Metazoan complexes |
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Details of SNX3 gene in Homo sapiens
IDs | |||||||||
---|---|---|---|---|---|---|---|---|---|
Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
| SNX3 | --- | O60493 | SNX3_HUMAN | 8724 | ENSG00000112335 | Sorting nexin-3 | SPROT |
Disease | |||||||||
---|---|---|---|---|---|---|---|---|---|
Disease | OMIM id | ||||||||
Microphthalmia, syndromic, 8 (MCOPS8) [MIM:601349]: A very rare congenital syndrome characterized by microcephaly, microphthalmia, ectrodactyly of the lower limbs and prognathism. Intellectual deficit has been reported. Microphthalmia is a disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. Note=The gene represented in this entry may be involved in disease pathogenesis. A chromosomal aberration involving SNX3 has been found in patients with syndromic microphthalmia. Translocation t(613)(q21q12). | 601349 |
Orthologs in other species | |||||||||
---|---|---|---|---|---|---|---|---|---|
M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
Snx3 | Snx3 | snx-3 | SPU_021342 |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
---|---|---|---|---|---|---|---|---|---|
SNX3 | AKR1A1 | 0.459826711 | SNX3 | AKR1A1 | cpx94; cpx46 | no | no | no | Novel |
SNX3 | HINT1 | 0.041999437 | SNX3 | HINT1 | cpx956 | no | no | no | Novel |
SNX3 | PIN1 | 0.982011948 | SNX3 | PIN1 | cpx956; cpx94 | no | yes | no | Known |
SNX3 | PPIL3 | 0.151489558 | SNX3 | PPIL3 | cpx94; cpx83 | no | no | no | Novel |
SNX3 | SNX12 | 0.037761409 | SNX3 | SNX12 | cpx94 | no | no | no | Novel |
UBE2L3 | SNX3 | 0.20328805 | UBE2L3 | SNX3 | cpx302 | no | no | no | Novel |
CAPG | SNX3 | 0.143025798 | CAPG | SNX3 | cpx46; cpx94 | no | no | no | Novel |
PIR | SNX3 | 0.128751513 | PIR | SNX3 | cpx83; cpx302 | no | no | no | Novel |
DAZAP1 | SNX3 | 0.104335782 | DAZAP1 | SNX3 | cpx46 | no | no | no | Novel |
GLOD4 | SNX3 | 0.091312313 | GLOD4 | SNX3 | cpx83 | no | no | no | Novel |
GOT1 | SNX3 | 0.121392223 | GOT1 | SNX3 | cpx83 | no | no | no | Novel |
SNX3 | TAGLN2 | 0.520219125 | SNX3 | TAGLN2 | cpx956 | no | yes | no | Known |
SNX3 | TAGLN3 | 0.316206691 | SNX3 | TAGLN3 | cpx956 | no | yes | no | Known |
SNX3 | TAGLN | 0.102349917 | SNX3 | TAGLN | cpx956 | no | yes | no | Known |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
---|---|---|---|---|
TRIP6 | SNX3 | 0.088306331 | TRIP6 | SNX3 |
CRIP1 | SNX3 | 0.205649926 | CRIP1 | SNX3 |
SNX3 | AKR1C2 | 0.110932451 | SNX3 | AKR1C2 |
SMEK1 | SNX3 | 0.081264791 | SMEK1 | SNX3 |
SNX3 | RBM12 | 0.115466968 | SNX3 | RBM12 |
HGS | SNX3 | 0.113582174 | HGS | SNX3 |
HEBP1 | SNX3 | 0.087912623 | HEBP1 | SNX3 |
MTAP | SNX3 | 0.105069868 | MTAP | SNX3 |
SNX3 | NME1-NME2 | 0.070764521 | SNX3 | NME1-NME2 |
DYNLL1 | SNX3 | 0.098815811 | DYNLL1 | SNX3 |