1. Gene
  2. CD6 - CD6 molecule Gene

CD6 - CD6 molecule Gene

Homo sapiens

Also known as TP120

Gene ID: 923 | Gene type: protein coding

About CD6

Cytogenetic location: 11q12.2 Genomic coordinates (GRCh38): 11:60,971,680-61,020,377 (from NCBI)

This gene has 14 transcripts (splice variants), 139 orthologues and 15 paralogues. Biased expression in lymph node (RPKM 22.7), appendix (RPKM 13.7) and 9 other tissues.

Summary

This gene encodes a protein found on the outer membrane of T-lymphocytes as well as some Other immune cells. The encoded protein contains three scavenger receptor cysteine-rich (SRCR) domains and a binding site for an activated leukocyte cell adhesion molecule. The gene product is important for continuation of T cell activation. This gene may be associated with susceptibility to multiple sclerosis (PMID: 19525953, 21849685). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

CD6 Products(3)

mRNA Protein Name
NM_001254750.2 NP_001241679.1 T-cell differentiation antigen CD6 isoform 2 precursor
NM_001254751.2 NP_001241680.1 T-cell differentiation antigen CD6 isoform 3 precursor
NM_006725.5 NP_006716.3 T-cell differentiation antigen CD6 isoform 1 precursor
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
26146185 GOA
enables lipopolysaccharide binding IDA
IDA: Inferred from direct assay
17601777 GOA
enables lipoteichoic acid binding IMP
IMP: Inferred from mutant phenotype
17601777 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
24584089 GOA
Biological Process GO Annotation Evidence Reference Source
involved in acute inflammatory response to antigenic stimulus IDA
IDA: Inferred from direct assay
17601777 GOA
involved in heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules IMP
IMP: Inferred from mutant phenotype
16352806 GOA
involved in immunological synapse formation IMP
IMP: Inferred from mutant phenotype
15294938 GOA
involved in lipopolysaccharide-mediated signaling pathway IDA
IDA: Inferred from direct assay
17601777 GOA
involved in positive regulation of T cell proliferation IMP
IMP: Inferred from mutant phenotype
15294938 GOA
involved in positive regulation of cytokine production involved in inflammatory response IDA
IDA: Inferred from direct assay
17601777 GOA
involved in response to lipopolysaccharide IDA
IDA: Inferred from direct assay
17601777 GOA
Cellular Component GO Annotation Evidence Reference Source
part of T cell receptor complex IDA
IDA: Inferred from direct assay
15294938 GOA
located in immunological synapse IDA
IDA: Inferred from direct assay
15294938 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
15294938 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

CD6 Protein Structure

SRCR

SRCR: Scavenger receptor cysteine-rich domain (48 - 155)

SRCR

SRCR: Scavenger receptor cysteine-rich domain (164 - 260)

SRCR

SRCR: Scavenger receptor cysteine-rich domain (268 - 361)

  • 0
  • 200
  • 400
  • 600
  • 668 a.a.
Protein Preferred Names Protein Names

T-cell differentiation antigen CD6

CD6 antigen

CD6 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
CD6 P30203 LGALS3 Homo sapiens P17931 24945728
Intra
CD6 P30203 LGALS3 Homo sapiens P17931 24945728
Intra
CD6 P30203 ALCAM Homo sapiens Q13740 26146185
Intra
CD6 P30203 ALCAM Homo sapiens Q13740 26146185
Intra
CD6 P30203 ALCAM Homo sapiens Q13740
GMS
26146185
Intra
CD6 P30203 ALCAM Homo sapiens Q13740 33961781
Intra
CD6 P30203 acn Yersinia pestis A0A380PDG1 20711500
Intra
CD6 P30203 CD6 Homo sapiens P30203 26146185
Intra
CD6 P30203 LCP2 Homo sapiens Q13094 24584089
Intra
CD6 P30203 Sdcbp Mus musculus O08992 16034076
Intra
CD6 P30203 CD6 Homo sapiens P30203
GMS
26146185
Intra
CD6 P30203 Sdcbp Mus musculus O08992 16034076
Intra
CD6 P30203 Sdcbp Mus musculus O08992 16034076
Intra
CD6 P30203 CD6 Homo sapiens P30203 26146185
Intra
CD6 P30203 GYG1 Homo sapiens P46976 21988832
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant CD6 Proteins

Cat. No. Product Name Accession Purity
HY-P72922 CD6 Protein, Human (HEK293, Fc) P30203 (H18-E398) ≥95%
HY-P700684 CD6 Protein, Human (HEK293, His) NP_006716.3 (H18-L402) ≥95%

Related Diseases

Diseases Alias
Inflammatory Bowel Disease 16

IBD16

Inflammatory Bowel Disease 16, Susceptibility To

Multiple Sclerosis

MS

Multiple Sclerosis, Susceptibility To

Disseminated Sclerosis

Multiple Sclerosis, Disease Progression, Modifier Of

Insular Sclerosis

Multiple Sclerosis Modifier Of Disease Progression

Multiple Sclerosis, Susceptibility To 1

Multiple Sclerosis, Susceptibility To, 1

Multiple Sclerosis 1

Generalized Multiple Sclerosis

Multiple Sclerosis Variant

Multiple Sclerosis Susceptibility To

Cerebrospinal Sclerosis

Generalised Multiple Sclerosis

Ms - [Multiple Sclerosis]

Disseminated Cerebrospinal Sclerosis

Disseminated Multiple Sclerosis

Disseminated Nervous System Myelosclerosis

Multiple Cerebrospinal Sclerosis

Multiple Combined Sclerosis

Multiple Sclerosis Generalised

Disseminated Brain Sclerosis

Disseminated Spinal Sclerosis

Insular Brain Sclerosis

Miliary Brain Sclerosis

Multiple Combined Sclerosis Of Spinal Cord

Multiple Ascending Sclerosis

Multiple Brain Sclerosis

Multiple Sclerosis Of Brain Stem

Multiple Sclerosis Of The Brain Stem

Multiple Sclerosis Of Cord

Sclérose En Plaques

Plaque Sclerosis

Multiple Sclerosis Of The Spinal Cord

Inflammatory Bowel Disease 18

IBD18

Diamond-Blackfan Anemia 1

Aase Syndrome

DBA1

Erythrogenesis Imperfecta

Aase-Smith Syndrome Ii

Dba

Blackfan-Diamond Syndrome

Bds

Anemia, Congenital Hypoplastic, Of Blackfan And Diamond

Anemia, Congenital Erythroid Hypoplastic

Red Cell Aplasia, Pure, Hereditary

Aregenerative Anemia, Chronic Congenital

Rps19-Related Diamond-Blackfan Anemia

Chronic Congenital Aregenerative Anemia

Congenital Erythroid Hypoplastic Anemia

Congenital Hypoplastic Anemia Of Blackfan And Diamond

Pure Hereditary Red Cell Aplasia

Anemia, Diamond-Blackfan, Type 1

Anemia, Diamond-Blackfan

Aase Smith Syndrome 2

Familial Hypoplastic Anaemia With Malformations

Constitutional Pure Red Cell Aplasia

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
Felis catus CD6 VGNC VGNC:60635
Rattus norvegicus CD6 RGD RGD:2312
Canis familiaris CD6 VGNC VGNC:38966
Mus musculus CD6 MGD MGI:103566
Macaca mulatta CD6 VGNC VGNC:100906
Bos taurus CD6 VGNC VGNC:27041
Macaca fascicularis CD6 NCBI NCBI:102143944
Susscrofa domestica CD6 NCBI
Leporidae CD6 NCBI
Others CD6 NCBI