40871-6LOINC 2.82
CNBP gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
CNBP Mut Anl Bld/T
Component
- CNBP gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; CCHC-type zinc finger, nucleic acid binding protein; Cellular nucleic acid binding protein (CNBP) (Zinc finger protein 9).; CNBP; CNBP1; DM2; Genetics; Heredity; Heritable; HGNC:2924; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; myotonic dystrophy type 2; Nominal; PCR; PDM; Point in time; PROMM; Proximal myotonic myopathy; Random; RNF163; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue; ZCCHC22; zinc finger protein 273; ZNF9
Index terms
- Blood
- CCHC-type zinc finger, nucleic acid binding protein
- Cellular nucleic acid binding protein (CNBP) (Zinc finger protein 9).
- CNBP
- CNBP gene targeted mutation analysis
- CNBP1
- DM2
- Genetics
- Heredity
- Heritable
- HGNC:2924
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- myotonic dystrophy type 2
- Nominal
- PCR
- PDM
- Point in time
- PROMM
- Proximal myotonic myopathy
- Random
- RNF163
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue
- ZCCHC22
- zinc finger protein 273
- ZNF9