Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
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Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
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Gene: Zfp532 ENSRNOG00000017116

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Description

zinc finger protein 532 [Source:RGD Symbol;Acc:1311719]

Gene Synonyms

LOC307362, Znf532

Location

Primary_assembly 18: 59,092,789-59,203,666 forward strand.

mRatBN7.2:CM026991.1

About this gene

This gene has 3 transcripts (splice variants), 237 orthologues and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000082403.2	Zfp532-202	5994	1353aa	ENSRNOP00000071139.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JZQ5	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,
ENSRNOT00000099718.1	Zfp532-203	7483	1031aa	ENSRNOP00000085177.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A3F9	-
ENSRNOT00000064250.2	Zfp532-201	5998	1332aa	ENSRNOP00000059551.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A659	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,

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Summary

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