2. Gene
  3. ITGBL1 - integrin subunit beta like 1 Gene

ITGBL1 - integrin subunit beta like 1 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as OSCP; TIED

Gene ID: 9358 | Gene type: protein coding

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
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  • 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) ≥95%

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
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS06973 ITGBL1 Human Pre-designed siRNA Set A / 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