RCBTB1
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RCBTB1
Summary
RCBTB1 is a gene[1]. RCBTB1 is known by 6 alternative names across languages and contexts.[2]
Key Facts
- RCBTB1's instance of is recorded as gene[3].
- RCBTB1 is a type of protein-coding gene[4].
- RCBTB1's HomoloGene ID is recorded as 10061[5].
- RCBTB1's ortholog is recorded as Rcbtb1[6].
- RCBTB1's ortholog is recorded as Rcbtb1[7].
- RCBTB1's ortholog is recorded as rcbtb1[8].
- RCBTB1's encodes is recorded as RCC1 and BTB domain containing protein 1[9].
- RCBTB1's found in taxon is recorded as Homo sapiens[10].
- RCBTB1's genetic association is recorded as retinal dystrophy with or without extraocular anomalies[11].
- RCBTB1's exact match is recorded as http://identifiers.org/ncbigene/55213[12].
Why It Matters
RCBTB1 is known by 6 alternative names across languages and contexts.[2]