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KLC1 (kinesin light chain 1)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3831
Gene nameGene Name - the full gene name approved by the HGNC.
Kinesin light chain 1
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
KLC1
SynonymsGene synonyms aliases
KLC, KNS2, KNS2A
ChromosomeChromosome number
14
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q32.33
SummarySummary of gene provided in NCBI Entrez Gene.
Conventional kinesin is a tetrameric molecule composed of two heavy chains and two light chains, and transports various cargos along microtubules toward their plus ends. The heavy chains provide the motor activity, while the light chains bind to various c
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT004189 hsa-miR-197-3p Microarray 16822819
MIRT025439 hsa-miR-34a-5p Proteomics 21566225
MIRT1095542 hsa-miR-105 CLIP-seq
MIRT1095543 hsa-miR-1289 CLIP-seq
MIRT1095544 hsa-miR-1321 CLIP-seq
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003774 Function Motor activity TAS 8786116
GO:0005515 Function Protein binding IPI 14970196, 16938850, 17332754, 19861499, 25416956, 25898167
GO:0005829 Component Cytosol ISS
GO:0005829 Component Cytosol TAS
GO:0005871 Component Kinesin complex ISS
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q07866
Protein name Kinesin light chain 1 (KLC 1)
Protein function Kinesin is a microtubule-associated force-producing protein that may play a role in organelle transport (PubMed:21385839). The light chain may function in coupling of cargo to the heavy chain or in the modulation of its ATPase activity (By simil
PDB 3NF1 , 5OJ8 , 7AI4 , 7AIE
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13424 TPR_12
211 287
Repeat
PF00515 TPR_1
297 329
Tetratricopeptide repeat
Repeat
PF13374 TPR_10
463 502
Repeat
Sequence
MYDNMSTMVYIKEDKLEKLTQDEIISKTKQVIQGLEALKNEHNSILQSLLETLKCLKKDD
ESNLVEEKSNMIRKSLEMLELGLSEAQVMMALSNHLNAVESEKQKLRAQVRRLCQENQWL
RDELANTQQKLQKSEQSVAQLEEEKKHLEFMNQLKKYDDDISPSEDKDTDSTKEPLDDLF
PNDEDDPGQGIQQQHSSAAAAAQQGGYEIPARLRTLHNLVIQYASQGRYEVAVPLCKQAL
EDLEKTSGHDHPDVATMLNILALVYRDQNKYKDAANLLNDALAIREK
TLGKDHPAVAATL
NNLAVLYGKRGKYKEAEPLCKRALEIREK
VLGKDHPDVAKQLNNLALLCQNQGKYEEVEY
YYQRALEIYQTKLGPDDPNVAKTKNNLASCYLKQGKFKQAETLYKEILTRAHEREFGSVD
DENKPIWMHAEEREECKGKQKDGTSFGEYGGWYKACKVDSPTVTTTLKNLGALYRRQGKF
EAAETLEEAAMRSRKQGLDNVH
KQRVAEVLNDPENMEKRRSRESLNVDVVKYESGPDGGE
EVSMSVEWNGGVSGRASFCGKRQQQQWPGRRHR
Sequence length 573
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Motor proteins
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Salmonella infection
  MHC class II antigen presentation
RHO GTPases activate KTN1
COPI-dependent Golgi-to-ER retrograde traffic
Kinesins
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Schizophrenia Schizophrenia rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 31268507, 30285260, 31374203, 25056061, 28540026, 26198764
Unknown
Disease name Disease term dbSNP ID References
Cytochrome-c oxidase deficiency Cytochrome-c Oxidase Deficiency rs28461189, rs267606883
Development disorder Child Development Disorders, Pervasive 28540026
Mental depression Major Depressive Disorder rs587778876, rs587778877 29662059

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