UniProt | Protein Name |
---|---|
O95427 |
|
A0A1W2PQA9 |
|
GO Term | Evidence Code | PMID |
---|---|---|
GPI anchor biosynthetic process | ||
preassembly of GPI anchor in ER membrane |
|
GO Term | Evidence Code | PMID |
---|---|---|
cytosol | ||
endoplasmic reticulum membrane | ||
plasma membrane | ||
membrane |
GO Term | Evidence Code | PMID |
---|---|---|
mannose-ethanolamine phosphotransferase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050453 | lissencephaly | |
DOID:0050778 | Meckel syndrome | |
DOID:0050841 | focal hand dystonia | |
DOID:0050908 | myelodysplastic syndrome | |
DOID:0060321 | umbilical hernia | |
DOID:0060327 | omphalocele | |
DOID:0060402 | chromosome 17p13.1 deletion syndrome | |
DOID:0060469 | Miller-Dieker lissencephaly syndrome | |
DOID:0060645 | chronic recurrent multifocal osteomyelitis | |
DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 |
HPO ID | HPO Term |
---|---|
HP:0000003 | Multicystic kidney dysplasia |
HP:0000007 | Autosomal recessive inheritance |
HP:0000028 | Cryptorchidism |
HP:0000034 | Hydrocele testis |
HP:0000047 | Hypospadias |
HP:0000072 | Hydroureter |
HP:0000073 | Ureteral duplication |
HP:0000076 | Vesicoureteral reflux |
HP:0000110 | Renal dysplasia |
HP:0000126 | Hydronephrosis |
Disease ID | Disease Name |
---|---|
ORPHA:280633 |
|
OMIM:614080 |
|
ORPHA:2059 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
171881 | WB:WBGene00021840 | ||
36049 | FB:FBgn0033479 | ||
41388 | FB:FBgn0037915 | ||
41389 | FB:FBgn0037916 | ||
42686 | FB:FBgn0039010 | ||
43303 | FB:FBgn0039518 | ||
100177059 | CIOIN02784 | ||
556797 | ZFIN:ZDB-GENE-080204-114 | DANRE26352 | |
103038036 | ASTMX06135 | ||
108256714 | ICTPU18201 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024