PCNX4
Pecanex-like protein 4
Also known as: C14orf135, PCNXL4, PCX4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q63HM2
- Gene
- PCNX4
- Ensembl
- ENSG00000126773
- Chromosome
- 14
- Canonical length
- 1172 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1172 residues, UniProt reviewed canonical sequence.
>Q63HM2|PCNX4
1 MSPDVPLLND YKQDFFLKRF PQTVLGGPRF KLGYCAPPYI YVNQIILFLM PWVWGGVGTL
61 LYQLGILKDY YTAALSGGLM LFTAFVIQFT SLYAKNKSTT VERILTTDIL AEEDEHEFTS
121 CTGAETVKFL IPGKKYVANT VFHSILAGLA CGLGTWYLLP NRITLLYGST GGTALLFFFG
181 WMTLCIAEYS LIVNTATETA TFQTQDTYEI IPLMRPLYIF FFVSVDLAHR FVVNMPALEH
241 MNQILHILFV FLPFLWALGT LPPPDALLLW AMEQVLEFGL GGSSMSTHLR LLVMFIMSAG
301 TAIASYFIPS TVGVVLFMTG FGFLLSLNLS DMGHKIGTKS KDLPSGPEKH FSWKECLFYI
361 IILVLALLET SLLHHFAGFS QISKSNSQAI VGYGLMILLI ILWILREIQS VYIIGIFRNP
421 FYPKDVQTVT VFFEKQTRLM KIGIVRRILL TLVSPFAMIA FLSLDSSLQG LHSVSVCIGF
481 TRAFRMVWQN TENALLETVI VSTVHLISST DIWWNRSLDT GLRLLLVGII RDRLIQFISK
541 LQFAVTVLLT SWTEKKQRRK TTATLCILNI VFSPFVLVII VFSTLLSSPL LPLFTLPVFL
601 VGFPRPIQSW PGAAGTTACV CADTVYYYQM VPRLTAVLQT AMAAGSLGLL LPGSHYLGRF
661 QDRLMWIMIL ECGYTYCSIN IKGLELQETS CHTAEARRVD EVFEDAFEQE YTRVCSLNEH
721 FGNVLTPCTV LPVKLYSDAR NVLSGIIDSH ENLKEFKGDL IKVLVWILVQ YCSKRPGMKE
781 NVHNTENKGK APLMLPALNT LPPPKSPEDI DSLNSETFND WSDDNIFDDE PTIKKVIEEK
841 HQLKDLPGTN LFIPGSVESQ RVGDHSTGTV PENDLYKAVL LGYPAVDKGK QEDMPYIPLM
901 EFSCSHSHLV CLPAEWRTSC MPSSKMKEMS SLFPEDWYQF VLRQLECYHS EEKASNVLEE
961 IAKDKVLKDF YVHTVMTCYF SLFGIDNMAP SPGHILRVYG GVLPWSVALD WLTEKPELFQ
1021 LALKAFRYTL KLMIDKASLG PIEDFRELIK YLEEYERDWY IGLVSDEKWK EAILQEKPYL
1081 FSLGYDSNMG IYTGRVLSLQ ELLIQVGKLN PEAVRGQWAN LSWELLYATN DDEERYSIQA
1141 HPLLLRNLTV QAAEPPLGYP IYSSKPLHIH LYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PCNX4 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Unknown
- Secreted
- No
- Transmembrane segments
- 15
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- retina: 17 nTPM
- fallopian tube: 12 nTPM
- endometrium: 12 nTPM
- kidney: 12 nTPM
- ovary: 11 nTPM
- prostate: 11 nTPM
Single-cell type
- renal collecting duct intercalated cells: 416 nCPM
- cardiomyocytes: 363 nCPM
- choroid plexus epithelial cells: 309 nCPM
- endometrial ciliated cells: 303 nCPM
- somatotrophs: 297 nCPM
- lactotrophs: 288 nCPM
Immune cell
- NK-cell: 8.4 nTPM
- MAIT T-cell: 6.5 nTPM
- non-classical monocyte: 5.3 nTPM
- gdT-cell: 4.8 nTPM
- myeloid DC: 4.4 nTPM
- naive CD8 T-cell: 4.4 nTPM
Brain region
- choroid plexus: 38 nTPM
- cerebellum: 26 nTPM
- hypothalamus: 25 nTPM
- midbrain: 25 nTPM
- white matter: 24 nTPM
- medulla oblongata: 23 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.24
- gnomAD pLI
- 0
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PCNX4 as an antibody target. Whether an autoantibody or antibody against PCNX4 could matter depends on whether native PCNX4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PCNX4 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label PCNX4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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