FAM126A (family with sequence similarity 126 member A)

2014-11-01  

Identity

HGNC
LOCATION
7p15.3
LOCUSID
ALIAS
DRCTNNB1A,HCC,HLD5,HYCC1
FUSION GENES

Other Information

Locus ID:

NCBI: 84668
MIM: 610531
HGNC: 24587
Ensembl: ENSG00000122591

Variants:

dbSNP: 84668
ClinVar: 84668
TCGA: ENSG00000122591
COSMIC: FAM126A

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000122591ENST00000409763B8ZZA2
ENSG00000122591ENST00000409923Q9BYI3
ENSG00000122591ENST00000432176Q9BYI3
ENSG00000122591ENST00000440481H7C0W7

Expression (GTEx)

0
5
10
15
20
25
30

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
353970542022CirRNA circFAM126A Exerts Oncogenic Functions in NSCLC to Upregulate IRS2.2
353970542022CirRNA circFAM126A Exerts Oncogenic Functions in NSCLC to Upregulate IRS2.2
301033152018TTC7 and Hyccin Regulate Neuronal Aβ42 Accumulation and its Associated Neural Deficits in Aβ42-Expressing Drosophila.1
301033152018TTC7 and Hyccin Regulate Neuronal Aβ42 Accumulation and its Associated Neural Deficits in Aβ42-Expressing Drosophila.1
265712112016The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane.61
265712112016The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane.61
244177972014Hypomyelinating leukodystrophy-associated missense mutant of FAM126A/hyccin/DRCTNNB1A aggregates in the endoplasmic reticulum.13
244177972014Hypomyelinating leukodystrophy-associated missense mutant of FAM126A/hyccin/DRCTNNB1A aggregates in the endoplasmic reticulum.13
227497242013Hypomyelination and congenital cataract: identification of novel mutations in two unrelated families.3
239989342013Novel FAM126A mutations in hypomyelination and congenital cataract disease.6
227497242013Hypomyelination and congenital cataract: identification of novel mutations in two unrelated families.3
239989342013Novel FAM126A mutations in hypomyelination and congenital cataract disease.6
219116992011Hypomyelination and congenital cataract: broadening the clinical phenotype.6
219116992011Hypomyelination and congenital cataract: broadening the clinical phenotype.6
179288152008A 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)