Loading…

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

Configure this page

Share this page

Bookmark this page

.

Gene: FAM171A2 ENSG00000161682

.

Description

family with sequence similarity 171, member A2 [Source:HGNC Symbol;Acc:30480]

Gene Synonyms

MGC34829

Location

Chromosome 17: 42,430,583-42,441,243 reverse strand.

GRCh37:CM000679.1

About this gene

This gene has 4 transcripts (splice variants) and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000293443.7	FAM171A2-001	3160	826aa	ENSP00000293443.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS45701	A8MVW0	NM_198475.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000589407.1	FAM171A2-004	1066	159aa	ENSP00000466195.1	Nonsense mediated decay		K7EMG4	-	-
ENST00000588067.1	FAM171A2-002	964	159aa	ENSP00000466493.1	Nonsense mediated decay		K7EMG4	-	-
ENST00000592560.1	FAM171A2-003	758	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

.

Summary

.

.