Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: FAM168B ENSOCUG00000017266

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Description

family with sequence similarity 168 member B [Source:HGNC Symbol;Acc:HGNC:27016]

Location

Chromosome 7: 60,403,111-60,464,249 reverse strand.

OryCun2.0:CM000796.1

About this gene

This gene has 3 transcripts (splice variants), 210 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000017269.3	FAM168B-201	1730	238aa	ENSOCUP00000014838.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1TDC6	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,
ENSOCUT00000059696.1	FAM168B-202	1337	227aa	ENSOCUP00000027532.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSOCUT00000043529.1	FAM168B-203	360	119aa	ENSOCUP00000046695.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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