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TMEM229A transmembrane protein 229A [ Homo sapiens (human) ]

Gene ID: 730130, updated on 23-Nov-2021

Summary

Official Symbol
TMEM229Aprovided by HGNC
Official Full Name
transmembrane protein 229Aprovided by HGNC
Primary source
HGNC:HGNC:37279
See related
Ensembl:ENSG00000234224
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
Orthologs
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Genomic context

See TMEM229A in Genome Data Viewer
Location:
7q31.32
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 7 NC_000007.14 (124030921..124033067, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (123670975..123673121, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene sperm adhesion molecule 1 Neighboring gene uncharacterized LOC105375483 Neighboring gene uncharacterized LOC105375484 Neighboring gene uncharacterized LOC107986841 Neighboring gene uncharacterized LOC101928211

Genomic regions, transcripts, and products

General gene information

Markers

Homology

Clone Names

  • MGC189723

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_001136002.2NP_001129474.1  transmembrane protein 229A

    See identical proteins and their annotated locations for NP_001129474.1

    Status: VALIDATED

    Source sequence(s)
    AC004690, BC157828, BU741231
    Consensus CDS
    CCDS47694.1
    UniProtKB/Swiss-Prot
    B2RXF0
    Related
    ENSP00000395244.1, ENST00000455783.3
    Conserved Domains (2) summary
    pfam06541
    Location:279362
    ABC_trans_CmpB; Putative ABC-transporter type IV
    cl01067
    Location:779
    Dyp_perox; Dyp-type peroxidase family

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_000007.14 Reference GRCh38.p13 Primary Assembly

    Range
    124030921..124033067 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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