ERLIN1
protein-coding gene in the species Homo sapiens
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ERLIN1
Summary
ERLIN1 is a gene[1].
Key Facts
- ERLIN1's instance of is recorded as gene[2].
- ERLIN1 is a type of protein-coding gene[3].
- ERLIN1's HomoloGene ID is recorded as 4716[4].
- ERLIN1's genomic start is recorded as 100150094[5].
- ERLIN1's genomic start is recorded as 101909851[6].
- ERLIN1's genomic end is recorded as 101948091[7].
- ERLIN1's genomic end is recorded as 100186033[8].
- ERLIN1's ortholog is recorded as Erlin1[9].
- ERLIN1's ortholog is recorded as Erlin1[10].
- ERLIN1's ortholog is recorded as erlin1[11].
- ERLIN1's ortholog is recorded as erl-1[12].
- ERLIN1's encodes is recorded as ER lipid raft associated 1[13].
- ERLIN1's encodes is recorded as Erlin-1[14].
- ERLIN1's found in taxon is recorded as Homo sapiens[15].
- ERLIN1's chromosome is recorded as human chromosome 10[16].
- ERLIN1's genetic association is recorded as hereditary spastic paraplegia 62[17].
- ERLIN1's strand orientation is recorded as reverse strand[18].
- ERLIN1's exact match is recorded as http://identifiers.org/ncbigene/10613[19].
- ERLIN1's cytogenetic location is recorded as 10q24.31[20].
- ERLIN1's expressed in is recorded as secondary oocyte[21].
- ERLIN1's expressed in is recorded as palpebral conjunctiva[22].
- ERLIN1's expressed in is recorded as gingival epithelium[23].
- ERLIN1's expressed in is recorded as tibia[24].
- ERLIN1's expressed in is recorded as bronchial epithelial cell[25].
- ERLIN1's expressed in is recorded as trabecular bone[26].