Personal tools

Difference between revisions of "TSS:Hg 101552.1"

From referenceTSS

Jump to: navigation, search
 
(2 intermediate revisions by the same user not shown)
Line 2: Line 2:
 
|FAC=
 
|FAC=
 
|FACC=
 
|FACC=
|all_trans=ENST00000289081.7:0 ENST00000490972.6:0 ENST00000474949.1:0 NM_000136:0 NM_001243744:0 uc004avh.4:0 uc004avi.5:0 uc064umh.1:0 BC015748:0 X66893:0 AK304887:0 AK222871:13 AK312548:109 NM_001243743:430 ENST00000375305.5:459 uc022bkl.2:459 X66894:459
+
|all_trans=HGNC:3584
 
|chr=chr9
 
|chr=chr9
 
|cpg_percent=0.14
 
|cpg_percent=0.14
Line 8: Line 8:
 
|distance_to_tss=4
 
|distance_to_tss=4
 
|end=95317726
 
|end=95317726
 +
|end_of_center_position=95317705
 
|entrez_id=2176
 
|entrez_id=2176
 
|gc_percent=0.661692
 
|gc_percent=0.661692
|gene_alias=FA3|FAC|FACC
+
|gene_alias=FA3{{!}}FAC{{!}}FACC
|gene_description=Fanconi anemia complementation group C
+
|gene_description=FA complementation group C
 
|gene_id=2176
 
|gene_id=2176
|gene_name=Fanconi anemia complementation group C
+
|gene_name=FA complementation group C
 
|gene_source=HGNC:3584
 
|gene_source=HGNC:3584
 
|gene_symbol=FANCC
 
|gene_symbol=FANCC
Line 20: Line 21:
 
|hgnc_mgi_id=HGNC:3584
 
|hgnc_mgi_id=HGNC:3584
 
|nearest_ensembl=ENSG00000158169
 
|nearest_ensembl=ENSG00000158169
|nearest_promoter_id=NM_000136
+
|nearest_promoter_id=NM_001243744
 
|nearest_refseq=NM_000136
 
|nearest_refseq=NM_000136
 
|nearest_unigene=Hs.494529
 
|nearest_unigene=Hs.494529
|num_trans=17
+
|num_trans=2176
 
|species=human
 
|species=human
 
|start=95317683
 
|start=95317683
 +
|start_of_center_position=95317704
 
|strand=-
 
|strand=-
|transcript_name=ENST00000289081.7 ENST00000490972.6 ENST00000474949.1 NM_000136 NM_001243744 uc004avh.4 uc004avi.5 uc064umh.1 BC015748 X66893 AK304887
+
|transcript_name=ENST00000289081.8 ENST00000474949.1 ENST00000649611.1 BC015748 X66893 AK304887
 
|tss_classification=yes
 
|tss_classification=yes
 
|tss_id=hg_101552.1
 
|tss_id=hg_101552.1
 
|tss_score=1
 
|tss_score=1
|uniprot_id=A0A024R9N2 A0A087WW44 B4E3W2 Q00597
+
|uniprot_id=A0A024R9N2 A0A3B3ITN9 B4E3W2 Q00597
 
}}
 
}}

Latest revision as of 18:07, 19 July 2021

Basic information about the TSS


TSS ID:hg_101552.1
Species:human
Chr:chr9
TSS Classification:yes
Start:95317683
End:95317726
Strand:-
TSS Score:1
Start of the center position in the TSS region:95317704
End of the center position in the TSS region:95317705



Gene and protein annotation


Transcript_name:ENST00000289081.8 ENST00000474949.1 ENST00000649611.1 BC015748 X66893 AK304887
Distance:0
GeneID:2176
HGNC/MGI_ID:HGNC:3584
UniProt_ID:A0A024R9N2 A0A3B3ITN9 B4E3W2 Q00597
Gene_name:FA complementation group C
Gene_symbol:FANCC
Gene_synonyms:FA3 FAC
Gene_source:HGNC:3584



Transcript annotation


Transcript_name:ENST00000289081.8 ENST00000474949.1 ENST00000649611.1 BC015748 X66893 AK304887
Distance:0
Num_trans:2176
All_trans:HGNC:3584



TATA-Box annotation


Distance to TSS:4
Nearest PromoterID:NM_001243744
Entrez ID:2176
Nearest Unigene:Hs.494529
Nearest Refseq:NM_000136
Nearest Ensembl:ENSG00000158169
Gene Name:FA complementation group C
Gene Alias:FA3|FAC|FACC
Gene Description:FA complementation group C
Gene Type:protein-coding
CpG%:0.14
GC%:0.661692
TATA-Box(TBP)/Promoter/Homer Distance From TSS(sequence,strand,conservation):