Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
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: MAD2L1BP ENSPTRG00000018207

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Description

MAD2L1 binding protein [Source:VGNC Symbol;Acc:VGNC:3373]

Location

Chromosome 6: 44,136,812-44,147,590 forward strand.

Pan_tro_3.0:CM000320.3

About this gene

This gene has 3 transcripts (splice variants) and 201 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000111252.1	MAD2L1BP-202	1005	334aa	ENSPTRP00000079675.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SSZ6	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,
ENSPTRT00000057220.4	MAD2L1BP-201	921	306aa	ENSPTRP00000050069.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XSR0 H2R790	-
ENSPTRT00000104564.1	MAD2L1BP-203	825	274aa	ENSPTRP00000086053.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2X2F6 K7A4V7	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,

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Summary

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