Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
89953
Gene name Gene Name - the full gene name approved by the HGNC.
Kinesin light chain 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KLC4
Synonyms (NCBI Gene) Gene synonyms aliases
CONDRHN, KNSL8, bA387M24.3
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018861 hsa-miR-335-5p Microarray 18185580
MIRT035911 hsa-miR-1180-3p CLASH 23622248
MIRT1095681 hsa-miR-15a CLIP-seq
MIRT1095682 hsa-miR-15b CLIP-seq
MIRT1095683 hsa-miR-16 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005737 Component Cytoplasm IEA
GO:0005871 Component Kinesin complex IEA
GO:0005874 Component Microtubule IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620909 21624 ENSG00000137171
Protein
UniProt ID Q9NSK0
Protein name Kinesin light chain 4 (KLC 4) (Kinesin-like protein 8)
Protein function Kinesin is a microtubule-associated force-producing protein that may play a role in organelle transport. The light chain may function in coupling of cargo to the heavy chain or in the modulation of its ATPase activity (By similarity). {ECO:00002
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13424 TPR_12 209 285 Repeat
PF13424 TPR_12 293 369 Repeat
PF13374 TPR_10 294 335 Repeat
PF13424 TPR_12 335 409 Repeat
PF13374 TPR_10 465 496 Repeat
Sequence
MSGLVLGQRDEPAGHRLSQEEILGSTRLVSQGLEALRSEHQAVLQSLSQTIECLQQGGHE
EGLVHEKARQLRRSMENIELGLSEAQVMLALASHLSTVESEKQKLRAQVRRLCQENQWLR
DELAGTQQRLQRSEQAVAQLEEEKKHLEFLGQLRQYDEDGHTSEEKEGDATKDSLDDLFP
NEEEEDPSNGLSRGQGATAAQQGGYEIPARLRTLHNLVIQYAAQGRYEVAVPLCKQALED
LERTSGRGHPDVATMLNILALVYRDQNKYKEAAHLLNDALSIRES
TLGPDHPAVAATLNN
LAVLYGKRGKYKEAEPLCQRALEIREKVLGTNHP
DVAKQLNNLALLCQNQGKYEAVERYY
QRALAIYEG
QLGPDNPNVARTKNNLASCYLKQGKYAEAETLYKEILTRA
HVQEFGSVDDD
HKPIWMHAEEREEMSKSRHHEGGTPYAEYGGWYKACKVSSPTVNTTLRNLGALYRRQGKL
EAAETLEECALRSRRQ
GTDPISQTKVAELLGESDGRRTSQEGPGDSVKFEGGEDASVAVE
WSGDGSGTLQRSGSLGKIRDVLRRSSELLVRKLQGTEPRPSSSNMKRAASLNYLNQPSAA
PLQVSRGLSASTMDLSSSS
Sequence length 619
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  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 Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
3m syndrome Miller-McKusick-Malvaux-Syndrome (3M Syndrome) rs121918215, rs1335171880, rs121918216, rs121918228, rs121918229, rs730880261, rs730880262, rs730880263, rs752254407, rs1568590155, rs201406974, rs786205651, rs61752334, rs762334954, rs749509661
View all (23 more)
30980518
Scoliosis Scoliosis, unspecified rs1057518828, rs147296805, rs758163506, rs1555613564, rs1596852902, rs1596853067, rs1596853085 30980518
Spastic paraplegia Spastic Paraplegia rs118204049, rs121918262, rs104894490, rs119476046, rs281865117, rs281865118, rs137853017, rs72554620, rs121908610, rs121908611, rs121908613, rs116171274, rs121434442, rs121434443, rs137852520
View all (368 more)
26423925
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Non Small Cell Lung Associate 32457423
Lung Neoplasms Associate 32457423