MedGen for PMC (Select 1287521) - MedGen - NCBI

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Items: 2

Select item 912801.

Chromosome breakage

Elevated rate of chromosomal breakage or interchanges occurring either spontaneously or following exposure to various DNA-damaging agents. This feature may be assayed by treatment of cultured lymphocytes with agents such as chemical mutagens, irradiation, and alkylating agents. [from HPO]

MedGen UID:: 91280
•Concept ID:: C0376628
•: Cell or Molecular Dysfunction

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 18259622.

Partial deletion of chromosome 7

MedGen UID:: 1825962
•Concept ID:: C5679655
•: Cell or Molecular Dysfunction

GTR
ClinVar
Genes
OMIM
GeneReviews

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MedGen for PMC (Select 1287521) (6)
MedGen
PMC Articles for MedGen (Select 1814320) (1)
PMC
Homo sapiens complement C1q C chain (C1QC), transcript variant 4, mRNA
Homo sapiens complement C1q C chain (C1QC), transcript variant 4, mRNA
gi|1675074598|ref|NM_001347620.2|

Nucleotide
microtubule associated protein EB1, putative (macronuclear) [Tetrahymena thermop...
microtubule associated protein EB1, putative (macronuclear) [Tetrahymena thermophila SB210]
gi|586731588|gnl|WGS:AAGF|cds.TTHER 58460A|gb|EAS02163.2|

Protein
GC-rich promoter binding protein 1, isoform CRA_c [Homo sapiens]
GC-rich promoter binding protein 1, isoform CRA_c [Homo sapiens]
gi|119575358|gb|EAW54963.1||gnl|WGS |hCP1814169

Protein

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