U.S. flag

An official website of the United States government

Wangler Lab (Baylor College of Medicine), WanglerLab

General information

Wangler Lab, WanglerLab
Baylor College of Medicine
1250 Moursund Avenue; Suite NR1050
Houston
Texas
United States - 77030
http://wanglerlab.org
Organization ID: 506171

Personnel

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 59

Gene

GeneSubmissionsLast Updated
ACTG24Nov 1, 2019
ADAR1Oct 28, 2022
ATP1A31Oct 6, 2022
ATP2B11Oct 14, 2022
CASR1Oct 27, 2022
CCDST1Oct 5, 2022
CDH232Dec 15, 2022
CHD81Oct 28, 2022
CLCN71Oct 14, 2022
CNOT31Nov 1, 2022
CTCF1Oct 6, 2022
DEPDC51Oct 28, 2022
DNM1L1Feb 20, 2019
DNMT3A1May 15, 2023
ERCC41Oct 28, 2022
FANCB3Jan 19, 2022
FAT21Oct 5, 2022
FBN11Oct 5, 2022
FGFR11Oct 28, 2022
FLG1Oct 5, 2022
GJB21Oct 5, 2022
GLRA28Jan 19, 2022
GNB11Oct 5, 2022
GRIN2A1Oct 28, 2022
ITGA2B1Oct 5, 2022
KDM5C1Oct 14, 2022
KMT2D2Dec 14, 2022
LOC1278142971Oct 27, 2022
METTL231Oct 27, 2022
MRTFB2Nov 15, 2022
MYH141Sep 28, 2022
MYLK1May 24, 2017
OTOA2Oct 5, 2022
OTOG1Oct 5, 2022
PACS11Dec 15, 2022
PEX13Apr 21, 2023
PEX62Apr 21, 2023
POU4F31Oct 27, 2022
RHOB1Oct 27, 2022
RPGR1Sep 28, 2022
TCF201Oct 6, 2022
TFAP2B1Oct 5, 2022
TOP2B1Oct 28, 2022
TRAPPC91Oct 28, 2022
YARS21Feb 20, 2019
ZIC21Oct 12, 2022

Condition

NameSubmissionsLast Updated
"See Cases"1Oct 27, 2022
Aicardi-Goutieres syndrome 61Oct 28, 2022
Alternating hemiplegia of childhood 21Oct 6, 2022
Autosomal dominant nonsyndromic hearing loss 151Oct 27, 2022
Autosomal recessive nonsyndromic hearing loss 122Dec 15, 2022
Autosomal recessive nonsyndromic hearing loss 18B1Oct 5, 2022
Autosomal recessive nonsyndromic hearing loss 1A1Oct 5, 2022
Autosomal recessive nonsyndromic hearing loss 222Oct 5, 2022
B-cell immunodeficiency, distal limb anomalies, and urogenital malformations1Oct 28, 2022
Char syndrome1Oct 5, 2022
Developmental delay with variable intellectual impairment and behavioral abnormalities1Oct 6, 2022
Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 11Feb 20, 2019
Epilepsy, familial focal, with variable foci 11Oct 28, 2022
Familial hypocalciuric hypercalcemia 11Oct 27, 2022
Hartsfield-Bixler-Demyer syndrome1Oct 28, 2022
Heyn-Sproul-Jackson syndrome1May 15, 2023
Holoprosencephaly 51Oct 12, 2022
Hypopigmentation, organomegaly, and delayed myelination and development1Oct 14, 2022
Ichthyosis vulgaris1Oct 5, 2022
Intellectual developmental disorder with autism and macrocephaly1Oct 28, 2022
Intellectual developmental disorder with speech delay, autism, and dysmorphic facies1Nov 1, 2022
Intellectual developmental disorder, autosomal dominant 661Oct 14, 2022
Intellectual disability, autosomal dominant 421Oct 5, 2022
Intellectual disability, autosomal recessive 131Oct 28, 2022
Intellectual disability, autosomal recessive 441Oct 27, 2022
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome1Oct 6, 2022
Kabuki syndrome 12Dec 14, 2022
Landau-Kleffner syndrome1Oct 28, 2022
MRTFB-related disorder2Nov 15, 2022
Marfan syndrome1Oct 5, 2022
Peroxisome biogenesis disorder 1A (Zellweger)3Apr 21, 2023
Peroxisome biogenesis disorder 4A (Zellweger)2Apr 21, 2023
Platelet-type bleeding disorder 161Oct 5, 2022
Primary dilated cardiomyopathy1Sep 28, 2022
Retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without deafness1Sep 28, 2022
Schuurs-Hoeijmakers syndrome1Dec 15, 2022
See cases8Jan 19, 2022
Spinocerebellar ataxia 451Oct 5, 2022
Syndromic X-linked intellectual disability Claes-Jensen type1Oct 14, 2022
Visceral myopathy 15Nov 1, 2019
Xeroderma pigmentosum, group F1Oct 28, 2022