer
Location:
1p34.2
Exon count:
6
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (42784991..42800827)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (43250703..43266489)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene prolyl 3-hydroxylase 1 Neighboring gene chromosome 1 open reading frame 50 Neighboring gene TMEM269 divergent transcript Neighboring gene uncharacterized LOC107984946 Neighboring gene small vasohibin binding protein Neighboring gene erythroblast membrane associated protein (Scianna blood group) Neighboring gene zinc finger protein 691

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Markers

Homology

Gene Ontology Provided by GOA

Component Evidence Code Pubs
located_in integral component of membrane IEA
Inferred from Electronic Annotation
more info
 

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001354602.2NP_001341531.2  transmembrane protein 269

    Status: VALIDATED

    Source sequence(s)
    AC098484
    Related
    ENSP00000490213.1, ENST00000637012.1
    Conserved Domains (1) summary
    COG1183
    Location:1188
    PssA; Phosphatidylserine synthase [Lipid transport and metabolism]

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    42784991..42800827
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001242750.1: Suppressed sequence

    Description
    NM_001242750.1: This RefSeq has been removed because currently there is insufficient support for the transcript and the protein.
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