GRIFIN
Chr 7galectin-related inter-fiber protein
Predicted to enable carbohydrate binding activity. [provided by Alliance of Genome Resources, Jul 2025]
18
ClinVar variants
13
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— GRIFIN
📋
ClinVar Variants
13 Pathogenic / Likely Pathogenic· 4 VUS of 18 total submissions
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
18 submitted variants in ClinVar
Classification Summary
Pathogenic13
VUS4
Likely Benign1
13
Pathogenic
4
VUS
1
Likely Benign
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | — | — | — | — | 13 |
Likely Pathogenic | — | — | — | — | 0 |
VUS | — | — | — | — | 4 |
Likely Benign | — | — | — | — | 1 |
Benign | — | — | — | — | 0 |
| Total | — | 18 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
GRIFIN · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
OMIM — Genotype-Phenotype Relationships
1 OMIM entry
GALECTIN-RELATED INTERFIBER PROTEIN; GRIFIN
MIM #619187 · *
External Resources
Links to major genomics databases and tools
Variant Interpretation
Population Databases
Gene Resources
Expert Curation
ClinGen
Expert-curated gene-disease validity
GenCC
Gene Curation Coalition — multi-curator classifications
Orphanet
Rare disease encyclopedia and gene-disease associations
PanelApp
Gene panels for rare disease diagnostics (Genomics England)
LOVD
Leiden Open Variation Database — variant listings
GeneReviews
Expert-authored summaries of heritable conditions (NCBI)
Clinical Literature
Landmark / reviewRecent case evidence
Key Publications
Landmark & review papers · by relevance
Interactions between small heat shock protein alpha-crystallin and galectin-related interfiber protein (GRIFIN) in the ocular lens.
Barton KA et al.·Biochemistry
2009
Unlike mammalian GRIFIN, the zebrafish homologue (DrGRIFIN) represents a functional carbohydrate-binding galectin.
Ahmed H et al.·Biochem Biophys Res Commun
2008Functional
Chicken GRIFIN: A homodimeric member of the galectin network with canonical properties and a unique expression profile.
García Caballero G et al.·Biochimie
2016
Expressed sequence tag analysis of guinea pig (Cavia porcellus) eye tissues for NEIBank.
Simpanya MF et al.·Mol Vis
2008
Transcriptomics Analysis of Lens from Patients with Posterior Subcapsular Congenital Cataract.
Lin X et al.·Genes (Basel)
2021Cohort
Identification and characterization of endogenous galectins expressed in Madin Darby canine kidney cells.
Poland PA et al.·J Biol Chem
2011
Twenty-five years of child and family homelessness: where are we now?
Grant R et al.·Am J Public Health
2013Review
Proportion of subjects with psychotic features in bipolar disorder correlated with treatment response by antipsychotics for acute mania.
Ikeda M et al.·Psychiatry Clin Neurosci
2022
Top 10 resultsSearch PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Chicken GRIFIN: binding partners, developmental course of localization and activation of its lens-specific gene expression by L-Maf/Pax6.
García Caballero G et al.·Cell Tissue Res
2019
Chicken GRIFIN: Structural characterization in crystals and in solution.
Ruiz FM et al.·Biochimie
2018🔓 Open Access
Top 5 resultsSearch Europe PMC ↗
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →External Resources
Links to major genomics databases and tools
Variant Interpretation
Population Databases
Gene Resources
Expert Curation
ClinGen
Expert-curated gene-disease validity
GenCC
Gene Curation Coalition — multi-curator classifications
Orphanet
Rare disease encyclopedia and gene-disease associations
PanelApp
Gene panels for rare disease diagnostics (Genomics England)
LOVD
Leiden Open Variation Database — variant listings
GeneReviews
Expert-authored summaries of heritable conditions (NCBI)