Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Cldnd1 ENSRNOG00000001657

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Description

claudin domain containing 1 [Source:RGD Symbol;Acc:1359273]

Gene Synonyms

MGC94479

Location

Primary_assembly 11: 55,352,321-55,358,907 reverse strand.

GRCr8:CM070401.1

About this gene

This gene has 2 transcripts (splice variants) and 284 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000002260.6	Cldnd1-201	2431	352aa	ENSRNOP00000002260.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3V674	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,
ENSRNOT00000167056.1	Cldnd1-202	2380	335aa	ENSRNOP00000104069.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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