2. Gene
  3. MYO1D - myosin ID Gene

MYO1D - myosin ID Gene

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

中文名称：肌球蛋白编号

种属: Homo sapiens

同用名: myr4; PPP1R108

基因 ID: 4642 | 基因类型: protein coding

关于 MYO1D

Cytogenetic location: 17q11.2 Genomic coordinates (GRCh38): 17:32,492,522-32,877,124 (from NCBI)

This gene has 16 transcripts (splice variants), 204 orthologues and 43 paralogues. Broad expression in colon (RPKM 49.5), small intestine (RPKM 32.7) and 22 other tissues.

功能概要

启用蛋白质域特异性结合活性。预计参与肌动蛋白丝组织；早期内体循环内体运输；和囊泡沿肌动蛋白丝运输。位于细胞外外泌体。 [由基因组资源联盟提供，2022 年 4 月]

Enables protein domain specific binding activity. Predicted to be involved in actin filament organization; early endosome to recycling endosome transport; and vesicle transport along actin filament. Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

MYO1D 基因产物(4)

mRNA Protein Name
NM_001303279.2 NP_001290208.1 unconventional myosin-Id isoform 2
NM_001303280.2 NP_001290209.1 unconventional myosin-Id isoform 3
NM_001411088.1 NP_001398017.1 unconventional myosin-Id isoform 4
NM_015194.3 NP_056009.1 unconventional myosin-Id isoform 1
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
28514442 GOA
enables protein domain specific binding IPI
IPI: 通过物理相互作用推断
22284616 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

MYO1D 蛋白结构

Myosin_head

Myosin_head: Myosin head (motor domain) (13 - 682)

IQ

IQ: IQ calmodulin-binding motif (700 - 719)

Myosin_TH1

Myosin_TH1: Unconventional myosin tail, actin- and lipid-binding (802 - 1004)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1006 a.a.
蛋白主名 其他名称

unconventional myosin-Id

myosin-I gamma

关联疾病

疾病名称 别名
Canavan Disease

Aspartoacylase Deficiency

Aminoacylase 2 Deficiency

Spongy Degeneration Of Central Nervous System

Aspa Deficiency

Acy2 Deficiency

Canavan-Van Bogaert-Bertrand Disease

Mild Canavan Disease

Asp Deficiency

Spongy Degeneration Of The Central Nervous System

Severe Canavan Disease

Von Bogaert-Bertrand Disease

Canavan'S Disease

Spongy Degeneration Of The Brain

Juvenile Canavan Disease

Infantile Canavan Disease

Neonatal Canavan Disease

CAND

Disease, Canavan

Canavan Disease, Juvenile

Canavan Disease, Infantile

Canavan Disease, Neonatal
Visceral Heterotaxy

Situs Ambiguus

Heterotaxia

Heterotaxy Syndrome

Heterotaxy

Lateralization Defect

Situs Ambiguous

Left Isomerism

Htx

Ivemark Syndrome

Right Isomerism

Situs Ambiguus Viscerum

Incomplete Situs Inversus

Partial Situs Inversus

Heterotaxy, Visceral

Asplenia Syndrome

Bilateral Left-Sidedness

Polysplenia Syndrome

Moller Syndrome
Situs Inversus

Situs Inversus Viscerum

Laterality Sequence

Complete Transposition

Siv
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-RS08940 MYO1D 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 MYO1D VGNC VGNC:68391
Canis familiaris MYO1D VGNC VGNC:43563
Mus musculus MYO1D MGD MGI:107728
Rattus norvegicus MYO1D RGD RGD:621321
Macaca mulatta MYO1D VGNC VGNC:75113
Bos taurus MYO1D VGNC VGNC:31819
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