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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: FAM161B ENSG00000156050

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Description

family with sequence similarity 161, member B [Source:HGNC Symbol;Acc:19854]

Gene Synonyms

C14orf44, FLJ31697, c14_5547

Location

Chromosome 14: 74,398,204-74,417,117 reverse strand.

GRCh37:CM000676.1

About this gene

This gene has 3 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
ENST00000286544.3	FAM161B-001	4078	710aa	ENSP00000286544.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS9822	Q96MY7	NM_152445.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000534936.1	FAM161B-201	2304	647aa	ENSP00000445326.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q96MY7	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000556794.1	FAM161B-003	1365	144aa	ENSP00000450889.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		-	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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