KIF26B - kinesin family member 26B Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 55083

About KIF26B

Cytogenetic location: 1q44 Genomic coordinates (GRCh38): 1:245,154,985-245,709,432 (from NCBI)

This gene has 4 transcripts (splice variants), 1 gene allele, 248 orthologues and 41 paralogues. Broad expression in placenta (RPKM 1.6), endometrium (RPKM 0.9) and 19 other tissues.

Summary

The protein encoded by this gene is an intracellular motor protein thought to transport organelles along microtubules. The encoded protein is required for kidney development. Elevated levels of this protein have been found in some breast and colorectal cancers. [provided by RefSeq, Mar 2017]

KIF26B Products (1)

mRNA Protein Name
NM_018012.4 NP_060482.2 kinesin-like protein KIF26B

KIF26B Protein Structure

Kinesin

Kinesin: Kinesin motor domain (495 - 798)

  • 0
  • 400
  • 800
  • 1200
  • 1600
  • 2000
  • 2108 a.a.
Protein Preferred Names Protein Names

kinesin-like protein KIF26B

Related Diseases

Diseases Alias
Autosomal Dominant Cerebellar Ataxia
  • Spinocerebellar Ataxia

  • Adca

  • Pierre Marie Cerebellar Ataxia

  • Ataxia, Spinocerebellar

  • Sca

  • Autosomal Dominant Spinocerebellar Ataxia

  • Spinocerebellar Ataxias

Spinocerebellar Ataxia, Autosomal Recessive 17
  • Autosomal Recessive Spinocerebellar Ataxia 17

  • SCAR17

  • Autosomal Recessive Cerebellar Ataxia Due To Cwf19l1 Deficiency

  • Spinocerebellar Ataxia Autosomal Recessive Type 17

  • Spinocerebellar Ataxia, Autosomal Recessive, 17

  • Ataxia, Spinocerebellar, Autosomal Recessive, Type 17

Bladder Urachal Carcinoma
  • Urachal Cancer

  • Urachal Carcinoma

Urachus Cancer
  • Malignant Tumor Of Urachus

Brittle Cornea Syndrome 1
  • Brittle Cornea Syndrome

  • Fragilitas Oculi With Joint Hyperextensibility

  • Dysgenesis Mesodermalis Corneae Et Sclerae

  • BCS1

  • Corneal Fragility, Keratoglobus, Blue Sclerae, Joint Hyperextensibility

  • Ehlers-Danlos Syndrome, Type Vib, Formerly

  • Eds6b, Formerly

  • Type Vib Ehlers-Danlos Syndrome

  • Eds Vib

  • Ehlers-Danlos Syndrome Type 6b

  • Corneal Fragility Keratoglobus Blue Sclerae Joint Hyperextensibility

  • Eds6b Formerly

  • Ehlers-Danlos Syndrome Type Vib Formerly

  • Ehlers-Danlos Syndrome Type 6

  • Cornea, Brittle, Syndrome

  • Cornea, Brittle, Syndrome, Type 1

  • Ehlers-Danlos Syndrome 6b

Keratoconus
  • Kc

  • Conical Cornea

  • Noninflammatory Corneal Thining

  • Bulging Cornea

  • Cornea Conical

  • Acquired Conus Of Cornea

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
Macaca mulatta KIF26B VGNC VGNC:99991
Bos taurus KIF26B VGNC VGNC:58385
Mus musculus KIF26B MGD MGI:2447076
Felis catus KIF26B VGNC VGNC:63116
Canis familiaris KIF26B VGNC VGNC:42400
Rattus norvegicus KIF26B RGD RGD:1560022