Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23057
Gene name Gene Name - the full gene name approved by the HGNC.
Nicotinamide nucleotide adenylyltransferase 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NMNAT2
Synonyms (NCBI Gene) Gene synonyms aliases
C1orf15, PNAT2
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q25.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene product belongs to the nicotinamide mononucleotide adenylyltransferase (NMNAT) enzyme family, members of which catalyze an essential step in NAD (NADP) biosynthetic pathway. Unlike the other human family member, which is localized to the nucleus
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs768849266 C>T Likely-pathogenic Missense variant, coding sequence variant
rs775499191 ->G Likely-pathogenic Coding sequence variant, frameshift variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT021432 hsa-miR-9-5p Microarray 17612493
MIRT023309 hsa-miR-122-5p Microarray 17612493
MIRT040033 hsa-miR-615-3p CLASH 23622248
MIRT040033 hsa-miR-615-3p CLASH 23622248
MIRT620702 hsa-miR-4328 HITS-CLIP 23824327
Transcription factors
Transcription factor Regulation Reference
CREB1 Unknown 22027994
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane TAS
GO:0000309 Function Nicotinamide-nucleotide adenylyltransferase activity IBA 21873635
GO:0004515 Function Nicotinate-nucleotide adenylyltransferase activity IBA 21873635
GO:0004515 Function Nicotinate-nucleotide adenylyltransferase activity IDA 16118205
GO:0005524 Function ATP binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608701 16789 ENSG00000157064
Protein
UniProt ID Q9BZQ4
Protein name Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 2 (NMN/NaMN adenylyltransferase 2) (EC 2.7.7.1) (EC 2.7.7.18) (Nicotinamide mononucleotide adenylyltransferase 2) (NMN adenylyltransferase 2) (Nicotinate-nucleotide adenylyltransferase 2) (NaM
Protein function Nicotinamide/nicotinate-nucleotide adenylyltransferase that acts as an axon maintenance factor (By similarity). Axon survival factor required for the maintenance of healthy axons: acts by delaying Wallerian axon degeneration, an evolutionarily c
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01467 CTP_transf_like 12 276 Cytidylyltransferase-like Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in brain, in particular in cerebrum, cerebellum, occipital lobe, frontal lobe, temporal lobe and putamen. Also found in the heart, skeletal muscle, pancreas and islets of Langerhans. {ECO:0000269|PubMed:12359228, ECO:0
Sequence
Sequence length 307
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Nicotinate and nicotinamide metabolism
Metabolic pathways
Biosynthesis of cofactors
  Nicotinate metabolism
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Erythromelalgia Erythromelalgia rs80356475, rs80356474, rs80356478, rs80356476, rs80356469, rs80356473, rs1553491169 31132363, 31136762
Hydrocephalus Hydrocephalus rs387907320, rs369384363, rs387907321, rs372127610, rs770273135, rs797045095, rs797045707, rs769795916, rs781251438, rs922703465, rs376078512, rs1567043467, rs1587149916, rs1586841546 31136762, 23082226
Hydrops fetalis Hydrops Fetalis rs28935477, rs1131691986 31136762, 23082226
Multiple congenital anomalies Multiple congenital anomalies rs1057517732 16118205, 12574164, 25560765, 28035283, 21615689, 23082226, 14516279, 24840802, 21940452, 12359228, 22842230, 24284888, 20943658
Unknown
Disease term Disease name Evidence References Source
Systemic lupus erythematosus Systemic lupus erythematosus GWAS
Schizophrenia Schizophrenia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Brain Stem Neoplasms Associate 28544218
Carcinogenesis Associate 27218101
Carcinoma Non Small Cell Lung Associate 24042441
Colorectal Neoplasms Stimulate 27218101
Colorectal Neoplasms Associate 38092774
Diabetic Retinopathy Inhibit 38222451
Lupus Erythematosus Systemic Associate 26783109
Psychotic Disorders Associate 28544218