ENST00000265983.8 HPX
Information
- Transcript ID
- ENST00000265983.8
- Genome
- hg19
- Position
- chr11:6,452,279-6,462,217
- Strand
- -
- CDS length
- 1,389
- Amino acid length
- 463
- Gene symbol
- HPX
- Gene type
- protein-coding
- Gene description
- hemopexin
- Gene Entrez Gene ID
- 3263
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 |
---|---|---|
10 | 6,452,279 | 6,452,700 |
9 | 6,452,871 | 6,453,033 |
8 | 6,453,117 | 6,453,247 |
7 | 6,458,276 | 6,458,407 |
6 | 6,458,670 | 6,458,882 |
5 | 6,459,586 | 6,459,739 |
4 | 6,461,395 | 6,461,516 |
3 | 6,461,697 | 6,461,768 |
2 | 6,461,902 | 6,461,960 |
1 | 6,462,111 | 6,462,217 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
10 | CDS | 6,452,441 | 6,452,700 |
9 | CDS | 6,452,871 | 6,453,033 |
8 | CDS | 6,453,117 | 6,453,247 |
7 | CDS | 6,458,276 | 6,458,407 |
6 | CDS | 6,458,670 | 6,458,882 |
5 | CDS | 6,459,586 | 6,459,739 |
4 | CDS | 6,461,395 | 6,461,516 |
3 | CDS | 6,461,697 | 6,461,768 |
2 | CDS | 6,461,902 | 6,461,960 |
1 | CDS | 6,462,111 | 6,462,193 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr11 | 6,431,049 | 6,440,987 | Link |
CDS sequence
ATGGCTAGGGTACTGGGAGCACCCGTTGCACTGGGGTTGTGGAGCCTATGCTGGTCTCTGGCCATTGCCACCCCTCTTCCTCCGACTAGTGCCCATGGGAATGTTGCTGAAGGCGAGACCAAGCCAGACCCAGACGTGACTGAACGCTGCTCAGATGGCTGGAGCTTTGATGCTACCACCCTGGATGACAATGGAACCATGCTGTTTTTTAAAGGGGAGTTTGTGTGGAAGAGTCACAAATGGGACCGGGAGTTAATCTCAGAGAGATGGAAGAATTTCCCCAGCCCTGTGGATGCTGCATTCCGTCAAGGTCACAACAGTGTCTTTCTGATCAAGGGGGACAAAGTCTGGGTATACCCTCCTGAAAAGAAGGAGAAAGGATACCCAAAGTTGCTCCAAGATGAATTTCCTGGAATCCCATCCCCACTGGATGCAGCTGTGGAATGTCACCGTGGAGAATGTCAAGCTGAAGGCGTCCTCTTCTTCCAAGGTGACCGCGAGTGGTTCTGGGACTTGGCTACGGGAACCATGAAGGAGCGTTCCTGGCCAGCTGTTGGGAACTGCTCCTCTGCCCTGAGATGGCTGGGCCGCTACTACTGCTTCCAGGGTAACCAATTCCTGCGCTTCGACCCTGTCAGGGGAGAGGTGCCTCCCAGGTACCCGCGGGATGTCCGAGACTACTTCATGCCCTGCCCTGGCAGAGGCCATGGACACAGGAATGGGACTGGCCATGGGAACAGTACCCACCATGGCCCTGAGTATATGCGCTGTAGCCCACATCTAGTCTTGTCTGCACTGACGTCTGACAACCATGGTGCCACCTATGCCTTCAGTGGGACCCACTACTGGCGTCTGGACACCAGCCGGGATGGCTGGCATAGCTGGCCCATTGCTCATCAGTGGCCCCAGGGTCCTTCAGCAGTGGATGCTGCCTTTTCCTGGGAAGAAAAACTCTATCTGGTCCAGGGCACCCAGGTATATGTCTTCCTGACAAAGGGAGGCTATACCCTAGTAAGCGGTTATCCGAAGCGGCTGGAGAAGGAAGTCGGGACCCCTCATGGGATTATCCTGGACTCTGTGGATGCGGCCTTTATCTGCCCTGGGTCTTCTCGGCTCCATATCATGGCAGGACGGCGGCTGTGGTGGCTGGACCTGAAGTCAGGAGCCCAAGCCACGTGGACAGAGCTTCCTTGGCCCCATGAGAAGGTAGACGGAGCCTTGTGTATGGAAAAGTCCCTTGGCCCTAACTCATGTTCCGCCAATGGTCCCGGCTTGTACCTCATCCATGGTCCCAATTTGTACTGCTACAGTGATGTGGAGAAACTGAATGCAGCCAAGGCCCTTCCGCAACCCCAGAATGTGACCAGTCTCCTGGGCTGCACTCACTGA
Amino sequence
MARVLGAPVALGLWSLCWSLAIATPLPPTSAHGNVAEGETKPDPDVTERCSDGWSFDATTLDDNGTMLFFKGEFVWKSHKWDRELISERWKNFPSPVDAAFRQGHNSVFLIKGDKVWVYPPEKKEKGYPKLLQDEFPGIPSPLDAAVECHRGECQAEGVLFFQGDREWFWDLATGTMKERSWPAVGNCSSALRWLGRYYCFQGNQFLRFDPVRGEVPPRYPRDVRDYFMPCPGRGHGHRNGTGHGNSTHHGPEYMRCSPHLVLSALTSDNHGATYAFSGTHYWRLDTSRDGWHSWPIAHQWPQGPSAVDAAFSWEEKLYLVQGTQVYVFLTKGGYTLVSGYPKRLEKEVGTPHGIILDSVDAAFICPGSSRLHIMAGRRLWWLDLKSGAQATWTELPWPHEKVDGALCMEKSLGPNSCSANGPGLYLIHGPNLYCYSDVEKLNAAKALPQPQNVTSLLGCTH*