Gene Gene information from NCBI Gene database.
Entrez ID 127687
Gene name Chromosome 1 open reading frame 122
Gene symbol C1orf122
Synonyms (NCBI Gene)
ALAESM
Chromosome 1
Chromosome location 1p34.3
miRNA miRNA information provided by mirtarbase database.
68
miRTarBase ID miRNA Experiments Reference
MIRT022665 hsa-miR-124-3p Microarray 18668037
MIRT023311 hsa-miR-122-5p Microarray 17612493
MIRT839472 hsa-miR-138 CLIP-seq
MIRT839473 hsa-miR-1913 CLIP-seq
MIRT839474 hsa-miR-194 CLIP-seq
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.
Q6ZSJ8
Protein name Uncharacterized protein C1orf122 (Protein ALAESM)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15855 DUF4726 10 110 Domain of unknown function (DUF4726) Family
Sequence
Sequence length 110
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
GALLOWAY-MOWAT SYNDROME 10 Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations