OFD1
protein-coding gene in the species Homo sapiens
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OFD1
Summary
OFD1 is a gene[1].
Key Facts
- OFD1's instance of is recorded as gene[2].
- OFD1 is a type of protein-coding gene[3].
- OFD1's HomoloGene ID is recorded as 2677[4].
- OFD1's genomic start is recorded as 13752832[5].
- OFD1's genomic start is recorded as 13734743[6].
- OFD1's genomic end is recorded as 13787480[7].
- OFD1's genomic end is recorded as 13777955[8].
- OFD1's ortholog is recorded as Ofd1[9].
- OFD1's ortholog is recorded as Ofd1[10].
- OFD1's ortholog is recorded as ofd1[11].
- OFD1's encodes is recorded as OFD1[12].
- OFD1's found in taxon is recorded as Homo sapiens[13].
- OFD1's chromosome is recorded as human X chromosome[14].
- OFD1's genetic association is recorded as Joubert syndrome 10[15].
- OFD1's genetic association is recorded as retinitis pigmentosa 23[16].
- OFD1's genetic association is recorded as ciliopathy[17].
- OFD1's genetic association is recorded as Simpson-Golabi-Behmel syndrome type 2[18].
- OFD1's genetic association is recorded as orofaciodigital syndrome I[19].
- OFD1's genetic association is recorded as Joubert syndrome with orofaciodigital defect[20].
- OFD1's strand orientation is recorded as forward strand[21].
- OFD1's exact match is recorded as http://identifiers.org/ncbigene/8481[22].
- OFD1's cytogenetic location is recorded as Xp22.2[23].
- OFD1's expressed in is recorded as sperm[24].
- OFD1's expressed in is recorded as bronchial epithelial cell[25].
- OFD1's expressed in is recorded as right uterine tube[26].