1. Gene
  2. KLC4 - kinesin light chain 4 Gene

KLC4 - kinesin light chain 4 Gene

Homo sapiens

Also known as KNSL8; bA387M24.3

Gene ID: 89953 | Gene type: protein coding

About KLC4

This gene has 19 transcripts (splice variants), 381 orthologues and 5 paralogues. Ubiquitous expression in duodenum (RPKM 24.3), small intestine (RPKM 22.1) and 25 other tissues.

Summary

Predicted to be located in cytoplasm and microtubule. Predicted to be part of Kinesin complex. [provided by Alliance of Genome Resources, Apr 2022]

KLC4 Products(6)

mRNA Protein Name
NM_001289034.2 NP_001275963.1 kinesin light chain 4 isoform a
NM_001289035.2 NP_001275964.1 kinesin light chain 4 isoform d
NM_138343.4 NP_612352.1 kinesin light chain 4 isoform c
NM_201521.3 NP_958929.1 kinesin light chain 4 isoform a
NM_201522.3 NP_958930.1 kinesin light chain 4 isoform a
NM_201523.3 NP_958931.1 kinesin light chain 4 isoform b
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

KLC4 Protein Structure

Rab5-bind

Rab5-bind: Rabaptin-like protein (79 - 252)

TPR_2

TPR_2: Tetratricopeptide repeat (256 - 282)

TPR_12

TPR_12: Tetratricopeptide repeat (291 - 368)

TPR_10

TPR_10: Tetratricopeptide repeat (378 - 408)

TPR_10

TPR_10: Tetratricopeptide repeat (465 - 496)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 619 a.a.
Protein Preferred Names Protein Names

kinesin light chain 4

kinesin-like protein 8

KLC4 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
KLC4 Q9NSK0 NECAB2 Homo sapiens Q7Z6G3-2 25416956
Intra
KLC4 Q9NSK0 NECAB2 Homo sapiens Q7Z6G3-2 32296183
Intra
KLC4 Q9NSK0 NECAB2 Homo sapiens Q7Z6G3-2 32296183
Intra
KLC4 Q9NSK0 CEP57L1 Homo sapiens Q8IYX8-2 25416956
Intra
KLC4 Q9NSK0 SLC16A9 Homo sapiens Q7RTY1 25416956
Intra
KLC4 Q9NSK0 ZNF343 Homo sapiens Q6P1L6 32296183
Intra
KLC4 Q9NSK0 ZNF343 Homo sapiens Q6P1L6 32296183
Intra
KLC4 Q9NSK0 KRT34 Homo sapiens O76011 32296183
Intra
KLC4 Q9NSK0 KRT34 Homo sapiens O76011 32296183
Intra
KLC4 Q9NSK0 KRT33B Homo sapiens Q14525 32296183
Intra
KLC4 Q9NSK0 KRT33B Homo sapiens Q14525 32296183
Intra
KLC4 Q9NSK0 CEP57 Homo sapiens Q86XR8-3 32296183
Intra
KLC4 Q9NSK0 CEP57 Homo sapiens Q86XR8-3 32296183
Intra
KLC4 Q9NSK0 KRT16 Homo sapiens P08779 32296183
Intra
KLC4 Q9NSK0 KRT16 Homo sapiens P08779 32296183
Intra
KLC4 Q9NSK0 YWHAE Homo sapiens P62258 36931259
Intra
KLC4 Q9NSK0 SYNE4 Homo sapiens Q8N205 25416956
Intra
KLC4 Q9NSK0 SYNE4 Homo sapiens Q8N205 25416956
Intra
KLC4 Q9NSK0 SYNE4 Homo sapiens Q8N205 25416956
Intra
KLC4 Q9NSK0 KRT15 Homo sapiens P19012 25416956
Intra
KLC4 Q9NSK0 KRT15 Homo sapiens P19012 25416956
Intra
KLC4 Q9NSK0 USHBP1 Homo sapiens Q8N6Y0 25416956
Intra
KLC4 Q9NSK0 TADA2A Homo sapiens O75478 25416956
Intra
KLC4 Q9NSK0 TADA2A Homo sapiens O75478 25416956
Intra
KLC4 Q9NSK0 KATNAL1 Homo sapiens Q9BW62 25416956
Intra
KLC4 Q9NSK0 KATNAL1 Homo sapiens Q9BW62 25416956
Intra
KLC4 Q9NSK0 KATNAL1 Homo sapiens Q9BW62 32296183
Intra
KLC4 Q9NSK0 KATNAL1 Homo sapiens Q9BW62 32296183
Intra
KLC4 Q9NSK0 MEOX2 Homo sapiens P50222 25416956
Intra
KLC4 Q9NSK0 MEOX2 Homo sapiens P50222 25416956
Intra
KLC4 Q9NSK0 SERTAD1 Homo sapiens Q9UHV2 32296183
Intra
KLC4 Q9NSK0 SERTAD1 Homo sapiens Q9UHV2 32296183
Intra
KLC4 Q9NSK0 SERTAD1 Homo sapiens Q9UHV2 32296183
Intra
KLC4 Q9NSK0 KRT31 Homo sapiens Q15323 32296183
Intra
KLC4 Q9NSK0 KRT31 Homo sapiens Q15323 25416956
Intra
KLC4 Q9NSK0 KRT31 Homo sapiens Q15323 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
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

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

Ehlers-Danlos Syndrome, Vascular Type

Eds Iv

Eds4

Vascular Ehlers-Danlos Syndrome

Veds

Sack-Barabas Syndrome

EDSVASC

Ehlers-Danlos Syndrome, Type Iv, Autosomal Dominant

Vascular Type Ehlers-Danlos Syndrome

Arterial-Ecchymotic Eds

Ehlers-Danlos Syndrome Type 4

Vascular Eds

Ehlers-Danlos Syndrome, Type 4

Ehlers-Danlos Syndrome, Type Iv

Ehlers-Danlos Syndrome, Arterial Type

Ehlers-Danlos Syndrome, Ecchymotic Type

Ehlers-Danlos Syndrome, Sack-Barabas Type

Autosomal Dominant Type Iv Ehlers-Danlos Syndrome

Eds Type Iv

Eds Type 4

Ehlers Danlos Syndrome, Sack-Barabas Type

Ehlers Danlos Syndrome, Arterial Type

Ehlers Danlos Syndrome, Ecchymotic Type

Ehlers-Danlos Syndrome Type Iv

Ehlers-Danlos Syndrome 4

Ehlers-Danlos Syndrome Arterial Type

Ehlers-Danlos Syndrome Ecchymotic Type

Ehlers-Danlos Syndrome, Type 4 Variant

Ehlers-Danlos, Vascular Type Syndrome

Diseases Alias
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

Orthologs Information

Species Symbol Source ID
Macaca mulatta KLC4 VGNC VGNC:73880
Felis catus KLC4 VGNC VGNC:63129
Canis familiaris KLC4 VGNC VGNC:42429
Rattus norvegicus KLC4 RGD RGD:1306555
Mus musculus KLC4 MGD MGI:1922014
Bos taurus KLC4 VGNC VGNC:30625