LAMB1 - laminin subunit beta 1 Gene

Also Known as CLM; LIS5

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 3912

About LAMB1

Cytogenetic location: 7q31.1 Genomic coordinates (GRCh38): 7:107,923,799-108,003,161 (from NCBI)

This gene has 37 transcripts (splice variants), 296 orthologues, 27 paralogues and is associated with 3 phenotypes. Broad expression in placenta (RPKM 75.7), fat (RPKM 65.2) and 23 other tissues.

Summary

Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins are composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively) and they form a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. Several isoforms of each chain have been described. Different alpha, beta and gamma chain isomers combine to give rise to different heterotrimeric laminin isoforms which are designated by Arabic numerals in the order of their discovery, i.e. alpha1beta1gamma1 heterotrimer is laminin 1. The biological functions of the different chains and trimer molecules are largely unknown, but some of the chains have been shown to differ with respect to their tissue distribution, presumably reflecting diverse functions in vivo. This gene encodes the beta chain isoform laminin, beta 1. The beta 1 chain has 7 structurally distinct domains which it shares with Other beta chain isomers. The C-terminal helical region containing domains I and II are separated by domain alpha, domains III and V contain several EGF-like repeats, and domains IV and VI have a globular conformation. Laminin, beta 1 is expressed in most tissues that produce basement membranes, and is one of the 3 chains constituting laminin 1, the first laminin isolated from Engelbreth-Holm-Swarm (EHS) tumor. A sequence in the beta 1 chain that is involved in cell attachment, chemotaxis, and binding to the laminin receptor was identified and shown to have the capacity to inhibit metastasis. [provided by RefSeq, Aug 2011]

LAMB1 Products (1)

mRNA Protein Name
NM_002291.3 NP_002282.2 laminin subunit beta-1 precursor

LAMB1 Protein Structure

Laminin_N

Laminin_N: Laminin N-terminal (Domain VI) (35 - 269)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (271 - 324)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (335 - 391)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (398 - 455)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (458 - 507)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (510 - 548)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (773 - 818)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (821 - 863)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (867 - 914)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (917 - 973)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (976 - 1025)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (1028 - 1081)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (1084 - 1126)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (1132 - 1172)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1500
  • 1786 a.a.
Protein Preferred Names Protein Names

laminin subunit beta-1

  • laminin B1 chain

LAMB1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
LAMB1 P07942 GPR152 Homo sapiens Q8TDT2 32296183
Intra
LAMB1 P07942 GPR152 Homo sapiens Q8TDT2 32296183
Intra
LAMB1 P07942 GPR152 Homo sapiens Q8TDT2 32296183
Intra
LAMB1 P07942 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
LAMB1 P07942 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
LAMB1 P07942 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
LAMB1 P07942 CD79A Homo sapiens P11912 32296183
Intra
LAMB1 P07942 CD79A Homo sapiens P11912 32296183
Intra
LAMB1 P07942 CD79A Homo sapiens P11912 32296183
Cross
LAMB1 P07942 c5mbe7_cantt Candida tropicalis C5MBE7 26438063
Cross
LAMB1 P07942 c5mbe7_cantt Candida tropicalis C5MBE7 26438063
Cross: Cross-species interaction Intra: Intraspecies interaction

LAMB1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P80439 Laminin beta 1 Antibody (YA312) WB, IHC-P, FC Human, Mouse
HY-P85254 Laminin beta 1 Antibody (YA4946) IHC-P, ELISA Human
HY-P85254A Laminin beta 1 Antibody (YA4946)(PBS only) IHC-P, ELISA Human
HY-P86418 Laminin beta 1 Antibody (YA6110) WB, IHC-P, ICC/IF, IP, ELISA Human, Mouse, Rat

Related Diseases

Diseases Alias
Lissencephaly 5
  • LIS5

  • Cobblestone Lissencephaly Without Muscular Or Ocular Involvement

  • Cobblestone Lissencephaly Without Muscular Or Eye Involvement

  • Lissencephaly Type 2 Without Muscular Or Eye Involvement

  • Lissencephaly Type 2 Without Muscular Or Ocular Involvement

  • Lissencephaly, Type 5

Cutis Laxa
  • Generalized Elastolysis

  • Loose Skin

  • Dermatolysis

  • Dermatomegaly

  • Cutis Laxa Syndrome

Band Heterotopia
  • Subcortical Band Heterotopia

  • Double Cortex Syndrome

  • Subcortical Laminar Heterotopia

  • Double Cortex

  • Band Heterotopia Of Brain

  • BH

  • Heco

  • Heterotopic Cortex

  • Familial Band Heterotopia

  • Dc

  • Dc Syndrome

  • Heterotopia, Subcortical Band

  • Sbh

  • Sclh

  • Bhy

Teratocarcinoma
  • Mixed Embryonal Carcinoma And Teratoma

Nephrotic Syndrome, Type 5, With Or Without Ocular Abnormalities
  • NPHS5

  • Nephrotic Syndrome Type 5

  • Nephrotic Syndrome Type 5, With Or Without Ocular Abnormalities

  • Nephrotic Syndrome 5 With Or Without Ocular Abnormalities

  • Nephrotic Syndrome, Type 5, With/Without Ocular Abnormalities

Junctional Epidermolysis Bullosa
  • Epidermolysis Bullosa, Junctional

  • Jeb

  • Epidermolysis Bullosa Atrophicans

  • Congenital Junctional Epidermolysis Bullosa

  • Epidermolysis Bullosa Junctional

  • Junctional Eb - [Epidermolysis Bullosa]

  • Jeb - [Junctional Epidermolysis Bullosa]

  • Lucidolytic Epidermolysis Bullosa

Embryonal Carcinoma
  • Embryonal Neoplasm

  • Embryonal Cancer

  • Primary Extragonadal Embryonal Carcinoma

  • Embryo Neoplasm

  • Carcinoma Embryonal

  • Cancer Embryonal

  • Carcinoma, Embryonal

  • Extragonadal Embryonal Carcinoma

  • Cancer, Embryonal

Supravalvular Aortic Stenosis
  • SVAS

  • Supravalvar Aortic Stenosis

  • Supravalvar Aortic Stenosis, Eisenberg Type

  • Aortic Supravalvular Stenosis

  • Aortic Stenosis, Supravalvular

  • Supra-Valvular Aortic Stenosis

  • Stenosis, Aortic Supravalvular

  • Stenosis, Supravalvular Aortic

  • Supravalvular Stenosis, Aortic

  • Aortic Stenosis Supravalvular

Hepatocellular Clear Cell Carcinoma
  • Clear Cell Carcinoma Of The Liver Cells

  • Hepatocellular Carcinoma, Clear Cell Type

  • Clear Cell Hepatocellular Carcinoma

Leiomyoma
  • Leiomyomatous Neoplasm

  • Leiomyomatous Tumor

  • Leiomyomas

  • Fibroid Tumor

  • Uterine Fibroids

Muscular Dystrophy
  • Muscular Dystrophies

  • Congenital Md

  • Congenital Muscular Dystrophy

  • Cmd

  • Mdc

  • Dystrophy, Muscular

  • Gower'S Muscular Dystrophy

  • Progressive Musclular Dystrophy

  • Pseudohypertrophic Atrophy

  • Pseudohypertrophic Muscle Paralysis

  • Pseudohypertrophic Muscular Atrophy

  • Pseudohypertrophic Muscular Dystrophy

  • Pseudohypertrophic Paralysis

  • Pseudomuscular Hypertrophy

Diffuse Mesangial Sclerosis
  • Familial Mesangial Sclerosis

  • Mesangial Sclerosis, Diffuse

  • Dms

  • Diffuse Isolated Mesangial Sclerosis

  • Isolated Diffuse Mesangial Sclerosis

  • Nephrotic Syndrome, Early Onset With Diffuse Mesangial Sclerosis

Leiomyomatosis
Lissencephaly
  • Pachygyria

  • Broad Gyri Of Cerebrum

  • Large Gyri Of Cerebrum

  • Macrogyria

Pierson Syndrome
  • Microcoria-Congenital Nephrotic Syndrome

  • Microcoria-Congenital Nephrosis Syndrome

  • PIERS

  • Microcoria - Congenital Nephrosis

  • Microcoria - Congenital Nephrotic Syndrome

  • PIERSS

Myopathy
  • Muscular Diseases

  • Myopathies

Autism Spectrum Disorder
  • Asd

  • Autism Spectrum Disorders

  • Autistic Continuum

  • Pervasive Developmental Disorder

  • Pervasive Development Disorder

  • Autistic Behavior

  • Autistic Disorder

  • Autistic

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Childhood Autism

  • Kanner Syndrome

  • Pervasive Developmental Delay Nos

  • Pervasive Developmental Disorder, Not Otherwise Specified

Walker-Warburg Syndrome
  • Hard Syndrome

  • Walker-Warburg Congenital Muscular Dystrophy

  • Cerebroocular Dysplasia-Muscular Dystrophy Syndrome

  • Cod-Md Syndrome

  • Chemke Syndrome

  • Hydrocephalus, Agyria And Retinal Dysplasia

  • Cerebroocular Dysgenesis

  • Cerebroocular Dysplasia Muscular Dystrophy Syndrome

  • Hard +/- E Syndrome

  • Pagon Syndrome

  • Warburg Syndrome

  • Hydrocephalus, Agyria, And Retinal Dysplasia

  • Mddga

  • Muscular Dystrophy-Dystroglycanopathy , Type A

  • Muscular Dystrophy-Dystroglycanopathy [With Brain And Eye Anomalies], Type A

  • Hydrocephalus-Agyria-Retinal Dysplasia Syndrome

  • Wws

  • Dystrophy, Muscular, Dystroglycanopathy, Type A

Autism
  • Autistic Disorder

  • Autism Susceptibility 1

  • Childhood Autism

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Kanner'S Syndrome

  • Autistic

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
Felis catus LAMB1 VGNC VGNC:68006
Bos taurus LAMB1 VGNC VGNC:30772
Rattus norvegicus LAMB1 RGD RGD:1306311
Macaca mulatta LAMB1 VGNC VGNC:74228
Canis familiaris LAMB1 VGNC VGNC:42567
Mus musculus LAMB1 MGD MGI:96743
Others LAMB1 NCBI