Loading…

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

Configure this page

Share this page

Bookmark this page

.

Gene: MAD2L1 ENSG00000164109

.

Description

MAD2 mitotic arrest deficient-like 1 (yeast) [Source:HGNC Symbol;Acc:6763]

Gene Synonyms

HSMAD2, MAD2

Location

Chromosome 4: 120,976,763-120,988,229 reverse strand.

GRCh37:CM000666.1

About this gene

This gene has 5 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000296509.6	MAD2L1-001	5468	205aa	ENSP00000296509.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS3715	Q13257	NM_002358.3	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,
ENST00000333047.5	MAD2L1-004	1277	90aa	ENSP00000332295.5	Nonsense mediated decay		Q13257	-	-
ENST00000504707.1	MAD2L1-003	764	41aa	ENSP00000425702.1	Nonsense mediated decay		D6RJE3	-	-
ENST00000512484.1	MAD2L1-005	626	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-
ENST00000511295.1	MAD2L1-002	528	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

.

Summary

.

.