ENST00000373095.6 EEIG1
Information
- Transcript ID
- ENST00000373095.6
- Genome
- hg19
- Position
- chr9:130,702,861-130,743,268
- 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 | 130,702,861 | 130,705,516 |
10 | 130,706,894 | 130,706,963 |
9 | 130,707,056 | 130,707,177 |
8 | 130,707,646 | 130,707,841 |
7 | 130,707,928 | 130,708,032 |
6 | 130,710,350 | 130,710,504 |
5 | 130,710,647 | 130,710,693 |
4 | 130,712,702 | 130,712,818 |
3 | 130,715,854 | 130,715,883 |
2 | 130,716,084 | 130,716,204 |
1 | 130,742,271 | 130,743,268 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
11 | CDS | 130,705,471 | 130,705,516 |
10 | CDS | 130,706,894 | 130,706,963 |
9 | CDS | 130,707,056 | 130,707,177 |
8 | CDS | 130,707,646 | 130,707,841 |
7 | CDS | 130,707,928 | 130,708,032 |
6 | CDS | 130,710,350 | 130,710,504 |
5 | CDS | 130,710,647 | 130,710,693 |
4 | CDS | 130,712,702 | 130,712,818 |
3 | CDS | 130,715,854 | 130,715,883 |
2 | CDS | 130,716,084 | 130,716,204 |
1 | CDS | 130,742,271 | 130,742,416 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr9 | 127,940,582 | 127,980,989 | Link |
CDS sequence
ATGGCTTTCTTGATGAAGAAGAAGAAATTCAAATTCCAAACTACTTTCACCCTGGAGGAGCTGACTGCGGTTCCCTTCGTGAACGGGGTCCTCTTCTGCAAGGTCCGGCTGCTGGATGGAGGGGATTTTGTCAGCTTGTCGTCAAGGGAGGAGGTACAGGAGAACTGTGTGCGGTGGCGAAAGAGGTTCACCTTCGTGTGTAAGATGAGTGCTAACCCGGCCACCGGCCTGCTGGACCCCTGTGTCTTCCGTGTGTCTGTGCGCAAGGAGCTGAAAGGCGGGAAGGCTTATTCCAAGCTGGGCTTCGCTGACTTGAACCTGGCCGAGTTTGCGGGCTCGGGCTCCACGGTGCGCTGCTGCCTGCTCGAGGGATATGACACGAAGAACACTCGCCAGGACAACTCCATCCTTAAGGTCACCATTGGTATGTTCCTGCTCTCTGGAGATCCCTGCTTCAAGACGCCACCATCGACTGCCAAGTCCATCTCCATCCCAGGCCAGGATTCCTCCCTGCAGCTGACGTGTAAGGGTGGTGGGACCAGCAGTGGGGGCAGCAGCACCAACTCCCTGACTGGGTCCCGGCCCCCCAAGGCTCGGCCCACTATTCTCAGCTCAGGGCTGCCAGAGGAACCCGACCAGAACCTGTCCAGCCCTGAGGAGGTGTTCCACTCTGGCCACTCCCGCAACTCCAGCTATGCCAGCCAGCAGTCCAAGATCTCCGGCTACAGCACAGAGCACTCGCGCTCCTCCAGCCTCTCAGACCTGACGCACCGCCGCAACACGTCCACCAGCAGCAGCGCCTCTGGGGGCCTTGGCATGACCGTGGAGGGCCCTGAGGGCAGTGAGCGGGAGCACCGGCCCCCGGAGAAGCCGCCGCGGCCACCCCGGCCCCTGCATCTGTCCGATCGCTCTTTCAGGCGGAAGAAGGACTCGGTGGAGAGCCACCCGACCTGGGTGGACGACACGCGGATCGATGCGGATGCCATCGTGGAGAAGATCGTGCAGAGCCAGGATTTCACAGATGGCAGCAACACCGAGGACAGCAACCTCCGGCTGTTCGTGAGCCGCGATGGCTCTGCCACGCTGAGCGGCATCCAGCTTGCCACCAGGGTCTCTTCTGGGGTCTACGAGCCAGTTGTGATTGAAAGCCATTGA
Amino sequence
MAFLMKKKKFKFQTTFTLEELTAVPFVNGVLFCKVRLLDGGDFVSLSSREEVQENCVRWRKRFTFVCKMSANPATGLLDPCVFRVSVRKELKGGKAYSKLGFADLNLAEFAGSGSTVRCCLLEGYDTKNTRQDNSILKVTIGMFLLSGDPCFKTPPSTAKSISIPGQDSSLQLTCKGGGTSSGGSSTNSLTGSRPPKARPTILSSGLPEEPDQNLSSPEEVFHSGHSRNSSYASQQSKISGYSTEHSRSSSLSDLTHRRNTSTSSSASGGLGMTVEGPEGSEREHRPPEKPPRPPRPLHLSDRSFRRKKDSVESHPTWVDDTRIDADAIVEKIVQSQDFTDGSNTEDSNLRLFVSRDGSATLSGIQLATRVSSGVYEPVVIESH*