Gene Gene information from NCBI Gene database.
Entrez ID 54503
Gene name ZDHHC palmitoyltransferase 13
Gene symbol ZDHHC13
Synonyms (NCBI Gene)
HIP14LHIP3RP
Chromosome 11
Chromosome location 11p15.1
miRNA miRNA information provided by mirtarbase database.
14
miRTarBase ID miRNA Experiments Reference
MIRT1507716 hsa-miR-146a CLIP-seq
MIRT1507717 hsa-miR-146b-5p CLIP-seq
MIRT1507718 hsa-miR-2054 CLIP-seq
MIRT1507719 hsa-miR-361-5p CLIP-seq
MIRT1507720 hsa-miR-365 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0000139 Component Golgi membrane ISS
GO:0005783 Component Endoplasmic reticulum IDA 16647879
GO:0005794 Component Golgi apparatus IEA
GO:0015095 Function Magnesium ion transmembrane transporter activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612815 18413 ENSG00000177054
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IUH4
Protein name Palmitoyltransferase ZDHHC13 (EC 2.3.1.225) (Huntingtin-interacting protein 14-related protein) (HIP14-related protein) (Huntingtin-interacting protein HIP3RP) (Putative MAPK-activating protein PM03) (Putative NF-kappa-B-activating protein 209) (Zinc fing
Protein function Palmitoyltransferase that could catalyze the addition of palmitate onto various protein substrates (By similarity). Palmitoyltransferase for HTT and GAD2. May play a role in Mg(2+) transport.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12796 Ank_2 53 146 Ankyrin repeats (3 copies) Repeat
PF13637 Ank_4 217 271 Repeat
PF01529 DHHC 421 559 DHHC palmitoyltransferase Family
Sequence
MEGPGLGSQCRNHSHGPHPPGFGRYGICAHENKELANAREALPLIEDSSNCDIVKATQYG
IFERCKELVEAGYDVRQPDKENVSLLHWAAINNRLDLVKFYISKGAVVDQLGGDLNSTPL
HWAIRQGHLPMVILLLQHGADPTLID
GEGFSSIHLAVLFQHMPIIAYLISKGQSVNMTDV
NGQTPLMLSAHKVIGPEPTGFLLKFNPSLNVVDKIHQNTPLHWAVAAGNVNAVDKLLEAG
SSLDIQNVKGETPLDMALQNKNQLIIHMLKT
EAKMRANQKFRLWRWLQKCELFLLLMLSV
ITMWAIGYILDFNSDSWLLKGCLLVTLFFLTSLFPRFLVGYKNLVYLPTAFLLSSVFWIF
MTWFILFFPDLAGAPFYFSFIFSIVAFLYFFYKTWATDPGFTKASEEEKKVNIITLAETG
SLDFRTFCTSCLIRKPLRSLHCHVCNCCVARYDQHCLWTGRCIGFGNHHYYIFFLFFLSM
VCGWIIYGSFIYLSSHCATTFKEDGLWTYLNQIVACSPWVLYILMLATFHFSWSTFLLLN
QLFQIAFLGLTSHERISLQ
KQSKHMKQTLSLRKTPYNLGFMQNLADFFQCGCFGLVKPCV
VDWTSQYTMVFHPAREKVLRSV
Sequence length 622
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
AMYLOIDOSIS CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LIVER CIRRHOSIS, EXPERIMENTAL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OSTEOPOROSIS CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Alopecia Alopecia CTD_human_DG 20548961
★☆☆☆☆
Found in Text Mining only
Alopecia Alopecia BEFREE 24637783
★☆☆☆☆
Found in Text Mining only
Alopecia, Male Pattern Alopecia, Male Pattern CTD_human_DG 20548961
★☆☆☆☆
Found in Text Mining only
Amyloidosis Amyloidosis CTD_human_DG 20548961
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Androgenetic Alopecia Androgenetic Alopecia CTD_human_DG 20548961
★☆☆☆☆
Found in Text Mining only
Dermatitis Dermatitis BEFREE 28017833, 31669413
★☆☆☆☆
Found in Text Mining only
Dermatitis, Atopic Dermatitis BEFREE 28017833
★☆☆☆☆
Found in Text Mining only
Eczema Eczema BEFREE 28017833
★☆☆☆☆
Found in Text Mining only
Huntington Disease Huntington Disease BEFREE 22155432, 25849918
★☆☆☆☆
Found in Text Mining only
Inflammatory dermatosis Dermatitis BEFREE 28017833, 31669413
★☆☆☆☆
Found in Text Mining only