CWF19L1
protein-coding gene in the species Homo sapiens
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CWF19L1
Summary
CWF19L1 is a gene[1].
Key Facts
- CWF19L1's instance of is recorded as gene[2].
- CWF19L1 is a type of protein-coding gene[3].
- CWF19L1's HomoloGene ID is recorded as 41244[4].
- CWF19L1's genomic start is recorded as 100232298[5].
- CWF19L1's genomic start is recorded as 101992055[6].
- CWF19L1's genomic end is recorded as 100267680[7].
- CWF19L1's genomic end is recorded as 102027437[8].
- CWF19L1's ortholog is recorded as Cwf19l1[9].
- CWF19L1's ortholog is recorded as Cwf19l1[10].
- CWF19L1's ortholog is recorded as cwf19l1[11].
- CWF19L1's ortholog is recorded as CG7741[12].
- CWF19L1's ortholog is recorded as cwf-19L1[13].
- CWF19L1's encodes is recorded as CWF19 like cell cycle control factor 1[14].
- CWF19L1's found in taxon is recorded as Homo sapiens[15].
- CWF19L1's chromosome is recorded as human chromosome 10[16].
- CWF19L1's genetic association is recorded as autosomal recessive spinocerebellar ataxia 17[17].
- CWF19L1's strand orientation is recorded as reverse strand[18].
- CWF19L1's exact match is recorded as http://identifiers.org/ncbigene/55280[19].
- CWF19L1's cytogenetic location is recorded as 10q24.31[20].
- CWF19L1's expressed in is recorded as monocyte[21].
- CWF19L1's expressed in is recorded as bone marrow[22].
- CWF19L1's expressed in is recorded as granulocyte[23].
- CWF19L1's expressed in is recorded as blood[24].
- CWF19L1's expressed in is recorded as skin of leg[25].
- CWF19L1's expressed in is recorded as right testis[26].