ACTG1P4 actin gamma 1 pseudogene 4 [Homo sapiens (human)] - Gene

Summary

Official Symbol: ACTG1P4provided by HGNC
Official Full Name: actin gamma 1 pseudogene 4provided by HGNC
Primary source: HGNC:HGNC:149
See related: AllianceGenome:HGNC:149
Gene type: pseudo
RefSeq status: VALIDATED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: ACTGP4
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Genomic context

Location:: 1p21.1

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	1	NC_000001.11 (103569404..103571391)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	1	NC_060925.1 (103418347..103420334)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	1	NC_000001.10 (104112026..104114013)

Chromosome 1 - NC_000001.11 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

GDB:181084 (e-PCR)
- UniSTS:155158

PMC85361P1 (e-PCR)
- UniSTS:273471

PMC133998P8 (e-PCR)
- UniSTS:270713

PMC20960P1 (e-PCR)
- UniSTS:272003

PMC224995P1 (e-PCR)
- UniSTS:272113

Other Names

ACTB pseudogene
actin, beta pseudogene
actin, gamma 2, smooth muscle, enteric pseudogene
actin, gamma pseudogene 4

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.