1. Gene
  2. SC5D - sterol-C5-desaturase Gene

SC5D - sterol-C5-desaturase Gene

中文名称:甾醇-C5-去饱和酶

种属: Homo sapiens

同用名: ERG3; S5DES; SC5DL

基因 ID: 6309 | 基因类型: protein coding

关于 SC5D

Cytogenetic location: 11q23.3-q24.1 Genomic coordinates (GRCh38): 11:121,292,771-121,313,410 (from NCBI)

This gene has 9 transcripts (splice variants), 251 orthologues, 3 paralogues and is associated with 3 phenotypes. Ubiquitous expression in liver (RPKM 29.7), prostate (RPKM 24.2) and 23 other tissues.

功能概要

该基因编码一种胆固醇生物合成酶。编码的蛋白质催化 lathosterol 转化为 7-脱氢胆固醇。该基因的突变与脂肪甾醇症有关。已经描述了编码相同蛋白质的可变剪接转录物变体。[RefSeq 提供,2008 年 7 月]

This gene encodes an Enzyme of Cholesterol biosynthesis. The encoded protein catalyzes the conversion of lathosterol into 7-dehydrocholesterol. Mutations in this gene have been associated with lathosterolosis. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]

SC5D 基因产物(2)

mRNA Protein Name
NM_001024956.3 NP_001020127.1 lathosterol oxidase
NM_006918.5 NP_008849.2 lathosterol oxidase
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 C-5 sterol desaturase activity EXP
EXP: 通过实验结果推断
12189593 GOA
enables delta7-sterol 5(6)-desaturase activity IDA
IDA: 通过直接分析推断
10786622 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cholesterol biosynthetic process via lathosterol IDA
IDA: 通过直接分析推断
10786622 GOA
involved in negative regulation of ferroptosis IMP
IMP: 通过突变表型推断
38297129 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
is active in endoplasmic reticulum membrane IDA
IDA: 通过直接分析推断
10786622 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

SC5D 蛋白结构

FA_hydroxylase

FA_hydroxylase: Fatty acid hydroxylase superfamily (124 - 233)

  • 0
  • 100
  • 200
  • 299 a.a.
蛋白主名 其他名称

lathosterol oxidase

3beta-hydroxysteroid-delta5-desaturase

关联疾病

疾病名称 别名
Lathosterolosis

Sterol C5-Desaturase Deficiency

LATHOS

Sc5d Deficiency

Congenital Hemidysplasia With Ichthyosiform Erythroderma And Limb Defects

Child Syndrome

Ichthyosiform Erythroderma, Unilateral, With Ipsilateral Malformations, Especially Absence Deformity Of Limbs

Child Nevus

Congenital Hemidysplasia With Ichthyosiform Nevus And Limbs Defects

Congenital Hemidysplasia With Ichthyosiform Nevus And Limb Defects

Ichthyosis, Child Syndrome

Child Syndrome Ichthyosis

CHILD

X-Linked Chondrodysplasia Punctata 2

Happle Syndrome

Cdpx2

Conradi-Hünermann Syndrome

Chondrodysplasia Punctata 2, X-Linked

X-Linked Dominant Chondrodysplasia Punctata

Conradi-Hunermann Syndrome

Conradi-Hünermann-Happle Syndrome

Cdpxd

Cpxd

Chondrodystrophia Calcificans Congenita

Conradi-Hunermann-Happle Syndrome

X-Linked Chondrodysplasia Punctata Type 2

Chondrodysplasia Punctata, X-Linked Dominant Type

Megalencephalic Leukoencephalopathy With Subcortical Cysts 2b

Megalencephalic Leukoencephalopathy With Subcortical Cysts 2b, Remitting, With Or Without Mental Retardation

Megalencephalic Leukoencephalopathy With Subcortical Cysts 2a

MLC2A

Leukoencephalopathy, Megalencephalic, With Subcortical Cysts, 2a

Leukoencephalopathy, Megalencephalic, With Subcortical Cysts, Type 2a

Smith-Lemli-Opitz Syndrome

SLOS

Rsh Syndrome

7-Dehydrocholesterol Reductase Deficiency

Slo Syndrome

Rutledge Lethal Multiple Congenital Anomaly Syndrome

Lethal Acrodysgenital Syndrome

Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobar Lung

Smith-Opitz-Inborn Syndrome

Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobular Lung

Smith Lemli Opitz Syndrome

Smith-Lemli-Opitz Syndrome, Type Ii

Ck Syndrome

CKS

X-Linked Intellectual Disability-Microcephaly-Cortical Malformation-Thin Habitus Syndrome

Mental Retardation, X-Linked, With Thin Body Habitus And Cortical Malformation

Frontometaphyseal Dysplasia

Fmd

Dysplasia, Frontometaphyseal

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

直系同源

种属 基因名 来源 基因 ID
Canis familiaris SC5D VGNC VGNC:45887
Mus musculus SC5D MGD MGI:1353611
Macaca mulatta SC5D VGNC VGNC:107638
Felis catus SC5D VGNC VGNC:81944
Rattus norvegicus SC5D RGD RGD:620775
Bos taurus SC5D VGNC VGNC:34312