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    RGMB repulsive guidance molecule BMP co-receptor b [ Homo sapiens (human) ]

    Gene ID: 285704, updated on 10-Dec-2024

    Summary

    Official Symbol
    RGMBprovided by HGNC
    Official Full Name
    repulsive guidance molecule BMP co-receptor bprovided by HGNC
    Primary source
    HGNC:HGNC:26896
    See related
    Ensembl:ENSG00000174136 MIM:612687; AllianceGenome:HGNC:26896
    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
    DRAGON
    Summary
    RGMB is a glycosylphosphatidylinositol (GPI)-anchored member of the repulsive guidance molecule family (see RGMA, MIM 607362) and contributes to the patterning of the developing nervous system (Samad et al., 2005 [PubMed 15671031]).[supplied by OMIM, Apr 2009]
    Expression
    Ubiquitous expression in brain (RPKM 10.1), skin (RPKM 10.1) and 24 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See RGMB in Genome Data Viewer
    Location:
    5q15
    Exon count:
    7
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (98768632..98796494)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (99271925..99299789)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (98104336..98132198)

    Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene CTBP2 pseudogene 4 Neighboring gene DEAD-box helicase 18 pseudogene 4 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr5:98102871-98103612 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr5:98103613-98104353 Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:98106065-98106565 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22835 Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:98109729-98110228 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22836 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr5:98114818-98116017 Neighboring gene RGMB antisense RNA 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:98175311-98175811 Neighboring gene uncharacterized LOC105379099 Neighboring gene casein kinase 1 alpha 1 pseudogene 3

    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

    EBI GWAS Catalog

    Description
    Genome-wide association study in NSAID-induced acute urticaria/angioedema in Spanish and Han Chinese populations.
    EBI GWAS Catalog
    Variants in several genomic regions associated with asperger disorder.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • FLJ90406, MGC86970, DKFZp434P228

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables coreceptor activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables identical protein binding ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in BMP signaling pathway IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in BMP signaling pathway ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in cell adhesion ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in positive regulation of DNA-templated transcription ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in signal transduction ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    Component Evidence Code Pubs
    located_in endoplasmic reticulum-Golgi intermediate compartment ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    located_in membrane raft IEA
    Inferred from Electronic Annotation
    more info
     
    is_active_in plasma membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in plasma membrane ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    located_in side of membrane IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    repulsive guidance molecule B
    Names
    DRG11-responsive axonal guidance and outgrowth of neurite
    RGM domain family, member B
    repulsive guidance molecule family member b

    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_001012761.3NP_001012779.2  repulsive guidance molecule B isoform 2

      See identical proteins and their annotated locations for NP_001012779.2

      Status: VALIDATED

      Source sequence(s)
      AC008522, AK054622, BC020513, BC067736
      Consensus CDS
      CCDS47251.1
      UniProtKB/TrEMBL
      J3KNF6
      Related
      ENSP00000308219.7, ENST00000308234.11
      Conserved Domains (2) summary
      pfam06534
      Location:267441
      RGM_C; Repulsive guidance molecule (RGM) C-terminus
      pfam06535
      Location:95262
      RGM_N; Repulsive guidance molecule (RGM) N-terminus
    2. NM_001366508.1NP_001353437.1  repulsive guidance molecule B isoform 1 precursor

      Status: VALIDATED

      Source sequence(s)
      AC008522
      Consensus CDS
      CCDS93751.1
      UniProtKB/Swiss-Prot
      D6R9A0, Q6NW40, Q8NC92
      Related
      ENSP00000423256.1, ENST00000513185.3
      Conserved Domains (2) summary
      pfam06534
      Location:226400
      RGM_C; Repulsive guidance molecule (RGM) C-terminus
      pfam06535
      Location:54221
      RGM_N; Repulsive guidance molecule (RGM) N-terminus
    3. NM_001366509.1NP_001353438.1  repulsive guidance molecule B isoform 2

      Status: VALIDATED

      Source sequence(s)
      AC008522
      Consensus CDS
      CCDS47251.1
      UniProtKB/TrEMBL
      J3KNF6
      Conserved Domains (2) summary
      pfam06534
      Location:267441
      RGM_C; Repulsive guidance molecule (RGM) C-terminus
      pfam06535
      Location:95262
      RGM_N; Repulsive guidance molecule (RGM) N-terminus
    4. NM_001366510.1NP_001353439.1  repulsive guidance molecule B isoform 2

      Status: VALIDATED

      Source sequence(s)
      AC008522
      Consensus CDS
      CCDS47251.1
      UniProtKB/TrEMBL
      J3KNF6
      Conserved Domains (2) summary
      pfam06534
      Location:267441
      RGM_C; Repulsive guidance molecule (RGM) C-terminus
      pfam06535
      Location:95262
      RGM_N; Repulsive guidance molecule (RGM) N-terminus
    5. NM_001366511.1NP_001353440.1  repulsive guidance molecule B isoform 3

      Status: VALIDATED

      Source sequence(s)
      AC008522
      Conserved Domains (2) summary
      pfam06534
      Location:266440
      RGM_C; Repulsive guidance molecule (RGM) C-terminus
      pfam06535
      Location:94261
      RGM_N; Repulsive guidance molecule (RGM) N-terminus

    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_000005.10 Reference GRCh38.p14 Primary Assembly

      Range
      98768632..98796494
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047417124.1XP_047273080.1  repulsive guidance molecule B isoform X1

    2. XM_047417125.1XP_047273081.1  repulsive guidance molecule B isoform X3

      UniProtKB/Swiss-Prot
      D6R9A0, Q6NW40, Q8NC92
    3. XM_011543345.3XP_011541647.1  repulsive guidance molecule B isoform X2

      See identical proteins and their annotated locations for XP_011541647.1

      UniProtKB/TrEMBL
      J3KNF6
      Conserved Domains (2) summary
      pfam06534
      Location:267441
      RGM_C; Repulsive guidance molecule (RGM) C-terminus
      pfam06535
      Location:95262
      RGM_N; Repulsive guidance molecule (RGM) N-terminus
    4. XM_011543346.3XP_011541648.1  repulsive guidance molecule B isoform X4

      Conserved Domains (2) summary
      pfam06534
      Location:185364
      RGM_C; Repulsive guidance molecule (RGM) C-terminus
      pfam06535
      Location:13180
      RGM_N; Repulsive guidance molecule (RGM) N-terminus

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060929.1 Alternate T2T-CHM13v2.0

      Range
      99271925..99299789
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054352457.1XP_054208432.1  repulsive guidance molecule B isoform X1

    2. XM_054352458.1XP_054208433.1  repulsive guidance molecule B isoform X4

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_173670.2: Suppressed sequence

      Description
      NM_173670.2: This RefSeq was permanently suppressed because there is insufficient support for the alternate terminal exon represented by this transcript.