PPIL3, (2q33.1) cyclophilin J, CYPJ
https://www.genecards.org/cgi-bin/carddisp.pl?gene=PPIL3&keywords=PPIL3
Aliases for PPIL3 Gene
Peptidylprolyl Isomerase Like 3
2
3
5
Cyclophilin J 2 3 4
Peptidylprolyl Isomerase (Cyclophilin)-Like 3 2 3
Peptidyl-Prolyl Cis-Trans Isomerase-Like 3 3 4
Cyclophilin-Like Protein PPIL3 3 4
Rotamase PPIL3 3 4
EC 5.2.1.8 4 52
PPIase 3 4
Peptidylprolyl Cis-Trans Isomerase-Like Protein 3 3
Cyclophilin-Like Protein 3 3
PPIase-Like Protein 3 3
CYPJ 3
CyPJ 4
Cyclophilin J 2 3 4
Peptidylprolyl Isomerase (Cyclophilin)-Like 3 2 3
Peptidyl-Prolyl Cis-Trans Isomerase-Like 3 3 4
Cyclophilin-Like Protein PPIL3 3 4
Rotamase PPIL3 3 4
EC 5.2.1.8 4 52
PPIase 3 4
Peptidylprolyl Cis-Trans Isomerase-Like Protein 3 3
Cyclophilin-Like Protein 3 3
PPIase-Like Protein 3 3
CYPJ 3
CyPJ 4
PPIL3 Gene: This gene encodes a member of the cyclophilin
family. Cyclophilins catalyze the cis-trans isomerization of
peptidylprolyl imide bonds in oligopeptides. They have been proposed to
act either as catalysts or as molecular chaperones in protein-folding
events. Alternative splicing results in multiple transcript variants.
[provided by RefSeq, Sep 2008]
Summary for PPIL3 Gene: Peptidylprolyl Isomerase Like 3 is a Protein Coding gene.
Gene Ontology (GO) annotations related to this gene include peptidyl-prolyl cis-trans isomerase activity.
An important paralog of this gene is PPIL2.
PPIases accelerate the folding of proteins. PPIL3
catalyzes the cis-trans isomerization of proline imidic peptide bonds
in oligopeptides. May be involved in pre-mRNA splicing. PPIL3_HUMAN,Q9H2H8
FKBP15, (9q32), FK506-Binding Protein 15
https://www.genecards.org/cgi-bin/carddisp.pl?gene=FKBP15&keywords=FKBP15
Aliases for FKBP15 Gene
FKBP15 Gene: FKBP Prolyl Isomerase 15 is a Protein Coding gene.
Diseases associated with FKBP15 include Megalencephalic Leukoencephalopathy With Subcortical Cysts 1 and Spinocerebellar Ataxia 11.
Gene Ontology (GO) annotations related to this gene include actin binding and peptidyl-prolyl cis-trans isomerase activity.
An important paralog of this gene is FKBP9.
FKBP Prolyl Isomerase 15
2
3
5
KIAA0674 2 3 4
Protein Phosphatase 1, Regulatory Subunit 76 2 3
FK506 Binding Protein 15, 133kDa 2 3
133 KDa FK506-Binding Protein 3 4
WASP And FKBP-Like Protein 2 3
FK506-Binding Protein 15 3 4
133 KDa FKBP 3 4
FKBP-133 3 4
FKBP-15 3 4
WAFL 3 4
FK506-Binding Protein 133kDa 3
WASP- And FKBP-Like Protein 4
FK506 Binding Protein 15 2
FKBP133 3
PPP1R76 3
KIAA0674 2 3 4
Protein Phosphatase 1, Regulatory Subunit 76 2 3
FK506 Binding Protein 15, 133kDa 2 3
133 KDa FK506-Binding Protein 3 4
WASP And FKBP-Like Protein 2 3
FK506-Binding Protein 15 3 4
133 KDa FKBP 3 4
FKBP-133 3 4
FKBP-15 3 4
WAFL 3 4
FK506-Binding Protein 133kDa 3
WASP- And FKBP-Like Protein 4
FK506 Binding Protein 15 2
FKBP133 3
PPP1R76 3
FKBP15 Gene n ay be involved in the cytoskeletal
organization of neuronal growth cones. Seems to be inactive as a PPIase
(By similarity). Involved in the transport of early endosomes at the
level of transition between microfilament-based and microtubule-based
movement. FKB15_HUMAN,Q5T1M5
FKBP10, ( 17q21.2), Peptidyl-Prolyl Cis-Trans Isomerase FKBP10
(SARS2 ORF8 proteiinin interaktioproteiini)
FK506 binding proteinb 10
https://www.genecards.org/cgi-bin/carddisp.pl?gene=FKBP10&keywords=FKBP10
Aliases for FKBP10 Gene
FKBP10 Gene: The protein encoded by this gene belongs to the
FKBP-type peptidyl-prolyl cis/trans isomerase (PPIase) family. This
protein localizes to the endoplasmic reticulum (ER) and acts as a molecular
chaperone. Alternatively spliced variants encoding different isoforms
have been reported, but their biological validity has not been
determined.[provided by RefSeq, Nov 2009]
FKBP Prolyl Isomerase 10
2
3
5
Peptidyl-Prolyl Cis-Trans Isomerase FKBP10 3 4
FK506 Binding Protein 10, 65 KDa 2 3
65 KDa FK506-Binding Protein 3 4
FK506-Binding Protein 10 3 4
Immunophilin FKBP65 3 4
PPIase FKBP10 3 4
65 KDa FKBP 3 4
EC 5.2.1.8 4 52
Rotamase 3 4
FKBP-10 3 4
FKBP-65 3 4
FKBP65 3 4
FK506 Binding Protein 10 (65 KDa) 2
FK506 Binding Protein 10 2
HFKBP65 3
PPIASE 3
BRKS1 3
OI11 3
OI6 3
Peptidyl-Prolyl Cis-Trans Isomerase FKBP10 3 4
FK506 Binding Protein 10, 65 KDa 2 3
65 KDa FK506-Binding Protein 3 4
FK506-Binding Protein 10 3 4
Immunophilin FKBP65 3 4
PPIase FKBP10 3 4
65 KDa FKBP 3 4
EC 5.2.1.8 4 52
Rotamase 3 4
FKBP-10 3 4
FKBP-65 3 4
FKBP65 3 4
FK506 Binding Protein 10 (65 KDa) 2
FK506 Binding Protein 10 2
HFKBP65 3
PPIASE 3
BRKS1 3
OI11 3
OI6 3
GeneCards Summary for FKBP10 Gene
FKBP10 (FKBP Prolyl Isomerase 10) is a Protein Coding gene.
Diseases associated with FKBP10 include Bruck Syndrome 1 and Osteogenesis Imperfecta, Type Xi.
Gene Ontology (GO) annotations related to this gene include calcium ion binding and FK506 binding.
An important paralog of this gene is FKBP9.
UniProtKB/Swiss-Prot Summary for FKBP10 Gene
PPIases accelerate the folding of proteins during protein synthesis. FKB10_HUMAN,Q96AY3
FKBP7 , (2q33.1), Peptidyl-Prolyl Cis-Trans Isomerase FKBP7
(SARS2 ORF8 ineraktioproteiini)
PPIases accelerate the folding of proteins during protein synthesis. FKB10_HUMAN,Q96AY3
FKBP7 , (2q33.1), Peptidyl-Prolyl Cis-Trans Isomerase FKBP7
(SARS2 ORF8 ineraktioproteiini)
Aliases for FKBP7 Gene
FKBP7 Gene: The protein encoded by this gene belongs to the
FKBP-type peptidyl-prolyl cis/trans isomerase (PPIase) family. Members
of this family exhibit PPIase activity and function as molecular
chaperones. A similar protein in mouse is located in the endoplasmic
reticulum and binds calcium. [provided by RefSeq, Jul 2008]
FKBP7 (FKBP Prolyl Isomerase 7) is a Protein Coding gene.
Diseases associated with FKBP7 include Cerebellar Ataxia, Cayman Type.
Gene Ontology (GO) annotations related to this gene include calcium ion binding and FK506 binding.
An important paralog of this gene is FKBP14.
Summary for FKBP7 Gene PPIases accelerate the folding of proteins during protein synthesis. FKBP7_HUMAN,Q9Y680
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