IL7 (interleukin 7)

Gene Gene information from NCBI Gene database.
Gene SNPs miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
Entrez ID 3574
Gene name Interleukin 7
Gene symbol IL7
Synonyms (NCBI Gene)
IL-7IMD130
Chromosome 8
Chromosome location 8q21.13
Summary The protein encoded by this gene is a cytokine important for B and T cell development. This cytokine and the hepatocyte growth factor (HGF) form a heterodimer that functions as a pre-pro-B cell growth-stimulating factor. IL7 is found to be a cofactor for
SNPs SNP information provided by dbSNP.
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Gene SNPs miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
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SNP ID Visualize variation Clinical significance Consequence
rs1486611027 T>A,C Risk-factor Coding sequence variant, stop gained, missense variant
miRNA miRNA information provided by mirtarbase database.
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Gene SNPs miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
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miRTarBase ID miRNA Experiments Reference
MIRT018556 hsa-miR-335-5p Microarray 18185580
MIRT022978 hsa-miR-124-3p Microarray 18668037
MIRT024567 hsa-miR-215-5p Microarray 19074876
MIRT026781 hsa-miR-192-5p Microarray 19074876
MIRT447670 hsa-miR-513b-3p PAR-CLIP 22100165
Transcription factors Transcription factors information provided by TRRUST V2 database.
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Gene SNPs miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
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Transcription factor Regulation Reference
MYB Activation 11675351
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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GO ID Ontology Definition Evidence Reference
GO:0001961 Process Positive regulation of cytokine-mediated signaling pathway IDA 11418668
GO:0002360 Process T cell lineage commitment IEA
GO:0005125 Function Cytokine activity IBA
GO:0005125 Function Cytokine activity IDA 11418668, 25870237
GO:0005125 Function Cytokine activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene SNPs miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
MIM HGNC e!Ensembl
146660 6023 ENSG00000104432
Protein Protein information from UniProt database.
Gene SNPs miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P13232
Protein name Interleukin-7 (IL-7)
Protein function Hematopoietic cytokine that plays an essential role in the development, expansion, and survival of naive and memory T-cells and B-cells thereby regulating the number of mature lymphocytes and maintaining lymphoid homeostasis (PubMed:25870237, Pu
PDB 3DI2 , 3DI3
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01415 IL7 26 → 177 Interleukin 7 Domain
Sequence
Sequence length 177
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
Gene SNPs miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
  KEGG  Reactome
  Cytokine-cytokine receptor interaction
PI3K-Akt signaling pathway
JAK-STAT signaling pathway
Hematopoietic cell lineage
Pathways in cancer 		  Interleukin-7 signaling
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Gene SNPs miRNA Transcription factors Gene ontology Other IDs Protein Pathways Associated diseases
Show/Hide Causal Diseases (1)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Epidermodysplasia verruciformis, susceptibility to, 5 Pathogenic rs1486611027 RCV000855443
Show/Hide Unknown Diseases (1)
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
IL7-related disorder Uncertain significance; Benign rs56222538, rs201412253, rs200025901, rs200683891 RCV003941401
RCV003934106
RCV003958180
RCV003970546
Show/Hide Text Mining Associations (193)
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Acute Coronary Syndrome Associate 32647892
Acute On Chronic Liver Failure Associate 33584648
Allan Herndon Dudley syndrome Associate 24768357
Alzheimer Disease Associate 30193587, 33194959
Angina Unstable Inhibit 12871422
Arterial Occlusive Diseases Associate 33776989
Arthritis Infectious Associate 23053510
Arthritis Juvenile Associate 15939793
Arthritis Rheumatoid Associate 10403280, 12525379, 15642153, 17185327, 17665400, 19714586, 20465565, 21647866, 22355377, 23325887, 24740301, 26314565, 9691097
Arthritis Rheumatoid Inhibit 15642146, 25533722