Human (GRCh37.p13)
Description

family with sequence similarity 47, member A [Source:HGNC Symbol;Acc:29962]

Gene Synonyms

MGC27003

Location

Chromosome X: 34,147,869-34,150,447 reverse strand.

GRCh37:CM000685.1

About this gene

This gene has 1 transcript (splice variant) and 4 paralogues.

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  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000346193.3FAM47A-0012579791aa
 
Protein coding
CCDS43926Q5JRC9 NM_203408.3Ensembl CanonicalGENCODE Basic
Name

FAM47A (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: Q5JRC9

CCDS

This gene is a member of the Human CCDS set: CCDS43926.1

Ensembl version

ENSG00000185448.9

Other assemblies

This gene maps to 34,129,752-34,132,330 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000021339 (version 1)

Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Contigs

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