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PLAC4 placenta enriched 4 [ Homo sapiens (human) ]

Gene ID: 191585, updated on 13-May-2022

Summary

Official Symbol
PLAC4provided by HGNC
Official Full Name
placenta enriched 4provided by HGNC
Primary source
HGNC:HGNC:14616
See related
Ensembl:ENSG00000280109 MIM:613770; AllianceGenome:HGNC:14616
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
PRED78; C21orf115
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Genomic context

See PLAC4 in Genome Data Viewer
Location:
21q22.2
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 21 NC_000021.9 (41175231..41185239, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (39563563..39573571, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 21 NC_000021.8 (42547158..42557166, complement)

Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 323 Neighboring gene microRNA 3197 Neighboring gene beta-secretase 2 Neighboring gene FAM3 metabolism regulating signaling molecule B Neighboring gene MX dynamin like GTPase 2

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Phenotypes

EBI GWAS Catalog

Description
Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies.
EBI GWAS Catalog

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Other Names

  • placenta specific 4

Clone Names

  • MGC126664, MGC126666

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_148920.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL773572
    Related
    ENST00000645185.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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
    41175231..41185239 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060945.1 Alternate T2T-CHM13v2.0

    Range
    39563563..39573571 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)