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Human (GRCh38.p14)
Description

paired like homeodomain 1 [Source:HGNC Symbol;Acc:HGNC:9004]

Gene Synonyms

BFT, POTX, PTX1

Location

Chromosome 5: 135,027,734-135,034,813 reverse strand.

GRCh38:CM000667.2

About this gene

This gene has 10 transcripts (splice variants), 194 orthologues, 51 paralogues and is associated with 9 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000265340.12PITX1-2012337314aaENSP00000265340.6
 
Protein coding
CCDS4182P78337 X5D9A5 NM_002653.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00001131942.1PITX1-2102518314aaENSP00000803743.1
 
Protein coding
CCDS4182X5D9A5 -Ensembl Canonical ExtendedGENCODE BasicAPPRIS P1
ENST00001009069.1PITX1-2072529170aaENSP00000678886.1
 
Protein coding
--GENCODE Basic
ENST00001125281.1PITX1-2092516144aaENSP00000795086.1
 
Protein coding
--GENCODE Basic
ENST00000506438.6PITX1-2052124314aaENSP00000427542.1
 
Protein coding
CCDS4182P78337 X5D9A5 -GENCODE BasicAPPRIS P1TSL:1
ENST00000502676.1PITX1-202666114aaENSP00000423624.1
 
Protein coding
D6R955 -TSL:3CDS 3' incomplete
ENST00000507253.5PITX1-206587130aaENSP00000422908.1
 
Protein coding
D6R9U1 -TSL:3CDS 3' incomplete
ENST00001125280.1PITX1-208263968aaENSP00000795085.1
 
Nonsense mediated decay
---
ENST00000503586.1PITX1-203624No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000504936.1PITX1-204770No protein-
 
Retained intron
--TSL:2