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Protein-coding gene in the species Homo sapiens
repeat domains protein 2 is a protein that in humans is encoded by the SHANK2 gene. Two alternative splice variants, encoding distinct isoforms, are reported
SHANK2
Book by Robert Kolker
on HBO called Six Schizophrenic Brothers. Studies implicated two genes, SHANK2 and CHRNA7, which were passed on to the boys from their mother. Hidden Valley
Hidden_Valley_Road
Neuron membrane protein
receptors and autism was also identified via the structural protein ProSAP1 SHANK2 and potentially ProSAP2 SHANK3. The study authors concluded that the study
Glutamate_receptor
Topics referred to by the same term
genus Tringa Shankh, a quantity in the Indian numbering system SHANK1, SHANK2, and SHANK3, types of protein Bud Shank, an American saxophonist Christopher
Shank
Small protein domain found in some kinases and GTPases
(potentially) STAC3 Some myosins SH3 and multiple ankyrin repeat domains: SHANK1, SHANK2, SHANK3 YAP1 ARHGAP12 vexin (VXN) TANGO1 Integrase Focal Adhesion Kinase
SH3_domain
Protein-coding gene in the species Homo sapiens
protein called guanylate kinase-associated protein (GKAP). GKAP binds to the SHANK2 and PSD-95 proteins, facilitating the assembly of the post-synaptic density
DLGAP1
Complex interplay of factors
disorders defined by genetics. One gene that has been linked to autism is SHANK2. Mutations in this gene act in a dominant fashion and appear to cause hyperconnectivity
Causes_of_autism
Protein-coding gene in the species Homo sapiens
SHANK2 is located on chromosome 11, and SHANK3 on chromosome 22. The locus of SHANK1, in particular, is less studied in relation to ASD than SHANK2 and
SHANK1
Southu Korean neuroscietnist (born 1961)
plasticity in the hippocampus is impaired in a mouse model of autism, the Shank2 knockout. When they treated the mice with drugs that upregulate NMDA receptor
Kaang_Bong-kiun
Protein-coding gene in the species Homo sapiens
channels. As with many other synaptic genes, including its binding partner SHANK2, DLGAP2 has been shown to be associated with autism. ENSG00000282152, ENSG00000282318
DLGAP2
Medical practice
frequently associated with intellectual disability. Mutations in SHANK1 and SHANK2 are generally linked to milder forms of disability. These mutations are
Prenatal_screening_for_autism
Q8TF17 14731 SH3YL1 HGNC:29546; Q96HL8 14732 SHANK1 HGNC:15474; Q9Y566 14733 SHANK2 HGNC:14295; Q9UPX8 14734 SHANK3 HGNC:14294; Q9BYB0 14735 SHARPIN HGNC:25321;
List of human protein-coding genes 7
List_of_human_protein-coding_genes_7
Protein domain
SAMD7; SAMD8; SAMD9; SARM1; SCMH1; SCML1; SCML2; SEC23IP; SGMS1; SHANK1; SHANK2; SHANK3; STARD13; UBP1; USH1G; ZCCHC14; p63; p73; Bork P, Ponting CP, Hofmann
Sterile_alpha_motif
Protein domain
PPP1R13L; PPP1R16A; PPP1R16B; PSMD10; RAI14; RFXANK; RIPK4; RNASEL; SHANK1; SHANK2; SHANK3; SNCAIP; TA-NFKBH; TEX14; TNKS; TNKS2; TNNI3K; TP53BP2; TRP7; TRPA1;
Ankyrin_repeat
Protein family
RAPGEF2 RGS12 RGS3 RHPN1 RIL RIMS1 RIMS2 SCN5A SCRIB SDCBP SDCBP2 SHANK1 SHANK2 SHANK3 SHROOM2 SHROOM3 SHROOM4 SIPA1 SIPA1L1 SIPA1L2 SIPA1L3 SLC9A3R1 SLC9A3R2
PDZ_domain
Mammalian protein found in Homo sapiens
KCNA2 KCNA4 KCNA5 KCNJ12 Kir2.1 LGI1 LRP1 LRP2 NLGN1 NOS1 PTK2B SEMA4C and SHANK2. Postsynaptic density GRCh38: Ensembl release 89: ENSG00000132535 – Ensembl
DLG4
Protein found in humans
Cortactin has been shown to interact with: ACTR3 ARPC2, CTNND1, FER, KCNA2, SHANK2, WASL, and WIPF1. actin gelsolin transferrin villin ENSG00000288401 GRCh38:
Cortactin
Protein-coding gene in the species Homo sapiens
cognitive functions. Somatostatin receptor 2 has been shown to interact with SHANK2. The somatostatin hormone itself can negatively affect the uptake of hormones
Somatostatin_receptor_2
Protein-coding gene in humans
activated via DHPH RhoGEF domain. The neuronal synapse adaptors SHANK1, SHANK2, and SHANK3 via PDZ Scribble via PDZ SNX27 via PDZ Rho family of GTPases
ARHGEF7
Canadian scientist (born 1964)
Hartmut; Sprengel, Rolf; Scherer, Stephen W. (May 16, 2010). "Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation"
Stephen_W._Scherer
South Korean neuroscientist
State University". Kim, Eunjoon (2012). "Autistic-like social behavior in Shank2-mutant mice improved by restoring NMDA receptor function". Nature. 486 (7402):
Eunjoon_Kim
Protein-coding gene in the species Homo sapiens
has not been determined. DNM2 has been shown to interact with: SHANK1, SHANK2, and SNX9. Mutations in this gene have been associated to cases of acute
DNM2
SHANK2
SHANK2
SHANK2
SHANK2
Surname or Lastname
English
English : from the Middle English personal name Wymer, Old English Wīgmǣr (composed of the elements wīg ‘war’ + mǣr ‘famous’), reinforced by the cognate Continental Germanic form Wigmar, introduced into England from France by the Normans. This also became confused with an Old Breton personal name, Wiumarch, composed of the elements uuiu ‘worthy’ + march ‘horse’.
Girl/Female
Tamil
Nithyasmithi | நீதà¯à®¯à®¸à¯à®®à¯€à®¤à¯€Â
Boy/Male
Indian
Forest
Boy/Male
Hindu, Indian
Name of a Saint
Boy/Male
Indian, Marathi, Modern
God
Boy/Male
Assamese, Hindu, Indian, Kannada, Oriya, Sanskrit, Telugu
Towards the Fire; A Son of Aitasa
Girl/Female
Arabic
Smell; Flavour
Girl/Female
Australian, French, Greek, Swiss
Marshy; White Blossom; Foreign Wealth
Girl/Female
English American Bavarian Hebrew
Boy/Male
Hindu, Indian
We Proud
SHANK2
SHANK2
SHANK2
SHANK2
SHANK2