APTR - Alu-mediated CDKN1A/p21 transcriptional regulator Gene

Also Known as RSBN1L-AS1

Species: Homo sapiens

Gene Type: ncRNA
Gene ID: 100505854

About 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.

Related Diseases

Diseases Alias
Liver Cirrhosis

  • Cirrhosis

  • Cirrhosis Of Liver

  • CIRRH

  • Cryptogenic Cirrhosis

  • Cirrhosis, Cryptogenic

  • Cirrhosis Nos
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
Diseases Alias
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

Orthologs Information

Species Symbol Source ID
Rattus norvegicus APTR RGD RGD:9685233