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    HEMGN hemogen [ Homo sapiens (human) ]

    Gene ID: 55363, updated on 3-Apr-2024

    Summary

    Official Symbol
    HEMGNprovided by HGNC
    Official Full Name
    hemogenprovided by HGNC
    Primary source
    HGNC:HGNC:17509
    See related
    Ensembl:ENSG00000136929 MIM:610715; AllianceGenome:HGNC:17509
    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
    Also known as
    NDR; EDAG; CT155; EDAG-1
    Summary
    Predicted to be involved in regulation of osteoblast differentiation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]
    Expression
    Biased expression in bone marrow (RPKM 77.2) and testis (RPKM 23.8) See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See HEMGN in Genome Data Viewer
    Location:
    9q22.33
    Exon count:
    5
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (97926791..97944852, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (110098729..110116790, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (100689073..100707134, complement)

    Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene VISTA enhancer hs1596 Neighboring gene forkhead box E1 Neighboring gene VISTA enhancers hs1597 and hs1717 Neighboring gene tRNA methyltransferase O Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28679 Neighboring gene Sharpr-MPRA regulatory region 4249 Neighboring gene CRISPRi-validated cis-regulatory element chr9.1594 Neighboring gene uncharacterized LOC124902226 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:100745493-100746375 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20107 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20108 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20109 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20110 Neighboring gene uncharacterized LOC124902225 Neighboring gene acidic nuclear phosphoprotein 32 family member B Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28680 Neighboring gene RNA, U6 small nuclear 918, pseudogene

    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

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
    EBI GWAS Catalog
    The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in cell differentiation IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in regulation of osteoblast differentiation IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Component Evidence Code Pubs
    is_active_in nucleoplasm IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
     

    General protein information

    Preferred Names
    hemogen
    Names
    erythroid differentiation-associated gene protein
    hemopoietic gene protein
    negative differentiation regulator protein

    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.

    mRNA and Protein(s)

    1. NM_018437.5NP_060907.2  hemogen

      See identical proteins and their annotated locations for NP_060907.2

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Variants 1 and 2 both encode the same protein.
      Source sequence(s)
      AF306682, AF322875, HY026328
      Consensus CDS
      CCDS6731.1
      UniProtKB/Swiss-Prot
      Q6XAR3, Q86XY5, Q9BXL5, Q9NPC0
      UniProtKB/TrEMBL
      A8K8S6
      Related
      ENSP00000259456.2, ENST00000259456.7
    2. NM_197978.3NP_932095.1  hemogen

      See identical proteins and their annotated locations for NP_932095.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longer transcript. Variants 1 and 2 both encode the same protein.
      Source sequence(s)
      AF306682
      Consensus CDS
      CCDS6731.1
      UniProtKB/Swiss-Prot
      Q6XAR3, Q86XY5, Q9BXL5, Q9NPC0
      UniProtKB/TrEMBL
      A8K8S6
      Related
      ENSP00000480020.1, ENST00000616898.2

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

      Range
      97926791..97944852 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060933.1 Alternate T2T-CHM13v2.0

      Range
      110098729..110116790 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054363238.1XP_054219213.1  hemogen isoform X1

      UniProtKB/Swiss-Prot
      Q6XAR3, Q86XY5, Q9BXL5, Q9NPC0
    2. XM_054363236.1XP_054219211.1  hemogen isoform X1

      UniProtKB/Swiss-Prot
      Q6XAR3, Q86XY5, Q9BXL5, Q9NPC0
    3. XM_054363237.1XP_054219212.1  hemogen isoform X1

      UniProtKB/Swiss-Prot
      Q6XAR3, Q86XY5, Q9BXL5, Q9NPC0