U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from GEO Profiles

    • Showing Current items.

    HOXC13 homeobox C13 [ Homo sapiens (human) ]

    Gene ID: 3229, updated on 10-Dec-2024

    Summary

    Official Symbol
    HOXC13provided by HGNC
    Official Full Name
    homeobox C13provided by HGNC
    Primary source
    HGNC:HGNC:5125
    See related
    Ensembl:ENSG00000123364 MIM:142976; AllianceGenome:HGNC:5125
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    HOX3; ECTD9; HOX3G
    Summary
    This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. The product of this gene may play a role in the development of hair, nail, and filiform papilla. [provided by RefSeq, Jul 2008]
    Expression
    Biased expression in skin (RPKM 1.8), testis (RPKM 0.2) and 1 other tissue See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See HOXC13 in Genome Data Viewer
    Location:
    12q13.13
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (53938831..53946544)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (53904353..53912048)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (54332615..54340328)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105378250 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:54141521-54142049 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:54142050-54142577 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:54144138-54144726 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4517 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4518 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6429 Neighboring gene chondrogenesis-associated transcript Neighboring gene RN7SK pseudogene 289 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr12:54242057-54243256 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_29403 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr12:54261991-54263190 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_29464 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_29460 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:54321787-54322624 Neighboring gene HOXC13 antisense RNA Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:54345326-54345913 Neighboring gene uncharacterized LOC105369775 Neighboring gene ReSE screen-validated silencer GRCh37_chr12:54355207-54355431 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:54360165-54361069 Neighboring gene NUP98-HOXC11 recombination region Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:54368136-54368730 Neighboring gene homeobox C12 Neighboring gene HOX transcript antisense RNA Neighboring gene homeobox C11

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    Associated conditions

    Description Tests
    Ectodermal dysplasia 9, hair/nail type
    MedGen: C3554127 OMIM: 614931 GeneReviews: Not available
    Compare labs

    EBI GWAS Catalog

    Description
    Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.
    EBI GWAS Catalog
    Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.
    EBI GWAS Catalog
    Genome-wide association study of selenium concentrations.
    EBI GWAS Catalog
    Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Component Evidence Code Pubs
    located_in chromatin ISA
    Inferred from Sequence Alignment
    more info
     
    located_in nucleus IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    homeobox protein Hox-C13
    Names
    NUP98/HOXC13
    homeo box 3G
    homeobox protein Hox-3G

    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_033026.1 RefSeqGene

      Range
      5040..12753
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_017410.3NP_059106.2  homeobox protein Hox-C13

      See identical proteins and their annotated locations for NP_059106.2

      Status: REVIEWED

      Source sequence(s)
      AA722686, AF255676, AF263466, BC090850, BU158600
      Consensus CDS
      CCDS8865.1
      UniProtKB/Swiss-Prot
      P31276, Q5BL02, Q96J32, Q9NR24, Q9NYD5
      Related
      ENSP00000243056.3, ENST00000243056.5
      Conserved Domains (2) summary
      smart00389
      Location:260312
      HOX; Homeodomain
      pfam12284
      Location:54166
      HoxA13_N; Hox protein A13 N terminal

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

      Range
      53938831..53946544
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060936.1 Alternate T2T-CHM13v2.0

      Range
      53904353..53912048
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)