COL2A1
protein-coding gene in the species Homo sapiens
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COL2A1
Summary
COL2A1 is a gene[1].
Key Facts
- COL2A1's instance of is recorded as gene[2].
- COL2A1 is a type of protein-coding gene[3].
- COL2A1's HomoloGene ID is recorded as 55607[4].
- COL2A1's genomic start is recorded as 48366748[5].
- COL2A1's genomic start is recorded as 47972967[6].
- COL2A1's genomic end is recorded as 48398269[7].
- COL2A1's genomic end is recorded as 48004554[8].
- COL2A1's ortholog is recorded as Col2a1[9].
- COL2A1's ortholog is recorded as Col2a1[10].
- COL2A1's ortholog is recorded as col2a1a[11].
- COL2A1's ortholog is recorded as col2a1b[12].
- COL2A1's encodes is recorded as Collagen type II alpha 1 chain[13].
- COL2A1's encodes is recorded as Chondrocalcin[14].
- COL2A1's found in taxon is recorded as Homo sapiens[15].
- COL2A1's chromosome is recorded as human chromosome 12[16].
- COL2A1's genetic association is recorded as spondyloepiphyseal dysplasia congenita[17].
- COL2A1's genetic association is recorded as spondyloepiphyseal dysplasia, Stanescu type[18].
- COL2A1's genetic association is recorded as spondyloepimetaphyseal dysplasia, Strudwick type[19].
- COL2A1's genetic association is recorded as Legg–Calvé–Perthes disease[20].
- COL2A1's genetic association is recorded as Kniest dysplasia[21].
- COL2A1's genetic association is recorded as mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis[22].
- COL2A1's genetic association is recorded as platyspondylic lethal skeletal dysplasia, Torrance type[23].
- COL2A1's genetic association is recorded as multiple epiphyseal dysplasia, Beighton type[24].
- COL2A1's genetic association is recorded as Spondyloperipheral dysplasia[25].
- COL2A1's genetic association is recorded as Czech dysplasia, metatarsal type[26].