LOXL1
protein-coding gene in the species Homo sapiens
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LOXL1
Summary
LOXL1 is a gene[1]. LOXL1 is known by 4 alternative names across languages and contexts.[2]
Key Facts
- LOXL1's instance of is recorded as gene[3].
- LOXL1 is a type of protein-coding gene[4].
- LOXL1's Commons category is recorded as LOXL1[5].
- LOXL1's HomoloGene ID is recorded as 4074[6].
- LOXL1's ortholog is recorded as Loxl1[7].
- LOXL1's ortholog is recorded as Loxl1[8].
- LOXL1's ortholog is recorded as loxl1[9].
- LOXL1's encodes is recorded as Lysyl oxidase like 1[10].
- LOXL1's found in taxon is recorded as Homo sapiens[11].
- LOXL1's genetic association is recorded as exfoliation syndrome[12].
- LOXL1's exact match is recorded as http://identifiers.org/ncbigene/4016[13].
- LOXL1's cytogenetic location is recorded as 15q24.1[14].
- LOXL1's expressed in is recorded as thoracic aorta[15].
- LOXL1's expressed in is recorded as ascending aorta[16].
- LOXL1's expressed in is recorded as stromal cell of endometrium[17].
- LOXL1's expressed in is recorded as right coronary artery[18].
- LOXL1's expressed in is recorded as urethra[19].
- LOXL1's expressed in is recorded as left coronary artery[20].
- LOXL1's expressed in is recorded as saphenous vein[21].
- LOXL1's expressed in is recorded as retinal pigment epithelium[22].
- LOXL1's expressed in is recorded as gallbladder[23].
- LOXL1's expressed in is recorded as anterior pituitary[24].
Why It Matters
LOXL1 is known by 4 alternative names across languages and contexts.[2]