ENSG00000239835.1, ENSG00000239835.1 (gene) Homo sapiens

Feature
Overview
NameENSG00000239835.1
Unique NameENSG00000239835.1
Typegene
OrganismHomo sapiens (Human)
Alignments
The following features are aligned
Aligned FeatureFeature TypeAlignment Location
chr3chromosomechr3:120028740..120029868 +
Analyses
This gene is derived from or has results from the following analyses
Analysis NameDate Performed
Gencode Annotation2017-03-01
Properties
Property NameValue
Gene idENSG00000239835.1
Gene typeprocessed_pseudogene
Gene nameRP11-767L7.1
Level1
Tagpseudo_consens
Havana geneOTTHUMG00000159402.1
Relationships

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

Feature NameUnique NameSpeciesType
ENST00000482027.1ENST00000482027.1Homo sapienstranscript


Sequences
The following sequences are available for this feature:

gene from alignment at chr3:120028740..120029868+

Legend: transcript
Hold the cursor over a type above to highlight its positions in the sequence below.
>ENSG00000239835.1 ID=ENSG00000239835.1|Name=ENSG00000239835.1|organism=Homo sapiens|type=gene|length=1129bp|location=Sequence derived from alignment at chr3:120028740..120029868+ (Homo sapiens)
ATGGCCTGGTGAGGCTGGGCAGAGAGAGGTTGGGGCAGCGACCAGGCGTG
GTCTCCGCCAGTGGGCGGCCGCAGCTGCAAGGAACTCACTGAGGCCCTAG
CCCCGCCACGGCTGCTCAGACGCAGGTTTGGCTTCTTCGCAAAAATGTGG
ATTCAGAAAAGCACCCAGGAAGGCTGAACCTCAAAGATCAGACACAGGCA
CAAGTGGTGAAGCATACAAGAGAAGTGCTTTGGTTCCTCCTGTGGAAGAA
ACGGCCTTTTATCCTTCTTTGTATCCTATAGGGACTCTCATAAAATCTTT
ATTTTTTACTGTTGGGTTTACAGGCTGTGCATTTGGATCAGCTACTATTT
GGCAATATGAATCACTGAAATCCAGGGTCCAGAGTTATTTTGATGATATA
AAAGCTGACGGTTGGGATAGCATAAGATCACAAAAAAGAGACTTCAGAAA
GGAGATTAACAAGTGGTAGAATAACCTAAGCGATGGCCACCAGACTATGA
CAGGTTATCACAGCTGCAAATGAATGTCTTTGTATTCTGTTTATAGAGAG
TACCTTCTCTGCAGCGGACAATGATCAGATATTTCGCATCTAATCCAGCC
TCAAAAGCCCTTTCTTTTCCAATGTTGCTGTCAACATTCAGTCATTTCTC
CTTATTTCACATGGCAGCAAATATCTTATGTTTTGTGGAGCTTCGCCTCC
AGCACAGTGAACATTCTGGATCAAGAGCAGTGTTATTATCTGCAGGTGTT
ATTTCCAATTGTGTCAGTTATGTGTGTAAAGTTGCCACAGGAAGATAGGG
ACCATCACTTGGTGCATCTGGCACCATCATGATGGTCTTTGCAGCTGTCT
GCACTAAGATCCCAGAAGGGAGGCTTGCCATTATTTCCCTTCAGATGTTC
ACATTCATAGCAGAGAATGCCCTAAAAGCCATTATGGCCATGGATACAGC
AGAAATCTTCATGGGATGGAAATTTTTTTATCATGCAGTGCATCCTGGGG
GAGCTCTCTTTGGAATATGGTATGTTACTTATGGTCATTAACTGTTTTGG
AAGAACAGGGAGCTTCTAGTGAAAATCTGGCACGAAATGAGGACTAATGG
CCCCCAAAAAAGGAGGTGGCTCTAAGTAA
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