1. Gene
  2. KLC3 - kinesin light chain 3 Gene

KLC3 - kinesin light chain 3 Gene

中文名称:驱动蛋白轻链 3

种属: Homo sapiens

同用名: KLC2; KLCt; KLC2L; KNS2B

基因 ID: 147700 | 基因类型: protein coding

关于 KLC3

Cytogenetic location: 19q13.32 Genomic coordinates (GRCh38): 19:45,340,750-45,351,519 (from NCBI)

This gene has 7 transcripts (splice variants), 373 orthologues and 5 paralogues. Biased expression in skin (RPKM 20.7), esophagus (RPKM 4.3) and 4 other tissues.

功能概要

该基因编码驱动蛋白轻链基因家族的成员。驱动蛋白是参与沿微管运输货物的分子马达,由两个驱动蛋白重链 (KHC) 和两个驱动蛋白轻链 (KLC) 分子组成。 KLC 被认为通常参与结合货物和调节驱动蛋白活性。在大鼠体内,一种类似于该基因产物的蛋白质在减数分裂后的精子细胞中表达,它与精子尾巴和线粒体的结构成分相关。[RefSeq 提供,2008 年 7 月]

This gene encodes a member of the Kinesin light chain gene family. Kinesins are molecular motors involved in the transport of cargo along microtubules, and are composed of two Kinesin heavy chain (KHC) and two Kinesin light chain (KLC) molecules. KLCs are thought to typically be involved in binding cargo and regulating Kinesin activity. In the rat, a protein similar to this gene product is expressed in post-meiotic spermatids, where it associates with structural components of sperm tails and mitochondria. [provided by RefSeq, Jul 2008]

KLC3 基因产物(1)

mRNA Protein Name
NM_177417.3 NP_803136.2 kinesin light chain 3
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
15161933 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

KLC3 蛋白结构

Rab5-bind

Rab5-bind: Rabaptin-like protein (79 - 248)

TPR_1

TPR_1: Tetratricopeptide repeat (252 - 280)

TPR_12

TPR_12: Tetratricopeptide repeat (287 - 365)

TPR_10

TPR_10: Tetratricopeptide repeat (374 - 402)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 504 a.a.
蛋白主名 其他名称

kinesin light chain 3

kinesin light chain 2

KLC3 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
KLC3 Q6P597 KRT13 Homo sapiens A1A4E9 25416956
种属内
KLC3 Q6P597 KRT13 Homo sapiens A1A4E9 25416956
种属内
KLC3 Q6P597 BICDL2 Homo sapiens A1A5D9 31515488
种属内
KLC3 Q6P597 BICDL2 Homo sapiens A1A5D9 25416956
种属内
KLC3 Q6P597 BICDL2 Homo sapiens A1A5D9 25416956
种属内
KLC3 Q6P597 ZNF572 Homo sapiens Q7Z3I7 25416956
种属内
KLC3 Q6P597 ZNF572 Homo sapiens Q7Z3I7 25416956
种属内
KLC3 Q6P597 NECAB2 Homo sapiens Q7Z6G3-2 25416956
种属内
KLC3 Q6P597 NECAB2 Homo sapiens Q7Z6G3-2 25416956
种属内
KLC3 Q6P597 CEP57L1 Homo sapiens Q8IYX8-2 25416956
种属内
KLC3 Q6P597 CEP57L1 Homo sapiens Q8IYX8-2 25416956
种属内
KLC3 Q6P597 MBIP Homo sapiens Q9NS73-5 25416956
种属内
KLC3 Q6P597 QARS1 Homo sapiens P47897-2 25416956
种属内
KLC3 Q6P597 FKBP1A Homo sapiens Q0VDC6 32814053
种属内
KLC3 Q6P597 FKBP1A Homo sapiens Q0VDC6 32814053
种属内
KLC3 Q6P597 FKBP1A Homo sapiens Q0VDC6 32814053
种属内
KLC3 Q6P597 SNAP47 Homo sapiens Q5SQN1 25416956
种属内
KLC3 Q6P597 SNAP47 Homo sapiens Q5SQN1 25416956
种属内
KLC3 Q6P597 SNAP47 Homo sapiens Q5SQN1 25416956
种属内
KLC3 Q6P597 PDE4DIP Homo sapiens Q5VU43 25416956
种属内
KLC3 Q6P597 TSNAX Homo sapiens Q99598 33961781
种属内
KLC3 Q6P597 TSNAX Homo sapiens Q99598 25416956
种属内
KLC3 Q6P597 TSNAX Homo sapiens Q99598 25416956
种属内
KLC3 Q6P597 TSNAX Homo sapiens Q99598 25416956
种属内
KLC3 Q6P597 APBB2 Homo sapiens Q92870-2 32814053
种属内
KLC3 Q6P597 APBB2 Homo sapiens Q92870-2 32814053
种属内
KLC3 Q6P597 APBB2 Homo sapiens Q92870-2 32814053
种属内
KLC3 Q6P597 CHAT Homo sapiens P28329-3 32814053
种属内
KLC3 Q6P597 CHAT Homo sapiens P28329-3 32814053
种属内
KLC3 Q6P597 CHAT Homo sapiens P28329-3 32814053
种属内
KLC3 Q6P597 VPS52 Homo sapiens Q8N1B4 25416956
种属内
KLC3 Q6P597 NUP58 Homo sapiens Q9BVL2 32814053
种属内
KLC3 Q6P597 NUP58 Homo sapiens Q9BVL2 32814053
种属内
KLC3 Q6P597 NUP58 Homo sapiens Q9BVL2 32814053
种属内
KLC3 Q6P597 BBS5 Homo sapiens Q8N3I7 25416956
种属内
KLC3 Q6P597 YWHAZ Homo sapiens P63104 33961781
种属内
KLC3 Q6P597 YWHAZ Homo sapiens P63104 15161933
种属内
KLC3 Q6P597 QARS1 Homo sapiens P47897 25416956
种属内
KLC3 Q6P597 FGFR3 Homo sapiens P22607 32814053
种属内
KLC3 Q6P597 FGFR3 Homo sapiens P22607 32814053
种属内
KLC3 Q6P597 FGFR3 Homo sapiens P22607 32814053
种属内
KLC3 Q6P597 HRAS Homo sapiens P01112 32814053
种属内
KLC3 Q6P597 HRAS Homo sapiens P01112 32814053
种属内
KLC3 Q6P597 HRAS Homo sapiens P01112 32814053
种属内
KLC3 Q6P597 YWHAE Homo sapiens P62258 33961781
种属内
KLC3 Q6P597 YWHAE Homo sapiens P62258 36931259
种属内
KLC3 Q6P597 HSPA2 Homo sapiens P54652 32814053
种属内
KLC3 Q6P597 HSPA2 Homo sapiens P54652 32814053
种属内
KLC3 Q6P597 HSPA2 Homo sapiens P54652 32814053
种属内
KLC3 Q6P597 YWHAG Homo sapiens P61981
SLC
36931259
种属内
KLC3 Q6P597 HTRA2 Homo sapiens O43464 32814053
种属内
KLC3 Q6P597 HTRA2 Homo sapiens O43464 32814053
种属内
KLC3 Q6P597 HTRA2 Homo sapiens O43464 32814053
种属内
KLC3 Q6P597 TCF4 Homo sapiens P15884 25416956
种属内
KLC3 Q6P597 TCF4 Homo sapiens P15884 25416956
种属内
KLC3 Q6P597 STX11 Homo sapiens O75558 25416956
种属内
KLC3 Q6P597 STX11 Homo sapiens O75558 25416956
种属内
KLC3 Q6P597 NDC80 Homo sapiens O14777 25416956
种属内
KLC3 Q6P597 NDC80 Homo sapiens O14777 25416956
种属内
KLC3 Q6P597 KRT15 Homo sapiens P19012 25416956
种属内
KLC3 Q6P597 DTX2 Homo sapiens Q86UW9 25416956
种属内
KLC3 Q6P597 DTX2 Homo sapiens Q86UW9 25416956
种属内
KLC3 Q6P597 ZNF417 Homo sapiens Q8TAU3 25416956
种属内
KLC3 Q6P597 ZNF417 Homo sapiens Q8TAU3 25416956
种属内
KLC3 Q6P597 ZNF417 Homo sapiens Q8TAU3 25416956
种属内
KLC3 Q6P597 CCNH Homo sapiens P51946 31515488
种属内
KLC3 Q6P597 CCNH Homo sapiens P51946 25416956
种属内
KLC3 Q6P597 CCNH Homo sapiens P51946 25416956
种属内
KLC3 Q6P597 CBY2 Homo sapiens Q8NA61 25416956
种属内
KLC3 Q6P597 ABI3 Homo sapiens Q9P2A4 25416956
种属内
KLC3 Q6P597 ABI3 Homo sapiens Q9P2A4 25416956
种属内
KLC3 Q6P597 ABI3 Homo sapiens Q9P2A4 25416956
种属内
KLC3 Q6P597 IMP3 Homo sapiens Q9NV31 25416956
种属内
KLC3 Q6P597 IMP3 Homo sapiens Q9NV31 25416956
种属内
KLC3 Q6P597 IMP3 Homo sapiens Q9NV31 25416956
种属内
KLC3 Q6P597 WAC Homo sapiens Q9BTA9 25416956
种属内
KLC3 Q6P597 WAC Homo sapiens Q9BTA9 25416956
种属内
KLC3 Q6P597 PRPH Homo sapiens P41219 32814053
种属内
KLC3 Q6P597 PRPH Homo sapiens P41219 32814053
种属内
KLC3 Q6P597 PRPH Homo sapiens P41219 32814053
种属内
KLC3 Q6P597 IHO1 Homo sapiens Q8IYA8 25416956
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
Spastic Paraplegia, Optic Atrophy, And Neuropathy

Spoan Syndrome

SPOAN

Spastic Paraplegia, Optic Atropy, And Neuropathy

Spastic Paraplegia, Optic Atropy, And Neuropathy Syndrome

Spastic Paraplegia-Optic Atrophy-Neuropathy Syndrome

Pituitary Adenoma 2, Growth Hormone-Secreting

PITA2

Acromegaly Due To Pituitary Adenoma 2

Acromegaly, X-Linked

Growth Hormone Secreting Pituitary Adenoma 2

Pituitary Adenoma, Growth Hormone-Secreting, 2

Pituitary Adenoma 2, Gh-Secreting

Gh-Secreting Pituitary Adenoma 2

X-Linked Acromegaly

Adenoma, Pituitary, Growth Hormone-Secreting, Type 2

Hereditary Spastic Paraplegia

Familial Spastic Paraplegia

Hereditary Spastic Paraparesis

Strumpell-Lorrain Disease

Familial Spastic Paraparesis

Hsp

Spg

Strümpell-Lorrain Disease

Spastic Paraplegia, Hereditary

French Settlement Disease

Strumpell-Lorrain Syndrome

Fsp

Spastic Paraplegia, Familial

Spastic Paraplegia Hereditary

Spastic Paraplegia 3, Autosomal Dominant

Spastic Paraparesis

Hereditary Spastic Paralysis

Familial Spastic Paralysis

Hereditary Spastic Ataxia

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 KLC3 MGD MGI:1277971
Macaca mulatta KLC3 VGNC VGNC:73870
Canis familiaris KLC3 VGNC VGNC:42428
Felis catus KLC3 VGNC VGNC:63128
Rattus norvegicus KLC3 RGD RGD:621432
Bos taurus KLC3 VGNC VGNC:30624