Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Fam227b ENSRNOG00000037124

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Description

family with sequence similarity 227, member B [Source:RGD Symbol;Acc:1359452]

Gene Synonyms

LOC296118, MGC108954, RGD1359452

Location

Primary_assembly 3: 133,686,605-133,845,717 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 2 transcripts (splice variants) and 85 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000117450.2	Fam227b-202	1741	574aa	ENSRNOP00000089612.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AC49	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,
ENSRNOT00000055995.4	Fam227b-201	1820	573aa	ENSRNOP00000052849.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6AXP3	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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