1. Gene
  2. KIFC3 - kinesin family member C3 Gene

KIFC3 - kinesin family member C3 Gene

Homo sapiens
Gene ID: 3801 | Gene type: protein coding

About KIFC3

Cytogenetic location: 16q21 Genomic coordinates (GRCh38): 16:57,758,217-57,862,858 (from NCBI)

This gene has 35 transcripts (splice variants), 202 orthologues and 41 paralogues. Broad expression in kidney (RPKM 11.2), testis (RPKM 9.9) and 24 other tissues.

Summary

This gene encodes a member of the Kinesin-14 family of microtubule motors. Members of this family play a role in the formation, maintenance and remodeling of the bipolar mitotic spindle. The protein encoded by this gene has cytoplasmic functions in the interphase cells. It may also be involved in the final stages of cytokinesis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]

KIFC3 Products(9)

mRNA Protein Name
NM_001130099.1 NP_001123571.1 kinesin-like protein KIFC3 isoform 3
NM_001130100.2 NP_001123572.1 kinesin-like protein KIFC3 isoform 2
NM_001318710.2 NP_001305639.1 kinesin-like protein KIFC3 isoform 4
NM_001318711.2 NP_001305640.1 kinesin-like protein KIFC3 isoform 5
NM_001318712.2 NP_001305641.1 kinesin-like protein KIFC3 isoform 6
NM_001318713.2 NP_001305642.1 kinesin-like protein KIFC3 isoform 7
NM_001318714.2 NP_001305643.1 kinesin-like protein KIFC3 isoform 3
NM_001318715.2 NP_001305644.1 kinesin-like protein KIFC3 isoform 3
NM_005550.4 NP_005541.3 kinesin-like protein KIFC3 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
20360068 GOA
Biological Process GO Annotation Evidence Reference Source
involved in epithelial cell-cell adhesion IMP
IMP: Inferred from mutant phenotype
19041755 GOA
involved in zonula adherens maintenance IMP
IMP: Inferred from mutant phenotype
19041755 GOA
Cellular Component GO Annotation Evidence Reference Source
located in centrosome IDA
IDA: Inferred from direct assay
19041755 GOA
located in zonula adherens IDA
IDA: Inferred from direct assay
19041755 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

KIFC3 Protein Structure

Kinesin

Kinesin: Kinesin motor domain (451 - 768)

  • 0
  • 200
  • 400
  • 600
  • 833 a.a.
Protein Preferred Names Protein Names

kinesin-like protein KIFC3

KIFC3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
KIFC3 Q9BVG8 CCDC102B Homo sapiens Q68D86 25416956
Intra
KIFC3 Q9BVG8 CCDC102B Homo sapiens Q68D86 25416956
Intra
KIFC3 Q9BVG8 CCDC102B Homo sapiens Q68D86 25416956
Intra
KIFC3 Q9BVG8 FLJ13057 Homo sapiens Q53SE7 25416956
Intra
KIFC3 Q9BVG8 MID2 Homo sapiens Q9UJV3-2 25416956
Intra
KIFC3 Q9BVG8 ZNF572 Homo sapiens Q7Z3I7 25416956
Intra
KIFC3 Q9BVG8 ZNF572 Homo sapiens Q7Z3I7 25416956
Intra
KIFC3 Q9BVG8 ZNF572 Homo sapiens Q7Z3I7 25416956
Intra
KIFC3 Q9BVG8 ITGB3BP Homo sapiens Q13352-5 25416956
Intra
KIFC3 Q9BVG8 ITGB3BP Homo sapiens Q13352-5 25416956
Intra
KIFC3 Q9BVG8 NEFL Homo sapiens I6L9F6 25416956
Intra
KIFC3 Q9BVG8 ZGPAT Homo sapiens Q8N5A5-2 25416956
Intra
KIFC3 Q9BVG8 ZGPAT Homo sapiens Q8N5A5-2 25416956
Intra
KIFC3 Q9BVG8 TPM3 Homo sapiens Q5VU62 25416956
Intra
KIFC3 Q9BVG8 TPM3 Homo sapiens Q5VU62 25416956
Intra
KIFC3 Q9BVG8 CCDC28A Homo sapiens Q7Z6N9 25416956
Intra
KIFC3 Q9BVG8 ICA1L Homo sapiens Q8NDH6 25416956
Intra
KIFC3 Q9BVG8 CYTH4 Homo sapiens Q8WWE8 25416956
Intra
KIFC3 Q9BVG8 CYTH4 Homo sapiens Q8WWE8 25416956
Intra
KIFC3 Q9BVG8 ZNF180 Homo sapiens Q9UJW8 25416956
Intra
KIFC3 Q9BVG8 ZNF180 Homo sapiens Q9UJW8 25416956
Intra
KIFC3 Q9BVG8 MFAP1 Homo sapiens P55081 25416956
Intra
KIFC3 Q9BVG8 MFAP1 Homo sapiens P55081 25416956
Intra
KIFC3 Q9BVG8 MFAP1 Homo sapiens P55081 25416956
Intra
KIFC3 Q9BVG8 RAD51D Homo sapiens O75771 31515488
Intra
KIFC3 Q9BVG8 RAD51D Homo sapiens O75771 25416956
Intra
KIFC3 Q9BVG8 ATF2 Homo sapiens P15336 25416956
Intra
KIFC3 Q9BVG8 ATF2 Homo sapiens P15336 25416956
Intra
KIFC3 Q9BVG8 CDR2 Homo sapiens Q01850 25416956
Intra
KIFC3 Q9BVG8 CDR2 Homo sapiens Q01850 25416956
Intra
KIFC3 Q9BVG8 FCHSD2 Homo sapiens O94868 25416956
Intra
KIFC3 Q9BVG8 FCHSD2 Homo sapiens O94868 25416956
Intra
KIFC3 Q9BVG8 PRKAA2 Homo sapiens P54646 25416956
Intra
KIFC3 Q9BVG8 PRKAA2 Homo sapiens P54646
Y2H
21516116
Intra
KIFC3 Q9BVG8 PRKAA2 Homo sapiens P54646 25416956
Intra
KIFC3 Q9BVG8 TRIM54 Homo sapiens Q9BYV2 25416956
Intra
KIFC3 Q9BVG8 FANCL Homo sapiens Q9NW38 25416956
Intra
KIFC3 Q9BVG8 FANCL Homo sapiens Q9NW38 25416956
Intra
KIFC3 Q9BVG8 HAUS1 Homo sapiens Q96CS2 25416956
Intra
KIFC3 Q9BVG8 HAUS1 Homo sapiens Q96CS2 25416956
Intra
KIFC3 Q9BVG8 KRT6C Homo sapiens P48668 25416956
Intra
KIFC3 Q9BVG8 KRT6C Homo sapiens P48668 25416956
Intra
KIFC3 Q9BVG8 ESRRG Homo sapiens P62508 25416956
Intra
KIFC3 Q9BVG8 ESRRG Homo sapiens P62508 25416956
Intra
KIFC3 Q9BVG8 ZGPAT Homo sapiens Q8N5A5 25416956
Intra
KIFC3 Q9BVG8 TSG101 Homo sapiens Q99816 25416956
Intra
KIFC3 Q9BVG8 TSG101 Homo sapiens Q99816 25416956
Intra
KIFC3 Q9BVG8 TSG101 Homo sapiens Q99816 25416956
Intra
KIFC3 Q9BVG8 NUP62 Homo sapiens P37198 25416956
Intra
KIFC3 Q9BVG8 CCDC28A Homo sapiens Q8IWP9 25416956
Intra
KIFC3 Q9BVG8 TRAF2 Homo sapiens Q12933 25416956
Intra
KIFC3 Q9BVG8 TRAF2 Homo sapiens Q12933 25416956
Intra
KIFC3 Q9BVG8 MCM7 Homo sapiens P33993 25416956
Intra
KIFC3 Q9BVG8 MCM7 Homo sapiens P33993 25416956
Intra
KIFC3 Q9BVG8 TNIP1 Homo sapiens Q15025 25416956
Intra
KIFC3 Q9BVG8 PSMB1 Homo sapiens P20618 31515488
Intra
KIFC3 Q9BVG8 MED4 Homo sapiens Q9NPJ6 25416956
Intra
KIFC3 Q9BVG8 MED4 Homo sapiens Q9NPJ6 25416956
Intra
KIFC3 Q9BVG8 SMARCE1 Homo sapiens Q969G3 25416956
Intra
KIFC3 Q9BVG8 SMARCE1 Homo sapiens Q969G3
Y2H
21516116
Intra
KIFC3 Q9BVG8 SMARCE1 Homo sapiens Q969G3 25416956
Intra
KIFC3 Q9BVG8 DTNBP1 Homo sapiens Q96EV8 25416956
Intra
KIFC3 Q9BVG8 DTNBP1 Homo sapiens Q96EV8 25416956
Intra
KIFC3 Q9BVG8 CLIP4 Homo sapiens Q8N3C7 25416956
Intra
KIFC3 Q9BVG8 GOLGA2 Homo sapiens Q08379 25416956
Intra
KIFC3 Q9BVG8 GOLGA2 Homo sapiens Q08379 25416956
Intra
KIFC3 Q9BVG8 ZNF655 Homo sapiens Q8N720 25416956
Intra
KIFC3 Q9BVG8 ZNF655 Homo sapiens Q8N720 25416956
Intra
KIFC3 Q9BVG8 ZNF655 Homo sapiens Q8N720 25416956
Intra
KIFC3 Q9BVG8 SYCE1 Homo sapiens Q8N0S2 25416956
Intra
KIFC3 Q9BVG8 KRT5 Homo sapiens P13647 25416956
Intra
KIFC3 Q9BVG8 KRT5 Homo sapiens P13647 25416956
Intra
KIFC3 Q9BVG8 KRT6A Homo sapiens P02538 25416956
Intra
KIFC3 Q9BVG8 KRT6A Homo sapiens P02538 25416956
Intra
KIFC3 Q9BVG8 ITGB3BP Homo sapiens Q13352 25416956
Intra
KIFC3 Q9BVG8 CBX8 Homo sapiens Q9HC52 25416956
Intra
KIFC3 Q9BVG8 CBX8 Homo sapiens Q9HC52 25416956
Intra
KIFC3 Q9BVG8 PHC2 Homo sapiens Q8IXK0 25416956
Intra
KIFC3 Q9BVG8 PHC2 Homo sapiens Q8IXK0 25416956
Intra
KIFC3 Q9BVG8 PHC2 Homo sapiens Q8IXK0 25416956
Intra
KIFC3 Q9BVG8 DCTN2 Homo sapiens Q13561 25416956
Intra
KIFC3 Q9BVG8 ZNF20 Homo sapiens P17024 25416956
Intra
KIFC3 Q9BVG8 ZNF20 Homo sapiens P17024 25416956
Intra
KIFC3 Q9BVG8 TLE5 Homo sapiens Q08117 25416956
Intra
KIFC3 Q9BVG8 TRIM27 Homo sapiens P14373 25416956
Intra
KIFC3 Q9BVG8 TRIM27 Homo sapiens P14373 25416956
Intra
KIFC3 Q9BVG8 TRIM41 Homo sapiens Q8WV44 25416956
Intra
KIFC3 Q9BVG8 LENG1 Homo sapiens Q96BZ8 25416956
Intra
KIFC3 Q9BVG8 KRT15 Homo sapiens P19012 25416956
Intra
KIFC3 Q9BVG8 TRIM23 Homo sapiens P36406 25416956
Intra
KIFC3 Q9BVG8 KANSL1 Homo sapiens Q7Z3B3 31515488
Intra
KIFC3 Q9BVG8 KRT6B Homo sapiens P04259 25416956
Intra
KIFC3 Q9BVG8 KRT6B Homo sapiens P04259 25416956
Intra
KIFC3 Q9BVG8 LZTS2 Homo sapiens Q9BRK4 25416956
Intra
KIFC3 Q9BVG8 CBY2 Homo sapiens Q8NA61 25416956
Intra
KIFC3 Q9BVG8 CBY2 Homo sapiens Q8NA61 25416956
Intra
KIFC3 Q9BVG8 ZBTB8A Homo sapiens Q96BR9 25416956
Intra
KIFC3 Q9BVG8 ZBTB8A Homo sapiens Q96BR9 25416956
Intra
KIFC3 Q9BVG8 KRT19 Homo sapiens P08727 25416956
Intra
KIFC3 Q9BVG8 USP2 Homo sapiens O75604 25416956
Intra
KIFC3 Q9BVG8 CEP170P1 Homo sapiens Q96L14 25416956
Intra
KIFC3 Q9BVG8 CEP170P1 Homo sapiens Q96L14 25416956
Intra
KIFC3 Q9BVG8 ABI2 Homo sapiens Q9NYB9 29892012
Intra
KIFC3 Q9BVG8 CDK18 Homo sapiens Q07002 25416956
Intra
KIFC3 Q9BVG8 TSR2 Homo sapiens Q969E8 25416956
Intra
KIFC3 Q9BVG8 TSR2 Homo sapiens Q969E8 25416956
Intra
KIFC3 Q9BVG8 SIAH1 Homo sapiens Q8IUQ4 25416956
Intra
KIFC3 Q9BVG8 SIAH1 Homo sapiens Q8IUQ4 25416956
Intra
KIFC3 Q9BVG8 SIAH1 Homo sapiens Q8IUQ4 25416956
Intra
KIFC3 Q9BVG8 CEP55 Homo sapiens Q53EZ4 25416956
Intra
KIFC3 Q9BVG8 RSPH14 Homo sapiens Q9UHP6 25416956
Intra
KIFC3 Q9BVG8 RSPH14 Homo sapiens Q9UHP6 25416956
Intra
KIFC3 Q9BVG8 DEUP1 Homo sapiens Q05D60 25416956
Intra
KIFC3 Q9BVG8 DEUP1 Homo sapiens Q05D60 25416956
Intra
KIFC3 Q9BVG8 HSBP1 Homo sapiens O75506 25416956
Intra
KIFC3 Q9BVG8 LIN37 Homo sapiens Q96GY3 25416956
Intra
KIFC3 Q9BVG8 LIN37 Homo sapiens Q96GY3 25416956
Intra
KIFC3 Q9BVG8 SCEL Homo sapiens O95171 25416956
Intra
KIFC3 Q9BVG8 BCL6 Homo sapiens P41182 25416956
Intra
KIFC3 Q9BVG8 BCL6 Homo sapiens P41182 25416956
Intra
KIFC3 Q9BVG8 AIRIM Homo sapiens Q9NX04 25416956
Intra
KIFC3 Q9BVG8 DCX Homo sapiens O43602 25416956
Intra
KIFC3 Q9BVG8 NDEL1 Homo sapiens Q9GZM8 25416956
Intra
KIFC3 Q9BVG8 NDEL1 Homo sapiens Q9GZM8 25416956
Intra
KIFC3 Q9BVG8 NDEL1 Homo sapiens Q9GZM8 25416956
Intra
KIFC3 Q9BVG8 KRT31 Homo sapiens Q15323 25416956
Intra
KIFC3 Q9BVG8 KRT31 Homo sapiens Q15323 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Retinitis Pigmentosa 63

RP63

Optic Atrophy 8

OPA8

Fanconi Anemia, Complementation Group C

Fanconi Anemia Complementation Group C

FANCC

Facc

Fac

Fa3

Fanconi Pancytopenia Type 3

Fanconi Pancytopenia, Type 3

Faces Syndrome

Facial Features , Anorexia, Cachexia, Eye And Skin Anomalies

Friedman-Goodman Syndrome

Abnormality Of The Face

Zellweger Syndrome

Cerebrohepatorenal Syndrome

Zellweger Leukodystrophy

Zs

Congenital Iron Overload

Chr

Zws

Severe Pbd-Zsd

Severe Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder

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
Canis familiaris KIFC3 VGNC VGNC:42416
Rattus norvegicus KIFC3 RGD RGD:1307693
Felis catus KIFC3 VGNC VGNC:67947
Mus musculus KIFC3 MGD MGI:109202
Macaca mulatta KIFC3 VGNC VGNC:74022
Bos taurus KIFC3 VGNC VGNC:30613