Version: 8.1.0Date: Fri Apr 18 2025
Category
Nyap2
(Mus musculus)Gene
Name: neuronal tyrosine-phophorylated phosphoinositide 3-kinase adaptor 2
Synonyms: 9430031J16Rik, RIKEN cDNA 9430031J16 gene, Jr6
Source: MGI:2443135
Biotype: protein coding gene
Symbol: Nyap2 (Mmu)
Symbol: Nyap2
Automated Gene Synopsis: Orthologous to human NYAP2 (neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2).
Strict Orthology Symbols: Nyap2
Alleles: Nyap2
Nyap2
(Rattus norvegicus)Gene
Name: neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2
Synonyms: NEWGENE_1305560, neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 2
Source: RGD:9171458
Biotype: protein coding gene
Symbol: Nyap2 (Rno)
Symbol: Nyap2
Gene Synopsis: Orthologous to human NYAP2 (neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2); INTERACTS
Automated Gene Synopsis: Orthologous to human NYAP2 (neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2).
Strict Orthology Symbols: Nyap2
NYAP2
(Homo sapiens)Gene
Name: neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2
Synonyms: hypothetical protein LOC57624, AC067961.1, KIAA1486, neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 2, uncharacterized protein KIAA1486
Source: HGNC:29291
Biotype: protein coding gene
Symbol: NYAP2 (Hsa)
Symbol: NYAP2
Strict Orthology Symbols: Nyap2
nyap2
(Xenopus tropicalis)Gene
Name: neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2
Synonyms: LOC108718135, neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2, LOC108716219, nyap2
Source: Xenbase:XB-GENE-1012710
Biotype: gene
Symbol: nyap2 (Xtr)
Symbol: nyap2
Automated Gene Synopsis: Orthologous to human NYAP2 (neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2).
Synonyms: nyap2...nyap2
Strict Orthology Symbols: Nyap2
nyap2a
(Danio rerio)Gene
Name: neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2a
Synonyms: si:dkeyp-51h1.2
Source: ZFIN:ZDB-GENE-131121-129
Biotype: protein coding gene
Symbol: nyap2a (Dre)
Automated Gene Synopsis: Orthologous to human NYAP2 (neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2).
Strict Orthology Symbols: Nyap2
Symbol: nyap2a
nyap2b
(Danio rerio)Gene
Name: neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2b
Synonyms: si:ch211-273k1.2
Source: ZFIN:ZDB-GENE-070705-169
Biotype: protein coding gene
Symbol: nyap2b (Dre)
Automated Gene Synopsis: Orthologous to human NYAP2 (neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2).
Strict Orthology Symbols: Nyap2
Symbol: nyap2b
Nyap2em2Gpt
(Mus musculus)Allele/Variant
Source: MGI:7303360
Genes: Nyap2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nyap2
Genes: Nyap2 (Mmu)
Symbol: Nyap2em2Gpt
Nyap2em1Gpt
(Mus musculus)Allele/Variant
Source: MGI:7303359
Genes: Nyap2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nyap2
Genes: Nyap2 (Mmu)
Symbol: Nyap2em1Gpt
Nyap2tm1Tya
(Mus musculus)Allele/Variant
Source: MGI:6107632
Genes: Nyap2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nyap2
Genes: Nyap2 (Mmu)
Symbol: Nyap2tm1Tya
Model
Id: MGI:6107635
Synonyms: Not Available
Genes: Nyap2 (Mmu)
Alleles: Nyap2
Name: Myo16/Myo16 Nyap1/Nyap1 Nyap2/Nyap2 [background:] B6.129P2...-Nyap2 Nyap1 Myo16
Symbol: Myo16/Myo16 Nyap1/Nyap1 Nyap2/Nyap2 [background:] B6.129P2
Source: GO:0043491
Synonyms:
- AKT signal transduction
- AKT signaling
Branch: biological process
Genes: NYAP2 (Hsa)...nyap2a (Dre)...nyap2b (Dre)...Nyap2 (Mmu)...Nyap2 (Rno)
Gene Ontology
Source: GO:0048812
Synonyms:
- neurite biosynthesis
- neurite formation
Branch: biological process
Genes: NYAP2 (Hsa)...nyap2a (Dre)...nyap2b (Dre)...Nyap2 (Mmu)...Nyap2 (Rno)
sa42599
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-8334
Genes: nyap2a (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: nyap2a (Dre)
Gene Ontology
Source: GO:0005515
Synonyms:
- glycoprotein binding
- protein amino acid binding
Branch: molecular function
Genes: Nyap2 (Mmu)...NYAP2 (Hsa)
(GRCh38)2:225582912C>G
(Homo sapiens)Allele/Variant
Source: rs371936878
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582912C>G
(GRCh38)2:225582966C>T
(Homo sapiens)Allele/Variant
Source: rs563650514
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582966C>T
(GRCh38)2:225651465C>T
(Homo sapiens)Allele/Variant
Source: rs200066611
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225651465C>T
(GRCh38)2:225627052G>A
(Homo sapiens)Allele/Variant
Source: rs1173602930
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225627052G>A
(GRCh38)2:225408941C>G
(Homo sapiens)Allele/Variant
Source: rs201512658
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225408941C>G
(GRCh38)2:225582543G>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.225582543G>C
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582543G>C
(GRCh38)2:225409074G>T
(Homo sapiens)Allele/Variant
Source: rs375169851
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225409074G>T
(GRCh38)2:225582730C>T
(Homo sapiens)Allele/Variant
Source: rs750626822
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582730C>T
(GRCh38)2:225651482C>T
(Homo sapiens)Allele/Variant
Source: rs1216355535
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225651482C>T
(GRCh38)2:225582611C>G
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.225582611C>G
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582611C>G
(GRCh38)2:225582622G>C
(Homo sapiens)Allele/Variant
Source: rs1692311648
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582622G>C
(GRCh38)2:225408986A>G
(Homo sapiens)Allele/Variant
Source: rs778592921
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225408986A>G
(GRCh38)2:225513499G>A
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.225513499G>A
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225513499G>A
(GRCh38)2:225582110G>A
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.225582110G>A
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582110G>A
(GRCh38)2:225582264G>T
(Homo sapiens)Allele/Variant
Source: rs760467083
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582264G>T
(GRCh38)2:225582517A>G
(Homo sapiens)Allele/Variant
Source: rs1395419658
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582517A>G
(GRCh38)2:225582576G>A
(Homo sapiens)Allele/Variant
Source: rs376429827
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582576G>A
(GRCh38)2:225626985A>G
(Homo sapiens)Allele/Variant
Source: rs781079866
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225626985A>G
(GRCh38)2:225541089C>G
(Homo sapiens)Allele/Variant
Source: rs207462884
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225541089C>G
(GRCh38)2:225651558G>A
(Homo sapiens)Allele/Variant
Source: rs200139665
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225651558G>A
(GRCh38)2:225582643C>G
(Homo sapiens)Allele/Variant
Source: rs367790714
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582643C>G
(GRCh38)2:225582129C>A
(Homo sapiens)Allele/Variant
Source: rs772989177
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582129C>A
(GRCh38)2:225582682G>A
(Homo sapiens)Allele/Variant
Source: rs377307715
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582682G>A
(GRCh38)2:225582859C>T
(Homo sapiens)Allele/Variant
Source: rs759695162
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582859C>T
(GRCh38)2:225582922C>T
(Homo sapiens)Allele/Variant
Source: rs773627897
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582922C>T
(GRCh38)2:225651472G>C
(Homo sapiens)Allele/Variant
Source: rs61753536
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225651472G>C
(GRCh38)2:225651519A>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.225651519A>T
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_lost
Diseases: Not Available
Variant Name: (GRCh38)2:225651519A>T
(GRCh38)2:225651533C>G
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.225651533C>G
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225651533C>G
(GRCh38)2:225582963A>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.225582963A>C
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582963A>C
(GRCh38)2:225513544G>T
(Homo sapiens)Allele/Variant
Source: rs766171317
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225513544G>T
(GRCh38)2:225582925G>A
(Homo sapiens)Allele/Variant
Source: rs138500026
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582925G>A
(GRCh38)2:225409058G>A
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.225409058G>A
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225409058G>A
(GRCh38)2:225513391G>A
(Homo sapiens)Allele/Variant
Source: rs771022509
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225513391G>A
(GRCh38)2:225582360C>T
(Homo sapiens)Allele/Variant
Source: rs567364084
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582360C>T
(GRCh38)2:225582964G>A
(Homo sapiens)Allele/Variant
Source: rs1420144648
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225582964G>A
(GRCh38)2:225626995A>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.225626995A>T
Genes: NYAP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:225626995A>T