KRTAP10-9

gene
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Also known as KAP10.9KAP18.9

Summary

KRTAP10-9 (keratin associated protein 10-9, HGNC:22971) is a protein-coding gene on chromosome 21q22.3, encoding Keratin-associated protein 10-9 (P60411). In the hair cortex, hair keratin intermediate filaments are embedded in an interfilamentous matrix, consisting of hair keratin-associated proteins (KRTAP), which are essential for the formation of a rigid and resistant hair shaft through their extensive disulfide bond cross-link…. It is a selective cancer dependency (DepMap: 34.1% of cell lines).

Predicted to be located in cytosol.

Source: NCBI Gene 386676 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 95 total
  • Cancer dependency (DepMap): dependent in 34.1% of screened cell lines
  • MANE Select transcript: NM_198690

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:22971
Approved symbolKRTAP10-9
Namekeratin associated protein 10-9
Location21q22.3
Locus typegene with protein product
StatusApproved
AliasesKAP10.9, KAP18.9
Ensembl geneENSG00000221837
Ensembl biotypeprotein_coding
Entrez386676

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 1 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000397911, ENST00000484861

RefSeq mRNA: 1 — MANE Select: NM_198690 NM_198690

CCDS: CCDS42961

Canonical transcript exons

ENST00000397911 — 1 exons

ExonStartEnd
ENSE000015306984462709344628378

Expression profiles

Bgee: expression breadth tissue_specific, 7 present calls, max score 37.20.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0190 / max 20.3556, expressed in 3 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1894930.01903

Top tissues by expression

116 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
colonic epitheliumUBERON:000039737.20gold quality
sural nerveUBERON:001548837.04gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
ganglionic eminenceUBERON:000402335.49gold quality
skeletal muscle tissueUBERON:000113433.38gold quality
skin of abdomenUBERON:000141632.99gold quality
zone of skinUBERON:000001432.27gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
bone marrowUBERON:000237131.74gold quality
skin of legUBERON:000151131.58gold quality
muscle tissueUBERON:000238531.06gold quality
liverUBERON:000210730.03gold quality
stromal cell of endometriumCL:000225529.87gold quality
monocyteCL:000057629.47gold quality
leukocyteCL:000073829.30gold quality
prefrontal cortexUBERON:000045129.25gold quality
urinary bladderUBERON:000125528.75gold quality
duodenumUBERON:000211428.14gold quality
lymph nodeUBERON:000002927.57gold quality
right lobe of liverUBERON:000111427.50gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.55gold quality
muscle of legUBERON:000138326.45gold quality
vermiform appendixUBERON:000115426.42gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
gastrocnemiusUBERON:000138825.58gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.20

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

14 targeting KRTAP10-9, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-185-3P99.9567.011743
HSA-MIR-449299.8768.253611
HSA-MIR-6756-5P99.8267.972466
HSA-MIR-76299.5866.611994
HSA-MIR-1207-5P99.4969.112983
HSA-MIR-444199.4966.563216
HSA-MIR-449899.4767.422360
HSA-MIR-450599.2767.812678
HSA-MIR-578799.2267.862628
HSA-MIR-6799-5P99.1465.722093
HSA-MIR-7160-5P99.1167.172207
HSA-MIR-5001-5P99.0566.761972
HSA-MIR-444897.0466.22752
HSA-MIR-390796.7665.04662

Functional genomics

DepMap (CRISPR cell-line fitness): dependent in 34.1% of screened cell lines.

Cross-species orthologs

36 orthologs

OrganismSymbolGene ID
mus_musculusKrtap5-2ENSMUSG00000054759
mus_musculusKrtap5-20ENSMUSG00000056885
mus_musculusKrtap10-4ENSMUSG00000069582
mus_musculusKrtap12-1ENSMUSG00000069583
mus_musculusKrtap12-23ENSMUSG00000069584
mus_musculusKrtap10-31ENSMUSG00000071195
mus_musculusKrtap12-22ENSMUSG00000094012
mus_musculusKrtap10-21ENSMUSG00000094120
mus_musculusKrtap12-21ENSMUSG00000094146
mus_musculusKrtap10-27ENSMUSG00000094913
mus_musculusKrtap10-26ENSMUSG00000095593
mus_musculusKrtap10-25ENSMUSG00000095721
mus_musculusKrtap10-22ENSMUSG00000095817
mus_musculusKrtap10-33ENSMUSG00000095970
mus_musculusKrtap10-29ENSMUSG00000096131
mus_musculusKrtap10-34ENSMUSG00000096380
mus_musculusKrtap12-20ENSMUSG00000096421
mus_musculusKrtap10-23ENSMUSG00000096481
mus_musculusKrtap5-26ENSMUSG00000109859
mus_musculusKrtap5-24ENSMUSG00000110324
mus_musculusKrtap10-24ENSMUSG00000111915
mus_musculusKrtap10-28ENSMUSG00000112170
mus_musculusKrtap10-10ENSMUSG00000112223
mus_musculusKrtap10-30ENSMUSG00000112380
mus_musculusGm49918ENSMUSG00000112600
mus_musculusKrtap10-35ENSMUSG00000112653
mus_musculusKrtap10-32ENSMUSG00000112864
rattus_norvegicusKrtap10-8l1ENSRNOG00000001218
rattus_norvegicusKrtap5-8ENSRNOG00000020131
rattus_norvegicusKrtap10-10ENSRNOG00000032530
rattus_norvegicusKrtap10-9ENSRNOG00000043302
rattus_norvegicusKrtap10-1l1ENSRNOG00000046538
rattus_norvegicusAABR07006049.1ENSRNOG00000046649
rattus_norvegicusKrtap10-1ENSRNOG00000047532
rattus_norvegicusLOC120098854ENSRNOG00000067436
rattus_norvegicusKrtap10-10l2ENSRNOG00000069553

Paralogs (47): KRTAP4-4 (ENSG00000171396), KRTAP9-7 (ENSG00000180386), KRTAP5-5 (ENSG00000185940), KRTAP12-1 (ENSG00000187175), KRTAP9-8 (ENSG00000187272), KRTAP10-8 (ENSG00000187766), KRTAP10-6 (ENSG00000188155), KRTAP1-1 (ENSG00000188581), KRTAP10-12 (ENSG00000189169), KRTAP4-3 (ENSG00000196156), KRTAP9-9 (ENSG00000198083), KRTAP4-6 (ENSG00000198090), KRTAP4-5 (ENSG00000198271), KRTAP4-1 (ENSG00000198443), KRTAP9-3 (ENSG00000204873), KRTAP4-8 (ENSG00000204880), KRTAP1-4 (ENSG00000204887), KRTAP12-3 (ENSG00000205439), KRTAP10-2 (ENSG00000205445), KRTAP5-6 (ENSG00000205864), KRTAP5-2 (ENSG00000205867), KRTAP16-1 (ENSG00000212657), KRTAP9-6 (ENSG00000212659), KRTAP4-11 (ENSG00000212721), KRTAP4-9 (ENSG00000212722), KRTAP2-3 (ENSG00000212724), KRTAP2-1 (ENSG00000212725), KRTAP10-3 (ENSG00000212935), KRTAP4-12 (ENSG00000213416), KRTAP2-4 (ENSG00000213417), KRTAP2-2 (ENSG00000214518), KRTAP10-4 (ENSG00000215454), KRTAP10-1 (ENSG00000215455), KRTAP1-5 (ENSG00000221852), KRTAP10-10 (ENSG00000221859), KRTAP12-2 (ENSG00000221864), KRTAP1-3 (ENSG00000221880), KRTAP9-2 (ENSG00000239886), KRTAP9-1 (ENSG00000240542), KRTAP4-7 (ENSG00000240871)

Protein

Protein identifiers

Keratin-associated protein 10-9P60411 (reviewed: P60411)

Alternative names: High sulfur keratin-associated protein 10.9, Keratin-associated protein 10.9, Keratin-associated protein 18-9, Keratin-associated protein 18.9

All UniProt accessions (1): P60411

UniProt curated annotations — full annotation on UniProt →

Function. In the hair cortex, hair keratin intermediate filaments are embedded in an interfilamentous matrix, consisting of hair keratin-associated proteins (KRTAP), which are essential for the formation of a rigid and resistant hair shaft through their extensive disulfide bond cross-linking with abundant cysteine residues of hair keratins. The matrix proteins include the high-sulfur and high-glycine-tyrosine keratins.

Subunit / interactions. Interacts with hair keratins.

Tissue specificity. Restricted to a narrow region of the hair fiber cuticle, lying approximately 20 cell layers above the apex of the dermal papilla of the hair root; not detected in any other tissues.

Similarity. Belongs to the KRTAP type 10 family.

Isoforms (1)

UniProt IDNamesCanonical?
P60411-11yes

RefSeq proteins (1): NP_941963* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR002494KAPFamily

Pfam: PF13885

UniProt features (30 total): repeat 25, sequence variant 2, chain 1, region of interest 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P60411-F137.450.00

Function

Pathways and Gene Ontology

Reactome pathways

2 pathways

IDPathway
R-HSA-6805567Keratinization
R-HSA-1266738Developmental Biology

MSigDB gene sets: 9 (showing top): chr21q22, GOCC_INTERMEDIATE_FILAMENT_CYTOSKELETON, GOCC_KERATIN_FILAMENT, GOCC_SUPRAMOLECULAR_COMPLEX, GOCC_POLYMERIC_CYTOSKELETAL_FIBER, REACTOME_KERATINIZATION, GOCC_SUPRAMOLECULAR_POLYMER, WP_VITAMIN_D_RECEPTOR_PATHWAY, GSE40685_NAIVE_CD4_TCELL_VS_FOXP3_KO_TREG_PRECURSOR_DN

GO Biological Process (0):

GO Molecular Function (1): protein binding (GO:0005515)

GO Cellular Component (3): cytosol (GO:0005829), keratin filament (GO:0045095), intermediate filament (GO:0005882)

Reactome top-level categories

Rollup of top-1 pathways:

CategoryPathways
Developmental Biology1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
binding1
cytoplasm1
cellular anatomical structure1
intermediate filament1
intermediate filament cytoskeleton1
polymeric cytoskeletal fiber1

Protein interactions and networks

STRING

212 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
KRTAP10-9OR1E1P30953573
KRTAP10-9KRTAP2-3P0C7H8506
KRTAP10-9KRT38O76015481
KRTAP10-9PRB3Q04118471
KRTAP10-9KRT26Q7Z3Y9447
KRTAP10-9IGFL1Q6UW32447
KRTAP10-9KRTAP1-1Q07627432
KRTAP10-9SAGE1Q9NXZ1371
KRTAP10-9FBN3Q75N90370
KRTAP10-9AGR3Q8TD06370
KRTAP10-9A0A087WZY1A0A087WZY1370
KRTAP10-9PRH1P02810358
KRTAP10-9HTN3P15516327
KRTAP10-9CLRN2A0PK11311
KRTAP10-9RTL1A6NKG5300

IntAct

900 interactions, top by confidence:

ABTypeScore
KRTAP10-9LCE1Bpsi-mi:“MI:0915”(physical association)0.780
OTX1KRTAP10-9psi-mi:“MI:0915”(physical association)0.740
KRTAP10-9KRTAP9-2psi-mi:“MI:0915”(physical association)0.740
KRTAP10-9LCE3Epsi-mi:“MI:0915”(physical association)0.740
KRTAP9-2KRTAP10-9psi-mi:“MI:0915”(physical association)0.740
NUFIP2KRTAP10-9psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9PRPF31psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9SPRY1psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9PRKAB2psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9FARS2psi-mi:“MI:0915”(physical association)0.720
KRTAP5-9KRTAP10-9psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9HPCAL1psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9HOXA1psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9SMCPpsi-mi:“MI:0915”(physical association)0.720
KRTAP10-9KRTAP12-1psi-mi:“MI:0915”(physical association)0.720
CXCL16KRTAP10-9psi-mi:“MI:0915”(physical association)0.720
GLRX3KRTAP10-9psi-mi:“MI:0915”(physical association)0.720
HOXA1KRTAP10-9psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9KRTAP10-7psi-mi:“MI:0915”(physical association)0.720
KRTAP10-8KRTAP10-9psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9CREB5psi-mi:“MI:0915”(physical association)0.720
ADAMTSL4KRTAP10-9psi-mi:“MI:0915”(physical association)0.720
CATSPER1KRTAP10-9psi-mi:“MI:0915”(physical association)0.720
MOBPKRTAP10-9psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9ZNF124psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9ZNF792psi-mi:“MI:0915”(physical association)0.720
KRTAP10-9LCE3Cpsi-mi:“MI:0915”(physical association)0.720
KRTAP10-9LCE4Apsi-mi:“MI:0915”(physical association)0.720

BioGRID (364): KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-11 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid), KRTAP10-9 (Two-hybrid)

ESM2 similar proteins: A5A6P5, A6QP35, A8MTY7, A8MVA2, A8MXZ3, O75690, P02438, P02441, P02442, P02443, P08131, P0C7H8, P26371, P59990, P59991, P60014, P60331, P60368, P60369, P60370, P60371, P60372, P60409, P60410, P60411, P60412, P60413, Q05B44, Q07627, Q3V2C1, Q6L8G4, Q6L8G8, Q6L8G9, Q6L8H2, Q701N4, Q8IUG1, Q9BQ66, Q9BYP9, Q9BYQ0, Q9BYQ2

Diamond homologs: P60014, P60331, P60368, P60369, P60370, P60371, P60409, P60411, P60412, P60413, P60372, A6QP35, P60410

SIGNOR signaling

0 interactions.

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 155 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.

Reactome pathways:

PathwayPartnersFoldFDR
Keratinization1810.9×1e-11
Formation of the cornified envelope87.6×7e-04

GO biological processes:

GO termPartnersFoldFDR
keratinization712.8×4e-04

Disease & clinical

Clinical variants and AI predictions

ClinVar

95 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance85
Likely benign10
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

424 predictions. Top by Δscore:

VariantEffectΔscore
21:44627319:G:GGdonor_gain0.8300
21:44627318:A:AGdonor_gain0.8200
21:44627228:G:GAdonor_gain0.7500
21:44627248:GCT:Gdonor_gain0.7500
21:44627227:T:TAdonor_gain0.7400
21:44627223:C:Tdonor_gain0.7000
21:44627251:G:GGdonor_gain0.6800
21:44627454:T:TAacceptor_gain0.6400
21:44627459:GCA:Gacceptor_gain0.6400
21:44627877:C:Aacceptor_gain0.6400
21:44628221:C:CAacceptor_gain0.6300
21:44628222:G:Aacceptor_gain0.6300
21:44627309:C:Adonor_gain0.6100
21:44628007:C:Aacceptor_gain0.6100
21:44627731:GCT:Gdonor_gain0.6000
21:44627734:G:GGdonor_gain0.5700
21:44627951:C:Gdonor_gain0.5500
21:44627380:G:GTdonor_gain0.5400
21:44627988:C:Aacceptor_gain0.5400
21:44627322:AGCC:Adonor_gain0.5300
21:44627323:GCCG:Gdonor_gain0.5300
21:44628013:G:GAacceptor_gain0.5300
21:44628222:GGGCA:Gacceptor_loss0.5200
21:44628223:GGCA:Gacceptor_loss0.5200
21:44628224:GCA:Gacceptor_loss0.5200
21:44628225:CAGGC:Cacceptor_loss0.5200
21:44628227:GGCGA:Gacceptor_gain0.5200
21:44627305:T:Adonor_gain0.5100
21:44627352:ACCT:Adonor_gain0.5000
21:44627458:A:AGacceptor_gain0.5000

AlphaMissense

1884 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
21:44627388:A:CS73R0.580
21:44627390:C:AS73R0.580
21:44627390:C:GS73R0.580
21:44627244:A:CS25R0.576
21:44627246:C:AS25R0.576
21:44627246:C:GS25R0.576

dbSNP variants (sampled 300 via entrez): RS1000201871 (21:44625788 G>A,T), RS1000651982 (21:44626035 G>C), RS1001535565 (21:44626367 T>C), RS1001565038 (21:44626517 G>A), RS1004776220 (21:44625468 G>C), RS1006218280 (21:44626944 G>A), RS1006417872 (21:44626425 C>A,G), RS1015094803 (21:44626729 G>A), RS1015484329 (21:44626433 G>A), RS1018759327 (21:44625320 C>T), RS1019203558 (21:44625485 T>C), RS1028766542 (21:44625764 T>A), RS1030432035 (21:44626994 T>C), RS1033130308 (21:44626042 A>G), RS1034522482 (21:44626117 G>A)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

2 total (human), top 2 by PubMed support.

ChemicalActions (top 5)PubMed papers
CGP 52608affects binding, increases reaction1
Benzo(a)pyreneaffects methylation1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.