PLEKHH1
Pleckstrin homology domain-containing family H member 1
Also known as: KIAA1200, PKHH1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9ULM0
- Gene
- PLEKHH1
- Ensembl
- ENSG00000054690
- Chromosome
- 14
- Canonical length
- 1364 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Centrosome
OverviewNCBI Gene
Predicted to be located in cytoskeleton. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1364 residues, UniProt reviewed canonical sequence.
>Q9ULM0|PLEKHH1
1 MAELKVEAPA SVDWQKRCLT LETQLFRFRL QASKIRELLA DKMQELEQRL LEAEQRAENA
61 ETQVGVMEEK VKLSNLKNVD SEGSLHRKYQ ELLKAIKGKD ELISQLEAQL EKQKQMRAEE
121 AKTVQEKAAK IKEWVTLKLA KLEMENQHLK SHNQRLVEQV GSLQDALEAI QIAPSRKLLV
181 PPYGAAEQDS VPSEPGIQPM GQDSGSQAQG LKAAVLAPSP GALQSKDSVS EAASPLEDSS
241 SSTVHSGETV EAKPLQPHLG RESPPHQPCM KLLTFRCSSA SWGEGLVTAQ RGMLPGTKTS
301 AREGGPGSSL TLPKVRAPGT PRDSIQLAKR HHSQPQVGHG HFGRVVNIET EAFSALHPSG
361 LPELESRARS REEPEKMEME EPPPAGKNEE RESPKALGAE LEEVELGNKP PTPPLHQFSS
421 WESRIYAVAT SGMRLSDMSP RSNTACCASS PPALVSPGSF SGLVYKNVTV PVYTALKGRA
481 TQISNMPFMD ESSGSDDDCS SQASFRISVP SSESRKTSGL GSPRAIKRGV SMSSLSSEGD
541 YAIPPDACSL DSDYSEPEHK LQRTSSYSTD GLGLGGESLE KSGYLLKMGS QVKTWKRRWF
601 VLRQGQIMYY KSPSDVIRKP QGQVDLNSRC QIVRGEGSQT FQLISEKKTY YLTADSPSLL
661 EEWIRVLQSL LKVQATGPPA LLRGGTKPTV KGWLTKVKHG HSKVVWCALV GKIFYYYRSH
721 EDKRPLGCLP VRDAHIEEVD RSCDSDEDYE AGGTRRLLSS HCTLVIHPTE HSPTYLLIGT
781 KHEKDTWLYH LTVAAGGSSA KVGTAYEQLI GKLMDGEGDP DSPLWRHPML CYSKDGLYAS
841 LTTLPSEALQ TEALKLFKSC QLFINVPVEA ASVDYHVSLA QTALQVCLVH PELQSEIYCQ
901 LMKQTSCRPP QKYSLMQCWQ LLALCAPLFL PQHHFLWYVK QQLQRHADPR SETGQYATYC
961 QRAVERTLRT GEREARPSRM EVVSILLRNP FHHSLPFSIP VHFTNGTYHV VGFDGSSTVD
1021 EFLQRLNQEI GMRKPSHSGF ALFTDDPSGR DLEHCLQGSV KICDAISKWE QAMKELHPGK
1081 SEGGTRVVKL MYKNRLYFRS QVKGETDRER LLLASQTSRE IVAGRFPINK ELALEMAALM
1141 AQVEYGDLEK PALPGPGGTS PAKAQHLLQQ VLDRFHPRRY RHGAPAEQLR HLADMLTTKW
1201 ATLQGCSPPE CIRIYLTVAR KWPFFGAKLF AAQPAQLSSK ENALVWIAVN EDGVSILDHN
1261 TMQVHITYPY SSVTTFGGCR DDFMLVIRSI PDKSSGKSHI EKLIFRMAAP KIAEATFIMA
1321 SYMNHCTTTV NPPTNPPGAC QLWELDGRQF FSSVSCATKG PTLLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLEKHH1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.43
- Highest tissue expression
- 42 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 42 nTPM
- thyroid gland: 35 nTPM
- cerebral cortex: 24 nTPM
- salivary gland: 22 nTPM
- hippocampal formation: 18 nTPM
- midbrain: 17 nTPM
Single-cell type
- oligodendrocytes: 855 nCPM
- retinal pigment epithelial cells: 239 nCPM
- pituitary stem cells: 169 nCPM
- salivary acinar cells: 110 nCPM
- cone photoreceptor cells: 110 nCPM
- prostatic glandular cells: 101 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 351 nTPM
- medulla oblongata: 199 nTPM
- basal ganglia: 180 nTPM
- cerebral cortex: 160 nTPM
- midbrain: 157 nTPM
- thalamus: 156 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)
- 0.54
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.96
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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 PLEKHH1 as an antibody target. Whether an autoantibody or antibody against PLEKHH1 could matter depends on whether native PLEKHH1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLEKHH1 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 PLEKHH1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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