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GM02292
cell line
GM-2292
GM 2292
GM2292A
GM02292B
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Statements
instance of
cell line
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
transformed cell line
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
autologous cell line
GM02290
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
GM02291
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
GM02338
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
described by source
Lesch-Nyhan syndrome. Repository identification Nos. GM-2290, 2291, 2292, 2338, 3115, 3116, and 3117
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
Mutator phenotype of Werner syndrome is characterized by extensive deletions
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
established from medical condition
Lesch-Nyhan syndrome
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
derived from organism type
Homo sapiens
sex or gender
male
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
exact match
http://purl.obolibrary.org/obo/CLO_0032131
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
Identifiers
Cell Line Ontology ID
CLO_0032131
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
Cellosaurus ID
CVCL_D868
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_D868
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