125850-131440 --- 136538-138360
| OMIM ID: disease or gene description | Ensembl Peptide ID | OrthoMCL Family | Jaccard Coefficient Cluster |
|---|---|---|---|
| 131530: OMIM gene: EPIDERMAL GROWTH FACTOR; EGF Gene map locus 4q25 (link from Ensembl BioMart) | ENSP00000265171 | ORTHOMCL14599 | jaccard_5 |
| 131550: OMIM gene: EPIDERMAL GROWTH FACTOR RECEPTOR; EGFR SPECIES ANTIGEN 7, INCLUDED; S7, INCLUDED Gene map locus 7p12.3-p12.1 (link from Ensembl BioMart) | ENSP00000345973 | ORTHOMCL901 | jaccard_512 |
| ENSP00000342376 | ORTHOMCL901 | jaccard_512 | |
| ENSP00000275493 | ORTHOMCL901 | jaccard_512 | |
| 131560: OMIM gene: FLOTILLIN 2; FLOT2 Gene map locus 17q11-q12 (link from Ensembl BioMart) | ENSP00000333941 | ORTHOMCL3640 | jaccard_1240 |
| 131705: OMIM phenotype: TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN; TBDN Gene map locus 3p21.3 (link from NCBI) | ENSP00000332371 | ORTHOMCL92 | jaccard_0 |
| 131750: OMIM phenotype: EPIDERMOLYSIS BULLOSA DYSTROPHICA, PASINI TYPE EPIDERMOLYSIS BULLOSA, PRETIBIAL, WITH LICHENOID FEATURES, INCLUDED Gene map locus 3p21.3 (link from NCBI) | ENSP00000332371 | ORTHOMCL92 | jaccard_0 |
| 131760: OMIM phenotype: EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE Gene map locus 17q12-q21, 12q13 (link from Ensembl BioMart) | ENSP00000167586 | ORTHOMCL971 | jaccard_0 |
| ENSP00000252242 | ORTHOMCL2248 | jaccard_0 | |
| 131800: OMIM phenotype: EPIDERMOLYSIS BULLOSA OF HANDS AND FEET Gene map locus 17q12-q21, 17q11-qter, 12q13 (link from NCBI) | ENSP00000252242 | ORTHOMCL2248 | jaccard_0 |
| ENSP00000344079 | ORTHOMCL7930 | jaccard_6244 | |
| ENSP00000167586 | ORTHOMCL971 | jaccard_0 | |
| ENSP00000200181 | ORTHOMCL7930 | jaccard_6244 | |
| 131850: OMIM phenotype: EPIDERMOLYSIS BULLOSA, PRETIBIAL Gene map locus 3p21.3 (link from NCBI) | ENSP00000332371 | ORTHOMCL92 | jaccard_0 |
| 131900: OMIM phenotype: EPIDERMOLYSIS BULLOSA SIMPLEX, KOEBNER TYPE; EBS2 Gene map locus 17q12-q21, 12q13 (link from Ensembl BioMart) | ENSP00000167586 | ORTHOMCL971 | jaccard_0 |
| ENSP00000252242 | ORTHOMCL2248 | jaccard_0 | |
| 131950: OMIM phenotype: EPIDERMOLYSIS BULLOSA SIMPLEX, OGNA TYPE Gene map locus 8q24 (link from NCBI) | ENSP00000347044 | ORTHOMCL82 | jaccard_3 |
| ENSP00000350277 | ORTHOMCL82 | jaccard_3 | |
| ENSP00000349868 | ORTHOMCL82 | jaccard_3 | |
| ENSP00000323856 | ORTHOMCL82 | jaccard_3 | |
| ENSP00000344848 | ORTHOMCL82 | jaccard_3 | |
| ENSP00000348702 | ORTHOMCL82 | jaccard_3 | |
| ENSP00000346602 | ORTHOMCL82 | jaccard_3 | |
| 131960: OMIM phenotype: EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION; EBS-MP Gene map locus 12q13 (link from NCBI) | ENSP00000252242 | ORTHOMCL2248 | jaccard_0 |
| 132000: OMIM phenotype: EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN AND DEFORMITY OF NAILS Gene map locus 3p21.3 (link from NCBI) | ENSP00000332371 | ORTHOMCL92 | jaccard_0 |
| 132350: OMIM gene: EPIMORPHIN; EPIM Gene map locus Chr.7 (link from Ensembl BioMart) | ENSP00000261653 | ORTHOMCL335 | jaccard_145 |
| ENSP00000342554 | ORTHOMCL335 | jaccard_145 | |
| 132400: OMIM phenotype: EPIPHYSEAL DYSPLASIA, MULTIPLE, 1; EDM1 EPIPHYSEAL DYSPLASIA, FAIRBANK TYPE, INCLUDED Gene map locus 19p13.1 (link from NCBI) | ENSP00000222271 | ORTHOMCL3522 | jaccard_1217 |
| 132450: OMIM phenotype: EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS (link from Ensembl BioMart) | ENSP00000338213 | ORTHOMCL106 | jaccard_0 |
| 132600: OMIM phenotype: PILOMATRIXOMA Gene map locus 1p34.3-p32.1, 3p22-p21.3 (link from NCBI) | ENSP00000255122 | ORTHOMCL2635 | jaccard_2579 |
| ENSP00000344456 | ORTHOMCL3117 | jaccard_134 | |
| 132700: OMIM phenotype: CYLINDROMATOSIS, FAMILIAL; CYLD CYLINDROMAS, DERMAL ECCRINE, INCLUDED Gene map locus 16q12-q13 (link from NCBI) | ENSP00000308928 | ORTHOMCL2720 | jaccard_1473 |
| 132810: OMIM gene: EPOXIDE HYDROLASE 1, MICROSOMAL; EPHX1 PHENYTOIN TOXICITY, INCLUDED Gene map locus 1q42.1 (link from Ensembl BioMart) | ENSP00000272167 | ORTHOMCL3743 | jaccard_2647 |
| 132811: OMIM gene: EPOXIDE HYDROLASE 2, CYTOSOLIC; EPHX2 Gene map locus 8p21-p12 (link from Ensembl BioMart) | ENSP00000315621 | ORTHOMCL1275 | jaccard_1291 |
| 132880: OMIM gene: NUCLEAR RECEPTOR SUBFAMILY 2, GROUP F, MEMBER 6; NR2F6 Gene map locus Chr.19 (link from Ensembl BioMart) | ENSP00000291442 | ORTHOMCL15809 | jaccard_18 |
| 132890: OMIM gene: NUCLEAR RECEPTOR SUBFAMILY 2, GROUP F, MEMBER 1; NR2F1 Gene map locus 5q14 (link from Ensembl BioMart) | ENSP00000325819 | ORTHOMCL4855 | jaccard_18 |
| 132900: OMIM phenotype: AORTIC ANEURYSM, FAMILIAL THORACIC 4 Gene map locus 16p13.13-p13.12 (link from NCBI) | ENSP00000300036 | ORTHOMCL32 | jaccard_3 |
| ENSP00000345136 | ORTHOMCL32 | jaccard_3 | |
| 133020: OMIM phenotype: ERYTHERMALGIA, PRIMARY Gene map locus 2q24 (link from Ensembl BioMart) | ENSP00000304748 | ORTHOMCL251 | jaccard_70 |
| 133090: OMIM gene: ERYTHROCYTE SURFACE PROTEIN BAND 7.2; EPB72 Gene map locus 9q34.1 (link from Ensembl BioMart) | ENSP00000339607 | ||
| ENSP00000286713 | ORTHOMCL2645 | jaccard_170 | |
| 133100: OMIM phenotype: ERYTHROCYTOSIS, FAMILIAL Gene map locus 19p13.3-p13.2 (link from NCBI) | ENSP00000222139 | ORTHOMCL15142 | jaccard_380 |
| 133170: OMIM gene: ERYTHROPOIETIN; EPO Gene map locus 7q21 (link from Ensembl BioMart) | ENSP00000252723 | ORTHOMCL11538 | jaccard_7525 |
| 133171: OMIM gene: ERYTHROPOIETIN RECEPTOR; EPOR Gene map locus 19p13.3-p13.2 (link from Ensembl BioMart) | ENSP00000222139 | ORTHOMCL15142 | jaccard_380 |
| 133200: OMIM phenotype: ERYTHROKERATODERMIA VARIABILIS; EKV ERYTHROKERATODERMIA VARIABILIS WITH ERYTHEMA GYRATUM REPENS, INCLUDED Gene map locus 1p35.1, 1p35.1 (link from NCBI) | ENSP00000343839 | ORTHOMCL10128 | jaccard_152 |
| ENSP00000345868 | ORTHOMCL16065 | jaccard_152 | |
| 133239: OMIM phenotype: ESOPHAGEAL CANCER ESOPHAGEAL SQUAMOUS CELL CARCINOMA, INCLUDED; ESCC, INCLUDED Gene map locus 16q23.3-q24.1, 13q12.11, 9q32, 8p22, 3p22-p21.3, 3p22 (link from NCBI) | ENSP00000265801 | ORTHOMCL12229 | jaccard_10403 |
| ENSP00000337480 | |||
| ENSP00000311671 | |||
| ENSP00000334295 | ORTHOMCL13764 | jaccard_9295 | |
| ENSP00000333406 | ORTHOMCL122 | jaccard_21 | |
| ENSP00000308597 | ORTHOMCL9601 | jaccard_6128 | |
| ENSP00000312908 | ORTHOMCL30 | jaccard_1391 | |
| ENSP00000348119 | jaccard_9295 | ||
| ENSP00000344073 | |||
| ENSP00000295754 | ORTHOMCL12399 | jaccard_285 | |
| ENSP00000351905 | |||
| ENSP00000269305 | ORTHOMCL10818 | jaccard_1112 | |
| ENSP00000315914 | ORTHOMCL9601 | jaccard_6128 | |
| ENSP00000340147 | ORTHOMCL13764 | ||
| ENSP00000342121 | ORTHOMCL30 | jaccard_1391 | |
| 133280: OMIM gene: ESTERASE D; ESD S-FORMYLGLUTATHIONE HYDROLASE, INCLUDED; FGH, INCLUDED Gene map locus 13q14.11 (link from Ensembl BioMart) | ENSP00000267160 | ORTHOMCL2813 | jaccard_2597 |
| 133430: OMIM gene: ESTROGEN RECEPTOR 1; ESR1 Gene map locus 6q25.1 (link from Ensembl BioMart) | ENSP00000352755 | jaccard_13727 | |
| ENSP00000206249 | ORTHOMCL9739 | jaccard_18 | |
| 133435: OMIM gene: CORE-BINDING FACTOR, ALPHA SUBUNIT 2, TRANSLOCATED TO, 1; CBFA2T1 ETO/AML FUSION GENE, INCLUDED Gene map locus 8q22 (link from Ensembl BioMart) | ENSP00000353504 | ORTHOMCL2387 | jaccard_745 |
| ENSP00000265814 | ORTHOMCL2387 | jaccard_745 | |
| 133440: OMIM gene: EUKARYOTIC TRANSLATION INITIATION FACTOR 4E; EIF4E Gene map locus 4q21-q25 (link from Ensembl BioMart) | ENSP00000280892 | ORTHOMCL531 | jaccard_396 |
| 133450: OMIM gene: EWING SARCOMA BREAKPOINT REGION 1; EWSR1 EWING SARCOMA, INCLUDED; EWS, INCLUDED; ES, INCLUDED Gene map locus 22q12 (link from Ensembl BioMart) | ENSP00000333122 | ORTHOMCL12464 | jaccard_18 |
| ENSP00000339627 | ORTHOMCL3300 | jaccard_351 | |
| ENSP00000238459 | ORTHOMCL12464 | jaccard_18 | |
| ENSP00000330516 | ORTHOMCL7454 | jaccard_0 | |
| ENSP00000349966 | jaccard_351 | ||
| ENSP00000242066 | ORTHOMCL17852 | jaccard_1265 | |
| ENSP00000330896 | ORTHOMCL20271 | jaccard_0 | |
| 133510: OMIM gene: EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 3; ERCC3 XERODERMA PIGMENTOSUM II, INCLUDED; XP2, INCLUDED Gene map locus 2q21 (link from Ensembl BioMart) | ENSP00000285398 | ORTHOMCL3770 | jaccard_3625 |
| 133520: OMIM gene: EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 4; ERCC4 Gene map locus 16p13.3-p13.13 (link from Ensembl BioMart) | ENSP00000310520 | ORTHOMCL4274 | jaccard_3679 |
| 133540: OMIM phenotype: COCKAYNE SYNDROME, TYPE B; CSB Gene map locus 10q11 (link from NCBI) | ENSP00000348089 | ORTHOMCL5416 | jaccard_48 |
| ENSP00000265899 | ORTHOMCL5416 | jaccard_48 | |
| 133550: OMIM gene: SOLUTE CARRIER FAMILY 1 (NEURONAL/EPITHELIAL HIGH AFFINITY GLUTAMATE TRANSPORTER), MEMBER 1; SLC1A1 Gene map locus 9p24 (link from Ensembl BioMart) | ENSP00000262352 | ORTHOMCL17096 | jaccard_453 |
| 133700: OMIM phenotype: EXOSTOSES, MULTIPLE, TYPE I Gene map locus 8q24.11-q24.13 (link from NCBI) | ENSP00000328662 | ORTHOMCL7596 | jaccard_1491 |
| 133701: OMIM phenotype: EXOSTOSES, MULTIPLE, TYPE II Gene map locus 11p12-p11 (link from NCBI) | ENSP00000342656 | ORTHOMCL5196 | jaccard_1491 |
| 133780: OMIM phenotype: EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT; EVR Gene map locus 11q14-q21, 11q13.4 (link from NCBI) | ENSP00000294304 | ORTHOMCL4085 | jaccard_5 |
| ENSP00000311581 | ORTHOMCL20527 | jaccard_407 | |
| 134350: OMIM gene: FACTOR D (link from Ensembl BioMart) | ENSP00000332139 | ORTHOMCL10993 | jaccard_10 |
| 134370: OMIM gene: COMPLEMENT FACTOR H; CFH FACTOR H-LIKE 1, INCLUDED; FHL1, INCLUDED Gene map locus 1q32 (link from Ensembl BioMart) | ENSP00000001567 | ORTHOMCL17861 | jaccard_34 |
| 134371: OMIM gene: COMPLEMENT FACTOR H-RELATED 1; CFHL1 Gene map locus 1q31-q32.1 (link from Ensembl BioMart) | ENSP00000314299 | ORTHOMCL18986 | jaccard_34 |
| 134390: OMIM gene: COAGULATION FACTOR III; F3 Gene map locus 1p22-p21 (link from Ensembl BioMart) | ENSP00000334145 | ORTHOMCL8515 | jaccard_1155 |
| 134500: OMIM phenotype: FACTOR VIII DEFICIENCY (link from Ensembl BioMart) | ENSP00000327895 | jaccard_1378 | |
| 134570: OMIM gene: FACTOR XIII, A1 SUBUNIT; F13A1 FACTOR XIII, A SUBUNIT, DEFICIENCY OF, INCLUDED Gene map locus 6p25-p24 (link from Ensembl BioMart) | ENSP00000264870 | ORTHOMCL12536 | jaccard_399 |
| 134580: OMIM gene: FACTOR XIII, B SUBUNIT; F13B FACTOR XIII, B SUBUNIT, DEFICIENCY OF, INCLUDED Gene map locus 1q31-q32.1 (link from Ensembl BioMart) | ENSP00000271509 | ORTHOMCL21317 | jaccard_34 |
| 134629: OMIM gene: FARNESYL DIPHOSPHATE SYNTHASE; FDPS FARNESYL DIPHOSPHATE SYNTHASE-LIKE 1 PSEUDOGENE, INCLUDED; FDPSL1, INCLUDED (link from Ensembl BioMart) | ENSP00000292252 | ORTHOMCL2962 | jaccard_1380 |
| ENSP00000349078 | ORTHOMCL2962 | jaccard_1380 | |
| 134635: OMIM gene: FARNESYLTRANSFERASE, CAAX BOX, ALPHA; FNTA Gene map locus 8p22-q11 (link from Ensembl BioMart) | ENSP00000303423 | ORTHOMCL3949 | jaccard_1197 |
| ENSP00000343931 | ORTHOMCL3949 | jaccard_1197 | |
| 134636: OMIM gene: FARNESYLTRANSFERASE, CAAX BOX, BETA; FNTB Gene map locus 14q23-q24 (link from Ensembl BioMart) | ENSP00000246166 | ORTHOMCL5362 | jaccard_1030 |
| 134637: OMIM gene: TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 6; TNFRSF6 Gene map locus 10q24.1 (link from Ensembl BioMart) | ENSP00000347426 | ORTHOMCL2837 | |
| ENSP00000318440 | ORTHOMCL2837 | jaccard_6236 | |
| ENSP00000349896 | ORTHOMCL2837 | jaccard_691 | |
| ENSP00000318464 | ORTHOMCL2837 | jaccard_6236 | |
| ENSP00000343487 | ORTHOMCL2837 | jaccard_6236 | |
| ENSP00000318239 | ORTHOMCL2837 | jaccard_691 | |
| ENSP00000345601 | ORTHOMCL2837 | jaccard_6236 | |
| ENSP00000347979 | ORTHOMCL2837 | jaccard_691 | |
| ENSP00000318609 | ORTHOMCL2837 | jaccard_6236 | |
| 134638: OMIM gene: TUMOR NECROSIS FACTOR LIGAND SUPERFAMILY, MEMBER 6; TNFSF6 Gene map locus 1q23 (link from Ensembl BioMart) | ENSP00000304123 | ORTHOMCL15192 | jaccard_950 |
| 134640: OMIM gene: FATTY ACID-BINDING PROTEIN 2; FABP2 Gene map locus 4q28-q31 (link from Ensembl BioMart) | ENSP00000274024 | ORTHOMCL16000 | jaccard_242 |
| 134650: OMIM gene: FATTY ACID-BINDING PROTEIN 1; FABP1 Gene map locus 2p11 (link from Ensembl BioMart) | ENSP00000295834 | ORTHOMCL14154 | jaccard_242 |
| 134651: OMIM gene: FATTY ACID-BINDING PROTEIN 3; FABP3 Gene map locus 1p33-p31 (link from Ensembl BioMart) | ENSP00000241156 | ORTHOMCL3705 | jaccard_242 |
| 134660: OMIM gene: GLUTATHIONE S-TRANSFERASE, PI; GSTP1 GLUTATHIONE S-TRANSFERASE PI PSEUDOGENE, INCLUDED; GSTPP, INCLUDED Gene map locus 11q13 (link from Ensembl BioMart) | ENSP00000196968 | ORTHOMCL1924 | jaccard_172 |
| 134690: OMIM gene: FAU GENE; FAU Gene map locus 11q13 (link from Ensembl BioMart) | ENSP00000279259 | ORTHOMCL1581 | jaccard_126 |
| 134770: OMIM gene: FERRITIN HEAVY CHAIN 1; FTH1 IRON OVERLOAD, AUTOSOMAL DOMINANT, INCLUDED Gene map locus 11q12-q13 (link from Ensembl BioMart) | ENSP00000273550 | ORTHOMCL674 | jaccard_254 |
| 134795: OMIM gene: FIBRILLARIN; FBL (link from Ensembl BioMart) | ENSP00000221801 | ORTHOMCL2533 | jaccard_1753 |
| 134797: OMIM gene: FIBRILLIN 1; FBN1 Gene map locus 15q21.1 (link from Ensembl BioMart) | ENSP00000325527 | ORTHOMCL2529 | jaccard_5 |
| 134820: OMIM gene: FIBRINOGEN, A ALPHA POLYPEPTIDE; FGA DYSFIBRINOGENEMIA CAUSING RECURRENT THROMBOSIS, INCLUDED Gene map locus 4q28 (link from Ensembl BioMart) | ENSP00000306361 | ORTHOMCL10482 | |
| 134830: OMIM gene: FIBRINOGEN, B BETA POLYPEPTIDE; FGB Gene map locus 4q28 (link from Ensembl BioMart) | ENSP00000306099 | ORTHOMCL16437 | jaccard_135 |
| 134850: OMIM gene: FIBRINOGEN, G GAMMA POLYPEPTIDE; FGG Gene map locus 4q28 (link from Ensembl BioMart) | ENSP00000336829 | ORTHOMCL9437 | jaccard_135 |
| 134920: OMIM gene: FIBROBLAST GROWTH FACTOR 2; FGF2 Gene map locus 4q25-q27 (link from Ensembl BioMart) | ENSP00000264498 | ORTHOMCL15845 | |
| 134921: OMIM gene: FIBROBLAST GROWTH FACTOR 6; FGF6 Gene map locus 12p13 (link from Ensembl BioMart) | ENSP00000228837 | ORTHOMCL10088 | jaccard_176 |
| 134934: OMIM gene: FIBROBLAST GROWTH FACTOR RECEPTOR 3; FGFR3 Gene map locus 4p16.3 (link from Ensembl BioMart) | ENSP00000260795 | ORTHOMCL6629 | jaccard_2 |
| ENSP00000231803 | ORTHOMCL329 | jaccard_2 | |
| 134935: OMIM gene: FIBROBLAST GROWTH FACTOR RECEPTOR 4; FGFR4 Gene map locus 5q35.1-qter (link from Ensembl BioMart) | ENSP00000292410 | ORTHOMCL17425 | jaccard_2 |
| ENSP00000292408 | ORTHOMCL17425 | jaccard_2 | |
| 135150: OMIM phenotype: BIRT-HOGG-DUBE SYNDROME; BHD Gene map locus 17p11.2 (link from NCBI) | ENSP00000285071 | ORTHOMCL5420 | jaccard_5134 |
| 135290: OMIM phenotype: DESMOID DISEASE, HEREDITARY Gene map locus 5q21-q22 (link from NCBI) | ENSP00000257430 | ORTHOMCL1440 | jaccard_5442 |
| 135300: OMIM phenotype: FIBROMATOSIS, GINGIVAL, 1; GINGF Gene map locus 2p22-p21, 5q13-q22 (link from NCBI) | ENSP00000263879 | ORTHOMCL1706 | jaccard_858 |
| 135600: OMIM gene: FIBRONECTIN 1; FN1 FNZ, INCLUDED Gene map locus 2q34 (link from Ensembl BioMart) | ENSP00000348285 | ORTHOMCL2007 | jaccard_2 |
| ENSP00000349509 | ORTHOMCL2007 | jaccard_2 | |
| ENSP00000338200 | ORTHOMCL2007 | jaccard_2 | |
| ENSP00000273049 | ORTHOMCL2007 | jaccard_2 | |
| ENSP00000350534 | ORTHOMCL2007 | jaccard_2 | |
| ENSP00000352696 | ORTHOMCL2007 | jaccard_2 | |
| ENSP00000265312 | ORTHOMCL2007 | jaccard_2 | |
| ENSP00000265313 | ORTHOMCL2007 | jaccard_2 | |
| ENSP00000323534 | ORTHOMCL2007 | jaccard_2 | |
| 135620: OMIM gene: INTEGRIN, ALPHA-5; ITGA5 Gene map locus 12q11-q13 (link from Ensembl BioMart) | ENSP00000293379 | ORTHOMCL15720 | jaccard_160 |
| 135630: OMIM gene: INTEGRIN, BETA-1; ITGB1 Gene map locus 10p11.2 (link from Ensembl BioMart) | ENSP00000302683 | ORTHOMCL3021 | jaccard_347 |
| ENSP00000339970 | ORTHOMCL3021 | jaccard_347 | |
| ENSP00000352630 | ORTHOMCL3021 | jaccard_347 | |
| ENSP00000303351 | ORTHOMCL3021 | jaccard_347 | |
| 135700: OMIM phenotype: FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1 Gene map locus 12q12 (link from NCBI) | ENSP00000354851 | ORTHOMCL1305 | jaccard_38 |
| ENSP00000354878 | ORTHOMCL1305 | jaccard_38 | |
| 135750: OMIM phenotype: LAURIN-SANDROW SYNDROME LAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED Gene map locus 14q13, 14q13 (link from NCBI) | ENSP00000333539 | ORTHOMCL18576 | |
| 135820: OMIM gene: FIBULIN 1; FBLN1 Gene map locus 22q13.3 (link from Ensembl BioMart) | ENSP00000331544 | ORTHOMCL1405 | jaccard_5 |
| ENSP00000262722 | ORTHOMCL1405 | jaccard_5 | |
| ENSP00000342212 | ORTHOMCL1405 | jaccard_5 | |
| ENSP00000262723 | ORTHOMCL1405 | jaccard_5 | |
| 135821: OMIM gene: FIBULIN 2; FBLN2 Gene map locus 3p25-p24 (link from Ensembl BioMart) | ENSP00000295761 | ORTHOMCL1405 | jaccard_5 |
| ENSP00000295760 | ORTHOMCL1405 | jaccard_5 | |
| 136120: OMIM phenotype: FISH-EYE DISEASE; FED Gene map locus 16q22.1 (link from NCBI) | ENSP00000264005 | ORTHOMCL13039 | jaccard_2024 |
| 136130: OMIM gene: FLAVIN-CONTAINING MONOOXYGENASE 1; FMO1 Gene map locus 1q23-q25 (link from Ensembl BioMart) | ENSP00000346901 | ORTHOMCL16921 | jaccard_279 |
| ENSP00000325815 | ORTHOMCL16921 | jaccard_279 | |
| 136131: OMIM gene: FLAVIN-CONTAINING MONOOXYGENASE 4; FMO4 Gene map locus 1q (link from Ensembl BioMart) | ENSP00000013916 | ORTHOMCL405 | jaccard_279 |
| 136132: OMIM gene: FLAVIN-CONTAINING MONOOXYGENASE 3; FMO3 Gene map locus 1q23-q25 (link from Ensembl BioMart) | ENSP00000008553 | ORTHOMCL405 | jaccard_279 |
| 136350: OMIM gene: FIBROBLAST GROWTH FACTOR RECEPTOR 1; FGFR1 FGFR1/BCR FUSION GENE, INCLUDED Gene map locus 8p11.2-p11.1 (link from Ensembl BioMart) | ENSP00000322945 | ||
| ENSP00000311337 | ORTHOMCL329 | jaccard_2 | |
| ENSP00000337247 | ORTHOMCL329 | jaccard_2 | |
| 136351: OMIM gene: FMS-RELATED TYROSINE KINASE 3; FLT3 Gene map locus 13q12 (link from Ensembl BioMart) | ENSP00000241453 | ORTHOMCL19565 | jaccard_2 |
| 136352: OMIM gene: FMS-LIKE TYROSINE KINASE 4; FLT4 Gene map locus 5q35.3 (link from Ensembl BioMart) | ENSP00000261937 | ORTHOMCL16243 | jaccard_2 |
| 136425: OMIM gene: FOLATE RECEPTOR 2, FETAL; FOLR2 Gene map locus 11q13.3-q13.5 (link from Ensembl BioMart) | ENSP00000298223 | ORTHOMCL12454 | jaccard_2138 |
| 136430: OMIM gene: FOLATE RECEPTOR 1, ADULT; FOLR1 Gene map locus 11q13.3-q13.5 (link from Ensembl BioMart) | ENSP00000308137 | ORTHOMCL12116 | jaccard_2138 |
| 136435: OMIM gene: FOLLICLE-STIMULATING HORMONE RECEPTOR; FSHR Gene map locus 2p21-p16 (link from Ensembl BioMart) | ENSP00000306780 | ORTHOMCL4624 | jaccard_415 |
| ENSP00000333908 | jaccard_415 | ||
| 136440: OMIM gene: FOLLICULAR LYMPHOMA VARIANT TRANSLOCATION 1; FVT1 Gene map locus 18q21.3 (link from Ensembl BioMart) | ENSP00000312939 | ORTHOMCL3878 | jaccard_21 |
| 136470: OMIM gene: FOLLISTATIN; FST Gene map locus 5q11.2 (link from Ensembl BioMart) | ENSP00000256759 | ORTHOMCL10180 | jaccard_864 |
| 136510: OMIM gene: FOLYLPOLYGLUTAMATE SYNTHETASE; FPGS GAT-MINUS AUXOTROPH, INCLUDED Gene map locus 9cen-q34 (link from Ensembl BioMart) | ENSP00000259403 | ORTHOMCL1336 | jaccard_1477 |
| 136515: OMIM gene: FOS-LIKE ANTIGEN 1; FOSL1 Gene map locus 11q13 (link from Ensembl BioMart) | ENSP00000310170 | ORTHOMCL19574 | jaccard_2326 |
| 136520: OMIM phenotype: FOVEAL HYPOPLASIA AND PRESENILE CATARACT SYNDROME FOVEAL HYPOPLASIA, ISOLATED, INCLUDED Gene map locus 11p13 (link from NCBI) | ENSP00000241001 | ORTHOMCL1064 | jaccard_273 |
| 136530: OMIM gene: FOLLICLE-STIMULATING HORMONE, BETA POLYPEPTIDE; FSHB Gene map locus 11p13 (link from Ensembl BioMart) | ENSP00000254122 | ORTHOMCL20343 | jaccard_1775 |
| 136533: OMIM gene: FORKHEAD BOX O1A; FOXO1A FKHR/PAX7 FUSION GENE, INCLUDED Gene map locus 13q14.1 (link from Ensembl BioMart) | ENSP00000280496 | ORTHOMCL1173 | jaccard_1145 |
| 136535: OMIM gene: FORMIN; FMN Gene map locus 15q13-q14 (link from Ensembl BioMart) | ENSP00000333950 | ORTHOMCL2197 | jaccard_131 |
| 136537: OMIM gene: FORMYL PEPTIDE RECEPTOR 1; FPR1 Gene map locus Chr.19 (link from Ensembl BioMart) | ENSP00000302707 | ORTHOMCL17705 | jaccard_6 |