Anatomical structure formation involved in morphogenesis
- ACTA1: actin, alpha 1, skeletal muscle
- ACVRL1: activin A receptor type II-like 1
- ANG: angiogenin, ribonuclease, RNase A family, 5
- ATP7A: ATPase, Cu++ transporting, alpha polypeptide
- BBS1: Bardet-Biedl syndrome 1
- BBS10: Bardet-Biedl syndrome 10
- BMPR1A: bone morphogenetic protein receptor, type IA
- BMPR2: bone morphogenetic protein receptor, type II (serine/threonine kinase)
- CAPN3: calpain 3, (p94)
- CAV3: caveolin 3
- CCM2: cerebral cavernous malformation 2
- CDC73: cell division cycle 73
- CEP290: centrosomal protein 290kDa
- COL4A3: collagen, type IV, alpha 3 (Goodpasture antigen)
- CTNNB1: catenin (cadherin-associated protein), beta 1, 88kDa
- CUL7: cullin 7
- DICER1: dicer 1, ribonuclease type III
- EGLN1: egl nine homolog 1 (C. elegans)
- ENG: endoglin
- ERAP1: endoplasmic reticulum aminopeptidase 1
- ERBB2: v-erb-b2 erythroblastic leukemia viral oncogene homolog 2, neuro/glioblastoma derived oncogene homolog (avian)
- FBN2: fibrillin 2
- FGFR2: fibroblast growth factor receptor 2
- FLNA: filamin A, alpha
- FLT4: fms-related tyrosine kinase 4
- FOXC1: forkhead box C1
- FOXC2: forkhead box C2 (MFH-1, mesenchyme forkhead 1)
- FOXG1: forkhead box G1
- FZD4: frizzled family receptor 4
- GATA1: GATA binding protein 1 (globin transcription factor 1)
- GTF2I: general transcription factor IIi
- HSPB1: heat shock 27kDa protein 1
- IL1A: interleukin 1, alpha
- JAG1: jagged 1
- KRIT1: KRIT1, ankyrin repeat containing
- KRT1: keratin 1
- MKKS: McKusick-Kaufman syndrome
- MYH9: myosin, heavy chain 9, non-muscle
- NF1: neurofibromin 1
- NTRK1: neurotrophic tyrosine kinase, receptor, type 1
- OCRL: oculocerebrorenal syndrome of Lowe
- OTX2: orthodenticle homeobox 2
- PAFAH1B1: platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
- PAX2: paired box 2
- PAX8: paired box 8
- PCNT: pericentrin
- PDGFRA: platelet-derived growth factor receptor, alpha polypeptide
- PDGFRB: platelet-derived growth factor receptor, beta polypeptide
- PKHD1: polycystic kidney and hepatic disease 1 (autosomal recessive)
- PML: promyelocytic leukemia
- PRICKLE1: prickle homolog 1 (Drosophila)
- PROK2: prokineticin 2
- RASA1: RAS p21 protein activator (GTPase activating protein) 1
- RPGR: retinitis pigmentosa GTPase regulator
- SALL1: sal-like 1 (Drosophila)
- SHH: sonic hedgehog
- SIX1: SIX homeobox 1
- SKI: v-ski sarcoma viral oncogene homolog (avian)
- SLC12A6: solute carrier family 12 (potassium/chloride transporters), member 6
- SNAI2: snail homolog 2 (Drosophila)
- SOX2: SRY (sex determining region Y)-box 2
- SOX9: SRY (sex determining region Y)-box 9
- T: T, brachyury homolog (mouse)
- TBX1: T-box 1
- TBX5: T-box 5
- TEK: TEK tyrosine kinase, endothelial
- TFAP2A: transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
- TFAP2B: transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
- TGFBI: transforming growth factor, beta-induced, 68kDa
- TGFBR2: transforming growth factor, beta receptor II (70/80kDa)
- TNNI3: troponin I type 3 (cardiac)
- TSC2: tuberous sclerosis 2
- TTN: titin
- TWIST1: twist basic helix-loop-helix transcription factor 1
- WNT3: wingless-type MMTV integration site family, member 3
- WT1: Wilms tumor 1
Source: Gene Ontology Consortium
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