Identity
HGNC
LOCATION
20p11.23
LOCUSID
ALIAS
CDA-II,CDAII,CDAN2,CWS7,HEMPAS,hSec23B
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 10483
MIM: 610512
HGNC: 10702
Ensembl: ENSG00000101310
Variants:
dbSNP: 10483
ClinVar: 10483
TCGA: ENSG00000101310
COSMIC: SEC23B
RNA/Proteins
Expression (GTEx)
Pathways
| Pathway | Source | External ID |
|---|---|---|
| Protein processing in endoplasmic reticulum | KEGG | ko04141 |
| Protein processing in endoplasmic reticulum | KEGG | hsa04141 |
| COPII complex | KEGG | hsa_M00404 |
| COPII complex | KEGG | M00404 |
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37204595 | 2023 | Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population. | 0 |
| 37373084 | 2023 | New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II. | 1 |
| 37204595 | 2023 | Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population. | 0 |
| 37373084 | 2023 | New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II. | 1 |
| 34954140 | 2022 | A common human missense mutation of vesicle coat protein SEC23B leads to growth restriction and chronic pancreatitis in mice. | 2 |
| 35163229 | 2022 | SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells. | 5 |
| 34954140 | 2022 | A common human missense mutation of vesicle coat protein SEC23B leads to growth restriction and chronic pancreatitis in mice. | 2 |
| 35163229 | 2022 | SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells. | 5 |
| 33753724 | 2021 | Non-canonical role of wild-type SEC23B in the cellular stress response pathway. | 1 |
| 33914262 | 2021 | Compound heterozygosity for two novel mutations of the SEC23B gene in congenital dyserythropoietic anemia type II. | 0 |
| 34365611 | 2021 | [Variant analysis of SEC23B gene in 4 families with congenital dyserythropoietic anemia]. | 0 |
| 33753724 | 2021 | Non-canonical role of wild-type SEC23B in the cellular stress response pathway. | 1 |
| 33914262 | 2021 | Compound heterozygosity for two novel mutations of the SEC23B gene in congenital dyserythropoietic anemia type II. | 0 |
| 34365611 | 2021 | [Variant analysis of SEC23B gene in 4 families with congenital dyserythropoietic anemia]. | 0 |
| 32123160 | 2020 | Mutations in the coat complex II component SEC23B promote colorectal cancer metastasis. | 5 |
Citation
Dessen P
SEC23B (SEC23 homolog B, COPII coat complex component)
Atlas Genet Cytogenet Oncol Haematol. 2015-03-01
Online version: http://atlasgeneticsoncology.org/gene/55636/sec23b-(sec23-homolog-b-copii-coat-complex-component)
