AIRN - antisense of IGF2R non-protein coding RNA Gene

Also Known as AIR; IGF2RAS; IGF2R-AS; IGF2R-AS1; NCRNA00088

Species: Homo sapiens

Gene Type: ncRNA
Gene ID: 100271873

About AIRN

Cytogenetic location: 6q25.3 Genomic coordinates (GRCh38): 6:160,003,291-160,007,664 (from NCBI)

This gene has 2 transcripts (splice variants). Low expression observed in reference dataset.

Summary

Both spliced and un-spliced long non-coding RNAs are transcribed from this gene. This gene overlaps on the opposite strand the second intron of the insulin-like growth factor 2 receptor gene; a CpG island associated with the second intron denotes an active promoter that drives the expression of this gene. The related mouse gene is responsible for silencing the insulin-like growth factor 2 receptor gene and flanking genes in the imprinted gene cluster of mice. This gene may be expressed in Wilms tumors. [provided by RefSeq, Feb 2013]

Related Diseases

Diseases Alias
Glioma Susceptibility 1
  • Astrocytoma

  • GLM1

  • Glioma, Susceptibility To, Somatic

  • Glioblastoma, Somatic

  • Glioma

  • Glioblastoma Multiforme

  • Oligodendroglioma

  • Glioma Somatic

  • Astrocytic Tumor

  • GLM

  • Familial Glioma Of Brain

  • Gbm

  • Glioma 1

  • Glioma, Susceptibility, Type 1

  • Cerebral Astrocytoma

  • Glioblastoma

  • Well Differentiated Oligodendroglioma

Wilms Tumor 1
  • Nephroblastoma

  • Wilms Tumor

  • WT1

  • Wilms' Tumor

  • Bilateral Wilms Tumor

  • Wilms Tumor, Type 1

  • Wilms Tumor, Somatic

  • Adult Nephroblastoma

  • Wt1 Disorder

  • Renal Embryonic Tumor

  • Adult Kidney Wilms Tumor

  • Childhood Kidney Wilms Tumor

  • Nonanaplastic Kidney Wilms Tumor

Alpha-Thalassemia
  • Alpha Thalassemia

  • Alpha Thalassaemia

  • Alpha Plus Thalassemia

  • Thalassemia, Alpha-

  • Thalassemias, Alpha-

  • A-Thalassemia

  • Α-Thalassemia

  • A-THAL

  • Thalassemia

  • Alpha Thalassaemia Syndrome

Beckwith-Wiedemann Syndrome
  • Wiedemann-Beckwith Syndrome

  • BWS

  • Exomphalos-Macroglossia-Gigantism Syndrome

  • Emg Syndrome

  • Beckwith-Wiedemann Syndrome Due To Cdkn1c Mutation

  • Emg Abnormality

  • Wbs

  • Exomphalos Macroglossia Gigantism Syndrome

  • Beckwith-Wiedemann Syndrome Due To Nsd1 Mutation

  • Macroglossia Exomphalos Gigantism

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
Mus musculus AIRN MGD MGI:1353471