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Gene Gene information from NCBI Gene database.
Entrez ID 4756
Gene name Neogenin 1
Gene symbol NEO1
Synonyms (NCBI Gene)
IGDCC2NGNNTN1R2
Chromosome 15
Chromosome location 15q24.1
Summary This gene encodes a cell surface protein that is a member of the immunoglobulin superfamily. The encoded protein consists of four N-terminal immunoglobulin-like domains, six fibronectin type III domains, a transmembrane domain and a C-terminal internal do
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs483352721 C>G Conflicting-interpretations-of-pathogenicity Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
297 Show/Hide all (297)
miRTarBase ID miRNA Experiments Reference
MIRT016178 hsa-miR-590-3p Sequencing 20371350
MIRT028322 hsa-miR-32-5p Sequencing 20371350
MIRT047083 hsa-miR-183-5p CLASH 23622248
MIRT044583 hsa-miR-320a CLASH 23622248
MIRT041971 hsa-miR-484 CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
35 Show/Hide all (35)
GO ID Ontology Definition Evidence Reference
GO:0001764 Process Neuron migration IBA
GO:0005515 Function Protein binding IPI 18335997, 22084112
GO:0005654 Component Nucleoplasm IDA
GO:0005794 Component Golgi apparatus IDA
GO:0005886 Component Plasma membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601907 7754 ENSG00000067141
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q92859
Protein name Neogenin (Immunoglobulin superfamily DCC subclass member 2)
Protein function Multi-functional cell surface receptor regulating cell adhesion in many diverse developmental processes, including neural tube and mammary gland formation, myogenesis and angiogenesis. Receptor for members of the BMP, netrin, and repulsive guida
PDB 1X5F , 1X5G , 1X5H , 1X5I , 1X5J , 1X5K , 3P4L
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00041 fn3 540 → 621 Fibronectin type III domain Domain
PF00041 fn3 635 → 721 Fibronectin type III domain Domain
PF00041 fn3 956 → 1044 Fibronectin type III domain Domain
PF00041 fn3 440 → 525 Fibronectin type III domain Domain
PF00041 fn3 740 → 820 Fibronectin type III domain Domain
PF00041 fn3 855 → 942 Fibronectin type III domain Domain
PF06583 Neogenin_C 1158 → 1461 Neogenin C-terminus Family
PF07679 I-set 341 → 427 Immunoglobulin I-set domain Domain
PF07679 I-set 249 → 337 Immunoglobulin I-set domain Domain
PF13895 Ig_2 55 → 148 Immunoglobulin domain Domain
PF13927 Ig_3 152 → 225 Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed and also in cancer cell lines.
Sequence
Sequence length 1461
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
KEGG Pathway
TGF-beta signaling pathway
Axon guidance
Cell adhesion molecules
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
17
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Show/Hide Unknown Diseases (17)
Phenotype Name Clinical Significance Source Reference Evidence Score
Acute myeloid leukemia Likely benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ALZHEIMER DISEASE — GWAS catalog 39998322
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ANTI-GAD65 AUTOIMMUNE NEUROLOGICAL SYNDROMES — GWAS catalog 35348614
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATRIAL FIBRILLATION — GWAS catalog 39537608
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cholangiocarcinoma Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (48)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Adenocarcinoma of lung (disorder) Lung adenocarcinoma BEFREE 15952876
★★★★★
★☆☆☆☆
Found in Text Mining only
Adult Acute Myeloblastic Leukemia Myeloblastic Leukemia BEFREE 19665076
★★★★★
★☆☆☆☆
Found in Text Mining only
Anemia Anemia BEFREE 28730177
★★★★★
★☆☆☆☆
Found in Text Mining only
Arrhythmogenic Right Ventricular Dysplasia Arrhythmogenic right ventricular cardiomyopathy Pubtator 31843279 Stimulate
★★★★★
★☆☆☆☆
Found in Text Mining only
Autism Spectrum Disorders Autism Spectrum Disorder BEFREE 26518331
★★★★★
★☆☆☆☆
Found in Text Mining only
Breast Carcinoma Breast Carcinoma BEFREE 25416629, 25998984
★★★★★
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 16324219, 25416629 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Carcinogenesis Pubtator 16324219 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Carcinoma Ductal Ductal carcinoma Pubtator 16324219 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Carcinoma, Basal Cell Carcinoma BEFREE 29137400
★★★★★
★☆☆☆☆
Found in Text Mining only