ENST00000706600.1 LAMP2
Information
- Transcript ID
- ENST00000706600.1
- Genome
- hg19
- Position
- chrX:119,564,870-119,603,152
- Strand
- -
- CDS length
- 1,365
- Amino acid length
- 455
- Gene symbol
- LAMP2
- Gene type
- protein-coding
- Gene description
- lysosomal associated membrane protein 2
- Gene Entrez Gene ID
- 3920
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
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Category | : |
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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 |
---|---|---|
9 | 119,564,870 | 119,566,541 |
8 | 119,575,585 | 119,575,749 |
7 | 119,576,454 | 119,576,517 |
6 | 119,580,160 | 119,580,282 |
5 | 119,581,696 | 119,581,880 |
4 | 119,582,825 | 119,582,983 |
3 | 119,589,212 | 119,589,425 |
2 | 119,590,506 | 119,590,624 |
1 | 119,602,961 | 119,603,152 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
9 | CDS | 119,566,270 | 119,566,541 |
8 | CDS | 119,575,585 | 119,575,749 |
7 | CDS | 119,576,454 | 119,576,517 |
6 | CDS | 119,580,160 | 119,580,282 |
5 | CDS | 119,581,696 | 119,581,880 |
4 | CDS | 119,582,825 | 119,582,983 |
3 | CDS | 119,589,212 | 119,589,425 |
2 | CDS | 119,590,506 | 119,590,624 |
1 | CDS | 119,602,961 | 119,603,024 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chrX | 120,431,015 | 120,469,297 | Link |
CDS sequence
ATGGTGTGCTTCCGCCTCTTCCCGGTTCCGGGCTCAGGGCTCGTTCTGGTCTGCCTAGTCCTGGGAGCTGTGCGGTCTTATGCATTGGAACTTAATTTGACAGATTCAGAAAATGCCACTTGCCTTTATGCAAAATGGCAGATGAATTTCACAGTACGCTATGAAACTACAAATAAAACTTATAAAACTGTAACCATTTCAGACCATGGCACTGTGACATATAATGGAAGCATTTGTGGGGATGATCAGAATGGTCCCAAAATAGCAGTGCAGTTCGGACCTGGCTTTTCCTGGATTGCGAATTTTACCAAGGCAGCATCTACTTATTCAATTGACAGCGTCTCATTTTCCTACAACACTGGTGATAACACAACATTTCCTGATGCTGAAGATAAAGGAATTCTTACTGTTGATGAACTTTTGGCCATCAGAATTCCATTGAATGACCTTTTTAGATGCAATAGTTTATCAACTTTGGAAAAGAATGATGTTGTCCAACACTACTGGGATGTTCTTGTACAAGCTTTTGTCCAAAATGGCACAGTGAGCACAAATGAGTTCCTGTGTGATAAAGACAAAACTTCAACAGTGGCACCCACCATACACACCACTGTGCCATCTCCTACTACAACACCTACTCCAAAGGAAAAACCAGAAGCTGGAACCTATTCAGTTAATAATGGCAATGATACTTGTCTGCTGGCTACCATGGGGCTGCAGCTGAACATCACTCAGGATAAGGTTGCTTCAGTTATTAACATCAACCCCAATACAACTCACTCCACAGGCAGCTGCCGTTCTCACACTGCTCTACTTAGACTCAATAGCAGCACCATTAAGTATCTAGACTTTGTCTTTGCTGTGAAAAATGAAAACCGATTTTATCTGAAGGAAGTGAACATCAGCATGTATTTGGTTAATGGCTCCGTTTTCAGCATTGCAAATAACAATCTCAGCTACTGGGATGCCCCCCTGGGAAGTTCTTATATGTGCAACAAAGAGCAGACTGTTTCAGTGTCTGGAGCATTTCAGATAAATACCTTTGATCTAAGGGTTCAGCCTTTCAATGTGACACAAGGAAAGTATTCTACAGAATGGCACCAGCATCTACATAATCAGTCAAGTGTGGAATTGGAAACCATTCTATTATCTCCTCCTCGTACACCCCCTACATCCGTTTGGTCAATTTTGCCTTCTAATTTGATCTCCAGTCTGTGCCTTCTGCTTTTCTTCTGCACTTCATTAATCCAGCTCAGGACAATATTATTGGTTACCTGGACTCTAGTGATAAAGATATGTCCTACCTTACTACCTCCATCTGCCATAACTTCTGAAATGAAATCCTGCTTAATATCCTGCTGCTGA
Amino sequence
MVCFRLFPVPGSGLVLVCLVLGAVRSYALELNLTDSENATCLYAKWQMNFTVRYETTNKTYKTVTISDHGTVTYNGSICGDDQNGPKIAVQFGPGFSWIANFTKAASTYSIDSVSFSYNTGDNTTFPDAEDKGILTVDELLAIRIPLNDLFRCNSLSTLEKNDVVQHYWDVLVQAFVQNGTVSTNEFLCDKDKTSTVAPTIHTTVPSPTTTPTPKEKPEAGTYSVNNGNDTCLLATMGLQLNITQDKVASVININPNTTHSTGSCRSHTALLRLNSSTIKYLDFVFAVKNENRFYLKEVNISMYLVNGSVFSIANNNLSYWDAPLGSSYMCNKEQTVSVSGAFQINTFDLRVQPFNVTQGKYSTEWHQHLHNQSSVELETILLSPPRTPPTSVWSILPSNLISSLCLLLFFCTSLIQLRTILLVTWTLVIKICPTLLPPSAITSEMKSCLISCC*