MYT1

MYT1
MYT1
사용 가능한 구조
PDBOrtholog 검색: PDBe RCSB
식별자
에일리어스MYT1, C20orf36, MTF1, MYTI, NZF2, PLPB1, ZC2HC4A, ZC2H2C1, 미엘린전사인자1
외부 IDOMIM: 600379 MGI: 1100535 HomoloGene: 3332 GeneCard: MYT1
맞춤법
종.인간마우스
엔트레즈
앙상블
유니프로트
RefSeq(mRNA)

NM_004535

NM_001171615
NM_001171616
NM_001171680
NM_008665

RefSeq(단백질)

NP_004526

NP_001165086
NP_001165087
NP_001165151
NP_032691

장소(UCSC)Chr 20: 64.1 ~64.24 MbChr 2: 181.76 ~181.83 Mb
PubMed 검색[3][4]
위키데이터
인간 보기/편집마우스 표시/편집

미엘린 전사인자 1은 인간의 MYT1 [5][6][7]유전자에 의해 암호화되는 단백질이다.

기능.

이 유전자에 의해 암호화된 단백질은 신경 특이적이고 아연 손가락을 포함하는 DNA 결합 단백질의 일원입니다.단백질은 중추신경계의 단백질 프로모터 영역에 결합하고 신경계를 [7]발달시키는 역할을 합니다.

인터랙티브 패스 맵

관련 기사를 방문하려면 아래의 유전자, 단백질, 대사물을 클릭하세요. [§ 1]

[[파일:
MECP2_and_Associated_Rett_Syndrome_WP3584Go to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to WikiPathwaysGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to article
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
[[
]]
MECP2_and_Associated_Rett_Syndrome_WP3584Go to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to WikiPathwaysGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to article
alt=MECP2 및 관련 Rett Syndrome 편집]
MECP2 및 관련 Rett Syndrome 편집
  1. ^ 대화형 경로 맵은 WikiPathways에서 편집할 수 있습니다."WP3584".

상호 작용

MYT1은 PIN1[8]상호 작용하는 으로 나타났습니다.

레퍼런스

  1. ^ a b c GRCh38: 앙상블 릴리즈 89: ENSG00000196132 - 앙상블, 2017년 5월
  2. ^ a b c GRCm38: 앙상블 릴리즈 89: ENSMUSG000010505 - 앙상블, 2017년 5월
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Kim JG, Hudson LD (December 1992). "Novel member of the zinc finger superfamily: A C2-HC finger that recognizes a glia-specific gene". Molecular and Cellular Biology. 12 (12): 5632–9. doi:10.1128/mcb.12.12.5632. PMC 360502. PMID 1280325.
  6. ^ Booher RN, Holman PS, Fattaey A (August 1997). "Human Myt1 is a cell cycle-regulated kinase that inhibits Cdc2 but not Cdk2 activity". The Journal of Biological Chemistry. 272 (35): 22300–6. doi:10.1074/jbc.272.35.22300. PMID 9268380.
  7. ^ a b "Entrez Gene: MYT1 myelin transcription factor 1".
  8. ^ Wells NJ, Watanabe N, Tokusumi T, Jiang W, Verdecia MA, Hunter T (October 1999). "The C-terminal domain of the Cdc2 inhibitory kinase Myt1 interacts with Cdc2 complexes and is required for inhibition of G(2)/M progression". Journal of Cell Science. 112 (19): 3361–71. doi:10.1242/jcs.112.19.3361. PMID 10504341.

추가 정보

외부 링크

이 기사에는 미국 국립 의학 도서관(미국 국립 의학 도서관)의 공공 도메인 텍스트가 포함되어 있습니다.