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JUST PUBLISHED ‒ Moving from information and collaboration to action: Report from the 5th International Dog Health Workshop in Helsinki, June 2024 ×

Anicom Specialty Medical Institute Inc.

In House Testing Non-Participant

General Information

Name
Anicom Specialty Medical Institute Inc.
Data Up to Date
22-Aug
GTP Code
anicom
URL
https://www.anicom-med.co.jp/
Email
anicom_med_info@ani-com.com
Telephone
-6644
Address
Sumitomo Fudosan Shinjuku Grand Tower 39F8-17-1
Address 2
Nishi-Shinjuku
City
Shinjukuku
State
Toyko
Zip Code/ Postal Code
160-0023
Country
Japan
Participant Since:
2019

People

Staff Counts
25
Lab/Company Director
Kosuke Kawamoto
Lab/Company Director Profile
CEO
Lead Scientist/ Geneticist
Genki Ishihara
Lead Scientist/ Geneticist Profile
Director
Lead Veterinarian
Ken Ohashi
Lead Veterinarian Profile
Manager
Laboratory Manager
Yuki Matsumoto
Qualified Laboratory Technicians
Yes
Description of Lab Tech Qualifications
national qualifications
Licensed veterinarian(s)
Yes

Quality Indicators - GTP

Non-Participant
Year Established
2014
In House Testing
Out Sourced Lab(s) in HGTD
N/A
Laboratory SOPs
Yes
Other Parentage Testing
Other Parentage Testing Details
Illumina 230K SNP array basedparentage testing
GTP Service Description
100% of tests done in house
Outsourced Lab(s) Accredited
N/A

Quality Indicators - Procedures/ Services

Sample collected by - GTP specific
Samples are owner-submitted
Sample Identification
Pedigree registration number and microchip number
Animal ID/ by GTP
Barcoding linked to sample ID
Test results provided to
Dog owners, and business partners
Test Faults Protocol
Yes
Faults Protocol Details
check on low DNA concentration
Results Query Protocol
re-testing sample
Laboratory Mishandling Protocol
Breeding Advice

Research

Ethics Committee/Board
N/A
Test Development In-House
Test Development More Info
Development of novel markers for testing the known loci
Research Collaborator
Dr. Miho Murayama-Inoue in Kyoto University

Phenes

Ataxia, Spinocerebellar, SPTBN2-related
Canine Leukocyte Adhesion Deficiency (CLAD)
Congenital Hypothyroidism
Congenital Stationary Night Blindness (CSNB)
Degenerative Myelopathy
Episodic Falling
Exercise-Induced Collapse / EIC
GM1 Gangliosidosis
Hyperuricosuria and Hyperuricemia (HUU)
Ichthyosis, PNPLA1-related
Imerslund-Grasbeck Syndrome (I-GS), CUBN related
Myotonia Congenita
Nasal Parakeratosis
Nephropathy
Neuroaxonal Dystrophy (NAD)
Neuronal Ceroid Lipofuscinosis 1 (NCL1)
Neuronal Ceroid Lipofuscinosis 5 (NCL5)
Neuronal Ceroid Lipofuscinosis 6 (NCL6)
Neuronal Ceroid Lipofuscinosis 8 (NCL8)
Osteogenesis Imperfecta
Prekallikrein Deficiency
Progressive Retinal Atrophy - CNGB1
Progressive Retinal Atrophy crd4 (PRA crd4) / cord1
Progressive Retinal Atrophy, GR PRA2
Progressive Retinal Atrophy, PRA1
Progressive Retinal Atrophy (PRA-prcd)
Progressive Retinal Atrophy rcd3 (PRA-rcd3)
Skeletal Dysplasia 2 (SD2)
Von Willebrand Disease I
Von Willebrand Disease II
Von Willebrand Disease III
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