ENSG00000267089.1, ENSG00000267089.1 (gene) Homo sapiens

Feature
Overview
NameENSG00000267089.1
Unique NameENSG00000267089.1
Typegene
OrganismHomo sapiens (Human)
Alignments
The following features are aligned
Aligned FeatureFeature TypeAlignment Location
chr19chromosomechr19:11841241..11842439 -
Analyses
This gene is derived from or has results from the following analyses
Analysis NameDate Performed
Gencode Annotation2017-03-01
Properties
Property NameValue
Gene idENSG00000267089.1
Gene typelincRNA
Gene nameCTC-499B15.8
Level2
Havana geneOTTHUMG00000182301.1
Relationships

The following transcript feature(s) are a part of this gene:

Feature NameUnique NameSpeciesType
ENST00000585694.1ENST00000585694.1Homo sapienstranscript


Sequences
The following sequences are available for this feature:

gene from alignment at chr19:11841241..11842439-

Legend: transcript
Hold the cursor over a type above to highlight its positions in the sequence below.
>ENSG00000267089.1 ID=ENSG00000267089.1|Name=ENSG00000267089.1|organism=Homo sapiens|type=gene|length=1199bp|location=Sequence derived from alignment at chr19:11841241..11842439- (Homo sapiens)
AAATGCCCAAGGCCTATTTATTTTTTGGGGTGGTATGTGTCTGAGTATTC
ATATTTTTATTATTTTGACTTGGCATAAAACAGCTTATTTCAAGAACTCA
TTTTCCTTCTTCAAACATTATCAAACTATTCACTAAGTTTCCAACCAGCT
AATTAAAATCCTAACACCCAAATCATAAAATAAAATTCTTAAATGTGGCC
AGGTGCAATGGCTAATGCCTGTAATCCTAGAACTTCGGGAGGCTGAGGCA
GGTGGATCACTTGAGGTCAGGACTTTGAGACCAGCCTGATCAACACGGTG
AAACTCCGTCACTACTAAAAACACACACAAAAATGAGCAGGGTGAGGTGG
CATGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGCAAGGAGAATCGTT
TGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGACTGCGCCACTCTACT
CCACCCTGGGCAACAGAGCGAGACTCTGTCTCAAAAAAAAAGAAGAAAAA
AAAAAAGAATCCCCCACCCTTTGTGTTGTGCAAGAGCACCTTACTGCAAT
GAAACACCCTTCGCATTATGACTTAGATTGTGCCACGTTTGTTACCTATG
ACAAACCAGATACAGATTAGACATTCCAGTATTTACCTCACAAACCATTA
GGTGAATAGCTTTGTCTTTAGTGATCAGTCAGAACGAAATATCTATTAAC
CAAAGCATGCTTCAGTTTCTCTCCTACCTCCAGGTCCCTGAACTTTTTTC
TTTTTTTGAGACAGTCTTGTTCTGTAGCCCAGGCTGGAGTGCAGTAGCAT
GATCTTGGCTCACTGCAACCTCCGCCTCCCTGGTGTTCAAGTGATTCTCA
TGCCTCAGTCGCCAGAGTAGCTGGGTTTACAGGTGTGTGCCATCATGCCC
AGTTAATTTTTATACTTTTCGTAGAGATGGGTTTTCATCATGCTGGCCAC
ACTTGTCTTCTGACCTCAAGTGATCTGCCCACCTCAGCCTCCCCAAGTGC
TGAGATTATGGGCATGAGCCACCACGACCAGTGGCCCCTGAATTTCTGAC
TGACCCATTCTAAGCCTATATACAACCCCATTTATTTATTTATTTATTTA
TTTATTTTTCGGGGGGACGAAGTCTAGCTCTTCCACCCAGGCTGGATTAC
AATGGCGTGATCTTGGCTCATTGCAACCTCCACCTCCCGGGTTCAAGCG
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