H-InvDB x AHG DB
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H-InvDB_9.0 released on May 27, 2015.
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H-Invitational ID: HIT000195630 Accession number: M35296 Created date: 26-Mar-2013 Last modified: 27-May-2015
Definition: Abelson tyrosine-protein kinase 2; EC=2.7.10.2; Abelson murine leukemia viral oncogene homolog 2; Abelson-related gene protein; Tyrosine-protein kinase ARG;
 
 

Gene function information  Gene family PPI viewer Similarity Search Tool TACT
H-Inv ID HIT000195630
H-Inv cluster ID Locus viewHIX0001374
Accession number M35296.1
CAGE tag ID NA
EST ID NA
Transcript feature  Help NO;  Splicing isoformSplicing isoform
Coding potential  Help Protein coding; 
Definition Abelson tyrosine-protein kinase 2; EC=2.7.10.2; Abelson murine leukemia viral oncogene homolog 2; Abelson-related gene protein; Tyrosine-protein kinase ARG;
Similarity category  Help Category: Identical to known human protein(Category I).
Identical to known human protein (P42684)  [Identity/coverage = 100.0%/100.0%] to Homo sapiens (Human). protein.
Experimental evidence Protein evidence
PubMed ID 219857137872601274829012775773147020391472917915489334157357351588609816678104167104141696424317306540173448461752533217974005181822991866964818691976188107621894567419369195196903322006823120841568214066922141734322297987ALL
Gene family/group Gene family H-Inv gene family/group ID NA
Gene family/group name NA
Evidence motif (InterPro) ID NA
Gene symbol/name HGNC symbol ABL2
HGNC aliases "v-abl Abelson murine leukemia viral oncogene homolog 2 (arg, Abelson-related gene)", "v-abl Abelson murine leukemia viral oncogene homolog 2", "c-abl oncogene 2, non-receptor tyrosine kinase"
HGNC name ABL proto-oncogene 2, non-receptor tyrosine kinase
DDBJ NA
UniProt ABL2
EC number EC 2.7.10.2non-specific protein-tyrosine kinase; 
GGDB
(GlycoGene Database)
Gene symbol NA
Familly NA
Designation NA
Expression NA
KEGG metabolic pathway 04020 :Calcium signaling pathway;  04360 :Axon guidance;  04370 :VEGF signaling pathway;  04510 :Focal adhesion;  04520 :Adherens junction;  04530 :Tight junction;  04540 :Gap junction;  04630 :Jak-STAT signaling pathway;  04660 :T cell receptor signaling pathway;  04662 :B cell receptor signaling pathway;  04664 :Fc epsilon RI signaling pathway;  04670 :Leukocyte transendothelial migration;  04730 :Long-term depression;  04810 :Regulation of actin cytoskeleton;  04912 :GnRH signaling pathway;  04920 :Adipocytokine signaling pathway;  05120 :Epithelial cell signaling in Helicobacter pylori infection;  05130 :Pathogenic Escherichia coli infection - EHEC;  05131 :Pathogenic Escherichia coli infection - EPEC; 
Protein-protein interaction (PPI) PPI viewer H-Inv protein ID HIP000059639
No. of interaction 10
Interaction partner(s) HIP000028444HIP000028444HIP000037309HIP000037309HIP000054177HIP000059105HIP000087997HIP000104670HIP000125446HIP000192588
BIND 177272;  258877;  258878;  58089;  58130; 
DIP 131587E;  131654E;  131745E;  131763E;  131975E;  132216E;  132385E;  288E;  58813E; 
MINT MINT-59458;  MINT-59459;  MINT-59461;  MINT-59462;  MINT-7041692;  MINT-74432;  MINT-74433;  MINT-74434;  MINT-74435;  MINT-74436;  MINT-74437;  MINT-74438;  MINT-74439;  MINT-74440;  MINT-74441;  MINT-74442;  MINT-74443;  MINT-74444;  MINT-74445;  MINT-74446;  MINT-74447;  MINT-74448;  MINT-74449;  MINT-74450;  MINT-74451;  MINT-74452;  MINT-74453;  MINT-74454;  MINT-74455;  MINT-74456;  MINT-74457;  MINT-74458;  MINT-7908314;  MINT-7908442;  MINT-8034736;  MINT-8110899;  MINT-8111655;  MINT-8112351;  MINT-8112867; 
HPRD 00579;  00796;  01281;  01398;  01809;  01819;  01820;  02533;  02740;  02767;  05142;  05813;  07338;  09352;  14381; 
IntAct NA
Database links RefSeq NA
Ensembl NA
Entrez Gene Entrez Gene ID:27
KEGG GENES KEGG GENES(27)
GeneCard GeneCardABL2*GeneCards is provided free to academic non-profit institutions.
etc H-GOLDHuman-Gene diversity Of Life-style related Diseases
Curation status Auto-annotated
Notes NA
Related H-InvDB links Gene familyGene family;  Similarity Search ToolSimilarity Search Tool;  TACTTACT
fRNAdb (The functional RNA database) : overlapping fRNAdb entries with H-InvDB transcripts based on the location of the genome. 
NA