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

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Gene: CD3D ENSBTAG00000006452

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Description

CD3 delta subunit of T-cell receptor complex [Source:VGNC Symbol;Acc:VGNC:27028]

Location

Primary_assembly 15: 29,016,437-29,024,370 reverse strand.

ARS-UCD2.0:CM008182.2

About this gene

This gene has 4 transcripts (splice variants), 144 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000107377.1	CD3D-201	771	191aa	ENSBTAP00000100667.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TQ17	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,
ENSBTAT00000091899.1	CD3D-204	1711	167aa	ENSBTAP00000097701.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TMX5	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,
ENSBTAT00000008462.5	CD3D-203	1476	168aa	ENSBTAP00000008462.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q28072	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,
ENSBTAT00000095713.1	CD3D-202	1236	98aa	ENSBTAP00000092806.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T4R8	-

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Summary

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