ATP1B3P1 ATPase Na+/K+ transporting subunit beta 3 pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: ATP1B3P1provided by HGNC
Official Full Name: ATPase Na+/K+ transporting subunit beta 3 pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:807
See related: AllianceGenome:HGNC:807
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:: 2p16.1

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	2	NC_000002.12 (60734390..60735925, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	2	NC_060926.1 (60740201..60741736, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	2	NC_000002.11 (60961525..60963060, complement)

Chromosome 2 - NC_000002.12 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?

Submit: New GeneRIF Correction

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

RH66869 (e-PCR)
- UniSTS:91696

G32213 (e-PCR)
- UniSTS:116820

SHGC-16162 (e-PCR)
- UniSTS:13732

RH66571 (e-PCR)
- UniSTS:54451

RH12662 (e-PCR)
- UniSTS:87279

Other Names

ATPase, Na+/K+ transporting, beta 3 polypeptide pseudogene
ATPase, Na+/K+ transporting, beta 3 pseudogene 1

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.