ZMP
dcbld1
Ensembl ID:
ZFIN ID:
Description:
discoidin, CUB and LCCL domain containing 1 [Source:RefSeq peptide;Acc:NP_001035066]
Human Orthologue:
DCBLD1
Human Description:
discoidin, CUB and LCCL domain containing 1 [Source:HGNC Symbol;Acc:21479]
Mouse Orthologue:
Dcbld1
Mouse Description:
discoidin, CUB and LCCL domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1913936]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23788 | Nonsense | Available for shipment | Available now |
| sa9772 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23788
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015801 | Nonsense | 113 | 703 | 3 | 15 |
| ENSDART00000099305 | Nonsense | 113 | 263 | 3 | 6 |
| ENSDART00000138640 | None | None | 445 | None | 8 |
| ENSDART00000139912 | Nonsense | 113 | 289 | 3 | 5 |
| ENSDART00000143993 | Nonsense | 88 | 207 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 42391420)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 42462579 |
| GRCz11 | 20 | 42359689 |
KASP Assay ID:
2261-4816.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCCTAGTGTACTGGGAGTACTGTGGTGATCCAATGCCCAAGCCCTCA[C/T]AGCTTCACACAGACTCCAATGAGCTGACCATTCGCTTTCGCAGCAGCCAA
Long Flanking Sequence:
AATTTATGTCAAGTTTATTCAAGTTTTATAGTTGATGTTCATTGTTGACTTCCATTGTATTTTTCGTGCACAACTGAGCCTGGTTTCTCTTGAGTTTTTTCCCTTGTCAATTGGTGAAGTTTTTTTCTTTGTCACTGTCACCGCTGACTTGCTTGGTTTGGGACTTGTGGAGCTGCGCATTGATGGATTTGCTCTTCAGTGTTTGGATTTTCAGCAGTGAAAATTGAACCACACTGAACTGAACTAAACTGAACTTTAACTCCGAAAACTGGACTGAAGCACTCTCAATTTTCTAGAACTTCTGTGTTAAGCTGCTTTGATACAATCTACATTGTAAAAGCGCTATTATTCTTGGATCGTTTCATTTATTCACTGCTACTGTAATACCCTAATAATACCTCAATATGATTCTGATTAATCTTTTATTAATTGTCCTTCACTTGCTTTCATTTCTCCTAGTGTACTGGGAGTACTGTGGTGATCCAATGCCCAAGCCCTCA[C/T]AGCTTCACACAGACTCCAATGAGCTGACCATTCGCTTTCGCAGCAGCCAACACATCACTGGAAGAGGATTCCTGCTTTCCTACTCCACAGAAAACCACAAAGGTATCCATACTGTAAAAGTTTAAGTGTGTATCACCTTAACATTACGTTGTACATACATTTGTACATTACATACAGTTGAAGTCGGAATTATTAGCCCTCCTGAATTATCAGCCCCTTCTTGTCTCTTGGTTGACCCTCATGTAAACCTCTGCTCTGTGGCTTGTTCCCTTTTCGTTCTTGAGATGCTTTTGGATCCTTTTGGGATGTTTCTTTAAACGACATGTTTGAACTCAACAGAGCAATTGATAAAAATATAATTGATGTAGAAATGAAAAGGCTGTTGGGTTTTATTCACCCTTATGTTGTTCTAAAGCTGGATGACTTTCATTCTCCAATGAAATGCAAAAAAAAGAGGAATGTCAAGGTCTATCTGTGATCTTCTATCTTTATTTAGTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9772
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015801 | Nonsense | 613 | 703 | 15 | 15 |
| ENSDART00000099305 | None | None | 263 | None | 6 |
| ENSDART00000138640 | Nonsense | 355 | 445 | 8 | 8 |
| ENSDART00000139912 | None | None | 289 | None | 5 |
| ENSDART00000143993 | None | None | 207 | None | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 42331692)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 42402851 |
| GRCz11 | 20 | 42299961 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGTGCTAAACAAAARCCCATCGTTTCGGGCAGTCGAAGGCGGGAACTG[T/A]AGGAAAGTGATYGGAGGGCTGGCCGGGGGCTACCAAACACCTCAAGTAAA
Long Flanking Sequence:
AAATGTGTTGAAAAAATTCTAAATATTCAGGGGGGCTATTAATTCTGACTTCAACTGTATATTAATTTTATCCCCAAGAATGTACATAAATATTACAGATATAATTTTAAATAGTACATTAAAAAAAAACGAATCTCCCACTAATCCCAGAGTTCTCTTTAGAACAACAATTCTAATTCCAGTTATTTCCCTTCTCAATTTTCTTCAGCAGAGTACCAACAACCACTGATGCTCGGCACGGACACAGTGTCCCGAAAAGGCTCAACGTTCAGACCGATGGACACCGAAACTAAAGACATGGAAAGTTCTCACTATGACCACCTGCAGACAGGCATCCAGTACGCCTTGCCACTGACCAATCAGGAGCCTGAATATGCCACACCCATAATCGAGCGCCACGCCTTCCGCAAAGACCCCTTCATCCCTGACGCTAGCTATAGTGTGCCAGGAGTGGTGCTAAACAAAAGCCCATCGTTTCGGGCAGTCGAAGGCGGGAACTG[T/A]AGGAAAGTGATTGGAGGGCTGGCCGGGGGCTACCAAACACCTCAAGTAAAGCCGGATCGAGGGAATTCCCCAGAGGACATCTATGATAGCCCTAAAATCCGCAAAGCTGTTGTCCTGAATGGCCCTGAATATCAGAGACCCCAGATTAAATCTCAGGATCAGGAGTGTTACTCAACTCCCAGAGATTGTGTTAGATTGCCTTTCTCCGGATTGAGACCAGATCCCGAAGGAAGCCGGTCTGAGCCTGAAGGCAGCAGCTCTGATGGAAGCTGAGATGAGTTTTACTGCCTTTTAATGTACCTGACTCAACAAAATCACCTCTTCGTAACTTATTTGAGTATTAGCGACATGTTTTTTAGTAAGTTCGCAGGAAAGGACTGTGGAGGCCAAAATTGGTTTGTTGTAATTTAATGGTTTTTATATGAGATTTTCTTTTTTTTTTGTCTTGATGAATCAATATTTTTTAAATTGTGCTGTTTATTTTATTATTAATATGCAGT
Associated Phenotype:
Not determined