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Anicom

In House Testing Sponsor

General Information

Name
Anicom
Alternative Name
Anicom Specialty Medical Insitute Inc.
Data Up to Date
19-Jul
GTP Code
anicom
URL
https://www.anicom-med.co.jp/
Email
anicom_med_info@ani-com.com
Telephone
-6644
Address
City Hards Chojamachi Blding., 5F, 2-6-3
Address 2
Chojamachi
City
Yokohamashi-Nakaku
State
Kanagawaken
Zip Code/ Postal Code
231-0033
Participant Since:
2019
Subsidiary Company

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
Description of Lab Tech Qualifications
national qualifications
Licensed veterinarian(s)
Yes

Quality Indicators - GTP

HGTD Leadership Sponsor
Sponsor
Supporter
Participant
Academic Participant
Non-participant
Year Established
2014
In House Testing
Out Sourced Testing
ISO Accredited/ GTP
ISO Accredited/LAB
ISO Accredited/tests
Other Recognized Accreditation
Other Parentage Testing
Other Parentage Testing Details
Illumina 230K SNP array basedparentage testing

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
Faults Protocol Details
check on low DNA concentration
Results Query Protocol
re-testing sample
Laboratory Mishandling Protocol
Breeding Advice

Research

Test Discovery- GTP
Test Development In-House
Test Development More Info
Development of novel markers for testing the known loci
Any Patents Held
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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