Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
80310
Gene name Gene Name - the full gene name approved by the HGNC.
Platelet derived growth factor D
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PDGFD
Synonyms (NCBI Gene) Gene synonyms aliases
IEGF, MSTP036, SCDGF-B, SCDGFB
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q22.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the platelet-derived growth factor family. The four members of this family are mitogenic factors for cells of mesenchymal origin and are characterized by a core motif of eight cysteines, seven of which are f
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT030746 hsa-miR-21-5p Microarray 18591254
MIRT053656 hsa-miR-145-5p Microarray 22942087
MIRT756188 hsa-miR-429 Western blotting, qRT-PCR 35509844
MIRT1221212 hsa-miR-1257 CLIP-seq
MIRT1221213 hsa-miR-125a-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane TAS
GO:0005161 Function Platelet-derived growth factor receptor binding IBA 21873635
GO:0005576 Component Extracellular region TAS
GO:0005615 Component Extracellular space IBA 21873635
GO:0005788 Component Endoplasmic reticulum lumen TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
609673 30620 ENSG00000170962
Protein
UniProt ID Q9GZP0
Protein name Platelet-derived growth factor D (PDGF-D) (Iris-expressed growth factor) (Spinal cord-derived growth factor B) (SCDGF-B) [Cleaved into: Platelet-derived growth factor D, latent form (PDGFD latent form); Platelet-derived growth factor D, receptor-binding f
Protein function Growth factor that plays an essential role in the regulation of embryonic development, cell proliferation, cell migration, survival and chemotaxis. Potent mitogen for cells of mesenchymal origin. Plays an important role in wound healing. Induces
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00431 CUB 53 167 CUB domain Domain
PF00341 PDGF 272 362 PDGF/VEGF domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed at high levels in the heart, pancreas, adrenal gland and ovary and at low levels in placenta, liver, kidney, prostate, testis, small intestine, spleen and colon. In the kidney, expressed by the visceral epithelial cells of th
Sequence
MHRLIFVYTLICANFCSCRDTSATPQSASIKALRNANLRRDESNHLTDLYRRDETIQVKG
NGYVQSPRFPNSYPRNLLLTWRLHSQENTRIQLVFDNQFGLEEAENDICRYDFVEVEDIS
ETSTIIRGRWCGHKEVPPRIKSRTNQIKITFKSDDYFVAKPGFKIYY
SLLEDFQPAAASE
TNWESVTSSISGVSYNSPSVTDPTLIADALDKKIAEFDTVEDLLKYFNPESWQEDLENMY
LDTPRYRGRSYHDRKSKVDLDRLNDDAKRYSCTPRNYSVNIREELKLANVVFFPRCLLVQ
RCGGNCGCGTVNWRSCTCNSGKTVKKYHEVLQFEPGHIKRRGRAKTMALVDIQLDHHERC
DC
ICSSRPPR
Sequence length 370
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  EGFR tyrosine kinase inhibitor resistance
MAPK signaling pathway
Ras signaling pathway
Rap1 signaling pathway
Calcium signaling pathway
Phospholipase D signaling pathway
PI3K-Akt signaling pathway
Focal adhesion
Gap junction
Regulation of actin cytoskeleton
Prostate cancer
Melanoma
Choline metabolism in cancer
  Signaling by PDGF
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Coronary artery disease Coronary Artery Disease rs137852988, rs121918313, rs121918529, rs121918531, rs137852340, rs1555800701, rs1215189537 21378988
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Cirrhosis Cirrhosis 25280005 ClinVar
Pulmonary arterial hypertension pulmonary arterial hypertension GenCC
Dementia Dementia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Acidosis Associate 26157007
Acne Vulgaris Associate 37018476
Adenocarcinoma Associate 29961751, 32869505
Adrenal Gland Neoplasms Associate 35568735
Airway Obstruction Associate 35568735
Arthritis Rheumatoid Associate 16508943, 24989895
Ascites Stimulate 22471482
Atherosclerosis Associate 26362023
Carcinogenesis Associate 26157007
Carcinoma Hepatocellular Associate 24158561, 25760076, 36308081, 37253627