SNX10
protein-coding gene in the species Homo sapiens
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SNX10
Summary
SNX10 is a gene[1].
Key Facts
- SNX10's instance of is recorded as gene[2].
- SNX10 is a type of protein-coding gene[3].
- SNX10's HomoloGene ID is recorded as 32171[4].
- SNX10's genomic start is recorded as 26331541[5].
- SNX10's genomic start is recorded as 26291862[6].
- SNX10's genomic end is recorded as 26413949[7].
- SNX10's genomic end is recorded as 26374383[8].
- SNX10's ortholog is recorded as Snx10[9].
- SNX10's ortholog is recorded as Snx10[10].
- SNX10's ortholog is recorded as snx10a[11].
- SNX10's ortholog is recorded as snx10b[12].
- SNX10's encodes is recorded as Sorting nexin 10[13].
- SNX10's encodes is recorded as Sorting nexin 10[14].
- SNX10's found in taxon is recorded as Homo sapiens[15].
- SNX10's chromosome is recorded as human chromosome 7[16].
- SNX10's genetic association is recorded as autosomal recessive osteopetrosis 8[17].
- SNX10's genetic association is recorded as Malignant infantile osteopetrosis[18].
- SNX10's strand orientation is recorded as forward strand[19].
- SNX10's exact match is recorded as http://identifiers.org/ncbigene/29887[20].
- SNX10's cytogenetic location is recorded as 7p15.2[21].
- SNX10's expressed in is recorded as lateral nuclear group of thalamus[22].
- SNX10's expressed in is recorded as pars compacta[23].
- SNX10's expressed in is recorded as pars reticulata[24].
- SNX10's expressed in is recorded as pons[25].
- SNX10's expressed in is recorded as monocyte[26].