SEZ6L (seizure related 6 homolog like)

2007-12-01  

Identity

HGNC
SEZ6L
LOCATION
22q12.1
LOCUSID
23544
ALIAS
-
FUSION GENES
Show Gene Fusions

Other Information

Locus ID:

NCBI: 23544
MIM: 607021
HGNC: 10763
Ensembl: ENSG00000100095

Variants:

dbSNP: 23544
ClinVar: 23544
TCGA: ENSG00000100095
COSMIC: SEZ6L

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000100095ENST00000248933Q9BYH1
ENSG00000100095ENST00000343706Q9BYH1
ENSG00000100095ENST00000360929Q9BYH1
ENSG00000100095ENST00000402979B0QYH5
ENSG00000100095ENST00000403121B0QYH4
ENSG00000100095ENST00000404234Q9BYH1
ENSG00000100095ENST00000529632B7ZLJ8
ENSG00000100095ENST00000629590Q9BYH1

Expression (GTEx)

0
10
20
30
40
50
60
Adipose - Subcutaneous
Adipose - Visceral
Adrenal Gland
Artery - Aorta
Artery - Tibial
Bladder
Brain - Amygdala
Brain - Anterior cingulate cortex
Brain - Caudate
Brain - Cerebellar Hemisphere
Brain - Cerebellum
Brain - Cortex
Brain - Frontal Cortex
Brain - Hippocampus
Brain - Hypothalamus
Brain - Nucleus accumbens
Brain - Putamen
Brain - Spinal cord
Brain - Substantia nigra
Breast - Mammary Tissue
Cells - Cultured fibroblasts
Cells - EBV - transformed lymphocytes
Cervix - Ectocervix
Cervix - Endocervix
Colon - Sigmoid
Colon - Transverse
Esophagus - Gastroesophageal Junction
Esophagus - Mucosa
Esophagus - Muscularis
Fallopian Tube
Heart - Atrial Appendage
Heart - Left Ventricle
Kidney - Cortex
Kidney - Medulla
Liver
Lung
Minor Salivary Gland
Muscle - Skeletal
Nerve - Tibial
Ovary
Pancreas
Pituitary
Prostate
Skin - Not Sun Exposed
Skin - Sun Exposed
Small Intestine - Terminal Ileum
Spleen
Stomach
Testis
Thyroid
Uterus
Vagina
Whole Blood

References

Pubmed IDYearTitleCitations
262049952015Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.33
262049952015Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.33
229207192013Polymorphisms in seizure 6-like gene are associated with bipolar disorder I: evidence of gene × gender interaction.11
229207192013Polymorphisms in seizure 6-like gene are associated with bipolar disorder I: evidence of gene × gender interaction.11
199554712010Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study.23
203796142010Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.78
204241292010Incorporation of a genetic factor into an epidemiologic model for prediction of individual risk of lung cancer: the Liverpool Lung Project.28
204241292010Incorporation of a genetic factor into an epidemiologic model for prediction of individual risk of lung cancer: the Liverpool Lung Project.28
206280862010Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.15
199554712010Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study.23
203796142010Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.78
204241292010Incorporation of a genetic factor into an epidemiologic model for prediction of individual risk of lung cancer: the Liverpool Lung Project.28
204241292010Incorporation of a genetic factor into an epidemiologic model for prediction of individual risk of lung cancer: the Liverpool Lung Project.28
206280862010Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.15
193365752009Genetic analysis of coronary artery disease single-nucleotide polymorphisms in diabetic nephropathy.3

Citation

Dessen P

SEZ6L (seizure related 6 homolog like)

Atlas Genet Cytogenet Oncol Haematol. 2007-12-01

Online version: http://atlasgeneticsoncology.org/gene/49889