microvillus Gene Set

Dataset COMPARTMENTS Curated Protein Localization Evidence Scores
Category structural or functional annotations
Type cellular component
Description Thin cylindrical membrane-covered projections on the surface of an animal cell containing a core bundle of actin filaments. Present in especially large numbers on the absorptive surface of intestinal cells. (Gene Ontology, GO_0005902)
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Genes

71 proteins localized to the microvillus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

Symbol Name Standardized Value
ITGAV integrin, alpha V 0.663342
GIF gastric intrinsic factor (vitamin B synthesis) 0.663342
MYO1A myosin IA 0.663342
VIL1 villin 1 0.663342
ANGPT1 angiopoietin 1 0.663342
CLIC4 chloride intracellular channel 4 0.663342
TEK TEK tyrosine kinase, endothelial 0.663342
CLRN1 clarin 1 0.663342
TBC1D10A TBC1 domain family, member 10A 0.663342
S100P S100 calcium binding protein P 0.663342
SLC9A3R1 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1 0.663342
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) 0.663342
ENPP7 ectonucleotide pyrophosphatase/phosphodiesterase 7 0.663342
AOC3 amine oxidase, copper containing 3 0.663342
KPTN kaptin (actin binding protein) 0.663342
DPEP1 dipeptidase 1 (renal) 0.663342
MYO1C myosin IC 0.663342
TSPEAR thrombospondin-type laminin G domain and EAR repeats 0.237908
PDGFA platelet-derived growth factor alpha polypeptide 0.237908
ATP6V1B1 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1 0.237908
TPRN taperin 0.237908
EPS8 epidermal growth factor receptor pathway substrate 8 0.237908
DFNB31 deafness, autosomal recessive 31 0.237908
MSN moesin 0.237908
USH1C Usher syndrome 1C (autosomal recessive, severe) 0.237908
GRXCR1 glutaredoxin, cysteine rich 1 0.237908
EZR ezrin 0.237908
LOXHD1 lipoxygenase homology domains 1 0.237908
HYAL2 hyaluronoglucosaminidase 2 0.237908
PODXL podocalyxin-like 0.237908
VCAM1 vascular cell adhesion molecule 1 0.237908
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa 0.098109
USH2A Usher syndrome 2A (autosomal recessive, mild) 0.098109
CDH23 cadherin-related 23 0.098109
DOCK4 dedicator of cytokinesis 4 0.098109
PCDH15 protocadherin-related 15 0.098109
PROM2 prominin 2 0.098109
TWF2 twinfilin actin binding protein 2 0.098109
CNP 2',3'-cyclic nucleotide 3' phosphodiesterase 0.03318
CRB1 crumbs family member 1, photoreceptor morphogenesis associated 0.03318
PROM1 prominin 1 0.03318
FOXA1 forkhead box A1 0.03318
MYO7A myosin VIIA 0.03318
ATP6V1A ATPase, H+ transporting, lysosomal 70kDa, V1 subunit A 0.03318
IQGAP2 IQ motif containing GTPase activating protein 2 0.03318
MYO6 myosin VI 0.03318
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) 0.03318
ATP6V1B2 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2 0.03318
RDX radixin 0.03318
SCARB1 scavenger receptor class B, member 1 0.03318
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10 0.03318
STARD10 StAR-related lipid transfer (START) domain containing 10 0.03318
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4 0.03318
PDGFRA platelet-derived growth factor receptor, alpha polypeptide 0.03318
CLIC5 chloride intracellular channel 5 0.03318
AQP5 aquaporin 5 0.03318
ATP6V1E1 ATPase, H+ transporting, lysosomal 31kDa, V1 subunit E1 0.03318
MYO15A myosin XVA 0.03318
CTSV cathepsin V 0.03318
CLCA1 chloride channel accessory 1 0.03318
SLC10A2 solute carrier family 10 (sodium/bile acid cotransporter), member 2 0.03318
MTTP microsomal triglyceride transfer protein 0.03318
SLC34A2 solute carrier family 34 (type II sodium/phosphate cotransporter), member 2 0.03318
ESPN espin 0.03318
FMN2 formin 2 0.03318
CA2 carbonic anhydrase II 0.03318
OXTR oxytocin receptor 0.03318
FSCN2 fascin actin-bundling protein 2, retinal 0.03318
ATP8B1 ATPase, aminophospholipid transporter, class I, type 8B, member 1 0.03318
PDZK1 PDZ domain containing 1 0.03318
DCXR dicarbonyl/L-xylulose reductase 0.03318