1. Gene
  2. TNFAIP1 - TNF alpha induced protein 1 Gene

TNFAIP1 - TNF alpha induced protein 1 Gene

Homo sapiens

Also known as B12; B61; EDP1; BTBD34; hBACURD2

Gene ID: 7126 | Gene type: protein coding

About TNFAIP1

Cytogenetic location: 17q11.2 Genomic coordinates (GRCh38): 17:28,335,761-28,347,009 (from NCBI)

This gene has 6 transcripts (splice variants), 223 orthologues and 2 paralogues. Ubiquitous expression in lung (RPKM 21.1), spleen (RPKM 20.2) and 25 other tissues.

Summary

This gene was identified as a gene whose expression can be induced by the tumor necrosis factor alpha (TNF) in umbilical vein endothelial cells. Studies of a similar gene in mouse suggest that the expression of this gene is developmentally regulated in a tissue-specific manner. [provided by RefSeq, Jul 2008]

TNFAIP1 Products(1)

mRNA Protein Name
NM_021137.5 NP_066960.1 BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
19615732 GOA
enables small GTPase binding IDA
IDA: Inferred from direct assay
19637314 GOA
contributes to ubiquitin-protein transferase activity IDA
IDA: Inferred from direct assay
19782033 GOA
Biological Process GO Annotation Evidence Reference Source
involved in cell migration IMP
IMP: Inferred from mutant phenotype
19782033 GOA
involved in immune response IEP
IEP: Inferred from expression pattern
1370465 GOA
involved in negative regulation of Rho protein signal transduction IMP
IMP: Inferred from mutant phenotype
19782033 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IDA
IDA: Inferred from direct assay
19782033 GOA
involved in protein ubiquitination IDA
IDA: Inferred from direct assay
19782033 GOA
involved in stress fiber assembly IMP
IMP: Inferred from mutant phenotype
19782033 GOA
Cellular Component GO Annotation Evidence Reference Source
part of Cul3-RING ubiquitin ligase complex IDA
IDA: Inferred from direct assay
19782033 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
19637314 GOA
located in endosome IDA
IDA: Inferred from direct assay
19637314 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

TNFAIP1 Protein Structure

BTB_2

BTB_2: BTB/POZ domain (30 - 120)

  • 0
  • 100
  • 200
  • 316 a.a.
Protein Preferred Names Protein Names

BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2

BTB/POZ domain-containing protein TNFAIP1

TNFAIP1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
TNFAIP1 Q13829 CAPN7 Homo sapiens Q7Z479 25416956
Intra
TNFAIP1 Q13829 CAPN7 Homo sapiens Q7Z479 25416956
Intra
TNFAIP1 Q13829 POLR1C Homo sapiens O15160 25416956
Intra
TNFAIP1 Q13829 POLR1C Homo sapiens O15160
Y2H
21988832
Intra
TNFAIP1 Q13829 JPH3 Homo sapiens Q8WXH2 32814053
Intra
TNFAIP1 Q13829 JPH3 Homo sapiens Q8WXH2 32814053
Intra
TNFAIP1 Q13829 JPH3 Homo sapiens Q8WXH2 32814053
Intra
TNFAIP1 Q13829 APOE Homo sapiens P02649 32814053
Intra
TNFAIP1 Q13829 APOE Homo sapiens P02649 32814053
Intra
TNFAIP1 Q13829 APOE Homo sapiens P02649 32814053
Intra
TNFAIP1 Q13829 CAPN7 Homo sapiens Q9Y6W3 32296183
Intra
TNFAIP1 Q13829 KCTD13 Homo sapiens Q8WZ19 25416956
Intra
TNFAIP1 Q13829 KCTD13 Homo sapiens Q8WZ19 32296183
Intra
TNFAIP1 Q13829 KCTD13 Homo sapiens Q8WZ19 32296183
Intra
TNFAIP1 Q13829 CUL3 Homo sapiens Q13618 25416956
Intra
TNFAIP1 Q13829 KCTD13 Homo sapiens Q8WZ19 33961781
Intra
TNFAIP1 Q13829 CUL3 Homo sapiens Q13618 25416956
Intra
TNFAIP1 Q13829 KCTD13 Homo sapiens Q8WZ19 32296183
Intra
TNFAIP1 Q13829 KCTD10 Homo sapiens Q9H3F6 32296183
Intra
TNFAIP1 Q13829 KCTD10 Homo sapiens Q9H3F6 32296183
Intra
TNFAIP1 Q13829 KCTD10 Homo sapiens Q9H3F6 33961781
Intra
TNFAIP1 Q13829 KCTD10 Homo sapiens Q9H3F6 32296183
Intra
TNFAIP1 Q13829 GATM Homo sapiens P50440 32814053
Intra
TNFAIP1 Q13829 GATM Homo sapiens P50440 32814053
Intra
TNFAIP1 Q13829 GATM Homo sapiens P50440 32814053
Intra
TNFAIP1 Q13829 CDC37 Homo sapiens Q16543 32296183
Intra
TNFAIP1 Q13829 PSMA1 Homo sapiens P25786 25416956
Intra
TNFAIP1 Q13829 EXOSC5 Homo sapiens Q9NQT4 32296183
Intra
TNFAIP1 Q13829 NXF1 Homo sapiens Q9UBU9 32296183
Intra
TNFAIP1 Q13829 GRB2 Homo sapiens P62993 32814053
Intra
TNFAIP1 Q13829 GRB2 Homo sapiens P62993 32814053
Intra
TNFAIP1 Q13829 GRB2 Homo sapiens P62993 32814053
Intra
TNFAIP1 Q13829 HEXIM2 Homo sapiens Q96MH2 32296183
Intra
TNFAIP1 Q13829 RHOB Homo sapiens P62745 19637314
Intra
TNFAIP1 Q13829 RHOB Homo sapiens P62745 19637314
Intra
TNFAIP1 Q13829 SRC Homo sapiens P12931 32814053
Intra
TNFAIP1 Q13829 SRC Homo sapiens P12931 32814053
Intra
TNFAIP1 Q13829 SRC Homo sapiens P12931 32814053
Intra
TNFAIP1 Q13829 EPM2AIP1 Homo sapiens Q7L775 25416956
Intra
TNFAIP1 Q13829 EPM2AIP1 Homo sapiens Q7L775 25416956
Intra
TNFAIP1 Q13829 EPM2AIP1 Homo sapiens Q7L775 25416956
Intra
TNFAIP1 Q13829 LNX1 Homo sapiens Q8TBB1 32296183
Intra
TNFAIP1 Q13829 NTAQ1 Homo sapiens Q96HA8 32296183
Intra
TNFAIP1 Q13829 ARMC7 Homo sapiens Q9H6L4 25416956
Intra
TNFAIP1 Q13829 ARMC7 Homo sapiens Q9H6L4 32296183
Intra
TNFAIP1 Q13829 ARMC7 Homo sapiens Q9H6L4 25416956
Intra
TNFAIP1 Q13829 ARMC7 Homo sapiens Q9H6L4 32296183
Intra
TNFAIP1 Q13829 GFAP Homo sapiens P14136 32814053
Intra
TNFAIP1 Q13829 GFAP Homo sapiens P14136 32814053
Intra
TNFAIP1 Q13829 GFAP Homo sapiens P14136 32814053
Intra
TNFAIP1 Q13829 ZMYND19 Homo sapiens Q96E35 32296183
Intra
TNFAIP1 Q13829 STK16 Homo sapiens O75716 25416956
Intra
TNFAIP1 Q13829 CARD9 Homo sapiens Q9H257 25416956
Intra
TNFAIP1 Q13829 CARD9 Homo sapiens Q9H257 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Pontocerebellar Hypoplasia, Type 16

PCH16

Pontocerebellar Hypoplasia Type 16

Pontocerebellar Hypoplasia 16

Doid:0112333

Neurotic Excoriation

Factitious Skin Disease

Dermatitis Artefacta

Dermatitis Factitia

Dermatitis Ficta

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 TNFAIP1 MGD MGI:104961
Felis catus TNFAIP1 VGNC VGNC:66397
Rattus norvegicus TNFAIP1 RGD RGD:3877
Canis familiaris TNFAIP1 VGNC VGNC:47648
Bos taurus TNFAIP1 VGNC VGNC:36154
Macaca mulatta TNFAIP1 VGNC VGNC:78578