Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79625
Gene name Gene Name - the full gene name approved by the HGNC.
Neuron derived neurotrophic factor
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NDNF
Synonyms (NCBI Gene) Gene synonyms aliases
C4orf31, HH25, NORD
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q27
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616506 26256 ENSG00000173376
Protein
UniProt ID 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 categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Hypogonadotropic Hypogonadism With Or Without Anosmia Hypogonadotropic hypogonadism 25 with anosmia rs1727077385, rs1726901153, rs1726871489 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Kallmann Syndrome Kallmann syndrome N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Diabetic Nephropathies Associate 36092962
Psychotic Disorders Inhibit 38340697