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TTTY14 testis expressed transcript, Y-linked 14 [ Homo sapiens (human) ]

Gene ID: 83869, updated on 10-Oct-2023

Summary

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Official Symbol
TTTY14provided by HGNC
Official Full Name
testis expressed transcript, Y-linked 14provided by HGNC
Primary source
HGNC:HGNC:18495
See related
Ensembl:ENSG00000176728 AllianceGenome:HGNC:18495
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
TTY14; CYorf14; PRO2834; NCRNA00137; NCRNA00185
Expression
Low expression observed in reference dataset See more
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Genomic context

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Location:
Yq11.222
Exon count:
11
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (18872501..19077547, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (19778988..19984049, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (21034387..21239433, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene OFD1 pseudogene 7 Y-linked Neighboring gene MT-CYB pseudogene 2 Neighboring gene zinc finger protein 839 pseudogene 1 Neighboring gene CD24 molecule pseudogene 4 Neighboring gene RNA, U6 small nuclear 255, pseudogene Neighboring gene uncharacterized LOC124905306 Neighboring gene glyceraldehyde 3 phosphate dehydrogenase pseudogene 19

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • 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

Bibliography

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Related articles in PubMed

  1. Expression of conjoined genes: another mechanism for gene regulation in eukaryotes. Prakash T, et al. PLoS One, 2010 Oct 12. PMID 20967262, Free PMC Article
  2. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Skaletsky H, et al. Nature, 2003 Jun 19. PMID 12815422
  3. The sequence of the human genome. Venter JC, et al. Science, 2001 Feb 16. PMID 11181995
  4. Transcriptome analysis of human gastric cancer. Oh JH, et al. Mamm Genome, 2005 Dec. PMID 16341674
  5. Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing. Fei T, et al. Proc Natl Acad Sci U S A, 2017 Jun 27. PMID 28611215, Free PMC Article

See all (7) citations in PubMed

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Other Names

  • testis-specific transcript, Y-linked 14 (non-protein coding)

Clone Names

  • FLJ32550

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_001543.4 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (5) lacks three exons and its transcription extends past a splice site used in the variant 1, resulting in a shorter transcript.
    Source sequence(s)
    AC007244, AC009235, AI674196

  2. NR_125733.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant:
    Source sequence(s)
    AF119903, DA411985, FY211594, FY213451

  3. NR_125734.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks two internal exons and contains an alternate internal exon, resulting in a shorter transcripts, compared to variant 1.
    Source sequence(s)
    AF119903, DA411985, FY211594

  4. NR_125735.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) lacks three internal exons and contains an alternate internal exon, resulting in a shorter transcripts, compared to variant 1.
    Source sequence(s)
    AF119903, BX280014, DA411985
    Related
    ENST00000454875.2

  5. NR_125736.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (4) differs in the 5' terminal exon, lacks two internal exons and contains two alternate internal exons, resulting in a shorter transcripts, compared to variant 1.
    Source sequence(s)
    AF119903, BM750145, HY121109
    Related
    ENST00000670354.1

  6. NR_125737.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (6) differs in the 5' terminal exon, lacks two exons and its transcription extends past a splice site used in the variant 1, resulting in a shorter transcript.
    Source sequence(s)
    AI674196, BM750145
    Related
    ENST00000651286.1

  7. NR_158640.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC007244, AC009235
    Related
    ENST00000670243.1

  8. NR_158641.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC007244, AC009235

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    18872501..19077547 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    19778988..19984049 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_031932.1: Suppressed sequence

    Description
    NM_031932.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.

  2. NR_001544.2: Suppressed sequence

    Description
    NR_001544.2: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript.
Nucleotide Protein
Heading Accession and Version

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