ENST00000309931.3 DAW1
Information
- Transcript ID
- ENST00000309931.3
- Genome
- hg19
- Position
- chr2:228,736,347-228,789,060
- Strand
- +
- CDS length
- 1,248
- Amino acid length
- 416
- Gene symbol
- DAW1
- Gene type
- protein-coding
- Gene description
- dynein assembly factor with WD repeats 1
- Gene Entrez Gene ID
- 164781
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 | 228,736,347 | 228,736,445 |
2 | 228,750,067 | 228,750,139 |
3 | 228,754,572 | 228,754,716 |
4 | 228,755,971 | 228,756,029 |
5 | 228,758,511 | 228,758,633 |
6 | 228,762,898 | 228,762,997 |
7 | 228,767,718 | 228,767,825 |
8 | 228,769,645 | 228,769,751 |
9 | 228,770,952 | 228,771,054 |
10 | 228,771,854 | 228,771,968 |
11 | 228,783,496 | 228,783,572 |
12 | 228,786,115 | 228,786,277 |
13 | 228,788,650 | 228,789,060 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
1 | CDS | 228,736,406 | 228,736,445 |
2 | CDS | 228,750,067 | 228,750,139 |
3 | CDS | 228,754,572 | 228,754,716 |
4 | CDS | 228,755,971 | 228,756,029 |
5 | CDS | 228,758,511 | 228,758,633 |
6 | CDS | 228,762,898 | 228,762,997 |
7 | CDS | 228,767,718 | 228,767,825 |
8 | CDS | 228,769,645 | 228,769,751 |
9 | CDS | 228,770,952 | 228,771,054 |
10 | CDS | 228,771,854 | 228,771,968 |
11 | CDS | 228,783,496 | 228,783,572 |
12 | CDS | 228,786,115 | 228,786,277 |
13 | CDS | 228,788,650 | 228,788,684 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr2 | 227,871,631 | 227,924,344 | Link |
CDS sequence
ATGAAGCTCAAGAGCCTCCTGCTCCGGTATTACCCGCCAGGAATTATGTTGGAATATGAAAAACATGGAGAATTAAAGACTAAGTCCATAGATTTGCTTGATCTTGGTCCCAGCACTGATGTCAGTGCGTTAGTAGAAGAAATCCAGAAGGCAGAACCTCTACTCACAGCTTCACGAACAGAGCAAGTCAAACTTTTGATACAGAGGTTGCAAGAGAAACTCGGCCAGAACAGCAATCACACGTTCTATCTTTTTAAGGTTCTCAAAGCACATATATTGCCACTGACTAATGTTGCACTTAACAAATCGGGCTCATGCTTTATCACAGGAAGCTATGATCGGACGTGCAAGCTCTGGGACACTGCGTCTGGAGAGGAGCTGAACACGCTGGAGGGCCACAGGAATGTGGTTTATGCCATAGCATTCAACAATCCTTACGGTGACAAAATCGCCACTGGGTCCTTTGATAAAACTTGTAAACTCTGGAGTGTGGAAACAGGAAAATGTTACCATACCTTCAGGGGTCATACAGCAGAAATAGTGTGTTTATCATTTAACCCTCAAAGCACATTGGTGGCGACTGGAAGTATGGACACAACAGCCAAATTGTGGGACATTCAGAATGGCGAGGAAGTTTACACCTTAAGAGGACATTCTGCCGAAATCATCTCCTTGTCATTTAACACCTCAGGAGACAGAATCATCACGGGGTCTTTTGATCATACCGTTGTAGTGTGGGACGCTGATACTGGAAGGAAGGTAAATATCTTAATTGGTCATTGTGCTGAGATTAGCAGTGCCTCATTCAATTGGGATTGCTCTCTAATATTAACTGGCTCTATGGACAAAACCTGCAAGCTGTGGGATGCTACAAATGGAAAATGTGTGGCAACCTTAACAGGCCATGATGATGAAATACTAGACAGCTGCTTTGATTACACTGGAAAGCTTATTGCAACTGCTTCAGCTGATGGAACAGCAAGAATTTTCAGTGCTGCCACAAGAAAATGCATTGCCAAACTGGAAGGTCATGAAGGTGAAATTTCAAAGATTTCTTTCAACCCTCAAGGGAACCATCTTCTAACTGGCAGCTCTGACAAAACGGCTAGAATCTGGGATGCTCAGACTGGCCAGTGCCTCCAGGTTCTTGAGGGGCACACTGATGAAATCTTTTCATGTGCTTTCAACTATAAAGGCAACATAGTCATTACAGGCAGCAAGGATAATACCTGTAGGATATGGCGTTGA
Amino sequence
MKLKSLLLRYYPPGIMLEYEKHGELKTKSIDLLDLGPSTDVSALVEEIQKAEPLLTASRTEQVKLLIQRLQEKLGQNSNHTFYLFKVLKAHILPLTNVALNKSGSCFITGSYDRTCKLWDTASGEELNTLEGHRNVVYAIAFNNPYGDKIATGSFDKTCKLWSVETGKCYHTFRGHTAEIVCLSFNPQSTLVATGSMDTTAKLWDIQNGEEVYTLRGHSAEIISLSFNTSGDRIITGSFDHTVVVWDADTGRKVNILIGHCAEISSASFNWDCSLILTGSMDKTCKLWDATNGKCVATLTGHDDEILDSCFDYTGKLIATASADGTARIFSAATRKCIAKLEGHEGEISKISFNPQGNHLLTGSSDKTARIWDAQTGQCLQVLEGHTDEIFSCAFNYKGNIVITGSKDNTCRIWR*