Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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2252 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Fibroblast growth factor 7 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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FGF7 |
SynonymsGene synonyms aliases
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HBGF-7, KGF |
ChromosomeChromosome number
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15 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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15q21.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein is a potent epithelial cell-specific growth factor, whose mitogenic activity is predominantly exhibited in keratinocytes but not in fibroblasts and endothelial cells. Studies of mouse and rat homologs of this gene implicated roles in morphogenesis of epithelium, reepithelialization of wounds, hair development and early lung organogenesis. [provided by RefSeq, Jul 2008] |
miRNAmiRNA information provided by mirtarbase database.
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Transcription factors
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
P21781 |
Protein name |
Fibroblast growth factor 7 (FGF-7) (Heparin-binding growth factor 7) (HBGF-7) (Keratinocyte growth factor) |
Protein function |
Plays an important role in the regulation of embryonic development, cell proliferation and cell differentiation. Required for normal branching morphogenesis. Growth factor active on keratinocytes. Possible major paracrine effector of normal epithelial cell proliferation. |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00167 |
FGF |
65 → 189 |
Fibroblast growth factor |
Domain |
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Sequence |
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Sequence length |
194 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Lung adenocarcinoma |
Adenocarcinoma of lung (disorder) |
rs-1, rs28934576, rs121913530, rs397516975, rs587776805, rs121913469, rs121913364, rs121913351, rs121913366, rs397516896, rs397516977, rs397516981, rs397517127, rs121913344, rs727504233, rs121913370, rs760043106, rs1057519788, rs1131692238, rs1131692237, rs1554350382 |
28604730 |
Pulmonary fibrosis |
Pulmonary Fibrosis |
rs121918666, rs199422300, rs121917737, rs121917834, rs199422294, rs201159197, rs199422297, rs199422305, rs751381953, rs876661305, rs878853260, rs863223336, rs786205702, rs1555811762, rs1060502990, rs1555903332, rs1554038539, rs1554042899, rs938938578 |
15677771 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Alveolitis |
Alveolitis, Fibrosing |
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15677771 |
Benign prostatic hyperplasia |
Benign Prostatic Hyperplasia |
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14999240 |
Liver cirrhosis |
Liver Cirrhosis |
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17692400 |
Liver fibrosis |
Fibrosis, Liver |
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17692400 |
Miscarriage |
Miscarriage |
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18539642 |
Prostatic adenoma |
Prostatic Adenoma |
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14999240 |
Prostatic hyperplasia |
Prostatic Hyperplasia |
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14999240 |
Prostatic hypertrophy |
Prostatic Hypertrophy |
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14999240 |
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