Identity
HGNC
LOCATION
7p15.3
LOCUSID
ALIAS
DRCTNNB1A,HCC,HLD5,HYCC1
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: 84668
MIM: 610531
HGNC: 24587
Ensembl: ENSG00000122591
Variants:
dbSNP: 84668
ClinVar: 84668
TCGA: ENSG00000122591
COSMIC: FAM126A
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000122591 | ENST00000409763 | B8ZZA2 |
| ENSG00000122591 | ENST00000409923 | Q9BYI3 |
| ENSG00000122591 | ENST00000432176 | Q9BYI3 |
| ENSG00000122591 | ENST00000440481 | H7C0W7 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35397054 | 2022 | CirRNA circFAM126A Exerts Oncogenic Functions in NSCLC to Upregulate IRS2. | 2 |
| 35397054 | 2022 | CirRNA circFAM126A Exerts Oncogenic Functions in NSCLC to Upregulate IRS2. | 2 |
| 30103315 | 2018 | TTC7 and Hyccin Regulate Neuronal Aβ42 Accumulation and its Associated Neural Deficits in Aβ42-Expressing Drosophila. | 1 |
| 30103315 | 2018 | TTC7 and Hyccin Regulate Neuronal Aβ42 Accumulation and its Associated Neural Deficits in Aβ42-Expressing Drosophila. | 1 |
| 26571211 | 2016 | The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane. | 61 |
| 26571211 | 2016 | The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane. | 61 |
| 24417797 | 2014 | Hypomyelinating leukodystrophy-associated missense mutant of FAM126A/hyccin/DRCTNNB1A aggregates in the endoplasmic reticulum. | 13 |
| 24417797 | 2014 | Hypomyelinating leukodystrophy-associated missense mutant of FAM126A/hyccin/DRCTNNB1A aggregates in the endoplasmic reticulum. | 13 |
| 22749724 | 2013 | Hypomyelination and congenital cataract: identification of novel mutations in two unrelated families. | 3 |
| 23998934 | 2013 | Novel FAM126A mutations in hypomyelination and congenital cataract disease. | 6 |
| 22749724 | 2013 | Hypomyelination and congenital cataract: identification of novel mutations in two unrelated families. | 3 |
| 23998934 | 2013 | Novel FAM126A mutations in hypomyelination and congenital cataract disease. | 6 |
| 21911699 | 2011 | Hypomyelination and congenital cataract: broadening the clinical phenotype. | 6 |
| 21911699 | 2011 | Hypomyelination and congenital cataract: broadening the clinical phenotype. | 6 |
| 17928815 | 2008 | A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract. | 3 |
Citation
Dessen P
FAM126A (family with sequence similarity 126 member A)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/63010/fam126a-(family-with-sequence-similarity-126-member-a)
