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C14orf132 chromosome 14 open reading frame 132 [ Homo sapiens (human) ]

Gene ID: 56967, updated on 11-Jun-2021

Summary

Official Symbol
C14orf132provided by HGNC
Official Full Name
chromosome 14 open reading frame 132provided by HGNC
Primary source
HGNC:HGNC:20346
See related
Ensembl:ENSG00000227051
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
C14orf88
Expression
Broad expression in brain (RPKM 28.5), endometrium (RPKM 10.8) and 14 other tissues See more
Orthologs
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Genomic context

See C14orf132 in Genome Data Viewer
Location:
14q32.2
Exon count:
4
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 14 NC_000014.9 (96039362..96093971)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (96505699..96560308)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370644 Neighboring gene TCL1 upstream neural differentiation-associated RNA Neighboring gene bradykinin receptor B2 Neighboring gene CDC28 protein kinase regulatory subunit 1B pseudogene 1 Neighboring gene bradykinin receptor B1

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

General gene information

Markers

Homology

Clone Names

  • FLJ10728, FLJ93483, DKFZp761F2014

Gene Ontology Provided by GOA

Component Evidence Code Pubs
located_in integral component of membrane IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
uncharacterized protein C14orf132

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.

mRNA and Protein(s)

  1. NM_001252507.3NP_001239436.1  uncharacterized protein C14orf132 isoform b

    See identical proteins and their annotated locations for NP_001239436.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks a portion of the 5' UTR and 5' coding region, and uses an alternate translational start codon, compared to variant 1. The encoded isoform (b) has a distinct N-terminus and is shorter than isoform a. Both variants 2 and 3 encode isoform b.
    Source sequence(s)
    AL137190, BC043593, CA434364, DB264577
    Consensus CDS
    CCDS81848.1
    UniProtKB/Swiss-Prot
    Q9NPU4
    Related
    ENSP00000490729.1, ENST00000555004.3
  2. NM_001282463.2NP_001269392.1  uncharacterized protein C14orf132 isoform a

    See identical proteins and their annotated locations for NP_001269392.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longest transcript and encodes isoform a.
    Source sequence(s)
    AL137190, CA434364, DA114412, DB264577
    Consensus CDS
    CCDS81849.1
    UniProtKB/TrEMBL
    A0A1B0GU51
    Related
    ENSP00000489964.1, ENST00000553764.1
  3. NM_001282464.2NP_001269393.1  uncharacterized protein C14orf132 isoform b

    See identical proteins and their annotated locations for NP_001269393.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) lacks a portion of the 5' UTR and 5' coding region, uses an alternate translational start codon, and differs in the 3' UTR, compared to variant 1. The encoded isoform (b) has a distinct N-terminus and is shorter than isoform a. Both variants 2 and 3 encode isoform b.
    Source sequence(s)
    BI791809, CA434364, DA811354, DB264577
    Consensus CDS
    CCDS81848.1
    UniProtKB/Swiss-Prot
    Q9NPU4
    Related
    ENSP00000490894.1, ENST00000556728.1
  4. NM_001289139.2NP_001276068.1  uncharacterized protein C14orf132 isoform c

    See identical proteins and their annotated locations for NP_001276068.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (4) contains multiple differences in the 5' UTR and 5' coding region, compared to variant 1, and uses an alternate translational start codon. The encoded isoform (c) has a distinct N-terminus and is longer than isoform a.
    Source sequence(s)
    AL137190, CA434364, DA249054, DA811354, DB264577
    Consensus CDS
    CCDS81847.1
    UniProtKB/TrEMBL
    A0A1B0GWH2
    Related
    ENSP00000490925.1, ENST00000553782.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000014.9 Reference GRCh38.p13 Primary Assembly

    Range
    96039362..96093971
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_017021469.1XP_016876958.1  uncharacterized protein C14orf132 isoform X1

    UniProtKB/TrEMBL
    A0A1B0GU51

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_020215.2: Suppressed sequence

    Description
    NM_020215.2: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.
  2. NR_023938.1: Suppressed sequence

    Description
    NR_023938.1: This RefSeq was permanently suppressed because it is now thought that this gene does encode a protein.
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