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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Cd1d1 ENSRNOG00000016451

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Description

CD1d1 molecule [Source:RGD Symbol;Acc:2296]

Gene Synonyms

Cd1, Cd1d

Location

Primary_assembly 2: 174,721,522-174,725,029 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 488 orthologues, 50 paralogues and is associated with 31 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000022150.4	Cd1d1-201	1901	358aa	ENSRNOP00000022150.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3V837	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 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,
ENSRNOT00000117073.2	Cd1d1-202	1442	205aa	ENSRNOP00000080498.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZPR1	-

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Paralogues

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