1. Gene
  2. YTHDC1 - YTH domain containing 1 Gene

YTHDC1 - YTH domain containing 1 Gene

中文名称:含 YTH 域 1

种属: Homo sapiens

同用名: YT521; YT521-B

基因 ID: 91746 | 基因类型: protein coding

关于 YTHDC1

Cytogenetic location: 4q13.2 Genomic coordinates (GRCh38): 4:68,310,387-68,350,090 (from NCBI)

This gene has 7 transcripts (splice variants), 1 gene allele, 204 orthologues and 3 paralogues. Ubiquitous expression in bone marrow (RPKM 22.7), ovary (RPKM 15.2) and 25 other tissues.

功能概要

启用含 N6-甲基腺苷的 RNA 结合活性。参与细胞核的 mRNA 输出; mRNA 剪接位点选择;和基因表达的调控。位于核斑点和质膜。 [由基因组资源联盟提供,2022 年 4 月]

Enables N6-methyladenosine-containing RNA binding activity. Involved in mRNA export from nucleus; mRNA splice site selection; and regulation of gene expression. Located in nuclear speck and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

YTHDC1 基因产物(3)

mRNA Protein Name
NM_001031732.4 NP_001026902.1 YTH domain-containing protein 1 isoform 1
NM_001330698.2 NP_001317627.1 YTH domain-containing protein 1 isoform 3
NM_133370.4 NP_588611.2 YTH domain-containing protein 1 isoform 2
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables N6-methyladenosine-containing RNA reader activity IDA
IDA: 通过直接分析推断
25242552 GOA
enables RNA binding IDA
IDA: 通过直接分析推断
20167602 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
15345239 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in dosage compensation by inactivation of X chromosome IDA
IDA: 通过直接分析推断
27602518 GOA
involved in mRNA export from nucleus IDA
IDA: 通过直接分析推断
28984244 GOA
involved in mRNA splice site recognition IDA
IDA: 通过直接分析推断
20167602 GOA
involved in regulation of mRNA splicing, via spliceosome IDA
IDA: 通过直接分析推断
26876937 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in nuclear speck IDA
IDA: 通过直接分析推断
26876937 GOA
located in nucleus IDA
IDA: 通过直接分析推断
20167602 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

YTHDC1 蛋白结构

YTH

YTH: YT521-B-like domain (355 - 492)

  • 0
  • 200
  • 400
  • 600
  • 727 a.a.
蛋白主名 其他名称

YTH domain-containing protein 1

putative splicing factor YT521

YTHDC1 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
YTHDC1 Q96MU7 RBMY1A1 Homo sapiens P0DJD3-2 32296183
种属内
YTHDC1 Q96MU7 RBMY1A1 Homo sapiens P0DJD3-2 32296183
种属内
YTHDC1 Q96MU7 KRTAP10-6 Homo sapiens P60371 32296183
种属内
YTHDC1 Q96MU7 KRTAP10-6 Homo sapiens P60371 32296183
种属内
YTHDC1 Q96MU7 PHF19 Homo sapiens Q5T6S3 32296183
种属内
YTHDC1 Q96MU7 PHF19 Homo sapiens Q5T6S3 32296183
种属内
YTHDC1 Q96MU7 HNRNPK Homo sapiens P61978 25416956
种属内
YTHDC1 Q96MU7 HNRNPK Homo sapiens P61978 29892012
种属内
YTHDC1 Q96MU7 ANKRD28 Homo sapiens O15084 32296183
种属内
YTHDC1 Q96MU7 ANKRD28 Homo sapiens O15084 32296183
种属内
YTHDC1 Q96MU7 SRPK1 Homo sapiens Q96SB4 23602568
种属内
YTHDC1 Q96MU7 SRPK2 Homo sapiens P78362 23602568
种属内
YTHDC1 Q96MU7 HNRNPK Homo sapiens P61978-2 32296183
种属内
YTHDC1 Q96MU7 HNRNPK Homo sapiens P61978-2 32296183
种属内
YTHDC1 Q96MU7 KHDRBS3 Homo sapiens O75525 32296183
种属内
YTHDC1 Q96MU7 KHDRBS3 Homo sapiens O75525 32296183
种属内
YTHDC1 Q96MU7 TRA2B Homo sapiens P62995 32296183
种属内
YTHDC1 Q96MU7 TRA2B Homo sapiens P62995 32296183
种属内
YTHDC1 Q96MU7 DVL3 Homo sapiens Q92997 25416956
种属内
YTHDC1 Q96MU7 DVL3 Homo sapiens Q92997 25416956
种属内
YTHDC1 Q96MU7 DVL3 Homo sapiens Q92997 32296183
种属内
YTHDC1 Q96MU7 DVL3 Homo sapiens Q92997 25416956
种属内
YTHDC1 Q96MU7 DVL3 Homo sapiens Q92997 32296183
种属内
YTHDC1 Q96MU7 SDCBP2 Homo sapiens Q9H190 32296183
种属内
YTHDC1 Q96MU7 SDCBP2 Homo sapiens Q9H190 25416956
种属内
YTHDC1 Q96MU7 SDCBP2 Homo sapiens Q9H190 32296183
种属内
YTHDC1 Q96MU7 SDCBP2 Homo sapiens Q9H190 31515488
种属内
YTHDC1 Q96MU7 SDCBP2 Homo sapiens Q9H190 25416956
种属内
YTHDC1 Q96MU7 SDCBP2 Homo sapiens Q9H190 32296183
种属内
YTHDC1 Q96MU7 KHDRBS2 Homo sapiens Q5VWX1 32296183
种属内
YTHDC1 Q96MU7 KHDRBS2 Homo sapiens Q5VWX1 25416956
种属内
YTHDC1 Q96MU7 KHDRBS2 Homo sapiens Q5VWX1 25416956
种属内
YTHDC1 Q96MU7 KHDRBS2 Homo sapiens Q5VWX1 32296183
种属内
YTHDC1 Q96MU7 CLK2 Homo sapiens P49760 32296183
种属内
YTHDC1 Q96MU7 CLK2 Homo sapiens P49760 32296183
种属内
YTHDC1 Q96MU7 PICK1 Homo sapiens Q9NRD5 32296183
种属内
YTHDC1 Q96MU7 PICK1 Homo sapiens Q9NRD5 32296183
种属内
YTHDC1 Q96MU7 PICK1 Homo sapiens Q9NRD5 32296183
种属内
YTHDC1 Q96MU7 RBMY1F Homo sapiens Q15415 25416956
种属内
YTHDC1 Q96MU7 RBMY1F Homo sapiens Q15415 32296183
种属内
YTHDC1 Q96MU7 RBMY1F Homo sapiens Q15415 32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Hepatoblastoma
Wilms Tumor 1

Nephroblastoma

Wilms Tumor

WT1

Wilms' Tumor

Bilateral Wilms Tumor

Wilms Tumor, Type 1

Wilms Tumor, Somatic

Adult Nephroblastoma

Wt1 Disorder

Renal Embryonic Tumor

Adult Kidney Wilms Tumor

Childhood Kidney Wilms Tumor

Nonanaplastic Kidney Wilms Tumor

Autism Spectrum Disorder

Asd

Autism Spectrum Disorders

Autistic Continuum

Pervasive Developmental Disorder

Pervasive Development Disorder

Autistic Behavior

Autistic Disorder

Autistic

Autistic Disorder Of Childhood Onset

Infantile Autism

Childhood Autism

Kanner Syndrome

Pervasive Developmental Delay Nos

Pervasive Developmental Disorder, Not Otherwise Specified

Leukemia, Acute Myeloid

Acute Myeloid Leukemia

Leukemia, Acute Myelogenous

Acute Myelogenous Leukemia

AML

Leukemia, Acute Myeloid, Susceptibility To

Acute Myeloblastic Leukemia

Leukemia, Acute Myeloid, Reduced Survival In, Somatic

Acute Myeloid Leukaemia

Leukemia, Myelocytic, Acute

Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

Secondary Aml

Acute Myelocytic Leukemia

Acute Myeloid Leukemia, Somatic

Leukemia, Acute Myeloid, Somatic

Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

Acute Myeloblastic Leukaemia

Acute Myelogenous Leukaemia

Aml - Acute Myeloid Leukemia

Acute Myeloid Leukemia With Cebpa Somatic Mutations

Aml With Cebpa Somatic Mutations

Inherited Acute Myeloid Leukemia

Familial Aml

Inherited Aml

Pure Familial Aml

Pure Familial Acute Myeloid Leukemia

Secondary Acute Myeloid Leukemia

Therapy-Related Aml And Myelodysplastic Syndrome

Acute Myeloid Leukemia, Secondary

Acute Non-Lymphoblastic Leukemia

Acute Non-Lymphocytic Leukemia

Acute Biphenotypic Leukemia

Acute Undifferentiated Leukemia

Acute Myeloblastic Leukaemia With Multilineage Dysplasia

Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

Acute Myeloid Leukaemia With Myelodysplasia-Related Features

Retinitis Pigmentosa

RP

Rod-Cone Dystrophy

Autosomal Recessive Retinitis Pigmentosa

Non-Syndromic Retinitis Pigmentosa

Pericentral Pigmentary Retinopathy

Pigmentary Retinopathy

Tapetoretinal Degeneration

Rcd

Retinitis Pigmentosa Autosomal Recessive

ARRP

Retinitis Pigmentosa, Autosomal Recessive

Retinitis Pigmentosa 1

疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Mus musculus YTHDC1 MGD MGI:2443713
Rattus norvegicus YTHDC1 RGD RGD:621706
Canis familiaris YTHDC1 VGNC VGNC:48503
Felis catus YTHDC1 VGNC VGNC:67150
Macaca mulatta YTHDC1 VGNC VGNC:79860
Bos taurus YTHDC1 VGNC VGNC:37039