1. Gene
  2. NCOA7 - nuclear receptor coactivator 7 Gene

NCOA7 - nuclear receptor coactivator 7 Gene

Homo sapiens

Also known as ESNA1; TLDC4; ERAP140; NCOA7-AS; Nbla00052; Nbla10993; dJ187J11.3

Gene ID: 135112 | Gene type: protein coding

About NCOA7

Cytogenetic location: 6q22.31-q22.32 Genomic coordinates (GRCh38): 6:125,781,115-125,932,034 (from NCBI)

This gene has 11 transcripts (splice variants), 295 orthologues and 3 paralogues. Ubiquitous expression in urinary bladder (RPKM 17.8), adrenal (RPKM 16.0) and 25 other tissues.

Summary

Enables nuclear receptor binding activity and nuclear receptor coactivator activity. Involved in positive regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

NCOA7 Products(6)

mRNA Protein Name
NM_001122842.3 NP_001116314.1 nuclear receptor coactivator 7 isoform 2
NM_001199619.2 NP_001186548.1 nuclear receptor coactivator 7 isoform 1
NM_001199620.2 NP_001186549.1 nuclear receptor coactivator 7 isoform 1
NM_001199621.2 NP_001186550.1 nuclear receptor coactivator 7 isoform 3
NM_001199622.2 NP_001186551.1 nuclear receptor coactivator 7 isoform 4
NM_181782.5 NP_861447.3 nuclear receptor coactivator 7 isoform 1

NCOA7 Protein Structure

LysM

LysM: LysM domain (120 - 158)

TLD

TLD: TLD (806 - 941)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 942 a.a.
Protein Preferred Names Protein Names

nuclear receptor coactivator 7

140 kDa estrogen receptor-associated protein

Related Diseases

Diseases Alias
Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, And Seizures Syndrome

Door Syndrome

Doors Syndrome

Digitorenocerebral Syndrome

Autosomal Recessive Deafness-Onychodystrophy Syndrome

Deafness-Onychoosteodystrophy-Intellectual Disability Syndrome

DOORS

Drc Syndrome

Eronen Syndrome

Deafness-Onychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

Brachydactyly Due To Absence Of Distal Phalanges

Deafness-Onychodystrophy-Osteodystrophy-Intellectual Disability-Seizures Syndrome

Deafness, Onychodystrophy, Osteodystrophy, And Mental Retardation Syndrome

Deafness-Oncychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

Autosomal Recessive Hearing Loss-Onychodystrophy Syndrome

Hearing Loss-Onychodystrophy-Osteodystrophy-Intellectual Disability Syndrome

Hearing Loss-Onychodystrophy-Osteodystrophy-Intellectual Disability-Seizures Syndrome

Hearing Loss-Onychoosteodystrophy-Intellectual Disability Syndrome

Deafness, Onychodystrophy, Osteodystrophy, Intellectual Disability, And Seizures Syndrome

Deafness, Congenital Onychodystrophy, Recessive Form

Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation Syndrome

Developmental And Epileptic Encephalopathy 16

DEE16

Epileptic Encephalopathy, Early Infantile, 16

Eiee16

Developmental And Epileptic Encephalopathy, 16

Early Infantile Epileptic Encephalopathy 16

Progressive Myoclonic Epilepsy With Dystonia

Pmed

Progressive Myoclonus Epilepsy With Dystonia

Encephalopathy, Epileptic, Early Infantile, Type 16

Brugada Syndrome

Sudden Unexpected Nocturnal Death Syndrome

Sudden Unexplained Nocturnal Death Syndrome

Bangungut

Brugada Type Idiopathic Ventricular Fibrillation

Pokkuri Death Syndrome

Sunds

Idiopathic Ventricular Fibrillation, Brugada Type

Sudden Unexplained Death

Dream Disease

Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome

Sudden Unexplained Death Syndrome

Suds

Sunds - [Sudden Unexplained Nocturnal Death Syndrome]

Martsolf Syndrome 1

Martsolf Syndrome

Cataract-Intellectual Disability-Hypogonadism Syndrome

MARTS1

Marts

Cataract-Mental Retardation-Hypogonadism

Martsolf

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 NCOA7 RGD RGD:1566426
Felis catus NCOA7 VGNC VGNC:63743
Macaca mulatta NCOA7 VGNC VGNC:74998
Mus musculus NCOA7 MGD MGI:2444847
Canis familiaris NCOA7 VGNC VGNC:43664
Bos taurus NCOA7 VGNC VGNC:108132