Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
22854
Gene name Gene Name - the full gene name approved by the HGNC.
Netrin G1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NTNG1
Synonyms (NCBI Gene) Gene synonyms aliases
Lmnt1, NetG1, NetrinG1
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p13.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a preproprotein that is processed into a secreted protein containing eukaroytic growth factor (EGF)-like domains. This protein acts to guide axon growth during neuronal development. Polymorphisms in this gene may be associated with schiz
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029912 hsa-miR-26b-5p Microarray 19088304
MIRT1196182 hsa-miR-583 CLIP-seq
MIRT1196183 hsa-miR-22 CLIP-seq
MIRT1196184 hsa-miR-3135b CLIP-seq
MIRT1196185 hsa-miR-338-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 14595443, 21946559
GO:0005576 Component Extracellular region TAS
GO:0005886 Component Plasma membrane IDA
GO:0005886 Component Plasma membrane TAS
GO:0007409 Process Axonogenesis ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608818 23319 ENSG00000162631
Protein
UniProt ID Q9Y2I2
Protein name Netrin-G1 (Laminet-1)
Protein function Involved in controlling patterning and neuronal circuit formation at the laminar, cellular, subcellular and synaptic levels. Promotes neurite outgrowth of both axons and dendrites.
PDB 3ZYJ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00055 Laminin_N 50 295 Laminin N-terminal (Domain VI) Family
PF00053 Laminin_EGF 297 343 Laminin EGF domain Domain
PF00053 Laminin_EGF 364 417 Laminin EGF domain Domain
PF00053 Laminin_EGF 420 467 Laminin EGF domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in the thalamus, with very low expression, if any, in other tissues. {ECO:0000269|PubMed:14595443, ECO:0000269|PubMed:15901489}.
Sequence
Sequence length 539
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Axon guidance
Cell adhesion molecules
  Post-translational modification: synthesis of GPI-anchored proteins
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
21278247
Colorectal neoplasms Colorectal Neoplasms rs28929483, rs63751108, rs28929484, rs63749831, rs63750047, rs63751207, rs63749811, rs1553350126, rs63750875, rs63750955, rs587776706, rs63750871, rs587776715, rs63751466, rs63750049
View all (1682 more)
21278247
Developmental regression Developmental regression rs1224421127
Mental retardation Intellectual Disability rs5742905, rs267607136, rs267607137, rs2131714307, rs267607038, rs267607042, rs80338685, rs137853127, rs80338815, rs28940893, rs387906309, rs121908096, rs121908099, rs587784365, rs121918315
View all (1024 more)
Unknown
Disease term Disease name Evidence References Source
Rett Syndrome atypical Rett syndrome GenCC
Neurodevelopmental Disorders complex neurodevelopmental disorder GenCC
Anorexia Anorexia GWAS
Metabolic Syndrome Metabolic Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Anorexia Nervosa Associate 27483138
Autism Spectrum Disorder Associate 22495309
Autistic Disorder Associate 22495309
Carcinogenesis Associate 28257124
Carcinogenesis Inhibit 33127842
Carcinoma Ovarian Epithelial Associate 33246661
Carcinoma Pancreatic Ductal Associate 33127842
Celiac Disease Associate 27483138
COVID 19 Associate 32503822
Delayed Cranial Ossification due to CBFB Haploinsufficiency Associate 19296131