Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
54503
Gene name Gene Name - the full gene name approved by the HGNC.
ZDHHC palmitoyltransferase 13
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZDHHC13
Synonyms (NCBI Gene) Gene synonyms aliases
HIP14L, HIP3RP
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11p15.1
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IBA 21873635
GO:0000139 Component Golgi membrane ISS
GO:0005783 Component Endoplasmic reticulum IDA 16647879
GO:0015095 Function Magnesium ion transmembrane transporter activity ISS
GO:0016020 Component Membrane HDA 19946888
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612815 18413 ENSG00000177054
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Amyloidosis Amyloidosis rs63750567, rs63750560, rs387906821, rs387906822, rs387906823, rs1561123748, rs140352180, rs770211260, rs763065333, rs1554300664, rs747723062, rs773435101 20548961
Osteoporosis Osteoporosis, Age-Related, Osteoporosis, Osteoporosis, Senile, Post-Traumatic Osteoporosis rs72658152, rs72667023, rs587776916, rs72656370, rs768615287 20548961