EntrezGene:10801

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Related TSS IDs


rfhg_199045.1
rfhg_199046.1
rfhg_199047.1
rfhg_199048.1
rfhg_199049.1
rfhg_199051.1
rfhg_199052.1
rfhg_199053.1
rfhg_199054.1
rfhg_199058.1
rfhg_199059.1
rfhg_199060.1
rfhg_199061.1
rfhg_199062.1
rfhg_199071.1
rfhg_199072.1
rfhg_199076.1
rfhg_199077.1
rfhg_199080.1
rfhg_199081.1
rfhg_199084.1
rfhg_199093.1
rfhg_199094.1
rfhg_199095.1
rfhg_199096.1
rfhg_199097.1
rfhg_199098.1
rfhg_199099.1
rfhg_199100.1
rfhg_199106.1
rfhg_199107.1
rfhg_199108.1
rfhg_199109.1
rfhg_199110.1
rfhg_199111.1
rfhg_199112.1
rfhg_199113.1
rfhg_199114.1
rfhg_199115.1
rfhg_199118.1
rfhg_199119.1
rfhg_199120.1
rfhg_199122.1
rfhg_199123.1
rfhg_199124.1
rfhg_199130.1
rfhg_199131.1


Basic information


GeneID:10801
Species:human
Gene name:septin 9
Gene symbol:SEPT9
Gene synonyms:AF17q25
MSF
MSF1
NAPB
PNUTL4
SINT1
SeptD1
Gene type:protein-coding
Old GeneIDs:8162


Links to external databases


HGNC/MGI_ID:HGNC:7323
Ensembl:Ensembl:ENSG00000184640
Vega:Vega:OTTHUMG00000177327
HPRD:HPRD:10360
miRBase:
IMGT/GENE-DB:
MIM:MIM:604061


Transcripts


Gencode transcripts:ENST00000589070.1
ENST00000427177.5
ENST00000591833.5
ENST00000591198.5
ENST00000590576.5
ENST00000449803.6
ENST00000431235.6
ENST00000587237.1
ENST00000329047.12
ENST00000590294.5
ENST00000588575.1
ENST00000590595.1
ENST00000591934.1
ENST00000588690.5
ENST00000592098.1
ENST00000423034.6
ENST00000590059.5
ENST00000587514.1
ENST00000590586.1
ENST00000592407.1
ENST00000427674.6
ENST00000589140.1
ENST00000590825.1
ENST00000586812.1
ENST00000592420.1
ENST00000585930.5
ENST00000591020.5
ENST00000586521.5
ENST00000588958.6
ENST00000586128.5
ENST00000541152.6
ENST00000591704.5
ENST00000592481.5
ENST00000591088.5
ENST00000590938.5
ENST00000592951.5
ENST00000586433.5
ENST00000585929.5
ENST00000590917.5
ENST00000591472.6
ENST00000593189.6
ENST00000427180.5
ENST00000589920.5
ENST00000585638.1
ENST00000589250.5
ENST00000586456.1
ENST00000589246.1
RefSeq transcripts:NM_001293695
NM_001113491
NM_001113492
NM_006640
NM_001113493
NM_001113494
NM_001293696
NM_001113496
NM_001293697
NM_001293698
NM_001113495
UCSC genes:uc060kph.1
uc002jts.5
uc060kpi.1
uc010wtk.3
uc060kpj.1
uc002jtt.5
uc060kpk.1
uc060kpl.1
uc002jtu.5
uc060kpm.1
uc060kpn.1
uc060kpp.1
uc060kpq.1
uc060kpr.1
uc002jtv.4
uc060kps.1
uc060kpu.1
uc060kpv.1
uc060kpw.1
uc002jtw.4
uc060kpx.1
uc060kpy.1
uc060kpz.1
uc060kqa.1
uc010wtl.3
uc060kqb.1
uc060kqc.1
uc060kqf.1
uc060kqg.1
uc002jty.5
uc060kqh.1
uc060kqi.1
uc010wtm.3
uc060kqj.1
uc010wtn.3
uc060kqk.1
uc060kql.1
uc060kqm.1
uc060kqn.1
uc060kqo.1
uc010dhd.4
uc060kqr.1
uc060kqs.1
uc060kqt.1
uc060kqu.1
uc060kqv.1
Other_mRNAs:AF189712
AF189713
AJ312323
AK300270
AK300268
BC054004
AK290368
AJ312321
AF123052
AF142408
BC021192
CU676864
DQ893792
BT007215
DQ890623
KU178538
KU178539
AJ312319
AK304143
AB023208
AJ312322
BC114550
AK303449
AJ312320
AK022493
AK299828
AK316473
AK056495
AL080131
BC128416
AF142569
BC064642
BC018877







Property "Other mrnas" (as page type) with input value "AF189712 AF189713 AJ312323 AK300270 AK300268 BC054004 AK290368 AJ312321 AF123052 AF142408 BC021192 CU676864 DQ893792 BT007215 DQ890623 KU178538 KU178539 AJ312319 AK304143 AB023208 AJ312322 BC114550 AK303449 AJ312320 AK022493 AK299828 AK316473 AK056495 AL080131 BC128416 AF142569 BC064642 BC018877" contains invalid characters or is incomplete and therefore can cause unexpected results during a query or annotation process.


Property "Ucsc genes" (as page type) with input value "uc060kph.1 uc002jts.5 uc060kpi.1 uc010wtk.3 uc060kpj.1 uc002jtt.5 uc060kpk.1 uc060kpl.1 uc002jtu.5 uc060kpm.1 uc060kpn.1 uc060kpp.1 uc060kpq.1 uc060kpr.1 uc002jtv.4 uc060kps.1 uc060kpu.1 uc060kpv.1 uc060kpw.1 uc002jtw.4 uc060kpx.1 uc060kpy.1 uc060kpz.1 uc060kqa.1 uc010wtl.3 uc060kqb.1 uc060kqc.1 uc060kqf.1 uc060kqg.1 uc002jty.5 uc060kqh.1 uc060kqi.1 uc010wtm.3 uc060kqj.1 uc010wtn.3 uc060kqk.1 uc060kql.1 uc060kqm.1 uc060kqn.1 uc060kqo.1 uc010dhd.4 uc060kqr.1 uc060kqs.1 uc060kqt.1 uc060kqu.1 uc060kqv.1" contains invalid characters or is incomplete and therefore can cause unexpected results during a query or annotation process.