Format

Send to:

Choose Destination

FGF7P8 fibroblast growth factor 7 pseudogene 8 [ Homo sapiens (human) ]

Gene ID: 100113421, updated on 12-Oct-2019

Summary

Official Symbol
FGF7P8provided by HGNC
Official Full Name
fibroblast growth factor 7 pseudogene 8provided by HGNC
Primary source
HGNC:HGNC:34516
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See FGF7P8 in Genome Data Viewer
Location:
9q13
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 9 NC_000009.12 (62888535..62892939)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (66544359..66548570)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene myosin VB pseudogene 2 Neighboring gene lncRNA negative regulator of fibroblast-like synoviocyte migration, SYNCRIP interacting Neighboring gene adhesion G protein-coupled receptor F5 pseudogene 1 Neighboring gene uncharacterized LOC728673 Neighboring gene CNTNAP3 pseudogene 1

Genomic regions, transcripts, and products

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.

Genomic

  1. NG_006615.4 

    Range
    101..4505
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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
    62888535..62892939
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center