WormBase Tree Display for Gene: HGNC:23096
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| HGNC:23096 | Identity | Name | CGC_name | Slc29a3 | Inferred_automatically | AGR_import |
|---|---|---|---|---|---|---|
| Other_name | RGD:1351725 | |||||
| Ent3 | ||||||
| FLJ11160 | ||||||
| hCLAP | ||||||
| HJCD | ||||||
| PHID | ||||||
| equilibrative nucleoside transporter 3 | ||||||
| solute carrier family 29 (equilibrative nucleoside transporter), member 3 | ||||||
| solute carrier family 29 (nucleoside transporters), member 3 | ||||||
| Public_name | Slc29a3 | |||||
| DB_info | Database | HGNC | id | 23096 | ||
| AGR | cURI | HGNC:23096 | ||||
| EnsEMBL | ENSEMBL_geneID | ENSG00000198246 | ||||
| UniProt | UniProt_AC | Q9BZD2 | ||||
| OMIM | gene | 612373 | ||||
| DO | id | DOID:0111278 | ||||
| Species | Homo sapiens | |||||
| Status | Live | |||||
| Gene_info | Biotype | SO:0001217 | ||||
| Ortholog | WBGene00009686 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | ||
| Inparanoid | ||||||
| OMA | ||||||
| OrthoInspector | ||||||
| PhylomeDB | ||||||
| SonicParanoid | ||||||
| WBGene00001320 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | |||
| Inparanoid | ||||||
| OrthoInspector | ||||||
| SonicParanoid | ||||||
| WBGene00008123 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | |||
| Inparanoid | ||||||
| OMA | ||||||
| OrthoInspector | ||||||
| SonicParanoid | ||||||
| WBGene00010510 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | |||
| Inparanoid | ||||||
| OrthoInspector | ||||||
| SonicParanoid | ||||||
| WBGene00010701 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | |||
| Inparanoid | ||||||
| OrthoInspector | ||||||
| SonicParanoid | ||||||
| WBGene00017532 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | |||
| Inparanoid | ||||||
| OMA | ||||||
| OrthoInspector | ||||||
| PhylomeDB | ||||||
| SonicParanoid | ||||||
| Structured_description | Automated_description | This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.[provided by RefSeq, Mar 2010] | Inferred_automatically | AGR_import |
