Homo sapiens (human): 3612 Help Entry 3612              CDS       T01001                                  Symbol IMPA1, IMP, IMPA, MRT59 Name (RefSeq) inositol monophosphatase 1   KO K01092   myo-inositol-1(or 4)-monophosphatase [EC:3.1.3.25] Organism hsa  Homo sapiens (human) Pathway hsa00562   Inositol phosphate metabolism hsa01100   Metabolic pathways hsa04070   Phosphatidylinositol signaling system Module hsa_M00131   Inositol phosphate metabolism, Ins(1,3,4,5)P4 => Ins(1,3,4)P3 => myo-inositol Disease H00768   Autosomal recessive intellectual developmental disorder Brite KEGG Orthology (KO) [BR:hsa00001]  09100 Metabolism   09101 Carbohydrate metabolism    00562 Inositol phosphate metabolism     3612 (IMPA1)  09130 Environmental Information Processing   09132 Signal transduction    04070 Phosphatidylinositol signaling system     3612 (IMPA1) Enzymes [BR:hsa01000]  3. Hydrolases   3.1  Acting on ester bonds    3.1.3  Phosphoric-monoester hydrolases     3.1.3.25  inositol-phosphate phosphatase      3612 (IMPA1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Inositol_P Motif Other DBs NCBI-GeneID:  3612 NCBI-ProteinID:  NP_005527 OMIM:  602064 HGNC:  6050 Ensembl:  ENSG00000133731 Pharos:  P29218(Tclin) UniProt:  P29218 A0A024R830 Structure PDB LinkDB All DBs Position 8:complement(81656914..81686325) Genome browser AA seq 277 aa AA seqDB search MADPWQECMDYAVTLARQAGEVVCEAIKNEMNVMLKSSPVDLVTATDQKVEKMLISSIKE KYPSHSFIGEESVAAGEKSILTDNPTWIIDPIDGTTNFVHRFPFVAVSIGFAVNKKIEFG VVYSCVEGKMYTARKGKGAFCNGQKLQVSQQEDITKSLLVTELGSSRTPETVRMVLSNME KLFCIPVHGIRSVGTAAVNMCLVATGGADAYYEMGIHCWDVAGAGIIVTEAGGVLMDVTG GPFDLMSRRVIAANNRILAERIAKEIQVIPLQRDDED NT seq 834 nt NT seq  +upstreamnt  +downstreamnt atggctgatccttggcaggaatgcatggattatgcagtaactctagcaagacaagctgga gaggtagtttgtgaagctataaaaaatgaaatgaatgttatgctgaaaagttctccagtt gatttggtaactgctacggaccaaaaagttgaaaaaatgcttatctcttccataaaggaa aagtatccatctcacagtttcattggtgaagaatctgtggcagctggggaaaaaagtatc ttaaccgacaaccccacatggatcattgaccctattgatggaacaactaactttgtacat agatttccttttgtagctgtttcaattggctttgctgtaaataaaaagatagaatttgga gttgtgtacagttgtgtggaaggcaagatgtacactgccagaaaaggaaaaggtgccttt tgtaatggtcaaaaactacaagtttcacaacaagaagatattaccaaatctctcttggtg actgagttgggctcttccagaacaccagagactgtgagaatggttctttctaatatggaa aagcttttttgcattcctgttcatgggatccggagtgttggaacagcagctgttaatatg tgccttgtggcaactggcggagcagatgcatattatgaaatgggaattcactgctgggat gttgcaggagctggcattattgttactgaagctggtggcgtgctaatggatgttacaggt ggaccatttgatttgatgtcacgaagagtaattgctgcaaataatagaatattagcagaa aggatagctaaagaaattcaggttatacctttgcaacgagacgacgaagattaa

Homo sapiens (human): 3613 Help Entry 3613              CDS       T01001                                  Symbol IMPA2 Name (RefSeq) inositol monophosphatase 2   KO K01092   myo-inositol-1(or 4)-monophosphatase [EC:3.1.3.25] Organism hsa  Homo sapiens (human) Pathway hsa00562   Inositol phosphate metabolism hsa01100   Metabolic pathways hsa04070   Phosphatidylinositol signaling system Module hsa_M00131   Inositol phosphate metabolism, Ins(1,3,4,5)P4 => Ins(1,3,4)P3 => myo-inositol Brite KEGG Orthology (KO) [BR:hsa00001]  09100 Metabolism   09101 Carbohydrate metabolism    00562 Inositol phosphate metabolism     3613 (IMPA2)  09130 Environmental Information Processing   09132 Signal transduction    04070 Phosphatidylinositol signaling system     3613 (IMPA2) Enzymes [BR:hsa01000]  3. Hydrolases   3.1  Acting on ester bonds    3.1.3  Phosphoric-monoester hydrolases     3.1.3.25  inositol-phosphate phosphatase      3613 (IMPA2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Inositol_P Motif Other DBs NCBI-GeneID:  3613 NCBI-ProteinID:  NP_055029 OMIM:  605922 HGNC:  6051 Ensembl:  ENSG00000141401 Pharos:  O14732(Tbio) UniProt:  O14732 Structure PDB LinkDB All DBs Position 18:11981507..12030877 Genome browser AA seq 288 aa AA seqDB search MKPSGEDQAALAAGPWEECFQAAVQLALRAGQIIRKALTEEKRVSTKTSAADLVTETDHL VEDLIISELRERFPSHRFIAEEAAASGAKCVLTHSPTWIIDPIDGTCNFVHRFPTVAVSI GFAVRQELEFGVIYHCTEERLYTGRRGRGAFCNGQRLRVSGETDLSKALVLTEIGPKRDP ATLKLFLSNMERLLHAKAHGVRVIGSSTLALCHLASGAADAYYQFGLHCWDLAAATVIIR EAGGIVIDTSGGPLDLMACRVVAASTREMAMLIAQALQTINYGRDDEK NT seq 867 nt NT seq  +upstreamnt  +downstreamnt atgaagccgagcggcgaggaccaggcggcgctggcggccggcccctgggaggagtgcttc caggcggccgtgcagctggcgctgcgggcaggacagatcatcagaaaagcccttactgag gaaaaacgtgtctcaacaaaaacatcagctgcagatcttgtgacagaaacagatcacctt gtggaagatttaattatttctgagttgcgagagaggtttccttcacacaggttcattgca gaagaggccgcggcttctggggccaagtgtgtgctcacccacagcccgacgtggatcatc gaccccatcgacggcacctgcaattttgtgcacagattcccgactgtggcggttagcatt ggatttgctgttcgacaagagcttgaattcggagtgatttaccactgcacagaggagcgg ctgtacacgggccggcggggtcggggcgccttctgcaatggccagcggctccgggtctcc ggggagacagatctctcaaaggccttggttctgacagaaattggccccaaacgtgaccct gcgaccctgaagctgttcctgagtaacatggagcggctgctgcatgccaaggcgcatggg gtccgagtgattggaagctccacattggcactctgccacctggcctcaggggccgcggat gcctattaccagtttggcctgcactgctgggatctggcggctgccacagtcatcatcaga gaagcaggcggcatcgtgatagacacttcgggtggacccctcgacctcatggcttgcaga gtggttgcggccagcacccgggagatggcgatgctcatagctcaggccttacagacgatt aactatgggcgggatgatgagaagtga

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