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Limb region 1 protein homolog is a protein that in humans is encoded by the LMBR1 gene.
Homeobox protein DLX-3 is a protein that in humans is encoded by the DLX3 gene.
Hermansky–Pudlak syndrome 1 protein is a protein that in humans is encoded by the HPS1 gene.
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Quaking homolog, KH domain RNA binding (mouse), also known as QKI, is a protein which in humans is encoded by the QKI gene.
T-cell leukemia homeobox protein 3 is a protein that in humans is encoded by the TLX3 gene.
Protein O-mannosyl-transferase 1 is an enzyme that in humans is encoded by the POMT1 gene. It is a member of the dolichyl-phosphate-mannose-protein mannosyltransferases.
Hermansky–Pudlak syndrome 4 protein is a protein that in humans is encoded by the HPS4 gene.
CD160 antigen is a protein that in humans is encoded by the CD160 gene.
DnaJ (Hsp40) homolog, subfamily C, member 13, also known as DNAJC13, is a human gene.
Protein cappuccino homolog is a protein that in humans is encoded by the CNO gene.
Neuralized-like protein 1 is a protein that in humans is encoded by the NEURL gene.
Bardet–Biedl syndrome 7 is a protein that in humans is encoded by the BBS7 gene.
Hermansky–Pudlak syndrome 6 (HPS6), also known as ruby-eye protein homolog (Ru), is a protein that in humans is encoded by the HPS6 gene.
Integrin alpha-10 also known as ITGA10 is a protein that in humans is encoded by the ITGA10 gene.
Polymerase (RNA) III polypeptide G (32kD)-like also known as POLR3GL is a protein which in humans is encoded by the POLR3GL gene.
N-acetyltransferase ESCO2, also known as establishment of cohesion 1 homolog 2 or ECO1 homolog 2, is an enzyme that in humans is encoded by the ESCO2 gene.
Ubiquinone biosynthesis protein COQ9, mitochondrial, also known as coenzyme Q9 homolog (COQ9), is a protein that in humans is encoded by the COQ9 gene.
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References
- ↑ "Entrez Gene: LIX1L Lix1 homolog (mouse)-like".
- ↑ Strausberg RL, Feingold EA, Grouse LH, et al. (December 2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi: 10.1073/pnas.242603899 . PMC 139241 . PMID 12477932.
- ↑ Klopocki E, Schulze H, Strauss G, et al. (February 2007). "Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome". Am. J. Hum. Genet. 80 (2): 232–40. doi:10.1086/510919. PMC 1785342 . PMID 17236129.
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