Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: FAM228B ENSBTAG00000030864

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Description

family with sequence similarity 228 member B [Source:NCBI gene (formerly Entrezgene);Acc:100125925]

Location

Primary_assembly 11: 74,947,565-74,990,076 reverse strand.

ARS-UCD1.3:CM008178.2

About this gene

This gene has 7 transcripts (splice variants), 112 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000108444.1	FAM228B-205	1643	384aa	ENSBTAP00000099169.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000111965.1	FAM228B-207	1401	282aa	ENSBTAP00000087237.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000101892.1	FAM228B-204	1382	297aa	ENSBTAP00000081902.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000109801.1	FAM228B-206	1308	338aa	ENSBTAP00000102344.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000043656.3	FAM228B-202	1300	264aa	ENSBTAP00000041212.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6QQ68	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,
ENSBTAT00000066406.2	FAM228B-201	1277	262aa	ENSBTAP00000063918.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M2B8	-
ENSBTAT00000104084.1	FAM228B-203	1214	241aa	ENSBTAP00000089672.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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