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Browse result for Autistic disorder

※ introduction

    Classic autism, also known as childhood autism, autistic disorder, (early) infantile autism, infantile psychosis, Kanner's autism, Kanner's syndrome, or (formerly) just autism, is a neurodevelopmental condition first described by Leo Kanner in 1943. It is characterized by atypical and impaired development in social interaction and communication as well as restricted, repetitive behaviors, activities, and interests. These symptoms first appear in early childhood and persist throughout life. It was last recognized as a diagnosis in the DSM-IV and ICD-10, and has been superseded by autism spectrum disorder in the DSM-5 (2013) and ICD-11 (2022). Globally, classic autism was estimated to affect 24.8 million people as of 2015. Autism is caused by a combination of genetic and environmental factors, with genetic factors thought to heavily predominate. Controversies surrounded other proposed environmental causes; for example, the vaccine hypothesis, which although disproved, continues to hold sway in certain communities. After DSM-5/ICD-11 the term "autism" has become more commonly used in reference to the autism spectrum more broadly.

Reference
Wiki: Autistic disorder



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD00452O004595296
PIK3R2
Phosphatidylinositol 3-kinase regulatory subunit beta
Homo sapiens
PTMD01045O753769611
NCOR1
Nuclear receptor corepressor 1
Homo sapiens
PTMD00506P05023476
ATP1A1
Sodium/potassium-transporting ATPase subunit alpha-1 /K ATPase alpha-1 subunit)
Homo sapiens
PTMD01001Q132242904
GRIN2B
Glutamate receptor ionotropic, NMDA 2B
Homo sapiens
PTMD00779Q96RK023152
CIC
Protein capicua homolog
Homo sapiens
PTMD01466P027667276
TTR
Transthyretin
Homo sapiens
PTMD01648P515326597
SMARCA4
Transcription activator BRG1
Homo sapiens
PTMD01724Q050867337
UBE3A
Ubiquitin-protein ligase E3A
Homo sapiens
PTMD01734Q128792903
GRIN2A
Glutamate receptor ionotropic, NMDA 2A
Homo sapiens
PTMD02402O146461105
CHD1
Chromodomain-helicase-DNA-binding protein 1
Homo sapiens
PTMD03227O759627204
TRIO
Triple functional domain protein
Homo sapiens
PTMD03874P083973145
HMBS
Porphobilinogen deaminase
Homo sapiens
PTMD04077P113622260
FGFR1
Fibroblast growth factor receptor 1
Homo sapiens
PTMD04366P185836651
SON
Protein SON
Homo sapiens
PTMD04548P23109270
AMPD1
AMP deaminase 1
Homo sapiens
PTMD05006P38606523
ATP6V1A
V-type proton ATPase catalytic subunit A
Homo sapiens
PTMD05085P422612890
GRIA1
Glutamate receptor 1
Homo sapiens
PTMD05206P47895220
ALDH1A3
Retinaldehyde dehydrogenase 3
Homo sapiens
PTMD06146Q022241062
CENPE
Centromere-associated protein E
Homo sapiens
PTMD06621Q137513914
LAMB3
Laminin subunit beta-3
Homo sapiens
PTMD07132Q1665010716
TBR1
T-box brain protein 1
Homo sapiens
PTMD07228Q2M1P537465
KIF7
Kinesin-like protein KIF7
Homo sapiens
PTMD08812Q7Z40679784
MYH14
Myosin-14
Homo sapiens
PTMD09426Q8IYD123708
GSPT2
Eukaryotic peptide chain release factor GTP-binding subunit ERF3B
Homo sapiens
PTMD10619Q8WWQ055023
PHIP
PH-interacting protein
Homo sapiens
PTMD10808Q927961741
DLG3
Disks large homolog 3
Homo sapiens
PTMD11768Q96ST325942
SIN3A
Paired amphipathic helix protein Sin3a
Homo sapiens
PTMD12495Q9C0K064919
BCL11B
B-cell lymphoma/leukemia 11B
Homo sapiens
PTMD13959Q9P2R6473
RERE
Arginine-glutamic acid dipeptide repeats protein
Homo sapiens
PTMD14830Q9Y4A58295
TRRAP
Transformation/transcription domain-associated protein
Homo sapiens
PTMD14961Q9Y5P410087
CERT1
Ceramide transfer protein
Homo sapiens