Gene Gene information from NCBI Gene database.
Entrez ID 102288414
Gene name Chromosome 11 open reading frame 98
Gene symbol C11orf98
Synonyms (NCBI Gene)
C11orf48
Chromosome 11
Chromosome location 11q12.3
Summary This gene shares three exons in common with another gene, LBH domain containing 1 (GeneID:79081), but the encoded protein uses a reading frame that is different from that of the LBH domain containing 1 gene. [provided by RefSeq, Nov 2017]
miRNA miRNA information provided by mirtarbase database.
356
miRTarBase ID miRNA Experiments Reference
MIRT741408 hsa-miR-1273h-5p PAR-CLIP 26701625
MIRT754654 hsa-miR-149-3p PAR-CLIP 26701625
MIRT741409 hsa-miR-30b-3p PAR-CLIP 26701625
MIRT741410 hsa-miR-3689a-3p PAR-CLIP 26701625
MIRT741411 hsa-miR-3689b-3p PAR-CLIP 26701625
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
E9PRG8
Protein name Uncharacterized protein C11orf98
PDB 8INF
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17719 DUF5564 1 98 Family of unknown function (DUF5564) Family
Sequence
Sequence length 123
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
IRRITABLE BOWEL SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations