Akt substrate,160kD (AS160, DKFZp779C0666, KIAA0603, TBC1 domain family member 4, Rab GAP)[Akt substrate,160kD]

• Catalog number
  MBS618672
• Price
  Please ask
• Size
  NA

• Products_type
  Antibody
• Reactivity
  Canine, Human, Mouse, Rat

• Gene target
  Akt   substrate   160kD   AS160   DKFZp779C0666   KIAA0603   TBC1   domain   family   member   Rab   GAP   [Akt   substrate   160kD]  
• Gene symbol
  TBC1D4, TBC1D1, GAP43, ARHGAP32, ITGA3, RASA1
• Short name
  Akt substrate 160kD (AS160, DKFZp779C0666, KIAA0603, TBC1 domain family member 4, Rab GAP)[Akt substrate 160kD]
• Host
  Rabbit
• Alternative name
  Akt substrate,160kD (AS160, DKFZp779C0666, KIAA0603, TBC1 domain family member 4, Rab GAP)[Akt substrate,160kD]

Gene info

• Identity
  HGNC:19165
• Gene
  TBC1D4
• Long gene name
  TBC1 domain family member 4
• Synonyms gene name
  • TBC1 domain family, member 4
• Synonyms
  • KIAA0603
  • AS160
  • DKFZp779C0666
• Synonyms name
  • Akt substrate of 160 kDa
• GenBank acession
  • AB011175
• Locus
  13q22.2
• Discovery year
  2002-08-29
• Entrez gene record
  9882
• Pubmed identfication
  • 11829485
  • 11994271
  • 15304337
• RefSeq identity
  • NM_014832
• VEGA ID
  OTTHUMG00000017088

Gene info

• Identity
  HGNC:11578
• Gene
  TBC1D1
• Long gene name
  TBC1 domain family member 1
• Synonyms gene name
  • TBC1 (tre-2/USP6, BUB2, cdc16) domain family, member 1
  • TBC1 domain family, member 1
• Synonyms
  • TBC
  • TBC1
  • KIAA1108
• GenBank acession
  • AB029031
• Locus
  4p14
• Discovery year
  2000-03-06
• Entrez gene record
  23216
• Pubmed identfication
  • 10965142
  • 18258599
• RefSeq identity
  • NM_015173
• VEGA ID
  OTTHUMG00000150302

Gene info

• Identity
  HGNC:4140
• Gene
  GAP43
• Long gene name
  growth associated protein 43
• Synonyms
  • B-50
  • PP46
  • GAP-43
• Synonyms name
  • neuron growth-associated protein 43
  • neuromodulin
  • nerve growth-related peptide GAP43
  • axonal membrane protein GAP-43
  • protein F1
  • calmodulin-binding protein P-57
  • neural phosphoprotein B-50
• Locus
  3q13.31
• Discovery year
  1990-07-10
• Entrez gene record
  2596
• Pubmed identfication
  • 3272162
  • 8231732
• RefSeq identity
  • NM_002045
• VEGA ID
  OTTHUMG00000133758

Gene info

• Identity
  HGNC:17399
• Gene
  ARHGAP32
• Long gene name
  Rho GTPase activating protein 32
• Synonyms
  • GRIT
  • KIAA0712
  • MGC1892
  • RICS
  • GC-GAP
• GenBank acession
  • AB018255
• Locus
  11q24.3
• Discovery year
  2010-02-19
• Entrez gene record
  9743
• Pubmed identfication
  • 12446789
  • 12819203
  • 17663722
• RefSeq identity
  • NM_014715
• Classification
  • Rho GTPase activating proteins
• VEGA ID
  OTTHUMG00000165774

Gene info

• Identity
  HGNC:6139
• Gene
  ITGA3
• Long gene name
  integrin subunit alpha 3
• Synonyms gene
  • MSK18
• Synonyms gene name
  • antigen identified by monoclonal antibody J143
  • integrin, alpha 3 (antigen CD49C, alpha 3 subunit of VLA-3 receptor)
• Synonyms
  • CD49c
  • VLA3a
  • VCA-2
  • GAP-B3
• Synonyms name
  • alpha 3 subunit of VLA-3 receptor
  • antigen CD49C
• GenBank acession
  • M59911
• Locus
  17q21.33
• Discovery year
  1992-02-27
• Entrez gene record
  3675
• Pubmed identfication
  • 1655803
  • 9704023
• RefSeq identity
  • NM_005501
• Classification
  • Integrin alpha subunits
  • CD molecules
• VEGA ID
  OTTHUMG00000161890

Gene info

• Identity
  HGNC:9871
• Gene
  RASA1
• Long gene name
  RAS p21 protein activator 1
• Synonyms gene
  • RASA
• Synonyms gene name
  • RAS p21 protein activator (GTPase activating protein) 1
• Synonyms
  • GAP
  • CM-AVM
  • p120GAP
  • p120RASGAP
  • p120
• Synonyms name
  • capillary malformation-arteriovenous malformation
  • p120 RAS GTPase activating protein
• Locus
  5q14.3
• Discovery year
  1989-06-30
• Entrez gene record
  5921
• Pubmed identfication
  • 15917201
• RefSeq identity
  • NM_002890
• Classification
  • SH2 domain containing
  • C2 and RasGAP domain containing
  • Pleckstrin homology domain containing
• VEGA ID
  OTTHUMG00000162605
• Locus Specific Databases
  • SH2base: Database for pathogenic SH2 domain mutations

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