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

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Gene: CORO7-PAM16 ENSG00000103426

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Description

CORO7-PAM16 readthrough [Source:HGNC Symbol;Acc:44424]

Location

Chromosome 16: 4,390,252-4,470,495 reverse strand.

GRCh37:CM000678.1

About this gene

This gene has 3 transcripts (splice variants) and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000572467.1	CORO7-PAM16-001	3284	1048aa	ENSP00000460885.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS58418	I3L258	NM_001201479.1	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000575334.1	CORO7-PAM16-002	3815	535aa	ENSP00000458607.1	Nonsense mediated decay		I3L167 I3L258	-	-
ENST00000572274.1	CORO7-PAM16-003	672	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-

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Summary

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