FSCN1P1 fascin actin-bundling protein 1 pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: FSCN1P1provided by HGNC
Official Full Name: fascin actin-bundling protein 1 pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:49669
See related: AllianceGenome:HGNC:49669
Gene type: pseudo
RefSeq status: INFERRED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

Location:: 15q14

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	15	NC_000015.10 (34494299..34497078)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	15	NC_060939.1 (32300019..32302798)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	15	NC_000015.9 (34786500..34789279)

Chromosome 15 - NC_000015.10 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

The fascin pseudogene is a conserved genomic locus with all the hallmarks of a fascin-derived processed retroposon, including target site duplications and lack of introns.
Title: The human fascin gene promoter is highly active in mature dendritic cells due to a stage-specific enhancer.

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Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See Variation Viewer (GRCh37.p13)

General gene information

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Markers

FSCN1__6758 (e-PCR)
- UniSTS:466191

G62033 (e-PCR)
- UniSTS:139123

RH28419 (e-PCR)
- UniSTS:84106

Other Names

fascin homolog 1, actin-bundling protein pseudogene
fascin 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.