RPS29
protein-coding gene in the species Homo sapiens
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RPS29
Summary
RPS29 is a gene[1].
Key Facts
- RPS29's instance of is recorded as gene[2].
- RPS29 is a type of protein-coding gene[3].
- RPS29's HomoloGene ID is recorded as 83197[4].
- RPS29's genomic start is recorded as 49570984[5].
- RPS29's genomic start is recorded as 50043390[6].
- RPS29's genomic end is recorded as 49599164[7].
- RPS29's genomic end is recorded as 50065408[8].
- RPS29's ortholog is recorded as Rps29[9].
- RPS29's ortholog is recorded as Rps29[10].
- RPS29's ortholog is recorded as rps-29[11].
- RPS29's ortholog is recorded as rps29[12].
- RPS29's ortholog is recorded as RpS29[13].
- RPS29's encodes is recorded as Ribosomal protein S29[14].
- RPS29's found in taxon is recorded as Homo sapiens[15].
- RPS29's chromosome is recorded as human chromosome 14[16].
- RPS29's genetic association is recorded as Diamond-Blackfan anemia[17].
- RPS29's strand orientation is recorded as reverse strand[18].
- RPS29's exact match is recorded as http://identifiers.org/ncbigene/6235[19].
- RPS29's cytogenetic location is recorded as 14q21.3[20].
- RPS29's expressed in is recorded as caput epididymis[21].
- RPS29's expressed in is recorded as human penis[22].
- RPS29's expressed in is recorded as parietal pleura[23].
- RPS29's expressed in is recorded as mucosa of sigmoid colon[24].
- RPS29's expressed in is recorded as superficial temporal artery[25].
- RPS29's expressed in is recorded as granulocyte[26].