Format

Send to:

Choose Destination

FAM47A family with sequence similarity 47 member A [ Homo sapiens (human) ]

Gene ID: 158724, updated on 11-Jun-2021

Summary

Official Symbol
FAM47Aprovided by HGNC
Official Full Name
family with sequence similarity 47 member Aprovided by HGNC
Primary source
HGNC:HGNC:29962
See related
Ensembl:ENSG00000185448
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
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See FAM47A in Genome Data Viewer
Location:
Xp21.1
Exon count:
1
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (34129752..34132314, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (34147869..34150431, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene lysosomal associated membrane protein 1 pseudogene Neighboring gene uncharacterized LOC105373153 Neighboring gene ferritin heavy chain 1 pseudogene 14 Neighboring gene uncharacterized LOC107985674

Genomic regions, transcripts, and products

Phenotypes

Associated conditions

Description Tests
Genome-wide association study of chronic periodontitis in a general German population.
GeneReviews: Not available

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Homology

Clone Names

  • MGC27003

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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.

Genomic

  1. NG_021359.1 RefSeqGene

    Range
    5001..7579
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_203408.4NP_981953.2  protein FAM47A

    See identical proteins and their annotated locations for NP_981953.2

    Status: VALIDATED

    Source sequence(s)
    AL591625
    Consensus CDS
    CCDS43926.1
    UniProtKB/Swiss-Prot
    Q5JRC9
    Related
    ENSP00000345029.3, ENST00000346193.5
    Conserved Domains (1) summary
    pfam14642
    Location:1255
    FAM47; FAM47 family

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    34129752..34132314 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center