Gene Gene information from NCBI Gene database.
Entrez ID 84272
Gene name Yip1 domain family member 4
Gene symbol YIPF4
Synonyms (NCBI Gene)
FinGER4Nbla11189YIPFalpha2
Chromosome 2
Chromosome location 2p22.3
miRNA miRNA information provided by mirtarbase database.
703
miRTarBase ID miRNA Experiments Reference
MIRT031780 hsa-miR-16-5p Proteomics 18668040
MIRT045777 hsa-miR-125a-5p CLASH 23622248
MIRT675783 hsa-miR-3664-5p HITS-CLIP 23824327
MIRT672496 hsa-miR-3929 HITS-CLIP 23824327
MIRT672495 hsa-miR-4419b HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16189514, 25416956, 28514442, 32296183
GO:0005783 Component Endoplasmic reticulum IDA
GO:0005794 Component Golgi apparatus IDA
GO:0005794 Component Golgi apparatus IEA
GO:0005802 Component Trans-Golgi network IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617534 28145 ENSG00000119820
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BSR8
Protein name Protein YIPF4 (YIP1 family member 4)
Protein function Involved in the maintenance of the Golgi structure.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04893 Yip1 95 242 Yip1 domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in keratinocytes (at protein level). {ECO:0000269|PubMed:26235900}.
Sequence
Sequence length 244
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
GOUT 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
Polycythemia Vera Polycythemia vera Pubtator 26235900 Associate
★☆☆☆☆
Found in Text Mining only