MEGF8
protein-coding gene in the species Homo sapiens
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MEGF8
Summary
MEGF8 is a gene[1].
Key Facts
- MEGF8's instance of is recorded as gene[2].
- MEGF8 is a type of protein-coding gene[3].
- MEGF8's HomoloGene ID is recorded as 15988[4].
- MEGF8's genomic start is recorded as 42325609[5].
- MEGF8's genomic start is recorded as 42829761[6].
- MEGF8's genomic end is recorded as 42378769[7].
- MEGF8's genomic end is recorded as 42882921[8].
- MEGF8's ortholog is recorded as Megf8[9].
- MEGF8's ortholog is recorded as Megf8[10].
- MEGF8's ortholog is recorded as Megf8[11].
- MEGF8's ortholog is recorded as megf8[12].
- MEGF8's encodes is recorded as Multiple EGF like domains 8[13].
- MEGF8's encodes is recorded as Multiple epidermal growth factor-like domains protein 8[14].
- MEGF8's found in taxon is recorded as Homo sapiens[15].
- MEGF8's chromosome is recorded as human chromosome 19[16].
- MEGF8's genetic association is recorded as Carpenter syndrome[17].
- MEGF8's strand orientation is recorded as forward strand[18].
- MEGF8's exact match is recorded as http://identifiers.org/ncbigene/1954[19].
- MEGF8's cytogenetic location is recorded as 19q13.2[20].
- MEGF8's expressed in is recorded as middle temporal gyrus[21].
- MEGF8's expressed in is recorded as prefrontal cortex[22].
- MEGF8's expressed in is recorded as right frontal lobe[23].
- MEGF8's expressed in is recorded as tendon of biceps brachii[24].
- MEGF8's expressed in is recorded as frontal pole[25].
- MEGF8's expressed in is recorded as primary visual cortex[26].