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FGF7P6 fibroblast growth factor 7 pseudogene 6 [ Homo sapiens (human) ]

Gene ID: 387628, updated on 12-Oct-2019

Summary

Official Symbol
FGF7P6provided by HGNC
Official Full Name
fibroblast growth factor 7 pseudogene 6provided by HGNC
Primary source
HGNC:HGNC:27852
See related
Ensembl:ENSG00000227449
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
KGFLP1
Expression
Ubiquitous expression in thyroid (RPKM 7.5), kidney (RPKM 5.1) and 24 other tissues See more

Genomic context

See FGF7P6 in Genome Data Viewer
Location:
9q13
Exon count:
4
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 9 NC_000009.12 (62376256..62435519)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (46687557..46746820)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379263 Neighboring gene RNA, 7SL, cytoplasmic 544, pseudogene Neighboring gene uncharacterized LOC102724238 Neighboring gene long intergenic non-protein coding RNA 1189 Neighboring gene fibroblast growth factor 7 pseudogene 7 Neighboring gene uncharacterized LOC103908604

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

NCBI Reference Sequences (RefSeq)

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_003674.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks an internal exon compared to variant 1.
    Source sequence(s)
    AF523265, AK307215, BC101842, CN274734
    Related
    ENST00000377614.7
  2. NR_047527.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AF523265, BC101842, CN274734, DB501751

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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
    62376256..62435519
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_174950.2: Suppressed sequence

    Description
    NM_174950.2: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
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