ENST00000218056.9 WDR13
Information
- Transcript ID
- ENST00000218056.9
- Genome
- hg38
- Position
- chrX:48,597,492-48,605,193
- Strand
- +
- CDS length
- 1,458
- Amino acid length
- 486
- Gene symbol
- WDR13
- Gene type
- protein-coding
- Gene description
- WD repeat domain 13
- Gene Entrez Gene ID
- 64743
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 | 48,597,492 | 48,598,037 |
| 2 | 48,598,717 | 48,598,957 |
| 3 | 48,599,353 | 48,599,462 |
| 4 | 48,599,587 | 48,599,717 |
| 5 | 48,600,319 | 48,600,626 |
| 6 | 48,601,784 | 48,601,964 |
| 7 | 48,602,065 | 48,602,206 |
| 8 | 48,604,272 | 48,604,390 |
| 9 | 48,604,848 | 48,605,193 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 48,597,997 | 48,598,037 |
| 2 | CDS | 48,598,717 | 48,598,957 |
| 3 | CDS | 48,599,353 | 48,599,462 |
| 4 | CDS | 48,599,587 | 48,599,717 |
| 5 | CDS | 48,600,319 | 48,600,626 |
| 6 | CDS | 48,601,784 | 48,601,964 |
| 7 | CDS | 48,602,065 | 48,602,206 |
| 8 | CDS | 48,604,272 | 48,604,390 |
| 9 | CDS | 48,604,848 | 48,605,032 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chrX | 48,455,880 | 48,463,581 | Link |
CDS sequence
ATGGCCGCGGTGTGGCAGCAAGTCTTAGCAGTGGACGCGAGGTACAACGCGTACCGCACACCAACGTTTCCACAGTTTCGGACGCAGTATATCCGCCGGCGCAGCCAGCTGCTGCGGGAGAATGCCAAGGCTGGGCACCCCCCAGCGCTGCGTCGGCAGTACCTGAGGCTTCGGGGGCAGCTGCTGGGCCAGCGCTACGGGCCCCTCTCCGAGCCAGGCAGTGCTCGTGCCTATAGCAACAGCATCGTCCGCAGTAGCCGCACTACTCTTGACCGCATGGAGGACTTTGAGGATGATCCTCGGGCCCTGGGGGCCCGTGGGCACCGTCGTTCTGTCAGCAGAGGCTCCTACCAGCTGCAGGCGCAGATGAACCGTGCCGTCTATGAGGACAGGCCCCCTGGCAGCGTGGTGCCCACGTCAGCAGCAGAGGCAAGTCGGGCCATGGCCGGGGACACGTCACTGAGCGAGAACTATGCCTTTGCGGGCATGTATCATGTTTTTGACCAGCACGTGGATGAGGCAGTCCCAAGGGTGCGCTTCGCCAATGATGACCGACACCGCCTGGCCTGCTGCTCACTCGACGGCAGCATCTCCCTGTGCCAGCTGGTGCCTGCCCCACCCACAGTGCTTCGCGTGCTACGGGGCCACACCCGTGGTGTCTCCGACTTCGCCTGGTCCCTCTCCAATGACATCCTCGTGTCCACCTCACTGGATGCCACCATGCGCATCTGGGCCTCTGAGGATGGTCGCTGCATCCGAGAGATCCCTGACCCCGATAGCGCTGAACTGCTCTGCTGCACCTTCCAGCCTGTCAACAACAACCTCACTGTGGTGGGGAACGCCAAGCACAACGTGCATGTCATGAACATCTCCACAGGCAAGAAAGTGAAGGGGGGCTCCAGCAAGCTGACAGGCCGTGTCCTTGCTCTGTCCTTTGATGCCCCTGGCCGGCTGCTCTGGGCGGGTGATGACCGTGGCAGTGTCTTCTCTTTCCTCTTTGATATGGCCACAGGGAAGCTGACCAAAGCCAAGCGTTTGGTGGTGCATGAGGGGAGCCCTGTGACCAGCATCTCAGCCCGGTCCTGGGTCAGCCGCGAGGCCCGGGATCCCTCACTGCTCATCAATGCTTGCCTCAACAAGTTGCTGCTCTACAGGGTGGTAGACAACGAGGGGACCCTGCAGCTGAAGAGAAGCTTCCCCATCGAGCAGAGCTCACATCCTGTGCGCAGCATCTTCTGTCCCCTCATGTCCTTCCGCCAGGGGGCCTGCGTGGTGACGGGCAGTGAGGACATGTGCGTGCACTTCTTTGATGTGGAGCGGGCGGCCAAGGCTGCTGTCAACAAGCTGCAGGGCCACAGTGCACCTGTGCTTGATGTCAGCTTCAACTGCGACGAGAGCCTACTGGCCTCCAGTGACGCCAGCGGCATGGTCATCGTCTGGAGGCGGGAGCAGAAGTAG
Amino sequence
MAAVWQQVLAVDARYNAYRTPTFPQFRTQYIRRRSQLLRENAKAGHPPALRRQYLRLRGQLLGQRYGPLSEPGSARAYSNSIVRSSRTTLDRMEDFEDDPRALGARGHRRSVSRGSYQLQAQMNRAVYEDRPPGSVVPTSAAEASRAMAGDTSLSENYAFAGMYHVFDQHVDEAVPRVRFANDDRHRLACCSLDGSISLCQLVPAPPTVLRVLRGHTRGVSDFAWSLSNDILVSTSLDATMRIWASEDGRCIREIPDPDSAELLCCTFQPVNNNLTVVGNAKHNVHVMNISTGKKVKGGSSKLTGRVLALSFDAPGRLLWAGDDRGSVFSFLFDMATGKLTKAKRLVVHEGSPVTSISARSWVSREARDPSLLINACLNKLLLYRVVDNEGTLQLKRSFPIEQSSHPVRSIFCPLMSFRQGACVVTGSEDMCVHFFDVERAAKAAVNKLQGHSAPVLDVSFNCDESLLASSDASGMVIVWRREQK*