U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

HAX1P1 HAX1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100129661, updated on 13-May-2022

Summary

Official Symbol
HAX1P1provided by HGNC
Official Full Name
HAX1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:55151
See related
AllianceGenome:HGNC:55151
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See HAX1P1 in Genome Data Viewer
Location:
Xq28
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (148197832..148198973, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (146464212..146465353, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (147279352..147280493, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene FMR1 neighbor Neighboring gene RNA, 5S ribosomal pseudogene 524 Neighboring gene ferritin heavy chain 1 pseudogene 8 Neighboring gene ribosomal protein L7 like 1 pseudogene 11 Neighboring gene origin of replication in 5' region of AFF2/FMR2 Neighboring gene fragile site, folic acid type, rare, fra(X)(q28) E

Genomic regions, transcripts, and products

Phenotypes

EBI GWAS Catalog

Description
Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study.
EBI GWAS Catalog

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_022646.3 

    Range
    101..1242
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    148197832..148198973 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    146464212..146465353 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)