Tissue | GTEx Coverage | GTEx Average TPM | GTEx Number of samples | TCGA Coverage | TCGA Average TPM | TCGA Number of samples |
---|---|---|---|---|---|---|
breast | 100% | 1940.68 | 459 / 459 | 100% | 28.45 | 1118 / 1118 |
esophagus | 100% | 1728.67 | 1445 / 1445 | 100% | 23.79 | 183 / 183 |
lung | 100% | 1721.58 | 578 / 578 | 100% | 26.92 | 1155 / 1155 |
ovary | 100% | 1797.05 | 180 / 180 | 100% | 20.86 | 430 / 430 |
prostate | 100% | 2030.32 | 245 / 245 | 100% | 22.22 | 502 / 502 |
stomach | 100% | 1455.88 | 359 / 359 | 100% | 25.21 | 286 / 286 |
uterus | 100% | 2100.63 | 170 / 170 | 100% | 27.06 | 459 / 459 |
intestine | 100% | 2235.55 | 966 / 966 | 100% | 27.63 | 526 / 527 |
bladder | 100% | 2127.33 | 21 / 21 | 100% | 24.44 | 503 / 504 |
brain | 100% | 1298.75 | 2634 / 2642 | 100% | 18.91 | 705 / 705 |
thymus | 100% | 1974.97 | 653 / 653 | 100% | 24.12 | 603 / 605 |
pancreas | 100% | 1008.71 | 327 / 328 | 99% | 21.30 | 177 / 178 |
adrenal gland | 100% | 2832.65 | 258 / 258 | 99% | 18.13 | 228 / 230 |
kidney | 100% | 1651.26 | 89 / 89 | 99% | 15.85 | 889 / 901 |
liver | 100% | 1138.40 | 226 / 226 | 99% | 11.68 | 400 / 406 |
skin | 100% | 1544.86 | 1808 / 1809 | 90% | 13.66 | 427 / 472 |
adipose | 100% | 1913.20 | 1204 / 1204 | 0% | 0 | 0 / 0 |
blood vessel | 100% | 2078.17 | 1335 / 1335 | 0% | 0 | 0 / 0 |
lymph node | 0% | 0 | 0 / 0 | 100% | 16.77 | 29 / 29 |
spleen | 100% | 1648.81 | 241 / 241 | 0% | 0 | 0 / 0 |
tonsil | 0% | 0 | 0 / 0 | 100% | 25.02 | 45 / 45 |
ureter | 0% | 0 | 0 / 0 | 100% | 5.93 | 1 / 1 |
muscle | 100% | 1382.55 | 801 / 803 | 0% | 0 | 0 / 0 |
heart | 98% | 979.01 | 847 / 861 | 0% | 0 | 0 / 0 |
peripheral blood | 78% | 752.65 | 720 / 929 | 0% | 0 | 0 / 0 |
eye | 0% | 0 | 0 / 0 | 65% | 5.83 | 52 / 80 |
abdomen | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
bone marrow | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
diaphragm | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
gingiva | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
nasal cavity | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
nasopharynx | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
nose | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
placenta | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
spinal column | 0% | 0 | 0 / 0 | 0% | 0 | 0 / 0 |
GO_0006325 | Biological process | chromatin organization |
GO_0055015 | Biological process | ventricular cardiac muscle cell development |
GO_0016567 | Biological process | protein ubiquitination |
GO_0001974 | Biological process | blood vessel remodeling |
GO_0000045 | Biological process | autophagosome assembly |
GO_0010040 | Biological process | response to iron(II) ion |
GO_1901096 | Biological process | regulation of autophagosome maturation |
GO_0071500 | Biological process | cellular response to nitrosative stress |
GO_0062029 | Biological process | positive regulation of stress granule assembly |
GO_0034727 | Biological process | piecemeal microautophagy of the nucleus |
GO_0009620 | Biological process | response to fungus |
GO_0016236 | Biological process | macroautophagy |
GO_2000378 | Biological process | negative regulation of reactive oxygen species metabolic process |
GO_0035973 | Biological process | aggrephagy |
GO_1902017 | Biological process | regulation of cilium assembly |
GO_0043687 | Biological process | post-translational protein modification |
GO_0051649 | Biological process | establishment of localization in cell |
GO_0039689 | Biological process | negative stranded viral RNA replication |
GO_0032480 | Biological process | negative regulation of type I interferon production |
GO_1904973 | Biological process | positive regulation of viral translation |
GO_0045824 | Biological process | negative regulation of innate immune response |
GO_0019883 | Biological process | antigen processing and presentation of endogenous antigen |
GO_0050765 | Biological process | negative regulation of phagocytosis |
GO_0048840 | Biological process | otolith development |
GO_0060047 | Biological process | heart contraction |
GO_0061684 | Biological process | chaperone-mediated autophagy |
GO_0050687 | Biological process | negative regulation of defense response to virus |
GO_0010659 | Biological process | cardiac muscle cell apoptotic process |
GO_0000422 | Biological process | autophagy of mitochondrion |
GO_0051279 | Biological process | regulation of release of sequestered calcium ion into cytosol |
GO_0000423 | Biological process | mitophagy |
GO_0006914 | Biological process | autophagy |
GO_0045060 | Biological process | negative thymic T cell selection |
GO_0010667 | Biological process | negative regulation of cardiac muscle cell apoptotic process |
GO_0009410 | Biological process | response to xenobiotic stimulus |
GO_0070254 | Biological process | mucus secretion |
GO_0042311 | Biological process | vasodilation |
GO_0006995 | Biological process | cellular response to nitrogen starvation |
GO_0061739 | Biological process | protein lipidation involved in autophagosome assembly |
GO_1902617 | Biological process | response to fluoride |
GO_0002718 | Biological process | regulation of cytokine production involved in immune response |
GO_0070257 | Biological process | positive regulation of mucus secretion |
GO_1904093 | Biological process | negative regulation of autophagic cell death |
GO_0031397 | Biological process | negative regulation of protein ubiquitination |
GO_0016020 | Cellular component | membrane |
GO_0034045 | Cellular component | phagophore assembly site membrane |
GO_0032991 | Cellular component | protein-containing complex |
GO_0005930 | Cellular component | axoneme |
GO_0044233 | Cellular component | mitochondria-associated endoplasmic reticulum membrane contact site |
GO_0005829 | Cellular component | cytosol |
GO_1990234 | Cellular component | transferase complex |
GO_0005776 | Cellular component | autophagosome |
GO_0005737 | Cellular component | cytoplasm |
GO_0030670 | Cellular component | phagocytic vesicle membrane |
GO_0061908 | Cellular component | phagophore |
GO_0034274 | Cellular component | Atg12-Atg5-Atg16 complex |
GO_0030424 | Cellular component | axon |
GO_0019776 | Molecular function | Atg8-family ligase activity |
GO_0005515 | Molecular function | protein binding |
Gene name | ATG5 |
Protein name | Autophagy protein 5 (APG5-like) (Apoptosis-specific protein) ATG5 variant 2 (Autophagy related 5) Autophagy protein 5 ATG5 variant 3 (Autophagy related 5) Autophagy related 5 |
Synonyms | DKFZp686F0183 APG5L ASP hCG_32959 |
Description | FUNCTION: Involved in autophagic vesicle formation. Conjugation with ATG12, through a ubiquitin-like conjugating system involving ATG7 as an E1-like activating enzyme and ATG10 as an E2-like conjugating enzyme, is essential for its function. The ATG12-ATG5 conjugate acts as an E3-like enzyme which is required for lipidation of ATG8 family proteins and their association to the vesicle membranes. Involved in mitochondrial quality control after oxidative damage, and in subsequent cellular longevity. Plays a critical role in multiple aspects of lymphocyte development and is essential for both B and T lymphocyte survival and proliferation. Required for optimal processing and presentation of antigens for MHC II. Involved in the maintenance of axon morphology and membrane structures, as well as in normal adipocyte differentiation. Promotes primary ciliogenesis through removal of OFD1 from centriolar satellites and degradation of IFT20 via the autophagic pathway. .; FUNCTION: May play an important role in the apoptotic process, possibly within the modified cytoskeleton. Its expression is a relatively late event in the apoptotic process, occurring downstream of caspase activity. Plays a crucial role in IFN-gamma-induced autophagic cell death by interacting with FADD. . FUNCTION: Involved in autophagic vesicle formation. Conjugation with ATG12, through a ubiquitin-like conjugating system involving ATG7 as an E1-like activating enzyme and ATG10 as an E2-like conjugating enzyme, is essential for its function. The ATG12-ATG5 conjugate acts as an E3-like enzyme which is required for lipidation of ATG8 family proteins and their association to the vesicle membranes. Involved in mitochondrial quality control after oxidative damage, and in subsequent cellular longevity. Plays a critical role in multiple aspects of lymphocyte development and is essential for both B and T lymphocyte survival and proliferation. Required for optimal processing and presentation of antigens for MHC II. Involved in the maintenance of axon morphology and membrane structures, as well as in normal adipocyte differentiation. Promotes primary ciliogenesis through removal of OFD1 from centriolar satellites and degradation of IFT20 via the autophagic pathway. .; FUNCTION: May play an important role in the apoptotic process, possibly within the modified cytoskeleton. Its expression is a relatively late event in the apoptotic process, occurring downstream of caspase activity. Plays a crucial role in IFN-gamma-induced autophagic cell death by interacting with FADD. .; FUNCTION: (Microbial infection) May act as a proviral factor. In association with ATG12, negatively regulates the innate antiviral immune response by impairing the type I IFN production pathway upon vesicular stomatitis virus (VSV) infection . Required for the translation of incoming hepatitis C virus (HCV) RNA and, thereby, for initiation of HCV replication, but not required once infection is established . . FUNCTION: Involved in autophagic vesicle formation. Conjugation with ATG12, through a ubiquitin-like conjugating system involving ATG7 as an E1-like activating enzyme and ATG10 as an E2-like conjugating enzyme, is essential for its function. The ATG12-ATG5 conjugate acts as an E3-like enzyme which is required for lipidation of ATG8 family proteins and their association to the vesicle membranes. Involved in mitochondrial quality control after oxidative damage, and in subsequent cellular longevity. Plays a critical role in multiple aspects of lymphocyte development and is essential for both B and T lymphocyte survival and proliferation. Required for optimal processing and presentation of antigens for MHC II. Involved in the maintenance of axon morphology and membrane structures, as well as in normal adipocyte differentiation. Promotes primary ciliogenesis through removal of OFD1 from centriolar satellites and degradation of IFT20 via the autophagic pathway. .; FUNCTION: May play an important role in the apoptotic process, possibly within the modified cytoskeleton. Its expression is a relatively late event in the apoptotic process, occurring downstream of caspase activity. Plays a crucial role in IFN-gamma-induced autophagic cell death by interacting with FADD. . FUNCTION: Involved in autophagic vesicle formation. Conjugation with ATG12, through a ubiquitin-like conjugating system involving ATG7 as an E1-like activating enzyme and ATG10 as an E2-like conjugating enzyme, is essential for its function. The ATG12-ATG5 conjugate acts as an E3-like enzyme which is required for lipidation of ATG8 family proteins and their association to the vesicle membranes. Involved in mitochondrial quality control after oxidative damage, and in subsequent cellular longevity. Plays a critical role in multiple aspects of lymphocyte development and is essential for both B and T lymphocyte survival and proliferation. Required for optimal processing and presentation of antigens for MHC II. Involved in the maintenance of axon morphology and membrane structures, as well as in normal adipocyte differentiation. Promotes primary ciliogenesis through removal of OFD1 from centriolar satellites and degradation of IFT20 via the autophagic pathway. .; FUNCTION: May play an important role in the apoptotic process, possibly within the modified cytoskeleton. Its expression is a relatively late event in the apoptotic process, occurring downstream of caspase activity. Plays a crucial role in IFN-gamma-induced autophagic cell death by interacting with FADD. . FUNCTION: Involved in autophagic vesicle formation. Conjugation with ATG12, through a ubiquitin-like conjugating system involving ATG7 as an E1-like activating enzyme and ATG10 as an E2-like conjugating enzyme, is essential for its function. The ATG12-ATG5 conjugate acts as an E3-like enzyme which is required for lipidation of ATG8 family proteins and their association to the vesicle membranes. Involved in mitochondrial quality control after oxidative damage, and in subsequent cellular longevity. Plays a critical role in multiple aspects of lymphocyte development and is essential for both B and T lymphocyte survival and proliferation. Required for optimal processing and presentation of antigens for MHC II. Involved in the maintenance of axon morphology and membrane structures, as well as in normal adipocyte differentiation. Promotes primary ciliogenesis through removal of OFD1 from centriolar satellites and degradation of IFT20 via the autophagic pathway. .; FUNCTION: May play an important role in the apoptotic process, possibly within the modified cytoskeleton. Its expression is a relatively late event in the apoptotic process, occurring downstream of caspase activity. Plays a crucial role in IFN-gamma-induced autophagic cell death by interacting with FADD. . FUNCTION: Involved in autophagic vesicle formation. Conjugation with ATG12, through a ubiquitin-like conjugating system involving ATG7 as an E1-like activating enzyme and ATG10 as an E2-like conjugating enzyme, is essential for its function. The ATG12-ATG5 conjugate acts as an E3-like enzyme which is required for lipidation of ATG8 family proteins and their association to the vesicle membranes. Involved in mitochondrial quality control after oxidative damage, and in subsequent cellular longevity. Plays a critical role in multiple aspects of lymphocyte development and is essential for both B and T lymphocyte survival and proliferation. Required for optimal processing and presentation of antigens for MHC II. Involved in the maintenance of axon morphology and membrane structures, as well as in normal adipocyte differentiation. Promotes primary ciliogenesis through removal of OFD1 from centriolar satellites and degradation of IFT20 via the autophagic pathway. .; FUNCTION: May play an important role in the apoptotic process, possibly within the modified cytoskeleton. Its expression is a relatively late event in the apoptotic process, occurring downstream of caspase activity. Plays a crucial role in IFN-gamma-induced autophagic cell death by interacting with FADD. . |
Accessions | ENST00000613993.1 ENST00000635758.2 [Q9H1Y0-2] ENST00000636437.1 ENST00000369076.8 [Q9H1Y0-1] ENST00000636335.1 ENST00000360666.6 ENST00000646025.1 A0A2R8Y718 L7UMD8 Q7Z3H3 ENST00000369070.5 L7UQJ2 ENST00000343245.7 [Q9H1Y0-1] Q9H1Y0 A0A1B0GUS1 A0A1B0GV54 A9UGY9 |