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:0003824 Function Catalytic activity IEA
GO:0005044 Function Scavenger receptor activity IEA
GO:0005575 Component Cellular_component ND
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
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Coronary artery disease CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1, Coronary Artery Disease rs137852988, rs121918313, rs121918529, rs121918531, rs137852340, rs1555800701, rs1215189537 23202125, 29212778, 21378990, 26343387, 28714975
Unknown
Disease term Disease name Evidence References Source
Coronary heart disease Coronary heart disease 21378990 ClinVar
Myocardial Infarction Myocardial Infarction GWAS
Coronary Heart Disease Coronary Heart Disease GWAS
Lung adenocarcinoma Lung adenocarcinoma Validation that loss of Tgfbr2 results in more aggressive and T cell-excluded KP lung tumors GWAS, CBGDA