ALB

Albumin

 

  • Alias                                 (According to NCBI)

 
  • DKFZp779N1935
  • PRO0883
  • PRO1341
  • albumin
  • Serum albumin precursor (PRO0903) (UNQ696/PRO1341).

  • Albumin is a soluble, monomeric protein which comprises about one-half of the blood serum protein. Albumin functions primarily as a carrier protein for steroids, fatty acids, and thyroid hormones and plays a role in stabilizing extracellular fluid volume. Mutations in this gene on chromosome 4 result in various anomalous proteins. Albumin is a globular unglycosylated serum protein of molecular weight 65,000. The human albumin gene is 16,961 nucleotides long from the putative 'cap' site to the first poly(A) addition site. It is split into 15 exons which are symmetrically placed within the 3 domains that are thought to have arisen by triplication of a single primordial domain. Albumin is synthesized in the liver as preproalbumin which has an N-terminal peptide that is removed before the nascent protein is released from the rough endoplasmic reticulum. The product, proalbumin, is in turn cleaved in the Golgi vesicles to produce the secreted albumin.
  • Location: 4q11-q13
  • Orientation: plus strand
  • Size: 17127  bp
  • 15 exons
  • DNA sequence (Human): NC_000004

  • CGH (4q11-q13):  Losses (%)  -15.0  Gain (%)  0.0   Amplifications (%) 0.0
  • Mutations and SNPs (According to HGMD and SNP)

 
  • HGMD (Human Gene Mutation Database): ALB
  • SNPs: ALB
  • m-RNA                       (According to NCBI and CGAP)

 

  • mRNA sequence (Human): NM_000477

  • Size: 2215  bp

  • cDNA libraries: ALB

 
  • Size: 609 amino acids; 69367 Da
  • Catalytic activity:

  • Subcellular location: Secreted.

  • Protein domains

 
  • Pathways and interactions (According to BioCarta, DIP)

  • Protein interactions:

 
  • Clinical                            (According to OMIM, PubMed)