about
Brain derived neurotrophic factorBrain derived neurotrophic factorNerve growth factorErb-b2 receptor tyrosine kinase 2Neurotrophin 3Neurotrophin 5ArteminGlial cell line derived neurotrophic factorAldehyde dehydrogenase 3 family member A2GDNF family receptor alpha 3Acid sensing ion channel subunit 2Erb-b2 receptor tyrosine kinase 3Early growth response 2Early growth response 3SRY-box transcription factor 10Neurogenin 3SRY-box transcription factor 8Adhesion G protein-coupled receptor B2Serpin family I member 1Sodium voltage-gated channel alpha subunit 8NeurofascinAdhesion G protein-coupled receptor B1Endothelin receptor type BSodium/myo-inositol cotransporterAdhesion G protein-coupled receptor B2Early growth response 3Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2Aldehyde dehydrogenase family 3, subfamily A2Endothelin receptor type BErb-b2 receptor tyrosine kinase 3Hairy/enhancer-of-split related with YRPW motif-likeOncostatin MNeurofibromin 1NeurofascinSRY (sex determining region Y)-box 8SRY (sex determining region Y)-box 10Solute carrier family 5 (inositol transporters), member 3UDP glycosyltransferase 8Neurotrophin 3Sodium voltage-gated channel alpha subunit 8
P682
Human neuroserpin (PI12): cDNA cloning and chromosomal localization to 3q26GFRalpha3 is an orphan member of the GDNF/neurturin/persephin receptor familyneurogenins, a novel family of atonal-related bHLH transcription factors, are putative mammalian neuronal determination genes that reveal progenitor cell heterogeneity in the developing CNS and PNSThe human gene CGT encoding the UDP-galactose ceramide galactosyl transferase (cerebroside synthase): cloning, characterization, and assignment to human chromosome 4, band q26Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathiesDejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene
P921
Q123045-8372FA6D-781A-4A84-A589-631B26F1F75AQ14863333-8725A439-80CF-44BB-9866-37E6062A85FFQ14873936-5AEFD328-9EB8-4203-9DA9-C62118CB5865Q14873936-7F7CD33C-8885-41A0-83DE-892B17BB04CFQ14877504-006C7828-DBAC-4ECC-B70F-F5F02B055BC6Q14904572-1C53FF63-52CA-4682-8331-5CFBAF4EB9ABQ14904572-3627CD75-A49C-4D88-BCA4-C7DBE32B7920Q14908136-6A072637-9CD6-438D-BDC3-D2E38C437D2FQ14912168-0CC645EE-7935-40E7-AA5F-D3BE380A716DQ14912168-72E964C7-194F-4BB6-A3AE-E40098F9958FQ14916288-D4E39694-F0AF-4040-AA39-1B9E9CB65B1CQ14916288-DABEDE86-54C7-4CF8-BD1E-F46127A4B976Q21097156-59CDF017-9077-43EB-9171-C90573302376Q21101567-5B2798AF-8DAD-442F-AC79-0A055BA3B05AQ21102082-6DD88049-AC34-4F22-BC99-344FEF6E13FAQ21104746-15A5BC3A-02B7-4598-B3B0-B20AC48DB3DDQ21110101-AE2FF0F7-B2F1-4BA3-9DA6-A16B12B5A279Q21110116-DE2218A2-E84D-4C0D-BBC4-20702BEB5550Q21118857-CAEC35DC-8548-4961-B7F2-6AD3AE724FCFQ21119142-6CADA58B-410D-4CFF-88C1-674B6F2290F3Q21127266-8A61B2FE-2944-48B2-9A70-A29C38015F4DQ21127266-A2FA01DD-BCF9-4883-9ABF-217686233A90Q21131642-2DED4E49-6303-453A-A92A-937412BA9865Q21131642-B8CEF967-0FF3-446D-939C-128543EAF959Q21134355-907F42F6-9E59-4C35-9F71-32553D6614E9Q21135479-4A0D76EB-E65F-4A6E-9C38-0B3CDA8C78D9Q21138888-7A00BE49-9F5E-4EB1-94EA-50F39C27BF94Q21172286-F2388C00-ED61-426B-A2EB-0AAA74AAAC19Q21173310-84350907-5F25-4232-A032-95919817B00CQ21208052-6EAB2697-6AE5-44EC-9A3E-37F1AD799A5AQ21494777-3F817ABA-D833-4C66-8D14-F7847A8CBCCBQ21494777-EBB0F88D-2F51-4E80-9D39-8CAE0BD7D6B1Q21498356-63FE4B45-D2CB-41AF-8AE3-3C4F885D506CQ21499275-5C34BFAF-6AF7-4BE2-9925-45CDE3972B45Q21981462-331AE2C4-C7ED-4B67-A6AE-0188DD4E2113Q21981791-EC48CC92-0CEB-4AC9-B4FB-5F6B51C43C23Q21984810-B70FA5B5-35D2-4BDA-BEA4-9C9C083394BFQ21985971-7291DEEF-A8FA-4816-8084-41186B0686D1Q21987345-212619BA-3633-448F-B708-B1C51A1DC374Q21987763-F1E7FDE0-608F-415F-B5AF-C42671E7CB7E
P682
description
The process whose specific out ...... system. Nerves in the PNS con
@en
biologisch proces
@nl
name
peripheral nervous system development
@en
type
label
peripheral nervous system development
@en
altLabel
GO:0007422
@en
prefLabel
peripheral nervous system development
@en
P2888
P686
GO:0007422