1. Gene
  2. TRHDE - thyrotropin releasing hormone degrading enzyme Gene

TRHDE - thyrotropin releasing hormone degrading enzyme Gene

中文名称:促甲状腺激素释放激素降解酶

种属: Homo sapiens

同用名: PAP-II; PGPEP2; TRH-DE

基因 ID: 29953 | 基因类型: protein coding

关于 TRHDE

Cytogenetic location: 12q21.1 Genomic coordinates (GRCh38): 12:72,087,266-72,670,758 (from NCBI)

This gene has 7 transcripts (splice variants), 241 orthologues and 11 paralogues. Broad expression in brain (RPKM 3.0), fat (RPKM 2.9) and 17 other tissues.

功能概要

该基因编码肽酶 M1 家族的一个成员。编码的蛋白质是一种细胞外肽酶,可特异性切割和灭活神经肽促甲状腺激素释放激素。[RefSeq 提供,2008 年 12 月]

This gene encodes a member of the peptidase M1 family. The encoded protein is an extracellular peptidase that specifically cleaves and inactivates the neuropeptide thyrotropin-releasing hormone.[provided by RefSeq, Dec 2008]

TRHDE 基因产物(1)

mRNA Protein Name
NM_013381.3 NP_037513.2 thyrotropin-releasing hormone-degrading ectoenzyme

TRHDE 蛋白结构

Peptidase_M1

Peptidase_M1: Peptidase family M1 domain (140 - 530)

ERAP1_C

ERAP1_C: ERAP1-like C-terminal domain (678 - 999)

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  • 1024 a.a.
蛋白主名 其他名称

thyrotropin-releasing hormone-degrading ectoenzyme

TRH-degrading ectoenzyme

关联疾病

疾病名称 别名
Thyroid Hormone Resistance, Generalized, Autosomal Dominant

Thyroid Hormone Resistance Syndrome

Thyroid Hormone Resistance

GRTHD

Gthr

Thyroid Hormone Unresponsiveness

Generalized Thyroid Hormone Resistance

Hyperthyroxinemia, Familial Euthyroid, Secondary To Pituitary And Peripheral Thyroid Hormones

Hyperthyroxinemia, Familial Euthyroid, Secondary To Pituitary And Peripheral Resistance To Thyroid Hormones

Refetoff Syndrome

Thyroid Hormone Responsiveness Defect

Familial Euthyroid Hyperthyroxinemia, Secondary To Pituitary And Peripheral Resistance To Thyroid Hormones

Thyroid Hormone Resistance, Generalized, Autosomal Recessive

Developmental And Epileptic Encephalopathy 2

Epileptic Encephalopathy, Early Infantile, 2

DEE2

Eiee2

Issx2

Developmental And Epileptic Encephalopathy, 2

Infantile Spasm Syndrome, X-Linked 2

Early Infantile Epileptic Encephalopathy 2

X-Linked Infantile Spasm Syndrome 2

Atypical Rett Syndrome Cdkl5-Related

Atypical Rett Syndrome Hanefeld Variant

Infantile Spasm Syndrome X-Linked 2

Rett Syndrome Early-Onset Seizure Variant

Rett Syndrome Variant With Infantile Spasms

Encephalopathy, Epileptic, Early Infantile, Type 2

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
Felis catus TRHDE VGNC VGNC:66525
Canis familiaris TRHDE VGNC VGNC:47798
Bos taurus TRHDE VGNC VGNC:36305
Mus musculus TRHDE MGD MGI:2384311
Rattus norvegicus TRHDE RGD RGD:728895
Macaca mulatta TRHDE VGNC VGNC:79872