RIN3
protein-coding gene in the species Homo sapiens
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RIN3
Summary
RIN3 is a gene[1].
Key Facts
- RIN3's instance of is recorded as gene[2].
- RIN3 is a type of protein-coding gene[3].
- RIN3's HomoloGene ID is recorded as 11748[4].
- RIN3's genomic start is recorded as 92980118[5].
- RIN3's genomic start is recorded as 92513781[6].
- RIN3's genomic end is recorded as 92688994[7].
- RIN3's genomic end is recorded as 93155339[8].
- RIN3's ortholog is recorded as Rin3[9].
- RIN3's ortholog is recorded as Rin3[10].
- RIN3's ortholog is recorded as rin3[11].
- RIN3's encodes is recorded as Ras and Rab interactor 3[12].
- RIN3's found in taxon is recorded as Homo sapiens[13].
- RIN3's chromosome is recorded as human chromosome 14[14].
- RIN3's genetic association is recorded as chronic obstructive pulmonary disease[15].
- RIN3's genetic association is recorded as mammary Paget's disease[16].
- RIN3's strand orientation is recorded as forward strand[17].
- RIN3's exact match is recorded as http://identifiers.org/ncbigene/79890[18].
- RIN3's cytogenetic location is recorded as 14q32.12[19].
- RIN3's expressed in is recorded as granulocyte[20].
- RIN3's expressed in is recorded as monocyte[21].
- RIN3's expressed in is recorded as blood[22].
- RIN3's expressed in is recorded as spleen[23].
- RIN3's expressed in is recorded as bone marrow cell[24].
- RIN3's expressed in is recorded as muscle layer of sigmoid colon[25].
- RIN3's expressed in is recorded as right lung[26].