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 |
GO Term | Evidence Code | PMID |
---|---|---|
protein homodimerization activity | ||
peptidase activity | ||
serine-type endopeptidase activity | ||
calcium ion binding | ||
calcium-dependent protein binding |
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:0000007 | Autosomal recessive inheritance |
HP:0000126 | Hydronephrosis |
HP:0000175 | Cleft palate |
HP:0000202 | Orofacial cleft |
HP:0000204 | Cleft upper lip |
HP:0000252 | Microcephaly |
HP:0000260 | Wide anterior fontanel |
HP:0000316 | Hypertelorism |
HP:0000365 | Hearing impairment |
HP:0000369 | Low-set ears |
Disease ID | Disease Name |
---|---|
ORPHA:293843 |
|
OMIM:257920 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
105470889 | MACNE16135 | ||
101017684 | PAPAN24166 | ||
105527857 | MANLE32144 | ||
101144543 | GORGO27859 | ||
100970830 | PANPA29480 | ||
100439814 | PONAB25475 | ||
488121 | CANLF13568 | ||
112926302 | VULVU20581 | ||
123801287 | URSAM23233 | ||
101674101 | MUSPF16510 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024