(Q21988157)

http://www.ebi.ac.uk/interpro/protein/Q3UHA3

Spatacsin, C-terminal domain, protein family

1 reference

based on heuristic

inferred from protein domain or family

1 reference

25 May 2022

1 reference

25 May 2022

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

3 references

2 references

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

2 references

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

4 references

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

14 February 2019

Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

4 references

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

14 February 2019

Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

regulation of synaptic plasticity

ISO

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

1 reference

14 February 2019

Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

chemical synaptic transmission

3 references

axo-dendritic transport

4 references

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

14 February 2019

Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

phagosome-lysosome fusion involved in apoptotic cell clearance

IEA

1 reference

14 February 2019

In Vivo Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

In Vivo Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11

lysosome organization

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

synaptic vesicle transport

3 references

1 reference

14 February 2019

In Vivo Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q3UHA3

Spatacsin, C-terminal domain

has part(s)

1 reference

stated in

InterPro Release 71.0