Gene Gene information from NCBI Gene database.
Entrez ID 90522
Gene name Yip1 interacting factor homolog B, membrane trafficking protein
Gene symbol YIF1B
Synonyms (NCBI Gene)
FinGER8KABAMAS
Chromosome 19
Chromosome location 19q13.2
miRNA miRNA information provided by mirtarbase database.
72
miRTarBase ID miRNA Experiments Reference
MIRT001396 hsa-miR-16-5p pSILAC 18668040
MIRT027066 hsa-miR-103a-3p Sequencing 20371350
MIRT001396 hsa-miR-16-5p Sequencing 20371350
MIRT001396 hsa-miR-16-5p Proteomics;Other 18668040
MIRT049802 hsa-miR-92a-3p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
24
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IBA
GO:0000139 Component Golgi membrane IEA
GO:0005515 Function Protein binding IPI 28298427, 30877195, 32296183, 33961781
GO:0005783 Component Endoplasmic reticulum IDA 26077767
GO:0005783 Component Endoplasmic reticulum IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619109 30511 ENSG00000167645
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5BJH7
Protein name Protein YIF1B (YIP1-interacting factor homolog B)
Protein function Functions in endoplasmic reticulum to Golgi vesicle-mediated transport and regulates the proper organization of the endoplasmic reticulum and the Golgi (By similarity). Plays a key role in targeting to neuronal dendrites receptors such as HTR1A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03878 YIF1 74 309 YIF1 Family
Sequence
Sequence length 314
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Kaya-Barakat-Masson syndrome Pathogenic rs1969221767, rs1969205933, rs750308729, rs564705275, rs1969205627, rs1969106432 RCV001270687
RCV001270684
RCV001270685
RCV001270686
RCV001270688
View all (1 more)
★★★★★
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
EBV-positive nodal T- and NK-cell lymphoma Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NEURODEVELOPMENTAL DISORDER-SPASTICITY-MOVEMENT DISORDER-EPILEPTIC SYNDROME Orphanet
★★☆☆☆
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
Breast Neoplasms Breast neoplasm Pubtator 32648580 Stimulate
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 32648580 Associate
★☆☆☆☆
Found in Text Mining only
Nervous System Diseases Nervous system disease Pubtator 32648580 Associate
★☆☆☆☆
Found in Text Mining only