The pahtway p1504 has 84 genes in the original annotation. Currently, there are 43 genes in SZGR (with evidence in schizophrenia) that are present at this pathway.
|
| Gene ID |
Symbol |
Synonyms |
Official Full Name |
Start Site |
End Site |
Location |
| 7465 | WEE1 | WEE1A | WEE1hu | WEE1 G2 checkpoint kinase | | | 11p15.4 |
| 283129 | C11orf85 | MAJIN | chromosome 11 open reading frame 85 | | | 11q13.1 |
| 116028 | RMI2 | BLAP18 | C16orf75 | RecQ mediated genome instability 2 | | | 16p13.13 |
| 51087 | YBX2 | CONTRIN | CSDA3 | DBPC | MSY2 | Y-box binding protein 2 | | | 17p13.1 |
| 146857 | SLFN13 | SLFN10 | schlafen family member 13 | | | 17q12 |
| 23217 | ZFR2 | KIAA1086 | zinc finger RNA binding protein 2 | | | 19p13.3 |
| 7398 | USP1 | UBP | ubiquitin specific peptidase 1 | | | 1p31.3 |
| 3633 | INPP5B | 5PTase | inositol polyphosphate-5-phosphatase B | | | 1p34 |
| 6118 | RPA2 | REPA2 | RP-A p32 | RP-A p34 | RPA32 | replication protein A2 | | | 1p35 |
| 3925 | STMN1 | C1orf215 | LAP18 | Lag | OP18 | PP17 | PP19 | PR22 | SMN | stathmin 1 | | | 1p36.11 |
| 3787 | KCNS1 | KV9.1 | potassium voltage-gated channel modifier subfamily S member 1 | | | 20q12 |
| 4744 | NEFH | NFH | neurofilament, heavy polypeptide | | | 22q12.2 |
| 150365 | MEI1 | SPATA38 | meiotic double-stranded break formation protein 1 | | | 22q13.2 |
| 4211 | MEIS1 | - | Meis homeobox 1 | | | 2p14 |
| 729967 | MORN2 | BLOCK27 | MOPT | MORN repeat containing 2 | | | 2p22.1 |
| 4175 | MCM6 | MCG40308 | Mis5 | P105MCM | minichromosome maintenance complex component 6 | | | 2q21 |
| 4292 | MLH1 | COCA2 | FCC2 | HNPCC | HNPCC2 | hMLH1 | mutL homolog 1 | | | 3p21.3 |
| 1951 | CELSR3 | ADGRC3 | CDHF11 | EGFL1 | FMI1 | HFMI1 | MEGF2 | RESDA1 | cadherin EGF LAG seven-pass G-type receptor 3 | | | 3p21.31 |
| 23225 | NUP210 | GP210 | POM210 | nucleoporin 210kDa | | | 3p25.1 |
| 152185 | SPICE1 | CCDC52 | SPICE | spindle and centriole associated protein 1 | | | 3q13.2 |
| 11073 | TOPBP1 | TOP2BP1 | topoisomerase (DNA) II binding protein 1 | | | 3q22.1 |
| 55167 | MSL2 | MSL-2 | MSL2L1 | RNF184 | male-specific lethal 2 homolog (Drosophila) | | | 3q22.3 |
| 256356 | GK5 | - | glycerol kinase 5 (putative) | | | 3q23 |
| 11235 | PDCD10 | CCM3 | TFAR15 | programmed cell death 10 | | | 3q26.1 |
| 55892 | MYNN | OSZF | SBBIZ1 | ZBTB31 | ZNF902 | myoneurin | | | 3q26.2 |
| 86 | ACTL6A | ACTL6 | ARPN-BETA | Arp4 | BAF53A | INO80K | actin like 6A | | | 3q26.33 |
| 8893 | EIF2B5 | CACH | CLE | EIF-2B | EIF2Bepsilon | LVWM | eukaryotic translation initiation factor 2B subunit epsilon | | | 3q27.1 |
| 90407 | TMEM41A | 2900010K02Rik | transmembrane protein 41A | | | 3q27.2 |
| 55171 | TBCCD1 | - | TBCC domain containing 1 | | | 3q27.3 |
| 5437 | POLR2H | RPABC3 | RPB17 | RPB8 | polymerase (RNA) II subunit H | | | 3q28 |
| 3280 | HES1 | HES-1 | HHL | HRY | bHLHb39 | hes family bHLH transcription factor 1 | | | 3q28-q29 |
| 205564 | SENP5 | - | SUMO1/sentrin specific peptidase 5 | | | 3q29 |
| 165918 | RNF168 | hRNF168 | ring finger protein 168, E3 ubiquitin protein ligase | | | 3q29 |
| 4976 | OPA1 | MGM1 | NPG | NTG | largeG | OPA1, mitochondrial dynamin like GTPase | | | 3q29 |
| 348793 | WDR53 | - | WD repeat domain 53 | | | 3q29 |
| 10874 | NMU | - | neuromedin U | | | 4q12 |
| 387103 | CENPW | C6orf173 | CENP-W | CUG2 | centromere protein W | | | 6q22.32 |
| 2146 | EZH2 | ENX-1 | ENX1 | EZH1 | EZH2b | KMT6 | KMT6A | WVS | WVS2 | enhancer of zeste 2 polycomb repressive complex 2 subunit | | | 7q35-q36 |
| 1029 | CDKN2A | ARF | CDK4I | CDKN2 | CMM2 | INK4 | INK4A | MLM | MTS-1 | MTS1 | P14 | P14ARF | P16 | P16-INK4A | P16INK4 | P16INK4A | P19 | P19ARF | TP16 | cyclin-dependent kinase inhibitor 2A | | | 9p21 |
| 55071 | C9orf40 | - | chromosome 9 open reading frame 40 | | | 9q21.13 |
| 65267 | WNK3 | PRKWNK3 | WNK lysine deficient protein kinase 3 | | | Xp11.22 |
| 54457 | TAF7L | CT40 | TAF2Q | TATA-box binding protein associated factor 7 like | | | Xq22.1 |
| 2332 | FMR1 | FMRP | FRAXA | POF | POF1 | fragile X mental retardation 1 | | | Xq27.3 |
