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    RAB43 RAB43, member RAS oncogene family [ Homo sapiens (human) ]

    Gene ID: 339122, updated on 25-Nov-2025
    Official Symbol
    RAB43provided by HGNC
    Official Full Name
    RAB43, member RAS oncogene familyprovided by HGNC
    Primary source
    HGNC:HGNC:19983
    See related
    Ensembl:ENSG00000172780 AllianceGenome:HGNC:19983
    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
    RAB41; RAB11B
    Summary
    Enables GTPase activity. Involved in Golgi organization; phagosome maturation; and retrograde transport, plasma membrane to Golgi. Located in Golgi apparatus and phagocytic vesicle. [provided by Alliance of Genome Resources, Jul 2025]
    Expression
    Ubiquitous expression in thyroid (RPKM 20.1), lung (RPKM 12.9) and 25 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table
    See RAB43 in Genome Data Viewer
    Location:
    3q21.3
    Exon count:
    8
    Annotation release Status Assembly Chr Location
    RS_2025_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (129087569..129122150, complement)
    RS_2025_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (131832460..131867053, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (128806412..128840993, complement)

    Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene glycoprotein IX platelet Neighboring gene small nucleolar RNA U13 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:128807293-128807837 Neighboring gene ISY1-RAB43 readthrough Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:128831162-128831662 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:128838731-128839676 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14717 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14718 Neighboring gene ISY1 spliceosome associated protein Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20503 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20504 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20505 Neighboring gene myotonic dystrophy type 2 repeat instability region Neighboring gene CCHC-type zinc finger nucleic acid binding protein

    • 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

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    Products Interactant Other Gene Complex Source Pubs Description

    Markers

    Clone Names

    • MGC90481

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables G protein activity IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    enables GTP binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables GTPase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables GTPase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables GTPase activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables nucleotide binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in Golgi organization IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in autophagosome assembly IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    acts_upstream_of_or_within cellular response to type II interferon IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in endoplasmic reticulum to Golgi vesicle-mediated transport IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in intracellular protein transport IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in phagosome maturation IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in regulation of Golgi organization IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in retrograde transport, plasma membrane to Golgi IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in virion assembly IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    is_active_in Golgi apparatus IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in Golgi apparatus IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in Golgi apparatus IEA
    Inferred from Electronic Annotation
    more info
     
    located_in Golgi membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    is_active_in cis-Golgi network membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in cis-Golgi network membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in cytoplasmic vesicle IEA
    Inferred from Electronic Annotation
    more info
     
    is_active_in endomembrane system IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    is_active_in endoplasmic reticulum membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in endoplasmic reticulum membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    is_active_in endoplasmic reticulum-Golgi intermediate compartment membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in endoplasmic reticulum-Golgi intermediate compartment membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in extracellular exosome HDA PubMed 
    located_in phagocytic vesicle IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in phagocytic vesicle IEA
    Inferred from Electronic Annotation
    more info
     
    located_in phagocytic vesicle membrane IEA
    Inferred from Electronic Annotation
    more info
     
    located_in trans-Golgi network membrane TAS
    Traceable Author Statement
    more info
     
    Preferred Names
    ras-related protein Rab-43
    Names
    ras-related protein Rab-41

    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_001204883.2NP_001191812.1  ras-related protein Rab-43 isoform a

      See identical proteins and their annotated locations for NP_001191812.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Variants 1-5 all encode the same isoform (a).
      Source sequence(s)
      AC108673, CA450364, DA317502, DA757569
      Consensus CDS
      CCDS33850.1
      UniProtKB/Swiss-Prot
      A8K4P9, E9PBQ0, Q86YS6
      Related
      ENSP00000376982.1, ENST00000393305.5
      Conserved Domains (1) summary
      cd01864
      Location:16180
      Rab19; Rab GTPase family 19 (Rab19)
    2. NM_001204884.2NP_001191813.1  ras-related protein Rab-43 isoform a

      See identical proteins and their annotated locations for NP_001191813.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) differs in the 5' UTR compared to variant 1. Variants 1-5 all encode the same isoform (a).
      Source sequence(s)
      AC108673, CA450364, DA008447
      Consensus CDS
      CCDS33850.1
      UniProtKB/Swiss-Prot
      A8K4P9, E9PBQ0, Q86YS6
      Related
      ENSP00000376984.1, ENST00000393307.5
      Conserved Domains (1) summary
      cd01864
      Location:16180
      Rab19; Rab GTPase family 19 (Rab19)
    3. NM_001204885.1NP_001191814.1  ras-related protein Rab-43 isoform a

      See identical proteins and their annotated locations for NP_001191814.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (4) differs in the 5' UTR compared to variant 1. Variants 1-5 all encode the same isoform (a).
      Source sequence(s)
      AC108673, CA450364, DA103180
      Consensus CDS
      CCDS33850.1
      UniProtKB/Swiss-Prot
      A8K4P9, E9PBQ0, Q86YS6
      Related
      ENSP00000376985.1, ENST00000393308.5
      Conserved Domains (1) summary
      cd01864
      Location:16180
      Rab19; Rab GTPase family 19 (Rab19)
    4. NM_001204886.2NP_001191815.1  ras-related protein Rab-43 isoform a

      See identical proteins and their annotated locations for NP_001191815.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (5) differs in the 5' UTR compared to variant 1. Variants 1-5 all encode the same isoform (a).
      Source sequence(s)
      AC108673, CA450364, DA339537
      Consensus CDS
      CCDS33850.1
      UniProtKB/Swiss-Prot
      A8K4P9, E9PBQ0, Q86YS6
      Related
      ENSP00000376981.1, ENST00000393304.5
      Conserved Domains (1) summary
      cd01864
      Location:16180
      Rab19; Rab GTPase family 19 (Rab19)
    5. NM_001204887.2NP_001191816.1  ras-related protein Rab-43 isoform b

      See identical proteins and their annotated locations for NP_001191816.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (6) includes an additional alternate exon that causes a frameshift in the 3' coding region, compared to variant 1. The encoded isoform (b) has a distinct and shorter C-terminus, compared to isoform a.
      Source sequence(s)
      AC108673, BX331971, CA450364, DB220260
      Consensus CDS
      CCDS56275.1
      UniProtKB/Swiss-Prot
      Q86YS6
      Related
      ENSP00000427632.1, ENST00000476465.5
      Conserved Domains (1) summary
      cl21455
      Location:16129
      P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
    6. NM_001204888.2NP_001191817.1  ras-related protein Rab-43 isoform c

      See identical proteins and their annotated locations for NP_001191817.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (7) uses an alternate splice site that causes a frameshift in the central and 3' coding regions, compared to variant 1. The encoded isoform (c) has a distinct and shorter C-terminus, compared to isoform a.
      Source sequence(s)
      AC108673, AK128345, CA450364, DB220260
      Conserved Domains (1) summary
      cl21455
      Location:1663
      P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
    7. NM_198490.3NP_940892.1  ras-related protein Rab-43 isoform a

      See identical proteins and their annotated locations for NP_940892.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) encodes the longest isoform (a). Variants 1-5 all encode the same isoform.
      Source sequence(s)
      AC108673, AY166852, CA450364, DB220260
      Consensus CDS
      CCDS33850.1
      UniProtKB/Swiss-Prot
      A8K4P9, E9PBQ0, Q86YS6
      Related
      ENSP00000319781.6, ENST00000315150.10
      Conserved Domains (1) summary
      cd01864
      Location:16180
      Rab19; Rab GTPase family 19 (Rab19)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2025_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

      Range
      129087569..129122150 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060927.1 Alternate T2T-CHM13v2.0

      Range
      131832460..131867053 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)