ENST00000394422.8 UTP14A
Information
- Transcript ID
- ENST00000394422.8
- Genome
- hg38
- Position
- chrX:129,906,164-129,929,752
- Strand
- +
- CDS length
- 2,316
- Amino acid length
- 772
- 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
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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 |
---|---|---|
1 | 129,906,164 | 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 | 129,911,766 | 129,911,921 |
7 | 129,919,175 | 129,919,294 |
8 | 129,919,395 | 129,919,489 |
9 | 129,920,457 | 129,920,580 |
10 | 129,920,675 | 129,920,752 |
11 | 129,921,194 | 129,921,587 |
12 | 129,924,795 | 129,925,195 |
13 | 129,925,919 | 129,926,112 |
14 | 129,926,240 | 129,926,339 |
15 | 129,929,336 | 129,929,752 |
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 | 129,911,766 | 129,911,921 |
7 | CDS | 129,919,175 | 129,919,294 |
8 | CDS | 129,919,395 | 129,919,489 |
9 | CDS | 129,920,457 | 129,920,580 |
10 | CDS | 129,920,675 | 129,920,752 |
11 | CDS | 129,921,194 | 129,921,587 |
12 | CDS | 129,924,795 | 129,925,195 |
13 | CDS | 129,925,919 | 129,926,112 |
14 | CDS | 129,926,240 | 129,926,339 |
15 | CDS | 129,929,336 | 129,929,608 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chrX | 129,040,140 | 129,063,728 | Link |
CDS sequence
ATGACTGCGAACCGGCTTGCAGAGAGCCTTCTGGCTTTGAGCCAACAGGAAGAACTAGCGGATTTGCCAAAAGACTACCTCTTGAGTGAGAGTGAAGATGAGGGGGACAATGATGGAGAGAGAAAGCATCAAAAGCTTCTGGAAGCAATCAGTTCCCTTGATGGAAAGAATAGGCGGAAATTGGCTGAGAGGTCTGAGGCTAGTCTGAAGGTGTCAGAGTTCAATGTCAGTTCTGAAGGATCAGGAGAAAAGCTGGTCCTTGCAGATCTGCTTGAGCCTGTTAAAACTTCATCTTCTTTGGCCACTGTGAAAAAGCAACTGAGTAGAGTCAAATCAAAGAAGACAGTGGAGTTACCTCTGAACAAAGAAGAGATTGAACGGATCCACAGAGAAGTAGCATTCAATAAAACCGCACAAGTCCTCTCCAAATGGGACCCTGTCGTCCTGAAGAACCGGCAGGCAGAGCAGCTGGTTTTTCCCCTGGAGAAAGAGGAGCCAGCCATTGCTCCCATTGAACATGTGCTCAGTGGCTGGAAGGCAAGAACTCCCCTGGAGCAGGAAATTTTCAACCTCCTCCATAAGAACAAGCAGCCAGTGACAGACCCTTTACTGACCCCTGTGGAAAAGGCCTCTCTCCGAGCCATGAGCCTAGAAGAGGCAAAGATGCGACGAGCAGAGCTTCAGAGGGCTCGGGCTCTGCAGTCCTACTATGAGGCCAAGGCTCGAAGAGAGAAGAAAATCAAAAGTAAAAAGTATCACAAAGTCGTGAAGAAAGGAAAGGCCAAGAAAGCCCTAAAAGAGTTTGAGCAGCTGCGGAAGGTTAATCCAGCTGCAGCACTAGAAGAACTGGAAAAAATTGAAAAGGCCAGAATGATGGAAAGAATGAGCCTTAAGCACCAAAACAGTGGGAAATGGGCCAAGTCAAAGGCAATTATGGCCAAATATGACCTGGAGGCTCGCCAAGCTATGCAGGAACAGTTGTCTAAGAACAAAGAACTGACACAGAAACTCCAGGTAGCCTCTGAGAGTGAGGAAGAGGAGGGAGGCACAGAAGATGTGGAAGAACTCCTTGTCCCTGATGTAGTGAATGAAGTGCAGATGAATGCAGATGGGCCGAATCCCTGGATGCTCAGGAGCTGCACCAGTGACACCAAAGAGGCTGCAACCCAGGAGGACCCTGAGCAACTGCCAGAGCTTGAGGCCCATGGAGTTTCTGAAAGTGAGGGAGAAGAAAGACCAGTGGCAGAAGAAGAAATTTTGTTGAGAGAATTTGAGGAAAGGCGATCCCTTAGAAAAAGATCTGAGCTCAGCCAAGATGCTGAGCCAGCAGGCAGTCAAGAAACAAAAGATTCTGGCAGCCAGGAGGTGCTGTCTGAATTGAGAGTACTATCTCAGAAATTGAAGGAAAACCATCAGTCCAGGAAGCAAAAAGCAAGTTCAGAGGGGACTATTCCCCAGGTCCAGAGAGAGGAACCTGCCCCAGAAGAAGAGGAGCCCCTGTTGCTACAGAGACCAGAGAGAGTACAGACGCTGGAAGAGCTAGAAGAGCTGGGAAAAGAAGAATGTTTTCAAAATAAGGAGCTTCCCAGACCTGTGTTAGAAGGGCAGCAGTCAGAGAGGACCCCAAATAATCGCCCTGATGCCCCTAAGGAGAAGAAAAAGAAGGAGCAAATGATCGACCTACAGAACCTCCTAACCACACAATCTCCCTCCGTGAAGTCTTTGGCAGTTCCCACAATAGAGGAGCTGGAAGATGAAGAGGAGAGAAACCATAGGCAGATGATAAAGGAAGCTTTTGCTGGGGATGATGTCATCAGAGATTTCTTGAAAGAGAAGAGGGAAGCTGTGGAGGCGAGTAAGCCAAAGGACGTGGACCTGACACTACCTGGCTGGGGCGAGTGGGGTGGTGTGGGCCTAAAGCCCAGTGCCAAGAAAAGACGCCGGTTTCTCATTAAAGCCCCTGAGGGTCCTCCAAGAAAAGATAAGAATTTGCCAAATGTGATTATCAATGAGAAGCGCAACATCCACGCAGCTGCTCATCAGGTACGAGTGCTTCCATATCCATTTACCCACCATTGGCAATTTGAAAGGACCATCCAGACCCCCATAGGATCCACATGGAACACCCAGAGGGCTTTCCAAAAGCTGACTACTCCCAAGGTCGTCACCAAGCCAGGCCATATCATTAACCCCATAAAAGCAGAAGACGTGGGCTACCGGTCTTCCTCAAGGTCGGACCTGTCTGTCATACAGAGGAATCCAAAACGAATCACCACACGTCACAAAAAACAGCTGAAGAAATGCTCTGTAGATTGA
Amino sequence
MTANRLAESLLALSQQEELADLPKDYLLSESEDEGDNDGERKHQKLLEAISSLDGKNRRKLAERSEASLKVSEFNVSSEGSGEKLVLADLLEPVKTSSSLATVKKQLSRVKSKKTVELPLNKEEIERIHREVAFNKTAQVLSKWDPVVLKNRQAEQLVFPLEKEEPAIAPIEHVLSGWKARTPLEQEIFNLLHKNKQPVTDPLLTPVEKASLRAMSLEEAKMRRAELQRARALQSYYEAKARREKKIKSKKYHKVVKKGKAKKALKEFEQLRKVNPAAALEELEKIEKARMMERMSLKHQNSGKWAKSKAIMAKYDLEARQAMQEQLSKNKELTQKLQVASESEEEEGGTEDVEELLVPDVVNEVQMNADGPNPWMLRSCTSDTKEAATQEDPEQLPELEAHGVSESEGEERPVAEEEILLREFEERRSLRKRSELSQDAEPAGSQETKDSGSQEVLSELRVLSQKLKENHQSRKQKASSEGTIPQVQREEPAPEEEEPLLLQRPERVQTLEELEELGKEECFQNKELPRPVLEGQQSERTPNNRPDAPKEKKKKEQMIDLQNLLTTQSPSVKSLAVPTIEELEDEEERNHRQMIKEAFAGDDVIRDFLKEKREAVEASKPKDVDLTLPGWGEWGGVGLKPSAKKRRRFLIKAPEGPPRKDKNLPNVIINEKRNIHAAAHQVRVLPYPFTHHWQFERTIQTPIGSTWNTQRAFQKLTTPKVVTKPGHIINPIKAEDVGYRSSSRSDLSVIQRNPKRITTRHKKQLKKCSVD*