ENST00000264434.7 C2orf42
Information
- Transcript ID
- ENST00000264434.7
- Genome
- hg38
- Position
- chr2:70,149,885-70,191,019
- Strand
- -
- CDS length
- 1,725
- Amino acid length
- 575
- Gene symbol
- C2orf42
- Gene type
- protein-coding
- Gene description
- chromosome 2 open reading frame 42
- Gene Entrez Gene ID
- 54980
Variants
Display target variant
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Exon
Exon number | Start | Stop |
---|---|---|
10 | 70,149,885 | 70,150,564 |
9 | 70,160,625 | 70,160,787 |
8 | 70,165,092 | 70,165,192 |
7 | 70,165,528 | 70,165,635 |
6 | 70,169,557 | 70,169,661 |
5 | 70,175,673 | 70,175,777 |
4 | 70,179,532 | 70,179,642 |
3 | 70,181,163 | 70,181,997 |
2 | 70,182,667 | 70,182,935 |
1 | 70,190,973 | 70,191,019 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
10 | CDS | 70,150,356 | 70,150,564 |
9 | CDS | 70,160,625 | 70,160,787 |
8 | CDS | 70,165,092 | 70,165,192 |
7 | CDS | 70,165,528 | 70,165,635 |
6 | CDS | 70,169,557 | 70,169,661 |
5 | CDS | 70,175,673 | 70,175,777 |
4 | CDS | 70,179,532 | 70,179,642 |
3 | CDS | 70,181,163 | 70,181,985 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr2 | 70,377,017 | 70,418,151 | Link |
CDS sequence
ATGGAACCAAATTCTCTGAGGACTAAAGTCCCAGCTTTCTTATCTGATTTGGGGAAGGCCACATTGAGGGGAATCAGAAAGTGTCCCCGATGTGGCACATACAATGGAACCCGGGGACTGAGCTGTAAGAACAAGACATGTGGAACCATATTCCGCTACGGTGCACGCAAGCAGCCTAGTGTTGAAGCTGTCAAAATCATTACAGGCTCTGATCTTCAGGTCTACTCAGTGCGGCAAAGAGACCGGGGCCCTGATTACCGATGCTTTGTGGAGCTCGGGGTTTCAGAGACAACAATCCAGACAGTGGATGGGACGATCATCACTCAGCTGAGCTCTGGACGGTGTTATGTCCCCTCATGCCTGAAAGCTGCCACTCAAGGCGTTGTGGAAAACCAGTGCCAGCACATCAAGCTGGCGGTGAACTGCCAGGCAGAGGCCACCCCTCTGACCCTGAAGAGCTCGGTCCTGAATGCAATGCAGGCCTCCCCGGAAACCAAACAGACCATCTGGCAGTTGGCCACGGAACCCACAGGTCCTCTGGTGCAGAGAATTACTAAAAACATCTTGGTGGTGAAATGCAAGGCAAGCCAGAAGCACAGTTTGGGGTATTTGCATACATCTTTTGTGCAGAAAGTCAGTGGCAAAAGCTTGCCTGAGCGCCGCTTCTTCTGCTCCTGTCAGACTCTGAAATCGCACAAGTCAAATGCCTCCAAGGATGAGACAGCCCAGAGATGCATTCATTTCTTTGCTTGCATCTGTGCCTTTGCCAGTGATGAGACACTGGCTCAGGAATTCTCAGACTTCCTAAATTTTGATTCCAGCGGTCTTAAAGAGATTATTGTACCCCAGTTAGGTTGCCATTCAGAATCAACAGTATCTGCTTGTGAGTCTACTGCCTCTAAGTCAAAGAAGAGGAGAAAGGATGAAGTATCTGGTGCACAGATGAACAGTTCACTACTGCCTCAAGATGCAGTGAGCAGTAATCTAAGGAAAAGTGGCCTGAAAAAGCCTGTGGTTGCTTCCTCGTTAAAAAGGCAGGCCTGTGGTCAGCTGTTAGATGAGGCACAAGTGACTTTATCCTTCCAAGACTGGCTGGCCAGTGTCACAGAACGCATCCATCAAACCATGCACTATCAGTTTGATGGCAAACCAGAACCATTGGTGTTCCACATTCCTCAGTCATTTTTTGATGCCCTGCAACAAAGAATATCTATAGGAAGTGCAAAAAAACGGCTCCCCAACTCCACCACAGCTTTTGTTCGGAAAGATGCCTTGCCACTGGGAACCTTTTCCAAGTATACTTGGCATATCACTAATATCCTGCAAGTTAAACAAATCTTAGATACCCCAGAGATGCCCTTGGAAATCACCCGTAGCTTTATCCAGAACCGAGATGGGACTTATGAGCTATTTAAATGCCCTAAAGTGGAAGTAGAAAGCATAGCAGAAACCTACGGTCGTATAGAAAAACAACCAGTGCTGCGACCCTTGGAACTAAAAACTTTTCTCAAAGTTGGCAACACTTCCCCAGATCAAAAGGAGCCAACACCTTTCATCATCGAGTGGATCCCAGATATCCTTCCCCAATCTAAGATTGGCGAGCTGCGGATCAAGTTTGAGTATGGCCACCACCGGAATGGGCATGTGGCGGAGTACCAAGACCAGCGGCCCCCCTTGGACCAGCCCTTGGAACTGGCCCCTCTGACCACTATTACTTTCCCTTAA
Amino sequence
MEPNSLRTKVPAFLSDLGKATLRGIRKCPRCGTYNGTRGLSCKNKTCGTIFRYGARKQPSVEAVKIITGSDLQVYSVRQRDRGPDYRCFVELGVSETTIQTVDGTIITQLSSGRCYVPSCLKAATQGVVENQCQHIKLAVNCQAEATPLTLKSSVLNAMQASPETKQTIWQLATEPTGPLVQRITKNILVVKCKASQKHSLGYLHTSFVQKVSGKSLPERRFFCSCQTLKSHKSNASKDETAQRCIHFFACICAFASDETLAQEFSDFLNFDSSGLKEIIVPQLGCHSESTVSACESTASKSKKRRKDEVSGAQMNSSLLPQDAVSSNLRKSGLKKPVVASSLKRQACGQLLDEAQVTLSFQDWLASVTERIHQTMHYQFDGKPEPLVFHIPQSFFDALQQRISIGSAKKRLPNSTTAFVRKDALPLGTFSKYTWHITNILQVKQILDTPEMPLEITRSFIQNRDGTYELFKCPKVEVESIAETYGRIEKQPVLRPLELKTFLKVGNTSPDQKEPTPFIIEWIPDILPQSKIGELRIKFEYGHHRNGHVAEYQDQRPPLDQPLELAPLTTITFP*