U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

HAVCR1P2 hepatitis A virus cellular receptor 1 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100421002, updated on 17-Sep-2024

Summary

Go to the top of the page Help
Official Symbol
HAVCR1P2provided by HGNC
Official Full Name
hepatitis A virus cellular receptor 1 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:44035
See related
Ensembl:ENSG00000271053 AllianceGenome:HGNC:44035
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

Go to the top of the page Help
See HAVCR1P2 in Genome Data Viewer
Location:
4q26
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (116858096..116858969)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (120159795..120160668)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (117779252..117780125)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377385 Neighboring gene uncharacterized LOC107986306 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:117701308-117701928 Neighboring gene RNA, U6 small nuclear 119, pseudogene Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr4:117901144-117902343 Neighboring gene uncharacterized LOC105377387 Neighboring gene uncharacterized LOC105377388 Neighboring gene translocation associated membrane protein 1 like 1

Genomic regions, transcripts, and products

Go to the top of the page Help

Go to nucleotide: Graphics FASTA GenBank

Bibliography

Go to the top of the pageHelp

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help

Review eQTL and phenotype association data in this region using PheGenI

Variation

Go to the top of the page Help

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

Go to the top of the page Help

NCBI Reference Sequences (RefSeq)

Go to the top of the page Help

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_025245.1 

    Range
    101..974
    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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    116858096..116858969
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    120159795..120160668
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases
Research Materials