MECP2
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MECP2
Summary
MECP2 is a gene[1]. MECP2 ranks in the top 0.77% of gene entities by monthly Wikipedia readership (215 views/month, #42 of 5,469).[2]
Key Facts
- MECP2's instance of is recorded as gene[3].
- MECP2 is a type of protein-coding gene[4].
- MECP2's HomoloGene ID is recorded as 3657[5].
- MECP2's genomic start is recorded as 154021573[6].
- MECP2's genomic start is recorded as 153287024[7].
- MECP2's genomic end is recorded as 154137103[8].
- MECP2's genomic end is recorded as 153363212[9].
- MECP2's ortholog is recorded as Mecp2[10].
- MECP2's ortholog is recorded as Mecp2[11].
- MECP2's ortholog is recorded as mecp2[12].
- MECP2's encodes is recorded as methyl-CpG binding protein 2[13].
- MECP2's encodes is recorded as Methyl-CpG-binding protein 2[14].
- MECP2's found in taxon is recorded as Homo sapiens[15].
- MECP2's chromosome is recorded as human X chromosome[16].
- MECP2's genetic association is recorded as Angelman syndrome[17].
- MECP2's genetic association is recorded as Rett syndrome[18].
- MECP2's genetic association is recorded as severe neonatal-onset encephalopathy with microcephaly[19].
- MECP2's genetic association is recorded as X-linked intellectual disability-psychosis-macroorchidism syndrome[20].
- MECP2's strand orientation is recorded as reverse strand[21].
- MECP2's exact match is recorded as http://identifiers.org/ncbigene/4204[22].
- MECP2's cytogenetic location is recorded as Xq28[23].
- MECP2's expressed in is recorded as paraflocculus of cerebellum[24].
- MECP2's expressed in is recorded as Brodmann area 10[25].
- MECP2's expressed in is recorded as sural nerve[26].
- MECP2's expressed in is recorded as frontal pole[27].
Why It Matters
MECP2 ranks in the top 0.77% of gene entities by monthly Wikipedia readership (215 views/month, #42 of 5,469).[2] MECP2 has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28] MECP2 is known by 21 alternative names across languages and contexts.[29]