MYO1D (myosin ID)

2014-11-01  

Identity

HGNC
LOCATION
17q11.2
LOCUSID
ALIAS
PPP1R108,myr4
FUSION GENES

Other Information

Locus ID:

NCBI: 4642
MIM: 606539
HGNC: 7598
Ensembl: ENSG00000176658

Variants:

dbSNP: 4642
ClinVar: 4642
TCGA: ENSG00000176658
COSMIC: MYO1D

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000176658ENST00000318217O94832
ENSG00000176658ENST00000394649K7EIG7
ENSG00000176658ENST00000577252J3QRR2
ENSG00000176658ENST00000579584J3QRN6
ENSG00000176658ENST00000583621J3KRL0

Expression (GTEx)

0
50
100
150
200
250
300
350

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
386846302024Identification of a novel MYO1D variant associated with laterality defects, congenital heart diseases, and sperm defects in humans.0
386846302024Identification of a novel MYO1D variant associated with laterality defects, congenital heart diseases, and sperm defects in humans.0
250067442014Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns.55
250067442014Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns.55
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
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
191655272009Prefrontal cortex shotgun proteome analysis reveals altered calcium homeostasis and immune system imbalance in schizophrenia.69
199131212009Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.105
191655272009Prefrontal cortex shotgun proteome analysis reveals altered calcium homeostasis and immune system imbalance in schizophrenia.69
199131212009Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.105
173767942007High density SNP association study of a major autism linkage region on chromosome 17.30
173767942007High density SNP association study of a major autism linkage region on chromosome 17.30

Citation

Dessen P

MYO1D (myosin ID)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/70629/teaching-explorer/humanGenome