1. Gene
  2. AIRN - antisense of IGF2R non-protein coding RNA Gene

AIRN - antisense of IGF2R non-protein coding RNA Gene

Homo sapiens

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

Gene ID: 100271873 | Gene type: ncRNA

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