Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Search help
21 results
  1. xmlghr-summaries.xml 
    https://medlineplus.gov/download/ghr-summaries.xml
    ... gene-summary ><gene-symbol >KIF1B</gene-symbol><name >kinesin family member 1B</name><ghr-page >https://medlineplus. ... gene provides instructions for making a protein called kinesin family member 1B, part of the kinesin family ...
  2. Congenital Fibrosis of the Extraocular Muscles Overview - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1348
    ... Engle EC. An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon ... Liu Q, Zhao C. Maternal germline mosaicism of kinesin family member 21A (KIF21A) mutation causes complex phenotypes ...
  3. xmlTopicIndex.xml 
    https://medlineplus.gov/download/TopicIndex.xml
    ... genetics/gene/khdc3l</url></topic><topic ><title >KIF1B: kinesin family member 1B</title><url >https://medlineplus.gov/genetics/gene/kif1b</url></topic><topic ><title >KIF21A: kinesin family member 21A</title><url >https://medlineplus.gov/ ...
  4. Hereditary Sensory and Autonomic Neuropathy Type II - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK49247
    ... Locus-Specific Databases HGMD ClinVar KIF1A 2q37 ​.3 Kinesin-like protein KIF1A KIF1A @ LOVD KIF1A KIF1A RETREG1 ... INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP 601255 KINESIN FAMILY MEMBER 1A; KIF1A 603415 SODIUM VOLTAGE-GATED ...
  5. Joubert Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1325
    ... 1 Protein TALPID3 KIAA0586 KIAA0586 KIF7 15q26 ​.1 Kinesin-like protein KIF7 KIF7 @ LOVD KIF7 KIF7 MKS1 ... SYNDROME 6; JBTS6 610937 RPGRIP1-LIKE; RPGRIP1L 611254 KINESIN FAMILY MEMBER 7; KIF7 611560 JOUBERT SYNDROME 7; ...
  6. DDX3X-Related Neurodevelopmental Disorder - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK561282
    ... PubMed : 22832583 ] Kanai Y, Dohmae N, Hirokawa N. Kinesin transports RNA: isolation and characterization of an RNA- ...
  7. Detailed Methods - Screening for Dyslipidemia in Younger Adults - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK396245
    ... Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and cardiovascular risk and efficacy ...
  8. Tubulinopathies Overview - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK350554
    ... Engle EC. Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. Cell. 2010;140:74– ...
  9. Cranioectodermal Dysplasia - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK154653
    ... IFT-B complex in association with the heterotrimeric kinesin-2 motor, while downward (i.e., tip-to- ...
  10. Spastic Paraplegia 3A - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK45978
    ... Pericak-Vance MA, Rubinsztein DC, Marchuk DA. A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia ( ...
previous · 1 · 2 · 3 · next