Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Zdhhc20 ENSRNOG00000011024

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Description

zinc finger DHHC-type palmitoyltransferase 20 [Source:RGD Symbol;Acc:1305755]

Gene Synonyms

LOC305923, MGC156467, RGD1305755

Location

Primary_assembly 15: 36,098,282-36,154,532 reverse strand.

GRCr8:CM070405.1

About this gene

This gene has 2 transcripts (splice variants), 283 orthologues and 17 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000063962.5	Zdhhc20-202	1968	444aa	ENSRNOP00000059785.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AR22 E9PT74	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,
ENSRNOT00000014820.5	Zdhhc20-201	2274	422aa	ENSRNOP00000014820.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7FM28	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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