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: Cldn10 ENSRNOG00000010085

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Description

claudin 10 [Source:RGD Symbol;Acc:1308027]

Gene Synonyms

LOC290485

Location

Primary_assembly 15: 102,269,858-102,361,589 forward strand.

GRCr8:CM070405.1

About this gene

This gene has 4 transcripts (splice variants), 421 orthologues, 30 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000013520.6	Cldn10-201	1331	286aa	ENSRNOP00000013520.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HUG9 G3V7A9	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,
ENSRNOT00000093403.3	Cldn10-203	1228	268aa	ENSRNOP00000076157.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1W2Q674	-
ENSRNOT00000083269.4	Cldn10-202	911	229aa	ENSRNOP00000070015.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JWU2 A6HUG8	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,
ENSRNOT00000127877.1	Cldn10-204	582	193aa	ENSRNOP00000112835.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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