1. Gene
  2. LIN7C - lin-7 homolog C, crumbs cell polarity complex component Gene

LIN7C - lin-7 homolog C, crumbs cell polarity complex component Gene

Homo sapiens

Also known as MALS3; VELI3; LIN-7C; MALS-3; LIN-7-C

Gene ID: 55327 | Gene type: protein coding

About LIN7C

Cytogenetic location: 11p14.1 Genomic coordinates (GRCh38): 11:27,494,418-27,506,769 (from NCBI)

This gene has 2 transcripts (splice variants), 213 orthologues and 3 paralogues. Ubiquitous expression in thyroid (RPKM 9.8), liver (RPKM 7.0) and 25 other tissues.

Summary

Enables L27 domain binding activity and cytoskeletal protein binding activity. Involved in morphogenesis of an epithelial sheet. Located in cell-cell junction; cytoplasm; and plasma membrane. Part of MPP7-DLG1-LIN7 complex. [provided by Alliance of Genome Resources, Apr 2022]

LIN7C Products(1)

mRNA Protein Name
NM_018362.4 NP_060832.1 protein lin-7 homolog C

LIN7C Protein Structure

L27

L27: L27 domain (14 - 68)

PDZ

PDZ: PDZ domain (Also known as DHR or GLGF) (94 - 172)

  • 0
  • 100
  • 197 a.a.
Protein Preferred Names Protein Names

protein lin-7 homolog C

LIN-7 protein 3

Related Diseases

Diseases Alias
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

Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome

Wagr Syndrome

11p Partial Monosomy Syndrome

Chromosome 11p13 Deletion Syndrome

Wilms Tumor, Aniridia, Genitourinary Anomalies And Mental Retardation Syndrome

11p Deletion Syndrome

Chromosome 11p Deletion Syndrome

Wagr Complex

Wilms Tumor-Aniridia-Genitourinary Anomalies-Intellectual Disability Syndrome

Deletion 11p13

WAGR

Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Syndrome

Chromosome 11p Deletion

11p Deletion

11p Monosomy

Deletion 11p

Monosomy 11p

Partial Monosomy 11p

Agr Triad

Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome

Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome

Wagr Contiguous Gene Syndrome

Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome

Wilms Tumor-Aniridia-Genitourinary Anomalies-Mr Syndrome

Del(11)(P13)

Monosomy 11p13

Chromosome 11, Deletion 11p

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 LIN7C VGNC VGNC:82034
Macaca mulatta LIN7C VGNC VGNC:74070
Mus musculus LIN7C MGD MGI:1330839
Rattus norvegicus LIN7C RGD RGD:621164
Bos taurus LIN7C VGNC VGNC:30897