hal_131977 Co-expression

Genes in hal_131977

Organism Gene name Common name Accession Description Start Stop Strand Chromosome
Halobacterium salinarum sp. NRC-1 VNG0811H VNG0811H NP_279789.1 Vng0811h 609288 608896 - NC_002607.1
Halobacterium salinarum sp. NRC-1 VNG1317H VNG1317H NP_280179.1 Vng1317h 984111 983914 - NC_002607.1
Halobacterium salinarum sp. NRC-1 VNG1833C VNG1833C NP_280561.1 Vng1833c 1353444 1352827 - NC_002607.1
Halobacterium salinarum sp. NRC-1 VNG1956H VNG1956H NP_280657.1 Vng1956h 1443507 1444004 + NC_002607.1
Halobacterium salinarum sp. NRC-1 VNG6191H VNG6191H NP_395722.1 Vng6191h 161740 161471 - NC_002608.1
Halobacterium salinarum sp. NRC-1 VNG6196G phoT2 NP_395726.1 sodium-dependent phosphate transporter 162665 163411 + NC_002608.1
Halobacterium salinarum sp. NRC-1 VNG6222H VNG6222H NP_395746.1 Vng6222h 183053 183622 + NC_002608.1
Halobacterium salinarum sp. NRC-1 VNG6292C VNG6292C NP_395794.1 Vng6292c 223370 222849 - NC_002608.1

Conditions in hal_131977

Condition ID Condition Name
hal_101 circadian_drk7_cycling_1980min_vs_NRC-1d.sig
hal_102 circadian_drk7_cycling_2160min_vs_NRC-1d.sig
hal_1051 O2_0258_-0001_L2H_vs_NRC1d.sig
hal_1052 O2_0258_0005_H_vs_NRC1d.sig
hal_1053 O2_0258_0010_H_vs_NRC1d.sig
hal_1055 O2_0258_0030_H_vs_NRC1d.sig
hal_1056 O2_0258_0045_H_vs_NRC1d.sig
hal_1058 O2_0258_0180_H_vs_NRC1d.sig
hal_107 circadian_drk7_cycling_3060min_vs_NRC-1d.sig
hal_108 circadian_drk7_cycling_3240min_vs_NRC-1d.sig
hal_1138 PQ_Const._set_1_0.25mM_-001m_vs_NRC-1f.sig
hal_1139 PQ_Const._set_1_0.25mM_000m_vs_NRC-1f.sig
hal_1141 PQ_Const._set_1_0.25mM_010m_vs_NRC-1f.sig
hal_1142 PQ_Const._set_1_0.25mM_020m_vs_NRC-1f.sig
hal_1143 PQ_Const._set_1_0.25mM_040m_vs_NRC-1f.sig
hal_1144 PQ_Const._set_1_0.25mM_080m_vs_NRC-1f.sig
hal_1145 PQ_Const._set_1_0.25mM_160m_vs_NRC-1f.sig
hal_1165 20060818_KO_ura3_rep2_0.189_vs_NRC-1e.sig
hal_1167 20060818_KO_ura3_rep2_0.828_vs_NRC-1e.sig
hal_1205 20060717_Cmyc_tbpF_rep1_0.401_vs_NRC-1d.sig
hal_1206 20060717_Cmyc_tbpF_rep1_0.829_vs_NRC-1d.sig
hal_127 circadian_20051021_cycling_dark_42oC_1440min_vs_NRC-1d.sig
hal_1276 20060308_KO_tbpA_rep1_0.398_vs_NRC-1e.sig
hal_1277 20060308_KO_tbpA_rep1_0.813_vs_NRC-1e.sig
hal_128 circadian_20051021_cycling_dark_42oC_1615min_vs_NRC-1d.sig
hal_129 circadian_20051021_cycling_dark_42oC_1800min_vs_NRC-1d.sig
hal_131 circadian_20051021_cycling_dark_42oC_2160min_vs_NRC-1d.sig
hal_1324 20050620_Cmyc_tfbG_rep2_0.170_vs_NRC-1d.sig
hal_1326 20050620_Cmyc_tfbG_rep2_1.000_vs_NRC-1d.sig
hal_133 circadian_20051021_cycling_dark_42oC_2515min_vs_NRC-1d.sig
hal_1339 20050620_Cmyc_tfbD_rep1_0.156_vs_NRC-1d.sig
hal_134 circadian_20051021_cycling_dark_42oC_2705min_vs_NRC-1d.sig
hal_1343 20050620_Cmyc_rep2_0.457_vs_NRC-1d.sig
hal_1344 20050620_Cmyc_rep2_1.072_vs_NRC-1d.sig
hal_135 circadian_20051021_cycling_dark_42oC_2880min_vs_NRC-1d.sig
hal_1377 NRC-1.2_0.1684_vs_NRC-1_h1.sig
hal_1378 NRC-1.2_0.3063_vs_NRC-1_h1.sig
hal_1398 NRC-1_0.3279_vs_NRC-1_h1.sig
hal_1428 sDura3D1179_pCu_d0.100mM_t+060m_vs_NRC-1h1.sig
hal_1429 sDura3D1179_pCu_d0.100mM_t+180m_vs_NRC-1h1.sig
hal_1453 sDura3D1179_pZn_d0.020mM_t+060m_vs_NRC-1h1.sig
hal_1456 sDura3D1179_pZn_d0.050mM_t+015m_vs_NRC-1h1.sig
hal_1457 sDura3D1179_pZn_d0.050mM_t+030m_vs_NRC-1h1.sig
hal_1458 sDura3D1179_pZn_d0.050mM_t+060m_vs_NRC-1h1.sig
hal_1459 sDura3D1179_pZn_d0.050mM_t+180m_vs_NRC-1h1.sig
hal_1460 sDura3D1179_pZn_d0.050mM_t-015m_vs_NRC-1h1.sig
hal_148 circadian_dark3_ctrl_1380min_vs_NRC-1d.sig
hal_1481 sDura3_pZn_d0.005mM_t+015m_vs_NRC-1h1.sig
hal_1483 sDura3_pZn_d0.005mM_t+060m_vs_NRC-1h1.sig
hal_1484 sDura3_pZn_d0.005mM_t+180m_vs_NRC-1h1.sig
hal_1485 sDura3_pZn_d0.005mM_t-015m_vs_NRC-1h1.sig
hal_1491 sDura3_pZn_d0.050mM_t+015m_vs_NRC-1h1.sig
hal_1492 sDura3_pZn_d0.050mM_t+030m_vs_NRC-1h1.sig
hal_1493 sDura3_pZn_d0.050mM_t+060m_vs_NRC-1h1.sig
hal_1494 sDura3_pZn_d0.050mM_t+180m_vs_NRC-1h1.sig
hal_150 circadian_dark3_ctrl_1500min_vs_NRC-1d.sig
hal_151 circadian_dark3_ctrl_1620min_vs_NRC-1d.sig
hal_152 circadian_dark3_ctrl_1800min_vs_NRC-1d.sig
hal_154 circadian_dark3_ctrl_2160min_vs_NRC-1d.sig
hal_156 circadian_dark3_ctrl_2340min_vs_NRC-1d.sig
hal_158 circadian_dark3_ctrl_2700min_vs_NRC-1d.sig
hal_159 circadian_dark3_ctrl_2880min_vs_NRC-1d.sig
hal_160 circadian_drk8_control_0000min_vs_NRC-1e.sig
hal_162 circadian_drk8_control_0360min_vs_NRC-1e.sig
hal_163 circadian_drk8_control_0540min_vs_NRC-1e.sig
hal_164 circadian_drk8_control_0720min_vs_NRC-1e.sig
hal_165 circadian_drk8_control_0900min_vs_NRC-1e.sig
hal_166 circadian_drk8_control_1080min_vs_NRC-1e.sig
hal_167 circadian_drk8_control_1260min_vs_NRC-1e.sig
hal_169 circadian_drk8_control_1620min_vs_NRC-1e.sig
hal_170 circadian_drk8_control_1800min_vs_NRC-1e.sig
hal_171 circadian_drk8_control_1980min_vs_NRC-1e.sig
hal_172 circadian_drk8_control_2160min_vs_NRC-1e.sig
hal_174 circadian_drk8_control_2520min_vs_NRC-1e.sig
hal_175 circadian_drk8_control_2700min_vs_NRC-1e.sig
hal_178 circadian_drk8_control_3240min_vs_NRC-1e.sig
hal_230 Circadian_Dark10_Cycling_-2873min_vs_NRC-1h1.sig
hal_232 Circadian_Dark10_Cycling_-2490min_vs_NRC-1h1.sig
hal_238 Circadian_Dark10_Cycling_-1410min_vs_NRC-1h1.sig
hal_239 Circadian_Dark10_Cycling_-1245min_vs_NRC-1h1.sig
hal_242 Circadian_Dark10_Cycling_-0690min_vs_NRC-1h1.sig
hal_243 Circadian_Dark10_Cycling_-0525min_vs_NRC-1h1.sig
hal_245 Circadian_Dark10_Cycling_-0165min_vs_NRC-1h1.sig
hal_246 Circadian_Dark10_Cycling_0000min_vs_NRC-1h1.sig
hal_249 Circadian_Dark10_Cycling_0560min_vs_NRC-1h1.sig
hal_251 Circadian_Dark10_Cycling_0915min_vs_NRC-1h1.sig
hal_252 Circadian_Dark10_Cycling_1100min_vs_NRC-1h1.sig
hal_253 Circadian_Dark10_Cycling_1270min_vs_NRC-1h1.sig
hal_259 Circadian_Dark10_Cycling_2345min_vs_NRC-1h1.sig
hal_262 Circadian_Dark10_Cycling_2895min_vs_NRC-1h1.sig
hal_263 Circadian_Dark10_Cycling_3070min_vs_NRC-1h1.sig
hal_264 Circadian_Dark10_Cycling_3252min_vs_NRC-1h1.sig
hal_266 Circadian_Dark10_Cycling_3630min_vs_NRC-1h1.sig
hal_270 Circadian_Dark10_Cycling_4330min_vs_NRC-1h1.sig
hal_285 Cu_020_vs_NRC-1.sig
hal_288 Cu_160_vs_NRC-1.sig
hal_363 Cu_ura3_KO_set2_010min_vs_NRC-1h1.sig
hal_366 Cu_ura3_KO_set2_080min_vs_NRC-1h1.sig
hal_367 Cu_ura3_KO_set2_160min_vs_NRC-1h1.sig
hal_369 Cu_vng700_KO_set2_000min_vs_NRC-1h1.sig
hal_371 Cu_vng700_KO_set2_010min_vs_NRC-1h1.sig
hal_375 Cu_vng700_KO_set2_160min_vs_NRC-1h1.sig
hal_462 feso4__-0001m_vs_NRC-1
hal_463 feso4__0000m_vs_NRC-1
hal_465 feso4__0010m_vs_NRC-1b
hal_468 feso4__0025m_vs_NRC-1b
hal_469 feso4__0040m_vs_NRC-1
hal_470 feso4__0080m_vs_NRC-1
hal_471 feso4__0160m_vs_NRC-1
hal_472 feso4__0320m_vs_NRC-1
hal_486 idr1_60min_+Fe_vs_NRC1-h1.sig
hal_512 tfbG_CHIS_over
hal_513 tfb_D_vs_NRC-1c
hal_514 tfb_C_vs_NRC-1c
hal_515 tfb_B_vs_NRC-1c
hal_516 tfb_A_vs_NRC-1c
hal_551 NRC-1__HO_D_vs_NRC-1
hal_554 NRC-1__LO_L_vs_NRC-1
hal_584 gamma4__0000gy-010min
hal_585 gamma4__0000gy-020min
hal_586 gamma4__0000gy-030min
hal_587 gamma4__0000gy-040min
hal_588 gamma4__0000gy-050min
hal_589 gamma4__0000gy-060min
hal_591 gamma4__0000gy-240min
hal_729 PQ_Recov._set_2_0mM_020min_vs_NRC-1f.sig
hal_750 H2O2_Const._set_1_0mM_000min_vs_NRC-1f.sig
hal_751 H2O2_Const._set_1_0mM_030min_vs_NRC-1f.sig
hal_833 NRC-1_control_2days_vs_NRC-1h1.sig
hal_919 PQ_Recov._set_2_4mM_000min_vs_NRC-1f.sig
hal_920 PQ_Recov._set_2_4mM_010min_vs_NRC-1f.sig
hal_924 PQ_Recov._set_2_4mM_050min_vs_NRC-1f.sig
hal_926 PQ_Recov._set_2_4mM_120min_vs_NRC-1f.sig
hal_927 PQ_Recov._set_2_4mM_240min_vs_NRC-1f.sig
hal_949 PQ_Recov._set_1_4mM_020min_vs_NRC-1f.sig
hal_95 circadian_drk7_cycling_0900min_vs_NRC-1d.sig
hal_950 PQ_Recov._set_1_4mM_030min_vs_NRC-1f.sig
hal_969 KO_trh6.1_0.1689_vs_NRC-1_h1.sig
hal_97 circadian_drk7_cycling_1260min_vs_NRC-1d.sig
hal_970 KO_trh6.1_0.3532_vs_NRC-1_h1.sig
hal_971 KO_trh6.1_0.4762_vs_NRC-1_h1.sig
hal_972 KO_trh6.1_0.7964_vs_NRC-1_h1.sig
hal_99 circadian_drk7_cycling_1620min_vs_NRC-1d.sig

De novo detected cis-regulatory motifs

CRM ID eval PSSM
hal_131977_1 230.0000
hal_131977_2 2500.0000

GREs assigned to hal_131977

GRE ID PSSM
hal_0
hal_0

Corems associated with hal_131977

Corem
hc15251
hc16269
hc18595
hc18596
hc23879
hc27530
hc35295
hc35473
hc36106
hc38369
hc9217
hc9222
hc9454