FAM138C
Chr 9family with sequence similarity 138 member C
Also known as: F379
I cannot provide a clinical summary for FAM138C as no functional or clinical information was provided in the data. This gene requires additional evidence regarding protein function, associated diseases, and inheritance patterns before a clinical summary can be written.
Clinical Summary— FAM138C
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
0 submitted variants in ClinVar
Protein Context — Lollipop Plot
FAM138C · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
3D Protein StructureAlphaFold
External Resources
Links to major genomics databases and tools
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →Clinical Literature
Open Research Assistant →Landmark / reviewRecent case evidence
Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
Identification of Copy Number Variants in a Southern Chinese Cohort of Patients with Congenital Scoliosis
Lai W et al.·Genes (Basel)
2021Cohort
Duplication of 9p24.3 in three unrelated patients and their phenotypes, considering affected genes, and similar recurrent variants
Capkova Z et al.·Mol Genet Genomic Med
2021Cohort
An immune infiltration-related prognostic model of kidney renal clear cell carcinoma with two valuable markers: CAPN12 and MSC
Xia G et al.·Front Oncol
2023Functional
From karyotypes to precision genomics in 9p deletion and duplication syndromes
Sams EI et al.·HGG Adv
2021
Top 5 full-text resultsSearch PubTator3 ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
No open access results found
Top 5 resultsSearch Europe PMC ↗
External Resources
Links to major genomics databases and tools