Intracellular non-membrane-bounded organelle

Intracellular non-membrane-bounded organelle

• ACTG1: actin, gamma 1
• ALMS1: Alstrom syndrome 1
• ALS2: amyotrophic lateral sclerosis 2 (juvenile)
• ANG: angiogenin, ribonuclease, RNase A family, 5
• APC: adenomatous polyposis coli
• APTX: aprataxin
• ATRX: alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae)
• BLM: Bloom syndrome, RecQ helicase-like
• BRCA1: breast cancer 1, early onset
• BRCA2: breast cancer 2, early onset
• CACNA1C: calcium channel, voltage-dependent, L type, alpha 1C subunit
• CBS: cystathionine-beta-synthase
• CDH1: cadherin 1, type 1, E-cadherin (epithelial)
• CDH23: cadherin-like 23
• CLIP2: CAP-GLY domain containing linker protein 2
• DCTN1: dynactin 1 (p150, glued homolog, Drosophila)
• DCX: doublecortin
• DFNB31: deafness, autosomal recessive 31
• DMD: dystrophin
• EDA: ectodysplasin A
• ERCC6: excision repair cross-complementing rodent repair deficiency, complementation group 6
• FLNA: filamin A, alpha
• FMR1: fragile X mental retardation 1
• FTL: ferritin, light polypeptide
• G6PD: glucose-6-phosphate dehydrogenase
• GAN: gigaxonin
• GFAP: glial fibrillary acidic protein
• GLI3: GLI family zinc finger 3
• GNE: glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
• HBA2: hemoglobin, alpha 2
• HSPB1: heat shock 27kDa protein 1
• IKBKAP: inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
• KIF1B: kinesin family member 1B
• KRT14: keratin 14
• KRT16: keratin 16
• KRT17: keratin 17
• KRT5: keratin 5
• LITAF: lipopolysaccharide-induced TNF factor
• LYST: lysosomal trafficking regulator
• MED12: mediator complex subunit 12
• MEFV: Mediterranean fever
• MEN1: multiple endocrine neoplasia I
• MID1: midline 1 (Opitz/BBB syndrome)
• MYCN: v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian)
• MYH7: myosin, heavy chain 7, cardiac muscle, beta
• MYO1A: myosin IA
• MYO6: myosin VI
• NBN: nibrin
• NDRG1: N-myc downstream regulated 1
• NEFH: neurofilament, heavy polypeptide
• NEFL: neurofilament, light polypeptide
• NEFM: neurofilament, medium polypeptide
• NF2: neurofibromin 2 (merlin)
• NR0B1: nuclear receptor subfamily 0, group B, member 1
• PAFAH1B1: platelet-activating factor acetylhydrolase, isoform Ib, subunit 1 (45kDa)
• PAX2: paired box 2
• PCDH15: protocadherin 15
• PKD2: polycystic kidney disease 2 (autosomal dominant)
• PKHD1: polycystic kidney and hepatic disease 1 (autosomal recessive)
• PLA2G6: phospholipase A2, group VI (cytosolic, calcium-independent)
• PROC: protein C (inactivator of coagulation factors Va and VIIIa)
• PRPH: peripherin
• PSEN1: presenilin 1
• RAD50: RAD50 homolog (S. cerevisiae)
• RAD51: RAD51 homolog (RecA homolog, E. coli) (S. cerevisiae)
• RB1: retinoblastoma 1
• RPL11: ribosomal protein L11
• RPL5: ribosomal protein L5
• RPS17: ribosomal protein S17
• RPS19: ribosomal protein S19
• RPS24: ribosomal protein S24
• RPS7: ribosomal protein S7
• SBDS: Shwachman-Bodian-Diamond syndrome
• SEPT9: septin 9
• SERPINA1: serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1
• SIX1: SIX homeobox 1
• SMC1A: structural maintenance of chromosomes 1A
• SMC3: structural maintenance of chromosomes 3
• SNCAIP: synuclein, alpha interacting protein
• TCOF1: Treacher Collins-Franceschetti syndrome 1
• TP53: tumor protein p53
• TRIOBP: TRIO and F-actin binding protein
• TSC1: tuberous sclerosis 1
• TTN: titin
• USH1C: Usher syndrome 1C (autosomal recessive, severe)
• USH1G: Usher syndrome 1G (autosomal recessive)
• VWF: von Willebrand factor
• WAS: Wiskott-Aldrich syndrome (eczema-thrombocytopenia)
• WRN: Werner syndrome, RecQ helicase-like

Source: Gene Ontology Consortium (June 2009).