ITGBL1 - integrin subunit beta like 1 Gene

Also Known as OSCP; TIED

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 9358

About ITGBL1

Cytogenetic location: 13q33.1 Genomic coordinates (GRCh38): 13:101,452,675-101,723,106 (from NCBI)

This gene has 6 transcripts (splice variants), 197 orthologues and 8 paralogues. Broad expression in gall bladder (RPKM 11.4), lung (RPKM 9.5) and 18 other tissues.

Summary

This gene encodes a beta integrin-related protein that is a member of the EGF-like protein family. The encoded protein contains integrin-like cysteine-rich repeats. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]

ITGBL1 Products (4)

mRNA Protein Name
NM_001271754.2 NP_001258683.1 integrin beta-like protein 1 isoform 4
NM_001271755.2 NP_001258684.1 integrin beta-like protein 1 isoform 2 precursor
NM_001271756.2 NP_001258685.1 integrin beta-like protein 1 isoform 3
NM_004791.3 NP_004782.1 integrin beta-like protein 1 isoform 1 precursor

ITGBL1 Protein Structure

EGF_2

EGF_2: EGF-like domain (96 - 126)

EGF_2

EGF_2: EGF-like domain (192 - 216)

EGF_2

EGF_2: EGF-like domain (281 - 310)

EGF_2

EGF_2: EGF-like domain (375 - 398)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 494 a.a.
Protein Preferred Names Protein Names

integrin beta-like protein 1

  • integrin beta like 1

Recombinant ITGBL1 Proteins

Cat. No. Product Name Accession Purity
HY-P71448 ITGBL1 Protein, Human (Myc, His) O95965 (V24-P494) ≥ 90%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Myasthenic Syndrome, Congenital, 13

  • Congenital Myasthenic Syndrome 13

  • CMS13

  • Cmsta2

  • Myasthenic Syndrome, Congenital, With Tubular Aggregates 2

  • Myasthenic Syndrome, Congenital, 13, With Tubular Aggregates

  • Congenital Myasthenic Syndrome 13 With Tubular Aggregates

  • Congenital Myasthenic Syndrome With Tubular Aggregates 2

  • Myasthenic Syndrome, Congenital, With Tubular Aggregates, 2

  • Myasthenic Syndrome, Congenital, With Tubular Aggregates, Type 2
Corneal Dystrophy, Posterior Polymorphous, 1

  • Posterior Polymorphous Corneal Dystrophy

  • Ppcd

  • Maumenee Corneal Dystrophy

  • Posterior Polymorphous Corneal Dystrophy 1

  • PPCD1

  • Corneal Dystrophy, Hereditary Polymorphous Posterior

  • Corneal Endothelial Dystrophy 1, Autosomal Dominant

  • Schlichting Dystrophy

  • Ched1

  • Corneal Endothelial Dystrophy 1, Autosomal Dominant, Formerly

  • Ched1, Formerly

  • Hereditary Polymorphus Posterior Corneal Dystrophy

  • Posterior Polymorphous Dystrophy

  • Hereditary Polymorphous Posterior Corneal Dystrophy

  • Dystrophy, Corneal, Posterior Polymorphous

  • Dystrophy, Corneal, Posterior Polymorphous, Type 1

  • Polymorphous Corneal Dystrophy

  • Corneal Endothelial Dystrophy 2
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (3)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS06973 ITGBL1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS16263 Itgbl1 Mouse Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS24673 Itgbl1 Rat Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Bos taurus ITGBL1 VGNC VGNC:53818
Macaca mulatta ITGBL1 VGNC VGNC:73792
Mus musculus ITGBL1 MGD MGI:2443439
Felis catus ITGBL1 VGNC VGNC:67858
Rattus norvegicus ITGBL1 RGD RGD:1560635
Canis familiaris ITGBL1 VGNC VGNC:42144
Others ITGBL1 NCBI