ENST00000420689.2 PHF21B
Information
- Transcript ID
- ENST00000420689.2
- Genome
- hg38
- Position
- chr22:44,882,881-45,008,986
- Strand
- -
- CDS length
- 1,434
- Amino acid length
- 478
- 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
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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 |
---|---|---|
13 | 44,882,881 | 44,883,304 |
12 | 44,885,426 | 44,885,529 |
11 | 44,885,863 | 44,885,938 |
10 | 44,887,963 | 44,888,121 |
9 | 44,889,760 | 44,889,782 |
8 | 44,891,306 | 44,891,360 |
7 | 44,893,457 | 44,893,533 |
6 | 44,896,032 | 44,896,083 |
5 | 44,913,822 | 44,913,962 |
4 | 44,916,280 | 44,916,630 |
3 | 44,920,398 | 44,920,490 |
2 | 45,008,545 | 45,008,610 |
1 | 45,008,794 | 45,008,986 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
13 | CDS | 44,883,086 | 44,883,304 |
12 | CDS | 44,885,426 | 44,885,529 |
11 | CDS | 44,885,863 | 44,885,938 |
10 | CDS | 44,887,963 | 44,888,121 |
9 | CDS | 44,889,760 | 44,889,782 |
8 | CDS | 44,891,306 | 44,891,360 |
7 | CDS | 44,893,457 | 44,893,533 |
6 | CDS | 44,896,032 | 44,896,083 |
5 | CDS | 44,913,822 | 44,913,962 |
4 | CDS | 44,916,280 | 44,916,630 |
3 | CDS | 44,920,398 | 44,920,490 |
2 | CDS | 45,008,545 | 45,008,610 |
1 | CDS | 45,008,794 | 45,008,811 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr22 | 45,278,761 | 45,404,867 | Link |
CDS sequence
ATGAGGCGGCAGCCACAGAACGGCGACCTCAAGAAGCAGCTCCACGAAAGGCAGCCGCGGATCGCCGCGCTCAGCGACAAACAAGCTTTGGGAACGATCACTGCAGTGCCTGTCACGGGTCCTCAGGTCAGCTCCTTGCAGAGGTTGGCCGGGCAAGGAGCGGCAGTGCTACCTCAGGTTAGGCCAAAGACTCTGATTCCAGACAGCCTCCCCGTTGCCCCGGGCCGGGACCGGCCACCCAAGCAGCCCCCAACATTCCAGAAGGCCACCGTGGTCAGCGTCAAGAACCCCAGCCCAGCCCTCCCCACCGCCAACAACACTGTCAGCCATGTGCCAGCGCCCGGCAGCCAGCCCCAGGCCCTCGCCGAGCCCGCCGCCCTCGCCTCTCCGCTGAGCAGTGCGGGGGTGGCCTACGCCATCATCTCCACCTCCCCCAGCAATGCCGCCGCCATGGCCCCCAGCACCGCCGTGTCTGTGGTCAGTGACAGCATCAAAGTCCAGCCCCTCCTCATCAGTGCTGACAACAAGGTCATCATCATTCAGCCTCAAGTGCAGACGCAGCCCGAGAGCACGGCAGAGTCGCGGCCGCCCACAGAGGAGCCATCTCAGGGAGCTCAGGCCACCAAAAAGAAGAAGGAAGACCGGCCCCCGACCCAGGAGAACCCCGAGAAAATCGCCTTCATGGTAGCGCTAGGCCTGGTTACCACGGAACATTTGGAAGAAATCCAGAGCAAGCGACAGGAGCGGAAGAGAAGAAGCACAGCCAACCCTGCCTACAGCGGCCTCCTGGAGACCGAGAGGAAACGGCTGGCCTCCAACTATCTCAACAACCCCCTGTTCCTCACAGCGAGAGCCAATGAGGACCCCTGCTGGAAGAACGAGATCACCCACGATGAGCACTGTGCCGCCTGCAAGCGAGGGGCCAACCTGCAGCCCTGCGGCACCTGCCCGGGGGCCTACCACCTCAGCTGCCTGGAGCCGCCCCTCAAGACGGCGCCCAAGGGCGTGTGGGTGTGCCCCAGGTGCCAGCAGAAGGCCTTAAAGAAAGACGAGGGTGTGCCCTGGACTGGGATGCTGGCCATCGTGCACTCTTATGTCACCCACAAGACAGTCAAAGAAGAGGAGAAGCAGAAGCTGCTGCAACGAGGCAGTGAGCTGCAGAACGAGCACCAGCAGCTGGAGGAGCGGGACCGGCGGCTGGCGTCAGCAGTGCAGAAATGCCTGGAGTTGAAGACAAGCCTGCTGGCCCGCCAGAGGGGCACCCAGTCATCCCTGGACCGCCTGCGGGCCCTCCTGAGACTGATACAGGGCGAGCAGCTGCTCCAGGTCACCATGACGACCACTAGCCCTGCCCCACTGCTGGCCGGGCCCTGGACCAAGCCCTCAGTGGCAGCCACACACCCCACCGTCCAGCACCCCCAGGGCCACAACTGA
Amino sequence
MRRQPQNGDLKKQLHERQPRIAALSDKQALGTITAVPVTGPQVSSLQRLAGQGAAVLPQVRPKTLIPDSLPVAPGRDRPPKQPPTFQKATVVSVKNPSPALPTANNTVSHVPAPGSQPQALAEPAALASPLSSAGVAYAIISTSPSNAAAMAPSTAVSVVSDSIKVQPLLISADNKVIIIQPQVQTQPESTAESRPPTEEPSQGAQATKKKKEDRPPTQENPEKIAFMVALGLVTTEHLEEIQSKRQERKRRSTANPAYSGLLETERKRLASNYLNNPLFLTARANEDPCWKNEITHDEHCAACKRGANLQPCGTCPGAYHLSCLEPPLKTAPKGVWVCPRCQQKALKKDEGVPWTGMLAIVHSYVTHKTVKEEEKQKLLQRGSELQNEHQQLEERDRRLASAVQKCLELKTSLLARQRGTQSSLDRLRALLRLIQGEQLLQVTMTTTSPAPLLAGPWTKPSVAATHPTVQHPQGHN*