FAM89B
protein-coding gene in the species Homo sapiens
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FAM89B
Summary
FAM89B is a gene[1].
Key Facts
- FAM89B's instance of is recorded as gene[2].
- FAM89B is a type of protein-coding gene[3].
- FAM89B's HomoloGene ID is recorded as 18749[4].
- FAM89B's genomic start is recorded as 65572349[5].
- FAM89B's genomic start is recorded as 65339820[6].
- FAM89B's genomic end is recorded as 65574198[7].
- FAM89B's genomic end is recorded as 65341669[8].
- FAM89B's ortholog is recorded as Fam89b[9].
- FAM89B's ortholog is recorded as Fam89b[10].
- FAM89B's ortholog is recorded as fam89b[11].
- FAM89B's encodes is recorded as Family with sequence similarity 89 member B[12].
- FAM89B's found in taxon is recorded as Homo sapiens[13].
- FAM89B's chromosome is recorded as human chromosome 11[14].
- FAM89B's strand orientation is recorded as forward strand[15].
- FAM89B's exact match is recorded as http://identifiers.org/ncbigene/23625[16].
- FAM89B's cytogenetic location is recorded as 11q13.1[17].
- FAM89B's expressed in is recorded as muscle of thigh[18].
- FAM89B's expressed in is recorded as gastrocnemius muscle[19].
- FAM89B's expressed in is recorded as right coronary artery[20].
- FAM89B's expressed in is recorded as granulocyte[21].
- FAM89B's expressed in is recorded as ganglionic eminence[22].
- FAM89B's expressed in is recorded as monocyte[23].
- FAM89B's expressed in is recorded as apex of heart[24].
- FAM89B's expressed in is recorded as thoracic aorta[25].
- FAM89B's expressed in is recorded as ascending aorta[26].