APTR - Alu-mediated CDKN1A/p21 transcriptional regulator Gene

中文名称：Alu 介导的 CDKN1A/p21 转录调节因子

种属: Homo sapiens

同用名: RSBN1L-AS1

基因 ID: 100505854 | 基因类型: ncRNA

关于 APTR

Cytogenetic location: 7q11.23 Genomic coordinates (GRCh38): 7:77,657,660-77,697,345 (from NCBI)

This gene has 14 transcripts (splice variants). Ubiquitous expression in thyroid (RPKM 5.3), testis (RPKM 4.2) and 25 other tissues.

疾病名称

别名

Liver Cirrhosis

Glioblastoma

Glioblastoma Multiforme	Gbm
Adult Glioblastoma Multiforme	Grade Iv Adult Astrocytic Tumor
Primary Glioblastoma Multiforme	Spongioblastoma Multiforme
Adult Glioblastoma	Primary Glioblastoma

High Molecular Weight Kininogen Deficiency

HMWK DEFICIENCY	Fitzgerald Trait
Congenital High-Molecular-Weight Kininogen Deficiency	Flaujeac Factor Deficiency
Kininogen Deficiency, High Molecular Weight	Kininogen Deficiency
Hmwk	High-Molecular-Weight Kininogen Deficiency, Congenital

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

种属	基因名	来源	基因 ID
Rattus norvegicus	APTR	RGD	RGD:9685233

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