IFT88
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IFT88
Summary
IFT88 is a gene[1]. IFT88 ranks in the top 2% of gene entities by monthly Wikipedia readership (6 views/month).[2]
Key Facts
- IFT88's instance of is recorded as gene[3].
- IFT88 is a type of protein-coding gene[4].
- IFT88's HomoloGene ID is recorded as 4761[5].
- IFT88's genomic start is recorded as 21140585[6].
- IFT88's genomic start is recorded as 20567138[7].
- IFT88's genomic end is recorded as 21265503[8].
- IFT88's genomic end is recorded as 20691444[9].
- IFT88's ortholog is recorded as Ift88[10].
- IFT88's ortholog is recorded as Ift88[11].
- IFT88's ortholog is recorded as nompB[12].
- IFT88's ortholog is recorded as osm-5[13].
- IFT88's ortholog is recorded as ift88[14].
- IFT88's encodes is recorded as Intraflagellar transport 88[15].
- IFT88's encodes is recorded as Intraflagellar transport protein 88 homolog[16].
- IFT88's found in taxon is recorded as Homo sapiens[17].
- IFT88's chromosome is recorded as human chromosome 13[18].
- IFT88's genetic association is recorded as bipolar disorder[19].
- IFT88's genetic association is recorded as schizophrenia[20].
- IFT88's genetic association is recorded as depression[21].
- IFT88's strand orientation is recorded as forward strand[22].
- IFT88's exact match is recorded as http://identifiers.org/ncbigene/8100[23].
Why It Matters
IFT88 ranks in the top 2% of gene entities by monthly Wikipedia readership (6 views/month).[2] IFT88 is known by 7 alternative names across languages and contexts.[24]