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Type
--
iPS Cell
ES Cell
Somatic Stem Cell
Cancer Stem Cell
Other
Race
--
Caucasian
African-American
Asian
Hispanic
African
Unknown
Other
Original Tissue
--
Skin
Peripheral Blood
Peripheral Blood(Cell Line)
Bone Marrow
Nervous System
Skeletal Muscle
Cardiac Tissue
Adipose Tissue
GastroIntestinal Tract
Cornea
Other
Vector
--
Retrovirus
Lentivirus
Adenovirus
AAV
Sendai virus
Plasmid
Vaccinia virus
Plasmid lipofection
Poxvirus
HSV1
Other
Disease Status
--
Normal
Diseased
Normal→Genome editing
Diseased→Genome editing
Gene carrier
Unknown
Feeder
--
Yes
No
Age
--
0-9
10-19
20-29
30-39
40-49
50-59
60-69
70-79
80-89
90-99
100-109
110-119
120-129
130-139
Fetus
Grade
--
Research Grade
Clinical Grade
Sex
--
Male
Female
Unknown
Database
--
hPSCreg
eagle-i
ICD10
--
A00-B99 Certain infectious and parasitic diseases
C00-D48 Neoplasms
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
E00-E90 Endocrine, nutritional and metabolic diseases
F00-F99 Mental and behavioural disorders
G00-G99 Diseases of the nervous system
H00-H59 Diseases of the eye and adnexa
H60-H95 Diseases of the ear and mastoid process
I00-I99 Diseases of the circulatory system
J00-J99 Diseases of the respiratory system
K00-K93 Diseases of the digestive system
L00-L99 Diseases of the skin and subcutaneous tissue
M00-M99 Diseases of the musculoskeletal system and connective tissue
N00-N99 Diseases of the genitourinary system
O00-O99 Pregnancy, childbirth and the puerperium
P00-P96 Certain conditions originating in the perinatal period
Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities
R00-R99 Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified
S00-T98 Injury, poisoning and certain other consequences of external causes
V01-Y98 External causes of morbidity and mortality
Z00-Z99 Factors influencing health status and contact with health services
U00-U89 Codes for special purposes
Free Words
Accession No
Pubmed ID/Title
Label：
Search Result (11 records)
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/ 1
Accession
Cell Line Name
Species
Type
Original Tissue
Disease
Status
Disease Name
Mutated Gene
Age
Sex
Race
Vector
Database
Summary
SKIP000544
Control 7
Human
iPS Cell
Skin
Normal
--
Male
Unknown
--
RNF213
R4810K
(rs112735431) induces genomic instability by mitotic abnormality. Hitomi T, Habu T
SKIP000545
Control 6
Human
iPS Cell
Skin
Normal
--
Female
Unknown
--
RNF213
R4810K
(rs112735431) induces genomic instability by mitotic abnormality. Hitomi T, Habu T
SKIP000546
Control 5
Human
iPS Cell
Skin
Normal
--
Male
Unknown
--
RNF213
R4810K
(rs112735431) induces genomic instability by mitotic abnormality. Hitomi T, Habu T
SKIP000547
Control 4
Human
iPS Cell
Skin
Normal
--
Female
Unknown
--
RNF213
R4810K
(rs112735431) induces genomic instability by mitotic abnormality. Hitomi T, Habu T
SKIP000548
Control 3
Human
iPS Cell
Skin
Normal
--
Male
Unknown
--
RNF213
R4810K
(rs112735431) induces genomic instability by mitotic abnormality. Hitomi T, Habu T
SKIP000549
Control 2
Human
iPS Cell
Skin
Normal
--
Female
Unknown
--
RNF213
R4810K
(rs112735431) induces genomic instability by mitotic abnormality. Hitomi T, Habu T
SKIP000550
Control 1
Human
iPS Cell
Skin
Normal
--
Female
Unknown
--
RNF213
R4810K
(rs112735431) induces genomic instability by mitotic abnormality. Hitomi T, Habu T
SKIP000551
Unaffected carrier
Human
iPS Cell
Skin
Normal
--
Male
Unknown
--
variant RNF213
R4810K
(rs112735431) induces genomic instability by mitotic abnormality. Hitomi T, Habu T
SKIP000552
Patient 1
Human
iPS Cell
Skin
Diseased
Moyamoya disease
--
Female
Unknown
--
R4810K
(rs112735431) induces genomic instability by mitotic abnormality. Hitomi T, Habu T, Kobayashi H
SKIP000553
Patient 2
Human
iPS Cell
Skin
Diseased
Moyamoya disease
--
Female
Unknown
--
R4810K
(rs112735431) induces genomic instability by mitotic abnormality. Hitomi T, Habu T, Kobayashi H
SKIP000554
Patient 3
Human
iPS Cell
Skin
Diseased
Moyamoya disease
--
Female
Unknown
--
R4810K
(rs112735431) induces genomic instability by mitotic abnormality. Hitomi T, Habu T, Kobayashi H