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GIT1 (GIT ArfGAP 1)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
28964
Gene nameGene Name - the full gene name approved by the HGNC.
GIT ArfGAP 1
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
GIT1
SynonymsGene synonyms aliases
p95-APP1
ChromosomeChromosome number
17
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q11.2
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT025756 hsa-miR-7-5p Microarray 19073608
MIRT042200 hsa-miR-484 CLASH 23622248
MIRT054625 hsa-miR-149-5p Immunofluorescence, Immunohistochemistry, Luciferase reporter assay, Microarray, qRT-PCR, Western blot 24608434
MIRT054625 hsa-miR-149-5p Immunofluorescence, Immunohistochemistry, Luciferase reporter assay, Microarray, qRT-PCR, Western blot 24608434
MIRT438167 hsa-miR-491-5p Immunofluorescence, Immunohistochemistry, Luciferase reporter assay, qRT-PCR, Western blot 24335959
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001957 Process Intramembranous ossification ISS
GO:0005096 Function GTPase activator activity IEA
GO:0005515 Function Protein binding IPI 15182672, 15383276, 16628223, 16717130, 16787945, 18369319, 19041750, 21295525, 21706016, 21900206, 23108400, 23455922, 25852190, 31980649
GO:0005739 Component Mitochondrion IDA
GO:0005829 Component Cytosol IDA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q9Y2X7
Protein name ARF GTPase-activating protein GIT1 (ARF GAP GIT1) (Cool-associated and tyrosine-phosphorylated protein 1) (CAT-1) (CAT1) (G protein-coupled receptor kinase-interactor 1) (GRK-interacting protein 1) (p95-APP1)
Protein function GTPase-activating protein for ADP ribosylation factor family members, including ARF1. Multidomain scaffold protein that interacts with numerous proteins and therefore participates in many cellular functions, including receptor internalization, f
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01412 ArfGap
1 120
Putative GTPase activating protein for Arf
Domain
PF12796 Ank_2
137 229
Ankyrin repeats (3 copies)
Repeat
PF08518 GIT_SHD
264 292
Spa2 homology domain (SHD) of GIT
Family
PF08518 GIT_SHD
328 356
Spa2 homology domain (SHD) of GIT
Family
PF16559 GIT_CC
409 474
GIT coiled-coil Rho guanine nucleotide exchange factor
Coiled-coil
PF12205 GIT1_C
638 754
G protein-coupled receptor kinase-interacting protein 1 C term
Domain
Sequence
MSRKGPRAEVCADCSAPDPGWASISRGVLVCDECCSVHRSLGRHISIVKHLRHSAWPPTL
LQMVHTLASNGANSIWEHSLLDPAQVQSGRRKANPQDKVHPIKSEFIRAKYQMLAFVHKL

PCRDDDGVTAKDLSKQLHSSVRTGNLETCLRLLSLGAQANFFHPEKGTTPLHVAAKAGQT
LQAELLVVYGADPGSPDVNGRTPIDYARQAGHHELAERLVECQYELTDR
LAFYLCGRKPD
HKNGHYIIPQMADSLDLSELAKAAKKKLQALSNRLFEELAMDVYDEVDRRENDAVWLATQ
NHSTLVTERSAVPFLPVNPEYSATRNQGRQKLARFNAREFATLIIDILSEAKRRQQGKSL
SSPTDNLELSLRSQSDLDDQHDYDSVASDEDTDQEPLRSTGATRSNRARSMDSSDLSDGA
VTLQEYLELKKALATSEAKVQQLMKVNSSLSDELRRLQREIHKLQAENLQLRQP
PGPVPT
PPLPSERAEHTPMAPGGSTHRRDRQAFSMYEPGSALKPFGGPPGDELTTRLQPFHSTELE
DDAIYSVHVPAGLYRIRKGVSASAVPFTPSSPLLSCSQEGSRHTSKLSRHGSGADSDYEN
TQSGDPLLGLEGKRFLELGKEEDFHPELESLDGDLDPGLPSTEDVILKTEQVTKNIQELL
RAAQEFKHDSFVPCSEKIHLAVTEMASLFPKRPALEPVRSSLRLLNASAYRLQSECRKTV
PPEPGAPVDFQLLTQQVIQCAYDIAKAAKQLVTI
TTREKKQ
Sequence length 761
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Endocytosis
Regulation of actin cytoskeleton
Epithelial cell signaling in Helicobacter pylori infection
  Ephrin signaling
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Attention deficit hyperactivity disorder Attention Deficit Disorder, Attention deficit hyperactivity disorder rs120074176, rs786205019 21499268
Unknown
Disease name Disease term dbSNP ID References
Memory disorders Memory Disorders 21499268
Age-related memory disorders Age-Related Memory Disorders 21499268
Minimal brain dysfunction Minimal Brain Dysfunction 21499268

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