ATAT1 (alpha tubulin acetyltransferase 1)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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79969 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Alpha tubulin acetyltransferase 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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ATAT1 |
SynonymsGene synonyms aliases
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C6orf134, MEC17, Nbla00487, TAT, alpha-TAT, alpha-TAT1 |
ChromosomeChromosome number
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6 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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6p21.33 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes a protein that localizes to clathrin-coated pits, where it acetylates alpha tubulin on lysine 40. This process may be important in microtubule growth, for instance during chemotaxis and the formation of cilium. Alternative splicing resul |
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 |
Q5SQI0 |
Protein name |
Alpha-tubulin N-acetyltransferase 1 (Alpha-TAT) (Alpha-TAT1) (TAT) (EC 2.3.1.108) (Acetyltransferase mec-17 homolog) |
Protein function |
Specifically acetylates 'Lys-40' in alpha-tubulin on the lumenal side of microtubules. Promotes microtubule destabilization and accelerates microtubule dynamics; this activity may be independent of acetylation activity. Acetylates alpha-tubulin |
PDB |
3VWD
,
3VWE
,
4B5O
,
4B5P
,
4GS4
,
4IF5
,
4PK2
,
4PK3
,
4U9Y
,
4U9Z
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF05301 |
Acetyltransf_16 |
8 → 190 |
GNAT acetyltransferase, Mec-17 |
Family |
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Sequence |
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Sequence length |
421 |
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 |
Prostate cancer |
Prostate carcinoma, Prostate cancer, familial |
rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 |
29892016 |
Prostate cancer, hereditary |
PROSTATE CANCER, HEREDITARY, 1 |
rs387906327, rs193929331, rs74315365, rs10993994, rs397516896, rs794729219, rs121913349, rs587782641, rs1114167673, rs1597371666, rs2073394466 |
29892016 |
Rheumatoid arthritis |
Rheumatoid Arthritis |
rs3766379, rs3792876, rs2071592, rs3087456, rs587776843, rs1566328963, rs2240340, rs1557787212 |
17804836, 19503088 |
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 |
28540026 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Development disorder |
Child Development Disorders, Pervasive |
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28540026 |
Vitiligo |
Vitiligo |
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20526339 |
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| © 2021, Biomedical Informatics Centre, NIRRH |
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Tel: +91-22-24192104, Fax No: +91-22-24139412 |