Human (GRCh37.p13)
Description

BPI fold containing family A, member 1 [Source:HGNC Symbol;Acc:15749]

Gene Synonyms

LUNX, NASG, PLUNC, SPLUNC1, SPURT, bA49G10.5

Location

Chromosome 20: 31,823,801-31,831,115 forward strand.

GRCh37:CM000682.1

About this gene

This gene has 3 transcripts (splice variants) and 1 paralogue.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000354297.4BPIFA1-0021079256aa
 
Protein coding
CCDS13217A6XMV5 Q9NP55 NM_130852.2Ensembl CanonicalGENCODE Basic
ENST00000375422.2BPIFA1-0031063256aa
 
Protein coding
CCDS13217A6XMV5 Q9NP55 NM_001243193.1GENCODE Basic
ENST00000375413.4BPIFA1-0011024256aa
 
Protein coding
CCDS13217A6XMV5 Q9NP55 NM_016583.3GENCODE Basic
Name

BPIFA1 (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: Q9NP55

CCDS

This gene is a member of the Human CCDS set: CCDS13217.1

Ensembl version

ENSG00000198183.7

Other assemblies

This gene maps to 33,235,995-33,243,309 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:
OTTHUMG00000032243 (version 2)

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