UBALD2 (UBA like domain containing 2)

Gene Gene information from NCBI Gene database.
Gene miRNA Other IDs Protein Associated diseases
Entrez ID 283991
Gene name UBA like domain containing 2
Gene symbol UBALD2
Synonyms (NCBI Gene)
FAM100B
Chromosome 17
Chromosome location 17q25.1
miRNA miRNA information provided by mirtarbase database.
15
Gene miRNA Other IDs Protein Associated diseases
Show/Hide all (15)
miRTarBase ID miRNA Experiments Reference
MIRT489449 hsa-miR-4738-5p PAR-CLIP 24398324
MIRT489449 hsa-miR-4738-5p PAR-CLIP 23592263
MIRT489449 hsa-miR-4738-5p PAR-CLIP 26701625
MIRT489449 hsa-miR-4738-5p PAR-CLIP 26701625
MIRT489449 hsa-miR-4738-5p PAR-CLIP 26701625
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
Gene miRNA Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IYN6
Protein name UBA-like domain-containing protein 2
PDB 2DZL
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14555 UBA_4 11 → 53 Domain
Sequence 
MSVNMDELRHQVMINQFVLAAGCAADQAKQLLQAAHWQFETALSTFFQETNIPNSHHHHQ
MMCTPSNTPATPPNFPDALAMFSKLRASEGLQSSNSPMTAAACSPPANFSPFWASSPPSH
QAPWIPPSSPTTFHHLHRPQPTWPPGAQQGGAQQKAMAAMDGQR
Sequence length 164
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Gene miRNA Other IDs Protein Associated diseases
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)
Show/Hide Unknown Diseases (1)
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
SCOLIOSIS — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations