ZMYM2 wt Allele

Preferred Label : ZMYM2 wt Allele;

NCIt synonyms : RP11-264J4.7; FIM; RAMP; SCLL; ZNF198; MYM; Zinc Finger Protein 198 Gene; Zinc Finger, MYM-Type 2 wt Allele; Zinc Finger MYM-Type Containing 2 wt Allele; Rearranged in an Atypical Myeloproliferative Disorder Gene; NECRC;

NCIt definition : Human ZMYM2 wild-type allele is located within 13q11-q12 and is approximately 133 kb in length. This allele, which encodes zinc finger MYM-type protein 2, is involved in the regulation of transcription. A chromosomal translocation t(8;13)(p11;q12) of the gene and the FGFR1 gene is associated with stem cell leukemia lymphoma syndrome.;

GenBank Accession Number : AF012126;

Details

Origin ID

C97874;

UMLS CUI

C3273671;

Automatic exact mappings (from CISMeF team)
- Assistive products for vertical accessibility, other and unspecified [ICHI extension code]
- Chromosome 8p11 myeloproliferative syndrome [OMIM Phenotype]
- Crawling [LOINC component]
- Denticleless e3 ubiquitin protein ligase homolog [OMIM gene]
- Myasthenic syndrome, congenital, 6, presynaptic [OMIM Phenotype]
- O-beta-ribosyl(1''--2')adenosine-5''-phosphate [MeSH Supplementary Concept]
- Ramp (physical object) [SNOMED CT concept]
- Ramping (qualifier value) [SNOMED CT concept]
- Zinc finger, mym-type 2 [OMIM gene]
- architectural accessibility [MeSH Descriptor]
- ramps [MeSH concept]
- ramps [EMDN type]
- ramps [medical devices type]
OMIM relation
- Zinc finger, mym-type 2 [OMIM gene]
See also inter- (CISMeF)
- congenital myasthenic syndrome 6 [DO Concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 13q11-q12 [NCIt concept]
gene_plays_role_in_process
- Transcriptional Regulation [NCIt concept]

Keyword's position in hierarchy(ies) :

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