about
ErythropoietinMyosin, heavy polypeptide 7, cardiac muscle, betaBone morphogenetic protein 10SMAD family member 7Transforming growth factor, beta 1Erythropoietin receptorForkhead box C2Transforming growth factor, beta receptor IIIFibroblast growth factor receptor 2Transforming growth factor beta 1Troponin T2, cardiac typeTropomyosin 1Troponin I3, cardiac typeFKBP prolyl isomerase 1AHeart and neural crest derivatives expressed 1Prospero homeobox 1ISL LIM homeobox 1Forkhead box C1Retinoid X receptor alphaTroponin I1, slow skeletal typeMyosin light chain 3Myosin heavy chain 6Myosin light chain 2Myosin binding protein C3Troponin C1, slow skeletal and cardiac typeCollagen type XI alpha 1 chainPentatricopeptide repeat domain 2Tropomyosin 1 (Alpha) isoform 4Pentatricopeptide repeat domain 2, isoform CRA_aMyosin-binding protein C, cardiac-typeHeart and neural crest derivatives expressed 1Myosin, light polypeptide 2, regulatory, cardiac, slowFK506 binding protein 1aRetinoid X receptor alphaCollagen, type XI, alpha 1Forkhead box C1ISL1 transcription factor, LIM/homeodomainMyosin, light polypeptide 3Myosin, heavy polypeptide 6, cardiac muscle, alphaLymphocyte antigen 6 complex, locus E
P682
Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderlyPrevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathyAlpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathyA loss-of-function mutation in the binding domain of HAND1 predicts hypoplasia of the human heartsMutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscleSingle-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study
P921
Q14852044-A18426BD-4436-4C6B-9233-C27374BE6047Q14876111-77817979-5DE4-4889-BE04-1F231F293299Q14903594-F7D60EFA-161C-42A1-846C-216B372B2720Q14904377-0943CBBD-05D4-401E-AB98-0F432BAF3045Q14904616-985819F5-DAB3-4FF2-A5D4-63CD0785EF0FQ14904901-8015903E-C369-4CB6-B8A4-698CAD9C38FEQ14905611-9EA52A0A-AFBB-4E05-A91E-31E58287B9B2Q14911566-13C22E25-963F-45CE-82F3-E1FF227DB2F4Q14911646-C608DC2A-1005-48A4-A9B0-7A289BAD5204Q2062543-68014EC8-2956-43A4-9D86-FAFA25052105Q21104681-90E15AD6-C2C2-4F95-925D-EC1861590EAEQ21105496-A2BD7F2E-580B-4C4F-990B-D7800ED39AA2Q21108986-26952E57-2A9A-4AC9-832C-C49622193A7BQ21110396-11E31440-1B58-4947-9C8C-34B270B4EE85Q21111001-AD45BD9B-A6AB-4937-9815-808EFE525106Q21114237-13144D9D-B000-4FF8-9003-096D5F6076C6Q21114762-CB21CD42-0EA2-41E7-930C-C3B4203C5C4AQ21116910-9977B161-1A31-4067-999E-B2FEDF28E50CQ21118710-E082E7D2-D7F3-482C-8854-1ED21150BDCDQ21119420-B590BAD8-6B93-459B-9415-55C6376FD116Q21119511-73BEBB82-11AC-4DAE-9BAF-5D02DB7C9496Q21119515-EA036147-9290-4ADB-A293-39371AE1C8B7Q21120852-9E03BB34-A66F-455C-8732-7CAE7356C0DEQ21120896-B1497B99-0200-4202-AA0A-5BD91CEF1497Q21124649-3B466B7E-20C3-485A-9B82-8A9B3993D383Q21131338-CCC24A1A-FD4C-4544-9B71-A41FBB218C09Q21135197-7968557B-DFDF-4EE2-931F-A98D8905DB91Q21136964-10E20EFF-9F22-4A24-80DC-18BEDA792520Q21137112-AC821836-93BC-4E72-8ED8-0BE8FAB33F80Q21491078-65DE7658-EED7-4D54-9D63-F22DCBE6313EQ21494520-92C76AB2-FDC3-4E64-9851-A3D2E43DCB44Q21494736-344ADE6D-B626-493C-A489-9A6021FD5F81Q21498441-20D08B64-72E8-41ED-BF26-FA2706EBB50BQ21499097-A3124879-FCA8-4AF9-BA54-83E39B484A7CQ21983046-7AEC9BB6-734B-460A-980D-BFDC5D7E688FQ21983987-C8A20A53-B3B6-4E34-8B88-13F253589336Q21986053-D12CA8BC-1A37-42EC-978F-80D23AE61AC4Q21986561-19ABC106-3A4C-46FE-A706-3FB6B0B1751EQ21986568-80EED98F-C13D-4A4F-A621-52A333F9BC1CQ21987650-2CEB12C2-CDDF-4726-BFEA-69FE4F063FDD
P682
description
The process in which the anato ...... le is generated and organized.
@en
biologisch proces
@nl
name
ventricular cardiac muscle tissue morphogenesis
@en
type
label
ventricular cardiac muscle tissue morphogenesis
@en
altLabel
GO:0055010
@en
cardiac ventricle muscle morphogenesis
@en
ventricular heart muscle morphogenesis
@en
prefLabel
ventricular cardiac muscle tissue morphogenesis
@en
P2888
P686
GO:0055010