ID: 80765 | StAR related lipid transfer domain containing 5 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (81309053..81324141, complement) | | 607050 |
ID: 51573 | glycerophosphodiester phosphodiesterase 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (19501693..19522098, complement) | 363E6.2, MIR16 | 605943 |
ID: 9416 | DEAD-box helicase 23 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48829756..48852163, complement) | PRPF28, SNRNP100, U5-100K, U5-100KD, prp28 | 612172 |
ID: 4285 | mitochondrial intermediate peptidase [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (23730189..23889400, complement) | COXPD31, HMIP, MIP | 602241 |
ID: 54925 | zinc finger and SCAN domain containing 32 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (3382085..3401004, complement) | HCCS-5, ZNF434 | |
ID: 542767 | prostate and testis expressed opposite C1QTNF9B and MIPEP [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (23888868..23892103) | C1QTNF9B-AS1 | 617122 |
ID: 374659 | HD domain containing 3 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (90929968..90932569, complement) | (ppGpp)ase, MESH1, MYNRL15 | |
ID: 116238 | TLC domain containing 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28724348..28727937, complement) | | 620966 |
ID: 403 | ARF like GTPase 3 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (102673731..102714397, complement) | ARFL3, JBTS35, RP83 | 604695 |
ID: 7126 | TNF alpha induced protein 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28335761..28347009) | B12, B61, BTBD34, EDP1, hBACURD2 | 191161 |
ID: 90410 | intraflagellar transport 20 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28328326..28335472, complement) | | 614394 |
ID: 84464 | SLX4 structure-specific endonuclease subunit [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (3581181..3611606, complement) | BTBD12, FANCP, MUS312 | 613278 |
ID: 23306 | nuclear envelope integral membrane protein 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (57055643..57088627, complement) | TMEM194, TMEM194A | 616496 |
ID: 84263 | hydroxysteroid dehydrogenase like 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (112380108..112472405) | C9orf99, SDR13C1 | |
ID: 210 | aminolevulinate dehydratase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (113386312..113401284, complement) | ALADH, PBGS | 125270 |
ID: 8509 | N-deacetylase and N-sulfotransferase 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (73801916..73811820, complement) | HSST2, N-HSST 2, NST2 | 603268 |
ID: 3709 | inositol 1,4,5-trisphosphate receptor type 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26335352..26833194, complement) | ANHD, CFAP48, INSP3R2, IP3R2 | 600144 |
ID: 51228 | glycolipid transfer protein [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109850945..109880541, complement) | | 608949 |
ID: 6921 | elongin C [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (73945119..73972287, complement) | SIII, TCEB1 | 600788 |
ID: 282991 | biogenesis of lysosomal organelles complex 1 subunit 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (100273278..100286680, complement) | BLOS2, BORCS2, CEAP, CEAP11 | 609768 |