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WangQJ Lab (Chinese People's Liberation Army General Hospital)

General information

WangQJ Lab
Chinese People's Liberation Army General Hospital
Beijing
China

Organization ID: 508192

Personnel

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 150

Gene

GeneSubmissionsLast Updated
ABHD14A-ACY11Jul 31, 2021
ACY11Jul 31, 2021
ADGRV16Jul 31, 2021
AIFM15Jan 8, 2024
ARID1B1Jul 31, 2021
ATP6V1B11Jul 31, 2021
CACNA1A1Jan 8, 2024
CCDC501Jul 31, 2021
CDH22Jan 8, 2024
CDH231Jul 31, 2021
COL2A11Jul 31, 2021
COL4A41Jul 31, 2021
EYA41Jul 31, 2021
FDXR2Jan 8, 2024
FLNA1Jul 31, 2021
GATA31Jul 31, 2021
GIPC31Jul 31, 2021
GJB22Dec 24, 2023
HARS22Jul 31, 2021
KCNQ11Jul 31, 2021
KCNQ1-AS11Jul 31, 2021
KIF5A1Jan 8, 2024
LOC1119828691Jul 31, 2021
LOC1128409213Jul 31, 2021
LOXHD11Jul 31, 2021
MARVELD22Jul 31, 2021
MFN21Jan 8, 2024
MYCN1Jul 31, 2021
MYO15A9Jul 31, 2021
MYO3A1Jul 31, 2021
MYO7A9Jan 8, 2024
NEFL1Jan 8, 2024
NOTCH32Jan 8, 2024
OPA15Jan 8, 2024
OTOA3Jul 31, 2021
OTOF34Jan 8, 2024
OTOG2Jul 31, 2021
OTOGL2Jul 31, 2021
P2RX21Jul 31, 2021
PAX31Jul 31, 2021
PCDH153Jul 31, 2021
POLR2F3Jul 31, 2021
PTPRQ6Jul 31, 2021
RAB33A5Jan 8, 2024
SLC26A42Jul 31, 2021
SLC52A21Jul 31, 2021
SLC52A32Jan 8, 2024
SOX103Jul 31, 2021
SPTB1Jul 31, 2021
STRC3Jul 31, 2021
SUCLG11Jul 31, 2021
TIMM8A2Jan 8, 2024
TMC13Jul 31, 2021
TP631Jan 8, 2024
TRIOBP1Jul 31, 2021
TRPV41Jan 8, 2024
TWNK2Jan 8, 2024
USH2A6Jul 31, 2021
USH2A-AS21Jul 31, 2021
WFS14Jan 8, 2024

Condition

NameSubmissionsLast Updated
Aminoacylase 1 deficiency1Jul 31, 2021
Auditory neuropathy52Jan 8, 2024
Auditory neuropathy spectrum disorder1Jul 31, 2021
Auditory neuropathy-optic atrophy syndrome1Jul 31, 2021
Autosomal dominant nonsyndromic hearing loss 101Jul 31, 2021
Autosomal dominant nonsyndromic hearing loss 411Jul 31, 2021
Autosomal dominant nonsyndromic hearing loss 441Jul 31, 2021
Autosomal recessive Alport syndrome1Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 121Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 151Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 163Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 18B2Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 1A2Dec 24, 2023
Autosomal recessive nonsyndromic hearing loss 26Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 221Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 233Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 281Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 39Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 301Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 42Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 492Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 75Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 771Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 84A6Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 84B2Jul 31, 2021
Autosomal recessive nonsyndromic hearing loss 911Jul 31, 2021
Brown-Vialetto-van Laere syndrome 21Jul 31, 2021
Coffin-Siris syndrome 11Jul 31, 2021
Deafness dystonia syndrome1Jul 31, 2021
Feingold syndrome type 11Jul 31, 2021
Frontometaphyseal dysplasia 11Jul 31, 2021
Hereditary spherocytosis type 21Jul 31, 2021
Hypoparathyroidism, deafness, renal disease syndrome1Jul 31, 2021
Jervell and Lange-Nielsen syndrome 11Jul 31, 2021
Mitochondrial DNA depletion syndrome 91Jul 31, 2021
Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy2Jul 31, 2021
Perrault syndrome 22Jul 31, 2021
Renal tubular acidosis with progressive nerve deafness1Jul 31, 2021
Stickler syndrome type 11Jul 31, 2021
Usher syndrome type 2A6Jul 31, 2021
Usher syndrome type 2C6Jul 31, 2021
Waardenburg syndrome type 11Jul 31, 2021
Waardenburg syndrome type 4C3Jul 31, 2021
Wolfram syndrome 11Jul 31, 2021