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GM11779
cell line
XVIII-23H-a
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Statements
instance of
cell line
1 reference
stated in
Cellosaurus release 49
retrieved
13 July 2024
Cellosaurus ID
CVCL_HM36
hybrid cell line
1 reference
stated in
Cellosaurus release 49
retrieved
13 July 2024
Cellosaurus ID
CVCL_HM36
parent cell line
V79/380-6
1 reference
stated in
Cellosaurus release 49
retrieved
13 July 2024
Cellosaurus ID
CVCL_HM36
described by source
Random X inactivation resulting in mosaic nullisomy of region Xp21.1----p21.3 associated with heterozygosity for ornithine transcarbamylase deficiency and for chronic granulomatous disease
1 reference
stated in
Cellosaurus release 49
retrieved
13 July 2024
Cellosaurus ID
CVCL_HM36
derived from organism type
Chinese hamster
1 reference
stated in
Cellosaurus release 49
retrieved
13 July 2024
Cellosaurus ID
CVCL_HM36
Homo sapiens
1 reference
stated in
Cellosaurus release 49
retrieved
13 July 2024
Cellosaurus ID
CVCL_HM36
exact match
http://purl.obolibrary.org/obo/CLO_0021421
1 reference
stated in
Cellosaurus release 49
retrieved
13 July 2024
Cellosaurus ID
CVCL_HM36
Identifiers
Cell Line Ontology ID
CLO_0021421
1 reference
stated in
Cellosaurus release 49
retrieved
13 July 2024
Cellosaurus ID
CVCL_HM36
Cellosaurus ID
CVCL_HM36
1 reference
stated in
Cellosaurus release 49
retrieved
13 July 2024
Cellosaurus ID
CVCL_HM36
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