Anatomical structure morphogenesis

Anatomical structure morphogenesis

• ACVRL1: activin A receptor type II-like 1
• ALS2: amyotrophic lateral sclerosis 2 (juvenile)
• AMELX: amelogenin (amelogenesis imperfecta 1, X-linked)
• ANG: angiogenin, ribonuclease, RNase A family, 5
• APOE: apolipoprotein E
• ATP7A: ATPase, Cu++ transporting, alpha polypeptide
• BCOR: BCL6 co-repressor
• BMPR2: bone morphogenetic protein receptor, type II (serine/threonine kinase)
• BRAF: v-raf murine sarcoma viral oncogene homolog B1
• CCM2: cerebral cavernous malformation 2
• CHRNB2: cholinergic receptor, nicotinic, beta 2 (neuronal)
• COL1A1: collagen, type I, alpha 1
• COL1A2: collagen, type I, alpha 2
• COL2A1: collagen, type II, alpha 1
• COL4A3: collagen, type IV, alpha 3 (Goodpasture antigen)
• COL5A1: collagen, type V, alpha 1
• COL5A2: collagen, type V, alpha 2
• COL9A1: collagen, type IX, alpha 1
• COMP: cartilage oligomeric matrix protein
• CUL7: cullin 7
• DCN: decorin
• ELN: elastin
• ENAM: enamelin
• ENG: endoglin
• ERBB2: v-erb-b2 erythroblastic leukemia viral oncogene homolog 2, neuro/glioblastoma derived oncogene homolog (avian)
• EYA1: eyes absent homolog 1 (Drosophila)
• EYA4: eyes absent homolog 4 (Drosophila)
• FBN2: fibrillin 2
• FGD1: FYVE, RhoGEF and PH domain containing 1
• FOXC2: forkhead box C2 (MFH-1, mesenchyme forkhead 1)
• GAA: glucosidase, alpha; acid
• GPC3: glypican 3
• HCCS: holocytochrome c synthase (cytochrome c heme-lyase)
• HRAS: v-Ha-ras Harvey rat sarcoma viral oncogene homolog
• HTT: huntingtin
• JAG1: jagged 1 (Alagille syndrome)
• KAL1: Kallmann syndrome 1 sequence
• MFN2: mitofusin 2
• MKKS: McKusick-Kaufman syndrome
• MMP20: matrix metallopeptidase 20
• MYH7: myosin, heavy chain 7, cardiac muscle, beta
• MYOC: myocilin, trabecular meshwork inducible glucocorticoid response
• NF1: neurofibromin 1
• NOTCH2: Notch homolog 2 (Drosophila)
• OPA1: optic atrophy 1 (autosomal dominant)
• PAFAH1B1: platelet-activating factor acetylhydrolase, isoform Ib, subunit 1 (45kDa)
• PAX2: paired box 2
• PAX3: paired box 3
• PAX6: paired box 6
• PAX8: paired box 8
• PKD1: polycystic kidney disease 1 (autosomal dominant)
• PKD2: polycystic kidney disease 2 (autosomal dominant)
• PROK2: prokineticin 2
• PTCH1: patched homolog 1 (Drosophila)
• ROBO3: roundabout, axon guidance receptor, homolog 3 (Drosophila)
• SALL1: sal-like 1 (Drosophila)
• SLC40A1: solute carrier family 40 (iron-regulated transporter), member 1
• SOD1: superoxide dismutase 1, soluble
• TBX1: T-box 1
• TBX5: T-box 5
• TGFB1: transforming growth factor, beta 1
• TGFBR2: transforming growth factor, beta receptor II (70/80kDa)
• TH: tyrosine hydroxylase
• TSC2: tuberous sclerosis 2
• TSHB: thyroid stimulating hormone, beta
• TTN: titin
• TWIST1: twist homolog 1 (Drosophila)
• VHL: von Hippel-Lindau tumor suppressor
• WHSC1: Wolf-Hirschhorn syndrome candidate 1

Source: Gene Ontology Consortium (June 2009).