300521-305990 --- 314370-600034
| OMIM ID: disease or gene description | Ensembl Peptide ID | OrthoMCL Family | Jaccard Coefficient Cluster |
|---|---|---|---|
| 306000: OMIM gene: GLYCOGEN STORAGE DISEASE VIII PHOSPHORYLASE KINASE, LIVER, ALPHA-2 SUBUNIT, INCLUDED; PHKA2, INCLUDED Gene map locus Xp22.2-p22.1 (link from Ensembl BioMart) | ENSP00000327131 | ORTHOMCL1127 | jaccard_930 |
| 306100: OMIM gene: GONADAL DYSGENESIS, XY FEMALE TYPE; GDXY TESTIS-DETERMINING FACTOR, X-CHROMOSOMAL, INCLUDED; TDFX, INCLUDED Gene map locus Xp22.11-p21.2 (link from Ensembl BioMart) | ENSP00000329362 | ||
| 306250: OMIM gene: COLONY-STIMULATING FACTOR 2 RECEPTOR, ALPHA; CSF2RA Gene map locus Xp22.32 (link from Ensembl BioMart) | ENSP00000354759 | ORTHOMCL5302 | jaccard_963 |
| ENSP00000348058 | ORTHOMCL5302 | jaccard_963 | |
| ENSP00000354836 | ORTHOMCL5302 | jaccard_963 | |
| ENSP00000346184 | ORTHOMCL5302 | jaccard_963 | |
| 306400: OMIM phenotype: GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CGD CYTOCHROME b-POSITIVE GRANULOMATOUS DISEASE, CHRONIC, X-LINKED, INCLUDED Gene map locus Xp21.1 (link from NCBI) | ENSP00000297870 | ORTHOMCL266 | jaccard_448 |
| 306480: OMIM gene: DXF68S1E Gene map locus Xp22.32 (link from Ensembl BioMart) | ENSP00000252304 | ORTHOMCL3399 | jaccard_1290 |
| 306700: OMIM gene: HEMOPHILIA A COAGULATION FACTOR VIIIC, PROCOAGULANT COMPONENT, INCLUDED; F8C, INCLUDED Gene map locus Xq28 (link from Ensembl BioMart) | ENSP00000353393 | ORTHOMCL3458 | jaccard_716 |
| ENSP00000327895 | jaccard_1378 | ||
| 306900: OMIM gene: HEMOPHILIA B; HEMB COAGULATION FACTOR IX, INCLUDED; F9, INCLUDED Gene map locus Xq27.1-q27.2 (link from Ensembl BioMart) | ENSP00000218099 | ORTHOMCL16028 | jaccard_10 |
| 306955: OMIM phenotype: HETEROTAXY, VISCERAL, X-LINKED Gene map locus Xq26.2 (link from NCBI) | ENSP00000287538 | ORTHOMCL14411 | jaccard_2734 |
| 307000: OMIM phenotype: HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS; HSAS HYDROCEPHALUS, X-LINKED, WITH CONGENITAL IDIOPATHIC INTESTINAL PSEUDOOBSTRUCTION, INCLUDED Gene map locus Xq28 (link from NCBI) | ENSP00000355380 | ORTHOMCL1418 | jaccard_2 |
| ENSP00000354712 | ORTHOMCL1418 | jaccard_2 | |
| 307030: OMIM phenotype: HYPERGLYCEROLEMIA Gene map locus Xp21.3-p21.2 (link from NCBI) | ENSP00000354642 | ORTHOMCL815 | jaccard_465 |
| 307200: OMIM phenotype: HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED Gene map locus Xq21.3-q22 (link from NCBI) | ENSP00000308176 | ORTHOMCL2323 | jaccard_54 |
| ENSP00000337233 | ORTHOMCL2323 | jaccard_54 | |
| 307800: OMIM phenotype: HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT Gene map locus Xp22.2-p22.1 (link from NCBI) | ENSP00000323863 | ORTHOMCL22330 | jaccard_189 |
| 308000: OMIM gene: HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1 HPRT Gene map locus Xq26-q27.2 (link from Ensembl BioMart) | ENSP00000355367 | ORTHOMCL5148 | jaccard_2195 |
| 308050: OMIM phenotype: CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS Gene map locus Xq28 (link from NCBI) | ENSP00000276346 | ORTHOMCL2304 | jaccard_238 |
| 308100: OMIM gene: ICHTHYOSIS, X-LINKED ARYLSULFATASE C, ISOZYME S, INCLUDED; ARSC1, INCLUDED Gene map locus Xp22.32 (link from Ensembl BioMart) | ENSP00000217961 | ORTHOMCL3888 | jaccard_197 |
| 308230: OMIM phenotype: IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 1; HIGM1 Gene map locus Xq26 (link from NCBI) | ENSP00000218368 | ORTHOMCL21741 | jaccard_950 |
| 308240: OMIM phenotype: LYMPHOPROLIFERATIVE SYNDROME, X-LINKED Gene map locus Xq25 (link from NCBI) | ENSP00000331181 | ORTHOMCL14508 | jaccard_2730 |
| 308300: OMIM phenotype: INCONTINENTIA PIGMENTI; IP Gene map locus Xq28 (link from NCBI) | ENSP00000263518 | ORTHOMCL17310 | |
| 308350: OMIM phenotype: INFANTILE SPASM SYNDROME, X-LINKED Gene map locus Xp22.13 (link from NCBI) | ENSP00000262697 | ORTHOMCL11520 | |
| ENSP00000005545 | ORTHOMCL6621 | jaccard_9621 | |
| 308370: OMIM phenotype: INFERTILE MALE SYNDROME (link from Ensembl BioMart) | ENSP00000313925 | ORTHOMCL8575 | jaccard_1435 |
| 308380: OMIM gene: INTERLEUKIN 2 RECEPTOR, GAMMA; IL2RG Gene map locus Xq13 (link from Ensembl BioMart) | ENSP00000276110 | ORTHOMCL14388 | jaccard_963 |
| 308700: OMIM gene: KALLMANN SYNDROME 1; KAL1 KALLMANN SYNDROME INTERVAL GENE 1, INCLUDED; KALIG1, INCLUDED Gene map locus Xp22.3 (link from Ensembl BioMart) | ENSP00000262648 | ORTHOMCL6724 | jaccard_4631 |
| 308800: OMIM phenotype: KERATOSIS FOLLICULARIS SPINULOSA DECALVANS; KFSD Gene map locus Xp22.1 (link from NCBI) | ENSP00000252349 | ORTHOMCL11127 | jaccard_1454 |
| 308840: OMIM gene: L1 CELL ADHESION MOLECULE; L1CAM Gene map locus Xq28 (link from Ensembl BioMart) | ENSP00000355380 | ORTHOMCL1418 | jaccard_2 |
| ENSP00000354712 | ORTHOMCL1418 | jaccard_2 | |
| 308930: OMIM phenotype: LEIGH SYNDROME, X-LINKED Gene map locus Xp22.2-p22.1 (link from NCBI) | ENSP00000254142 | ORTHOMCL1589 | jaccard_838 |
| ENSP00000348062 | ORTHOMCL245 | jaccard_1212 | |
| 308940: OMIM phenotype: LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY Gene map locus Xq22.3 (link from NCBI) | ENSP00000355057 | ORTHOMCL92 | jaccard_0 |
| ENSP00000334733 | ORTHOMCL92 | jaccard_0 | |
| ENSP00000355107 | ORTHOMCL92 | jaccard_0 | |
| 308990: OMIM phenotype: PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS (link from Ensembl BioMart) | ENSP00000343213 | ORTHOMCL1034 | jaccard_243 |
| ENSP00000304257 | ORTHOMCL1034 | jaccard_243 | |
| 309060: OMIM gene: LYSOSOME-ASSOCIATED MEMBRANE PROTEIN 2; LAMP2 Gene map locus Xq24 (link from Ensembl BioMart) | ENSP00000200639 | ORTHOMCL9626 | jaccard_1947 |
| ENSP00000007752 | ORTHOMCL9626 | jaccard_1947 | |
| 309400: OMIM phenotype: MENKES DISEASE Gene map locus Xq12-q13 (link from NCBI) | ENSP00000345728 | ORTHOMCL817 | jaccard_30 |
| 309500: OMIM phenotype: RENPENNING SYNDROME 1; RENS1 Gene map locus Xp11.23 (link from NCBI) | ENSP00000218224 | ORTHOMCL4785 | jaccard_3874 |
| ENSP00000308619 | ORTHOMCL3160 | jaccard_48 | |
| 309510: OMIM phenotype: PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS Gene map locus Xp22.13 (link from NCBI) | ENSP00000005545 | ORTHOMCL6621 | jaccard_9621 |
| 309548: OMIM gene: FRAGILE SITE, FOLIC ACID TYPE, RARE, FRA(X)(q28); FRAXE FRAGILE SITE MENTAL RETARDATION 2 GENE, INCLUDED; FMR2, INCLUDED Gene map locus Xq28 (link from Ensembl BioMart) | ENSP00000286437 | ORTHOMCL6311 | jaccard_9168 |
| 309549: OMIM phenotype: MENTAL RETARDATION, X-LINKED 9; MRX9 Gene map locus Xp11.23 (link from NCBI) | ENSP00000326948 | ORTHOMCL3049 | jaccard_1275 |
| ENSP00000019019 | ORTHOMCL3049 | jaccard_1275 | |
| 309550: OMIM gene: FRAGILE SITE MENTAL RETARDATION 1 GENE; FMR1 FRAGILE X SYNDROME, INCLUDED Gene map locus Xq27.3 (link from Ensembl BioMart) | ENSP00000345039 | jaccard_936 | |
| 309580: OMIM phenotype: MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED Gene map locus Xq13 (link from NCBI) | ENSP00000308619 | ORTHOMCL3160 | jaccard_48 |
| ENSP00000319106 | ORTHOMCL3160 | jaccard_48 | |
| 309583: OMIM phenotype: MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE Gene map locus Xp22.1 (link from NCBI) | ENSP00000354731 | ORTHOMCL5810 | jaccard_1100 |
| 309845: OMIM gene: MOESIN; MSN Gene map locus Xq11.2-q12 (link from Ensembl BioMart) | ENSP00000275995 | ORTHOMCL490 | jaccard_63 |
| ENSP00000353408 | ORTHOMCL490 | jaccard_63 | |
| 309850: OMIM gene: MONOAMINE OXIDASE A; MAOA BRUNNER SYNDROME, INCLUDED Gene map locus Xp11.23 (link from Ensembl BioMart) | ENSP00000340684 | ORTHOMCL16775 | jaccard_298 |
| 309860: OMIM gene: MONOAMINE OXIDASE B; MAOB Gene map locus Xp11.23 (link from Ensembl BioMart) | ENSP00000265833 | ORTHOMCL15477 | jaccard_298 |
| 309900: OMIM gene: MUCOPOLYSACCHARIDOSIS TYPE II IDURONATE 2-SULFATASE, INCLUDED; IDS, INCLUDED Gene map locus Xq28 (link from Ensembl BioMart) | ENSP00000355289 | jaccard_197 | |
| ENSP00000339801 | ORTHOMCL10939 | jaccard_197 | |
| 310200: OMIM phenotype: MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD Gene map locus Xp21.2, 12q21 (link from NCBI) | ENSP00000354464 | ORTHOMCL994 | jaccard_644 |
| ENSP00000350765 | ORTHOMCL994 | jaccard_3 | |
| ENSP00000352894 | ORTHOMCL994 | jaccard_3 | |
| ENSP00000355035 | ORTHOMCL994 | jaccard_644 | |
| ENSP00000228641 | ORTHOMCL7577 | jaccard_2085 | |
| ENSP00000340057 | ORTHOMCL994 | jaccard_3 | |
| ENSP00000354923 | ORTHOMCL994 | jaccard_3 | |
| ENSP00000354515 | ORTHOMCL994 | jaccard_644 | |
| 310300: OMIM phenotype: EMERY-DREIFUSS MUSCULAR DYSTROPHY, X-LINKED; EDMD Gene map locus Xq28 (link from NCBI) | ENSP00000218240 | ORTHOMCL21487 | jaccard_1524 |
| 310400: OMIM phenotype: MYOTUBULAR MYOPATHY 1; MTM1 Gene map locus Xq28 (link from NCBI) | ENSP00000301919 | ORTHOMCL1691 | jaccard_221 |
| 310468: OMIM phenotype: NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE; XRN Gene map locus Xp11.22 (link from NCBI) | ENSP00000343213 | ORTHOMCL1034 | jaccard_243 |
| ENSP00000304257 | ORTHOMCL1034 | jaccard_243 | |
| 310500: OMIM phenotype: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1; CSNB1 NYCTALOPIA, INCLUDED Gene map locus Xp11.4 (link from NCBI) | ENSP00000340328 | ORTHOMCL16152 | jaccard_7 |
| 310600: OMIM gene: NORRIE DISEASE; ND NDP GENE, INCLUDED; NDP, INCLUDED Gene map locus Xp11.4 (link from Ensembl BioMart) | ENSP00000244349 | ORTHOMCL11321 | jaccard_7332 |
| 311030: OMIM gene: MCF.2 CELL LINE-DERIVED TRANSFORMING SEQUENCE; MCF2 Gene map locus Xq27 (link from Ensembl BioMart) | ENSP00000355405 | ORTHOMCL7871 | jaccard_55 |
| 311040: OMIM gene: ELK1, MEMBER OF ETS ONCOGENE FAMILY; ELK1 ELK2, MEMBER OF ETS ONCOGENE FAMILY, PSEUDOGENE 1, INCLUDED Gene map locus Xp11.2 (link from Ensembl BioMart) | ENSP00000247161 | ORTHOMCL24934 | jaccard_464 |
| 311150: OMIM phenotype: OPTICOACOUSTIC NERVE ATROPHY WITH DEMENTIA Gene map locus Xq22 (link from NCBI) | ENSP00000247385 | ORTHOMCL2050 | jaccard_1309 |
| 311200: OMIM phenotype: OROFACIODIGITAL SYNDROME I; OFD1 Gene map locus Xp22.3-p22.2 (link from NCBI) | ENSP00000319207 | ORTHOMCL10464 | jaccard_3 |
| ENSP00000344314 | |||
| 311240: OMIM gene: ORNITHINE AMINOTRANSFERASE-LIKE 1; OATL1 Gene map locus Xp11.3-p11.23 (link from Ensembl BioMart) | ENSP00000156097 | ORTHOMCL13441 | jaccard_8884 |
| 311250: OMIM phenotype: ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO VALPROATE SENSITIVITY, INCLUDED Gene map locus Xp21.1 (link from NCBI) | ENSP00000039007 | ORTHOMCL8419 | jaccard_4550 |
| 311550: OMIM gene: PCTAIRE PROTEIN KINASE 1; PCTK1 Gene map locus Xp11.3-p11.23 (link from Ensembl BioMart) | ENSP00000352776 | ORTHOMCL9751 | jaccard_28 |
| ENSP00000276052 | ORTHOMCL9751 | jaccard_28 | |
| ENSP00000349762 | ORTHOMCL9751 | jaccard_28 | |
| 311770: OMIM gene: PHOSPHATIDYLINOSITOL GLYCAN, CLASS A; PIGA PAROXYSMAL NOCTURNAL HEMOGLOBINURIA, INCLUDED; PNH, INCLUDED Gene map locus Xp22.1 (link from Ensembl BioMart) | ENSP00000297902 | ORTHOMCL4273 | jaccard_2193 |
| ENSP00000351532 | jaccard_2193 | ||
| 311790: OMIM gene: 6-@PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE 1; PFKFB1 Gene map locus Xp11.21 (link from Ensembl BioMart) | ENSP00000289537 | ORTHOMCL424 | jaccard_601 |
| 311800: OMIM gene: PHOSPHOGLYCERATE KINASE 1; PGK1 PHOSPHOGLYCERATE KINASE 1 PSEUDOGENE 1, INCLUDED; PGK1P1, INCLUDED Gene map locus Xq13 (link from Ensembl BioMart) | ENSP00000218265 | ORTHOMCL1504 | jaccard_1440 |
| 311850: OMIM gene: PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE I; PRPS1 GOUT, PRPS-RELATED, INCLUDED Gene map locus Xq22-q24 (link from Ensembl BioMart) | ENSP00000276174 | ORTHOMCL765 | jaccard_452 |
| 311860: OMIM gene: PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE II; PRPS2 Gene map locus Xp22.3-p22.2 (link from Ensembl BioMart) | ENSP00000218027 | ORTHOMCL765 | jaccard_452 |
| 311870: OMIM gene: PHOSPHORYLASE KINASE, MUSCLE, ALPHA-1 SUBUNIT; PHKA1 Gene map locus Xq13 (link from Ensembl BioMart) | ENSP00000262840 | ORTHOMCL1127 | jaccard_930 |
| 312040: OMIM gene: POLYMERASE, DNA, ALPHA; POLA Gene map locus Xp22.3-p21.1 (link from Ensembl BioMart) | ENSP00000314415 | ORTHOMCL3926 | jaccard_998 |
| 312060: OMIM phenotype: PROPERDIN DEFICIENCY, X-LINKED PROPERDIN DEFICIENCY, TYPE II, INCLUDED Gene map locus Xp11.4-p11.23 (link from NCBI) | ENSP00000247153 | ORTHOMCL20958 | jaccard_41 |
| 312070: OMIM gene: UBIQUITIN-LIKE 4; UBL4 Gene map locus Xq28 (link from Ensembl BioMart) | ENSP00000218299 | ORTHOMCL12998 | jaccard_126 |
| 312080: OMIM phenotype: PELIZAEUS-MERZBACHER DISEASE; PMD Gene map locus Xq22 (link from NCBI) | ENSP00000354860 | ORTHOMCL7313 | jaccard_981 |
| ENSP00000305152 | ORTHOMCL7313 | jaccard_981 | |
| 312090: OMIM gene: PROTEIN P3 Gene map locus Xq28 (link from Ensembl BioMart) | ENSP00000263512 | ORTHOMCL4383 | jaccard_863 |
| 312095: OMIM gene: PSEUDOAUTOSOMAL GENE XE7 Gene map locus Xp22.32 (link from Ensembl BioMart) | ENSP00000324827 | ORTHOMCL5516 | |
| 312170: OMIM phenotype: PYRUVATE DECARBOXYLASE DEFICIENCY LACTIC ACIDEMIA, THIAMINE-RESPONSIVE, INCLUDED Gene map locus Xp22.2-p22.1 (link from NCBI) | ENSP00000254142 | ORTHOMCL1589 | jaccard_838 |
| ENSP00000348062 | ORTHOMCL245 | jaccard_1212 | |
| ENSP00000307241 | ORTHOMCL2270 | jaccard_1289 | |
| 312173: OMIM gene: RIBOSOMAL PROTEIN L10; RPL10 Gene map locus Xq28 (link from Ensembl BioMart) | ENSP00000341730 | ORTHOMCL1806 | jaccard_1218 |
| 312180: OMIM gene: UBIQUITIN-CONJUGATING ENZYME E2A; UBE2A Gene map locus Xq24-q25 (link from Ensembl BioMart) | ENSP00000335027 | jaccard_42 | |
| ENSP00000161284 | ORTHOMCL1871 | jaccard_42 | |
| ENSP00000338634 | |||
| 312300: OMIM phenotype: REIFENSTEIN SYNDROME (link from Ensembl BioMart) | ENSP00000313925 | ORTHOMCL8575 | jaccard_1435 |
| 312420: OMIM gene: RENIN-BINDING PROTEIN; RENBP Gene map locus Xq28 (link from Ensembl BioMart) | ENSP00000218151 | ORTHOMCL15088 | jaccard_11781 |
| 312600: OMIM gene: RETINITIS PIGMENTOSA 2, X-LINKED; RP2 RP2 GENE, INCLUDED; RP2, INCLUDED Gene map locus Xp11.3 (link from Ensembl BioMart) | ENSP00000218340 | ORTHOMCL7222 | jaccard_2110 |
| 312610: OMIM gene: RETINITIS PIGMENTOSA GTPase REGULATOR; RPGR Gene map locus Xp21.1 (link from Ensembl BioMart) | ENSP00000343671 | ORTHOMCL3294 | jaccard_13711 |
| ENSP00000322219 | ORTHOMCL3294 | jaccard_2932 | |
| ENSP00000339531 | ORTHOMCL3294 | jaccard_231 | |
| 312700: OMIM gene: RETINOSCHISIS 1, X-LINKED, JUVENILE; RS1 RETINOSCHISIS 1 GENE, INCLUDED; RS1 GENE, INCLUDED Gene map locus Xp22.2-p22.1 (link from Ensembl BioMart) | ENSP00000218225 | ORTHOMCL16709 | jaccard_1378 |
| 312750: OMIM phenotype: RETT SYNDROME; RTT RETT SYNDROME, PRESERVED SPEECH VARIANT, INCLUDED Gene map locus Xq28, Xp22 (link from NCBI) | ENSP00000262697 | ORTHOMCL11520 | |
| ENSP00000301948 | ORTHOMCL12144 | jaccard_8147 | |
| 312760: OMIM gene: RIBOSOMAL PROTEIN S4, X-LINKED; RPS4X SINGLE-COPY ABUNDANT mRNA; SCAR Gene map locus Xq13.1 (link from Ensembl BioMart) | ENSP00000352322 | ORTHOMCL2015 | jaccard_1270 |
| 312820: OMIM gene: SARCOMA, SYNOVIAL, X BREAKPOINT 1; SSX1 SARCOMA, SYNOVIAL, INCLUDED Gene map locus Xp11.2 (link from Ensembl BioMart) | ENSP00000290501 | ORTHOMCL222 | jaccard_557 |
| 312861: OMIM gene: 5-@HYDROXYTRYPTAMINE RECEPTOR 2C; HTR2C Gene map locus Xq24 (link from Ensembl BioMart) | ENSP00000276198 | ORTHOMCL10103 | jaccard_19 |
| 312863: OMIM phenotype: COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX Gene map locus Xq13 (link from NCBI) | ENSP00000276110 | ORTHOMCL14388 | jaccard_963 |
| 312865: OMIM gene: SHORT STATURE HOMEOBOX; SHOX PSEUDOAUTOSOMAL HOMEOBOX-CONTAINING OSTEOGENIC GENE, INCLUDED; PHOG, INCLUDED Gene map locus Xpter-p22.32 (link from Ensembl BioMart) | ENSP00000341131 | ORTHOMCL18208 | |
| 312870: OMIM phenotype: SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1 Gene map locus Xq26 (link from NCBI) | ENSP00000276212 | ORTHOMCL15238 | jaccard_1068 |
| 312920: OMIM phenotype: SPASTIC PARAPLEGIA 2, X-LINKED; SPG2 Gene map locus Xq22 (link from NCBI) | ENSP00000354860 | ORTHOMCL7313 | jaccard_981 |
| ENSP00000305152 | ORTHOMCL7313 | jaccard_981 | |
| 313020: OMIM gene: SPERMIDINE/SPERMINE N(1)-ACETYLTRANSFERASE; SAT Gene map locus Xp22.1 (link from Ensembl BioMart) | ENSP00000252349 | ORTHOMCL11127 | jaccard_1454 |
| 313200: OMIM phenotype: SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1; SMAX1 SPINAL MUSCULAR ATROPHY, BENIGN, WITH HYPERTROPHY OF CALVES, INCLUDED Gene map locus Xq11-q12 (link from NCBI) | ENSP00000313925 | ORTHOMCL8575 | jaccard_1435 |
| 313400: OMIM phenotype: SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT Gene map locus Xp22.2-p22.1 (link from NCBI) | ENSP00000310153 | ORTHOMCL6772 | jaccard_1553 |
| ENSP00000350472 | ORTHOMCL13735 | jaccard_1553 | |
| 313430: OMIM gene: SRY-BOX 3; SOX3 INFUNDIBULAR HYPOPLASIA AND HYPOPITUITARISM, INCLUDED Gene map locus Xq26.3 (link from Ensembl BioMart) | ENSP00000257018 | ORTHOMCL5215 | jaccard_12290 |
| 313440: OMIM gene: SYNAPSIN I; SYN1 Gene map locus Xp11.4-p11.2 (link from Ensembl BioMart) | ENSP00000263237 | ORTHOMCL699 | jaccard_8100 |
| ENSP00000295987 | ORTHOMCL699 | jaccard_1109 | |
| ENSP00000343206 | ORTHOMCL699 | jaccard_8100 | |
| 313475: OMIM gene: SYNAPTOPHYSIN; SYP Gene map locus Xp11.23-p11.22 (link from Ensembl BioMart) | ENSP00000263233 | ORTHOMCL8566 | jaccard_1177 |
| 313650: OMIM gene: TAF1 RNA POLYMERASE II, TATA BOX-BINDING PROTEIN-ASSOCIATED FACTOR, 250-KD; TAF1 TRANSCRIPTION FACTOR IID, INCLUDED; TFIID, INCLUDED; TF2D, INCLUDED Gene map locus Xq13 (link from Ensembl BioMart) | ENSP00000276072 | ORTHOMCL2081 | jaccard_2262 |
| 313700: OMIM gene: ANDROGEN RECEPTOR; AR Gene map locus Xq11-q12 (link from Ensembl BioMart) | ENSP00000313925 | ORTHOMCL8575 | jaccard_1435 |
| 313900: OMIM phenotype: THROMBOCYTOPENIA 1; THC1 THROMBOCYTOPENIA, X-LINKED, INTERMITTENT, INCLUDED Gene map locus Xp11.23-p11.22 (link from NCBI) | ENSP00000317862 | ORTHOMCL13483 | jaccard_11979 |
| 314200: OMIM gene: THYROXINE-BINDING GLOBULIN OF SERUM; TBG THYROXINE-BINDING GLOBULIN DEFICIENCY, INCLUDED Gene map locus Xq22.2 (link from Ensembl BioMart) | ENSP00000329374 | ORTHOMCL20519 | jaccard_51 |
| 314310: OMIM gene: TRANSCRIPTION FACTOR FOR IMMUNOGLOBULIN HEAVY-CHAIN ENHANCER 3; TFE3 TFE3/ASPSCR1 FUSION GENE, INCLUDED Gene map locus Xp11.22 (link from Ensembl BioMart) | ENSP00000314129 | ORTHOMCL6275 | jaccard_531 |
| ENSP00000338360 | ORTHOMCL6275 | jaccard_531 |