Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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4862 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Neuronal PAS domain protein 2 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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NPAS2 |
SynonymsGene synonyms aliases
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MOP4, PASD4, bHLHe9 |
ChromosomeChromosome number
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2 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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2q11.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH)-PAS family of transcription factors. A similar mouse protein may play a regulatory role in the acquisition of specific types of memory. It also may function as a part of a m |
miRNAmiRNA information provided by mirtarbase database.
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Transcription factors
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Transcription factor |
Regulation |
Reference |
KAT2B |
Unknown |
14645221 |
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
Q99743 |
Protein name |
Neuronal PAS domain-containing protein 2 (Neuronal PAS2) (Basic-helix-loop-helix-PAS protein MOP4) (Class E basic helix-loop-helix protein 9) (bHLHe9) (Member of PAS protein 4) (PAS domain-containing protein 4) |
Protein function |
Transcriptional activator which forms a core component of the circadian clock. The circadian clock, an internal time-keeping system, regulates various physiological processes through the generation of approximately 24 hour circadian rhythms in g |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00010 |
HLH |
10 → 60 |
Helix-loop-helix DNA-binding domain |
Domain |
PF00989 |
PAS |
84 → 176 |
PAS fold |
Domain |
PF14598 |
PAS_11 |
248 → 355 |
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Domain |
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Sequence |
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Sequence length |
824 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Autism |
Autistic Disorder |
rs121964908, rs121912597, rs2710102, rs7794745, rs142990298, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699, rs1553510219, rs1684182454, rs1559060428, rs1553510677, rs1576352885, rs1574152522, rs1574152672, rs1696658542, rs1751123722, rs1750373491, rs1751075634 |
17264841 |
Non-obstructive azoospermia |
Non-obstructive azoospermia |
rs587777872, rs879253743, rs1600840291, rs1600877766, rs753462162, rs1588618614, rs1602684496, rs377712900 |
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Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
19839995 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Bipolar disorder |
Bipolar Disorder |
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20072116, 16528748, 21835597, 24389266, 22538398 |
Mental depression |
Mental Depression, Depressive disorder |
rs587778876, rs587778877 |
19693801, 19693801, 22538398 |
Schizoaffective disorder |
Schizoaffective Disorder |
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19839995 |
Seasonal affective disorder |
Seasonal Affective Disorder |
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21835597, 22538398, 22137330, 17969870 |
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