1. Gene
  2. APTR - Alu-mediated CDKN1A/p21 transcriptional regulator Gene

APTR - Alu-mediated CDKN1A/p21 transcriptional regulator Gene

Homo sapiens

Also known as RSBN1L-AS1

Gene ID: 100505854 | Gene type: ncRNA

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