ENST00000373095.6 EEIG1
Information
- Transcript ID
- ENST00000373095.6
- Genome
- hg38
- Position
- chr9:127,940,582-127,980,989
- Strand
- -
- CDS length
- 1,155
- Amino acid length
- 385
- Gene symbol
- EEIG1
- Gene type
- protein-coding
- Gene description
- estrogen-induced osteoclastogenesis regulator 1
- Gene Entrez Gene ID
- 399665
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 |
---|---|---|
11 | 127,940,582 | 127,943,237 |
10 | 127,944,615 | 127,944,684 |
9 | 127,944,777 | 127,944,898 |
8 | 127,945,367 | 127,945,562 |
7 | 127,945,649 | 127,945,753 |
6 | 127,948,071 | 127,948,225 |
5 | 127,948,368 | 127,948,414 |
4 | 127,950,423 | 127,950,539 |
3 | 127,953,575 | 127,953,604 |
2 | 127,953,805 | 127,953,925 |
1 | 127,979,992 | 127,980,989 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
11 | CDS | 127,943,192 | 127,943,237 |
10 | CDS | 127,944,615 | 127,944,684 |
9 | CDS | 127,944,777 | 127,944,898 |
8 | CDS | 127,945,367 | 127,945,562 |
7 | CDS | 127,945,649 | 127,945,753 |
6 | CDS | 127,948,071 | 127,948,225 |
5 | CDS | 127,948,368 | 127,948,414 |
4 | CDS | 127,950,423 | 127,950,539 |
3 | CDS | 127,953,575 | 127,953,604 |
2 | CDS | 127,953,805 | 127,953,925 |
1 | CDS | 127,979,992 | 127,980,137 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr9 | 130,702,861 | 130,743,268 | Link |
CDS sequence
ATGGCTTTCTTGATGAAGAAGAAGAAATTCAAATTCCAAACTACTTTCACCCTGGAGGAGCTGACTGCGGTTCCCTTCGTGAACGGGGTCCTCTTCTGCAAGGTCCGGCTGCTGGATGGAGGGGATTTTGTCAGCTTGTCGTCAAGGGAGGAGGTACAGGAGAACTGTGTGCGGTGGCGAAAGAGGTTCACCTTCGTGTGTAAGATGAGTGCTAACCCGGCCACCGGCCTGCTGGACCCCTGTGTCTTCCGTGTGTCTGTGCGCAAGGAGCTGAAAGGCGGGAAGGCTTATTCCAAGCTGGGCTTCGCTGACTTGAACCTGGCCGAGTTTGCGGGCTCGGGCTCCACGGTGCGCTGCTGCCTGCTCGAGGGATATGACACGAAGAACACTCGCCAGGACAACTCCATCCTTAAGGTCACCATTGGTATGTTCCTGCTCTCTGGAGATCCCTGCTTCAAGACGCCACCATCGACTGCCAAGTCCATCTCCATCCCAGGCCAGGATTCCTCCCTGCAGCTGACGTGTAAGGGTGGTGGGACCAGCAGTGGGGGCAGCAGCACCAACTCCCTGACTGGGTCCCGGCCCCCCAAGGCTCGGCCCACTATTCTCAGCTCAGGGCTGCCAGAGGAACCCGACCAGAACCTGTCCAGCCCTGAGGAGGTGTTCCACTCTGGCCACTCCCGCAACTCCAGCTATGCCAGCCAGCAGTCCAAGATCTCCGGCTACAGCACAGAGCACTCGCGCTCCTCCAGCCTCTCAGACCTGACGCACCGCCGCAACACGTCCACCAGCAGCAGCGCCTCTGGGGGCCTTGGCATGACCGTGGAGGGCCCTGAGGGCAGTGAGCGGGAGCACCGGCCCCCGGAGAAGCCGCCGCGGCCACCCCGGCCCCTGCATCTGTCCGATCGCTCTTTCAGGCGGAAGAAGGACTCGGTGGAGAGCCACCCGACCTGGGTGGACGACACGCGGATCGATGCGGATGCCATCGTGGAGAAGATCGTGCAGAGCCAGGATTTCACAGATGGCAGCAACACCGAGGACAGCAACCTCCGGCTGTTCGTGAGCCGCGATGGCTCTGCCACGCTGAGCGGCATCCAGCTTGCCACCAGGGTCTCTTCTGGGGTCTACGAGCCAGTTGTGATTGAAAGCCATTGA
Amino sequence
MAFLMKKKKFKFQTTFTLEELTAVPFVNGVLFCKVRLLDGGDFVSLSSREEVQENCVRWRKRFTFVCKMSANPATGLLDPCVFRVSVRKELKGGKAYSKLGFADLNLAEFAGSGSTVRCCLLEGYDTKNTRQDNSILKVTIGMFLLSGDPCFKTPPSTAKSISIPGQDSSLQLTCKGGGTSSGGSSTNSLTGSRPPKARPTILSSGLPEEPDQNLSSPEEVFHSGHSRNSSYASQQSKISGYSTEHSRSSSLSDLTHRRNTSTSSSASGGLGMTVEGPEGSEREHRPPEKPPRPPRPLHLSDRSFRRKKDSVESHPTWVDDTRIDADAIVEKIVQSQDFTDGSNTEDSNLRLFVSRDGSATLSGIQLATRVSSGVYEPVVIESH*