NTNG2 netrin G2
Gene ID: 84628, updated on 17-Sep-2024Gene type: protein coding
Also known as: Lmnt2; NTNG1; NEDBASH; LHLL9381; NetrinG2; bA479K20.1
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- Go to complete Gene record for NTNG2
- Go to Variation Viewer for NTNG2 variants
Summary
Predicted to be involved in several processes, including basement membrane assembly; cell morphogenesis involved in differentiation; and regulation of cell projection organization. Located in Flemming body; intercellular bridge; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. GeneReviews: Not available | |
| Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia | not available |
Genomic context
- Location:
- 9q34.13
- Sequence:
- Chromosome: 9; NC_000009.12 (132161689..132244526)
- Total number of exons:
- 22
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for NTNG2 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- NTNG2 @ LOVD
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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