about
24-dehydrocholesterol reductaseSonic hedgehogA disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 2Collagen, type I, alpha 1ATPase, Cu++ transporting, alpha polypeptideInterferon regulatory factor 6Catenin (cadherin associated protein), beta 1DesmoplakinCollagen, type III, alpha 1Excision repair cross-complementing rodent repair deficiency, complementation group 2Integrin alpha 3Transcription factor 7 like 2, T cell specific, HMG boxPolycystin 1, transient receptor poteintial channel interactingCollagen, type V, alpha 1Collagen, type V, alpha 2Cartilage oligomeric matrix proteinCatenin beta 1Polycystin 1, transient receptor potential channel interactingGuanine nucleotide-binding protein G(s) subunit alpha isoforms XLasCollagen type V alpha 3 chainIntegrin subunit beta 4Arrestin domain containing 3BAF chromatin remodeling complex subunit BCL11BFraser extracellular matrix complex subunit 1Integrin subunit alpha 6Achaete-scute family bHLH transcription factor 4Aspartic peptidase retroviral like 1Gap junction protein beta 3ATP binding cassette subfamily B member 6 (Langereis blood group)ATPase phospholipid transporting 8A2Solute carrier family 27 member 4Ovo like transcriptional repressor 1Platelet derived growth factor subunit AWnt family member 10ASLIT and NTRK like family member 5SRY-box transcription factor 21StratifinDishevelled binding antagonist of beta catenin 2Transcription factor 15Patched 2
P682
The pro-alpha3(V) collagen chain. Complete primary structure, expression domains in adult and developing tissues, and comparison to the structures and expression domains of the other types V and XI procollagen chainsMutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasiaRecessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegiaMolecular characterization of the body site-specific human epidermal cytokeratin 9: cDNA cloning, amino acid sequence, and tissue specificity of gene expressionHash4, a novel human achaete-scute homologue found in fetal skinA point mutation in an intronic branch site results in aberrant splicing of COL5A1 and in Ehlers-Danlos syndrome type II in two British familiesMutations of the alpha2(V) chain of type V collagen impair matrix assembly and produce ehlers-danlos syndrome type IMutations in the COL3A1 gene result in the Ehlers-Danlos syndrome type IV and alterations in the size and distribution of the major collagen fibrils of the dermisRegional Control of Hairless versus Hair-Bearing Skin by Dkk2
P921
Q14599665-FE3BE768-5D53-4666-B64D-1806EF1FC65DQ14860215-FEB0A117-D207-47DA-8861-808F5EFE3EE9Q14881711-E344A190-CE09-4415-B32B-4F5C23271841Q14881727-5402AADD-E638-4D18-99E1-2E918DAFFB31Q14881727-BAD53367-FE19-429D-8024-403985B5500DQ14884615-5383BC81-580D-440F-9A22-414123940F1AQ14890131-97DB2C67-80B4-424F-A8F4-67CD68C8C3B8Q14902827-851336B3-AAF2-47F1-AAAA-02C5B8FDDC6AQ14906114-00143A9D-088F-4680-8401-15FC84F7C6FAQ14906114-E2BA978B-9D27-462C-BDF5-5B7B6036EC89Q14906850-8A8B571B-3DE3-44FF-B7B3-D157704D19C6Q14908100-4209B7E4-F023-426B-80F5-3A686DEAFED0Q14912141-1FB80B36-F865-480D-934E-31D0BBF827FCQ14913903-F8815B8B-DC88-4CBB-B74E-163FFDD7FEF6Q14914569-8CD70B6C-629E-4A45-9B96-6E4019AD1BD7Q15311977-8BD3CAB9-A152-44F8-B959-D67AB6BA35FEQ15312000-5529BA64-535B-46A6-A62F-68EEFFCBD965Q15312000-7EE11EDB-5D48-42BE-B92B-9D1A8D3D1FA0Q15320351-8AD0128C-C21F-436E-B9EB-CB4213A3F2A2Q1634046-4CE87806-39D6-41D2-A612-BE9CF86AFEE6Q2044253-AE3F5BDB-C2E6-4D6F-AC59-E9BB1EF397EDQ21102044-8B052E67-EAF7-4F83-8F38-88DA93E04BF5Q21102491-54DFE670-B6B3-4D22-8D81-BC8AB7EC18B2Q21105257-C3049C09-9D25-46F5-B9B8-A0341F29FB7CQ21105275-CC5A7F3A-31CF-4F8E-BCEB-9A17B3D55371Q21105437-34C44D78-C15D-42F5-BE91-5AE6808E95F6Q21107452-A53E3A8E-1491-4A00-A27B-C58E46F6102EQ21107772-4F8B620E-3D4D-43A9-8DF8-72C1B7D27416Q21111618-55CCCECF-7A3E-4816-8986-15FB7254D3B4Q21112684-94A8175E-A602-4F48-AF49-1750228F1D38Q21113099-F77F3E8E-BBB9-4D5D-A9A7-AAFCD87B1D10Q21115261-6A36CD1D-801E-4FBE-8A6F-962C59904841Q21115361-10D056FC-8043-4EE4-ACB5-483C299193E6Q21121313-F87F8769-B7B4-4CE8-8A50-05BA82387DF1Q21122431-F394C253-E297-470E-995B-123F5CDABD16Q21123233-1BFCC54E-5981-4B3A-8B84-A5D743AF5D88Q21123978-98459188-A465-4DCA-995B-68034E32E6B0Q21124492-702CE14C-6DD5-4BEE-B019-577486744C4EQ21127271-BF010ACA-1BF3-4536-8C2C-295112716E0AQ21131010-005207BA-9502-436C-AC29-B864D7E03FEC
P682
Q22253347-3FA6AA85-DF24-49DB-B04D-5F8C7FF5E1BAQ24293212-D5359A3D-432E-4ED0-9467-A568FB815866Q24297910-C3C1744A-110E-4FFE-BFEE-AEA6FF7ECAD2Q24305039-6F6E86E0-2520-4BB6-B095-5343988C9B59Q24306737-3A85F70A-D978-4580-8E21-393C06334033Q24318493-6679AA60-FDE8-4A92-9635-50D19FD7756EQ24318955-0E01FD62-691A-438D-91A1-0F5D22A248F4Q24320166-CEB85F14-C7E2-417C-95A3-E15D185E8E6DQ64384866-3EC5282C-E6E8-4731-8AE9-5FC25413B818
P921
description
The process whose specific out ...... ists of two layers, an outer n
@en
biologisch proces
@nl
name
skin development
@en
развитие кожи
@ru
type
label
skin development
@en
развитие кожи
@ru
altLabel
GO:0043588
@en
animal skin development
@en
prefLabel
skin development
@en
развитие кожи
@ru
P2888
P686
GO:0043588