ENST00000517724.5 SEMA4G
Information
- Transcript ID
- ENST00000517724.5
- Genome
- hg19
- Position
- chr10:102,732,469-102,745,015
- Strand
- +
- CDS length
- 2,109
- Amino acid length
- 703
- Gene symbol
- SEMA4G
- Gene type
- protein-coding
- Gene description
- semaphorin 4G
- Gene Entrez Gene ID
- 57715
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 | 102,732,469 | 102,732,793 |
| 2 | 102,732,886 | 102,733,034 |
| 3 | 102,733,304 | 102,733,366 |
| 4 | 102,737,389 | 102,737,487 |
| 5 | 102,738,052 | 102,738,145 |
| 6 | 102,738,284 | 102,738,397 |
| 7 | 102,738,606 | 102,738,775 |
| 8 | 102,738,859 | 102,739,028 |
| 9 | 102,739,605 | 102,739,749 |
| 10 | 102,739,879 | 102,740,101 |
| 11 | 102,740,335 | 102,740,450 |
| 12 | 102,740,579 | 102,740,754 |
| 13 | 102,740,925 | 102,740,986 |
| 14 | 102,744,247 | 102,745,015 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 102,732,670 | 102,732,793 |
| 2 | CDS | 102,732,886 | 102,733,034 |
| 3 | CDS | 102,733,304 | 102,733,366 |
| 4 | CDS | 102,737,389 | 102,737,487 |
| 5 | CDS | 102,738,052 | 102,738,145 |
| 6 | CDS | 102,738,284 | 102,738,397 |
| 7 | CDS | 102,738,606 | 102,738,775 |
| 8 | CDS | 102,738,859 | 102,739,028 |
| 9 | CDS | 102,739,605 | 102,739,749 |
| 10 | CDS | 102,739,879 | 102,740,101 |
| 11 | CDS | 102,740,335 | 102,740,450 |
| 12 | CDS | 102,740,579 | 102,740,754 |
| 13 | CDS | 102,740,925 | 102,740,986 |
| 14 | CDS | 102,744,247 | 102,744,650 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr10 | 100,972,712 | 100,985,258 | Link |
CDS sequence
ATGTGGGGGAGGCTCTGGCCCCTCCTCCTCAGCATCCTCACAGCAACTGCAGTCCCAGGACCCTCACTGCGGAGACCGTCTAGAGAACTAGATGCCACCCCTCGGATGACCATACCCTATGAAGAGCTCTCTGGGACCCGGCACTTCAAGGGCCAAGCCCAGAACTACTCAACACTGCTGCTGGAGGAGGCCTCAGCAAGGCTGCTGGTGGGAGCCCGAGGTGCCCTGTTCTCTCTCAGTGCCAACGACATAGGAGATGGGGCTCACAAAGAGATCCACTGGGAAGCCTCCCCAGAGATGCAAAGCAAATGTCATCAAAAAGGGAAAAACAACCAGACGGAGTGCTTTAACCATGTGCGGTTCCTGCAGCGGCTCAATTCTACCCACCTCTATGCATGTGGGACTCACGCCTTCCAGCCCCTCTGTGCAGCCATTGATGCTGAGGCCTTCACCTTGCCAACCAGCTTCGAGGAGGGGAAGGAGAAGTGTCCTTATGACCCAGCCCGTGGCTTCACAGGCCTCATCATTGATGGAGGCCTCTACACAGCCACTAGGTATGAATTCCGGAGCATTCCTGACATCCGCCGGAGCCGCCACCCACACTCCCTGAGAACTGAGGAGACACCAATGCATTGGCTCAATGATGCGGAGTTTGTGTTCTCCGTCCTCGTGCGGGAGAGCAAGGCCAGTGCAGTGGGTGATGATGACAAGGTGTACTACTTCTTCACGGAGCGTGCCACTGAGGAGGGCTCTGGCAGCTTCACTCAGAGCCGCAGCAGTCACCGTGTGGCCCGTGTGGCTCGTGTCTGCAAGGGAGACCTGGGAGGGAAGAAGATCCTGCAGAAGAAGTGGACTTCCTTCCTGAAAGCCCGTCTCATCTGCCACATTCCACTGTATGAGACACTGCGTGGGGTCTGCAGCCTGGATGCTGAAACCTCAAGCCGTACACACTTCTATGCAGCCTTCACGCTGAGCACACAGTGGAAGACCCTGGAGGCCTCAGCCATCTGCCGCTATGACCTGGCAGAGATCCAGGCTGTCTTTGCAGGACCCTATATGGAATACCAGGATGGTTCCCGGCGCTGGGGTCGCTATGAGGGTGGGGTGCCTGAGCCCCGGCCTGGCTCGTGTATCACAGATTCATTGCGCAGCCAAGGCTACAATTCATCCCAAGACTTGCCATCCCTGGTCCTGGACTTTGTAAAGTTGCACCCACTGATGGCTCGGCCCGTTGTGCCCACACGTGGACGGCCCCTGCTGCTCAAGCGCAACATACGCTACACACACCTTACAGGGACACCTGTCACCACGCCTGCTGGACCTACCTATGACCTGCTCTTTCTGGGCACAGCTGATGGCTGGATCCACAAGGCCGTAGTCCTGGGCTCTGGGATGCACATTATTGAAGAGACACAAGTGTTCAGGGAGTCCCAGTCTGTGGAAAATCTAGTCATCTCTCTATTGCAGCACAGCCTCTATGTGGGGGCTCCTAGCGGAGTCATCCAGCTACCACTCTCCAGCTGCTCCCGCTACCGATCCTGCTATGACTGCATCTTGGCCCGAGACCCCTACTGTGGCTGGGACCCTGGCACCCATGCCTGCGCAGCAGCCACCACCATAGCCAACAGGTCCCAGGGAAGCAGGACAGCACTGATACAGGACATAGAGAGAGGAAATCGAGGCTGTGAGAGCAGCAGGGATACAGGCAGGGCTCTGCAGGTCCATATGGGCTCAATGTCACCACCCTCTGCATGGCCCTGTGTGCTGGATGGTCCTGAAACCAGACAAGACCTCTGCCAGCCACCTAAGCCCTGCGTACATTCACATGCACACATGGAAGAATGTTTATCGGCTGGGCTGCAGTGCCCCCACCCTCACCTTCTCCTGGTGCATTCTTGTTTCATCCCTGCTTCTGGACTTGGGGTACCCTCCCAATTGCCACATCCTATCTGGTCCTCTTCCCCAGCCCCATGTGGTGACCTCTTTGTCAAGAGCTTGGGAACGGGCCAGCCTGGGGAGGTAAGACTGCATCACTCCCCTCCTCTCCCTTCCTGTGTGGCCCTTGTGAATCAGCCTCCCCACTCTCCTTGGTCATTCTCAAGAGTATGA
Amino sequence
MWGRLWPLLLSILTATAVPGPSLRRPSRELDATPRMTIPYEELSGTRHFKGQAQNYSTLLLEEASARLLVGARGALFSLSANDIGDGAHKEIHWEASPEMQSKCHQKGKNNQTECFNHVRFLQRLNSTHLYACGTHAFQPLCAAIDAEAFTLPTSFEEGKEKCPYDPARGFTGLIIDGGLYTATRYEFRSIPDIRRSRHPHSLRTEETPMHWLNDAEFVFSVLVRESKASAVGDDDKVYYFFTERATEEGSGSFTQSRSSHRVARVARVCKGDLGGKKILQKKWTSFLKARLICHIPLYETLRGVCSLDAETSSRTHFYAAFTLSTQWKTLEASAICRYDLAEIQAVFAGPYMEYQDGSRRWGRYEGGVPEPRPGSCITDSLRSQGYNSSQDLPSLVLDFVKLHPLMARPVVPTRGRPLLLKRNIRYTHLTGTPVTTPAGPTYDLLFLGTADGWIHKAVVLGSGMHIIEETQVFRESQSVENLVISLLQHSLYVGAPSGVIQLPLSSCSRYRSCYDCILARDPYCGWDPGTHACAAATTIANRSQGSRTALIQDIERGNRGCESSRDTGRALQVHMGSMSPPSAWPCVLDGPETRQDLCQPPKPCVHSHAHMEECLSAGLQCPHPHLLLVHSCFIPASGLGVPSQLPHPIWSSSPAPCGDLFVKSLGTGQPGEVRLHHSPPLPSCVALVNQPPHSPWSFSRV*