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FAM47C family with sequence similarity 47 member C [ Homo sapiens (human) ]

Gene ID: 442444, updated on 11-Jun-2021

Summary

Official Symbol
FAM47Cprovided by HGNC
Official Full Name
family with sequence similarity 47 member Cprovided by HGNC
Primary source
HGNC:HGNC:25301
See related
Ensembl:ENSG00000198173
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
This gene encodes a product belonging to a family of proteins with unknown function. The coding sequence of this family member includes several tandemly repeated regions. [provided by RefSeq, Sep 2011]
Orthologs
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Genomic context

See FAM47C 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 (37008366..37011664)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (37026439..37029737)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene TFDP1 pseudogene 2 Neighboring gene LanC like 3 pseudogene Neighboring gene ferritin heavy chain like 18, pseudogene Neighboring gene ferritin, heavy polypeptide-like 17 pseudogene

Genomic regions, transcripts, and products

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.

Genomic

  1. NG_021373.1 RefSeqGene

    Range
    5001..8308
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001013736.3NP_001013758.1  putative protein FAM47C

    See identical proteins and their annotated locations for NP_001013758.1

    Status: VALIDATED

    Source sequence(s)
    BX842568
    Consensus CDS
    CCDS35227.1
    UniProtKB/Swiss-Prot
    Q5HY64
    Related
    ENSP00000367913.3, ENST00000358047.5
    Conserved Domains (1) summary
    pfam14642
    Location:1257
    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
    37008366..37011664
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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