2. Gene
  3. ZDHHC14 - zinc finger DHHC-type palmitoyltransferase 14 Gene

ZDHHC14 - zinc finger DHHC-type palmitoyltransferase 14 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：锌指 DHHC 型棕榈酰转移酶 14

种属: Homo sapiens

同用名: NEW1CP

基因 ID: 79683 | 基因类型: protein coding

关于 ZDHHC14

Cytogenetic location: 6q25.3 Genomic coordinates (GRCh38): 6:157,381,190-157,678,157 (from NCBI)

This gene has 9 transcripts (splice variants), 198 orthologues and 17 paralogues. Ubiquitous expression in brain (RPKM 2.5), endometrium (RPKM 2.3) and 24 other tissues.

功能概要

启用棕榈酰转移酶活性。参与肽基-L-半胱氨酸 S-棕榈酰化。位于内质网。 [由基因组资源联盟提供，2022 年 4 月]

Enables palmitoyltransferase activity. Involved in peptidyl-L-cysteine S-palmitoylation. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Apr 2022]

ZDHHC14 基因产物(2)

mRNA Protein Name
NM_024630.3 NP_078906.2 palmitoyltransferase ZDHHC14 isoform 1
NM_153746.2 NP_714968.1 palmitoyltransferase ZDHHC14 isoform 2
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables palmitoyltransferase activity IDA
IDA: 通过直接分析推断
23034182 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in peptidyl-L-cysteine S-palmitoylation IMP
IMP: 通过突变表型推断
27481942 GOA
involved in protein palmitoylation IDA
IDA: 通过直接分析推断
23034182 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in endoplasmic reticulum IDA
IDA: 通过直接分析推断
16647879 GOA
EXP：通过实验结果推断 IDA：通过直接分析推断 IPI：通过物理相互作用推断 IMP：通过突变表型推断 IGI：通过遗传相互作用推断 IEP：通过表达模式推断

ZDHHC14 蛋白结构

DHHC

DHHC: DHHC palmitoyltransferase (109 - 287)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 488 a.a.
蛋白主名 其他名称

palmitoyltransferase ZDHHC14

DHHC domain-containing cysteine-rich protein 14

关联疾病

疾病名称 别名
Chromosome 6q24-Q25 Deletion Syndrome

Chromosome 6q25-Q25 Deletion Syndrome

6q25 Microdeletion Syndrome

Monosomy 6q25

Del(6)(Q25)
Trichothiodystrophy 3, Photosensitive

TTD3

Trichothiodystrophy, Complementation Group A

Ttda

Photosensitive Trichothiodystrophy 3

Trichothiodystrophy Complementation Group A
Coffin-Siris Syndrome 1

Coffin-Siris Syndrome

Fifth Digit Syndrome

Css

CSS1

Mrd12

Mental Retardation, Autosomal Dominant 12

Hhid

Dwarfism-Onychodysplasia

Hypertrichosis, Hyperkeratosis, Mental Retardation, And Distinctive Facial Features

Autosomal Dominant Mental Retardation 12

Short Stature-Onychodysplasia.

Intellectual Disability With Absent Fifth Fingernail And Terminal Phalanx

Mental Retardation With Hypoplastic Fifth Fingernails And Toenails

Short Stature-Onychodysplasia

Coffin-Siris Syndrome, Type 1

Mental Retardation, Autosomal Dominant, Type 12
Lung Acinar Adenocarcinoma

Acinar Adenocarcinoma Of The Lung
疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS16014 ZDHHC14 Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Felis catus ZDHHC14 VGNC VGNC:67203
Rattus norvegicus ZDHHC14 RGD RGD:1565877
Mus musculus ZDHHC14 MGD MGI:2653229
Bos taurus ZDHHC14 VGNC VGNC:37129
Macaca mulatta ZDHHC14 VGNC VGNC:82270
Canis familiaris ZDHHC14 VGNC VGNC:48580
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