Daryl Scott Lab (Baylor College of Medicine)

General information

Daryl Scott Lab
Baylor College of Medicine
R813, One Baylor Plaza, BCM225
Houston
Texas
United States - 77030
https://www.bcm.edu/people/view/daryl-scott-m-d-ph-d/b174cc0d-ffed-11e2-be68-080027880ca6
Organization ID: 505993

Personnel

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 86

Gene

GeneSubmissionsLast Updated
ABL11Nov 12, 2020
ACO21Apr 6, 2020
ALG123Nov 12, 2020
ANKRD111Nov 12, 2020
B3GALT62Nov 12, 2020
BAZ2B6Sep 11, 2019
BRCA22Nov 12, 2020
CCNH1Nov 12, 2020
CLTRN1Oct 2, 2019
DDX3X1Nov 12, 2020
DKC11Nov 12, 2020
EP3002Nov 12, 2020
FANCI1Nov 12, 2020
FGFRL12Jan 5, 2021
FOXC21Nov 12, 2020
FOXP11Nov 12, 2020
FRAS13Nov 9, 2016
FREM24Nov 9, 2016
GLI31Nov 9, 2016
HCCS1Nov 12, 2020
IDS1Nov 12, 2020
KMT2D5Nov 12, 2020
LMX1B1Nov 12, 2020
LOC1060501021Nov 12, 2020
LRP22Nov 12, 2020
MCPH11Nov 12, 2020
MED121Nov 12, 2020
MYRF4Nov 12, 2020
NONO3Mar 17, 2020
PAX59Aug 23, 2021
PDHA11Nov 12, 2020
POGZ1Nov 12, 2020
POLR3H1Apr 6, 2020
RASA11Nov 12, 2020
RERE10Sep 12, 2017
ROBO41Nov 9, 2016
SLC2A101Nov 12, 2020
SMARCA41Nov 12, 2020
SMARCC21Nov 12, 2020
SOS11Nov 12, 2020
TCF121Nov 12, 2020
TRAF71Nov 12, 2020
ZFPM22Nov 12, 2020
ZFPM2-AS12Nov 12, 2020

Condition

NameSubmissionsLast Updated
ALG12-congenital disorder of glycosylation3Nov 12, 2020
Aminoaciduria2Oct 2, 2019
Arterial tortuosity syndrome1Nov 12, 2020
Capillary malformation-arteriovenous malformation 11Nov 12, 2020
Cardiac, facial, and digital anomalies with developmental delay1Nov 12, 2020
Cardiac-urogenital syndrome4Nov 12, 2020
Coffin-Siris syndrome 81Nov 12, 2020
Congenital diaphragmatic hernia11Jan 5, 2021
Congenital heart defects and skeletal malformations syndrome1Nov 12, 2020
Craniosynostosis 31Nov 12, 2020
Diaphragmatic hernia 32Nov 12, 2020
Distichiasis-lymphedema syndrome1Nov 12, 2020
Donnai-Barrow syndrome2Nov 12, 2020
Dyskeratosis congenita, X-linked1Nov 12, 2020
Ehlers-Danlos syndrome, progeroid type, 22Nov 12, 2020
Fanconi anemia, complementation group D12Nov 12, 2020
Fanconi anemia, complementation group I1Nov 12, 2020
KBG syndrome1Nov 12, 2020
Kabuki syndrome 15Nov 12, 2020
Linear skin defects with multiple congenital anomalies 11Nov 12, 2020
MED12-related disorder1Nov 12, 2020
Mental retardation with language impairment and with or without autistic features1Nov 12, 2020
Mental retardation, X-linked 1021Nov 12, 2020
Mental retardation, X-linked, syndromic 343Mar 17, 2020
Mental retardation, autosomal dominant 161Nov 12, 2020
Mucopolysaccharidosis, MPS-II1Nov 12, 2020
Nail-patella syndrome1Nov 12, 2020
Neurodevelopmental disorder15Aug 23, 2021
Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart10Sep 12, 2017
Noonan syndrome 41Nov 12, 2020
Optic atrophy 91Apr 6, 2020
Primary autosomal recessive microcephaly 11Nov 12, 2020
Pyruvate dehydrogenase E1-alpha deficiency1Nov 12, 2020
Rubinstein-Taybi syndrome 22Nov 12, 2020
See cases1Apr 16, 2021
White-sutton syndrome1Nov 12, 2020
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