SAMSN1
protein-coding gene in the species Homo sapiens
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Summary
SAMSN1 is a gene[1].
Key Facts
- SAMSN1's instance of is recorded as gene[2].
- SAMSN1 is a type of protein-coding gene[3].
- SAMSN1's HomoloGene ID is recorded as 11148[4].
- SAMSN1's genomic start is recorded as 14485228[5].
- SAMSN1's genomic start is recorded as 15857549[6].
- SAMSN1's genomic end is recorded as 15955723[7].
- SAMSN1's genomic end is recorded as 14658821[8].
- SAMSN1's ortholog is recorded as Samsn1[9].
- SAMSN1's ortholog is recorded as Samsn1[10].
- SAMSN1's ortholog is recorded as samsn1b[11].
- SAMSN1's encodes is recorded as SAM domain, SH3 domain and nuclear localization signals 1[12].
- SAMSN1's found in taxon is recorded as Homo sapiens[13].
- SAMSN1's chromosome is recorded as human chromosome 21[14].
- SAMSN1's strand orientation is recorded as reverse strand[15].
- SAMSN1's exact match is recorded as http://identifiers.org/ncbigene/64092[16].
- SAMSN1's cytogenetic location is recorded as 21q11.2[17].
- SAMSN1's expressed in is recorded as bone marrow[18].
- SAMSN1's expressed in is recorded as appendix[19].
- SAMSN1's expressed in is recorded as bone marrow cell[20].
- SAMSN1's expressed in is recorded as monocyte[21].
- SAMSN1's expressed in is recorded as right lung[22].
- SAMSN1's expressed in is recorded as blood[23].
- SAMSN1's expressed in is recorded as spleen[24].
- SAMSN1's expressed in is recorded as lymph node[25].
- SAMSN1's expressed in is recorded as epithelium of nasopharynx[26].