AmyCo

The Amyloidoses Collection

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Basic Information

Disease Name:

Hereditary lysozyme Amyloidosis

ISA Name:

ALys Amyloidosis

Alternative Names:

Familial amyloid nephropathy due to lysozyme variant
Familial renal amyloidosis due to lysozyme variant
Hereditary amyloid nephropathy due to lysozyme variant
Hereditary renal amyloidosis due to lysozyme variant
Lysozyme amyloidosis
Hereditary Lysozyme Amyloidosis
Amyloidosis VIII
Ostertag Type Amyloidosis
German Type Amyloidosis
Amyloidosis, Familial renal
Amyloidosis, Familial visceral
Amyloidosis, Systemic Non-neuropathic

MeSH Description:

No information available

Type:

Amyloidosis

ICD-10 Classification

Amyloidosis

Tissue:

Liver, Kidney, Gastrointestinal Tract, Spleen, Lymph Node, Skin, Lachrymal Gland, Salivary Gland, Heart

Precursor Proteins:

Primary Name:	Lysozyme C
Gene Name:	LYZ
Alternative Protein Names:	Lysozyme C (EC 3.2.1.17) (1,4-beta-N-acetylmuramidase C)
ISA Nomenclature:	ALys
Protein Length:	148
Precursor Protein Sequence:	MKALIVLGLVLLSVTVQGKVFERCELARTLKRLGMDGYRGISLANWMCLAKWESGYNTRATNYNAGDRSTDYGIFQINSRYWCNDGKTPGAVNACHLSCSALLQDNIADAVACAKRVVRDPQGIRAWVAWRNRCQNRDVRQYVQGCGV
UniProt AC:	P61626
UniProt ID:	LYSC_HUMAN
AmyPro:	AP00016

Co-deposited Proteins:

No information available

Interaction Network

Right click on Protein Nodes to go to UniProt.
Red Colored Edges indicate a connection between the disease and a precursor protein, while Blue Colored Edges indicate a connection with co-deposited proteins

Cross-References

MeSH:
ICD:
OMIM:
PubMed:

National and Kapodistrian University of Athens

Department of Biology

Biophysics & Bioinformatics Laboratory

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