G KYNU | |||
Description: kynureninase Associations 76 Studies 53 |
T DCXR/KYNU protein level ratio in blood OBA_2054068 | |||
A compound attribute that is the ratio of amount of L-xylulose reductase (human) in blood to amount of kynureninase (human) in blood. Associations 2 Studies 1 |
T KYNU/SCLY protein level ratio in blood OBA_2055544 | |||
A compound attribute that is the ratio of amount of kynureninase (human) in blood to amount of selenocysteine lyase (human) in blood. Associations 3 Studies 1 |
T ACY1/KYNU protein level ratio in blood OBA_2055784 | |||
A compound attribute that is the ratio of amount of aminoacylase-1 (human) in blood to amount of kynureninase (human) in blood. Associations 0 Studies 1 |
T ADH4/KYNU protein level ratio in blood OBA_2053758 | |||
A compound attribute that is the ratio of amount of all-trans-retinol dehydrogenase [NAD(+)] ADH4 (human) in blood to amount of kynureninase (human) in blood. Associations 1 Studies 1 |
V rs352889 | |||
Location: 2:143002122 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs9013 | |||
Location: 2:143040620 Cytogenetic region:2q22.2 Most severe consequence: Missense variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs3768844 | |||
Location: 2:143039125 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 2 Studies 2 |
V rs3816193 | |||
Location: 2:143042338 Cytogenetic region:2q22.2 Most severe consequence: 3 prime utr variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs16858410 | |||
Location: 2:142962382 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs77035103 | |||
Location: 2:142878150 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs78201785 | |||
Location: 2:142917663 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs7425446 | |||
Location: 2:143019929 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs60431337 | |||
Location: 2:143032297 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 4 Studies 4 |
V rs59441438 | |||
Location: 2:143044106 Cytogenetic region:2q22.2 Most severe consequence: 3 prime utr variant Mapped gene(s): KYNU Associations 4 Studies 4 |
V rs12477146 | |||
Location: 2:143036245 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs352890 | |||
Location: 2:143001888 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs201957970 | |||
Location: 2:143043760 Cytogenetic region:2q22.2 Most severe consequence: 3 prime utr variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs199546957 | |||
Location: 2:143042078 Cytogenetic region:2q22.2 Most severe consequence: Missense variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs1371516 | |||
Location: 2:142991224 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs2043931 | |||
Location: 2:143038112 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs11678380 | |||
Location: 2:143030653 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs73961715 | |||
Location: 2:143046278 Cytogenetic region:2q22.2 Most severe consequence: 3 prime utr variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs354687 | |||
Location: 2:143043175 Cytogenetic region:2q22.2 Most severe consequence: 3 prime utr variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs17808482 | |||
Location: 2:143033224 Cytogenetic region:2q22.2 Most severe consequence: Splice polypyrimidine tract variant Mapped gene(s): KYNU Associations 2 Studies 2 |
V rs352925 | |||
Location: 2:143020781 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs3845642 | |||
Location: 2:143041434 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs2083189 | |||
Location: 2:142907166 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs73961713 | |||
Location: 2:143043636 Cytogenetic region:2q22.2 Most severe consequence: 3 prime utr variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs352931 | |||
Location: 2:143017266 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 2 Studies 2 |
V rs150818198 | |||
Location: 2:143030220 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs71423227 | |||
Location: 2:142972005 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs182808856 | |||
Location: 2:142990451 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs183916915 | |||
Location: 2:143016892 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs115952468 | |||
Location: 2:143046374 Cytogenetic region:2q22.2 Most severe consequence: 3 prime utr variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs12993448 | |||
Location: 2:142968486 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs74390986 | |||
Location: 2:142987885 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs62169949 | |||
Location: 2:143030652 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs16858549 | |||
Location: 2:143043227 Cytogenetic region:2q22.2 Most severe consequence: 3 prime utr variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs187469176 | |||
Location: 2:143037422 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs74847330 | |||
Location: 2:143074030 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 14 Studies 14 |
V rs79645820 | |||
Location: 2:143086939 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs112376172 (rs756711255) | |||
Location: 2:143017146 Cytogenetic region:2q22.2 Most severe consequence: Intron variant Mapped gene(s): KYNU Associations 1 Studies 1 |
V rs139354053 | |||
Location: 2:142874099 Cytogenetic region:2q22.2 Most severe consequence: Regulatory region variant Mapped gene(s): RRN3P4,KYNU Associations 1 Studies 1 |
V rs114960420 | |||
Location: 2:143057159 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs80055389 | |||
Location: 2:143061536 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs76089189 | |||
Location: 2:143064481 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs78776446 | |||
Location: 2:143064911 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs143910373 | |||
Location: 2:143074716 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs114260278 | |||
Location: 2:143080790 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs115457883 | |||
Location: 2:143056563 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs75241114 | |||
Location: 2:143066161 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs74478510 | |||
Location: 2:143077639 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs114081378 | |||
Location: 2:143081995 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs79246999 | |||
Location: 2:143084068 Cytogenetic region:2q22.2 Most severe consequence: Regulatory region variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs116072987 | |||
Location: 2:143089788 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs79836088 | |||
Location: 2:143074878 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs79256433 | |||
Location: 2:143083328 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
V rs1561542 | |||
Location: 2:143088180 Cytogenetic region:2q22.2 Most severe consequence: Intergenic variant Mapped gene(s): ARHGAP15,KYNU Associations 1 Studies 1 |
T kynureninase measurement EFO_0008201 | |||
quantification of the amount of kynureninase in a sample Associations 37 Studies 10 |
T blood protein measurement EFO_0007937 | |||
quantification of the levels of some protein in a blood sample Associations 20444 Studies 8346 |