XYLB - xylulokinase Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 9942

About XYLB

Cytogenetic location: 3p22.2 Genomic coordinates (GRCh38): 3:38,346,785-38,453,041 (from NCBI)

This gene has 7 transcripts (splice variants), 196 orthologues and 6 paralogues. Broad expression in liver (RPKM 5.0), kidney (RPKM 3.6) and 18 other tissues.

Summary

The protein encoded by this gene shares 22% sequence identity with Hemophilus influenzae xylulokinase, and even higher identity to Other gene products in C.elegans (45%) and yeast (31-35%), which are thought to belong to a family of Enzymes that include fucokinase, gluconokinase, glycerokinase and xylulokinase. These proteins play important roles in energy metabolism. [provided by RefSeq, Aug 2009]

XYLB Products (4)

mRNA Protein Name
NM_001349178.2 NP_001336107.1 xylulose kinase isoform 1
NM_001349179.2 NP_001336108.1 xylulose kinase isoform 3
NM_001349180.2 NP_001336109.1 xylulose kinase isoform 4
NM_005108.4 NP_005099.2 xylulose kinase isoform 2

XYLB Protein Structure

FGGY_N

FGGY_N: FGGY family of carbohydrate kinases, N-terminal domain (10 - 287)

FGGY_C

FGGY_C: FGGY family of carbohydrate kinases, C-terminal domain (296 - 480)

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  • 536 a.a.
Protein Preferred Names Protein Names

xylulose kinase

  • D-xylulokinase

Related Diseases

Diseases Alias
Pentosuria
  • Xylitol Dehydrogenase Deficiency

  • L-Xylulosuria

  • L-Xylulose Reductase Deficiency

  • Essential Pentosuria

  • PNTSU

  • Essential Benign Pentosuria

Terminal Osseous Dysplasia
  • Terminal Osseous Dysplasia And Pigmentary Defects

  • Terminal Osseous Dysplasia-Pigmentary Defects Syndrome

  • Todpd

  • TOD

  • Odpd

  • Odpf Syndrome

  • Osseous Dysplasia, Digital, With Facial Pigmentary Defects And Multiple Frenula

  • Odpf

  • Digital Osseous Dysplasia With Facial Pigmentary Defects And Multiple Frenula

  • Terminal Osseous Dysplasia With Pigmentary Defects

  • Dcd

  • Digitocutaneous Dysplasia

  • Terminal Osseous Dysplasia And Pigmentary Defect Syndrome

  • Osseous Dysplasia And Pigmentary Defects

Iminoglycinuria
  • Iminoglycinuria, Digenic

  • IG

Neutropenia, Severe Congenital, X-Linked
  • X-Linked Severe Congenital Neutropenia

  • XLN

  • SCNX

  • Severe Congenital Neutropenia X-Linked

  • Neutropenia, Congenital, Severe, X-Linked

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 XYLB VGNC VGNC:78815
Bos taurus XYLB VGNC VGNC:37011
Rattus norvegicus XYLB RGD RGD:1307372
Mus musculus XYLB MGD MGI:2142985
Felis catus XYLB VGNC VGNC:97690
Canis familiaris XYLB VGNC VGNC:48474