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

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Gene: CARD14 ENSBTAG00000015261

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Description

caspase recruitment domain family member 14 [Source:VGNC Symbol;Acc:VGNC:26762]

Location

Primary_assembly 19: 52,430,398-52,460,270 reverse strand.

ARS-UCD2.0:CM008186.2

About this gene

This gene has 5 transcripts (splice variants), 184 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000020297.4	CARD14-205	3266	1019aa	ENSBTAP00000020297.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BHS1	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,
ENSBTAT00000112556.1	CARD14-201	4226	997aa	ENSBTAP00000081649.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S6N0	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,
ENSBTAT00000074938.2	CARD14-204	3437	972aa	ENSBTAP00000074596.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MRV5	-
ENSBTAT00000081030.2	CARD14-202	3301	1002aa	ENSBTAP00000068087.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MGF0	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,
ENSBTAT00000109786.1	CARD14-203	3179	962aa	ENSBTAP00000087404.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9STD9	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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