Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
11067
Gene name Gene Name - the full gene name approved by the HGNC.
DEPP autophagy regulator 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DEPP1
Synonyms (NCBI Gene) Gene synonyms aliases
C10orf10, DEPP, FIG, Fseg
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q11.21
Summary Summary of gene provided in NCBI Entrez Gene.
The expression of this gene is induced by fasting as well as by progesterone. The protein encoded by this gene contains a t-synaptosome-associated protein receptor (SNARE) coiled-coil homology domain and a peroxisomal targeting signal. Production of the e
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IDA 25261981
GO:0005739 Component Mitochondrion IBA 21873635
GO:0005739 Component Mitochondrion IDA 25261981
GO:0005777 Component Peroxisome IDA 25261981
GO:0006914 Process Autophagy IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611309 23355 ENSG00000165507
Protein
UniProt ID Q9NTK1
Protein name Protein DEPP1 (Decidual protein induced by progesterone) (Fasting-induced gene protein) (FIG)
Protein function Acts as a critical modulator of FOXO3-induced autophagy via increased cellular ROS.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15343 DEPP 25 212 Decidual protein induced by progesterone family Family
Tissue specificity TISSUE SPECIFICITY: Expressed in various tissues, including pancreas, placenta, ovary, testis and kidney. {ECO:0000269|PubMed:16123073}.
Sequence
Sequence length 212
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  FoxO signaling pathway  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast cancer Malignant neoplasm of breast rs587776547, rs1137887, rs137853007, rs587776650, rs80359351, rs80359714, rs121917783, rs104886456, rs121964878, rs80359874, rs80357868, rs80357508, rs387906843, rs80357569, rs80358158
View all (309 more)
16298037
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451
View all (71 more)
16298037
Marfan syndrome Mammary Carcinoma, Human rs137854456, rs137854457, rs267606796, rs137854458, rs137854459, rs137854460, rs137854470, rs137854471, rs267606797, rs137854461, rs137854462, rs137854463, rs869025419, rs137854464, rs137854465
View all (942 more)
16298037
Unknown
Disease term Disease name Evidence References Source
Endometriosis Endometriosis 20864642 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Inhibit 24936657
Glioma Associate 37385612
Hepatitis B Associate 24936657
Hypoxia Stimulate 31963726, 37385612
Hypoxia Brain Stimulate 31963726
Neuroblastoma Associate 25261981, 28545464
Osteoarthritis Associate 38423139
Retinal Diseases Associate 31963726
Retinitis Associate 31963726
Thyroid Cancer Papillary Associate 30278442