ENST00000294964.6 PKDCC
Information
- Transcript ID
- ENST00000294964.6
- Genome
- hg19
- Position
- chr2:42,275,161-42,285,657
- Strand
- +
- CDS length
- 1,482
- Amino acid length
- 494
- Gene symbol
- PKDCC
- Gene type
- protein-coding
- Gene description
- protein kinase domain containing, cytoplasmic
- Gene Entrez Gene ID
- 91461
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 | 42,275,161 | 42,275,978 |
2 | 42,280,379 | 42,280,501 |
3 | 42,281,176 | 42,281,447 |
4 | 42,282,081 | 42,282,160 |
5 | 42,282,426 | 42,282,533 |
6 | 42,284,361 | 42,284,534 |
7 | 42,284,743 | 42,285,657 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
1 | CDS | 42,275,340 | 42,275,978 |
2 | CDS | 42,280,379 | 42,280,501 |
3 | CDS | 42,281,176 | 42,281,447 |
4 | CDS | 42,282,081 | 42,282,160 |
5 | CDS | 42,282,426 | 42,282,533 |
6 | CDS | 42,284,361 | 42,284,534 |
7 | CDS | 42,284,743 | 42,284,828 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr2 | 42,048,021 | 42,058,517 | Link |
CDS sequence
ATGCGGCGCCGGCGGGCGGCAGTGGCCGCGGGTTTCTGCGCCTCCTTCCTGCTGGGCTCCGTCCTCAACGTGCTCTTCGCTCCGGGCTCGGAGCCTCCGAGGCCAGGCCAGTCCCCTGAGCCTTCGCCGGCCCCGGGTCCGGGCCGTCGCGGGGGCCGCGGGGAGCTGGCCCGGCAGATCCGGGCGCGCTACGAGGAGGTGCAGCGCTATTCCCGCGGGGGCCCCGGGCCCGGGGCGGGCCGGCCGGAGCGGCGGCGCCTGATGGACCTGGCTCCGGGCGGGCCCGGCCTGCCGCGCCCCCGGCCCCCTTGGGCCCGGCCCCTGTCCGACGGCGCCCCAGGCTGGCCCCCGGCTCCCGGCCCAGGCTCCCCCGGCCCGGGCCCGCGCCTGGGCTGCGCCGCGCTTCGCAACGTGTCCGGCGCGCAGTACATGGGCTCAGGCTACACCAAGGCCGTGTACCGGGTCCGCCTGCCCGGCGGTGCCGCGGTGGCGCTCAAGGCGGTGGACTTTAGCGGCCACGATCTGGGCAGCTGCGTGCGCGAGTTCGGGGTACGGAGGGGCTGCTATCGGCTGGCGGCCCACAAGCTGCTTAAGGAGATGGTGCTGCTGGAGCGGCTGCGGCACCCCAACGTGCTGCAGCTCTATGGCTACTGCTACCAGGACAGCGAGGACATCCCAGACACCCTGACCACCATCACGGAGCTGGGCGCCCCTGTAGAAATGATCCAGCTGCTGCAAACTTCCTGGGAGGATCGATTCCGAATCTGCCTGAGCCTGGGCCGCCTCCTCCACCACCTGGCCCACTCCCCACTGGGCTCCGTCACTCTGCTGGACTTCCGCCCTCGGCAGTTTGTGCTGGTGGATGGGGAGCTCAAAGTGACGGACCTGGATGACGCACGTGTGGAGGAGACGCCGTGTGCAGGCAGCACCGACTGCATACTCGAGTTTCCGGCCAGGAACTTCACCCTGCCCTGCTCAGCCCAGGGCTGGTGCGAGGGCATGAACGAGAAGCGGAACCTCTATAATGCCTACAGGTTTTTCTTCACATACCTCCTGCCTCACAGTGCCCCGCCTTCACTGCGTCCTCTGCTGGACAGCATCGTCAACGCCACAGGAGAGCTCGCCTGGGGGGTGGACGAGACCCTGGCCCAGCTGGAGAAGGTGCTGCACCTGTACCGGAGCGGGCAGTATCTGCAGAACTCCACGGCAAGCAGCAGTACCGAGTACCAGTGTATCCCAGACAGCACCATCCCCCAGGAAGACTACCGCTGCTGGCCATCCTACCACCACGGGAGCTGCCTCCTTTCAGTGTTCAACCTGGCTGAGGCTGTGGATGTCTGTGAGAGCCATGCCCAGTGTCGGGCCTTTGTGGTCACCAACCAGACCACCTGGACAGGTCGGCAGCTGGTCTTTTTCAAGACTGGATGGAGCCAAGTGGTCCCTGATCCCAACAAGACCACATATGTGAAGGCCTCTGGCTGA
Amino sequence
MRRRRAAVAAGFCASFLLGSVLNVLFAPGSEPPRPGQSPEPSPAPGPGRRGGRGELARQIRARYEEVQRYSRGGPGPGAGRPERRRLMDLAPGGPGLPRPRPPWARPLSDGAPGWPPAPGPGSPGPGPRLGCAALRNVSGAQYMGSGYTKAVYRVRLPGGAAVALKAVDFSGHDLGSCVREFGVRRGCYRLAAHKLLKEMVLLERLRHPNVLQLYGYCYQDSEDIPDTLTTITELGAPVEMIQLLQTSWEDRFRICLSLGRLLHHLAHSPLGSVTLLDFRPRQFVLVDGELKVTDLDDARVEETPCAGSTDCILEFPARNFTLPCSAQGWCEGMNEKRNLYNAYRFFFTYLLPHSAPPSLRPLLDSIVNATGELAWGVDETLAQLEKVLHLYRSGQYLQNSTASSSTEYQCIPDSTIPQEDYRCWPSYHHGSCLLSVFNLAEAVDVCESHAQCRAFVVTNQTTWTGRQLVFFKTGWSQVVPDPNKTTYVKASG*