Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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9638 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Fasciculation and elongation protein zeta 1 |
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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FEZ1 |
SynonymsGene synonyms aliases
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UNC-76 |
ChromosomeChromosome number
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11 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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11q24.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene is an ortholog of the C. elegans unc-76 gene, which is necessary for normal axonal bundling and elongation within axon bundles. Expression of this gene in C. elegans unc-76 mutants can restore to the mutants partial locomotion and axonal fascicu |
miRNAmiRNA information provided by mirtarbase database.
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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 |
Q99689 |
Protein name |
Fasciculation and elongation protein zeta-1 (Zygin I) (Zygin-1) |
Protein function |
May be involved in axonal outgrowth as component of the network of molecules that regulate cellular morphology and axon guidance machinery. Able to restore partial locomotion and axonal fasciculation to C.elegans unc-76 mutants in germline trans |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF07763 |
FEZ |
58 → 297 |
FEZ-like protein |
Family |
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Sequence |
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Sequence length |
392 |
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 |
Attention deficit hyperactivity disorder |
Attention deficit hyperactivity disorder |
rs120074176, rs786205019 |
23453885 |
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 |
23453885, 16936715, 22099459, 22688191, 18647754, 21926974 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Bipolar disorder |
Bipolar Disorder |
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23453885 |
Development disorder |
Child Development Disorders, Pervasive |
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23453885 |
Mental depression |
Major Depressive Disorder |
rs587778876, rs587778877 |
23453885 |
Psychosis |
Psychotic Disorders |
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22099459 |
Vascular diseases |
Peripheral Arterial Diseases |
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27082954 |
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