Gene: KIF1B (kinesin family member 1B)  Homo sapiens
Symbol: KIF1B
Name: kinesin family member 1B
Description: This gene encodes a motor protein that transports mitochondria and synaptic vesicle precursors. Mutations in this gene cause Charcot-Marie-Tooth disease, type 2A1. [provided by RefSeq, Jul 2008]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: CMT2; CMT2A; CMT2A1; FLJ23699; HMSNII; KIAA0591; KIAA1448; kinesin superfamily protein KIF1B; kinesin-like protein KIF1B; KLP; MGC134844; NBLST1; OTTHUMP00000001772; OTTHUMP00000001773; OTTHUMP00000001774; OTTHUMP00000001775; OTTHUMP00000001776
Orthologs: Mus musculus : Kif1b (kinesin family member 1B)  MGI
Rattus norvegicus : Kif1b (kinesin family member 1B)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_1110,288,750 - 10,459,836+NCBI
Human Genome Assembly HuRef19,426,051 - 9,595,334+NCBI
Human Genome Assembly GRCh37110,270,764 - 10,441,661+NCBI
Human Genome Assembly Build 36110,193,418 - 10,364,242+NCBI
Human Cytogenetic Map1p36.2 NCBI
Human Genome Assembly110,205,096 - 10,301,081 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)

Annotation    (Toggle Detail/Summary View)

Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
  
More on KIF1B
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 732615
Created: 2004-01-12
Species: Homo sapiens
Last Modified: 2013-03-06
Status: ACTIVE



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