EntrezGene:9949
From referenceTSS
Related TSS IDs
| rfhg_238367.1 |
| rfhg_238368.1 |
| rfhg_238369.1 |
| rfhg_238378.1 |
| rfhg_238379.1 |
| rfhg_238380.1 |
Basic information
| GeneID: | 9949 |
|---|---|
| Species: | human |
| Gene name: | Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 |
| Gene symbol: | AMMECR1 |
| Gene synonyms: | AMMERC1 |
| Gene type: | protein-coding |
| Old GeneIDs: | 23656 286505 |
Links to external databases
| HGNC/MGI_ID: | HGNC:467 |
|---|---|
| Ensembl: | Ensembl:ENSG00000101935 |
| Vega: | Vega:OTTHUMG00000022197 |
| HPRD: | HPRD:02182 |
| miRBase: | |
| IMGT/GENE-DB: | |
| MIM: | MIM:300195 |
Transcripts
| Gencode transcripts: | ENST00000262844.9 ENST00000372059.6 ENST00000372057.1 ENST00000473662.1 ENST00000496695.1 |
|---|---|
| RefSeq transcripts: | NM_015365 NM_001171689 NM_001025580 |
| UCSC genes: | uc004eoo.4 uc004eop.4 uc004eoq.4 uc065arq.1 uc065art.1 |
| Other_mRNAs: | BC065214 BC051895 AK055321 BC037983 BC024762 BC060813 AK023637 BX648797 AK001703 AK091430 AJ007014 AK314596 HQ448514 KU178496 KU178497 CU687440 |