NNAT - neuronatin Gene

Also Known as Peg5

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 4826

About NNAT

Cytogenetic location: 20q11.23 Genomic coordinates (GRCh38): 20:37,521,250-37,523,690 (from NCBI)

This gene has 5 transcripts (splice variants) and 70 orthologues. Biased expression in placenta (RPKM 54.6), brain (RPKM 50.1) and 3 other tissues.

Summary

The protein encoded by this gene is a proteolipid that may be involved in the regulation of ion channels during brain development. The encoded protein may also play a role in forming and maintaining the structure of the nervous system. This gene is found within an intron of another gene, bladder Cancer associated protein, but on the opposite strand. This gene is imprinted and is expressed only from the paternal allele. [provided by RefSeq, Apr 2016]

NNAT Products (3)

mRNA Protein Name
NM_001322802.2 NP_001309731.1 neuronatin isoform gamma
NM_005386.4 NP_005377.1 neuronatin isoform alpha
NM_181689.3 NP_859017.1 neuronatin isoform beta
Protein Preferred Names Protein Names

neuronatin

NNAT Antibodies

Art. -Nr. Produktname Anwendung Reactivity
HY-P82690 Neuronatin Antibody (YA2435) WB Human, Mouse

Related Diseases

Diseases Alias
Alopecia-Mental Retardation Syndrome 1

  • APMR1

  • Alopecia-Intellectual Disability Syndrome 1

  • Amr Syndrome

  • Alopecia-Intellectual Disability Syndrome

  • Amr Syndrome 1

  • Alopecia With Severe Intellectual Deficit

  • Apmr

  • Alopecia Intellectual Disbility Syndrome 1

  • Perniola-Krajewska-Carnevale Syndrome

  • Alopecia - Intellectual Disability Syndrome

  • Alopecia With Mental Retardation Syndrome 1

  • Perniola Krajewska Carnevale Syndrome
Myoclonic Epilepsy Of Lafora

  • Lafora Disease

  • Epilepsy, Progressive Myoclonic 2b

  • EPM2

  • Melf

  • Epilepsy, Progressive Myoclonic 2a

  • Epm2a

  • Lafora'S Disease

  • Lafora Body Disease

  • Lbd

  • Epilepsy, Progressive Myoclonic, 2a

  • Lafora Progressive Myoclonic Epilepsy

  • Epilepsy Progressive Myoclonic 2

  • Lafora Body Disorder

  • Pme Type 2

  • Progressive Myoclonic Epilepsy Type 2

  • Progressive Myoclonus Epilepsy Type 2

  • Epilepsy, Progressive Myoclonic 2

  • Epm2b

  • Ld

  • Progressive Myoclonic Epilepsy 2

  • Progressive Myoclonic Epilepsy 2a

  • Progressive Myoclonic Epilepsy 2b

  • Progressive Myoclonic Epilepsy Lafora Type

  • Epilepsy, Myoclonic, Of Lafora
Distal Muscular Dystrophy With Anterior Tibial Onset

  • Dmat
Transient Neonatal Diabetes Mellitus

  • Diabetes Mellitus, Transient Neonatal

  • Tndm

  • Chromosome 6-Associated Transient Diabetes Mellitus

  • Dmtn

  • Diabetes Mellitus, 6q24-Related Transient Neonatal

  • Tndm1

  • Neonatal Diabetes Mellitus, Transient

  • Tndm -[Transient Neonatal Diabetes Mellitus]
Progressive Myoclonus Epilepsy

  • Pme

  • Progressive Myoclonic Epilepsy

  • Myoclonic Epilepsies, Progressive

  • Unverricht-Lundborg Syndrome
Hemoglobin H Disease

  • HBH

  • Hemoglobin H Disease, Nondeletional

  • Hemoglobin H Disease, Deletional

  • Alpha-Thalassemia Intermedia

  • Haemoglobin H Disease

  • Alpha-Thalassemia, Hemoglobin H Type

  • Hemoglobin H Disease, Deletional And Nondeletional

  • Alpha Thalassemia, Haemoglobin H Type

  • Alpha Thalassemia, Hemoglobin H Type

  • Haemoglobin H Disease, Deletional

  • Hbh Disease

  • Alpha-Thalassemia Hemoglobin H Type

  • Hemoglobin H Disease Deletional

  • Hemoglobin H Disease Non-Deletional

  • Alpha-Thalassemia

  • Alpha - /- - Or Mutational Forms Of Alpha-Thalassaemia

  • Alpha Thalassaemia Intermedia
Silver-Russell Syndrome 1

  • Silver-Russell Syndrome

  • Russell-Silver Syndrome

  • Silver-Russell Dwarfism

  • Rss

  • SRS1

  • Srs

  • Silver Russell Dwarfism

  • Russell Silver Syndrome

  • Silver Russell Syndrome
Medulloblastoma

  • MDB

  • Cpnet

  • Localized Primitive Neuroectodermal Tumor

  • Classic Medulloblastoma

  • Medulloblastoma Predisposition Syndrome

  • Medulloblastoma, Somatic

  • Brain Medulloblastoma

  • Cns Pnet

  • Infratentorial Primitive Neuroectodermal Tumor

  • Neuroectodermal Tumors, Primitive

  • Medulloblastomas

  • Desmoplastic Medulloblastoma

  • Medulloblastoma, With Extensive Nodularity

  • Medulloblastoma Of Unspecified Site

  • Medullomyoblastoma Of Unspecified Site
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (7)
Art. -Nr. Produktname
Wirkung
Reinheit
Rare Diseases
HY-145476 N-Nitrosoanatabine 99.70% Unkown
HY-145476S N-Nitrosoanatabine-d4 / Unkown
HY-145476S2 N-Nitrosoanatabine-d3 / Unkown
HY-RS09394 NNAT Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS20310 Nnat Mouse Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS26818 Nnat Rat Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-W653722 (S)-N-Nitrosoanatabine / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus NNAT VGNC VGNC:81132
Mus musculus NNAT MGD MGI:104716
Bos taurus NNAT VGNC VGNC:32142
Canis familiaris NNAT VGNC VGNC:43868
Rattus norvegicus NNAT RGD RGD:620155
Others NNAT NCBI