ENST00000326974.9 KLHDC3
Information
- Transcript ID
- ENST00000326974.9
- Genome
- hg19
- Position
- chr6:42,981,987-42,989,032
- Strand
- +
- CDS length
- 1,149
- Amino acid length
- 383
- Gene symbol
- KLHDC3
- Gene type
- protein-coding
- Gene description
- kelch domain containing 3
- Gene Entrez Gene ID
- 116138
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| 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 | 42,981,987 | 42,982,086 |
| 2 | 42,984,872 | 42,985,084 |
| 3 | 42,985,257 | 42,985,433 |
| 4 | 42,985,591 | 42,985,706 |
| 5 | 42,985,883 | 42,985,954 |
| 6 | 42,986,081 | 42,986,294 |
| 7 | 42,986,371 | 42,986,457 |
| 8 | 42,986,601 | 42,986,709 |
| 9 | 42,986,830 | 42,986,903 |
| 10 | 42,987,026 | 42,987,104 |
| 11 | 42,988,405 | 42,989,032 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 2 | CDS | 42,984,931 | 42,985,084 |
| 3 | CDS | 42,985,257 | 42,985,433 |
| 4 | CDS | 42,985,591 | 42,985,706 |
| 5 | CDS | 42,985,883 | 42,985,954 |
| 6 | CDS | 42,986,081 | 42,986,294 |
| 7 | CDS | 42,986,371 | 42,986,457 |
| 8 | CDS | 42,986,601 | 42,986,709 |
| 9 | CDS | 42,986,830 | 42,986,903 |
| 10 | CDS | 42,987,026 | 42,987,104 |
| 11 | CDS | 42,988,405 | 42,988,471 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr6 | 43,014,249 | 43,021,294 | Link |
CDS sequence
ATGTTACGGTGGACAGTGCACCTGGAGGGCGGGCCCCGCAGGGTGAACCATGCTGCAGTGGCTGTCGGGCATCGGGTATACTCCTTCGGGGGTTACTGCTCTGGTGAAGACTATGAGACACTGCGTCAGATAGATGTGCACATTTTCAATGCAGTGTCCTTGCGTTGGACAAAGCTGCCCCCGGTGAAGTCTGCCATCCGTGGGCAAGCTCCTGTGGTACCCTACATGCGCTATGGACACTCAACCGTCCTCATCGACGACACAGTCCTCCTTTGGGGCGGGCGGAATGACACCGAAGGGGCCTGCAATGTGCTCTATGCCTTTGACGTCAATACGCACAAGTGGTTCACACCCCGAGTGTCAGGGACAGTTCCTGGGGCCCGGGATGGACATTCAGCCTGTGTCCTAGGCAAGATCATGTACATTTTTGGGGGCTACGAGCAGCAGGCGGACTGTTTTTCCAATGACATTCACAAGCTAGATACCAGCACCATGACATGGACTCTTATCTGTACAAAGGGCAGCCCTGCACGCTGGAGGGACTTCCACTCAGCCACAATGCTGGGAAGTCACATGTATGTCTTTGGGGGCCGTGCCGACCGCTTTGGGCCATTCCATTCCAACAATGAGATTTACTGCAACCGCATTCGAGTCTTTGACACCAGAACTGAGGCTTGGCTGGACTGTCCCCCGACTCCAGTGCTGCCTGAGGGGCGCCGGAGCCACTCGGCCTTTGGCTACAATGGGGAGCTGTACATCTTTGGTGGTTATAATGCAAGGCTGAACCGGCACTTCCATGACCTCTGGAAGTTTAATCCTGTGTCCTTTACCTGGAAAAAGATTGAACCGAAGGGGAAGGGGCCATGTCCCCGCCGGCGCCAGTGCTGCTGTATTGTTGGTGACAAGATTGTCCTCTTTGGGGGTACCAGTCCATCTCCTGAGGAAGGCCTGGGAGATGAATTTGACCTTATAGATCATTCTGACTTACACATTTTGGACTTTAGCCCTAGTCTGAAGACTCTGTGCAAACTGGCCGTGATTCAGTATAACCTAGACCAGTCCTGTTTGCCTCATGATATCAGGTGGGAGCTGAATGCCATGACCACCAACAGCAATATCAGTCGCCCCATCGTCTCCTCCCATGGGTAG
Amino sequence
MLRWTVHLEGGPRRVNHAAVAVGHRVYSFGGYCSGEDYETLRQIDVHIFNAVSLRWTKLPPVKSAIRGQAPVVPYMRYGHSTVLIDDTVLLWGGRNDTEGACNVLYAFDVNTHKWFTPRVSGTVPGARDGHSACVLGKIMYIFGGYEQQADCFSNDIHKLDTSTMTWTLICTKGSPARWRDFHSATMLGSHMYVFGGRADRFGPFHSNNEIYCNRIRVFDTRTEAWLDCPPTPVLPEGRRSHSAFGYNGELYIFGGYNARLNRHFHDLWKFNPVSFTWKKIEPKGKGPCPRRRQCCCIVGDKIVLFGGTSPSPEEGLGDEFDLIDHSDLHILDFSPSLKTLCKLAVIQYNLDQSCLPHDIRWELNAMTTNSNISRPIVSSHG*