InnateDB Protein
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IDBP-20766.5
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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NRTN
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Protein Name
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neurturin
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Synonyms
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NTN;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000302648
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InnateDB Gene
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IDBG-20764 (NRTN)
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Protein Structure
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Function |
Supports the survival of sympathetic neurons in culture. May regulate the development and maintenance of the CNS. Might control the size of non-neuronal cell population such as haemopoietic cells.
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Subcellular Localization |
Secreted.
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Disease Associations |
Note=Genetic variations in NRTN may contribute to Hirschsprung disease, in association with mutations of RET gene, and possibly mutations in other loci. Hirschsprung disease is a disorder of neural crest development is characterized by the absence of intramural ganglion cells in the hindgut, often resulting in intestinal obstruction.
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Tissue Specificity |
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated |
Total |
3
[view]
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Protein-Protein |
3
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Predicted by orthology |
Total |
1 [view]
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR001839
Transforming growth factor-beta, C-terminal
IPR029034
Cystine-knot cytokine
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PFAM |
PF00019
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PRINTS |
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PIRSF |
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SMART |
SM00204
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TIGRFAMs |
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Modification |
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SwissProt |
Q99748
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PhosphoSite |
PhosphoSite-
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TrEMBL |
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UniProt Splice Variant |
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Entrez Gene |
4902
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UniGene |
Hs.234775
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RefSeq |
NP_004549
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HUGO |
HGNC:8007
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OMIM |
602018
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CCDS |
CCDS12151
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HPRD |
03604
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IMGT |
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EMBL |
AL161995
BC137399
BC137400
CH471139
U78110
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GenPept |
AAC50898
AAI37400
AAI37401
CAB82327
EAW69140
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