2. Gene
  3. SCGB2A1 - secretoglobin family 2A member 1 Gene

SCGB2A1 - secretoglobin family 2A member 1 Gene

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

中文名称：分泌珠蛋白家族 2A 成员 1

种属: Homo sapiens

同用名: LPHC; LPNC; MGB2; UGB3

基因 ID: 4246 | 基因类型: protein coding

关于 SCGB2A1

Cytogenetic location: 11q12.3 Genomic coordinates (GRCh38): 11:62,208,673-62,213,943 (from NCBI)

This gene has 1 transcript (splice variant), 106 orthologues and 1 paralogue. Biased expression in endometrium (RPKM 28.0), stomach (RPKM 15.9) and 4 other tissues.

功能概要

参与雄激素受体信号通路。位于细胞外空间。 [由基因组资源联盟提供，2022 年 4 月]

Involved in Androgen Receptor signaling pathway. Located in extracellular space. [provided by Alliance of Genome Resources, Apr 2022]

SCGB2A1 基因产物(1)

mRNA Protein Name
NM_002407.3 NP_002398.1 mammaglobin-B precursor
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 protein binding IPI
IPI: 通过物理相互作用推断
9720917 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in androgen receptor signaling pathway IDA
IDA: 通过直接分析推断
16020486 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in extracellular space IDA
IDA: 通过直接分析推断
9720917 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

SCGB2A1 蛋白结构

Uteroglobin

Uteroglobin: Uteroglobin family (22 - 90)

  • 0
  • 95 a.a.
蛋白主名 其他名称

mammaglobin-B

lacryglobin

重组 SCGB2A1 蛋白

目录号 产品名 蛋白编号 纯度
HY-P77076 SCGB2A1 Protein, Human (HEK293, Fc) O75556/NP_002398.1 (D19-N95) ≥95%

关联疾病

疾病名称 别名
Hypotrichosis 13

HYPT13

Hypotrichosis With Woolly Hair

Hypotrichosis, Type 13
Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type

Methylcobalamin Deficiency, Cblg Type

HMAG

Methionine Synthase Deficiency

Methylcobalamin Deficiency Type Cblg

Homocystinuria-Megaloblastic Anemia Due To Defect In Cobalamin Metabolism, Cblg Complementation Type

Homocystinuria-Megaloblastic Anemia Cblg Type

Homocystinuria-Megaloblastic Anemia Due To Defect In Cobalamin Metabolism Cblg Complementation Type

Methylcobalamin Deficiency Cbl G Type

Homocystinuria Due To Defect In Methylation Cbl G

Cblg

Functional Methionine Synthase Deficiency Type Cblg

Methylcobalamin Deficiency Cblg Type

Arakawa Syndrome 2
Ovarian Cancer

Ovarian Carcinoma

Ovarian Neoplasm

Malignant Tumour Of Ovary

Cancer Of The Ovary

Epithelial Ovarian Cancer

Neoplasm Of Ovary

Ovarian Neoplasms

Ovarian Cancers

Malignant Neoplasm Of Ovary

Primary Malignant Neoplasm Of Ovary

Ovarian Cancer, Somatic

Malignant Ovarian Tumor

Ovary Neoplasm

Primary Ovarian Cancer

Tumor Of The Ovary

Malignant Neoplasm Of The Ovary

Malignant Tumor Of The Ovary

Ovarian Malignant Tumor

OC

Ovarian Carcinomas

Cancer, Ovarian

Cancer Of Ovary

Ovary Cancer

Ca Ovary
Brachydactyly, Type C

Brachydactyly Type C

BDC

Brachydactyly Haws Type

Brachydactyly, Haws Type

Brachydactyly C
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-RS12505 SCGB2A1 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Mus musculus SCGB2A1 MGD MGI:3780828
Rattus norvegicus SCGB2A1 RGD RGD:735031
Others SCGB2A1 NCBI
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