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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: FTH1P21 ENSG00000249013

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Description

ferritin, heavy polypeptide 1 pseudogene 21 [Source:HGNC Symbol;Acc:3997]

Gene Synonyms

FTHL21, FTHP2

Location

Chromosome 4: 156,927,630-156,928,140 forward strand.

GRCh37:CM000666.1

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
ENST00000512179.1	FTH1P21-001	511	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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