ENST00000344636.6 PLEKHG7
Information
- Transcript ID
- ENST00000344636.6
- Genome
- hg38
- Position
- chr12:92,702,989-92,772,455
- Strand
- +
- CDS length
- 2,076
- Amino acid length
- 692
- Gene symbol
- PLEKHG7
- Gene type
- protein-coding
- Gene description
- pleckstrin homology and RhoGEF domain containing G7
- Gene Entrez Gene ID
- 440107
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| 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 | 92,702,989 | 92,703,132 |
| 2 | 92,706,471 | 92,707,138 |
| 3 | 92,707,650 | 92,707,672 |
| 4 | 92,728,993 | 92,729,120 |
| 5 | 92,732,233 | 92,732,273 |
| 6 | 92,736,482 | 92,736,577 |
| 7 | 92,737,378 | 92,737,521 |
| 8 | 92,740,853 | 92,740,948 |
| 9 | 92,741,491 | 92,741,592 |
| 10 | 92,745,478 | 92,745,591 |
| 11 | 92,754,090 | 92,754,264 |
| 12 | 92,755,825 | 92,755,940 |
| 13 | 92,756,298 | 92,756,391 |
| 14 | 92,761,752 | 92,761,831 |
| 15 | 92,764,041 | 92,764,194 |
| 16 | 92,768,983 | 92,769,080 |
| 17 | 92,770,088 | 92,772,455 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 2 | CDS | 92,706,632 | 92,707,138 |
| 3 | CDS | 92,707,650 | 92,707,672 |
| 4 | CDS | 92,728,993 | 92,729,120 |
| 5 | CDS | 92,732,233 | 92,732,273 |
| 6 | CDS | 92,736,482 | 92,736,577 |
| 7 | CDS | 92,737,378 | 92,737,521 |
| 8 | CDS | 92,740,853 | 92,740,948 |
| 9 | CDS | 92,741,491 | 92,741,592 |
| 10 | CDS | 92,745,478 | 92,745,591 |
| 11 | CDS | 92,754,090 | 92,754,264 |
| 12 | CDS | 92,755,825 | 92,755,940 |
| 13 | CDS | 92,756,298 | 92,756,391 |
| 14 | CDS | 92,761,752 | 92,761,831 |
| 15 | CDS | 92,764,041 | 92,764,194 |
| 16 | CDS | 92,768,983 | 92,769,080 |
| 17 | CDS | 92,770,088 | 92,770,195 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr12 | 93,096,765 | 93,166,231 | Link |
CDS sequence
ATGGAGAAAACAGAGTCATTCTGTCCAGAGGTGCCACCCCAAGACTGTGGAGCCTCTCCTCGGCCCTCGCTGAGGAGCCTGCCAAAGAACCAGGGGAGTCTCCTCCAGTTTGACCGGCAAGCCCCAGGCCGCATCTCCACCTCGCCCACTTTGAGGAGATTAAGGACCCGTGGCTGTGGGACAAGGCAGGATGCCTGGCAGGTGACCACCTGGGGAAGCTGGGGAGCTCCTGTGGGCTTCCCATGTTACCTTTCGAAGAGCCTGCCAGGAAGCCCAAAGGATTCTTCACACTTGCTGTCACCCTTGAGACTCCACTCAAGATTGACCTCTGAACCTGAAAGGGCCCTGAATGCAGCTGACTCACTGGAGCCCCAAACCCGGCCCACTGACAAGTATCTCCCTCCTGAGCTTCAGCCTGTCAATGAAGGGTCCCTTCACCAGGCCTCTCTTCGGCAGCAAGAAGGCCACTTCCTGCCCAGCCCCACCCTACGACACCCTAGTCCTCAGGGAGAAGAATTGCACCCATCCAGGTTCTACGAGCACAGGCGGAGTTCTGTGGTGCTGAACTTACCTGGACTTGAGGTGTTCCCCGGGGACCTTCTGGTGTCAGATGGAGCTGCTGATTACCTATGCCATCCACTTCTGCTGCTGAATTCAGAATCCAAAAAGCCAAGATGGCCTTTCTCCAAAAGAGGAGTGGGCAAAGACAAACACAAGCACATATCTGATCTGGAAAACTGCCTGTCCTCTGTGAAAATTACCAGCTTCAGGGGCTATGACTTCTACGGTCTTAAGGATAAGACCTGGGATGAAGTCTTGGAAACACATCACAAACTCCCGACCGATCAATTAGACCTGAAAAAGCAGCAAGAGGCCGTGTGGGAACTTTTCACAAGTGAATGCACCTATTTTTTGGACCATTTATTAGTTCTTAAGATGATCTTTATGAATACACTAAGATATCTGCAAACTCATGAATATCTCCTAGATGTGGATTTATGGAGACTTTTTGCAAACCTGGAGGAGTTAACTCAGACAAGCCTTGGTTTTGTGAACAGTCTCTTTGGCATCATCAAGGACTATGTAGACGCTTCTGAGATTTCCTCATCACTGGATTTTATTTCCGTGCTCACAAAGTATTTCCGAGGGAGTCTCTGTCAGAGCCACCAGACCTACTGCCTGAACTATTCAGCTGCTATCTTTTATCTTGAGAGCCTGAGGCAGAGAGATGACTTTGGAATTTATTTAAAATGGTGTGAGCAGAATGAACAATGCAGACGGCTCCACGTGCCAGAGCTGCTAGTGGCCCCACTACAGAGGCTCACTCGATATCCGTTGTTGCTGAAGAATATCTGGAAAAGGAGCATGGACTCTGCTGAGAAAATCATGATCTACTCCATCAAGGAAAAGGTGGAAAAGTCCATCCGGGACCTTGAAGGAAAAGTGAAGTGGCTGGACAATTTCCAAAAATTTAGATATCTACAGGAGATTATAGTGTGGCCACCGCTTTGGGATAGAGATAAAAGGTTTTTCATTCCAGAGTGTTTGAAACACATTTTTAAAGAACACATGGCAGAAAACATCTTGTCACCAACCAGCAGACACCTTCTCTATGAAGGAAAATTAACTCTTGCAGAAAGCACGAGATTCCTAGATGTTTATCTGTTTCTCTTCAATGATTTCCTCTTAGTTACGAAAACTAAGTGCAACAAAAAGAAACTTGGAGGCTCAGACCCTGGTTTAATGTGTCCTTCTCTTACTCCTGAGTTGCAAGCAGTAATAAAAGAGGGTGGTTCGTGTACAGTACTCGATCAGCCTATTCCACTAGATAGATTGGTAGTCAAAAGTATTGAACCACTCCATGTGTCAGTCTTTGGGCTGAGAAATGCTTTTCTTATACAACACGAAAACAGATATCGACAGTGTATAGCAGCATTCTTATTACAAGCCCAAACGGAAAACATCAAAAAAACATGGATGGCACAAATAACAACTGCAATTTCTTGCTTTACCAAGAGTCAGGAAACCAAGAAAATATCTTTATTCACATTGCCCGCAGAATCCTCTGAAATTTAG
Amino sequence
MEKTESFCPEVPPQDCGASPRPSLRSLPKNQGSLLQFDRQAPGRISTSPTLRRLRTRGCGTRQDAWQVTTWGSWGAPVGFPCYLSKSLPGSPKDSSHLLSPLRLHSRLTSEPERALNAADSLEPQTRPTDKYLPPELQPVNEGSLHQASLRQQEGHFLPSPTLRHPSPQGEELHPSRFYEHRRSSVVLNLPGLEVFPGDLLVSDGAADYLCHPLLLLNSESKKPRWPFSKRGVGKDKHKHISDLENCLSSVKITSFRGYDFYGLKDKTWDEVLETHHKLPTDQLDLKKQQEAVWELFTSECTYFLDHLLVLKMIFMNTLRYLQTHEYLLDVDLWRLFANLEELTQTSLGFVNSLFGIIKDYVDASEISSSLDFISVLTKYFRGSLCQSHQTYCLNYSAAIFYLESLRQRDDFGIYLKWCEQNEQCRRLHVPELLVAPLQRLTRYPLLLKNIWKRSMDSAEKIMIYSIKEKVEKSIRDLEGKVKWLDNFQKFRYLQEIIVWPPLWDRDKRFFIPECLKHIFKEHMAENILSPTSRHLLYEGKLTLAESTRFLDVYLFLFNDFLLVTKTKCNKKKLGGSDPGLMCPSLTPELQAVIKEGGSCTVLDQPIPLDRLVVKSIEPLHVSVFGLRNAFLIQHENRYRQCIAAFLLQAQTENIKKTWMAQITTAISCFTKSQETKKISLFTLPAESSEI*