ENSMUSG00000066072
Mus musculus | |
Features
Gene ID: | ENSMUSG00000066072 | | | Biological name : | Cyp4a10 | | | Synonyms : | Cyp4a10 / Cytochrome P450 4A10 / O88833 | | | Possible biological names infered from orthology : | CYP4A11 / CYP4A22 / cytochrome P450 family 4 subfamily A member 11 / cytochrome P450 family 4 subfamily A member 22 / Q02928 / Q5TCH4 | | | Species: | Mus musculus | | | Chr. number: | 4 | Strand: | 1 | Band: | D1 | Gene start: | 115518264 | Gene end: | 115533649 | | | Corresponding Affymetrix probe sets: | 10507163 (MoGene1.0st) 10507177 (MoGene1.0st) 1424853_s_at (Mouse Genome 430 2.0 Array) | | | Cross references: | Ensembl peptide - ENSMUSP00000092486 Ensembl peptide - ENSMUSP00000061126 NCBI entrez gene - 13117
See in Manteia.
MGI - MGI:88611 RefSeq - NM_010011 RefSeq Peptide - NP_034141 swissprot - A2A977 swissprot - O88833 Ensembl - ENSMUSG00000066072
| | | See expression report in BioGPS See gene description in Wikigenes See co-cited genes in PubMed
Ortholog prediction (from Ensembl)
Paralog prediction (from Ensembl)
Cyp4a32 / cytochrome P450, family 4, subfamily a, polypeptide 32 / Q5TCH4* / Q02928* / CYP4A11* / CYP4A22* / cytochrome P450 family 4 subfamily A member 22* / cytochrome P450 family 4 subfa... | ENSMUSG00000063929 | 96 | Cyp4a31 / cytochrome P450, family 4, subfamily a, polypeptide 31 / Q5TCH4* / Q02928* / CYP4A11* / CYP4A22* / cytochrome P450 family 4 subfamily A member 22* / cytochrome P450 family 4 subfa... | ENSMUSG00000028712 | 94 | Cyp4a12b / cytochrome P450, family 4, subfamily a, polypeptide 12B / Q5TCH4* / Q02928* / CYP4A11* / CYP4A22* / cytochrome P450 family 4 subfamily A member 22* / cytochrome P450 family 4 sub... | ENSMUSG00000078597 | 78 | Q91WL5 / Cyp4a12a / Cytochrome P450 4A12A / Q02928* / Q5TCH4* / CYP4A11* / CYP4A22* / cytochrome P450 family 4 subfamily A member 22* / cytochrome P450 family 4 subfamily A member 11* | ENSMUSG00000066071 | 77 | O35728 / Cyp4a14 / Cytochrome P450 4A14 / Q5TCH4* / Q02928* / CYP4A11* / CYP4A22* / cytochrome P450 family 4 subfamily A member 22* / cytochrome P450 family 4 subfamily A member 11* | ENSMUSG00000028715 | 71 | Cyp4a30b / cytochrome P450, family 4, subfamily a, polypeptide 30b / Q5TCH4* / Q02928* / CYP4A11* / CYP4A22* / cytochrome P450 family 4 subfamily A member 22* / cytochrome P450 family 4 sub... | ENSMUSG00000084346 | 69 | Cyp4a29 / cytochrome P450, family 4, subfamily a, polypeptide 29 / Q5TCH4* / Q02928* / CYP4A11* / CYP4A22* / cytochrome P450 family 4 subfamily A member 22* / cytochrome P450 family 4 subfa... | ENSMUSG00000083138 | 69 | Cyp4b1 / Q64462 / Cytochrome P450 4B1 / P13584* / cytochrome P450 family 4 subfamily B member 1* | ENSMUSG00000028713 | 52 | Cyp4x1 / Q6A152 / Cytochrome P450 4X1 / Q8N118* / cytochrome P450 family 4 subfamily X member 1* | ENSMUSG00000047155 | 50 | Q99N16 / Cyp4f18 / Leukotriene-B(4) omega-hydroxylase 2 / CYP4F3* / Q08477* / cytochrome P450 family 4 subfamily F member 3* | ENSMUSG00000003484 | 45 | Cyp4f15 / cytochrome P450, family 4, subfamily f, polypeptide 15 | ENSMUSG00000073424 | 44 | Cyp4f13 / cytochrome P450, family 4, subfamily f, polypeptide 13 | ENSMUSG00000024055 | 44 | Cyp4f40 / cytochrome P450, family 4, subfamily f, polypeptide 40 | ENSMUSG00000090700 | 44 | Cyp4f17 / cytochrome P450, family 4, subfamily f, polypeptide 17 | ENSMUSG00000091586 | 44 | Q9EP75 / Cyp4f14 / Mus musculus cytochrome P450, family 4, subfamily f, polypeptide 14 (Cyp4f14), transcript variant 6, mRNA. | ENSMUSG00000024292 | 44 | Cyp4f16 / cytochrome P450, family 4, subfamily f, polypeptide 16 | ENSMUSG00000048440 | 43 | Cyp4f39 / cytochrome P450, family 4, subfamily f, polypeptide 39 / Q6NT55* / CYP4F22* / cytochrome P450 family 4 subfamily F member 22* | ENSMUSG00000061126 | 42 | Cyp4f37 / cytochrome P450, family 4, subfamily f, polypeptide 37 | ENSMUSG00000062464 | 42 | Q9DBW0 / Cyp4v3 / Cytochrome P450 4V2 / CYP4V2* / Q6ZWL3* / cytochrome P450 family 4 subfamily V member 2* | ENSMUSG00000079057 | 31 |
Protein motifs (from Interpro)
Gene Ontology (GO)
Pathways (from Reactome)
Phenotype (from MGI, Zfin or HPO)
MP:0000231 | hypertension | "sustained high blood pressure at a level that is likely to result in cardiovascular disease and/or other pathological states" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Ednrbtm1Myks/Ednrbtm1Myks Genetic Background: involves: 129P2/OlaHsd
| MP:0000676 | abnormal water content | "more or less than the normal total amount of water retained in the body" [il:Ira Lu, Mouse Genome Informatics Curator] |
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Allelic Composition: Ednrbtm1Myks/Ednrbtm1Myks Genetic Background: involves: 129P2/OlaHsd
| MP:0003620 | decreased urine output | "decreased volume of urine produced and excreted" [ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: Ednrbtm1Myks/Ednrbtm1Myks Genetic Background: involves: 129P2/OlaHsd
| MP:0004217 | salt-sensitive hypertension | "sustained high blood pressure that is maintained with a normal or increase in the amount of salt consumed in the diet; blood pressure may return to normotensive with a low salt diet" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ednrbtm1Myks/Ednrbtm1Myks Genetic Background: involves: 129P2/OlaHsd
| MP:0005618 | decreased potassium excretion | "less than the normal amount of this alkaline metallic element, the most abundant intracellular ion, voided by the kidneys" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, RGD:Rat Genome Database submission] |
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Allelic Composition: Ednrbtm1Myks/Ednrbtm1Myks Genetic Background: involves: 129P2/OlaHsd
| MP:0006144 | increased systolic blood pressure | "abnormal increase in the pressure in the arteries as the heart contracts and pumps blood into the arteries" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Ednrbtm1Myks/Ednrbtm1Myks Genetic Background: involves: 129P2/OlaHsd
| MP:0010109 | abnormal renal sodium reabsorption | "any anomaly in the process by which sodium ions are transported out of the renal tubules back into the bloodstream" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ednrbtm1Myks/Ednrbtm1Myks Genetic Background: involves: 129P2/OlaHsd
| MP:0011442 | abnormal renal sodium ion transport | "any anomaly in the directed movement of sodium ions (Na+) by the kidney" [GO:0003096] |
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Allelic Composition: Ednrbtm1Myks/Ednrbtm1Myks Genetic Background: involves: 129P2/OlaHsd
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Interacting proteins (from Reactome) No match
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