ENST00000430297.7 RETREG2
Information
- Transcript ID
- ENST00000430297.7
- Genome
- hg19
- Position
- chr2:220,042,997-220,050,197
- Strand
- +
- CDS length
- 1,632
- Amino acid length
- 544
- Gene symbol
- RETREG2
- Gene type
- protein-coding
- Gene description
- reticulophagy regulator family member 2
- Gene Entrez Gene ID
- 79137
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 | 220,042,997 | 220,043,355 |
2 | 220,043,644 | 220,043,750 |
3 | 220,044,455 | 220,044,485 |
4 | 220,044,832 | 220,044,967 |
5 | 220,045,392 | 220,045,476 |
6 | 220,045,784 | 220,045,927 |
7 | 220,046,091 | 220,046,185 |
8 | 220,046,362 | 220,046,497 |
9 | 220,046,735 | 220,050,197 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
1 | CDS | 220,043,075 | 220,043,355 |
2 | CDS | 220,043,644 | 220,043,750 |
3 | CDS | 220,044,455 | 220,044,485 |
4 | CDS | 220,044,832 | 220,044,967 |
5 | CDS | 220,045,392 | 220,045,476 |
6 | CDS | 220,045,784 | 220,045,927 |
7 | CDS | 220,046,091 | 220,046,185 |
8 | CDS | 220,046,362 | 220,046,497 |
9 | CDS | 220,046,735 | 220,047,351 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr2 | 219,178,275 | 219,185,475 | Link |
CDS sequence
ATGGCGAGCGGCGGTGGCGGGGGTAACACTGGCGCGGGTGGGGGGCCGGGGATGGGCCTGAGCCTGGGCCTGGGTCTGGGTCTGAGCCTAGGCATGAGTGAGGCCACCAGTGAGGCAGAGGAGGAGGCGGCCACGGCCGAGGCGGTGGGACGCCTGGCCACGACGCTGTGGCTGCGGCTCCGCGGCTGGGAGGCGGTGCTGGCGGCGGCGCAGCGGTTGCTGGTGTGGGAGAAGCCGCTGCACAGCCTGGTCACGGCGGCCGCGCTCAACGGCCTCTTCTGGTTGCTGTCTTCCTCGTCCCTCCGGCCCTTCTTCCTACTCAGCGTCTCACTTTTGGCCTATTTTCTGCTGGATCTCTGGCAGCCTCGCTTTCTCCCTGACGTTTCAGCATCATCCCCAGAGGAGCCACACTCTGACAGTGAGGGTGCGGGGTCAGGCGCCCGGCCGCACCTGCTGAGTGTGCCCGAGTTGTGCAGATACCTGGCTGAGAGCTGGCTCACCTTCCAGATTCACCTGCAGGAGCTGCTGCAGTACAAGAGGCAGAATCCAGCTCAGTTCTGCGTTCGAGTCTGCTCTGGCTGTGCTGTGTTGGCTGTGTTGGGACACTATGTTCCAGGGATTATGATTTCCTACATTGTCTTGTTGAGTATCCTGCTGTGGCCCCTGGTGGTTTATCATGAGCTGATCCAGAGGATGTACACTCGCCTGGAGCCCCTGCTCATGCAGCTGGACTACAGCATGAAGGCAGAAGCCAATGCCCTGCATCACAAACACGACAAGAGGAAGCGTCAGGGGAAGAATGCACCCCCAGGAGGTGATGAGCCACTGGCAGAGACAGAGAGTGAAAGCGAGGCAGAGCTGGCTGGCTTCTCCCCAGTGGTGGATGTGAAGAAAACAGCATTGGCCTTGGCCATTACAGACTCAGAGCTGTCAGATGAGGAGGCTTCTATCTTGGAGAGTGGTGGCTTCTCCGTATCCCGGGCCACAACTCCGCAGCTGACTGATGTCTCCGAGGATTTGGACCAGCAGAGCCTGCCAAGTGAACCAGAGGAGACCCTAAGCCGGGACCTAGGGGAGGGAGAGGAGGGAGAGCTGGCCCCTCCCGAAGACCTACTAGGCCGTCCTCAAGCTCTGTCAAGGCAAGCCCTGGACTCGGAGGAAGAGGAAGAGGATGTGGCAGCTAAGGAAACCTTGTTGCGGCTCTCATCCCCCCTCCACTTTGTGAACACGCACTTCAATGGGGCAGGGTCCCCCCCAGATGGAGTGAAATGCTCCCCTGGAGGACCAGTGGAGACACTGAGCCCCGAGACAGTGAGTGGTGGCCTCACTGCTCTGCCCGGCACCCTGTCACCTCCACTTTGCCTTGTTGGAAGTGACCCAGCCCCCTCCCCTTCCATTCTCCCACCTGTTCCCCAGGACTCACCCCAGCCCCTGCCTGCCCCTGAGGAAGAAGAGGCACTCACCACTGAGGACTTTGAGTTGCTGGATCAGGGGGAGCTGGAGCAGCTGAATGCAGAGCTGGGCTTGGAGCCAGAGACACCGCCAAAACCCCCTGATGCTCCACCCCTGGGGCCCGACATCCATTCTCTGGTACAGTCAGACCAAGAAGCTCAGGCCGTGGCAGAGCCATGA
Amino sequence
MASGGGGGNTGAGGGPGMGLSLGLGLGLSLGMSEATSEAEEEAATAEAVGRLATTLWLRLRGWEAVLAAAQRLLVWEKPLHSLVTAAALNGLFWLLSSSSLRPFFLLSVSLLAYFLLDLWQPRFLPDVSASSPEEPHSDSEGAGSGARPHLLSVPELCRYLAESWLTFQIHLQELLQYKRQNPAQFCVRVCSGCAVLAVLGHYVPGIMISYIVLLSILLWPLVVYHELIQRMYTRLEPLLMQLDYSMKAEANALHHKHDKRKRQGKNAPPGGDEPLAETESESEAELAGFSPVVDVKKTALALAITDSELSDEEASILESGGFSVSRATTPQLTDVSEDLDQQSLPSEPEETLSRDLGEGEEGELAPPEDLLGRPQALSRQALDSEEEEEDVAAKETLLRLSSPLHFVNTHFNGAGSPPDGVKCSPGGPVETLSPETVSGGLTALPGTLSPPLCLVGSDPAPSPSILPPVPQDSPQPLPAPEEEEALTTEDFELLDQGELEQLNAELGLEPETPPKPPDAPPLGPDIHSLVQSDQEAQAVAEP*