SPTBN2
protein-coding gene in the species Homo sapiens
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SPTBN2
Summary
SPTBN2 is a gene[1]. SPTBN2 ranks in the top 2% of gene entities by monthly Wikipedia readership (9 views/month).[2]
Key Facts
- SPTBN2's instance of is recorded as gene[3].
- SPTBN2 is a type of protein-coding gene[4].
- SPTBN2's HomoloGene ID is recorded as 48482[5].
- SPTBN2's genomic start is recorded as 66452719[6].
- SPTBN2's genomic start is recorded as 66682497[7].
- SPTBN2's genomic end is recorded as 66496697[8].
- SPTBN2's genomic end is recorded as 66744670[9].
- SPTBN2's ortholog is recorded as Sptbn2[10].
- SPTBN2's ortholog is recorded as Sptbn2[11].
- SPTBN2's ortholog is recorded as LOC558044[12].
- SPTBN2's ortholog is recorded as beta-Spec[13].
- SPTBN2's encodes is recorded as Spectrin beta, non-erythrocytic 2[14].
- SPTBN2's found in taxon is recorded as Homo sapiens[15].
- SPTBN2's chromosome is recorded as human chromosome 11[16].
- SPTBN2's genetic association is recorded as spinocerebellar ataxia type 5[17].
- SPTBN2's genetic association is recorded as autosomal recessive spinocerebellar ataxia 14[18].
- SPTBN2's strand orientation is recorded as reverse strand[19].
- SPTBN2's exact match is recorded as http://identifiers.org/ncbigene/6712[20].
- SPTBN2's cytogenetic location is recorded as 11q13.2[21].
- SPTBN2's expressed in is recorded as right hemisphere of cerebellum[22].
- SPTBN2's expressed in is recorded as right frontal lobe[23].
- SPTBN2's expressed in is recorded as skin of leg[24].
- SPTBN2's expressed in is recorded as skin of abdomen[25].
- SPTBN2's expressed in is recorded as ganglionic eminence[26].
- SPTBN2's expressed in is recorded as prefrontal cortex[27].
Why It Matters
SPTBN2 ranks in the top 2% of gene entities by monthly Wikipedia readership (9 views/month).[2] SPTBN2 is known by 5 alternative names across languages and contexts.[28]