ENST00000619701.5 ABCG4
Information
- Transcript ID
- ENST00000619701.5
- Genome
- hg19
- Position
- chr11:119,019,762-119,033,362
- Strand
- +
- CDS length
- 1,941
- Amino acid length
- 647
- Gene symbol
- ABCG4
- Gene type
- protein-coding
- Gene description
- ATP binding cassette subfamily G member 4
- Gene Entrez Gene ID
- 64137
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| 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 | 119,019,762 | 119,020,073 |
| 2 | 119,020,664 | 119,020,913 |
| 3 | 119,024,736 | 119,024,853 |
| 4 | 119,024,970 | 119,025,102 |
| 5 | 119,025,235 | 119,025,285 |
| 6 | 119,025,480 | 119,025,625 |
| 7 | 119,027,039 | 119,027,162 |
| 8 | 119,027,274 | 119,027,388 |
| 9 | 119,027,582 | 119,027,724 |
| 10 | 119,028,944 | 119,029,042 |
| 11 | 119,029,267 | 119,029,435 |
| 12 | 119,029,539 | 119,029,639 |
| 13 | 119,030,937 | 119,031,095 |
| 14 | 119,031,248 | 119,031,366 |
| 15 | 119,031,591 | 119,033,362 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 2 | CDS | 119,020,676 | 119,020,913 |
| 3 | CDS | 119,024,736 | 119,024,853 |
| 4 | CDS | 119,024,970 | 119,025,102 |
| 5 | CDS | 119,025,235 | 119,025,285 |
| 6 | CDS | 119,025,480 | 119,025,625 |
| 7 | CDS | 119,027,039 | 119,027,162 |
| 8 | CDS | 119,027,274 | 119,027,388 |
| 9 | CDS | 119,027,582 | 119,027,724 |
| 10 | CDS | 119,028,944 | 119,029,042 |
| 11 | CDS | 119,029,267 | 119,029,435 |
| 12 | CDS | 119,029,539 | 119,029,639 |
| 13 | CDS | 119,030,937 | 119,031,095 |
| 14 | CDS | 119,031,248 | 119,031,366 |
| 15 | CDS | 119,031,591 | 119,031,816 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr11 | 119,149,052 | 119,162,653 | Link |
CDS sequence
ATGGCGGAGAAGGCGCTGGAGGCCGTGGGCTGTGGACTAGGGCCGGGGGCTGTGGCCATGGCCGTGACGCTGGAGGACGGGGCGGAACCCCCTGTGCTGACCACGCACCTGAAGAAGGTGGAGAACCACATCACTGAAGCCCAGCGCTTCTCCCACCTACCCAAGCGCTCAGCCGTGGACATCGAGTTCGTGGAGCTGTCCTATTCCGTGCGGGAGGGGCCCTGCTGGCGCAAAAGGGGTTATAAGACCCTTCTCAAGTGCCTCTCAGGTAAATTCTGCCGCCGGGAGCTGATTGGCATCATGGGCCCCTCAGGGGCTGGCAAGTCTACATTCATGAACATCTTGGCAGGATACAGGGAGTCTGGAATGAAGGGGCAGATCCTGGTTAATGGAAGGCCACGGGAGCTGAGGACCTTCCGCAAGATGTCCTGCTACATCATGCAAGATGACATGCTGCTGCCGCACCTCACGGTGTTGGAAGCCATGATGGTCTCTGCTAACCTGAAGCTGAGTGAGAAGCAGGAGGTGAAGAAGGAGCTGGTGACAGAGATCCTGACGGCACTGGGCCTGATGTCGTGCTCCCACACGAGGACAGCCCTGCTCTCTGGCGGGCAGAGGAAGCGTCTGGCCATCGCCCTGGAGCTGGTCAACAACCCGCCTGTCATGTTCTTTGATGAGCCCACCAGTGGTCTGGATAGCGCCTCTTGTTTCCAAGTGGTGTCCCTCATGAAGTCCCTGGCACAGGGGGGCCGTACCATCATCTGCACCATCCACCAGCCCAGTGCCAAGCTCTTTGAGATGTTTGACAAGCTCTACATCCTGAGCCAGGGTCAGTGCATCTTCAAAGGCGTGGTCACCAACCTGATCCCCTATCTAAAGGGACTCGGCTTGCATTGCCCCACCTACCACAACCCGGCTGACTTCATCATCGAGGTGGCCTCTGGCGAGTATGGAGACCTGAACCCCATGTTGTTCAGGGCTGTGCAGAATGGGCTGTGCGCTATGGCTGAGAAGAAGAGCAGCCCTGAGAAGAACGAGGTCCCTGCCCCATGCCCTCCTTGTCCTCCGGAAGTGGATCCCATTGAAAGCCACACCTTTGCCACCAGCACCCTCACACAGTTCTGCATCCTCTTCAAGAGGACCTTCCTGTCCATCCTCAGGGACACGGTCCTGACCCACCTACGGTTCATGTCCCACGTGGTTATTGGCGTGCTCATCGGCCTCCTCTACCTGCATATTGGCGACGATGCCAGCAAGGTCTTCAACAACACCGGCTGCCTCTTCTTCTCCATGCTGTTCCTCATGTTCGCCGCCCTCATGCCAACTGTGCTCACCTTCCCCTTAGAGATGGCGGTCTTCATGAGGGAGCACCTCAACTACTGGTACAGCCTCAAAGCGTATTACCTGGCCAAGACCATGGCTGACGTGCCCTTTCAGGTGGTGTGTCCGGTGGTCTACTGCAGCATTGTGTACTGGATGACGGGCCAGCCCGCTGAGACCAGCCGCTTCCTGCTCTTCTCAGCCCTGGCCACCGCCACCGCCTTGGTGGCCCAATCTTTGGGGCTGCTGATCGGAGCTGCTTCCAACTCCCTACAGGTGGCCACTTTTGTGGGCCCAGTTACCGCCATCCCTGTCCTCTTGTTCTCCGGCTTCTTTGTCAGCTTCAAGACCATCCCCACTTACCTGCAATGGAGCTCCTATCTCTCCTATGTCAGGTATGGCTTTGAGGGTGTGATCCTGACGATCTATGGCATGGAGCGAGGAGACCTGACATGTTTAGAGGAACGCTGCCCGTTCCGGGAGCCACAGAGCATCCTCCGAGCGCTGGATGTGGAGGATGCCAAGCTCTACATGGACTTCCTGGTCTTGGGCATCTTCTTCCTAGCCCTGCGGCTGCTGGCCTACCTTGTGCTGCGTTACCGGGTCAAGTCAGAGAGATAG
Amino sequence
MAEKALEAVGCGLGPGAVAMAVTLEDGAEPPVLTTHLKKVENHITEAQRFSHLPKRSAVDIEFVELSYSVREGPCWRKRGYKTLLKCLSGKFCRRELIGIMGPSGAGKSTFMNILAGYRESGMKGQILVNGRPRELRTFRKMSCYIMQDDMLLPHLTVLEAMMVSANLKLSEKQEVKKELVTEILTALGLMSCSHTRTALLSGGQRKRLAIALELVNNPPVMFFDEPTSGLDSASCFQVVSLMKSLAQGGRTIICTIHQPSAKLFEMFDKLYILSQGQCIFKGVVTNLIPYLKGLGLHCPTYHNPADFIIEVASGEYGDLNPMLFRAVQNGLCAMAEKKSSPEKNEVPAPCPPCPPEVDPIESHTFATSTLTQFCILFKRTFLSILRDTVLTHLRFMSHVVIGVLIGLLYLHIGDDASKVFNNTGCLFFSMLFLMFAALMPTVLTFPLEMAVFMREHLNYWYSLKAYYLAKTMADVPFQVVCPVVYCSIVYWMTGQPAETSRFLLFSALATATALVAQSLGLLIGAASNSLQVATFVGPVTAIPVLLFSGFFVSFKTIPTYLQWSSYLSYVRYGFEGVILTIYGMERGDLTCLEERCPFREPQSILRALDVEDAKLYMDFLVLGIFFLALRLLAYLVLRYRVKSER*