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Human (GRCh38.p14)
Description

placenta enriched 1 [Source:HGNC Symbol;Acc:HGNC:9044]

Gene Synonyms

CT92, OOSP2B, OOSP2L

Location

Chromosome X: 134,565,837-134,764,355 reverse strand.

GRCh38:CM000685.2

About this gene

This gene has 9 transcripts (splice variants), 66 orthologues and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000359237.9PLAC1-2011119212aaENSP00000352173.4
 
Protein coding
CCDS14642Q9HBJ0 NM_021796.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000917138.1PLAC1-2071176212aaENSP00000587197.1
 
Protein coding
CCDS14642--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000878501.1PLAC1-2051110212aaENSP00000548560.1
 
Protein coding
CCDS14642--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000950374.1PLAC1-2091075212aaENSP00000620433.1
 
Protein coding
CCDS14642--GENCODE BasicAPPRIS P1
ENST00000917139.1PLAC1-2081056212aaENSP00000587198.1
 
Protein coding
CCDS14642--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000917137.1PLAC1-2061025212aaENSP00000587196.1
 
Protein coding
CCDS14642--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000476971.5PLAC1-2041138No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000466797.1PLAC1-202740No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000473897.1PLAC1-203333No protein-
 
Protein coding CDS not defined
--TSL:5