ENST00000468427.2 MPHOSPH10
Information
- Transcript ID
- ENST00000468427.2
- Genome
- hg38
- Position
- chr2:71,130,310-71,150,087
- Strand
- +
- CDS length
- 1,626
- Amino acid length
- 542
- Gene symbol
- MPHOSPH10
- Gene type
- protein-coding
- Gene description
- M-phase phosphoprotein 10
- Gene Entrez Gene ID
- 10199
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 |
---|---|---|
1 | 71,130,310 | 71,130,845 |
2 | 71,132,898 | 71,133,576 |
3 | 71,133,948 | 71,134,105 |
4 | 71,134,626 | 71,134,797 |
5 | 71,138,490 | 71,138,631 |
6 | 71,139,795 | 71,139,862 |
7 | 71,141,232 | 71,141,369 |
8 | 71,144,428 | 71,144,538 |
9 | 71,147,999 | 71,148,106 |
10 | 71,149,223 | 71,149,453 |
11 | 71,149,866 | 71,150,087 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
2 | CDS | 71,133,229 | 71,133,576 |
3 | CDS | 71,133,948 | 71,134,105 |
4 | CDS | 71,134,626 | 71,134,797 |
5 | CDS | 71,138,490 | 71,138,631 |
6 | CDS | 71,139,795 | 71,139,862 |
7 | CDS | 71,141,232 | 71,141,369 |
8 | CDS | 71,144,428 | 71,144,538 |
9 | CDS | 71,147,999 | 71,148,106 |
10 | CDS | 71,149,223 | 71,149,453 |
11 | CDS | 71,149,866 | 71,150,015 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr2 | 71,357,440 | 71,377,217 | Link |
CDS sequence
ATGGGTAATGATGATCCTGAAATGGGTGAGAGAGCTGAAAACTCAAGCAAATCTGATCTGAGGAAAAGCCCCGTTTTCAGTGATGAGGATTCTGACCTTGACTTTGATATCAGCAAATTGGAACAGCAGAGCAAGGTGCAAAACAAAGGACAGGGAAAACCAAGAGAAAAGTCCATAGTAGATGATAAATTCTTCAAACTCTCTGAAATGGAGGCCTATTTAGAAAACATAGAAAAAGAAGAGGAACGAAAAGATGATAATGATGAGGAGGAGGAAGATATTGATTTTTTTGAAGATATTGATTCTGATGAAGATGAAGGGGGACTGTTTGGAAGTAAAAAACTTAAGTCAGGTAAAAGTTCCAGAAATCTGAAATACAAAGATTTTTTTGATCCAGTTGAAAGTGATGAAGACATAACAAATGTTCATGATGATGAGCTGGATTCAAACAAAGAAGATGATGAAATTGCTGAAGAAGAAGCAGAAGAACTAAGTATTTCGGAAACGGATGAAGATGATGACCTTCAAGAAAATGAAGACAATAAACAACATAAAGAAAGCTTGAAAAGAGTGACCTTTGCTTTACCAGATGATGCGGAAACTGAAGATACAGGTGTTTTAAATGTAAAGAAAAATTCTGATGAAGTTAAATCCTCCTTTGAAAAAAGACAGGAAAAGATGAATGAAAAAATTGCATCTTTAGAAAAAGAGTTGTTAGAAAAAAAGCCGTGGCAGCTTCAGGGGGAAGTGACAGCACAGAAGAGGCCAGAGAACAGCCTCCTGGAGGAGACCCTACACTTTGACCATGCTGTCCGGATGGCACCTGTGATTACAGAGGAAACCACCCTTCAACTGGAAGATATCATTAAACAGAGGATAAGAGATCAGGCTTGGGATGATGTAGTACGTAAAGAAAAACCTAAAGAGGATGCATATGAATATAAAAAGCGTTTAACCTTAGACCATGAGAAGAGTAAATTGAGCCTTGCTGAAATTTATGAACAGGAGTACATCAAACTCAACCAGCAAAAAACAGCAGAAGAAGAAAATCCAGAACATGTAGAAATTCAGAAGATGATGGATTCCCTCTTCTTAAAATTGGATGCCCTCTCAAACTTCCACTTTATCCCTAAACCGCCTGTACCAGAGATTAAAGTTGTGTCAAATCTGCCAGCCATAACCATGGAGGAAGTAGCCCCAGTGAGTGTTAGTGATGCAGCTCTCCTGGCCCCAGAGGAGATCAAGGAGAAAAATAAAGCTGGAGATATAAAAACAGCTGCTGAAAAAACAGCTACAGACAAGAAACGAGAGCGAAGGAAAAAGAAATATCAAAAGCGTATGAAAATAAAAGAGAAGGAGAAGCGGAGAAAACTGCTTGAAAAGAGCAGTGTAGATCAAGCAGGGAAATACAGCAAAACAGTAGCTTCGGAGAAGTTAAAACAGCTGACCAAAACTGGCAAAGCTTCCTTCATAAAGGATGAAGGTAAAGACAAGGCCTTAAAGTCCTCTCAAGCATTCTTTTCTAAATTACAAGATCAAGTAAAAATGCAAATCAATGATGCAAAGAAAACAGAAAAGAAAAAGAAGAAAAGACAGGATATTTCTGTTCATAAATTAAAGCTGTAA
Amino sequence
MGNDDPEMGERAENSSKSDLRKSPVFSDEDSDLDFDISKLEQQSKVQNKGQGKPREKSIVDDKFFKLSEMEAYLENIEKEEERKDDNDEEEEDIDFFEDIDSDEDEGGLFGSKKLKSGKSSRNLKYKDFFDPVESDEDITNVHDDELDSNKEDDEIAEEEAEELSISETDEDDDLQENEDNKQHKESLKRVTFALPDDAETEDTGVLNVKKNSDEVKSSFEKRQEKMNEKIASLEKELLEKKPWQLQGEVTAQKRPENSLLEETLHFDHAVRMAPVITEETTLQLEDIIKQRIRDQAWDDVVRKEKPKEDAYEYKKRLTLDHEKSKLSLAEIYEQEYIKLNQQKTAEEENPEHVEIQKMMDSLFLKLDALSNFHFIPKPPVPEIKVVSNLPAITMEEVAPVSVSDAALLAPEEIKEKNKAGDIKTAAEKTATDKKRERRKKKYQKRMKIKEKEKRRKLLEKSSVDQAGKYSKTVASEKLKQLTKTGKASFIKDEGKDKALKSSQAFFSKLQDQVKMQINDAKKTEKKKKKRQDISVHKLKL*