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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
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: FAM168B ENSG00000152102

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Description

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

Gene Synonyms

KIAA0280L, MANI

Location

Chromosome 2: 131,805,449-131,851,033 reverse strand.

GRCh37:CM000664.1

About this gene

This gene has 2 transcripts (splice variants) and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000409185.1	FAM168B-001	5285	195aa	ENSP00000387051.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS42755	A1KXE4	NM_001009993.2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000389915.3	FAM168B-003	944	195aa	ENSP00000374565.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS42755	A1KXE4	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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