Gene Gene information from NCBI Gene database.
Entrez ID 29125
Gene name Chromosome 11 open reading frame 21
Gene symbol C11orf21
Synonyms (NCBI Gene)
-
Chromosome 11
Chromosome location 11p15.5
miRNA miRNA information provided by mirtarbase database.
120
miRTarBase ID miRNA Experiments Reference
MIRT829401 hsa-miR-1205 CLIP-seq
MIRT829402 hsa-miR-1236 CLIP-seq
MIRT829403 hsa-miR-1257 CLIP-seq
MIRT829404 hsa-miR-125a-5p CLIP-seq
MIRT829405 hsa-miR-125b CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611033 13231 ENSG00000110665
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9P2W6
Protein name Uncharacterized protein C11orf21
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15399 DUF4620 20 132 Domain of unknown function (DUF4620) Family
Tissue specificity TISSUE SPECIFICITY: Expressed exclusively in heart.
Sequence
Sequence length 132
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
9
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
CHRONIC LYMPHOCYTIC LEUKEMIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LEUKEMIA, LYMPHOCYTIC, CHRONIC, B-CELL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OBESITY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OROFACIAL CLEFT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Autistic Disorder Autism Pubtator 25180572 Associate
★☆☆☆☆
Found in Text Mining only
Beckwith-Wiedemann Syndrome Beckwith-Wiedemann Syndrome BEFREE 11054561
★☆☆☆☆
Found in Text Mining only
Bipolar Disorder Bipolar Disorder GWASCAT_DG 29064472
★☆☆☆☆
Found in Text Mining only
Chronic Lymphocytic Leukemia Lymphocytic Leukemia GWASDB_DG 23770605
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Chronic Lymphocytic Leukemia Lymphocytic Leukemia CTD_human_DG 23770605
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Chronic Lymphocytic Leukemia Lymphocytic Leukemia GWASCAT_DG 26956414, 28165464
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Schizoaffective Disorder Schizoaffective Disorder GWASCAT_DG 29064472
★☆☆☆☆
Found in Text Mining only
Schizophrenia Schizophrenia GWASCAT_DG 29064472
★☆☆☆☆
Found in Text Mining only
Small Lymphocytic Lymphoma Lymphocytic Leukemia GWASCAT_DG 26956414, 28165464
★☆☆☆☆
Found in Text Mining only