ACTBP2 ACTB pseudogene 2 [Homo sapiens (human)] - Gene

Summary

Official Symbol: ACTBP2provided by HGNC
Official Full Name: ACTB pseudogene 2provided by HGNC
Primary source: HGNC:HGNC:135
See related: AllianceGenome:HGNC:135
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:: 5q14.1

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	5	NC_000005.10 (77784803..77786597)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	5	NC_060929.1 (78266784..78268576)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	5	NC_000005.9 (77080627..77082421)

Chromosome 5 - NC_000005.10 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?

The detection of polymorphism in the SE33 locus is very useful in DNA profiling.
Title: [Polymorphism in the SE33 locus in the Polish population].

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

PMC193670P1 (e-PCR)
- UniSTS:271752

PMC86716P1 (e-PCR)
- UniSTS:273551

PMC317352P1 (e-PCR)
- UniSTS:273088

Actb-rs1 (e-PCR), detects polymorphism
- UniSTS:141017

PMC26753P1 (e-PCR)
- UniSTS:272350

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.