Skip Navigation
Genetics Home Reference: your guide to understanding genetic conditions About   Site Map   Contact Us
 
Home A service of the U.S. National Library of Medicine®

Establishment of protein localization

Establishment of protein localization

  • ABCA1: ATP-binding cassette, sub-family A (ABC1), member 1
  • AGXT: alanine-glyoxylate aminotransferase
  • AKT1: v-akt murine thymoma viral oncogene homolog 1
  • ANG: angiogenin, ribonuclease, RNase A family, 5
  • ANK1: ankyrin 1, erythrocytic
  • APOA1: apolipoprotein A-I
  • AR: androgen receptor
  • ATP6V0A2: ATPase, H+ transporting, lysosomal V0 subunit a2
  • BARD1: BRCA1 associated RING domain 1
  • BBS1: Bardet-Biedl syndrome 1
  • BMPR1A: bone morphogenetic protein receptor, type IA
  • CDH1: cadherin 1, type 1, E-cadherin (epithelial)
  • CEP290: centrosomal protein 290kDa
  • CSF1R: colony stimulating factor 1 receptor
  • CTSA: cathepsin A
  • CYLD: cylindromatosis (turban tumor syndrome)
  • DNAJC19: DnaJ (Hsp40) homolog, subfamily C, member 19
  • DNM2: dynamin 2
  • DRD3: dopamine receptor D3
  • EGR2: early growth response 2
  • EMD: emerin
  • FLNA: filamin A, alpha
  • FOXP3: forkhead box P3
  • GDAP1: ganglioside induced differentiation associated protein 1
  • HTT: huntingtin
  • IL1A: interleukin 1, alpha
  • INS: insulin
  • JAK2: Janus kinase 2
  • LDLRAP1: low density lipoprotein receptor adaptor protein 1
  • MCOLN1: mucolipin 1
  • MFN2: mitofusin 2
  • MYH9: myosin, heavy chain 9, non-muscle
  • MYO6: myosin VI
  • NCF1: neutrophil cytosolic factor 1
  • NF1: neurofibromin 1
  • NLRP1: NLR family, pyrin domain containing 1
  • NLRP12: NLR family, pyrin domain containing 12
  • NLRP3: NLR family, pyrin domain containing 3
  • NOD2: nucleotide-binding oligomerization domain containing 2
  • PEX1: peroxisomal biogenesis factor 1
  • PEX7: peroxisomal biogenesis factor 7
  • PKD1: polycystic kidney disease 1 (autosomal dominant)
  • PKD2: polycystic kidney disease 2 (autosomal dominant)
  • PML: promyelocytic leukemia
  • PNP: purine nucleoside phosphorylase
  • PPT1: palmitoyl-protein thioesterase 1
  • PRICKLE1: prickle homolog 1 (Drosophila)
  • PTCH1: patched 1
  • RAB23: RAB23, member RAS oncogene family
  • RAB7A: RAB7A, member RAS oncogene family
  • RPGR: retinitis pigmentosa GTPase regulator
  • RPL11: ribosomal protein L11
  • RPL35A: ribosomal protein L35a
  • RPL5: ribosomal protein L5
  • RPS10: ribosomal protein S10
  • RPS17: ribosomal protein S17
  • RPS19: ribosomal protein S19
  • RPS24: ribosomal protein S24
  • RPS26: ribosomal protein S26
  • RPS7: ribosomal protein S7
  • RYR2: ryanodine receptor 2 (cardiac)
  • SAA1: serum amyloid A1
  • SIL1: SIL1 homolog, endoplasmic reticulum chaperone (S. cerevisiae)
  • SMAD3: SMAD family member 3
  • SMAD4: SMAD family member 4
  • SNAI2: snail homolog 2 (Drosophila)
  • STAT3: signal transducer and activator of transcription 3 (acute-phase response factor)
  • TCIRG1: T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
  • TGFB1: transforming growth factor, beta 1
  • TGFBR1: transforming growth factor, beta receptor 1
  • TIMM8A: translocase of inner mitochondrial membrane 8 homolog A (yeast)
  • TRPS1: trichorhinophalangeal syndrome I
  • TSC2: tuberous sclerosis 2
  • TWIST1: twist basic helix-loop-helix transcription factor 1
  • VCP: valosin containing protein
  • VLDLR: very low density lipoprotein receptor
  • WFS1: Wolfram syndrome 1 (wolframin)
  • WNT4: wingless-type MMTV integration site family, member 4
  • YWHAE: tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide

Source: Gene Ontology ConsortiumThis link leads to a site outside Genetics Home Reference..

 
Published: May 20, 2013