Gene Gene information from NCBI Gene database.
Entrez ID 79625
Gene name Neuron derived neurotrophic factor
Gene symbol NDNF
Synonyms (NCBI Gene)
C4orf31HH25NORD
Chromosome 4
Chromosome location 4q27
miRNA miRNA information provided by mirtarbase database.
116
miRTarBase ID miRNA Experiments Reference
MIRT655970 hsa-miR-6865-3p HITS-CLIP 23824327
MIRT655969 hsa-miR-1224-3p HITS-CLIP 23824327
MIRT655968 hsa-miR-6892-3p HITS-CLIP 23824327
MIRT655967 hsa-miR-3183 HITS-CLIP 23824327
MIRT655966 hsa-miR-4723-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
30
GO ID Ontology Definition Evidence Reference
GO:0001525 Process Angiogenesis IDA 24706764
GO:0001764 Process Neuron migration IDA 20969804
GO:0002931 Process Response to ischemia IEA
GO:0005539 Function Glycosaminoglycan binding IEA
GO:0005539 Function Glycosaminoglycan binding ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616506 26256 ENSG00000173376
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TB73
Protein name Protein NDNF (Neuron-derived neurotrophic factor)
Protein function Secretory protein that plays a role in various cellular processes (PubMed:20969804, PubMed:24706764, PubMed:31883645). Acts as a chemorepellent acting on gonadotropin-releasing hormone (GnRH) expressing neurons regulating their migration to the
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10179 DUF2369 291 383 Uncharacterised conserved protein (DUF2369) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in neurons along the gonadotropin-releasing hormone (GnRH) expressing neurons migratory route. {ECO:0000269|PubMed:31883645}.
Sequence
MVLLHWCLLWLLFPLSSRTQKLPTRDEELFQMQIRDKAFFHDSSVIPDGAEISSYLFRDT
PKRYFFVVEEDNTPLSVTVTPCDAPLEWKLSLQELPEDRSGEGSGDLEPLEQQKQQIINE
EGTELFSYKGNDVEYFISSSSPSGLYQLDLLSTEKDTHFKVYATTTPESDQPYPELPYDP
RVDVTSLGRTTVTLAWKPSPTASLLKQPIQYCVVINKEHNFKSLCAVEAKLSADDAFMMA
PKPGLDFSPFDFAHFGFPSDNSGKERSFQAKPSPKLGRHVYSRPKVDIQKICIGNKNIFT
VSDLKPDTQYYFDVFVVNINSNMSTAYVGTFARTKEEAKQKTVELKDGKITDVFVKRKGA
KFLRFAPVSSHQKVTFFIHSCLD
AVQIQVRRDGKLLLSQNVEGIQQFQLRGKPKAKYLVR
LKGNKKGASMLKILATTRPTKQSFPSLPEDTRIKAFDKLRTCSSATVAWLGTQERNKFCI
YKKEVDDNYNEDQKKREQNQCLGPDIRKKSEKVLCKYFHSQNLQKAVTTETIKGLQPGKS
YLLDVYVIGHGGHSVKYQSKVVKTRKFC
Sequence length 568
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
13
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Hypogonadotropic hypogonadism 25 with anosmia Likely pathogenic; Pathogenic rs2476439283, rs1727077385, rs1726901153, rs1726871489 RCV002290153
RCV001034704
RCV001034705
RCV001034706
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Diabetic Nephropathies Associate 36092962
Psychotic Disorders Inhibit 38340697