HMGA1P6 high mobility group AT-hook 1 pseudogene 6 [Homo sapiens (human)] - Gene

Summary

Official Symbol: HMGA1P6provided by HGNC
Official Full Name: high mobility group AT-hook 1 pseudogene 6provided by HGNC
Primary source: HGNC:HGNC:19121
See related: AllianceGenome:HGNC:19121
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: HMGA1L6
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Genomic context

Location:: 13q12.12

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	13	NC_000013.11 (23134168..23135879)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	13	NC_060937.1 (22340966..22342677)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	13	NC_000013.10 (23708307..23710018)

Chromosome 13 - NC_000013.11 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?

Overexpression of pseudogenes HMGA1P6 and HMGA1P7 could contribute to increase HMGA1 levels in human pituitary tumors, and then to pituitary tumorigenesis.
Title: HMGA1-pseudogene expression is induced in human pituitary tumors.
HMGA1P6 and HMGA1P7 are potential proto-oncogenic competitive endogenous RNAs in thyroid and ovarian neoplasms.
Title: HMGA1 pseudogenes as candidate proto-oncogenic competitive endogenous RNAs.

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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 studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

high mobility group AT-hook 1-like 6
high mobility group protein gene A1-like 6

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.