ENST00000379643.10 MAP7D2
Information
- Transcript ID
- ENST00000379643.10
- Genome
- hg19
- Position
- chrX:20,024,831-20,135,025
- Strand
- -
- CDS length
- 2,322
- Amino acid length
- 774
- Gene symbol
- MAP7D2
- Gene type
- protein-coding
- Gene description
- MAP7 domain containing 2
- Gene Entrez Gene ID
- 256714
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 |
---|---|---|
17 | 20,024,831 | 20,026,516 |
16 | 20,028,895 | 20,029,170 |
15 | 20,030,467 | 20,030,653 |
14 | 20,031,172 | 20,031,250 |
13 | 20,031,687 | 20,031,743 |
12 | 20,033,341 | 20,033,445 |
11 | 20,034,212 | 20,034,443 |
10 | 20,043,069 | 20,043,201 |
9 | 20,043,799 | 20,044,070 |
8 | 20,060,620 | 20,060,747 |
7 | 20,062,482 | 20,062,642 |
6 | 20,068,942 | 20,069,064 |
5 | 20,070,996 | 20,071,106 |
4 | 20,074,798 | 20,074,909 |
3 | 20,081,532 | 20,081,695 |
2 | 20,082,846 | 20,082,923 |
1 | 20,134,868 | 20,135,025 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
16 | CDS | 20,028,921 | 20,029,170 |
15 | CDS | 20,030,467 | 20,030,653 |
14 | CDS | 20,031,172 | 20,031,250 |
13 | CDS | 20,031,687 | 20,031,743 |
12 | CDS | 20,033,341 | 20,033,445 |
11 | CDS | 20,034,212 | 20,034,443 |
10 | CDS | 20,043,069 | 20,043,201 |
9 | CDS | 20,043,799 | 20,044,070 |
8 | CDS | 20,060,620 | 20,060,747 |
7 | CDS | 20,062,482 | 20,062,642 |
6 | CDS | 20,068,942 | 20,069,064 |
5 | CDS | 20,070,996 | 20,071,106 |
4 | CDS | 20,074,798 | 20,074,909 |
3 | CDS | 20,081,532 | 20,081,695 |
2 | CDS | 20,082,846 | 20,082,923 |
1 | CDS | 20,134,868 | 20,134,997 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chrX | 20,006,713 | 20,116,907 | Link |
CDS sequence
ATGGAGCGCGGCGGCGGCGGCTCCGGGACGGGATCCCGGCCTGAGGGGACTGCGCGGGGAACCTCTCTCCCAGGGAAGATCGCAGAACCGGGCGCGGTGCGGACCTCTCAGCCCAACTACCGGCCTCAAGGCATGGAGGGATTTTTGAAATCAGATGAGAGGCAGAGATTGGCCAAAGAAAGACGAGAAGAAAGAGAAAAATGTCTGGCTGCTCGGGAGCAACAGATCCTGGAGAAACAGAAAAGAGCCAGGCTGCAGTACGAAAAGCAAATGGAGGAGCGATGGCGAAAACTGGAAGAGCAGCGGCAGCGGGAGGACCAAAAGAGAGCTGCTGTGGAAGAGAAAAGGAAACAGAAGCTCCGGGAGGAGGAGGAACGGCTGGAGGCGATGATGCGCCGGTCCCTGGAGCGCACACAGCAGCTGGAGCTGAAAAAGAAGTATTCGTGGGGAGCACCACTGGCCATTGGACCCGGAGGACATGATGCATGTGACAAACTTTCAACATCAACTATGAGTTTGCCAAAGCCAACGGAGCCTCCCATGAATAAACGCCTGTCTTCATCCACCGTGGCAATATCCTATTCCCCAGACCGAGCTCATCACATGCACCTTAGTCCAATGGAAGCCATTCTTGTTTCGCGACTGTTGACACCCACACAGTCTTCTTTAGCCAGAAGCAGAGCTTCAGTCATGCTCTCTGGGCAGGCCAATGATTCAGTATTCCATGTCTGTCCTCGTTTAGCTCCTCTTGGCCCTCTTAACCCTTCTTACAAGTCTTCACCCACTCGAAACATTGAGAAGAAGAAAGCTACATCTACGTCTACATCTGGTGCAGGAGATGTTGGGAAAGAAGCCCTTTCAGGAGGAGAGGCCTCTCTGGTGGAGAAGGTGAAGCGGGGGCAACGAACAGCAACTTCTCTTCCTGTTGTGAACTTCGGGTCCCCTCTGAGAAGATGTGAGTTTTCTGGAGGCATTCCTAAGAGACCATCTTCTCCTGTGATATCCAAGACAGCTACTAAAGCTTATCCACAGTCTCCAAAGACAACGAAACCTCCCTACCCAGGGTCTCCTGTGAAGTACCGCTTACCTGCCCTTTCTGGCCAAGACATGCCCAAGAGGAAAGCGGAGAAAGAGAAGAGCAACAAGGAAAGGGAAGGTACCTTGGCTCAGCAGGCTGCTGGCCCGCAAGGAGAGGAAGCCCTAGAGAAGCATGTAGTGGACAAGCATGCCAGCGAGAAGCATGCTGCTGCCGCAGGAGGGAAAGCCGAAAACAGCGCAGCCTTGGGGAAGCCCACAGCAGGCACCACTGATGCAGGAGAGGCTGCGAAGATCTTGGCTGAAAAGAGAAGACAGGCCCGGCTGCAGAAGGAACAGGAGGAGCAAGAACGACTGGAGAAGGAAGAACAAGATAGGCTGGAGAGAGAGGAATTGAAAAGAAAGGCAGAGGAGGAAAGGCTTCGCCTAGAAGAGGAAGCCCGAAAGCAGGAAGAAGAAAGGAAGCGGCAGGAAGAGGAAAAGAAAAAACAGGAAGGGGAAGAGAAAAGAAAGGCAGGCGAGGAGGCCAAGCGGAAGGCTGAGGAGGAGCTGTTGTTGAAAGAAAAGCAAGAACAAGAAAAACAAGAGAAAGCCATGATTGAAAAGCAGAAAGAAGCAGCAGAAACAAAGGCCCGGGAGGTAGCTGAACAGATGCGTCTCGAGAGAGAACAGATTATGCTGCAGATTGAGCAGGAGAGACTGGAGAGAAAGAAGAGAATAGATGAAATCATGAAGAGAACAAGGAAAAGTGATGTGTCTCCACAAGTGAAGAAAGAAGACCCCAAAGTGGGGGTCCAGCCTGCTGTGTGTGTGGAAAAGAAGACAAAACTGGTTGTCCCCAACAAAATGGAAATCAATGGATTGAACACCTGCCAGGAAGTTAATGGTGTGGATCACGCTGCCCCAGAAACTTATCCCCAAGACATTTTCTCTAATGGGCTTAAGCCAGCTGGGGGACTCATTCATCTGGATGCCCTTGATGGGAAATCAAATAGCCTGGATGATTCAACTGAAGAAGTTCAGTCTATGGATGTGAGTCCTGTTTCAAAAGAAGAGCTTATCTCTATCCCGGAATTTTCACCAGTGAGTGAAATGATTCCTGGGGTGTCTCTGGACCAAAATGGAACTGGTAATGCCCGAGCACTTCAAGATCTCTTAGATTTCACTGGTCCCCCGACATTCCCCAAGAGATCCAGTGAAAATCTCAGCCTGGACGACTGTAACAAAAACCTTATCGAAGGATTTAACAGTCCTGGCCAAGAAACTCCTCTCAACACCTTCTGTTGA
Amino sequence
MERGGGGSGTGSRPEGTARGTSLPGKIAEPGAVRTSQPNYRPQGMEGFLKSDERQRLAKERREEREKCLAAREQQILEKQKRARLQYEKQMEERWRKLEEQRQREDQKRAAVEEKRKQKLREEEERLEAMMRRSLERTQQLELKKKYSWGAPLAIGPGGHDACDKLSTSTMSLPKPTEPPMNKRLSSSTVAISYSPDRAHHMHLSPMEAILVSRLLTPTQSSLARSRASVMLSGQANDSVFHVCPRLAPLGPLNPSYKSSPTRNIEKKKATSTSTSGAGDVGKEALSGGEASLVEKVKRGQRTATSLPVVNFGSPLRRCEFSGGIPKRPSSPVISKTATKAYPQSPKTTKPPYPGSPVKYRLPALSGQDMPKRKAEKEKSNKEREGTLAQQAAGPQGEEALEKHVVDKHASEKHAAAAGGKAENSAALGKPTAGTTDAGEAAKILAEKRRQARLQKEQEEQERLEKEEQDRLEREELKRKAEEERLRLEEEARKQEEERKRQEEEKKKQEGEEKRKAGEEAKRKAEEELLLKEKQEQEKQEKAMIEKQKEAAETKAREVAEQMRLEREQIMLQIEQERLERKKRIDEIMKRTRKSDVSPQVKKEDPKVGVQPAVCVEKKTKLVVPNKMEINGLNTCQEVNGVDHAAPETYPQDIFSNGLKPAGGLIHLDALDGKSNSLDDSTEEVQSMDVSPVSKEELISIPEFSPVSEMIPGVSLDQNGTGNARALQDLLDFTGPPTFPKRSSENLSLDDCNKNLIEGFNSPGQETPLNTFC*