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  2. TAPBPL - TAP binding protein like Gene

TAPBPL - TAP binding protein like Gene

Homo sapiens

Also known as TAPBPR; TAPBP-R

Gene ID: 55080 | Gene type: protein coding

About TAPBPL

Cytogenetic location: 12p13.31 Genomic coordinates (GRCh38): 12:6,451,649-6,472,006 (from NCBI)

This gene has 8 transcripts (splice variants), 182 orthologues and 2 paralogues. Ubiquitous expression in duodenum (RPKM 8.1), small intestine (RPKM 7.3) and 25 other tissues.

Summary

Tapasin, or TAPBP (MIM 601962), is a member of the variable-constant Ig superfamily that links major histocompatibility complex (MHC) class I molecules to the transporter associated with antigen processing (TAP; see MIM 170260) in the endoplasmic reticulum (ER). The TAPBP gene is located near the MHC complex on chromosome 6p21.3. TAPBPL is a member of the Ig superfamily that is localized on chromosome 12p13.3, a region somewhat paralogous to the MHC.[supplied by OMIM, Mar 2008]

TAPBPL Products(2)

mRNA Protein Name
NM_001351355.2 NP_001338284.1 tapasin-related protein isoform 2
NM_018009.5 NP_060479.3 tapasin-related protein isoform 1 precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables MHC class I protein complex binding IDA
IDA: Inferred from direct assay
23401559 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
23401559 GOA
Biological Process GO Annotation Evidence Reference Source
involved in negative regulation of antigen processing and presentation of peptide antigen via MHC class I IDA
IDA: Inferred from direct assay
23401559 GOA
involved in peptide antigen assembly with MHC class I protein complex IDA
IDA: Inferred from direct assay
26869717 GOA
Cellular Component GO Annotation Evidence Reference Source
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
23401559 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

TAPBPL Protein Structure

V-set

V-set: Immunoglobulin V-set domain (194 - 294)

C1-set

C1-set: Immunoglobulin C1-set domain (317 - 392)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 468 a.a.
Protein Preferred Names Protein Names

tapasin-related protein

TAP binding protein related

TAPBPL Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
TAPBPL Q9BX59 KRTAP10-8 Homo sapiens P60410 32296183
Intra
TAPBPL Q9BX59 KRTAP10-8 Homo sapiens P60410 32296183
Intra
TAPBPL Q9BX59 HLA-B Homo sapiens P01889 26439010
Intra
TAPBPL Q9BX59 KRT34 Homo sapiens O76011 32296183
Intra
TAPBPL Q9BX59 KRT34 Homo sapiens O76011 32296183
Intra
TAPBPL Q9BX59 KRT35 Homo sapiens Q92764 32296183
Intra
TAPBPL Q9BX59 KRT35 Homo sapiens Q92764 32296183
Intra
TAPBPL Q9BX59 TEPSIN Homo sapiens Q96N21 32296183
Intra
TAPBPL Q9BX59 TEPSIN Homo sapiens Q96N21 32296183
Intra
TAPBPL Q9BX59 PM20D2 Homo sapiens Q8IYS1 32296183
Intra
TAPBPL Q9BX59 PM20D2 Homo sapiens Q8IYS1 32296183
Intra
TAPBPL Q9BX59 TCF4 Homo sapiens P15884-3 32296183
Intra
TAPBPL Q9BX59 TCF4 Homo sapiens P15884-3 32296183
Intra
TAPBPL Q9BX59 NOTCH2NLC Homo sapiens P0DPK4 32296183
Intra
TAPBPL Q9BX59 NOTCH2NLC Homo sapiens P0DPK4 32296183
Intra
TAPBPL Q9BX59 HLA-A Homo sapiens P01892 26439010
Intra
TAPBPL Q9BX59 HLA-A Homo sapiens P01892 24163410
Intra
TAPBPL Q9BX59 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
TAPBPL Q9BX59 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
TAPBPL Q9BX59 KRT31 Homo sapiens Q15323 32296183
Intra
TAPBPL Q9BX59 KRT31 Homo sapiens Q15323 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Spastic Ataxia 1, Autosomal Dominant

SPAX1

Ataxia, Spastic, 1, Autosomal Dominant

Autosomal Dominant Spastic Ataxia Type 1

Ataxia, Spastic, Type 1, Autosomal Dominant

Spastic Ataxia 1
Myasthenic Syndrome, Congenital, 25, Presynaptic

CMS25

Myasthenic Syndrome, Congenital, 25

Congenital Myasthenic Syndrome

Congenital Myasthenia

Congenital Myasthenic Syndromes

Cms

Myasthenic Syndromes, Congenital

Myasthenic Syndromes Congenital

Myasthenic Syndrome, Congenital

Congenital Myasthenic Syndrome Ib

Congenital And Developmental Myasthenia

Developmental Myasthenia

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 TAPBPL MGD MGI:2384853
Felis catus TAPBPL VGNC VGNC:65953
Rattus norvegicus TAPBPL RGD RGD:1307893
Canis familiaris TAPBPL VGNC VGNC:47107
Bos taurus TAPBPL VGNC VGNC:35600
Macaca mulatta TAPBPL NCBI NCBI:712626
Others TAPBPL NCBI