CNGB3
protein-coding gene in the species Homo sapiens
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CNGB3
Summary
CNGB3 is a gene[1].
Key Facts
- CNGB3's instance of is recorded as gene[2].
- CNGB3 is a type of protein-coding gene[3].
- CNGB3's Commons category is recorded as Cyclic nucleotide gated channel beta 3[4].
- CNGB3's HomoloGene ID is recorded as 40908[5].
- CNGB3's genomic start is recorded as 86553977[6].
- CNGB3's genomic start is recorded as 87566205[7].
- CNGB3's genomic end is recorded as 86743675[8].
- CNGB3's genomic end is recorded as 87755903[9].
- CNGB3's ortholog is recorded as Cngb3[10].
- CNGB3's ortholog is recorded as Cngb3[11].
- CNGB3's ortholog is recorded as LOC562466[12].
- CNGB3's ortholog is recorded as cngb3.1[13].
- CNGB3's encodes is recorded as Cyclic nucleotide gated channel subunit beta 3[14].
- CNGB3's found in taxon is recorded as Homo sapiens[15].
- CNGB3's chromosome is recorded as human chromosome 8[16].
- CNGB3's genetic association is recorded as Stargardt disease[17].
- CNGB3's genetic association is recorded as achromatopsia 3[18].
- CNGB3's genetic association is recorded as achromatopsia[19].
- CNGB3's strand orientation is recorded as reverse strand[20].
- CNGB3's exact match is recorded as http://identifiers.org/ncbigene/54714[21].
- CNGB3's cytogenetic location is recorded as 8q21.3[22].
- CNGB3's expressed in is recorded as testicle[23].
- CNGB3's expressed in is recorded as retinal pigment epithelium[24].
- CNGB3's expressed in is recorded as gonad[25].
- CNGB3's expressed in is recorded as Achilles tendon[26].