KRT9
Keratin, type I cytoskeletal 9
Also known as: CK-9, EPPK, K1C9_HUMAN, K9
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P35527
- Gene
- KRT9
- Ensembl
- ENSG00000171403
- Chromosome
- 17
- Canonical length
- 623 aa
- Protein class
- Disease related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes the type I keratin 9, an intermediate filament chain expressed only in the terminally differentiated epidermis of palms and soles. Mutations in this gene cause epidermolytic palmoplantar keratoderma. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
623 residues, UniProt reviewed canonical sequence.
>P35527|KRT9
1 MSCRQFSSSY LSRSGGGGGG GLGSGGSIRS SYSRFSSSGG GGGGGRFSSS SGYGGGSSRV
61 CGRGGGGSFG YSYGGGSGGG FSASSLGGGF GGGSRGFGGA SGGGYSSSGG FGGGFGGGSG
121 GGFGGGYGSG FGGFGGFGGG AGGGDGGILT ANEKSTMQEL NSRLASYLDK VQALEEANND
181 LENKIQDWYD KKGPAAIQKN YSPYYNTIDD LKDQIVDLTV GNNKTLLDID NTRMTLDDFR
241 IKFEMEQNLR QGVDADINGL RQVLDNLTME KSDLEMQYET LQEELMALKK NHKEEMSQLT
301 GQNSGDVNVE INVAPGKDLT KTLNDMRQEY EQLIAKNRKD IENQYETQIT QIEHEVSSSG
361 QEVQSSAKEV TQLRHGVQEL EIELQSQLSK KAALEKSLED TKNRYCGQLQ MIQEQISNLE
421 AQITDVRQEI ECQNQEYSLL LSIKMRLEKE IETYHNLLEG GQEDFESSGA GKIGLGGRGG
481 SGGSYGRGSR GGSGGSYGGG GSGGGYGGGS GSRGGSGGSY GGGSGSGGGS GGGYGGGSGG
541 GHSGGSGGGH SGGSGGNYGG GSGSGGGSGG GYGGGSGSRG GSGGSHGGGS GFGGESGGSY
601 GGGEEASGSG GGYGGGSGKS SHSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KRT9 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.62
- Highest tissue expression
- 11 nTPM
Expression across tissuesHPA
Tissue
- thymus: 11 nTPM
- skin: 2.3 nTPM
- adrenal gland: 0.5 nTPM
- vagina: 0.3 nTPM
- breast: 0.2 nTPM
- esophagus: 0.2 nTPM
Single-cell type
- adrenal medulla cells: 11 nCPM
- breast myoepithelial cells: 7.7 nCPM
- extravillous trophoblasts: 3.3 nCPM
- basal keratinocytes: 2.5 nCPM
- salivary myoepithelial cells: 1.9 nCPM
- ocular epithelial cells: 1 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
- spinal cord: 0.2 nTPM
- midbrain: 0.1 nTPM
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about KRT9.
Disease | AllUniProt
Conditions KRT9 is implicated in, by any mechanism.
- Palmoplantar keratoderma, epidermolytic, 1 (EPPK1) MIM:144200
Disease | GeneticClinVar
19 pathogenic / likely-pathogenic of 238 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Epidermolytic palmoplantar keratoderma, 1
- Palmoplantar keratoderma, epidermolytic
- Inborn genetic diseases
- Palmoplantar keratoderma
- Palmoplantar keratodermas
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)
- 0.92
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.2
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- epidermis development
- epithelial cell differentiation
- intermediate filament organization
- morphogenesis of an epithelium
- skin development
- spermatogenesis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads KRT9 as an antibody target. Whether an autoantibody or antibody against KRT9 could matter depends on whether native KRT9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KRT9 is annotated as secreted, so native KRT9 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label KRT9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...