Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Matn2 ENSRNOG00000006060

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Description

matrilin 2 [Source:RGD Symbol;Acc:1305353]

Gene Synonyms

LOC299996

Location

Primary_assembly 7: 67,380,168-67,530,153 forward strand.

GRCr8:CM070397.1

About this gene

This gene has 4 transcripts (splice variants), 193 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000008361.9	Matn2-201	3892	912aa	ENSRNOP00000008361.9	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LXS3	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, 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,
ENSRNOT00000100118.2	Matn2-203	3494	911aa	ENSRNOP00000076610.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5YBE6	-
ENSRNOT00000106400.2	Matn2-204	3451	910aa	ENSRNOP00000092408.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GJR4	-
ENSRNOT00000098862.2	Matn2-202	1101	280aa	ENSRNOP00000094117.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ALH2	-

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data