ENST00000688520.1 WDR12
Information
- Transcript ID
- ENST00000688520.1
- Genome
- hg19
- Position
- chr2:203,738,984-203,776,949
- Strand
- -
- CDS length
- 1,272
- Amino acid length
- 424
- Gene symbol
- WDR12
- Gene type
- protein-coding
- Gene description
- WD repeat domain 12
- Gene Entrez Gene ID
- 55759
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 |
|---|---|---|
| 13 | 203,738,984 | 203,745,660 |
| 12 | 203,747,434 | 203,747,506 |
| 11 | 203,748,332 | 203,748,464 |
| 10 | 203,748,921 | 203,749,026 |
| 9 | 203,749,118 | 203,749,258 |
| 8 | 203,757,340 | 203,757,425 |
| 7 | 203,759,304 | 203,759,349 |
| 6 | 203,760,788 | 203,760,942 |
| 5 | 203,762,023 | 203,762,138 |
| 4 | 203,764,254 | 203,764,360 |
| 3 | 203,765,748 | 203,765,842 |
| 2 | 203,772,588 | 203,772,682 |
| 1 | 203,776,159 | 203,776,949 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 13 | CDS | 203,745,583 | 203,745,660 |
| 12 | CDS | 203,747,434 | 203,747,506 |
| 11 | CDS | 203,748,332 | 203,748,464 |
| 10 | CDS | 203,748,921 | 203,749,026 |
| 9 | CDS | 203,749,118 | 203,749,258 |
| 8 | CDS | 203,757,340 | 203,757,425 |
| 7 | CDS | 203,759,304 | 203,759,349 |
| 6 | CDS | 203,760,788 | 203,760,942 |
| 5 | CDS | 203,762,023 | 203,762,138 |
| 4 | CDS | 203,764,254 | 203,764,360 |
| 3 | CDS | 203,765,748 | 203,765,842 |
| 2 | CDS | 203,772,588 | 203,772,682 |
| 1 | CDS | 203,776,159 | 203,776,199 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr2 | 202,874,261 | 202,912,226 | Link |
CDS sequence
ATGGCTCAGCTCCAAACACGCTTCTACACTGATAACAAGAAATATGCCGTAGATGATGTTCCCTTCTCAATCCCTGCTGCCTCTGAAATTGCCGACCTTAGTAACATCATCAATAAACTACTAAAGGACAAAAATGAGTTCCACAAACATGTGGAGTTTGATTTCCTTATTAAGGGCCAGTTTCTGCGAATGCCCTTGGACAAACACATGGAAATGGAGAACATCTCATCAGAAGAAGTTGTGGAAATAGAATACGTGGAGAAGTATACTGCACCCCAGCCAGAGCAATGCATGTTCCATGATGACTGGATCAGTTCAATTAAAGGGGCAGAGGAATGGATCTTGACTGGTTCTTATGATAAGACTTCTCGGATCTGGTCCTTGGAAGGAAAGTCAATAATGACAATTGTGGGACATACGGATGTTGTAAAAGATGTGGCCTGGGTGAAAAAAGATAGTTTGTCCTGCTTATTATTGAGTGCTTCTATGGATCAGACTATTCTCTTATGGGAGTGGAATGTAGAGAGAAACAAAGTGAAAGCCCTACACTGCTGTAGAGGTCATGCTGGAAGTGTAGATTCTATAGCTGTTGATGGCTCAGGAACTAAATTTTGCAGTGGCTCCTGGGATAAGATGCTAAAGATCTGGTCTACAGTCCCTACAGATGAAGAAGATGAAATGGAGGAGTCCACAAATCGACCAAGAAAGAAACAGAAGACAGAACAGTTGGGACTAACAAGGACTCCCATAGTGACCCTCTCTGGCCACATGGAGGCAGTTTCCTCAGTTCTGTGGTCAGATGCTGAAGAAATCTGCAGTGCATCTTGGGACCATACAATTAGAGTGTGGGATGTTGAGTCTGGCAGTCTTAAGTCAACTTTGACAGGAAATAAAGTGTTTAATTGTATTTCCTATTCTCCACTTTGTAAACGTTTAGCATCTGGAAGCACAGATAGGCATATCAGACTGTGGGATCCCCGAACTAAAGATGGTTCTTTGGTGTCGCTGTCCCTAACGTCACATACTGGTTGGGTGACATCAGTAAAATGGTCTCCTACCCATGAACAGCAGCTGATTTCAGGATCTTTAGATAACATTGTTAAGCTGTGGGATACAAGAAGTTGTAAGGCTCCTCTCTATGATCTGGCTGCTCATGAAGACAAAGTTCTGAGTGTAGACTGGACAGACACAGGGCTACTTCTGAGTGGAGGAGCAGACAATAAATTGTATTCCTACAGATATTCACCTACCACTTCCCATGTTGGGGCATGA
Amino sequence
MAQLQTRFYTDNKKYAVDDVPFSIPAASEIADLSNIINKLLKDKNEFHKHVEFDFLIKGQFLRMPLDKHMEMENISSEEVVEIEYVEKYTAPQPEQCMFHDDWISSIKGAEEWILTGSYDKTSRIWSLEGKSIMTIVGHTDVVKDVAWVKKDSLSCLLLSASMDQTILLWEWNVERNKVKALHCCRGHAGSVDSIAVDGSGTKFCSGSWDKMLKIWSTVPTDEEDEMEESTNRPRKKQKTEQLGLTRTPIVTLSGHMEAVSSVLWSDAEEICSASWDHTIRVWDVESGSLKSTLTGNKVFNCISYSPLCKRLASGSTDRHIRLWDPRTKDGSLVSLSLTSHTGWVTSVKWSPTHEQQLISGSLDNIVKLWDTRSCKAPLYDLAAHEDKVLSVDWTDTGLLLSGGADNKLYSYRYSPTTSHVGA*