PLEKHA6
Pleckstrin homology domain-containing family A member 6
Also known as: KIAA0969, PEPP3, PKHA6_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y2H5
- Gene
- PLEKHA6
- Ensembl
- ENSG00000143850
- Chromosome
- 1
- Canonical length
- 1048 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles,Cell Junctions
OverviewNCBI Gene
No narrative summary is available for PLEKHA6 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
1048 residues, UniProt reviewed canonical sequence.
>Q9Y2H5|PLEKHA6
1 MSNKTGGKRP ATTNSDIPNH NMVSEVPPER PSVRATRTAR KAVAFGKRSH SMKRNPNAPV
61 TKAGWLFKQA SSGVKQWNKR WFVLVDRCLF YYKDEKEESI LGSIPLLSFR VAAVQPSDNI
121 SRKHTFKAEH AGVRTYFFSA ESPEEQEAWI QAMGEAARVQ IPPAQKSVPQ AVRHSHEKPD
181 SENVPPSKHH QQPPHNSLPK PEPEAKTRGE GDGRGCEKAE RRPERPEVKK EPPVKANGLP
241 AGPEPASEPG SPYPEGPRVP GGGEQPAQPN GWQYHSPSRP GSTAFPSQDG ETGGHRRSFP
301 PRTNPDKIAQ RKSSMNQLQQ WVNLRRGVPP PEDLRSPSRF YPVSRRVPEY YGPYSSQYPD
361 DYQYYPPGVR PESICSMPAY DRISPPWALE DKRHAFRNGG GPAYQLREWK EPASYGRQDA
421 TVWIPSPSRQ PVYYDELDAA SSSLRRLSLQ PRSHSVPRSP SQGSYSRARI YSPVRSPSAR
481 FERLPPRSED IYADPAAYVM RRSISSPKVP PYPEVFRDSL HTYKLNEQDT DKLLGKLCEQ
541 NKVVREQDRL VQQLRAEKES LESALMGTHQ ELEMFGSQPA YPEKLRHKKD SLQNQLINIR
601 VELSQATTAL TNSTIEYEHL ESEVSALHDD LWEQLNLDTQ NEVLNRQIQK EIWRIQDVME
661 GLRKNNPSRG TDTAKHRGGL GPSATYSSNS PASPLSSASL TSPLSPFSLV SGSQGSPTKP
721 GSNEPKANYE QSKKDPHQTL PLDTPRDISL VPTRQEVEAE KQAALNKVGV VPPRTKSPTD
781 DEVTPSAVVR RNASGLTNGL SSQERPKSAV FPGEGKVKMS VEEQIDRMRR HQSGSMREKR
841 RSLQLPASPA PDPSPRPAYK VVRRHRSIHE VDISNLEAAL RAEEPGGHAY ETPREEIARL
901 RKMELEPQHY DVDINKELST PDKVLIPERY IDLEPDTPLS PEELKEKQKK VERIKTLIAK
961 SSMQNVVPIG EGDSVDVPQD SESQLQEQEK RIEISCALAT EASRRGRMLS VQCATPSPPT
1021 SPASPAPPAN PLSSESPRGA DSSYTMRVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLEKHA6 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
- 0
- Mean surface accessibility (rSASA)
- 0.6
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- stomach: 38 nTPM
- cerebellum: 33 nTPM
- spinal cord: 32 nTPM
- colon: 30 nTPM
- pituitary gland: 30 nTPM
- cerebral cortex: 29 nTPM
Single-cell type
- proximal tubule cells: 565 nCPM
- esophageal apical cells: 281 nCPM
- retinal amacrine cells: 272 nCPM
- thyrotrophs: 220 nCPM
- retinal bipolar cells: 217 nCPM
- lactotrophs: 216 nCPM
Immune cell
- memory B-cell: 0.1 nTPM
- myeloid DC: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- thalamus: 114 nTPM
- cerebral cortex: 108 nTPM
- midbrain: 91 nTPM
- pons: 89 nTPM
- medulla oblongata: 88 nTPM
- white matter: 86 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)
- 0.42
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.71
- DepMap mean gene effect
- 0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PLEKHA6 as an antibody target. Whether an autoantibody or antibody against PLEKHA6 could matter depends on whether native PLEKHA6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLEKHA6 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 PLEKHA6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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