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FGF7P2 fibroblast growth factor 7 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 394217, updated on 10-Oct-2023

Summary

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Official Symbol
FGF7P2provided by HGNC
Official Full Name
fibroblast growth factor 7 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:17193
See related
AllianceGenome:HGNC:17193
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
FGF7L; PRED3
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Genomic context

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Location:
21q11.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 21 NC_000021.9 (13349265..13353660)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (11693617..11698003)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 21 NC_000021.8 (14721586..14725981)

Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene ankyrin repeat domain 30B pseudogene 2 Neighboring gene zinc finger protein 355, pseudogene Neighboring gene BNIP3 pseudogene 43 Neighboring gene ankyrin repeat domain 30B pseudogene 1 Neighboring gene microRNA 3156-3 Neighboring gene general transcription factor IIi pseudogene 2

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Fluorescence in situ hybridization analysis of keratinocyte growth factor gene amplification and dispersion in evolution of great apes and humans. Zimonjic DB, et al. Proc Natl Acad Sci U S A, 1997 Oct 14. PMID 9326632, Free PMC Article

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 studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • fibroblast growth factor 7 (keratinocyte growth factor) pseudogene

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.

Genomic

  1. NG_005961.5 

    Range
    101..4496
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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_000021.9 Reference GRCh38.p14 Primary Assembly

    Range
    13349265..13353660
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060945.1 Alternate T2T-CHM13v2.0

    Range
    11693617..11698003
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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