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

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Gene: ZCCHC12 ENSPTRG00000022215

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Description

zinc finger CCHC-type containing 12 [Source:VGNC Symbol;Acc:VGNC:7622]

Location

Chromosome X: 118,400,580-118,401,788 forward strand.

Pan_tro_3.0:CM000336.3

About this gene

This gene has 1 transcript (splice variant), 629 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000041405.4	ZCCHC12-201	1209	402aa	ENSPTRP00000038246.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XPX0 H2QZ15	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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