Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84439
Gene name Gene Name - the full gene name approved by the HGNC.
HHIP like 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HHIPL1
Synonyms (NCBI Gene) Gene synonyms aliases
KIAA1822, UNQ9245
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q32.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein that belongs to the glucose/sorbosone dehydrogenase family. The encoded protein also contains a domain that binds folate and reduced folic acid derivatives. [provided by RefSeq, Jul 2016]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT641073 hsa-miR-362-5p HITS-CLIP 23824327
MIRT641072 hsa-miR-500b-5p HITS-CLIP 23824327
MIRT641071 hsa-miR-501-5p HITS-CLIP 23824327
MIRT641070 hsa-miR-885-5p HITS-CLIP 23824327
MIRT647356 hsa-miR-877-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005515 Function Protein binding IPI 32296183
GO:0005575 Component Cellular_component ND
GO:0005576 Component Extracellular region IEA
GO:0005576 Component Extracellular region IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q96JK4
Protein name HHIP-like protein 1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03024 Folate_rec 22 183 Folate receptor family Domain
PF07995 GSDH 193 527 Glucose / Sorbosone dehydrogenase Domain
PF00530 SRCR 679 776 Scavenger receptor cysteine-rich domain Domain
Sequence
Sequence length 782
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Carpal Tunnel Syndrome Carpal tunnel syndrome N/A N/A GWAS
Coronary artery disease Coronary artery disease N/A N/A GWAS
Coronary Heart Disease Coronary heart disease N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS