Human (GRCh37.p13)
Description

family with sequence similarity 161, member A [Source:HGNC Symbol;Acc:25808]

Gene Synonyms

FLJ13305, RP28

Location

Chromosome 2: 62,051,989-62,081,278 reverse strand.

GRCh37:CM000664.1

About this gene

This gene has 7 transcripts (splice variants), 1 paralogue and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000404929.1FAM161A-0053762716aaENSP00000385158.1
 
Protein coding
CCDS56120Q3B820 NM_001201543.1GENCODE basic
ENST00000405894.3FAM161A-0013684660aaENSP00000385893.3
 
Protein coding
CCDS42687Q3B820 NM_032180.2GENCODE basic
ENST00000418113.1FAM161A-0044027601aaENSP00000416861.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000456262.1FAM161A-0023579142aaENSP00000396105.1
 
Nonsense mediated decay
F8WCZ8 --
ENST00000307507.3FAM161A-003189775aaENSP00000303170.3
 
Nonsense mediated decay
F8W731 --
ENST00000496369.1FAM161A-008699No protein-
 
Retained intron
---
ENST00000478494.1FAM161A-009630No protein-
 
Retained intron
---