ENST00000648610.2 C2CD2L
Information
- Transcript ID
- ENST00000648610.2
- Genome
- hg38
- Position
- chr11:119,107,344-119,118,544
- Strand
- +
- CDS length
- 2,121
- Amino acid length
- 707
- Gene symbol
- C2CD2L
- Gene type
- protein-coding
- Gene description
- C2CD2 like
- Gene Entrez Gene ID
- 9854
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 | 119,107,344 | 119,108,095 |
| 2 | 119,110,104 | 119,110,199 |
| 3 | 119,110,561 | 119,110,680 |
| 4 | 119,110,847 | 119,110,957 |
| 5 | 119,111,052 | 119,111,168 |
| 6 | 119,111,263 | 119,111,374 |
| 7 | 119,111,521 | 119,111,629 |
| 8 | 119,112,328 | 119,112,392 |
| 9 | 119,112,482 | 119,112,609 |
| 10 | 119,112,700 | 119,112,874 |
| 11 | 119,113,611 | 119,113,712 |
| 12 | 119,113,855 | 119,113,988 |
| 13 | 119,114,080 | 119,114,365 |
| 14 | 119,116,045 | 119,118,544 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 119,107,742 | 119,108,095 |
| 2 | CDS | 119,110,104 | 119,110,199 |
| 3 | CDS | 119,110,561 | 119,110,680 |
| 4 | CDS | 119,110,847 | 119,110,957 |
| 5 | CDS | 119,111,052 | 119,111,168 |
| 6 | CDS | 119,111,263 | 119,111,374 |
| 7 | CDS | 119,111,521 | 119,111,629 |
| 8 | CDS | 119,112,328 | 119,112,392 |
| 9 | CDS | 119,112,482 | 119,112,609 |
| 10 | CDS | 119,112,700 | 119,112,874 |
| 11 | CDS | 119,113,611 | 119,113,712 |
| 12 | CDS | 119,113,855 | 119,113,988 |
| 13 | CDS | 119,114,080 | 119,114,365 |
| 14 | CDS | 119,116,045 | 119,116,256 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr11 | 118,978,054 | 118,989,254 | Link |
CDS sequence
ATGGATCCGGGCTGGGGGCAGCGGGACGTGGGCTGGGCGGCCTTGCTGATCCTCTTCGCCGCCTCGCTGCTCACGGTGTTCGCCTGGCTGCTGCAATATGCCCGGGGCTTGTGGCTGGCGCGGGCCCGCGGGGACCGGGGCCCGGGACCCGCCTTAGCCGGGGAACCCGCGGGTTCCCTGCGGGAGCTGGGCGTGTGGCGCTCGCTGCTGCGGCTGCGGGCGACTCGGGCTGGCGCCGCCGAGGAGCCAGGAGTCCGGGGCCTCCTGGCGTCACTCTTCGCCTTCAAGTCTTTCCGGGAGAACTGGCAGCGGGCTTGGGTGCGAGCGCTGAACGAGCAGGCCTGCAGAAACGGGAGCTCCATCCAAATCGCCTTTGAGGAGGTGCCCCAACTCCCACCCAGAGCCAGCATCAGTCATGTGACCTGCGTAGACCAATCTGAGCATACCATGGTGCTGCGTTGCCAGCTCTCTGCTGAGGAGGTGCGGTTCCCAGTCTCTGTGACCCAGCAGTCCCCCGCTGCCGTCTCCATGGAGACCTACCACGTCACTCTGACACTGCCACCAACACAGTTGGAAGTCAACCTGGAGGAAATCCCTGGTGAGGGGCTGCTCATATCCTGGGCCTTCACTGATCGCCCAGATCTCAGCCTAACGGTGCTTCCCAAGCTTCAGGCCAGGGAGAGAGGTGAAGAACAAGTGGAGCTCTCCACAATTGAGGAACTGATCAAGGATGCCATAGTCAGCACCCAGCCAGCCATGATGGTCAACCTCAGGGCTTGCTCTGCCCCAGGAGGCCTGGTACCCAGTGAGAAGCCACCCATGATGCCCCAGGCTCAGCCAGCCATCCCCAGACCTAACCGGTTATTCCTACGGCAGCTTCGGGCATCTCACTTGGGAAATGAGCTGGAAGGCACCGAGGAACTGTGCTGTGTAGCTGAACTCGACAACCCCATGCAGCAGAAGTGGACCAAGCCCGCGAGGGCTGGATCCGAGGTGGAGTGGACAGAAGACCTGGCACTGGATCTGGGCCCCCAGAGCCGGGAGCTGACCCTCAAAGTGCTGAGGAGCAGCAGCTGTGGAGACACCGAACTCCTAGGCCAGGCCACACTGCCTGTGGGCTCCCCCTCCAGACCACTGTCTCGAAGACAGTTGTGCCCACTCACCCCAGGGCCAGGGAAAGCCCTGGGACCAGCAGCCACCATGGCAGTGGAGCTTCACTATGAGGAGGGCTCTCCCCGGAACCTGGGTACTCCCACCTCCTCCACTCCACGCCCCAGCATCACACCTACCAAGAAGATTGAGCTTGACCGGACCATCATGCCCGATGGCACCATTGTCACCACAGTCACCACTGTCCAGTCCCGGCCCCGTATAGACGGCAAATTAGACTCCCCCTCCCGCTCCCCGTCCAAGGTGGAGGTGACCGAGAAGACGACAACTGTGCTGAGTGAGAGCAGTGGCCCCAGCAATACCTCCCATAGCAGCAGCCGGGACAGCCACCTTTCCAACGGCTTGGACCCTGTAGCAGAGACAGCGATTCGCCAGCTGACAGAGCCCAGTGGGCGGGTGGCCAAGAAGACACCCACCAAGCGCAGCACTCTCATCATCTCTGGTGTTTCCAAGGTGCCCATTGCTCAGGACGAGTTGGCGCTATCCCTGGGCTATGCGGCATCCCTGGAAGCCTCAGTGCAGGATGATGCAGGGACCAGCGGAGGCCCCTCTTCACCTCCCTCAGACCCACCAGCCATGTCTCCAGGACCGCTAGATGCCCTCTCTAGTCCCACAAGTGTCCAGGAAGCAGACGAGACAACCCGTTCGGATATTTCTGAGAGGCCATCTGTGGATGATATTGAGTCGGAAACGGGGTCCACTGGTGCCCTGGAGACCCGCAGCCTCAAGGATCACAAAGTGAGTTTCCTGCGCAGCGGCACTAAGCTCATCTTCCGCCGGAGGCCTAGGCAGAAGGAAGCTGGCCTGAGCCAATCACACGATGACCTCTCCAACGCAACGGCCACGCCCAGTGTCCGAAAGAAGGCCGGCAGCTTTTCTCGCCGCCTTATCAAGCGCTTTTCCTTCAAATCCAAACCCAAGGCCAATGGTAACCCCAGCCCCCAGCTCTGA
Amino sequence
MDPGWGQRDVGWAALLILFAASLLTVFAWLLQYARGLWLARARGDRGPGPALAGEPAGSLRELGVWRSLLRLRATRAGAAEEPGVRGLLASLFAFKSFRENWQRAWVRALNEQACRNGSSIQIAFEEVPQLPPRASISHVTCVDQSEHTMVLRCQLSAEEVRFPVSVTQQSPAAVSMETYHVTLTLPPTQLEVNLEEIPGEGLLISWAFTDRPDLSLTVLPKLQARERGEEQVELSTIEELIKDAIVSTQPAMMVNLRACSAPGGLVPSEKPPMMPQAQPAIPRPNRLFLRQLRASHLGNELEGTEELCCVAELDNPMQQKWTKPARAGSEVEWTEDLALDLGPQSRELTLKVLRSSSCGDTELLGQATLPVGSPSRPLSRRQLCPLTPGPGKALGPAATMAVELHYEEGSPRNLGTPTSSTPRPSITPTKKIELDRTIMPDGTIVTTVTTVQSRPRIDGKLDSPSRSPSKVEVTEKTTTVLSESSGPSNTSHSSSRDSHLSNGLDPVAETAIRQLTEPSGRVAKKTPTKRSTLIISGVSKVPIAQDELALSLGYAASLEASVQDDAGTSGGPSSPPSDPPAMSPGPLDALSSPTSVQEADETTRSDISERPSVDDIESETGSTGALETRSLKDHKVSFLRSGTKLIFRRRPRQKEAGLSQSHDDLSNATATPSVRKKAGSFSRRLIKRFSFKSKPKANGNPSPQL*