Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Gene tree
  - Orthologues
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Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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Genetic Variation
- Variant table
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- Structural variants
Gene expression
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Gene: Ms4a6b ENSRNOG00000047349

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Description

membrane-spanning 4-domains, subfamily A, member 6B [Source:RGD Symbol;Acc:1311761]

Gene Synonyms

AABR07006269.1, LOC293750, Ms4a6a

Location

Primary_assembly 1: 217,705,961-217,727,450 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 355 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000032937.7	Ms4a6b-201	1872	265aa	ENSRNOP00000035907.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZZ58	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000049574.3	Ms4a6b-202	1728	247aa	ENSRNOP00000047278.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7FJ62	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Summary

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