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

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Gene: MEP1B ENSG00000141434

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Description

meprin A, beta [Source:HGNC Symbol;Acc:7020]

Location

Chromosome 18: 29,765,032-29,800,367 forward strand.

GRCh37:CM000680.1

About this gene

This gene has 4 transcripts (splice variants) and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000269202.6	MEP1B-001	2312	701aa	ENSP00000269202.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS45846	J3KRK1 Q16820	NM_005925.2	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,
ENST00000581447.1	MEP1B-002	2308	700aa	ENSP00000463280.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		J3KRK1 J3QKX5	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000581184.1	MEP1B-004	483	114aa	ENSP00000462038.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		J3KRK1	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000579919.1	MEP1B-003	563	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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