ENST00000425117.6 UTP14A
Information
- Transcript ID
- ENST00000425117.6
- Genome
- hg38
- Position
- chrX:129,906,121-129,929,761
- Strand
- +
- CDS length
- 2,160
- Amino acid length
- 720
- Gene symbol
- UTP14A
- Gene type
- protein-coding
- Gene description
- UTP14A small subunit processome component
- Gene Entrez Gene ID
- 10813
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 | 129,906,121 | 129,906,236 |
| 2 | 129,907,367 | 129,907,442 |
| 3 | 129,908,060 | 129,908,130 |
| 4 | 129,908,670 | 129,908,734 |
| 5 | 129,911,008 | 129,911,150 |
| 6 | 129,919,175 | 129,919,294 |
| 7 | 129,919,395 | 129,919,489 |
| 8 | 129,920,457 | 129,920,580 |
| 9 | 129,920,675 | 129,920,752 |
| 10 | 129,921,194 | 129,921,587 |
| 11 | 129,924,795 | 129,925,195 |
| 12 | 129,925,919 | 129,926,112 |
| 13 | 129,926,240 | 129,926,339 |
| 14 | 129,929,336 | 129,929,761 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 129,906,211 | 129,906,236 |
| 2 | CDS | 129,907,367 | 129,907,442 |
| 3 | CDS | 129,908,060 | 129,908,130 |
| 4 | CDS | 129,908,670 | 129,908,734 |
| 5 | CDS | 129,911,008 | 129,911,150 |
| 6 | CDS | 129,919,175 | 129,919,294 |
| 7 | CDS | 129,919,395 | 129,919,489 |
| 8 | CDS | 129,920,457 | 129,920,580 |
| 9 | CDS | 129,920,675 | 129,920,752 |
| 10 | CDS | 129,921,194 | 129,921,587 |
| 11 | CDS | 129,924,795 | 129,925,195 |
| 12 | CDS | 129,925,919 | 129,926,112 |
| 13 | CDS | 129,926,240 | 129,926,339 |
| 14 | CDS | 129,929,336 | 129,929,608 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chrX | 129,040,097 | 129,063,737 | Link |
CDS sequence
ATGACTGCGAACCGGCTTGCAGAGAGCCTTCTGGCTTTGAGCCAACAGGAAGAACTAGCGGATTTGCCAAAAGACTACCTCTTGAGTGAGAGTGAAGATGAGGGGGACAATGATGGAGAGAGAAAGCATCAAAAGCTTCTGGAAGCAATCAGTTCCCTTGATGGAAAGAATAGGCGGAAATTGGCTGAGAGGTCTGAGGCTAGTCTGAAGGTGTCAGAGTTCAATGTCAGTTCTGAAGGATCAGGAGAAAAGCTGGTCCTTGCAGATCTGCTTGAGCCTGTTAAAACTTCATCTTCTTTGGCCACTGTGAAAAAGCAACTGAGTAGAGTCAAATCAAAGAAGACAGTGGAGTTACCTCTGAACAAAGAAGAGATTGAACGGGCAAGAACTCCCCTGGAGCAGGAAATTTTCAACCTCCTCCATAAGAACAAGCAGCCAGTGACAGACCCTTTACTGACCCCTGTGGAAAAGGCCTCTCTCCGAGCCATGAGCCTAGAAGAGGCAAAGATGCGACGAGCAGAGCTTCAGAGGGCTCGGGCTCTGCAGTCCTACTATGAGGCCAAGGCTCGAAGAGAGAAGAAAATCAAAAGTAAAAAGTATCACAAAGTCGTGAAGAAAGGAAAGGCCAAGAAAGCCCTAAAAGAGTTTGAGCAGCTGCGGAAGGTTAATCCAGCTGCAGCACTAGAAGAACTGGAAAAAATTGAAAAGGCCAGAATGATGGAAAGAATGAGCCTTAAGCACCAAAACAGTGGGAAATGGGCCAAGTCAAAGGCAATTATGGCCAAATATGACCTGGAGGCTCGCCAAGCTATGCAGGAACAGTTGTCTAAGAACAAAGAACTGACACAGAAACTCCAGGTAGCCTCTGAGAGTGAGGAAGAGGAGGGAGGCACAGAAGATGTGGAAGAACTCCTTGTCCCTGATGTAGTGAATGAAGTGCAGATGAATGCAGATGGGCCGAATCCCTGGATGCTCAGGAGCTGCACCAGTGACACCAAAGAGGCTGCAACCCAGGAGGACCCTGAGCAACTGCCAGAGCTTGAGGCCCATGGAGTTTCTGAAAGTGAGGGAGAAGAAAGACCAGTGGCAGAAGAAGAAATTTTGTTGAGAGAATTTGAGGAAAGGCGATCCCTTAGAAAAAGATCTGAGCTCAGCCAAGATGCTGAGCCAGCAGGCAGTCAAGAAACAAAAGATTCTGGCAGCCAGGAGGTGCTGTCTGAATTGAGAGTACTATCTCAGAAATTGAAGGAAAACCATCAGTCCAGGAAGCAAAAAGCAAGTTCAGAGGGGACTATTCCCCAGGTCCAGAGAGAGGAACCTGCCCCAGAAGAAGAGGAGCCCCTGTTGCTACAGAGACCAGAGAGAGTACAGACGCTGGAAGAGCTAGAAGAGCTGGGAAAAGAAGAATGTTTTCAAAATAAGGAGCTTCCCAGACCTGTGTTAGAAGGGCAGCAGTCAGAGAGGACCCCAAATAATCGCCCTGATGCCCCTAAGGAGAAGAAAAAGAAGGAGCAAATGATCGACCTACAGAACCTCCTAACCACACAATCTCCCTCCGTGAAGTCTTTGGCAGTTCCCACAATAGAGGAGCTGGAAGATGAAGAGGAGAGAAACCATAGGCAGATGATAAAGGAAGCTTTTGCTGGGGATGATGTCATCAGAGATTTCTTGAAAGAGAAGAGGGAAGCTGTGGAGGCGAGTAAGCCAAAGGACGTGGACCTGACACTACCTGGCTGGGGCGAGTGGGGTGGTGTGGGCCTAAAGCCCAGTGCCAAGAAAAGACGCCGGTTTCTCATTAAAGCCCCTGAGGGTCCTCCAAGAAAAGATAAGAATTTGCCAAATGTGATTATCAATGAGAAGCGCAACATCCACGCAGCTGCTCATCAGGTACGAGTGCTTCCATATCCATTTACCCACCATTGGCAATTTGAAAGGACCATCCAGACCCCCATAGGATCCACATGGAACACCCAGAGGGCTTTCCAAAAGCTGACTACTCCCAAGGTCGTCACCAAGCCAGGCCATATCATTAACCCCATAAAAGCAGAAGACGTGGGCTACCGGTCTTCCTCAAGGTCGGACCTGTCTGTCATACAGAGGAATCCAAAACGAATCACCACACGTCACAAAAAACAGCTGAAGAAATGCTCTGTAGATTGA
Amino sequence
MTANRLAESLLALSQQEELADLPKDYLLSESEDEGDNDGERKHQKLLEAISSLDGKNRRKLAERSEASLKVSEFNVSSEGSGEKLVLADLLEPVKTSSSLATVKKQLSRVKSKKTVELPLNKEEIERARTPLEQEIFNLLHKNKQPVTDPLLTPVEKASLRAMSLEEAKMRRAELQRARALQSYYEAKARREKKIKSKKYHKVVKKGKAKKALKEFEQLRKVNPAAALEELEKIEKARMMERMSLKHQNSGKWAKSKAIMAKYDLEARQAMQEQLSKNKELTQKLQVASESEEEEGGTEDVEELLVPDVVNEVQMNADGPNPWMLRSCTSDTKEAATQEDPEQLPELEAHGVSESEGEERPVAEEEILLREFEERRSLRKRSELSQDAEPAGSQETKDSGSQEVLSELRVLSQKLKENHQSRKQKASSEGTIPQVQREEPAPEEEEPLLLQRPERVQTLEELEELGKEECFQNKELPRPVLEGQQSERTPNNRPDAPKEKKKKEQMIDLQNLLTTQSPSVKSLAVPTIEELEDEEERNHRQMIKEAFAGDDVIRDFLKEKREAVEASKPKDVDLTLPGWGEWGGVGLKPSAKKRRRFLIKAPEGPPRKDKNLPNVIINEKRNIHAAAHQVRVLPYPFTHHWQFERTIQTPIGSTWNTQRAFQKLTTPKVVTKPGHIINPIKAEDVGYRSSSRSDLSVIQRNPKRITTRHKKQLKKCSVD*