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    FOLH1B folate hydrolase 1B (pseudogene) [ Homo sapiens (human) ]

    Gene ID: 219595, updated on 2-Nov-2024

    Summary

    Official Symbol
    FOLH1Bprovided by HGNC
    Official Full Name
    folate hydrolase 1B (pseudogene)provided by HGNC
    Primary source
    HGNC:HGNC:13636
    See related
    MIM:609020; AllianceGenome:HGNC:13636
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    PSM; FOLH2; FOLHP; PSMAL; PSMA-LIKE
    Summary
    Enables metallocarboxypeptidase activity. Involved in C-terminal protein deglutamylation. Located in extracellular exosome. [provided by Alliance of Genome Resources, Nov 2024]
    Expression
    Biased expression in duodenum (RPKM 38.8), prostate (RPKM 20.3) and 6 other tissues See more
    Orthologs
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    Genomic context

    See FOLH1B in Genome Data Viewer
    Location:
    11q14.3
    Exon count:
    14
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (89659268..89698718)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (89578945..89618403)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (89392436..89431886)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene NADPH oxidase 4 Neighboring gene H3 histone pseudogene 34 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:89304186-89305004 Neighboring gene Sharpr-MPRA regulatory region 15382 Neighboring gene uncharacterized LOC124902843 Neighboring gene UBTF like 10 (pseudogene) Neighboring gene tripartite motif containing 77

    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

    Markers

    Other Names

    • N-acetylated-alpha-linked-acidic dipeptidase
    • cell growth-inhibiting gene 26 protein
    • folate hydrolase 2
    • prostate-specific membrane antigen-like protein
    • putative N-acetylated-alpha-linked acidic dipeptidase
    • putative folate hydrolase 1B

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables dipeptidase activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables metal ion binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables metallocarboxypeptidase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in C-terminal protein deglutamylation IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in proteolysis IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    located_in cytoplasm IEA
    Inferred from Electronic Annotation
    more info
     
    located_in extracellular exosome HDA PubMed 
    located_in plasma membrane TAS
    Traceable Author Statement
    more info
     

    NCBI Reference Sequences (RefSeq)

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    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.

    RNA

    1. NR_175944.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AP003122

    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_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      89659268..89698718
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      89578945..89618403
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NG_003258.2: Suppressed sequence

      Description
      NG_003258.2: This RefSeq was permanently suppressed because it is primarily UTR sequence.
    2. NM_001395847.1: Suppressed sequence

      Description
      NM_001395847.1: This RefSeq was removed because currently there is insufficient support for the transcript and the protein.
    3. NM_153696.3: Suppressed sequence

      Description
      NM_153696.3: This RefSeq was removed because currently there is support for the transcript but not for the protein.