EXOC6B - exocyst complex component 6B Gene

Also Known as SEC15B; SEC15L2; SEMDJL3

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 23233

About EXOC6B

Cytogenetic location: 2p13.2 Genomic coordinates (GRCh38): 2:72,175,984-72,826,033 (from NCBI)

This gene has 9 transcripts (splice variants), 219 orthologues, 1 paralogue and is associated with 2 phenotypes. Ubiquitous expression in heart (RPKM 12.8), brain (RPKM 8.7) and 23 other tissues.

Summary

This gene encodes a protein which is a part of the evolutionarily conserved exocyst, a multimeric protein complex necessary for exocytosis, which in turn, is crucial for cell growth, polarity and migration. Disruption of this gene may be associated with phenotypes exhibiting multiple symptoms including intellectual disability and developmental delay (DD). [provided by RefSeq, Jun 2016]

EXOC6B Products (6)

mRNA Protein Name
NM_001321729.2 NP_001308658.1 exocyst complex component 6B isoform 1
NM_001321730.2 NP_001308659.1 exocyst complex component 6B isoform 3
NM_001321731.2 NP_001308660.1 exocyst complex component 6B isoform 4
NM_001321733.2 NP_001308662.1 exocyst complex component 6B isoform 5
NM_001321734.2 NP_001308663.1 exocyst complex component 6B isoform 6
NM_015189.3 NP_056004.1 exocyst complex component 6B isoform 2
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
27173435 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

EXOC6B Protein Structure

Sec15

Sec15: Exocyst complex subunit Sec15-like (465 - 772)

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

exocyst complex component 6B

  • SEC15 homolog B

EXOC6B Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
EXOC6B Q9Y2D4 SHTN1 Homo sapiens A0MZ66-4 32296183
Intra
EXOC6B Q9Y2D4 SHTN1 Homo sapiens A0MZ66-4 32296183
Intra
EXOC6B Q9Y2D4 EXOC5 Homo sapiens O00471 33961781
Intra
EXOC6B Q9Y2D4 EXOC5 Homo sapiens O00471
TAP
27173435
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3
  • SEMDJL3

  • Spondyloepimetaphyseal Dysplasia With Joint Laxity Type 3

  • Spondyloepimetaphyseal Dysplasia With Joint Laxity, 3

Spondyloepimetaphyseal Dysplasia With Joint Laxity
  • Dysplasia, Spondyloepimetaphyseal, With Joint Laxity

  • Semdjl

  • Spondyloepimetaphyseal Dysplasia Joint Laxity

  • Semd-Jl

  • Semdjl1

  • Spondyloepimetaphyseal Dysplasia With Joint Laxity Type 1

  • Spondyloepimetaphyseal Dysplasia With Joint Laxity, Beighton Type

Spondyloepimetaphyseal Dysplasia
  • Dysplasia, Spondyloepimetaphyseal

Spondyloepimetaphyseal Dysplasia, X-Linked
  • X-Linked Spondyloepimetaphyseal Dysplasia

  • SEMDX

  • Semd, X-Linked

  • Semd X-Linked

  • Spondyloepimetaphyseal Dysplasia X-Linked

  • Spondylo-Epimetaphyseal Dysplasia

Laurin-Sandrow Syndrome
  • Sandrow Syndrome

  • Tetramelic Mirror-Image Polydactyly

  • Mirror-Image Polydactyly

  • Mirror Hands And Feet With Nasal Defects

  • Tmip

  • LSS

  • Mip

  • Mirror Hands And Feets-Nasal Defects Syndrome

  • Fibula And Ulna, Duplication Of, With Absence Of Tibia And Radius

  • Miccor Hands And Feet With Nasal Defects

  • Mipduplication Of Fibuland Ulna With Absence Of Tibia And Radius

  • Fibula Ulna Duplication Tibia Radius Absence

  • Laurin Sandrow Syndrome

  • Duplication Of Fibula And Ulna With Absence Of Tibia And Radius

  • Segmental Laurin-Sandrow Syndrome

  • Laurin-Sandrow Syndrome, Segmental

Scoliosis
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 EXOC6B VGNC VGNC:62003
Rattus norvegicus EXOC6B RGD RGD:1560638
Macaca mulatta EXOC6B VGNC VGNC:106160
Bos taurus EXOC6B VGNC VGNC:28651
Canis familiaris EXOC6B VGNC VGNC:40517
Mus musculus EXOC6B MGD MGI:1923164
Others EXOC6B NCBI