LIN7A - lin-7 homolog A, crumbs cell polarity complex component Gene

Also Known as LIN7; MALS1; VELI1; LIN-7A; MALS-1; TIP-33

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 8825

About LIN7A

Cytogenetic location: 12q21.31 Genomic coordinates (GRCh38): 12:80,792,520-80,937,934 (from NCBI)

This gene has 4 transcripts (splice variants), 210 orthologues and 3 paralogues. Broad expression in bone marrow (RPKM 7.9), brain (RPKM 5.7) and 20 other tissues.

Summary

The protein encoded by this gene is involved in generating and maintaining the asymmetric distribution of channels and receptors at the cell membrane. The encoded protein also is required for the localization of some specific channels and can be part of a protein complex that couples synaptic vesicle exocytosis to cell adhesion in the brain. [provided by RefSeq, May 2016]

LIN7A Products (2)

mRNA Protein Name
NM_001324423.2 NP_001311352.1 protein lin-7 homolog A isoform 2
NM_004664.4 NP_004655.1 protein lin-7 homolog A isoform 1
Molecular Function GO Annotation Evidence References Source
enables L27 domain binding IPI
IPI: Inferred from physical interaction
17237226 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11311936 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

LIN7A Protein Structure

L27

L27: L27 domain (28 - 83)

PDZ

PDZ: PDZ domain (Also known as DHR or GLGF) (109 - 187)

  • 0
  • 100
  • 200
  • 233 a.a.
Protein Preferred Names Protein Names

protein lin-7 homolog A

  • mammalian lin-seven protein 1

LIN7A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
LIN7A O14910 FAM9B Homo sapiens Q8IZU0 25416956
Intra
LIN7A O14910 MPP2 Homo sapiens Q14168-2 31515488
Intra
LIN7A O14910 MPP2 Homo sapiens Q14168-2 25416956
Intra
LIN7A O14910 MPP2 Homo sapiens Q14168-2 25416956
Intra
LIN7A O14910 CASK Homo sapiens O14936-4 32296183
Intra
LIN7A O14910 CASK Homo sapiens O14936-4 32296183
Intra
LIN7A O14910 CASK Homo sapiens O14936-4 32296183
Intra
LIN7A O14910 CASK Homo sapiens O14936 25416956
Intra
LIN7A O14910 CASK Homo sapiens O14936 24366813
Intra
LIN7A O14910 CASK Homo sapiens O14936 25416956
Intra
LIN7A O14910 MPP2 Homo sapiens Q14168-4 32296183
Intra
LIN7A O14910 MPP2 Homo sapiens Q14168-4 32296183
Intra
LIN7A O14910 MPP2 Homo sapiens Q14168-4 32296183
Intra
LIN7A O14910 PALS1 Homo sapiens Q8N3R9 24366813
Intra
LIN7A O14910 PALS1 Homo sapiens Q8N3R9 31515488
Intra
LIN7A O14910 PALS1 Homo sapiens Q8N3R9 25416956
Intra
LIN7A O14910 PALS1 Homo sapiens Q8N3R9 32296183
Intra
LIN7A O14910 MPP7 Homo sapiens Q5T2T1 32296183
Intra
LIN7A O14910 MPP7 Homo sapiens Q5T2T1 24366813
Intra
LIN7A O14910 MPP7 Homo sapiens Q5T2T1 32296183
Intra
LIN7A O14910 MPP7 Homo sapiens Q5T2T1 32296183
Intra
LIN7A O14910 PALS2 Homo sapiens Q9NZW5 32296183
Intra
LIN7A O14910 PALS2 Homo sapiens Q9NZW5 32296183
Intra
LIN7A O14910 PALS2 Homo sapiens Q9NZW5 24366813
Intra
LIN7A O14910 PALS2 Homo sapiens Q9NZW5 32296183
Intra
LIN7A O14910 ZYX Homo sapiens Q15942 25416956
Intra
LIN7A O14910 ZYX Homo sapiens Q15942 25416956
Intra
LIN7A O14910 ZYX Homo sapiens Q15942 25416956
Intra
LIN7A O14910 MPP3 Homo sapiens Q13368 32296183
Intra
LIN7A O14910 MPP3 Homo sapiens Q13368 32296183
Intra
LIN7A O14910 MPP3 Homo sapiens Q13368 32296183
Intra
LIN7A O14910 MDFI Homo sapiens Q99750 32296183
Intra
LIN7A O14910 MDFI Homo sapiens Q99750 32296183
Intra
LIN7A O14910 MDFI Homo sapiens Q99750 32296183
Intra
LIN7A O14910 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Intra
LIN7A O14910 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Intra
LIN7A O14910 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Intra
LIN7A O14910 CHRD Homo sapiens Q9H2X0 32296183
Intra
LIN7A O14910 ECM1 Homo sapiens Q16610 32296183
Intra
LIN7A O14910 ECM1 Homo sapiens Q16610 32296183
Intra
LIN7A O14910 ECM1 Homo sapiens Q16610 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Chronic Tubotympanic Suppurative Otitis Media
  • Chronic Tubotympanic Disease

  • Benign Chronic Suppurative Otitis Media

Chronic Atticoantral Disease
  • Chronic Atticoantral Suppurative Otitis Media

  • Persistent Mucosal Disease

  • Chronic Atticoantral Disorder

Syndromic X-Linked Intellectual Disability Najm Type
  • Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia

  • Micpch

  • X-Linked Intellectual Disability-Microcephaly-Pontocerebellar Hypoplasia Syndrome

Adhesive Otitis Media
  • Adhesive Middle Ear Disease

  • Chronic Adhesive Otitis Media

  • Adhesive Otitis

  • Fibrotic Adhesive Otitis Media

  • Adhesive Disorder Of Middle Ear

Retinitis Pigmentosa 12
  • RP12

  • Retinitis Pigmentosa With Or Without Paraarteriolar Preservation Of Retinal Pigment Epithelium

  • Rp With Or Without Preserved Paraarteriole Retinal Pigment Epithelium

  • Rp With Or Without Pprpe

  • Retinitis Pigmentosa-12

Attention Deficit-Hyperactivity Disorder
  • Attention Deficit Hyperactivity Disorder

  • ADHD

  • Attention Deficit Disorder

  • Attention Deficit-Hyperactivity Disorder, Susceptibility To

  • Attention Deficit Disorder With Hyperactivity

  • Hyperkinetic Disorder

  • Hyperactivity Of Childhood

  • Attention-Deficit/Hyperactivity Disorder

  • Add

  • Addh

  • Attention Deficit

  • Attention Deficit Disorder Of Childhood With Hyperactivity

  • Attention Deficit Disorder With Hyperactivity Syndrome

  • Hyperkinetic Syndrome

  • Attention-Deficit Hyperactivity Disorder

  • Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type

  • Disturbance Of Activity And Attention

  • Disorder Of Activity And Attention

  • Adhd - [Attention Deficit Hyperactivity Disorder]

  • Hyperkinetic Disorders

  • Disorder Of Activity And Attention With Hyperkinesia

  • Attention Deficit Syndrome With Hyperactivity

Opitz-Kaveggia Syndrome
  • Fg Syndrome

  • Fgs1

  • Fgs

  • Keller Syndrome

  • OKS

  • Fg Syndrome 1

  • Fg Syndrome Type 1

  • Mental Retardation, Large Head, Imperforate Anus, Congenital Hypotonia, And Partial Agenesis Of Corpus Callosum

  • Intellectual Disability, Large Head, Imperforate Anus, Congenital Hypotonia, And Partial Agenesis Of Corpus Callosum

  • Mental Retardation, Large Head, Imperforate Anus, Congenital Hypotonia, And Partial Agenesis Of The Corpus Callosum

Leber Plus Disease
  • Leber Congenital Amaurosis

  • Lca

  • Leber'S Amaurosis

  • Leber'S Disease

  • Amaurosis Congenita Of Leber

  • Amaurosis Congenita Of Leber, Type 1

  • Lhon Plus Disease

  • Congenital Absence Of The Rods And Cones

  • Congenital Retinal Blindness

  • Crb

  • Congenital Amaurosis Of Retinal Origin

  • Leber'S Congenital Amaurosis

  • Leber Congenital Amaurosis 1

  • Leber'S Congenital Tapetoretinal Degeneration

  • Leber'S Congenital Tapetoretinal Dysplasia

  • Lca1

  • Leber Congenital Amaurosis Type 1

  • Retinal Blindness, Congenital

  • Amaurosis, Leber Congenital

  • Dysgenesis Neuroepithelialis Retinae

  • Hereditary Epithelial Dysplasia Of Retina

  • Hereditary Retinal Aplasia

  • Heredoretinopathia Congenitalis

  • Leber Abiotrophy

  • Leber Congenital Tapetoretinal Degeneration

  • Lebers Congenital Amaurosis

  • Optic Atrophy, Hereditary, Leber

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

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 LIN7A VGNC VGNC:74068
Mus musculus LIN7A MGD MGI:2135609
Bos taurus LIN7A VGNC VGNC:30895
Felis catus LIN7A VGNC VGNC:63233
Rattus norvegicus LIN7A RGD RGD:621256
Canis familiaris LIN7A VGNC VGNC:42686
Others LIN7A NCBI