SEC23A - SEC23 homolog A, COPII coat complex component Gene

Also Known as CLSD; hSec23A

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10484

About SEC23A

Cytogenetic location: 14q21.1 Genomic coordinates (GRCh38): 14:39,031,919-39,103,235 (from NCBI)

This gene has 15 transcripts (splice variants), 131 orthologues, 1 paralogue and is associated with 3 phenotypes. Ubiquitous expression in duodenum (RPKM 27.6), small intestine (RPKM 25.4) and 24 other tissues.

Summary

The protein encoded by this gene is a member of the SEC23 subfamily of the SEC23/SEC24 family. It is part of a protein complex and found in the ribosome-free transitional face of the endoplasmic reticulum (ER) and associated vesicles. This protein has similarity to yeast Sec23p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. The encoded protein is suggested to play a role in the ER-Golgi protein trafficking. [provided by RefSeq, Jul 2008]

SEC23A Products (1)

mRNA Protein Name
NM_006364.4 NP_006355.2 protein transport protein Sec23A
Molecular Function GO Annotation Evidence Références Source
enables protein binding IPI
IPI: Inferred from physical interaction
10075675 GOA
enables zinc ion binding IDA
IDA: Inferred from direct assay
18843296 GOA
Biological Process GO Annotation Evidence Références Source
involved in COPII-coated vesicle cargo loading IDA
IDA: Inferred from direct assay
17499046 GOA
involved in COPII-coated vesicle cargo loading IGI
IGI: Inferred from genetic interaction
8898360 GOA
Cellular Component GO Annotation Evidence Références Source
part of COPII vesicle coat IDA
IDA: Inferred from direct assay
17499046 GOA
located in ER to Golgi transport vesicle membrane IGI
IGI: Inferred from genetic interaction
8898360 GOA
located in cytosol IDA
IDA: Inferred from direct assay
8898360 GOA
located in endoplasmic reticulum exit site IDA
IDA: Inferred from direct assay
8898360 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

SEC23A Protein Structure

zf-Sec23_Sec24

zf-Sec23_Sec24: Sec23/Sec24 zinc finger (57 - 98)

Sec23_trunk

Sec23_trunk: Sec23/Sec24 trunk domain (126 - 390)

Sec23_BS

Sec23_BS: Sec23/Sec24 beta-sandwich domain (401 - 504)

Sec23_helical

Sec23_helical: Sec23/Sec24 helical domain (519 - 619)

Gelsolin

Gelsolin: Gelsolin repeat (631 - 718)

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

protein transport protein Sec23A

  • SEC23-related protein A

SEC23A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Références
Intra
SEC23A Q15436 CADPS Homo sapiens A2RRN7 32296183
Intra
SEC23A Q15436 CADPS Homo sapiens A2RRN7 32296183
Intra
SEC23A Q15436 MFF Homo sapiens Q9GZY8-5 32296183
Intra
SEC23A Q15436 MFF Homo sapiens Q9GZY8-5 32296183
Intra
SEC23A Q15436 MFF Homo sapiens Q9GZY8-5 32296183
Intra
SEC23A Q15436 CLEC17A Homo sapiens Q6ZS10 32296183
Intra
SEC23A Q15436 CLEC17A Homo sapiens Q6ZS10 32296183
Intra
SEC23A Q15436 CLEC17A Homo sapiens Q6ZS10 32296183
Intra
SEC23A Q15436 MINAR1 Homo sapiens Q9UPX6 32296183
Intra
SEC23A Q15436 MINAR1 Homo sapiens Q9UPX6 32296183
Intra
SEC23A Q15436 MINAR1 Homo sapiens Q9UPX6 32296183
Intra
SEC23A Q15436 SF1 Homo sapiens Q15637-4 32296183
Intra
SEC23A Q15436 SF1 Homo sapiens Q15637-4 32296183
Intra
SEC23A Q15436 SF1 Homo sapiens Q15637-4 32296183
Intra
SEC23A Q15436 GJA8 Homo sapiens P48165 32296183
Intra
SEC23A Q15436 GJA8 Homo sapiens P48165 32296183
Intra
SEC23A Q15436 SEC23IP Homo sapiens Q9Y6Y8 32296183
Intra
SEC23A Q15436 SEC23IP Homo sapiens Q9Y6Y8 32296183
Intra
SEC23A Q15436 SEC23IP Homo sapiens Q9Y6Y8 32296183
Intra
SEC23A Q15436 SEC23IP Homo sapiens Q9Y6Y8 33961781
Intra
SEC23A Q15436 SUCLA2 Homo sapiens Q9P2R7 32296183
Intra
SEC23A Q15436 MIA3 Homo sapiens Q5JRA6 32296183
Intra
SEC23A Q15436 MIA3 Homo sapiens Q5JRA6 32296183
Intra
SEC23A Q15436 MIA3 Homo sapiens Q5JRA6 32296183
Intra
SEC23A Q15436 RNF19B Homo sapiens Q6ZMZ0 32296183
Intra
SEC23A Q15436 RNF19B Homo sapiens Q6ZMZ0 32296183
Intra
SEC23A Q15436 RNF19B Homo sapiens Q6ZMZ0 32296183
Intra
SEC23A Q15436 DNM2 Homo sapiens P50570 32296183
Intra
SEC23A Q15436 DNM2 Homo sapiens P50570 32296183
Intra
SEC23A Q15436 PIAS2 Homo sapiens O75928-2 32296183
Intra
SEC23A Q15436 PIAS2 Homo sapiens O75928-2 32296183
Intra
SEC23A Q15436 ERLIN1 Homo sapiens O75477 32296183
Intra
SEC23A Q15436 ERLIN1 Homo sapiens O75477 32296183
Intra
SEC23A Q15436 TMEM45B Homo sapiens Q96B21 32296183
Intra
SEC23A Q15436 TMEM45B Homo sapiens Q96B21 32296183
Intra
SEC23A Q15436 TMEM45B Homo sapiens Q96B21 32296183
Intra
SEC23A Q15436 SLC7A1 Homo sapiens P30825 32296183
Intra
SEC23A Q15436 SLC7A1 Homo sapiens P30825 32296183
Intra
SEC23A Q15436 FASLG Homo sapiens P48023 32296183
Intra
SEC23A Q15436 FASLG Homo sapiens P48023 32296183
Intra
SEC23A Q15436 TNFSF14 Homo sapiens O43557 32296183
Intra
SEC23A Q15436 TNFSF14 Homo sapiens O43557 32296183
Intra
SEC23A Q15436 WBP11 Homo sapiens Q9Y2W2 32296183
Intra
SEC23A Q15436 WBP11 Homo sapiens Q9Y2W2 32296183
Intra
SEC23A Q15436 WBP11 Homo sapiens Q9Y2W2 32296183
Intra
SEC23A Q15436 CDK16 Homo sapiens Q00536 16091426
Intra
SEC23A Q15436 CDK16 Homo sapiens Q00536
Y2H
16091426
Intra
SEC23A Q15436 DTX2 Homo sapiens Q86UW9 32296183
Intra
SEC23A Q15436 DTX2 Homo sapiens Q86UW9 32296183
Intra
SEC23A Q15436 DTX2 Homo sapiens Q86UW9 32296183
Intra
SEC23A Q15436 SEC23B Homo sapiens Q15437 32296183
Intra
SEC23A Q15436 SEC23B Homo sapiens Q15437 33961781
Intra
SEC23A Q15436 SEC23B Homo sapiens Q15437 32296183
Intra
SEC23A Q15436 SEC23B Homo sapiens Q15437 32296183
Intra
SEC23A Q15436 FATE1 Homo sapiens Q969F0 32296183
Intra
SEC23A Q15436 FATE1 Homo sapiens Q969F0 32296183
Intra
SEC23A Q15436 FATE1 Homo sapiens Q969F0 32296183
Intra
SEC23A Q15436 SEC24D Homo sapiens O94855 33961781
Intra
SEC23A Q15436 SEC24D Homo sapiens O94855 35271311
Intra
SEC23A Q15436 BNIP3 Homo sapiens Q12983 32296183
Intra
SEC23A Q15436 BNIP3 Homo sapiens Q12983 32296183
Intra
SEC23A Q15436 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
SEC23A Q15436 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
SEC23A Q15436 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
SEC23A Q15436 SEC24B Homo sapiens O95487 35271311
Intra
SEC23A Q15436 SEC24B Homo sapiens O95487 33961781
Intra
SEC23A Q15436 SEC24C Homo sapiens P53992 18692470
Intra
SEC23A Q15436 SEC24C Homo sapiens P53992 33961781
Intra
SEC23A Q15436 SEC24C Homo sapiens P53992
EM
18692470
Intra
SEC23A Q15436 SEC24C Homo sapiens P53992
Y2H
10075675
Cross: Cross-species interaction Intra: Intraspecies interaction

SEC23A Anticorps

Cat. No. Nom du produit Application Reactivity
HY-P81799 SEC23A Antibody (YA1544) WB, FC Human

Related Diseases

Diseases Alias
Craniolenticulosutural Dysplasia
  • Boyadjiev-Jabs Syndrome

  • CLSD

  • Cranio-Lenticulo-Sutural Dysplasia

  • Cranio-Lenticulo-Sutural Dysplasia, Clsd

Spondyloepiphyseal Dysplasia Tarda, X-Linked
  • Spondyloepiphyseal Dysplasia Tarda

  • X-Linked Spondyloepiphyseal Dysplasia Tarda

  • SEDT

  • Sed Tarda, X-Linked

  • Spondyloepiphyseal Dysplasia, Late

  • Spondyloepiphyseal Dysplasia Tarda X-Linked

  • Sed

  • X Linked Spondyloepiphyseal Dysplasia Tarda

  • X-Linked Spondyloepiphyseal Dysplasia

  • Late Onset Spondyloepiphyseal Dysplasia

  • Sed Tarda

  • X-Linked Sed

  • X-Linked Sedt

  • Dysplasia, Spondyloepiphyseal, Tarda

  • Spondyloepiphyseal Dysplasia

Anemia, Congenital Dyserythropoietic, Type Ii
  • Congenital Dyserythropoietic Anemia Type Ii

  • CDAN2

  • Cda Ii

  • Hereditary Erythroblastic Multinuclearity With Positive Acidified-Serum Test

  • Cda Type Ii

  • Congenital Dyserythropoietic Anemia Type 2

  • Hereditary Erythroblastic Multinuclearity With A Positive Acidified-Serum Test

  • Sec23b-Cdg

  • Congenital Dyserythropoietic Anemia, Type Ii

  • Dyserythropoietic Anemia, Hempas Type

  • Hempas

  • Cda Type 2

  • Dyserythropoietic Anemia, Congenital, Type Ii

  • Cda, Type Ii

  • Congenital Dyserythropoietic Anaemia Type 2

  • Congenital Dyserythropoietic Anaemia Type Ii

  • Anemia, Dyserythropoietic, Congenital Type 2

  • Hempas Anemia

  • Dyserythropoietic Anemia, Congenital Type 2

  • Anemia, Congenital Dyserythropoietic, 2

  • Dyserythropoietic Anemia Hempas Type

  • Anemia, Dyserythropoietic Congenital, Type Ii

  • Anemia, Dyserythropoietic, Congenital, Type Ii

Camptodactyly-Tall Stature-Scoliosis-Hearing Loss Syndrome
  • Catshl Syndrome

  • Camptodactyly-Tall Stature-Scoliosis-Deafness Syndrome

Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type
  • Spondyloepimetaphyseal Dysplasia-Short Limb-Abnormal Calcification Syndrome

  • Smed-Sl

  • Smed-Sl/Ac

  • Smed Short Limb-Abnormal Calcification Type

  • Smed Short Limb-Hand Type

  • Spondylometaepiphyseal Dysplasia Short Limb-Hand Type

  • Smed, Type Ii

  • Smed Type 2

  • Spondylometaepiphyseal Dysplasia Short Limb-Abnormal Calcification Type

  • Smed, Short Limb-Hand Type

  • Spondylometaepiphyseal Dysplasia, Short Limb-Abnormal Calcification Type

  • Smed, Short Limb-Abnormal Calcification Type

  • Spondyloepimetaphyseal Dysplasia - Short Limb - Abnormal Calcification

  • Spondyloepimetaphyseal Dysplasia, Short Limb-Hand Type

  • SEMD-SL

  • Smed Type Ii

  • Dysplasia, Spondylometaepiphyseal, Short Limb-Hand Type

Cole-Carpenter Syndrome
  • Cole Carpenter Syndrome

  • Bone Fragility Craniosynostosis Proptosis Hydrocephalus

  • Bone Fragility With Craniosynostosis, Ocular Proptosis, Hydrocephalus, And Distinctive Facial Features

  • Bone Fragility-Craniosynostosis-Proptosis-Hydrocephalus Syndrome

Spondyloepiphyseal Dysplasia Congenita
  • SEDC

  • Sed Congenita

  • Spondyloepiphyseal Dysplasia, Congenital Type

  • Late Spondyloepiphyseal Dysplasia

  • Sed, Congenital Type

  • Congenital Spondyloepiphyseal Dysplasia

  • Spranger-Wiedemann Disease

  • Spondyloepiphyseal Dysplasia Congenital Type

  • Dysplasia, Spondyloepiphyseal, Congenita

  • Spondyloepiphyseal Dysplasia, Congenita

  • Spondyloepiphyseal Dysplasia Tarda, X-Linked

Geroderma Osteodysplasticum
  • Gerodermia Osteodysplastica

  • Geroderma Osteodysplastica

  • GO

  • Walt Disney Dwarfism

  • Type Of Gerodermia Osteodysplastica

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
Rattus norvegicus SEC23A RGD RGD:1309103
Bos taurus SEC23A VGNC VGNC:34410
Canis familiaris SEC23A VGNC VGNC:45969
Mus musculus SEC23A MGD MGI:1349635
Felis catus SEC23A VGNC VGNC:64966
Macaca mulatta SEC23A VGNC VGNC:77150
Others SEC23A NCBI