Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Ensembl protein families
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: ANP32B ENSPTRG00000021172

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Description

acidic nuclear phosphoprotein 32 family member B [Source:VGNC Symbol;Acc:VGNC:4614]

Location

Chromosome 9: 75,715,619-75,747,850 forward strand.

Pan_tro_3.0:CM000323.3

About this gene

This gene has 2 transcripts (splice variants), 295 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ANP32B-201	ENSPTRT00000039151.4	1497	251aa	ENSPTRP00000036180.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WMJ4 H2QXJ7	<p>APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant.</p><p>APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene.</p>APPRIS P5,
ANP32B-202	ENSPTRT00000107748.1	717	238aa	ENSPTRP00000079977.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SSR6	<p>APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species.</p><p>APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene.</p>APPRIS ALT2,

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Summary

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Gene-based displays