Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: ZCCHC10 ENSBTAG00000030616

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Description

zinc finger CCHC-type containing 10 [Source:VGNC Symbol;Acc:VGNC:37115]

Location

Primary_assembly 7: 44,565,898-44,595,423 reverse strand.

ARS-UCD1.3:CM008174.2

About this gene

This gene has 6 transcripts (splice variants) and 177 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000116420.1	ZCCHC10-202	2292	227aa	ENSBTAP00000077659.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000101583.1	ZCCHC10-203	2281	162aa	ENSBTAP00000085657.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000112727.1	ZCCHC10-204	2189	181aa	ENSBTAP00000079774.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000106679.1	ZCCHC10-201	2102	161aa	ENSBTAP00000083967.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000035343.5	ZCCHC10-205	948	170aa	ENSBTAP00000035219.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q2TBL3	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,
ENSBTAT00000106615.1	ZCCHC10-206	495	156aa	ENSBTAP00000088697.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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