SAMN38448004
External Id
dbGaP
INSDC center name
2023-11-27T12:12:15.970Z
INSDC first public
2023-12-15T06:11:16.590Z
INSDC last update
SRS19721119
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS19721119
SRA accession
DNA
analyte type
NIDDK_PruneBellySyndrome
biospecimen repository
PBS-01
biospecimen repository sample id
BLOOD Lymphocytes
body site
phs003475
gap_accession
1
gap_consent_code
GRU-IRB
gap_consent_short_name
5703315
gap_sample_id
4647064
gap_subject_id
No
is tumor
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
male
sex
Case Set
study design
PIEZO1 Loss of Function Compound Heterozygous Mutation in the Rare Congenital Human Disorder Prune Belly Syndrome
study name
PBS-01
submitted sample id
PBS-01
submitted subject id
NIDDK_PruneBellySyndrome
submitter handle
Non-tumor DNA sample from BLOOD Lymphocytes of a human male participant in the dbGaP study "PIEZO1 Loss of Function Compound Heterozygous Mutation in the Rare Congenital Human Disorder Prune Belly Syndrome"
title