Preferred Name

Nibrin

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C21171

code

C21171

Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116977

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C142799

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C142800

Contributing_Source

CTRP

DEFINITION

Nibrin (754 aa, ~85 kDa) is encoded by the human NBN gene. This protein is involved in cell cycle checkpoint control, DNA damage responses and meiotic recombination.

Display_Name

Nibrin

FULL_SYN

NBS1

Cell Cycle Regulatory Protein P95

ATV

Nijmegen Breakage Syndrome Protein 1

AT-V2

NBN

AT-V1

p95 Protein of the MRE11/RAD50 Complex

NBS

MRE11/RAD50 Complex p95 Protein

Nibrin

label

Nibrin

Legacy Concept Name

Nibrin

OMIM_Number

602667

Preferred_Name

Nibrin

prefixIRI

Thesaurus:C21171

prefLabel

Nibrin

Semantic_Type

Amino Acid, Peptide, or Protein

Swiss_Prot

O60934

UMLS_CUI

C0674679

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C21170

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/602667 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://www.orpha.net/ORDO/Orphanet_123688 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.obolibrary.org/obo/PR_000011014 Protein Ontology / 蛋白质本体 LOOM