UniProt | Protein Name |
---|---|
P48740 |
|
GO Term | Evidence Code | PMID |
---|---|---|
complement activation, lectin pathway | ||
zymogen activation |
GO Term | Evidence Code | PMID |
---|---|---|
cytosol | ||
extracellular region |
|
|
extracellular space | ||
nucleoplasm |
DO ID | Disease Name | Source |
---|---|---|
DOID:0040085 | bacterial sepsis | |
DOID:0050865 | tongue squamous cell carcinoma | |
DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | |
DOID:0060193 | amyotrophic lateral sclerosis type 1 | |
DOID:0060198 | amyotrophic lateral sclerosis type 6 | |
DOID:0060225 | 3MC syndrome | |
DOID:0060249 | scoliosis | |
DOID:0060260 | ptosis | |
DOID:0060261 | congenital ptosis | |
DOID:0060262 | gallbladder disease |
HPO ID | HPO Term |
---|---|
HP:0001540 | Diastasis recti |
HP:0001629 | Ventricular septal defect |
HP:0001631 | Atrial septal defect |
HP:0001643 | Patent ductus arteriosus |
HP:0001769 | Broad foot |
HP:0001773 | Short foot |
HP:0002265 | Large fleshy ears |
HP:0002553 | Highly arched eyebrow |
HP:0002558 | Supernumerary nipple |
HP:0002650 | Scoliosis |
Disease ID | Disease Name |
---|---|
ORPHA:293843 |
|
OMIM:257920 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100038300 | Xenbase:XB-GENE-984453 | ||
101942804 | CHRPI11561 | ||
109308542 | CROPO15376 | ||
100551064 | MELGA02751 | ||
103815377 | SERCA08976 | ||
100082252 | ORNAN25025 | ||
100407253 | CALJA11916 | ||
105575210 | CERAT15715 | ||
101866962 | MACFA25802 | ||
708206 | MACMU29120 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024