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FAM237A family with sequence similarity 237 member A [ Homo sapiens (human) ]

Gene ID: 200726, updated on 22-Sep-2022

Summary

Official Symbol
FAM237Aprovided by HGNC
Official Full Name
family with sequence similarity 237 member Aprovided by HGNC
Primary source
HGNC:HGNC:52388
See related
Ensembl:ENSG00000235118 AllianceGenome:HGNC:52388
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
Summary
Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]
Expression
Low expression observed in reference dataset See more
Orthologs
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Genomic context

See FAM237A in Genome Data Viewer
Location:
2q33.3
Exon count:
3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (206642487..206649365)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (207124596..207131470)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (207507211..207514089)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene heterogeneous nuclear ribonucleoprotein A1 pseudogene 51 Neighboring gene ADAM metallopeptidase domain 23 Neighboring gene dystrotelin Neighboring gene VPS26C pseudogene 1 Neighboring gene malate dehydrogenase 1B

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

Homology

Clone Names

  • AC010731.4

Gene Ontology Provided by GOA

Component Evidence Code Pubs
located_in 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_001102659.3NP_001096129.1  protein FAM237A

    See identical proteins and their annotated locations for NP_001096129.1

    Status: VALIDATED

    Source sequence(s)
    AC010731
    Consensus CDS
    CCDS82560.1
    UniProtKB/Swiss-Prot
    A0A1B0GTK4
    Related
    ENSP00000490802.1, ENST00000441223.4

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    206642487..206649365
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    207124596..207131470
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)