LGTN

protein-coding

ligatin

Gene summary

Ligatin is a peripheral membrane protein found in mammalian and avian tissues during embryonic development and in early differentiated states. It is a receptor that localizes phosphoglycoproteins within endosomes and at the cell periphery where they participate in specific metabolic processes, as well as intercellular adhesion. Ligatin is, therefore, a trafficking receptor for phosphoglycoproteins (summary by Jakoi et al., 1989 [PubMed 2482295]).[supplied by OMIM, Jan 2011]

MANE transcript

N/A

Inheritance

—

ClinVar variants

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Top phenotype

—

Max pathogenic AF

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External References & Databases

GenCC Phenotypes & Disease Associations

Curated gene-disease validity assertions and inheritance patterns

No GenCC data available for this gene.

ClinVar Associated Diseases & Phenotypes

Reported disease conditions connected to LGTN variants in ClinVar

0 Conditions Cataloged

No annotated ClinVar phenotypes.

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript . Only rare variants are included.

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
0
missense
0
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
0
Total000000
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Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 0 of 0 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
No transcripts match your selected source or search query.
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