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Palindrome (Gene Kavoshgaran Aria), PLN

General information

Palindrome, PLN
Gene Kavoshgaran Aria
SadatAbad
Isfahan
Esfahan
Iran - 8164934409
https://palinlab.com/
Organization ID: 508498

Personnel

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 113

Gene

GeneSubmissionsLast Updated
ABCA41May 30, 2024
ACER31Jul 14, 2024
ADAM91Mar 30, 2024
ADGRV11May 30, 2024
AHDC11May 30, 2024
ALMS11Apr 15, 2022
ALX31Mar 30, 2024
ARID1A1May 30, 2024
ARL61Mar 30, 2024
ASAH11Dec 17, 2024
ASPM1May 30, 2024
AUTS21Jun 26, 2024
BEST11Dec 17, 2024
BRCA11Jul 14, 2024
BRCA21Jul 14, 2024
C17orf1071Oct 13, 2024
CAMK2A1Jul 14, 2024
CEP2901Jul 14, 2024
CFAP4181May 30, 2024
CHD71Jul 14, 2024
CHRNE1Oct 13, 2024
CLCN11Jan 22, 2025
CLDN161May 30, 2024
CNGA31Mar 30, 2024
COL17A11Jan 22, 2025
COL4A31Jun 26, 2024
COL7A12Jun 26, 2024
CTNS1Oct 13, 2024
CTNS-AS11Oct 13, 2024
CTSC1May 30, 2024
CUL71Oct 13, 2024
DDOST1Oct 13, 2024
DMD1Dec 17, 2024
DNAH111May 30, 2024
DOCK71Dec 17, 2024
EDAR1Dec 17, 2024
EXT11Jul 14, 2024
FANCA1May 30, 2024
FBN11Jun 26, 2024
FKBP101Oct 13, 2024
FLVCR11Feb 23, 2025
FOLR11Apr 15, 2022
FOXE31May 30, 2024
GJB11May 30, 2024
GNAI31Dec 17, 2024
GORAB1Dec 17, 2024
GPI1Jan 22, 2025
GPT21Mar 30, 2024
HBA-LCR1Jun 26, 2024
HEXB2Jun 26, 2024
HGSNAT2Jan 22, 2025
IGHMBP21Jul 14, 2024
ITGA2B1Mar 30, 2024
KCNQ11Feb 19, 2025
KCNQ21Jun 26, 2024
KIDINS2201Jan 22, 2025
KLHL241Feb 19, 2025
LAMA22Jul 14, 2024
LAMB31Oct 13, 2024
LARP71Oct 13, 2024
LINC013891May 30, 2024
LOC1125336721Oct 13, 2024
LOC1239562101Feb 19, 2025
LOC1299340691Mar 12, 2025
LOC1299925851Jan 22, 2025
LOC1300678641May 30, 2024
MACF11Feb 19, 2025
MC2R1Jan 22, 2025
MFF-DT1Jun 26, 2024
MFSD81Feb 19, 2025
MIR302CHG1Oct 13, 2024
MLH11Oct 13, 2024
MOCS21Jan 22, 2025
MTHFS1Mar 17, 2022
MYO7A1May 30, 2024
NBN1Jun 26, 2024
NEU11Jul 14, 2024
NF11May 30, 2024
NPR21Jan 22, 2025
NPRL31Jun 26, 2024
NR1H41May 30, 2024
NSD11Jun 26, 2024
OTOG1Jun 26, 2024
PAPSS21Apr 15, 2022
PCARE1Feb 19, 2025
PCDHG@1Jun 26, 2024
PCDHGA11Jun 26, 2024
PCDHGA101Jun 26, 2024
PCDHGA111Jun 26, 2024
PCDHGA121Jun 26, 2024
PCDHGA21Jun 26, 2024
PCDHGA31Jun 26, 2024
PCDHGA41Jun 26, 2024
PCDHGA51Jun 26, 2024
PCDHGA61Jun 26, 2024
PCDHGA71Jun 26, 2024
PCDHGA81Jun 26, 2024
PCDHGA91Jun 26, 2024
PCDHGB11Jun 26, 2024
PCDHGB21Jun 26, 2024
PCDHGB31Jun 26, 2024
PCDHGB41Jun 26, 2024
PCDHGB51Jun 26, 2024
PCDHGB61Jun 26, 2024
PCDHGB71Jun 26, 2024
PCDHGC31Jun 26, 2024
PCDHGC41Jun 26, 2024
PDE6B1Dec 17, 2024
PDE6C1Jul 14, 2024
PHF61Jun 26, 2024
PIK3R11Feb 19, 2025
PLEC3Feb 19, 2025
PLEKHG51Jun 26, 2024
PMP221Dec 17, 2024
POLR1A1Jan 22, 2025
POMC1Feb 19, 2025
RANBP21Dec 17, 2024
RARS21Jun 26, 2024
RPGRIP11Oct 13, 2024
SCN1A1Jun 26, 2024
SELENON1Oct 13, 2024
SERPINF11Oct 13, 2024
SGCB1Jan 22, 2025
SHOC21Oct 13, 2024
SLC26A41Feb 19, 2025
SLC2A21Oct 13, 2024
SPAST1Jan 22, 2025
SPR1Mar 12, 2025
SPTBN22Dec 17, 2024
SRD5A31Feb 19, 2025
ST20-MTHFS1Mar 17, 2022
STK111Jan 22, 2025
SYNE11Oct 13, 2024
TYMP1May 30, 2024
UNC13D1Oct 13, 2024
VPS13B1Jan 22, 2025
VWF1Mar 30, 2024
WFS11Jul 14, 2024
XPC1Jan 22, 2025
ZEB21May 30, 2024

Condition

NameSubmissionsLast Updated
3M syndrome 11Oct 13, 2024
AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome1May 30, 2024
Achromatopsia 21Mar 30, 2024
Acromesomelic dysplasia 1, Maroteaux type1Jan 22, 2025
Alkaline ceramidase 3 deficiency1Jul 14, 2024
Alstrom syndrome1Apr 15, 2022
Atrial fibrillation, familial, 31Feb 19, 2025
Auriculocondylar syndrome 11Dec 17, 2024
Autism spectrum disorder due to AUTS2 deficiency1Jun 26, 2024
Autosomal dominant Alport syndrome1Jun 26, 2024
Autosomal recessive ataxia, Beauce type1Oct 13, 2024
Autosomal recessive bestrophinopathy1Dec 17, 2024
Autosomal recessive limb-girdle muscular dystrophy type 2E1Jan 22, 2025
Autosomal recessive nonsyndromic hearing loss 18B1Jun 26, 2024
Autosomal recessive nonsyndromic hearing loss 21May 30, 2024
Autosomal recessive nonsyndromic hearing loss 41Feb 19, 2025
Autosomal recessive spinocerebellar ataxia 142Dec 17, 2024
Becker muscular dystrophy1Dec 17, 2024
Borjeson-Forssman-Lehmann syndrome1Jun 26, 2024
Breast-ovarian cancer, familial, susceptibility to, 11Jul 14, 2024
Breast-ovarian cancer, familial, susceptibility to, 21Jul 14, 2024
CHARGE syndrome1Jul 14, 2024
Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies1Feb 19, 2025
Cerebral folate transport deficiency1Apr 15, 2022
Charcot-Marie-Tooth disease X-linked dominant 11May 30, 2024
Charcot-Marie-Tooth disease axonal type 2S1Jul 14, 2024
Charcot-Marie-Tooth disease, type IA1Dec 17, 2024
Cholestasis, progressive familial intrahepatic, 51May 30, 2024
Cohen syndrome1Jan 22, 2025
Colorectal cancer, hereditary nonpolyposis, type 21Oct 13, 2024
Cone dystrophy 41Jul 14, 2024
Cone-rod dystrophy 131Oct 13, 2024
Cone-rod dystrophy 161May 30, 2024
Cone-rod dystrophy 91Mar 30, 2024
Congenital disorder of glycosylation type Ir1Oct 13, 2024
Congenital myasthenic syndrome 4B1Oct 13, 2024
Congenital myotonia, autosomal recessive form1Jan 22, 2025
Congenital primary aphakia1May 30, 2024
Developmental and epileptic encephalopathy, 231Dec 17, 2024
Dopa-responsive dystonia due to sepiapterin reductase deficiency1Mar 12, 2025
Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive1Dec 17, 2024
Ectopia lentis 1, isolated, autosomal dominant1Jun 26, 2024
Eichsfeld type congenital muscular dystrophy1Oct 13, 2024
Epidermolysis bullosa simplex 5C, with pyloric atresia1Feb 19, 2025
Epidermolysis bullosa simplex with nail dystrophy2Oct 13, 2024
Epidermolysis bullosa, junctional 4, intermediate1Jan 22, 2025
Epilepsy, familial focal, with variable foci 31Jun 26, 2024
Exostoses, multiple, type 11Jul 14, 2024
Familial hemophagocytic lymphohistiocytosis 31Oct 13, 2024
Fanconi anemia complementation group A1May 30, 2024
Fanconi-Bickel syndrome1Oct 13, 2024
Farber lipogranulomatosis1Dec 17, 2024
Frontorhiny1Mar 30, 2024
Generalized epilepsy with febrile seizures plus, type 21Jun 26, 2024
Geroderma osteodysplastica1Dec 17, 2024
Glanzmann thrombasthenia 11Mar 30, 2024
Glucocorticoid deficiency 11Jan 22, 2025
Glutamate pyruvate transaminase 2 deficiency1Mar 30, 2024
Hemolytic anemia due to glucophosphate isomerase deficiency1Jan 22, 2025
Hereditary spastic paraplegia 41Jan 22, 2025
Intellectual disability, autosomal dominant 141May 30, 2024
Intellectual disability, autosomal dominant 531Jul 14, 2024
Joubert syndrome 51Jul 14, 2024
Junctional epidermolysis bullosa gravis of Herlitz1Oct 13, 2024
Kahrizi syndrome1Feb 19, 2025
Leukodystrophy, hypomyelinating, 271Jan 22, 2025
Lissencephaly 9 with complex brainstem malformation1Feb 19, 2025
Merosin deficient congenital muscular dystrophy2Jul 14, 2024
Microcephalic primordial dwarfism, Alazami type1Oct 13, 2024
Microcephaly 5, primary, autosomal recessive1May 30, 2024
Microcephaly, normal intelligence and immunodeficiency1Jun 26, 2024
Mitochondrial DNA depletion syndrome 11May 30, 2024
Mowat-Wilson syndrome1May 30, 2024
Mucopolysaccharidosis, MPS-III-C2Jan 22, 2025
Nephropathic cystinosis1Oct 13, 2024
Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination1Mar 17, 2022
Neurodevelopmental disorder with poor growth and skeletal anomalies1Jun 26, 2024
Neurofibromatosis, type 11May 30, 2024
Neuronal ceroid lipofuscinosis 71Feb 19, 2025
Neuronopathy, distal hereditary motor, autosomal recessive 41Jun 26, 2024
Noonan syndrome-like disorder with loose anagen hair 11Oct 13, 2024
Obesity due to pro-opiomelanocortin deficiency1Feb 19, 2025
Osteogenesis imperfecta type 111Oct 13, 2024
Osteogenesis imperfecta type 61Oct 13, 2024
Papillon-Lefèvre syndrome1May 30, 2024
Peutz-Jeghers syndrome1Jan 22, 2025
Pontocerebellar hypoplasia type 61Jun 26, 2024
Posterior column ataxia-retinitis pigmentosa syndrome1Feb 23, 2025
Primary ciliary dyskinesia 71May 30, 2024
Primary hypomagnesemia1May 30, 2024
Recessive dystrophic epidermolysis bullosa2Jun 26, 2024
Retinitis pigmentosa 401Dec 17, 2024
Retinitis pigmentosa 541Feb 19, 2025
Retinitis pigmentosa 551Mar 30, 2024
SHORT syndrome1Feb 19, 2025
Sandhoff disease2Jun 26, 2024
Seizures, benign familial neonatal, 11Jun 26, 2024
Severe early-childhood-onset retinal dystrophy1May 30, 2024
Sialidosis type 21Jul 14, 2024
Sotos syndrome1Jun 26, 2024
Spastic paraplegia, intellectual disability, nystagmus, and obesity1Jan 22, 2025
Spondyloepimetaphyseal dysplasia, PAPSS2 type1Apr 15, 2022
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B1Jan 22, 2025
Usher syndrome type 2C1May 30, 2024
Wolfram syndrome 11Jul 14, 2024
Xeroderma pigmentosum, group C1Jan 22, 2025
von Willebrand disease type 31Mar 30, 2024