Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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Molecular interactions
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ID History
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Gene: ZNF132 ENSBTAG00000003267

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Description

zinc finger protein 132 [Source:VGNC Symbol;Acc:VGNC:52982]

Location

Primary_assembly 18: 65,691,530-65,701,844 reverse strand.

ARS-UCD2.0:CM008185.2

About this gene

This gene has 5 transcripts (splice variants), 66 orthologues and 122 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000119320.1	ZNF132-201	3468	730aa	ENSBTAP00000077435.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S2A3	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, 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. 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. APPRIS ALT2,
ENSBTAT00000103196.1	ZNF132-203	3334	729aa	ENSBTAP00000079860.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S1V2	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. 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. APPRIS ALT2,
ENSBTAT00000094002.1	ZNF132-202	3309	702aa	ENSBTAP00000084556.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SKZ9	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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. APPRIS P2,
ENSBTAT00000114094.1	ZNF132-204	3271	696aa	ENSBTAP00000098188.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TIP6	-
ENSBTAT00000004230.7	ZNF132-205	3068	674aa	ENSBTAP00000004230.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MY83	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. 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. APPRIS ALT2,

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Summary

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