ENST00000414269.2 PHF21B
Information
- Transcript ID
- ENST00000414269.2
- Genome
- hg38
- Position
- chr22:44,883,086-45,009,999
- Strand
- -
- CDS length
- 984
- Amino acid length
- 328
- Gene symbol
- PHF21B
- Gene type
- protein-coding
- Gene description
- PHD finger protein 21B
- Gene Entrez Gene ID
- 112885
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| 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 |
|---|---|---|
| 11 | 44,883,086 | 44,883,304 |
| 10 | 44,885,426 | 44,885,529 |
| 9 | 44,885,863 | 44,885,938 |
| 8 | 44,887,963 | 44,888,121 |
| 7 | 44,889,760 | 44,889,782 |
| 6 | 44,891,306 | 44,891,360 |
| 5 | 44,893,457 | 44,893,533 |
| 4 | 44,896,032 | 44,896,083 |
| 3 | 44,913,822 | 44,913,962 |
| 2 | 44,916,280 | 44,916,450 |
| 1 | 45,009,949 | 45,009,999 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 11 | CDS | 44,883,086 | 44,883,304 |
| 10 | CDS | 44,885,426 | 44,885,529 |
| 9 | CDS | 44,885,863 | 44,885,938 |
| 8 | CDS | 44,887,963 | 44,888,121 |
| 7 | CDS | 44,889,760 | 44,889,782 |
| 6 | CDS | 44,891,306 | 44,891,360 |
| 5 | CDS | 44,893,457 | 44,893,533 |
| 4 | CDS | 44,896,032 | 44,896,083 |
| 3 | CDS | 44,913,822 | 44,913,962 |
| 2 | CDS | 44,916,280 | 44,916,357 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr22 | 45,278,966 | 45,405,880 | Link |
CDS sequence
ATGGCCCCCAGCACCGCCGTGTCTGTGGTCAGTGACAGCATCAAAGTCCAGCCCCTCCTCATCAGTGCTGACAACAAGGTCATCATCATTCAGCCTCAAGTGCAGACGCAGCCCGAGAGCACGGCAGAGTCGCGGCCGCCCACAGAGGAGCCATCTCAGGGAGCTCAGGCCACCAAAAAGAAGAAGGAAGACCGGCCCCCGACCCAGGAGAACCCCGAGAAAATCGCCTTCATGGTAGCGCTAGGCCTGGTTACCACGGAACATTTGGAAGAAATCCAGAGCAAGCGACAGGAGCGGAAGAGAAGAAGCACAGCCAACCCTGCCTACAGCGGCCTCCTGGAGACCGAGAGGAAACGGCTGGCCTCCAACTATCTCAACAACCCCCTGTTCCTCACAGCGAGAGCCAATGAGGACCCCTGCTGGAAGAACGAGATCACCCACGATGAGCACTGTGCCGCCTGCAAGCGAGGGGCCAACCTGCAGCCCTGCGGCACCTGCCCGGGGGCCTACCACCTCAGCTGCCTGGAGCCGCCCCTCAAGACGGCGCCCAAGGGCGTGTGGGTGTGCCCCAGGTGCCAGCAGAAGGCCTTAAAGAAAGACGAGGGTGTGCCCTGGACTGGGATGCTGGCCATCGTGCACTCTTATGTCACCCACAAGACAGTCAAAGAAGAGGAGAAGCAGAAGCTGCTGCAACGAGGCAGTGAGCTGCAGAACGAGCACCAGCAGCTGGAGGAGCGGGACCGGCGGCTGGCGTCAGCAGTGCAGAAATGCCTGGAGTTGAAGACAAGCCTGCTGGCCCGCCAGAGGGGCACCCAGTCATCCCTGGACCGCCTGCGGGCCCTCCTGAGACTGATACAGGGCGAGCAGCTGCTCCAGGTCACCATGACGACCACTAGCCCTGCCCCACTGCTGGCCGGGCCCTGGACCAAGCCCTCAGTGGCAGCCACACACCCCACCGTCCAGCACCCCCAGGGCCACAACTGA
Amino sequence
MAPSTAVSVVSDSIKVQPLLISADNKVIIIQPQVQTQPESTAESRPPTEEPSQGAQATKKKKEDRPPTQENPEKIAFMVALGLVTTEHLEEIQSKRQERKRRSTANPAYSGLLETERKRLASNYLNNPLFLTARANEDPCWKNEITHDEHCAACKRGANLQPCGTCPGAYHLSCLEPPLKTAPKGVWVCPRCQQKALKKDEGVPWTGMLAIVHSYVTHKTVKEEEKQKLLQRGSELQNEHQQLEERDRRLASAVQKCLELKTSLLARQRGTQSSLDRLRALLRLIQGEQLLQVTMTTTSPAPLLAGPWTKPSVAATHPTVQHPQGHN*