ENST00000380486.4 C2CD2
Information
- Transcript ID
- ENST00000380486.4
- Genome
- hg38
- Position
- chr21:41,885,112-41,954,018
- Strand
- -
- CDS length
- 2,091
- Amino acid length
- 697
- Gene symbol
- C2CD2
- Gene type
- protein-coding
- Gene description
- C2 calcium dependent domain containing 2
- Gene Entrez Gene ID
- 25966
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
|
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 |
---|---|---|
14 | 41,885,112 | 41,889,344 |
13 | 41,899,053 | 41,899,362 |
12 | 41,901,622 | 41,901,749 |
11 | 41,905,724 | 41,905,837 |
10 | 41,906,992 | 41,907,166 |
9 | 41,907,660 | 41,907,784 |
8 | 41,909,459 | 41,909,523 |
7 | 41,912,332 | 41,912,440 |
6 | 41,914,598 | 41,914,721 |
5 | 41,918,105 | 41,918,227 |
4 | 41,918,856 | 41,918,960 |
3 | 41,921,972 | 41,922,085 |
2 | 41,942,147 | 41,942,245 |
1 | 41,953,370 | 41,954,018 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
14 | CDS | 41,889,124 | 41,889,344 |
13 | CDS | 41,899,053 | 41,899,362 |
12 | CDS | 41,901,622 | 41,901,749 |
11 | CDS | 41,905,724 | 41,905,837 |
10 | CDS | 41,906,992 | 41,907,166 |
9 | CDS | 41,907,660 | 41,907,784 |
8 | CDS | 41,909,459 | 41,909,523 |
7 | CDS | 41,912,332 | 41,912,440 |
6 | CDS | 41,914,598 | 41,914,721 |
5 | CDS | 41,918,105 | 41,918,227 |
4 | CDS | 41,918,856 | 41,918,960 |
3 | CDS | 41,921,972 | 41,922,085 |
2 | CDS | 41,942,147 | 41,942,245 |
1 | CDS | 41,953,370 | 41,953,648 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr21 | 43,305,221 | 43,374,127 | Link |
CDS sequence
ATGGCCATGGCCCGGCTGGGCTCGTGGCTCGGGGAGGCGCAGTGGCTCGCGCTGGTGTCGCTCTTCGTCGCGGCCCTGGCCACGGTAGGCCTGTACCTGGCGCAGTGGGCGCTGGCCAGGGCGCGACCCCAGCCCCAGCGGCGGGCGGTGGAGCCTGGAGAGGGGCCGCGCCCGGGGTCCGACGCGCTGCTCTCCTGGATCCTGACGCTGGGCAGCTGGAGGAGCCAGTGGCAGGCGGCCTGGGTGACCGCCCTGAACGAGGAGGCCGAGAGGAAAGGGGGCCCACCTTTCCTGTCCTTTGAGGAGGACCCGCGGCAGCAGGCACTGGAGCTGGTGGTGCAGGAGGTCTCCAGCGTGCTCAGGTCGGCGGAGGAGAAGGTGGTGGTCTGTCACGTGGTGGGCCAGGCTATTCAGTTCTTGGTCAGCGAGACGCCTGCCTTGGGTGCTGGATGCCGGCTGTACGACATGCGGCTCTCCCCTTTCCATTTACAGCTGGAGTTCCACATGAAGGAGAAGAGAGAGGACCTCCAGATTAGCTGGTCTTTCATCAGTGTGCCGGAAATGGCCGTTAATATCCAGCCCAAAGCACTGGGGGAGGACCAGGTGGCTGAGACAAGTGCGATGTCTGACGTTCTCAAGGACATCTTGAAGCATTTGGCTGGTTCTGCCTCTCCATCAGTGGTTCTGATTACCAAGCCCACGACTGTAAAGGAAGCTCAGAACTTACAGTGTGCTGCATCTACTGCTCAGGAATCCTGTCCTCCTAAACCTCCAAGGGCTCACGAGCTGAAGCTACTGGTGAGGAACATCCACGTCTTGCTGCTCAGCGAGCCCGGTGCCTCAGGCCACATTAATGCAGTGTGCGTCGTGCAGCTGAACGATCCTGTTCAGAGGTTCTCCAGCACCCTGACGAAAAACACTCCGGACCTCATGTGGGAAGAGGAATTCACCTTCGAGTTGAATGCCAAGTCGAAGGAGTTACACCTGCAGATTTCAGAGGCTGGGCGATCCTCAGAAGGTCTGCTGGCGACGGCGACAGTTCCTCTGGACTTATTTAAGAAGCAGCCTTCTGGGCCACAGAGCTTCACGCTGACCAGCGGGTCTGCCTGCGGCAGCTCGGTGCTGGGCTCGGTCACGGCAGAGTTCTCTTACATGGAACCTGGTGAATTGAAATCCTGGCCCATCCCTCCCCCTGTTCCTGCTGCAAAAATAGAAAAGGACCGCACGGTGATGCCCTGTGGGACTGTGGTCACTACTGTCACTGCTGTGAAGACCAAGCCTCGCGTCGACGTGGGGAGGGCGTCCCCGCTGAGCTCTGATTCTCCGGTGAAGACTCCCATCAAGGTGAAGGTGATCGAGAAGGACATCTCTGTCCAGGCCATCGCCTGCCGCAGCGCCCCCGTCAGCAAAACACTCTCTTCTTCAGACACAGAATTGTTGGTGTTGAATGGTTCGGATCCAGTGGCTGAAGTGGCCATTCGACAGCTCAGTGAATCTTCAAAGCTGAAACTCAAGTCGCCACGGAAGAAAAGCACTATTATCATATCAGGGATCTCCAAGACCTCACTATCTCAGGACCACGACGCTGCCCTGATGCAGGGCTACACGGCCTCTGTGGACAGCACCCACCAGGAGGACGCCCCATCCCATCCGGAGAGGGCGGCAGCCTCTGCCCCGCCAGAGGAAGCCGAGTCAGCCCAGGCATCCCTTGCCCCCAAGCCCCAGGAGGACGAGCTAGACTCCTGGGACTTGGAGAAGGAGCCACAGGCCGCGGCATGGAGCAGCCAGGTCCTGCTGGACCCCGACGGTGATGAGCTGTCAGAGAGCTCCATGAGTGTCTTGGAGCCGGGCACTGCCAAAAAGCATAAAGGAGGAATTCTAAGGAAAGGTGCAAAGCTGTTCTTCCGCCGGCGGCATCAACAGAAAGACCCAGGCATGAGTCAGTCACACAATGACCTTGTGTTCCTGGAGCAGCCAGAGGGTTCCCGGAGGAAAGGCATCACCCTCACCAGGATCCTGAACAAGAAGCTGCTCTCCAGGCACAGAAACAAGAACACCATGAACGGTGCCCCCGTGGAGCCCTGCACGTAG
Amino sequence
MAMARLGSWLGEAQWLALVSLFVAALATVGLYLAQWALARARPQPQRRAVEPGEGPRPGSDALLSWILTLGSWRSQWQAAWVTALNEEAERKGGPPFLSFEEDPRQQALELVVQEVSSVLRSAEEKVVVCHVVGQAIQFLVSETPALGAGCRLYDMRLSPFHLQLEFHMKEKREDLQISWSFISVPEMAVNIQPKALGEDQVAETSAMSDVLKDILKHLAGSASPSVVLITKPTTVKEAQNLQCAASTAQESCPPKPPRAHELKLLVRNIHVLLLSEPGASGHINAVCVVQLNDPVQRFSSTLTKNTPDLMWEEEFTFELNAKSKELHLQISEAGRSSEGLLATATVPLDLFKKQPSGPQSFTLTSGSACGSSVLGSVTAEFSYMEPGELKSWPIPPPVPAAKIEKDRTVMPCGTVVTTVTAVKTKPRVDVGRASPLSSDSPVKTPIKVKVIEKDISVQAIACRSAPVSKTLSSSDTELLVLNGSDPVAEVAIRQLSESSKLKLKSPRKKSTIIISGISKTSLSQDHDAALMQGYTASVDSTHQEDAPSHPERAAASAPPEEAESAQASLAPKPQEDELDSWDLEKEPQAAAWSSQVLLDPDGDELSESSMSVLEPGTAKKHKGGILRKGAKLFFRRRHQQKDPGMSQSHNDLVFLEQPEGSRRKGITLTRILNKKLLSRHRNKNTMNGAPVEPCT*