FAM167B (family with sequence similarity 167 member B)

Gene Gene information from NCBI Gene database.
Gene miRNA Other IDs Protein Associated diseases
Entrez ID 84734
Gene name Family with sequence similarity 167 member B
Gene symbol FAM167B
Synonyms (NCBI Gene)
C1orf90DIORA-2
Chromosome 1
Chromosome location 1p35.2
miRNA miRNA information provided by mirtarbase database.
49
Gene miRNA Other IDs Protein Associated diseases
Show/Hide all (49)
miRTarBase ID miRNA Experiments Reference
MIRT658452 hsa-miR-330-5p HITS-CLIP 23824327
MIRT658451 hsa-miR-326 HITS-CLIP 23824327
MIRT658450 hsa-miR-6832-3p HITS-CLIP 23824327
MIRT658449 hsa-miR-877-3p HITS-CLIP 23824327
MIRT658448 hsa-miR-4287 HITS-CLIP 23824327
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.
Q9BTA0
Protein name Protein FAM167B
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF11652 FAM167 90 → 163 FAM167 Family
Sequence 
MSLGLLKFQAVGEEDEEDEEGESLDSVKALTAKLQLQTRRPSYLEWTAQVQSQAWRRAQA
KPGPGGPGDICGFDSMDSALEWLRRELREMQAQDRQLAGQLLRLRAQLHRLKMDQACHLH
QELLDEAELELELEPGAGLALAPLLRHLGLTRMNISARRFTLC
Sequence length 163
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
LIVER CIRRHOSIS, EXPERIMENTAL — CTD
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations