1. Gene
  2. KIF3B - kinesin family member 3B Gene

KIF3B - kinesin family member 3B Gene

中文名称:驱动蛋白家族成员 3B

种属: Homo sapiens

同用名: FLA8; RP89; HH0048; KLP-11

基因 ID: 9371 | 基因类型: protein coding

关于 KIF3B

Cytogenetic location: 20q11.21 Genomic coordinates (GRCh38): 20:32,277,651-32,335,011 (from NCBI)

This gene has 1 transcript (splice variant), 206 orthologues, 41 paralogues and is associated with 2 phenotypes. Ubiquitous expression in brain (RPKM 22.2), kidney (RPKM 21.4) and 25 other tissues.

功能概要

由该基因编码的蛋白质作为驱动蛋白家族成员 3A 的异二聚体,有助于有丝分裂和减数分裂期间的染色体运动。编码的蛋白质是一个正端定向的微管马达,可以与 cohesin 复合物的 SMC3 亚基相互作用。此外,编码的蛋白质可能参与膜细胞器的细胞内运动。这种蛋白质和驱动蛋白家族成员 3A 形成驱动蛋白超家族的驱动蛋白 II 亚家族。[RefSeq 提供,2008 年 7 月]

The protein encoded by this gene acts as a heterodimer with Kinesin family member 3A to aid in chromosome movement during mitosis and meiosis. The encoded protein is a plus end-directed microtubule motor and can interact with the SMC3 subunit of the cohesin complex. In addition, the encoded protein may be involved in the intracellular movement of membranous organelles. This protein and Kinesin family member 3A form the Kinesin II subfamily of the Kinesin superfamily. [provided by RefSeq, Jul 2008]

KIF3B 基因产物(1)

mRNA Protein Name
NM_004798.4 NP_004789.1 kinesin-like protein KIF3B

KIF3B 蛋白结构

Kinesin

Kinesin: Kinesin motor domain (15 - 340)

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

kinesin-like protein KIF3B

microtubule plus end-directed kinesin motor 3B

KIF3B 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
KIF3B O15066 CLCN5 Homo sapiens P51795 19940036
种属内
KIF3B O15066 ARHGEF10 Homo sapiens O15013
IF
19635168
种属内
KIF3B O15066 ARHGEF10 Homo sapiens O15013 19635168
种属内
KIF3B O15066 KIFAP3 Homo sapiens Q92845 16298999
种属内
KIF3B O15066 KIFAP3 Homo sapiens Q92845
TAP
27173435
种属内
KIF3B O15066 KIFAP3 Homo sapiens Q92845 35271311
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
Retinitis Pigmentosa 89

RP89

Retinitis Pigmentosa, Type 89

Myasthenic Syndrome, Congenital, 16

Congenital Myasthenic Syndrome 16

CMS16

Myasthenic Syndrome, Congenital, Acetazolamide-Responsive

Congenital Myasthenic Syndrome Acetazolamide-Responsive

Congenital Myasthenic Syndrome Due To Mutation In Scn4a

Congenital Myasthenic Syndrome Scn4a-Related

Polydactyly

Non-Syndromic Polydactyly

Polydactyly, Postaxial

Postaxial Polydactyly

Supernumerary Digit

Extra Digits

Hyperdactyly

Polydactylia

Polydactylism

Supernumerary Digits

Kartagener Syndrome

Kartagener'S Syndrome

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

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

Asphyxiating Thoracic Dystrophy

Jeune Thoracic Dystrophy

Jeune Syndrome

Asphyxiating Thoracic Dysplasia

Short-Rib Thoracic Dysplasia With Or Without Polydactyly

Thoracic Pelvic Phalangeal Dystrophy

Asphyxiating Thoracic Chondrodystrophy

Atd

Chondroectodermal Dysplasia-Like Syndrome

Infantile Thoracic Dystrophy

Jeune Thoracic Dysplasia

Thoracic Asphyxiant Dystrophy

Thoracic-Pelvic-Phalangeal Dystrophy

Short-Rib Thoracic Dysplasia Without Polydactyly

Asphyxiating Thoracic Dystrophy Of The Newborn

Asphyxiating Thorax Dystrophy

Situs Inversus

Situs Inversus Viscerum

Laterality Sequence

Complete Transposition

Siv

Cystic Kidney Disease

Renal Cyst

Simple Renal Cyst

Kidney Cysts

Kidney Diseases, Cystic

Renal Cysts

Kidney Cyst

Cystic Kidney

Congenital Cystic Kidney Disease

Cystic Kidney Diseases

Bosniak 1 Cyst

Primary Ciliary Dyskinesia

Immotile Cilia Syndrome

Kartagener Syndrome

Dextrocardia Bronchiectasis And Sinusitis

Pcd

Ciliary Motility Disorders

Ciliary Motility Disorder

Immotile Ciliary Syndrome

Ciliary Dyskinesia Primary

Ics

Polynesian Bronchiectasis

Dextrocardia-Bronchiectasis-Sinusitis Syndrome

Immotile Cilia Syndrome, Kartagener Type

Primary Ciliary Dyskinesia And Situs Inversus

Primary Ciliary Dyskinesia, Kartagener Type

Siewert Syndrome

Dyskinesia, Ciliary, Primary

Meckel Syndrome, Type 1

Meckel-Gruber Syndrome

Meckel Syndrome

Dysencephalia Splanchnocystica

Meckel Syndrome 1

MKS1

Mks

Gruber Syndrome

Meckel-Gruber Syndrome, Type 1

Mes

Dysencephalia Splachnocystica

Meckel Gruber Syndrome

Meckel Syndrome Type 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

Polycystic Kidney Disease

Polycystic Kidney Diseases

Pkd

Polycystic Renal Disease

Kidney Disease, Polycystic

Polycystic Kidney, Autosomal Dominant

Joubert Syndrome 1

Joubert Syndrome

Jbts

Cerebellooculorenal Syndrome 1

JBTS1

Joubert-Boltshauser Syndrome

Cerebelloparenchymal Disorder Iv

Cpd4

Cors1

Joubert Syndrome And Related Disorders

Jsrd

Familial Aplasia Of The Vermis

Joubert Syndrome Related Disorders

Js

Cerebellar Vermis Agenesis

Cerebelloparenchymal Disorder 4

Agenesis Of Cerebellar Vermis

Cerebello-Oculo-Renal Syndrome

Cors

Joubert-Bolthauser Syndrome

Cpd Iv

Classic Joubert Syndrome

Joubert Syndrome Type A

Pure Joubert Syndrome

Cerebello-Oculo-Renal Syndrome 1

Joubert Syndrome-1

Joubert Syndrome, Type 1

Joubert'S Syndrome

Fundus Dystrophy

Retinal Dystrophy

Retinal Dystrophies

Dystrophy, Retinal

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 KIF3B MGD MGI:107688
Bos taurus KIF3B VGNC VGNC:30603
Rattus norvegicus KIF3B RGD RGD:1306815
Canis familiaris KIF3B VGNC VGNC:42405
Felis catus KIF3B VGNC VGNC:67942
Macaca mulatta KIF3B VGNC VGNC:74018