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Protein-coding gene in the species Homo sapiens
critical region protein 1 is a protein that in humans is encoded by the CECR1 gene. This gene encodes a member of a subfamily of the adenosine deaminase
CECR1
Genetic partial duplication of chromosome 22
supernumerary marker chromosomes in cat eye syndrome). This area contains the CECR1, SLC25A18, and ATP6V1E1 genes which are strong candidate genes for causing
Cat_eye_syndrome
Human chromosome
encoding chromobox protein homolog 7 CDC42EP1: CDC42 effector protein 1 CECR1: cat eye syndrome critical region protein 1 CHEK2 (22q12) COMT:
Chromosome_22
Abnormal partial or mixed chromosome
located on its q arm at bands 11.1 through ll.23. This area contains the CECR1, SLC22A18, and ATP6V1E1 genes which are strong candidate genes for causing
Small supernumerary marker chromosome
Small_supernumerary_marker_chromosome
Medical condition
is caused by mutations in DNA encoding the gene ADA2, formerly known as CECR1. The ADA2 gene is located on chromosome 22q11.1. Many different kinds of
Adenosine deaminase 2 deficiency
Adenosine_deaminase_2_deficiency
CECR1
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Surname or Lastname
English (Kent)
English (Kent) : unexplained.
Boy/Male
Hindu
Girl/Female
Hebrew Biblical
God's glory.
Boy/Male
Hindu, Indian, Marathi, Sanskrit
Fragrant; Famous
Boy/Male
Indian, Telugu
Little
Girl/Female
Latin American
Industrious; striving.
Girl/Female
Indian
Sublime, Lofty, High
Boy/Male
British, English
Son of Walter
Boy/Male
Arthurian Legend
Guinevere's father.
Girl/Female
Hindu
Of the sea
CECR1
CECR1
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