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Items: 1 to 20 of 96

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    Name/Gene IDDescriptionLocationAliasesMIM
    ID: 9749
    phosphatase and actin regulator 2 [Homo sapiens (human)]Chromosome 6, NC_000006.12 (143536878..143831185)C6orf56608724
    ID: 56928
    signal peptide peptidase like 2B [Homo sapiens (human)]Chromosome 19, NC_000019.10 (2328684..2355095)IMP-4, IMP4, PSH4, PSL1608239
    ID: 51690
    LSM7 homolog, U6 small nuclear RNA and mRNA degradation associated [Homo sapiens (human)]Chromosome 19, NC_000019.10 (2321521..2328586, complement)YNL147W607287
    ID: 84498
    family with sequence similarity 120 member B [Homo sapiens (human)]Chromosome 6, NC_000006.12 (170290703..170407067)CCPG, KIAA1838, PGCC1, SAN1, dJ894D12.1612266
    ID: 6326
    sodium voltage-gated channel alpha subunit 2 [Homo sapiens (human)]Chromosome 2, NC_000002.12 (165239414..165392304)BFIC3, BFIS3, BFNIS, DEE11, EA9, EIEE11, HBA, HBSCI, HBSCII, NAC2, Na(v)1.2, Nav1.21, SCN2A2, SCN2A182390
    ID: 552891
    DNAJC25-GNG10 readthrough [Homo sapiens (human)]Chromosome 9, NC_000009.12 (111631334..111670226)
    ID: 548645
    DnaJ heat shock protein family (Hsp40) member C25 [Homo sapiens (human)]Chromosome 9, NC_000009.12 (111631334..111654345)bA16L21.2.1
    ID: 8731
    RNA guanine-7 methyltransferase [Homo sapiens (human)]Chromosome 18, NC_000018.10 (13726673..13764556)CMT1, CMT1c, MET, Met, N7-MTase, RG7MT1, cm1p, hCMT1, hMet603514
    ID: 65005
    mitochondrial ribosomal protein L9 [Homo sapiens (human)]Chromosome 1, NC_000001.11 (151759647..151763496, complement)L9mt, bL9m611824
    ID: 1392
    corticotropin releasing hormone [Homo sapiens (human)]Chromosome 8, NC_000008.11 (66176376..66178464, complement)CRF1, CRH122560
    ID: 114984
    FLYWCH family member 2 [Homo sapiens (human)]Chromosome 16, NC_000016.10 (2883195..2899382)
    ID: 84306
    programmed cell death 2 like [Homo sapiens (human)]Chromosome 19, NC_000019.10 (34404399..34426168)615661
    ID: 55638
    syntabulin [Homo sapiens (human)]Chromosome 8, NC_000008.11 (109573978..109691600, complement)GOLSYN, OCSYN, SNPHL611568
    ID: 284131
    endonuclease V [Homo sapiens (human)]Chromosome 17, NC_000017.11 (80415167..80438086)619821
    ID: 2948
    glutathione S-transferase mu 4 [Homo sapiens (human)]Chromosome 1, NC_000001.11 (109656099..109667727)GSTM4-4, GTM4138333
    ID: 9024
    BR serine/threonine kinase 2 [Homo sapiens (human)]Chromosome 11, NC_000011.10 (1389934..1462689)C11orf7, PEN11B, SAD-A, SAD1, SADA, STK29609236
    ID: 10142
    A-kinase anchoring protein 9 [Homo sapiens (human)]Chromosome 7, NC_000007.14 (91940862..92110673)AKAP-9, AKAP350, AKAP450, CG-NAP, HYPERION, LQT11, MU-RMS-40.16A, PPP1R45, PRKA9, YOTIAO604001
    ID: 30850
    cerebellar degeneration related protein 2 like [Homo sapiens (human)]Chromosome 17, NC_000017.11 (74987632..75005800)HUMPPA
    ID: 8209
    glutamine amidotransferase class 1 domain containing 3 [Homo sapiens (human)]Chromosome 21, NC_000021.9 (44133683..44145711)C21orf33, ES1A, GT335, HES1, KNPH, KNPI, GATD3601659
    ID: 8925
    HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 [Homo sapiens (human)]Chromosome 15, NC_000015.10 (63608618..63833948, complement)MDFPMR, p532, p619605109
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