Preferred Label : USH1G wt Allele;

NCIt synonyms : Sans; FLJ33924; Usher Syndrome 1G (Autosomal Recessive) wt Allele; ANKS4A;

NCIt definition : Human USH1G wild-type allele is located in the vicinity of 17q25.1 and is approximately 7 kb in length. This allele, which encodes Usher syndrome type-1G protein, is involved in the development of both the retina and cochlear hair cells. Mutation of the gene is associated with Usher syndrome 1G.;

NCIt note : There is a report of a chromosomal aberration involving the HN1 gene and the USH1G gene, which is associated with breast cancer. (COSMIC);

GenBank Accession Number : AK091243;

Details


Keyword's position in hierarchy(ies) : arborescence

Main resources

You can consult :


https://www.has-sante.fr/jcms/p_3511526/fr/flash-securite-patient-surveillance-des-patients-en-service-de-soins-critiques-une-veille-sans-faille-pour-qu-aucun-patient-ne-defaille
2024
France
guideline
Risk Factor History Negative
Null
Drug Accumulation Less than 1.2
None Device
Desmosine
critical care
patient care
CASP8AP2 wt Allele
No Hand Mobility
Patient Care
Use_For
No Support Needed
patients
patient safety
Non-Neoplastic Finding Absent
No Exacerbating Factor to Chief Complaint
custodial care
WWOX wt Allele
Safety Monitoring
No Signs and Symptoms Associated with Chief Complaint
professional practice
Care Of
Professional Practice
No Alleviating Factor to Chief Complaint
failure, nos
USH1G wt Allele
Patient Monitoring
Patient
No Effort
Human Papillomavirus Negative
has patient

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15/05/2024


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