KLHL29
protein-coding gene in the species Homo sapiens
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KLHL29
Summary
KLHL29 is a gene[1].
Key Facts
- KLHL29's instance of is recorded as gene[2].
- KLHL29 is a type of protein-coding gene[3].
- KLHL29's HomoloGene ID is recorded as 66272[4].
- KLHL29's genomic start is recorded as 23608088[5].
- KLHL29's genomic start is recorded as 23385179[6].
- KLHL29's genomic end is recorded as 23708611[7].
- KLHL29's genomic end is recorded as 23931481[8].
- KLHL29's ortholog is recorded as Klhl29[9].
- KLHL29's ortholog is recorded as Klhl29[10].
- KLHL29's ortholog is recorded as LOC100334314[11].
- KLHL29's encodes is recorded as Kelch like family member 29[12].
- KLHL29's found in taxon is recorded as Homo sapiens[13].
- KLHL29's chromosome is recorded as human chromosome 2[14].
- KLHL29's genetic association is recorded as coronary artery disease[15].
- KLHL29's strand orientation is recorded as forward strand[16].
- KLHL29's exact match is recorded as http://identifiers.org/ncbigene/114818[17].
- KLHL29's cytogenetic location is recorded as 2p24.1[18].
- KLHL29's expressed in is recorded as tibia[19].
- KLHL29's expressed in is recorded as middle temporal gyrus[20].
- KLHL29's expressed in is recorded as sural nerve[21].
- KLHL29's expressed in is recorded as Brodmann area 23[22].
- KLHL29's expressed in is recorded as synovial joint[23].
- KLHL29's expressed in is recorded as retinal pigment epithelium[24].
- KLHL29's expressed in is recorded as trigeminal ganglion[25].
- KLHL29's expressed in is recorded as lateral nuclear group of thalamus[26].