CEP120
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CEP120
Summary
CEP120 is a gene[1]. CEP120 is known by 5 alternative names across languages and contexts.[2]
Key Facts
- CEP120's instance of is recorded as gene[3].
- CEP120 is a type of protein-coding gene[4].
- CEP120's HomoloGene ID is recorded as 27415[5].
- CEP120's genomic start is recorded as 123344885[6].
- CEP120's genomic start is recorded as 122680579[7].
- CEP120's genomic end is recorded as 123423592[8].
- CEP120's genomic end is recorded as 122759286[9].
- CEP120's ortholog is recorded as Cep120[10].
- CEP120's ortholog is recorded as Cep120[11].
- CEP120's ortholog is recorded as cep120[12].
- CEP120's encodes is recorded as Centrosomal protein 120[13].
- CEP120's found in taxon is recorded as Homo sapiens[14].
- CEP120's chromosome is recorded as human chromosome 5[15].
- CEP120's genetic association is recorded as short-rib thoracic dysplasia 13 with or without polydactyly[16].
- CEP120's genetic association is recorded as Joubert syndrome 31[17].
- CEP120's genetic association is recorded as Joubert syndrome[18].
- CEP120's strand orientation is recorded as reverse strand[19].
- CEP120's exact match is recorded as http://identifiers.org/ncbigene/153241[20].
- CEP120's cytogenetic location is recorded as 5q23.2[21].
- CEP120's expressed in is recorded as Achilles tendon[22].
- CEP120's expressed in is recorded as pancreatic epithelial cell[23].
- CEP120's expressed in is recorded as mucosa of paranasal sinus[24].
- CEP120's expressed in is recorded as thymus[25].
- CEP120's expressed in is recorded as germinal epithelium[26].
- CEP120's expressed in is recorded as superficial temporal artery[27].
Why It Matters
CEP120 is known by 5 alternative names across languages and contexts.[2]