EFNB1
protein-coding gene in the species Homo sapiens
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EFNB1
Summary
EFNB1 is a gene[1].
Key Facts
- EFNB1's instance of is recorded as gene[2].
- EFNB1 is a type of protein-coding gene[3].
- EFNB1's HomoloGene ID is recorded as 3263[4].
- EFNB1's genomic start is recorded as 68048840[5].
- EFNB1's genomic start is recorded as 68829021[6].
- EFNB1's genomic end is recorded as 68061990[7].
- EFNB1's genomic end is recorded as 68842160[8].
- EFNB1's ortholog is recorded as Efnb1[9].
- EFNB1's ortholog is recorded as Efnb1[10].
- EFNB1's ortholog is recorded as efnb1[11].
- EFNB1's encodes is recorded as Ephrin B1[12].
- EFNB1's found in taxon is recorded as Homo sapiens[13].
- EFNB1's chromosome is recorded as human X chromosome[14].
- EFNB1's genetic association is recorded as craniofrontonasal dysplasia[15].
- EFNB1's strand orientation is recorded as forward strand[16].
- EFNB1's exact match is recorded as http://identifiers.org/ncbigene/1947[17].
- EFNB1's cytogenetic location is recorded as Xq13.1[18].
- EFNB1's expressed in is recorded as ventricular zone[19].
- EFNB1's expressed in is recorded as right lung[20].
- EFNB1's expressed in is recorded as ganglionic eminence[21].
- EFNB1's expressed in is recorded as mucosa of transverse colon[22].
- EFNB1's expressed in is recorded as skin of abdomen[23].
- EFNB1's expressed in is recorded as skin of leg[24].
- EFNB1's expressed in is recorded as upper lobe of left lung[25].
- EFNB1's expressed in is recorded as tibial nerve[26].