148210-153615 --- 158320-162332
| OMIM ID: disease or gene description | Ensembl Peptide ID | OrthoMCL Family | Jaccard Coefficient Cluster |
|---|---|---|---|
| 153618: OMIM gene: MACROPHAGE MANNOSE RECEPTOR; MRC1 Gene map locus 10p13 (link from Ensembl BioMart) | ENSP00000239761 | ORTHOMCL417 | jaccard_23 |
| 153619: OMIM gene: LECTIN, GALACTOSIDE-BINDING, SOLUBLE, 3; LGALS3 Gene map locus 14q21-q22 (link from Ensembl BioMart) | ENSP00000254301 | ORTHOMCL14260 | jaccard_169 |
| 153620: OMIM gene: MACROPHAGE MIGRATION INHIBITORY FACTOR; MIF Gene map locus 22q11.2 (link from Ensembl BioMart) | ENSP00000215754 | ORTHOMCL3254 | jaccard_1609 |
| 153622: OMIM gene: MACROPHAGE SCAVENGER RECEPTOR; MSR1 Gene map locus 8p22 (link from Ensembl BioMart) | ENSP00000308757 | ORTHOMCL6067 | jaccard_1514 |
| ENSP00000262100 | ORTHOMCL6067 | jaccard_1514 | |
| ENSP00000347430 | ORTHOMCL6067 | jaccard_1514 | |
| ENSP00000262101 | ORTHOMCL6067 | jaccard_1514 | |
| 153634: OMIM gene: MACROPHAGE ANTIGEN CD68; CD68 Gene map locus 17p13 (link from Ensembl BioMart) | ENSP00000250092 | ORTHOMCL21551 | jaccard_1947 |
| 153640: OMIM phenotype: FECHTNER SYNDROME; FTNS Gene map locus 22q11.2 (link from NCBI) | ENSP00000216181 | ORTHOMCL32 | jaccard_3 |
| 153650: OMIM phenotype: EPSTEIN SYNDROME ALPORT SYNDROME WITH MACROTHROMBOCYTOPENIA, INCLUDED; APSM, INCLUDED Gene map locus 22q11.2 (link from NCBI) | ENSP00000216181 | ORTHOMCL32 | jaccard_3 |
| 153670: OMIM phenotype: BERNARD-SOULIER SYNDROME, BENIGN AUTOSOMAL DOMINANT (link from Ensembl BioMart) | ENSP00000329380 | ORTHOMCL20235 | |
| 153700: OMIM phenotype: MACULAR DYSTROPHY, VITELLIFORM; VMD Gene map locus 11q13 (link from NCBI) | ENSP00000301774 | ORTHOMCL236 | jaccard_494 |
| 153800: OMIM phenotype: MACULAR DEGENERATION, AGE-RELATED, 2; ARMD2 Gene map locus 1p21-p13 (link from NCBI) | ENSP00000355303 | ORTHOMCL110 | jaccard_161 |
| 153870: OMIM phenotype: MACULAR DYSTROPHY, CONCENTRIC ANNULAR Gene map locus 11q13 (link from NCBI) | ENSP00000301774 | ORTHOMCL236 | jaccard_494 |
| 154020: OMIM phenotype: HYPOMAGNESEMIA 2, RENAL; HOMG2 Gene map locus 11q23 (link from NCBI) | ENSP00000292079 | ORTHOMCL9740 | jaccard_1264 |
| ENSP00000260287 | ORTHOMCL9740 | jaccard_1264 | |
| 154030: OMIM gene: NUCLEASE-SENSITIVE ELEMENT-BINDING PROTEIN 1; NSEP1 Gene map locus 1p34 (link from Ensembl BioMart) | ENSP00000163282 | ORTHOMCL11977 | jaccard_703 |
| 154045: OMIM gene: LENS INTRINSIC MEMBRANE PROTEIN 2, 19-KD; LIM2 CATARACT, CORTICAL PULVERULENT, LATE-ONSET, INCLUDED Gene map locus 19q13.4 (link from Ensembl BioMart) | ENSP00000221973 | ORTHOMCL8942 | jaccard_742 |
| 154050: OMIM gene: MAJOR INTRINSIC PROTEIN OF LENS FIBER; MIP CATARACT, POLYMORPHIC AND LAMELLAR, INCLUDED Gene map locus 12q13 (link from Ensembl BioMart) | ENSP00000257979 | ORTHOMCL997 | jaccard_122 |
| 154100: OMIM gene: MALATE DEHYDROGENASE, MITOCHONDRIAL; MDH2 Gene map locus 7cen-q22 (link from Ensembl BioMart) | ENSP00000327070 | ORTHOMCL2237 | jaccard_234 |
| 154200: OMIM gene: MALATE DEHYDROGENASE, SOLUBLE; MDH1 Gene map locus 2p16 (link from Ensembl BioMart) | ENSP00000233114 | ORTHOMCL2398 | jaccard_234 |
| 154235: OMIM gene: MALE GERM CELL-ASSOCIATED KINASE; MAK Gene map locus 6q22 (link from Ensembl BioMart) | ENSP00000313021 | ORTHOMCL1753 | jaccard_14652 |
| ENSP00000346484 | ORTHOMCL1753 | jaccard_14652 | |
| 154250: OMIM gene: MALIC ENZYME 1; ME1 Gene map locus 6q12 (link from Ensembl BioMart) | ENSP00000265285 | ORTHOMCL998 | jaccard_847 |
| 154270: OMIM gene: MALIC ENZYME 2; ME2 Gene map locus 18q21 (link from Ensembl BioMart) | ENSP00000321070 | ORTHOMCL998 | jaccard_847 |
| 154360: OMIM gene: MALTASE-GLUCOAMYLASE; MGAM Gene map locus 7q34 (link from Ensembl BioMart) | ENSP00000316431 | ORTHOMCL648 | jaccard_371 |
| 154365: OMIM gene: PROTEASOME 26S SUBUNIT, ATPase, 2; PSMC2 Gene map locus 7q22.1-q22.3 (link from Ensembl BioMart) | ENSP00000292644 | ORTHOMCL3860 | jaccard_60 |
| 154500: OMIM phenotype: TREACHER COLLINS-FRANCESCHETTI SYNDROME; TCOF Gene map locus 5q32-q33.1 (link from NCBI) | ENSP00000325223 | ORTHOMCL11308 | jaccard_6848 |
| ENSP00000314349 | ORTHOMCL11308 | jaccard_6848 | |
| 154540: OMIM gene: MANNOSE 6-PHOSPHATE RECEPTOR, CATION-DEPENDENT; M6PR Gene map locus 12p13 (link from Ensembl BioMart) | ENSP00000000412 | ORTHOMCL13571 | jaccard_7030 |
| 154545: OMIM gene: LECTIN, MANNOSE-BINDING, SOLUBLE, 2; MBL2 MANNOSE-BINDING PROTEIN DEFICIENCY, INCLUDED Gene map locus 10q11.2-q21 (link from Ensembl BioMart) | ENSP00000298244 | ORTHOMCL10790 | jaccard_23 |
| 154550: OMIM gene: MANNOSEPHOSPHATE ISOMERASE; MPI Gene map locus 15q22-qter (link from Ensembl BioMart) | ENSP00000318318 | ORTHOMCL2107 | jaccard_2641 |
| 154580: OMIM gene: MANNOSIDASE, ALPHA, CLASS 2C, MEMBER 1; MAN2C1 Gene map locus 15q11-q13 (link from Ensembl BioMart) | ENSP00000267978 | ORTHOMCL12135 | jaccard_7513 |
| 154582: OMIM gene: MANNOSIDASE, ALPHA, CLASS 2A, MEMBER 1; MAN2A1 Gene map locus 5q21-q22 (link from Ensembl BioMart) | ENSP00000261483 | ORTHOMCL1155 | jaccard_589 |
| 154700: OMIM phenotype: MARFAN SYNDROME; MFS Gene map locus 15q21.1 (link from NCBI) | ENSP00000325527 | ORTHOMCL2529 | jaccard_5 |
| 154705: OMIM phenotype: MARFAN SYNDROME, TYPE II; MFS2 Gene map locus 3p25-p24.2 (link from Ensembl BioMart) | ENSP00000295754 | ORTHOMCL12399 | jaccard_285 |
| 154780: OMIM phenotype: MARSHALL SYNDROME Gene map locus 1p21 (link from NCBI) | ENSP00000351163 | ORTHOMCL106 | jaccard_0 |
| ENSP00000302551 | ORTHOMCL106 | jaccard_0 | |
| ENSP00000193186 | ORTHOMCL106 | jaccard_0 | |
| 154870: OMIM gene: MATRIX GAMMA-CARBOXYGLUTAMIC ACID; MGP Gene map locus 12p13.1-p12.3 (link from Ensembl BioMart) | ENSP00000228938 | ORTHOMCL19890 | jaccard_11498 |
| 154950: OMIM gene: MAX PROTEIN; MAX Gene map locus 14q23 (link from Ensembl BioMart) | ENSP00000351490 | ORTHOMCL4984 | jaccard_942 |
| ENSP00000246163 | ORTHOMCL18710 | jaccard_14732 | |
| ENSP00000342482 | ORTHOMCL18710 | jaccard_14732 | |
| ENSP00000284165 | ORTHOMCL12281 | jaccard_942 | |
| ENSP00000351175 | ORTHOMCL4984 | jaccard_942 | |
| 155100: OMIM phenotype: MAY-HEGGLIN ANOMALY; MHA Gene map locus 22q11.2 (link from NCBI) | ENSP00000216181 | ORTHOMCL32 | jaccard_3 |
| 155120: OMIM gene: A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 11; ADAM11 Gene map locus 17q21.3 (link from Ensembl BioMart) | ENSP00000200557 | ORTHOMCL4035 | jaccard_41 |
| 155240: OMIM phenotype: THYROID CARCINOMA, FAMILIAL MEDULLARY; MTC Gene map locus 1q21-q22, 10q11.2 (link from NCBI) | ENSP00000344798 | ORTHOMCL3899 | jaccard_3163 |
| ENSP00000352570 | ORTHOMCL8964 | jaccard_2 | |
| ENSP00000351486 | ORTHOMCL8964 | jaccard_2 | |
| 155255: OMIM phenotype: MEDULLOBLASTOMA MEDULLOBLASTOMA, DESMOPLASTIC, INCLUDED Gene map locus 17p13.1-p12, 10q25.3-q26.1, 10q24-q25, 1p32 (link from NCBI) | ENSP00000305179 | ORTHOMCL11462 | jaccard_6533 |
| ENSP00000327747 | ORTHOMCL354 | ||
| ENSP00000303909 | ORTHOMCL1978 | jaccard_3239 | |
| ENSP00000257430 | ORTHOMCL1440 | jaccard_5442 | |
| ENSP00000331522 | ORTHOMCL354 | jaccard_186 | |
| ENSP00000267071 | ORTHOMCL8430 | ||
| ENSP00000236083 | ORTHOMCL2524 | jaccard_272 | |
| ENSP00000344456 | ORTHOMCL3117 | jaccard_134 | |
| ENSP00000343175 | ORTHOMCL354 | jaccard_186 | |
| ENSP00000291107 | ORTHOMCL1978 | jaccard_3239 | |
| ENSP00000339752 | ORTHOMCL354 | jaccard_186 | |
| ENSP00000342500 | ORTHOMCL354 | jaccard_186 | |
| ENSP00000342210 | ORTHOMCL354 | jaccard_186 | |
| ENSP00000345836 | ORTHOMCL354 | ||
| 155540: OMIM gene: MELANOCORTIN 3 RECEPTOR; MC3R Gene map locus 20q13.2 (link from Ensembl BioMart) | ENSP00000243911 | ORTHOMCL14539 | jaccard_19 |
| 155541: OMIM gene: MELANOCORTIN 4 RECEPTOR; MC4R Gene map locus 18q22 (link from Ensembl BioMart) | ENSP00000299766 | ORTHOMCL14667 | jaccard_19 |
| 155550: OMIM gene: SILVER, MOUSE, HOMOLOG OF; SILV Gene map locus 12q13-q14 (link from Ensembl BioMart) | ENSP00000353940 | ORTHOMCL5270 | jaccard_2570 |
| 155555: OMIM gene: MELANOCORTIN 1 RECEPTOR; MC1R Gene map locus 16q24.3 (link from Ensembl BioMart) | ENSP00000302777 | jaccard_92 | |
| 155600: OMIM phenotype: MELANOMA, CUTANEOUS MALIGNANT; CMM MELANOMA, CUTANEOUS MALIGNANT, 1, INCLUDED; CMM1, INCLUDED Gene map locus 1p22, 1p36 (link from Ensembl BioMart) | ENSP00000257904 | ORTHOMCL23597 | jaccard_28 |
| 155601: OMIM phenotype: MELANOMA, CUTANEOUS MALIGNANT, 2; CMM2 Gene map locus 9p21 (link from NCBI) | ENSP00000307101 | ORTHOMCL15852 | jaccard_11 |
| ENSP00000355153 | ORTHOMCL15311 | jaccard_7703 | |
| ENSP00000354638 | ORTHOMCL15311 | jaccard_7703 | |
| 155730: OMIM gene: CHEMOKINE, CXC MOTIF, LIGAND 1; CXCL1 Gene map locus 4q12-q13 (link from Ensembl BioMart) | ENSP00000296031 | ORTHOMCL8759 | jaccard_514 |
| 155735: OMIM gene: MELANOMA ADHESION MOLECULE; MCAM (link from Ensembl BioMart) | ENSP00000264036 | ORTHOMCL9889 | jaccard_2 |
| 155740: OMIM gene: CD63 ANTIGEN; CD63 Gene map locus 12q12-q13 (link from Ensembl BioMart) | ENSP00000257857 | ORTHOMCL5460 | jaccard_75 |
| 155750: OMIM gene: MELANOMA-ASSOCIATED ANTIGEN p97; MFI2 Gene map locus 3q29 (link from Ensembl BioMart) | ENSP00000296350 | ORTHOMCL5056 | jaccard_1216 |
| ENSP00000296351 | jaccard_1216 | ||
| 155755: OMIM phenotype: MELANOMA-ASTROCYTOMA SYNDROME Gene map locus 9p21 (link from NCBI) | ENSP00000307101 | ORTHOMCL15852 | jaccard_11 |
| ENSP00000355153 | ORTHOMCL15311 | jaccard_7703 | |
| ENSP00000354638 | ORTHOMCL15311 | jaccard_7703 | |
| 155760: OMIM gene: AGGRECAN 1; AGC1 Gene map locus 15q26.1 (link from Ensembl BioMart) | ENSP00000268134 | ORTHOMCL10102 | jaccard_0 |
| ENSP00000341615 | ORTHOMCL10102 | jaccard_0 | |
| 155950: OMIM phenotype: MELORHEOSTOSIS MELORHEOSTOSIS WITH OSTEOPOIKILOSIS, INCLUDED Gene map locus 12q14 (link from NCBI) | ENSP00000308369 | ORTHOMCL9024 | jaccard_9416 |
| 155970: OMIM gene: MEMBRANE GLYCOPROTEIN MRC OX-2; MOX2 Gene map locus 3q12-q13 (link from Ensembl BioMart) | ENSP00000312766 | ORTHOMCL10368 | jaccard_12524 |
| 156000: OMIM phenotype: MENIERE DISEASE Gene map locus 14q12-q13 (link from Ensembl BioMart) | ENSP00000216361 | ORTHOMCL10455 | jaccard_2 |
| 156100: OMIM gene: MENINGIOMA 1 GENE; MN1 MN1/TEL FUSION GENE, INCLUDED Gene map locus 22q12.3-qter (link from Ensembl BioMart) | ENSP00000304956 | ORTHOMCL20025 | jaccard_0 |
| 156225: OMIM gene: LAMININ, ALPHA-2; LAMA2 MEROSIN, INCLUDED Gene map locus 6q22-q23 (link from Ensembl BioMart) | ENSP00000347393 | ORTHOMCL1793 | jaccard_5 |
| ENSP00000346769 | ORTHOMCL1793 | jaccard_5 | |
| 156349: OMIM gene: METALLOTHIONEIN 1B; MT1B Gene map locus 16q13 (link from Ensembl BioMart) | ENSP00000334998 | ORTHOMCL906 | jaccard_5 |
| 156350: OMIM gene: METALLOTHIONEIN 1A; MT1A Gene map locus 16q13 (link from Ensembl BioMart) | ENSP00000290705 | ORTHOMCL906 | jaccard_5 |
| 156352: OMIM gene: METALLOTHIONEIN 1F; MT1F Gene map locus 16q13 (link from Ensembl BioMart) | ENSP00000334872 | ORTHOMCL906 | jaccard_5 |
| 156353: OMIM gene: METALLOTHIONEIN 1G; MT1G Gene map locus 16q13 (link from Ensembl BioMart) | ENSP00000245183 | ORTHOMCL906 | jaccard_5 |
| 156354: OMIM gene: METALLOTHIONEIN 1H; MT1H Gene map locus 16q13 (link from Ensembl BioMart) | ENSP00000330587 | ORTHOMCL906 | jaccard_5 |
| 156355: OMIM gene: METALLOTHIONEIN 1I; MT1I Gene map locus 16q13 (link from Ensembl BioMart) | ENSP00000245183 | ORTHOMCL906 | jaccard_5 |
| 156360: OMIM gene: METALLOTHIONEIN 2A; MT2A METALLOTHIONEIN II PROCESSED PSEUDOGENE; MT2P1, INCLUDED Gene map locus 16q13 (link from Ensembl BioMart) | ENSP00000245185 | ORTHOMCL906 | jaccard_5 |
| 156400: OMIM phenotype: METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE Gene map locus 3p22-p21.1 (link from NCBI) | ENSP00000321999 | ORTHOMCL15677 | jaccard_59 |
| 156490: OMIM gene: NONMETASTATIC CELLS 1, PROTEIN EXPRESSED IN; NME1 NM23H1B, INCLUDED Gene map locus 17q21.3 (link from Ensembl BioMart) | ENSP00000013034 | ORTHOMCL1481 | jaccard_408 |
| ENSP00000337060 | ORTHOMCL1481 | jaccard_408 | |
| 156491: OMIM gene: NONMETASTATIC CELLS 2, PROTEIN EXPRESSED IN; NME2 Gene map locus 17q21.3 (link from Ensembl BioMart) | ENSP00000312446 | ORTHOMCL1481 | jaccard_408 |
| 156500: OMIM phenotype: METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS (link from Ensembl BioMart) | ENSP00000327368 | ORTHOMCL11172 | jaccard_0 |
| ENSP00000243222 | ORTHOMCL12767 | jaccard_0 | |
| 156535: OMIM gene: METHYL-CpG-BINDING DOMAIN PROTEIN 1; MBD1 METHYL-CpG-BINDING PROTEIN 1 COMPLEX, INCLUDED Gene map locus 18q21.1 (link from Ensembl BioMart) | ENSP00000269468 | ORTHOMCL3339 | jaccard_3522 |
| ENSP00000269469 | ORTHOMCL3339 | jaccard_3522 | |
| ENSP00000269471 | ORTHOMCL3339 | jaccard_3522 | |
| ENSP00000342531 | ORTHOMCL3339 | jaccard_3522 | |
| ENSP00000285102 | ORTHOMCL3339 | jaccard_3522 | |
| 156540: OMIM gene: METHYLTHIOADENOSINE PHOSPHORYLASE; MTAP Gene map locus 9p21 (link from Ensembl BioMart) | ENSP00000297736 | ORTHOMCL6377 | jaccard_1008 |
| 156550: OMIM phenotype: KNIEST DYSPLASIA Gene map locus 12q13.11-q13.2 (link from NCBI) | ENSP00000346511 | ORTHOMCL106 | jaccard_0 |
| ENSP00000338213 | ORTHOMCL106 | jaccard_0 | |
| 156560: OMIM gene: METHIONYL-tRNA SYNTHETASE; MARS Gene map locus Chr.12 (link from Ensembl BioMart) | ENSP00000262027 | ORTHOMCL5933 | jaccard_1794 |
| 156565: OMIM gene: N-@METHYLPURINE DNA GLYCOSYLASE; MPG Gene map locus 16pter-p13.3 (link from Ensembl BioMart) | ENSP00000348809 | ORTHOMCL5744 | jaccard_4979 |
| ENSP00000219431 | ORTHOMCL5744 | jaccard_4979 | |
| 156569: OMIM gene: METHYLGUANINE-DNA METHYLTRANSFERASE; MGMT Gene map locus 10q26 (link from Ensembl BioMart) | ENSP00000302111 | ORTHOMCL8219 | jaccard_7800 |
| 156570: OMIM gene: 5-@METHYLTETRAHYDROFOLATE-HOMOCYSTEINE S-METHYLTRANSFERASE; MTR Gene map locus 1q43 (link from Ensembl BioMart) | ENSP00000264178 | ORTHOMCL12567 | jaccard_8713 |
| 156575: OMIM phenotype: MEVALONATE UPTAKE FACILITATOR; MEV (link from Ensembl BioMart) | ENSP00000285753 | ORTHOMCL9651 | jaccard_184 |
| 156790: OMIM gene: MICROFIBRIL-ASSOCIATED PROTEIN 2; MFAP2 Gene map locus 1p36.1-p35 (link from Ensembl BioMart) | ENSP00000235772 | ORTHOMCL18544 | jaccard_6099 |
| 156845: OMIM gene: MICROPHTHALMIA-ASSOCIATED TRANSCRIPTION FACTOR; MITF Gene map locus 3p14.1-p12.3 (link from Ensembl BioMart) | ENSP00000327867 | ORTHOMCL13787 | jaccard_531 |
| ENSP00000324443 | ORTHOMCL13787 | jaccard_531 | |
| ENSP00000295600 | ORTHOMCL6275 | jaccard_531 | |
| ENSP00000324246 | ORTHOMCL1414 | jaccard_531 | |
| 157129: OMIM gene: MICROTUBULE-ASSOCIATED PROTEIN 1B; MAP1B Gene map locus 5q13 (link from Ensembl BioMart) | ENSP00000296755 | ORTHOMCL7212 | jaccard_7025 |
| 157130: OMIM gene: MICROTUBULE-ASSOCIATED PROTEIN 2; MAP2 Gene map locus 2q34-q35 (link from Ensembl BioMart) | ENSP00000199940 | ORTHOMCL3214 | jaccard_1395 |
| ENSP00000353508 | ORTHOMCL8390 | jaccard_8853 | |
| ENSP00000352460 | ORTHOMCL8390 | jaccard_8853 | |
| ENSP00000355290 | ORTHOMCL16181 | jaccard_1395 | |
| 157132: OMIM gene: MICROTUBULE-ASSOCIATED PROTEIN 4; MAP4 Gene map locus 3p21 (link from Ensembl BioMart) | ENSP00000264724 | ORTHOMCL8626 | |
| ENSP00000353375 | ORTHOMCL8626 | jaccard_8563 | |
| 157140: OMIM gene: MICROTUBULE-ASSOCIATED PROTEIN TAU; MAPT TAUOPATHY AND RESPIRATORY FAILURE, INCLUDED Gene map locus 17q21.1 (link from Ensembl BioMart) | ENSP00000302706 | ORTHOMCL5812 | jaccard_1395 |
| ENSP00000334886 | ORTHOMCL12646 | jaccard_1395 | |
| ENSP00000303214 | ORTHOMCL3214 | jaccard_1395 | |
| ENSP00000262410 | ORTHOMCL3214 | ||
| 157145: OMIM gene: MICROSEMINOPROTEIN, BETA; MSMB Gene map locus 10q11.2 (link from Ensembl BioMart) | ENSP00000298239 | ||
| ENSP00000351363 | ORTHOMCL21240 | jaccard_10998 | |
| 157147: OMIM gene: MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN, 88-KD; MTP Gene map locus 4q22-q24 (link from Ensembl BioMart) | ENSP00000265517 | ORTHOMCL7908 | jaccard_5930 |
| 157170: OMIM phenotype: HOLOPROSENCEPHALY 2; HPE2 MIDLINE CLEFT SYNDROME, INCLUDED Gene map locus 2p21 (link from NCBI) | ENSP00000260653 | ORTHOMCL3865 | jaccard_791 |
| 157300: OMIM phenotype: MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1 Gene map locus 6q25.1, 6p21.3, 4q31.2, 4q24 (link from NCBI) | ENSP00000352755 | jaccard_13727 | |
| ENSP00000315011 | ORTHOMCL19555 | jaccard_6 | |
| ENSP00000206249 | ORTHOMCL9739 | jaccard_18 | |
| 157640: OMIM phenotype: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 1 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH HYPOGONADISM, INCLUDED Gene map locus 15q25, 4q35 (link from NCBI) | ENSP00000281456 | ORTHOMCL410 | jaccard_27 |
| ENSP00000268124 | ORTHOMCL6276 | jaccard_4616 | |
| 157655: OMIM gene: NADH-UBIQUINONE OXIDOREDUCTASE Fe-S PROTEIN 1; NDUFS1 Gene map locus 2q33-q34 (link from Ensembl BioMart) | ENSP00000233190 | ORTHOMCL4067 | jaccard_3321 |
| 157680: OMIM gene: CELL DIVISION CYCLE 25C; CDC25C Gene map locus 5q31 (link from Ensembl BioMart) | ENSP00000345205 | ORTHOMCL2273 | jaccard_1152 |
| ENSP00000321656 | ORTHOMCL2273 | jaccard_1152 | |
| 157970: OMIM gene: PROTEASOME 26S SUBUNIT, NON-ATPase, 7; PSMD7 MOLONEY LEUKEMIA VIRUS 34 PROVIRAL INTEGRATION SITE, MOUSE, HOMOLOG OF, INCLUDED; MOV34, INCLUDED Gene map locus 16q23-q24 (link from Ensembl BioMart) | ENSP00000219313 | ORTHOMCL5096 | jaccard_1065 |
| 158000: OMIM phenotype: MONILETHRIX Gene map locus 12q13, 12q13 (link from NCBI) | ENSP00000293525 | ORTHOMCL2218 | jaccard_0 |
| 158070: OMIM gene: SOLUTE CARRIER FAMILY 3 (ACTIVATOR OF DIBASIC AND NEUTRAL AMINO ACID TRANSPORT), MEMBER 2; SLC3A2 MONOCLONAL ANTIBODY 44D7, INCLUDED Gene map locus 11q13 (link from Ensembl BioMart) | ENSP00000340815 | ORTHOMCL9685 | jaccard_738 |
| 158105: OMIM gene: CHEMOKINE, CC MOTIF, LIGAND 2; CCL2 Gene map locus 17q11.2-q12 (link from Ensembl BioMart) | ENSP00000225831 | ORTHOMCL6503 | jaccard_248 |
| 158106: OMIM gene: CHEMOKINE, CC MOTIF, LIGAND 7; CCL7 Gene map locus 17q11.2-q12 (link from Ensembl BioMart) | ENSP00000200307 | ORTHOMCL6503 | jaccard_248 |
| 158120: OMIM gene: MONOCYTE DIFFERENTIATION ANTIGEN CD14; CD14 Gene map locus 5q31.1 (link from Ensembl BioMart) | ENSP00000304236 | ORTHOMCL23039 | jaccard_11803 |
| 158270: OMIM gene: MOTILIN; MLN Gene map locus 6p21.3 (link from Ensembl BioMart) | ENSP00000266003 | ||
| 158300: OMIM phenotype: TRISMUS-PSEUDOCAMPTODACTYLY SYNDROME Gene map locus 17p13.1 (link from NCBI) | ENSP00000252173 | ORTHOMCL32 | jaccard_3 |