1. Gene
  2. KIF11 - kinesin family member 11 Gene

KIF11 - kinesin family member 11 Gene

中文名称:驱动蛋白家族成员 11

种属: Homo sapiens

同用名: EG5; HKSP; KNSL1; MCLMR; TRIP5

基因 ID: 3832 | 基因类型: protein coding

关于 KIF11

Cytogenetic location: 10q23.33 Genomic coordinates (GRCh38): 10:92,593,130-92,655,395 (from NCBI)

This gene has 5 transcripts (splice variants), 203 orthologues, 41 paralogues and is associated with 4 phenotypes. Broad expression in lymph node (RPKM 9.9), bone marrow (RPKM 8.6) and 18 other tissues.

功能概要

该基因编码属于驱动蛋白样蛋白家族的运动蛋白。已知该蛋白质家族的成员参与各种纺锤体动力学。该基因产物的功能包括染色体定位、中心体分离和在细胞有丝分裂期间建立双极纺锤体。[RefSeq 提供,2008 年 7 月]

This gene encodes a motor protein that belongs to the kinesin-like protein family. Members of this protein family are known to be involved in various kinds of spindle dynamics. The function of this gene product includes chromosome positioning, centrosome separation and establishing a bipolar spindle during cell Mitosis. [provided by RefSeq, Jul 2008]

KIF11 基因产物(1)

mRNA Protein Name
NM_004523.4 NP_004514.2 kinesin-like protein KIF11
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 protein binding IPI
IPI: 通过物理相互作用推断
21303978 GOA
enables protein kinase binding IPI
IPI: 通过物理相互作用推断
19001501 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in mitotic spindle assembly IDA
IDA: 通过直接分析推断
19001501 GOA
involved in mitotic spindle assembly IMP
IMP: 通过突变表型推断
15843429 GOA
involved in regulation of mitotic centrosome separation IMP
IMP: 通过突变表型推断
15843429 GOA
involved in spindle organization IMP
IMP: 通过突变表型推断
14718566 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in microtubule IDA
IDA: 通过直接分析推断
21525035 GOA
part of protein-containing complex IPI
IPI: 通过物理相互作用推断
17707232 GOA
located in spindle IDA
IDA: 通过直接分析推断
19001501 GOA
colocalizes with spindle microtubule IDA
IDA: 通过直接分析推断
14718566 GOA
colocalizes with spindle pole IDA
IDA: 通过直接分析推断
14718566 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

KIF11 蛋白结构

Kinesin

Kinesin: Kinesin motor domain (24 - 359)

Microtub_bind

Microtub_bind: Kinesin-associated microtubule-binding (916 - 1053)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1056 a.a.
蛋白主名 其他名称

kinesin-like protein KIF11

TR-interacting protein 5

KIF11 抗体

目录号 产品名 应用 反应物种
HY-P80647 Eg5 Antibody (YA776) WB, ICC/IF, IP Human
HY-P85489 Eg5 Antibody (YA5181) WB, IP, ICC Human

关联疾病

疾病名称 别名
Microcephaly With Or Without Chorioretinopathy, Lymphedema, Or Mental Retardation

Lymphedema, Microcephaly And Chorioretinopathy Syndrome

Microcephaly With Or Without Chorioretinopathy, Lymphedema, Or Intellectual Disability

MCLMR

Microcephaly, Lymphedema, Chorioretinal Dysplasia Syndrome

Mlcrd Syndrome

Cdmmr Syndrome

Lymphedema And Retinal Folds With Microcephaly And Microphthalmos

Chorioretinal Dysplasia-Microcephaly-Mental Retardation Syndrome

Microcephaly Lymphedema Chorioretinal Dysplasia

Microcephaly And Chorioretinopathy With Or Without Mental Retardation, Autosomal Dominant

Lymphedema, Microcephaly, Chorioretinopathy Syndrome

Lymphedema And Retinal Folds With Ficrocephaly And Microphthalmos

Chorioretinal Dysplasia-Microcephaly-Intellectual Disability Syndrome

Microcephaly-Lymphedema-Chorioretinopathy Syndrome

Mlcrd

Lymphedema Microcephaly Chorioretinopathy Syndrome

Microcephaly Lymphedema Chorioretinal Dysplasia Syndrome

Microcephaly With Or Without Chorioretinopathy, Lymphedema Or Intellectual Disability

Microcephaly With/Without Chorioretinopathy, Lymphedema, Or Mental Retardation

Syndromic Rod-Cone Dystrophy

Syndromic Retinitis Pigmentosa

Microcephaly And Chorioretinopathy 1
Microcephaly And Chorioretinopathy, Autosomal Recessive, 1

MCCRP1

Microcephaly And Chorioretinopathy, Autosomal Recessive, Type 1

Chorioretinal Dysplasia-Microcephaly-Mental Retardation Syndrome

Lymphedema, Microcephaly And Chorioretinopathy Syndrome

Microcephaly

Microencephaly

Microcephalus

Microcephalic

Nanocephaly

Congenital Microcephaly

Brain Hypoplasia

Brain Nondevelopment

Cephalic Hypoplasia

Undeveloped Cerebrum

Undeveloped Brain

Micrencephalon

Micrencephaly

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

Cone-Rod Dystrophy 2

Cone-Rod Dystrophy

CORD2

Cone-Rod Retinal Dystrophy

Rcrd2

Cone-Rod Retinal Dystrophy 2

Crd2

Cord

Crd

Retinal Cone-Rod Dystrophy

Cone-Rod Retinal Dystrophy-2

Retinal Cone-Rod Dystrophy 2

Tapetoretinal Degeneration

Cone-Rod Degeneration

Cone Rod Dystrophy

Dystrophy, Cone-Rod

Dystrophy, Cone-Rod, Type 2

Retinitis Pigmentosa

Retinitis Pigmentosa 2

Progressive Cone-Rod Dystrophy

Congenital Lymphedema

Lymphedema, Congenital

Milroy Disease

Microcephaly, Autosomal Dominant

Autosomal Dominant Microcephaly

Microcephaly Autosomal Dominant

Autosomal Dominant Primary Microcephaly

Microcephaly With Autosomal Dominant Inheritance

Astigmatism
Invasive Bladder Transitional Cell Carcinoma

Invasive Bladder Urothelial Carcinoma

Infiltrating Bladder Urothelial Carcinoma

Fundus Dystrophy

Retinal Dystrophy

Retinal Dystrophies

Dystrophy, Retinal

Exudative Vitreoretinopathy

Familial Exudative Vitreoretinopathy

Fevr

Criswick-Schepens Syndrome

Exudative Vitreoretinopathy, Familial

Vitreoretinopathy, Exudative )

Exudative Vitreoretinopathy 1

Norrie Disease

Atrophia Bulborum Hereditaria

Episkopi Blindness

Pseudoglioma

ND

Norrie-Warburg Disease

Anderson-Warburg Syndrome

Fetal Iritis Syndrome

Norrie Syndrome

Norrie-Warburg Syndrome

Ndp

Congenital Progressive Oculo-Acoustico-Cerebral Degeneration

Norrie'S Disease

Oligophrenia Microphthalmus

Pseudoglioma Congenita

Whitnall-Norman Syndrome

Microphthalmia

Microphthalmos

Isolated Anophthalmia-Microphthalmia Syndrome

Isolated Microphthalmia-Anophthalmia-Coloboma

Simple Microphthalmos

Clinical Anophthalmia

Isolated Anophthalmia - Microphthalmia

Isolated Pure Microphthalmia

Mac Spectrum

Microphthalmia-Anophthalmia-Coloboma Spectrum

Primitive Anophthalmia

Globe Of Eye Small

Small Eyeball

Hypoplasia Of Eye

Isolated Nanophthalmos

Rudimentary Eye

Dysplasia Of Eye

Primary Autosomal Recessive Microcephaly

Autosomal Recessive Primary Microcephaly

Mcph

True Microcephaly

Microcephalia Vera

Microcephaly Vera

Microcephaly Primary Hereditary

Microcephaly, Primary, Autosomal Recessive

Primary Microcephaly

Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder

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
Canis familiaris KIF11 VGNC VGNC:42379
Rattus norvegicus KIF11 RGD RGD:621258
Macaca mulatta KIF11 VGNC VGNC:74030
Bos taurus KIF11 VGNC VGNC:30580
Mus musculus KIF11 MGD MGI:1098231
Felis catus KIF11 VGNC VGNC:67971
Others KIF11 NCBI