Description

claudin 10 [Source:HGNC Symbol;Acc:HGNC:2033]

Synonyms

CPETRL3, OSP-L

Location
INSDC coordinates

chromosome:GRCh38:CM000675.2:95433604:95579759:1

Transcripts



This gene has 3 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
CLDN10-001ENST000003768732656226 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS9475P78369 Q5W075 NM_001160100
NM_182848
NP_001153572
NP_878268
TSL:2

TSL2: The best supporting mRNA is flagged as suspect or the support is from multiple ESTs.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
CLDN10-002ENST00000299339949228 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS9476P78369 Q5W075 NM_006984
NP_008915
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS PIAPPRIS principal isoform [01-09-2014]
Glossary entry for APPRIS
APPRIS website
CLDN10-003ENST0000037685570173 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-Q5W075 -TSL:2

TSL2: The best supporting mRNA is flagged as suspect or the support is from multiple ESTs.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

Gene-based displays