U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

PSIP1P1 PSIP1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 353329, updated on 17-Sep-2024

Summary

Official Symbol
PSIP1P1provided by HGNC
Official Full Name
PSIP1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:31132
See related
AllianceGenome:HGNC:31132
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
PSIP1P
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See PSIP1P1 in Genome Data Viewer
Location:
9p22.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (15054967..15056600)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (15064777..15066410)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (15054965..15056598)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene histone PARylation factor 1 pseudogene Neighboring gene chloride voltage-gated channel 3 pseudogene 1 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:15138267-15138798 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:15138799-15139330 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:15139331-15139861 Neighboring gene uncharacterized LOC124902123 Neighboring gene RNA, U6 small nuclear 559, pseudogene

Genomic regions, transcripts, and products

Phenotypes

EBI GWAS Catalog

Description
Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study.
EBI GWAS Catalog

General gene information

Markers

Other Names

  • PC4 and SFRS1 interacting protein 1 pseudogene 1
  • PC4 and SFRS1 interacting protein pseudogene

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_002792.4 

    Range
    101..1734
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    15054967..15056600
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    15064777..15066410
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)