ENSMUSG00000038567
 Mus musculus | |
Features
Gene ID: | ENSMUSG00000038567 | | | Biological name : | Cyp24a1 | | | Synonyms : | 1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial / Cyp24a1 / Q64441 | | | Possible biological names infered from orthology : | cytochrome P450 family 24 subfamily A member 1 / Q07973 | | | Species: | Mus musculus | | | Chr. number: | 2 | Strand: | -1 | Band: | H3 | Gene start: | 170482708 | Gene end: | 170497145 | | | Corresponding Affymetrix probe sets: | 10490080 (MoGene1.0st) 1418866_at (Mouse Genome 430 2.0 Array) 1418867_at (Mouse Genome 430 2.0 Array) | | | Cross references: | Ensembl peptide - ENSMUSP00000047954 NCBI entrez gene - 13081
See in Manteia.
MGI - MGI:88593 RefSeq - NM_009996 RefSeq Peptide - NP_034126 swissprot - Q3TWW0 swissprot - Q64441 Ensembl - ENSMUSG00000038567
| | | See expression report in BioGPS See gene description in Wikigenes See co-cited genes in PubMed
Ortholog prediction (from Ensembl)
Paralog prediction (from Ensembl)
Q9DBG1 / Cyp27a1 / Sterol 26-hydroxylase, mitochondrial / Q02318* / cytochrome P450 family 27 subfamily A member 1* | ENSMUSG00000026170 | 30 | O35084 / Cyp27b1 / 25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial / O15528* / cytochrome P450 family 27 subfamily B member 1* | ENSMUSG00000006724 | 29 | Cyp11b2 / cytochrome P450, family 11, subfamily b, polypeptide 2 / P19099* / P15538* / CYP11B1* / cytochrome P450 family 11 subfamily B member 1* / cytochrome P450 family 11 subfamily B member 2* | ENSMUSG00000022589 | 24 | Cyp11b1 / cytochrome P450, family 11, subfamily b, polypeptide 1 / P15538* / P19099* / CYP11B2* / cytochrome P450 family 11 subfamily B member 2* / cytochrome P450 family 11 subfamily B member 1* | ENSMUSG00000075604 | 24 | Q9QZ82 / Cyp11a1 / Cholesterol side-chain cleavage enzyme, mitochondrial / P05108* / cytochrome P450 family 11 subfamily A member 1* | ENSMUSG00000032323 | 23 | Q64464 / Cyp3a13 / Cytochrome P450 3A13 / Q9HB55* / CYP3A4* / CYP3A5* / CYP3A7* / P08684* / P20815* / P24462* / CYP3A43* / CYP3A7-CYP3A51P* / CYP3A7-CYP3A51P readthrough* / cytochrome P450... | ENSMUSG00000029727 | 21 | Cyp3a44 / cytochrome P450, family 3, subfamily a, polypeptide 44 / CYP3A4* / CYP3A5* / CYP3A7* / P08684* / P20815* / P24462* / Q9HB55* / CYP3A43* / CYP3A7-CYP3A51P* / CYP3A7-CYP3A51P readth... | ENSMUSG00000054417 | 20 | Q64459 / Cyp3a11 / Cytochrome P450 3A11 / Q9HB55* / CYP3A4* / CYP3A5* / CYP3A7* / P08684* / P20815* / P24462* / CYP3A43* / CYP3A7-CYP3A51P* / CYP3A7-CYP3A51P readthrough* / cytochrome P450... | ENSMUSG00000056035 | 20 | Q9JMA7 / Cyp3a41a / Cytochrome P450 3A41 / CYP3A4* / CYP3A5* / CYP3A7* / P08684* / P20815* / P24462* / Q9HB55* / CYP3A43* / CYP3A7-CYP3A51P* / CYP3A7-CYP3A51P readthrough* / cytochrome P45... | ENSMUSG00000075551 | 20 | Q9JMA7 / Cyp3a41b / Cytochrome P450 3A41 / CYP3A4* / CYP3A5* / CYP3A7* / P08684* / P20815* / P24462* / Q9HB55* / CYP3A43* / CYP3A7-CYP3A51P* / CYP3A7-CYP3A51P readthrough* / cytochrome P45... | ENSMUSG00000075552 | 20 | Q9WVK8 / Cyp46a1 / Cholesterol 24-hydroxylase / Q9Y6A2* / cytochrome P450 family 46 subfamily A member 1* | ENSMUSG00000021259 | 19 | O09158 / Cyp3a25 / Cytochrome P450 3A25 / Q9HB55* / CYP3A4* / CYP3A5* / CYP3A7* / P08684* / P20815* / P24462* / CYP3A43* / CYP3A7-CYP3A51P* / CYP3A7-CYP3A51P readthrough* / cytochrome P450... | ENSMUSG00000029630 | 19 | Q64481 / Cyp3a16 / Cytochrome P450 3A16 / Q9HB55* / CYP3A4* / CYP3A5* / CYP3A7* / P08684* / P20815* / P24462* / CYP3A43* / CYP3A7-CYP3A51P* / CYP3A7-CYP3A51P readthrough* / cytochrome P450... | ENSMUSG00000038656 | 19 | Cyp3a57 / cytochrome P450, family 3, subfamily a, polypeptide 57 / CYP3A4* / CYP3A5* / CYP3A7* / P08684* / P20815* / P24462* / Q9HB55* / CYP3A43* / CYP3A7-CYP3A51P* / CYP3A7-CYP3A51P readth... | ENSMUSG00000070419 | 19 | Cyp3a59 / cytochrome P450, family 3, subfamily a, polypeptide 59 / CYP3A4* / CYP3A5* / CYP3A7* / P08684* / P20815* / P24462* / Q9HB55* / CYP3A43* / CYP3A7-CYP3A51P* / CYP3A7-CYP3A51P readth... | ENSMUSG00000061292 | 18 | P36423 / Tbxas1 / thromboxane A synthase 1, platelet / P24557* / thromboxane A synthase 1* | ENSMUSG00000029925 | 17 |
Protein motifs (from Interpro)
Gene Ontology (GO)
Pathways (from Reactome)
Phenotype (from MGI, Zfin or HPO)
MP:0000194 | hypercalcemia | "abnormally high concentration of calcium ions in the circulating blood " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Atp2b2wri/Atp2b2wri Genetic Background: involves: BALB/cAnN
| MP:0001265 | reduced body size | "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170] |
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Allelic Composition: Atp2b2wri/Atp2b2wri Genetic Background: involves: BALB/cAnN
| MP:0002082 | postnatal lethality | "premature death anytime after postnatal day 1 to weaning age (3 weeks)" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Atp2b2wri/Atp2b2wri Genetic Background: involves: BALB/cAnN
| MP:0002135 | abnormal kidney morphology | "abnormal development of the kidney resulting in structural abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Atp2b2wri/Atp2b2wri Genetic Background: involves: BALB/cAnN
| MP:0002705 | dilated renal tubules | "enlarged lumens of the loops of Henle and/or collecting ducts of the kidney" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Atp2b2wri/Atp2b2wri Genetic Background: involves: BALB/cAnN
| MP:0005441 | hypercalciuria | "excretion of abnormally large amounts of calcium in the urine" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:86949] |
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Allelic Composition: Atp2b2wri/Atp2b2wri Genetic Background: involves: BALB/cAnN
| MP:0008271 | abnormal bone ossification | "any anomaly in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance" [GO:0001503] |
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Allelic Composition: Atp2b2wri/Atp2b2wri Genetic Background: involves: BALB/cAnN
| MP:0011228 | abnormal vitamin D level | "any anomaly in the concentration of vitamin D, any of a group of related, fat-soluble compounds that are derived from delta-5,7 steroids and play a central role in calcium metabolism; specific forms of vitamin D include calciferol (ergocalciferol; vitamin D2) and cholecalciferol (calciol; vitamin D3)" [GO:0042368] |
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Allelic Composition: Atp2b2wri/Atp2b2wri Genetic Background: involves: BALB/cAnN
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Interacting proteins (from Reactome) No match
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