NR2C2AP - nuclear receptor 2C2 associated protein Gene

Also Known as TRA16

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 126382

About NR2C2AP

Cytogenetic location: 19p13.11 Genomic coordinates (GRCh38): 19:19,201,409-19,203,414 (from NCBI)

This gene has 7 transcripts (splice variants) and 194 orthologues. Ubiquitous expression in ovary (RPKM 9.3), skin (RPKM 8.7) and 25 other tissues.

Summary

Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

NR2C2AP Products (2)

mRNA Protein Name
NM_001300945.2 NP_001287874.1 nuclear receptor 2C2-associated protein isoform 1
NM_176880.6 NP_795361.1 nuclear receptor 2C2-associated protein isoform 2
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
12486131 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

NR2C2AP Protein Structure

F5_F8_type_C

F5_F8_type_C: F5/8 type C domain (15 - 99)

  • 0
  • 100
  • 139 a.a.
Protein Preferred Names Protein Names

nuclear receptor 2C2-associated protein

  • TR4 orphan receptor associated protein TRA16

NR2C2AP Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
NR2C2AP Q86WQ0 REL Homo sapiens Q04864-2 32296183
Intra
NR2C2AP Q86WQ0 REL Homo sapiens Q04864-2 32296183
Intra
NR2C2AP Q86WQ0 TEPSIN Homo sapiens Q96N21 32296183
Intra
NR2C2AP Q86WQ0 TEPSIN Homo sapiens Q96N21 32296183
Intra
NR2C2AP Q86WQ0 TEPSIN Homo sapiens Q96N21 32296183
Intra
NR2C2AP Q86WQ0 VPS52 Homo sapiens Q8N1B4 32296183
Intra
NR2C2AP Q86WQ0 VPS52 Homo sapiens Q8N1B4 32296183
Intra
NR2C2AP Q86WQ0 VPS52 Homo sapiens Q8N1B4 32296183
Intra
NR2C2AP Q86WQ0 REL Homo sapiens Q04864 25416956
Intra
NR2C2AP Q86WQ0 TCF4 Homo sapiens P15884 25416956
Intra
NR2C2AP Q86WQ0 DDIT4L Homo sapiens Q96D03 32296183
Intra
NR2C2AP Q86WQ0 DDIT4L Homo sapiens Q96D03 32296183
Intra
NR2C2AP Q86WQ0 DDIT4L Homo sapiens Q96D03 32296183
Intra
NR2C2AP Q86WQ0 SLC16A3 Homo sapiens O15427 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Bare Lymphocyte Syndrome, Type Ii
  • Mhc Class Ii Deficiency

  • Bare Lymphocyte Syndrome

  • Major Histocompatibility Complex Class Ii Deficiency

  • Bare Lymphocyte Syndrome 2

  • Bare Lymphocyte Syndrome Type 2

  • Severe Combined Immunodeficiency, Hla Class Ii-Negative

  • Bare Lymphocyte Syndrome, Type Ii, Complementation Group C

  • Bare Lymphocyte Syndrome, Type Ii, Complementation Group D

  • Bare Lymphocyte Syndrome Type Ii

  • Scid, Hla Class Ii-Negative

  • Bare Lymphocyte Syndrome, Type Ii, Complementation Group A

  • Bare Lymphocyte Syndrome, Type Ii, Complementation Group B

  • Scid Due To Absent Class Ii Hla Antigens

  • Hla Class 1 Deficiency

  • Scid, Hla Class 2-Negative

  • Bls Type Ii

  • Bare Lymphocyte Syndrome Type 2, Complementation Group A

  • Bare Lymphocyte Syndrome Type 2, Complementation Group E

  • Severe Combined Immunodeficiency

  • Bls, Type Ii

  • Bls

  • Bare Lymphocyte Syndrome, Type Ii, Complementation Group E

  • Blsii

  • Bls Type 1

  • Bls 2

  • Scid Due To Absence Of Class Ii Hla Antigens

  • Severe Combined Immunodeficiency Due To Absent Class Ii Human Leukocyte Antigens

  • Immunodeficiency By Defective Expression Of Mhc Class Ii

  • BLS2

  • Bare Lymphocyte Syndrome Type Ii Complementation Group A

  • Bare Lymphocyte Syndrome Type Ii Complementation Group B

  • Bare Lymphocyte Syndrome Type Ii Complementation Group C

  • Bare Lymphocyte Syndrome Type Ii Complementation Group D

  • Bare Lymphocyte Syndrome Type Ii Complementation Group E

  • Bls Ii

  • Hereditary Mhc Class Ii Deficiency

  • Hla Class Ii Deficient Combined Immunodeficiency

  • Mhc-Ii Deficiency

  • Scid Hla Class Ii-Negative

  • Severe Combined Immunodeficiency Hla Class Ii-Negative

  • Bl-2

  • Immunodeficiency By Defective Expression Of Hla Class 2

  • Hla Class 2-Negative Severe Combined Immunodeficiency

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
Bos taurus NR2C2AP VGNC VGNC:32237
Macaca mulatta NR2C2AP VGNC VGNC:75495
Felis catus NR2C2AP VGNC VGNC:63877
Rattus norvegicus NR2C2AP RGD RGD:1561190
Mus musculus NR2C2AP MGD MGI:1922942
Canis familiaris NR2C2AP VGNC VGNC:43948
Others NR2C2AP NCBI