2. Gene
  3. VILL - villin like Gene

VILL - villin like Gene

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

中文名称：小人样

种属: Homo sapiens

基因 ID: 50853 | 基因类型: protein coding

关于 VILL

Cytogenetic location: 3p22.2 Genomic coordinates (GRCh38): 3:37,987,978-38,007,185 (from NCBI)

This gene has 10 transcripts (splice variants), 196 orthologues and 7 paralogues. Broad expression in stomach (RPKM 21.1), small intestine (RPKM 13.2) and 17 other tissues.

功能概要

该基因编码的蛋白质属于绒毛蛋白/凝溶胶蛋白家族。它包含 6 个凝溶胶蛋白样重复序列和一个头盔结构域。它可能在肌动蛋白捆绑中发挥作用。[RefSeq 提供，2008 年 7 月]

The protein encoded by this gene belongs to the villin/gelsolin family. It contains 6 gelsolin-like repeats and a headpiece domain. It may play a role in actin-bundling. [provided by RefSeq, Jul 2008]

VILL 基因产物(5)

mRNA Protein Name
NM_001370264.1 NP_001357193.1 villin-like protein isoform 2
NM_001370265.1 NP_001357194.1 villin-like protein isoform 3
NM_001385038.1 NP_001371967.1 villin-like protein isoform 1
NM_001385039.1 NP_001371968.1 villin-like protein isoform 1
NM_015873.4 NP_056957.3 villin-like protein 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
32814053 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

VILL 蛋白结构

Gelsolin

Gelsolin: Gelsolin repeat (23 - 105)

Gelsolin

Gelsolin: Gelsolin repeat (147 - 217)

Gelsolin

Gelsolin: Gelsolin repeat (270 - 340)

Gelsolin

Gelsolin: Gelsolin repeat (403 - 482)

Gelsolin

Gelsolin: Gelsolin repeat (521 - 588)

Gelsolin

Gelsolin: Gelsolin repeat (627 - 699)

VHP

VHP: Villin headpiece domain (821 - 856)

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

villin-like protein

关联疾病

疾病名称 别名
Hyperekplexia

Hereditary Hyperekplexia

Kok Disease

Congenital Stiff Man Syndrome

Familial Startle Disease

Sthe

Stiff-Baby Syndrome

Hereditary Hyperexplexia

Startle Disease

Exaggerated Startle Reaction

Hyperexplexia Hereditary

Startle Disease, Familial

Startle Reaction, Exaggerated

Stiff-Man Syndrome, Congenital

Stiff-Person Syndrome, Congenital

Congenital Stiff-Man Syndrome

Congenital Stiff-Person Syndrome

Familial Hyperekplexia

Startle Syndrome

Stiff Baby Syndrome

Hyperekplexia, Hereditary

Stiff-Person Syndrome
Amyloidosis, Finnish Type

Finnish Type Amyloidosis

Meretoja Syndrome

Amyloidosis V

Amyloidosis, Meretoja Type

Amyloid Cranial Neuropathy With Lattice Corneal Dystrophy

Lattice Corneal Dystrophy Type Ii

Familial Amyloidosis, Finnish Type

Familial Amyloid Polyneuropathy Type Iv

Amyloidosis Due To Mutant Gelsolin

Agel Amyloidosis

Gelsolin Amyloidosis

Hereditary Gelsolin Amyloidosis

Lattice Corneal Dystrophy Type Ii Finnish

Gelsolin-Related Amyloidosis

Kymenlaakso Syndrome

Lattice Corneal Dystrophy, Gelsolin Type

Hereditary Amyloidosis, Finnish Type

Lattice Corneal Dystrophy Type 2

Amyloidosis 5

AMYL5

Agel

Familial Amyloidosis Finnish Type

Meretoja Type Amyloidosis

Type Iv Familial Amyloid Polyneuropathy

Familial Amyloid Polyneuropathy, Type V

Familial Amyloid Polyneuropathy, Type Iv
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 (3)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS15651 VILL Human Pre-designed siRNA Set A Pre-designed Set / 否
HY-RS21456 Vill Mouse Pre-designed siRNA Set A Pre-designed Set / 否
HY-RS27974 Vill Rat Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Bos taurus VILL VGNC VGNC:36795
Felis catus VILL VGNC VGNC:102865
Canis familiaris VILL VGNC VGNC:48262
Mus musculus VILL MGD MGI:1201781
Rattus norvegicus VILL RGD RGD:1304843
Macaca mulatta VILL VGNC VGNC:79897
Others VILL NCBI
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