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CFAP95-DT CFAP95 divergent transcript [ Homo sapiens (human) ]

Gene ID: 494558, updated on 23-Nov-2021

Summary

Official Symbol
CFAP95-DTprovided by HGNC
Official Full Name
CFAP95 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:48713
See related
Ensembl:ENSG00000225626
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
C9orf135-DT; C9orf135-AS1
Expression
Restricted expression toward testis (RPKM 22.7) See more
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Genomic context

See CFAP95-DT in Genome Data Viewer
Location:
9q21.12
Exon count:
2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 9 NC_000009.12 (69819405..69820739, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (72434321..72435655, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376076 Neighboring gene Sharpr-MPRA regulatory region 12610 Neighboring gene cilia and flagella associated protein 95 Neighboring gene RNA, 7SL, cytoplasmic 570, pseudogene Neighboring gene MAM domain containing 2 Neighboring gene MAMDC2 antisense RNA 1

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

Other Names

  • C9orf135 antisense RNA 1 (head to head)
  • C9orf135 divergent transcript

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_038833.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC039385, BG717523, BI830190
    Related
    ENST00000652595.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p13 Primary Assembly

    Range
    69819405..69820739 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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