ELOA3BP elongin A3 family member B, pseudogene [Homo sapiens (human)] - Gene

Summary

Official Symbol: ELOA3BPprovided by HGNC
Official Full Name: elongin A3 family member B, pseudogeneprovided by HGNC
Primary source: HGNC:HGNC:31007
See related: Ensembl:ENSG00000288607 AllianceGenome:HGNC:31007
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: ELOA3; ELOA3B; EloA3C; HsT828; TCEB3C; ELOA3CP; ELOA3L1; TCEB3CL; TCEB3L2; Elongin-A3; eloA3-like-1
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Genomic context

Location:: 18q21.1

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	18	NC_000018.10 (47022187..47024027, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	18	NC_060942.1 (47212455..47214295, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	18	NC_000018.9 (44548558..44550398, complement)

Chromosome 18 - NC_000018.10 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See Variation Viewer (GRCh37.p13)

Interactions

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Products	Interactant	Other Gene	Complex	Source	Pubs	Description

General gene information

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Other Names

Putative elongin-A3 member C
RNA polymerase II transcription factor SIII subunit A3
RNA polymerase II transcription factor SIII subunit A3-like-1
Transcription elongation factor B polypeptide 3C
elongin A3 like 1
elongin-A3 member B
transcription elongation factor B polypeptide 3C-like-1
transcription elongation factor B subunit 3C like

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.