2. Gene
  3. MAGOH - mago homolog, exon junction complex subunit Gene

MAGOH - mago homolog, exon junction complex subunit Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：mago 同系物，外显子连接复合亚基

种属: Homo sapiens

同用名: MAGOH1; MAGOHA

基因 ID: 4116 | 基因类型: protein coding

关于 MAGOH

Cytogenetic location: 1p32.3 Genomic coordinates (GRCh38): 1:53,226,900-53,238,518 (from NCBI)

This gene has 4 transcripts (splice variants), 215 orthologues and 1 paralogue. Ubiquitous expression in bone marrow (RPKM 28.8), colon (RPKM 24.3) and 25 other tissues.

功能概要

其 mago nashi (无孙) 基因发生突变的果蝇产生的后代在种质组装和种系发育方面存在缺陷。该基因编码哺乳动物 mago nashi 同系物。在哺乳动物中，mRNA 表达不限于种质，而是在成体组织中普遍表达，并且可以通过静止成纤维细胞的血清刺激来诱导。[RefSeq 提供，2008 年 7 月]

Drosophila that have mutations in their mago nashi (grandchildless) gene produce progeny with defects in germplasm assembly and germline development. This gene encodes the mammalian mago nashi homolog. In mammals, mRNA expression is not limited to the germ plasm, but is expressed ubiquitously in adult tissues and can be induced by serum stimulation of quiescent fibroblasts. [provided by RefSeq, Jul 2008]

MAGOH 基因产物(1)

mRNA Protein Name
NM_002370.4 NP_002361.1 protein mago nashi homolog

MAGOH 蛋白结构

Mago_nashi

Mago_nashi: Mago nashi protein (4 - 146)

  • 0
  • 100
  • 146 a.a.
蛋白主名 其他名称

protein mago nashi homolog

mago homolog, exon junction complex core component

重组 MAGOH 蛋白

目录号 产品名 蛋白编号 纯度
HY-P76484 MAGOH Protein, Human (His) P61326-1/NP_002361.1 (M1-I146) ≥95%

关联疾病

疾病名称 别名
Metaphyseal Chondrodysplasia, Schmid Type

MCDS

Schmid Metaphyseal Chondrodysplasia

Metaphyseal Chondrodysplasia Schmid Type

Spondylometaphyseal Dysplasia, Japanese Type

Japanese Type Spondylometaphyseal Dysplasia

Schmid Type Metaphyseal Dysplasia

Metaphyseal Chondrodysplasia Type Schmid

Schmid Type Metaphyseal Chondrodysplasia

SMCD

Chondrodysplasia, Metaphyseal, Schmid Type

Corneal Dystrophy, Subepithelial Mucinous
Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder
Primary Autosomal Recessive Microcephaly

Autosomal Recessive Primary Microcephaly

Mcph

True Microcephaly

Microcephalia Vera

Microcephaly Vera

Microcephaly Primary Hereditary

Microcephaly, Primary, Autosomal Recessive

Primary Microcephaly
Microcephaly

Microencephaly

Microcephalus

Microcephalic

Nanocephaly

Congenital Microcephaly

Brain Hypoplasia

Brain Nondevelopment

Cephalic Hypoplasia

Undeveloped Cerebrum

Undeveloped Brain

Micrencephalon

Micrencephaly
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS07985 MAGOH Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Felis catus MAGOH VGNC VGNC:107580
Rattus norvegicus MAGOH RGD RGD:1305174
Mus musculus MAGOH MGD MGI:1330312
Others MAGOH NCBI
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