Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
254359
Gene name Gene Name - the full gene name approved by the HGNC.
ZDHHC palmitoyltransferase 24
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZDHHC24
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q13.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT664102 hsa-miR-508-5p HITS-CLIP 23824327
MIRT664101 hsa-miR-589-3p HITS-CLIP 23824327
MIRT664100 hsa-miR-1273g-3p HITS-CLIP 23824327
MIRT664099 hsa-miR-221-5p HITS-CLIP 23824327
MIRT664098 hsa-miR-8073 HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005783 Component Endoplasmic reticulum IBA
GO:0005794 Component Golgi apparatus IBA
GO:0006612 Process Protein targeting to membrane IBA
GO:0016020 Component Membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q6UX98
Protein name Probable palmitoyltransferase ZDHHC24 (EC 2.3.1.225) (Zinc finger DHHC domain-containing protein 24)
Protein function Probable palmitoyltransferase that could catalyze the addition of palmitate onto various protein substrates.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01529 DHHC 91 234 DHHC palmitoyltransferase Family
Sequence
MGQPWAAGSTDGAPAQLPLVLTALWAAAVGLELAYVLVLGPGPPPLGPLARALQLALAAF
QLLNLLGNVGLFLRSDPSIRGVMLAGRGLGQGWAYCYQCQSQVPPRSGHCSACRVCILRR
DHHCRLLGRCVGFGNYRPFLCLLLHAAGVLLHVSVLLGPALSALLRAHTPLHMAALLLLP
WLMLLTGRVSLAQFALAFVTDTCVAGALLCGAGLLFHGMLLLRGQTTWEWARGQ
HSYDLG
PCHNLQAALGPRWALVWLWPFLASPLPGDGITFQTTADVGHTAS
Sequence length 284
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Insomnia Insomnia N/A N/A GWAS