MEG8 - maternally expressed 8, small nucleolar RNA host gene Gene

Also Known as Bsr; Irm; Rian; SNHG23; SNHG24; lnc-MGC; LINC00024; NCRNA00024

Species: Homo sapiens

Gene Type: ncRNA
Gene ID: 79104

About MEG8

Cytogenetic location: 14q32.2-q32.31 Genomic coordinates (GRCh38): 14:100,889,649-100,999,113 (from NCBI)

Summary

This gene is located in a cluster of imprinted genes on chromosome 14q32.3. It encodes a a non-protein coding transcript that is preferentially expressed from the maternal allele in skeletal muscle, and appears to be coordinately regulated with Other imprinted genes in this region. [provided by RefSeq, Oct 2010]

Related Diseases

Diseases Alias
Microvascular Complications Of Diabetes 3

  • Diabetic Nephropathy

  • Microvascular Complications Of Diabetes, Susceptibility To, 3

  • MVCD3

  • Nephropathy, Diabetic

  • Nephropathy, Diabetic, Susceptibility To

  • End-Stage Renal Disease, Diabetic

  • End-Stage Renal Disease, Diabetic, Susceptibility To

  • Diabetic End-Stage Renal Disease

  • Diabetic Nephropathies
Endocrine System Disease

  • Abnormality Of The Endocrine System

  • Disorder Of Endocrine System

  • Endocrine System Diseases
Retinitis Pigmentosa 11

  • RP11

  • Retinitis Pigmentosa-11

  • Retinitis Pigmentosa, Type 11
Temple Syndrome

  • Uniparental Disomy, Maternal, Chromosome 14

  • Temple Syndrome Due To Paternal 14q32.2 Microdeletion

  • Paternal Del(14)(Q32.2)

  • Temple Syndrome Due To Paternal 14q32.2 Hypomethylation

  • Temple Syndrome Due To Maternal Uniparental Disomy Of Chromosome 14

  • Upd(14)Mat
Kagami-Ogata Syndrome

  • Paternal Uniparental Disomy Of Chromosome 14

  • Uniparental Disomy, Paternal, Chromosome 14

  • Kos

  • Mca Due To 14q32.2 Maternally Expressed Gene Defect

  • Paternal Uniparental Disomy 14

  • Kagami-Ogata Syndrome Due To Maternal 14q32.2 Microdeletion

  • Maternal Del(14)(Q32.2)

  • Maternal Monosomy 14q32.2

  • Kagami-Ogata Syndrome Due To Maternal 14q32.2 Hypermethylation

  • Kagami-Ogata Syndrome Due To Paternal Uniparental Disomy Of Chromosome 14

  • Upd(14)Pat
Premature Ovarian Failure 18

  • POF18

  • Primary Ovarian Insufficiency 18

  • Ovarian Failure, Premature, Type 18
Israeli Tick Typhus

  • Israeli Spotted Fever
Pituitary Cancer

  • Pituitary Carcinoma

  • Malignant Pituitary Neoplasm

  • Malignant Tumor Of Pituitary Gland

  • Neoplasm Of Pituitary Gland

  • Pituitary Gland Cancer

  • Pituitary Gland Neoplasm

  • Pituitary Neoplasm

  • Carcinoma Of The Pituitary Gland

  • Neoplasm Of The Pituitary Gland

  • Pituitary Neoplasms

  • Malignant Neoplasm Of Pituitary Gland
Pituitary Gland Disease

  • Pituitary Diseases

  • Pituitary Dysfunction

  • Pituitary Disease

  • Pituitary Deficiency

  • Pituitary Disorders
Basilar Artery Insufficiency

  • Basilar Artery Syndrome
Endocrine Organ Benign Neoplasm
Angelman Syndrome

  • AS

  • Happy Puppet Syndrome

  • Happy Puppet Syndrome, Formerly

  • Puppetlike Syndrome
Acromesomelic Dysplasia 2a

  • Chondrodysplasia, Grebe Type

  • Acromesomelic Dysplasia, Grebe Type

  • Grebe Chondrodysplasia

  • Amdg

  • Grebe Syndrome

  • AMD2A

  • Grebe Dysplasia

  • Achondrogenesis, Brazilian

  • Achondrogenesis, Type Ii, Formerly

  • Acromesomelic Dysplasia-2a

  • Achondrogenesis Type Ii

  • Brazilian Achondrogenesis

  • Acromesomelic Chondrodysplasia, Grebe Type
Developmental And Epileptic Encephalopathy 66

  • DEE66

  • Epileptic Encephalopathy, Early Infantile, 66

  • Eiee66

  • Developmental And Epileptic Encephalopathy, 66

  • Early Infantile Epileptic Encephalopathy 66

  • Encephalopathy, Epileptic, Early Infantile, Type 66
Large Intestine Cancer
Eye Degenerative Disease
Brooke-Spiegler Syndrome

  • Cyld Cutaneous Syndrome

  • Spiegler-Brooke Syndrome

  • Familial Cylindromatosis

  • BRSS

  • Bss

  • Sbs

  • Multiple Familial Trichoepithelioma

  • Ancell-Spiegler Cylindromas

  • Familial Multiple Trichoepithelioma

  • Trichoepithelioma

  • Fc

  • Mft

  • Multiple Familial Trichoepitheliomas

  • Ccs

  • Turban Tumor Syndrome

  • Schilbach-Rott Syndrome

  • Eccrine Dermal Cylindroma

  • Familial Multiple Trichoepitheliomata
Cell Type Benign Neoplasm
Physical Disorder

  • Physical Illness
Eye Disease

  • Eye Diseases

  • Abnormality Of The Eye

  • Toxoplasma Oculopathy
Retinitis Pigmentosa

  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1
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 MEG8 MGD MGI:1922995