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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Paralogues
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: HMGN1P32 ENSG00000237589

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Description

high mobility group nucleosome binding domain 1 pseudogene 32 [Source:HGNC Symbol;Acc:39376]

Location

Chromosome 19: 54,271,225-54,271,807 reverse strand.

GRCh37:CM000681.1

About this gene

This gene has 1 transcript (splice variant).

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	RefSeq	Flags
ENST00000441744.1	HMGN1P32-001	256	No protein	-	Pseudogene that lack introns and is thought to arise from reverse transcription of mRNA followed by reinsertion of DNA into the genome.Processed pseudogene		-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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