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    TIMM23B translocase of inner mitochondrial membrane 23 homolog B [ Homo sapiens (human) ]

    Gene ID: 100652748, updated on 3-Nov-2024

    Summary

    Official Symbol
    TIMM23Bprovided by HGNC
    Official Full Name
    translocase of inner mitochondrial membrane 23 homolog Bprovided by HGNC
    Primary source
    HGNC:HGNC:23581
    See related
    Ensembl:ENSG00000204152 MIM:620758; AllianceGenome:HGNC:23581
    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
    Predicted to enable protein transmembrane transporter activity. Predicted to be involved in protein import into mitochondrial matrix. Located in mitochondrion. [provided by Alliance of Genome Resources, Nov 2024]
    Expression
    Ubiquitous expression in testis (RPKM 3.8), bone marrow (RPKM 3.7) and 25 other tissues See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See TIMM23B in Genome Data Viewer
    Location:
    10q11.23
    Exon count:
    9
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (49942053..49974850)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (50791695..50824486)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (51371399..51734610)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene ribosomal protein L21 pseudogene 89 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr10:51038955-51039720 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr10:51039721-51040484 Neighboring gene Sharpr-MPRA regulatory region 10647 Neighboring gene poly(ADP-ribose) glycohydrolase Neighboring gene ribosomal protein L35a pseudogene 24 Neighboring gene H3K27ac hESC enhancer GRCh37_chr10:51133929-51134429 Neighboring gene TIMM23B-AGAP6 readthrough (NMD candidate) Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3355 Neighboring gene small nucleolar RNA, H/ACA box 74C-2 Neighboring gene RNA, 5S ribosomal pseudogene 317 Neighboring gene ArfGAP with GTPase domain, ankyrin repeat and PH domain 6

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues 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

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Readthrough TIMM23B-AGAP6

    Readthrough gene: TIMM23B-AGAP6, Included gene: AGAP6

    Clone Names

    • FLJ40725, FLJ56773, FLJ57933, FLJ60010, FLJ79448, MGC22767

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables protein transmembrane transporter activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Process Evidence Code Pubs
    involved_in protein import into mitochondrial matrix IBA
    Inferred from Biological aspect of Ancestor
    more info
     

    General protein information

    Preferred Names
    mitochondrial import inner membrane translocase subunit Tim23B
    Names
    putative mitochondrial import inner membrane translocase subunit Tim23B

    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_001290117.2NP_001277046.1  mitochondrial import inner membrane translocase subunit Tim23B isoform 1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) encodes the longer isoform (1).
      Source sequence(s)
      AK098044, AK293228, AL542628, BU620107, BU928648, DC419977
      Consensus CDS
      CCDS73131.1
      UniProtKB/Swiss-Prot
      B4DDK6, E7EP42, Q5SRD1, Q5SRD2
      UniProtKB/TrEMBL
      B4DI18
      Related
      ENSP00000502369.1, ENST00000651259.3
      Conserved Domains (1) summary
      cl02381
      Location:46171
      Tim17; Tim17/Tim22/Tim23/Pmp24 family
    2. NM_001290118.2NP_001277047.1  mitochondrial import inner membrane translocase subunit Tim23B isoform 2

      See identical proteins and their annotated locations for NP_001277047.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) lacks two exons in the coding region, compared to variant 1, which results in a shorter protein (isoform 2), compared to isoform 1.
      Source sequence(s)
      AK098044, AK293228, BU620107, BU928648, DA019889, DC419977
      Consensus CDS
      CCDS76301.1
      UniProtKB/TrEMBL
      B4DDK6
      Related
      ENSP00000502146.1, ENST00000652716.1
      Conserved Domains (1) summary
      cl02381
      Location:46123
      Tim17; Tim17/Tim22/Tim23/Pmp24 family
    3. NM_001365871.1NP_001352800.1  mitochondrial import inner membrane translocase subunit Tim23B isoform 3

      Status: VALIDATED

      Source sequence(s)
      AL442003, FO393433, FP565721
      Conserved Domains (1) summary
      cl02381
      Location:187
      Tim17; Tim17/Tim22/Tim23/Pmp24 family

    RNA

    1. NR_110767.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) contains an alternate exon, compared to variant 1. This variant is represented as non-coding because the use of the expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AK098044, AK293228, AL542628, BU620107, BU928648, DC419977
      Related
      ENST00000478381.5
    2. NR_158651.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL442003, FO393433, FP565721
    3. NR_158652.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL442003, FO393433, FP565721

    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_000010.11 Reference GRCh38.p14 Primary Assembly

      Range
      49942053..49974850
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      50791695..50824486
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NR_135475.1: Suppressed sequence

      Description
      NR_135475.1: This RefSeq has been removed because it is thought to be partial.