ZMP
dcbld2
Ensembl ID:
ZFIN ID:
Description:
discoidin, CUB and LCCL domain containing 2 [Source:RefSeq peptide;Acc:NP_001073640]
Human Orthologue:
DCBLD2
Human Description:
discoidin, CUB and LCCL domain containing 2 [Source:HGNC Symbol;Acc:24627]
Mouse Orthologue:
Dcbld2
Mouse Description:
discoidin, CUB and LCCL domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1920629]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21503 | Nonsense | Available for shipment | Available now |
| sa41444 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa8562 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21503
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 |
|---|---|---|---|---|---|
| ENSDART00000089582 | None | None | 235 | None | 9 |
| ENSDART00000113710 | Nonsense | 396 | 671 | 10 | 15 |
| ENSDART00000139863 | Nonsense | 396 | 661 | 10 | 15 |
| ENSDART00000140040 | None | None | 42 | None | 9 |
Genomic Location (Zv9):
Chromosome 9 (position 31055841)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 30211787 |
| GRCz11 | 9 | 30022533 |
KASP Assay ID:
2260-1955.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGGAGGTGCGAAACAACTTTATTCCTCCAATTGAGGCACGCTTTCTC[C/T]GAATATGTCCCTTACAGTGGCACCAGAGGATCGCCCTTAAAATGGAACTG
Long Flanking Sequence:
GCCTGTCAATCTCATGTTCCATCCTTCCCTCACTCATGAACTGTTTTATTTTATTTTATTTTATTTTATTTTAGCAGAAATTGAATTTGGCCAACACAAGCTTAGCTGAAAGCATATCCAGCTGAGTTTGTTTTGAAGCAGTGTGTTTTGTGTTTGTGTGGTGTGAATAAAGTGTTGGTATTGTCACTGCTGCAGAATGACATCACTTTCTTTGTATATTTGTAGGAAAAAAAGGGTTTTACATTCTTGAGGTTTTAGGAGGCTGAAATGAAAGTGCACTCTGTGGTCATTAATAATGAATGTCCATCGACTGTCAGCGGGCTTAACGAGAGATGCATTGATTAGGCGTAAATAAGACGAACCTTGAGCTGAGGCCAAATGTTCTTTGTTGCTAAAGCCTCGTTGTCCTTGTGTCTCTGAAACAGATTTTCCAAGGTAACACCCACTATCTGCAGGAGGTGCGAAACAACTTTATTCCTCCAATTGAGGCACGCTTTCTC[C/T]GAATATGTCCCTTACAGTGGCACCAGAGGATCGCCCTTAAAATGGAACTGCTGGGCTGCCAACCCCATGCAGGTGAGAAAACCGCTCACTTGTTCACTCATTCACTAATCCCTATATAGTGGATGGCAGCTTGAGTTGACTATATTAGGAAAGAGGGGATGAAAATGAGTGAGTGAATTTAGACGGTGGTTAAAATAGTGTGACCCAGAAAACAGTCTGTGCCGACTATTTGGTGATAAACATTACACGTTGTAATACAGTGGGCGGGGAAATTATTCAACACGTCAAGTTTTTTTTTTTTTCTTGGGAAAAATGTTCTAAAGGAGCTGTTGAGATGGAATTGAACCAGAATTTGGTAAAAACCCAAACAATACAAACATAAAAATAAAACAAAACAAAAAAGTGCAATGTTTTTGTGTAATAGCAATGGAATGATACTAGGAGAAAGTAATGAACTACTGAAATGTATTTAATACTTTTATATTAAATAAGAAATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41444
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089582 | None | None | 235 | None | 9 |
| ENSDART00000113710 | Nonsense | 452 | 671 | 11 | 15 |
| ENSDART00000139863 | Nonsense | 452 | 661 | 11 | 15 |
| ENSDART00000140040 | None | None | 42 | None | 9 |
Genomic Location (Zv9):
Chromosome 9 (position 31052656)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 30208602 |
| GRCz11 | 9 | 30019348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCACAACACCGCCAGCGCAGGACAGGACCACACACACACCCAACATC[C/T]GAAACTCCACCATGCCTCCACACTCCCATGACGGTAAGATATTCTGCATT
Long Flanking Sequence:
ATTTCACAGGAGGGCAAACAATATAATATTAACTAAATAGCAGAATATGCTGTAGTTATAATAGAAAGTATAAATCTATTAAAATAAAGAAACCCTTCATACTATATGAACATGAAATATTCTGAGATATGAACAACAAAATTAAATGAGCCAAAATTCATGTCAATCATGCTTCTTTTTCATTTTTTAATATTGCTTCTATAAGTCTGAAATTTGTGAAAATGTTGCTTTATTGAATGAAATTCATGTGAATTACTGTCAAAAAAGTAGTGAAAAAATTTAGGGTATAAAGTCACTCACTTTATAGTGGATAGAGAGTGGTTTCAGACACCACTTGAGAAATTGCTATCAGATTTGCTCAATTAGTCATGTTTGGAAGCTTGATTGGATCTTTGTCTTTGTCAGCGAGGCCCAGAATCTTCCACCCAGGCCCTGCACCTCCTCGCAGGAAGAGCACAACACCGCCAGCGCAGGACAGGACCACACACACACCCAACATC[C/T]GAAACTCCACCATGCCTCCACACTCCCATGACGGTAAGATATTCTGCATTCACTACAGCAACATTACATCACTACAAGCTCTGTTATAAGCCTGCCTCCGTCCTTCATACAGAGTCTGTTCTTATGTTTAAAAATGCAGGCCAGTGGAATAAATAAATAAAATCAACTAGAAGAAACATTTTCAAAGTTGAACTTCTTTCAATTTAAGTTGCCGGTTCTTTGGATGTTGTGTCGAGAGCCTTGCAACTTGTAATTTCTGAAAACAGCAGAAAATACAGTTGAAAACAGGGAATTTTCCAGATATCCTAGAATTTTGCCAAATGGGTTAATAATCAGAACTGACATTGTACACCAAATCTATCTATTATATGGATTAATGTCTGTGAATTTAAAAGCGTAAACCACTATATGGTCTTACTCATCTACACAAGTGGATTCACGACATCTTGTTGAAATAAAAATTCTGTTTAGTTTAAAGAAATTCTGATACACATGGCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8562
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089582 | None | None | 235 | None | 9 |
| ENSDART00000113710 | Essential Splice Site | 462 | 671 | 11 | 15 |
| ENSDART00000139863 | Essential Splice Site | 462 | 661 | 11 | 15 |
| ENSDART00000140040 | None | None | 42 | None | 9 |
Genomic Location (Zv9):
Chromosome 9 (position 31052622)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 30208568 |
| GRCz11 | 9 | 30019314 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACACACCCAACATCCGAAACTCCACCATGCCTCCACACTCCCATGACG[G/T]TAAGATATTCTGCATTCACTACAGCAACATTACATCACTACRAGCTCTGT
Long Flanking Sequence:
AAATAGCAGAATATGCTGTAGTTATAATAGAAAGTATAAATCTATTAAAATAAAGAAACCCTTCATACTATATGAACATGAAATATTCTGAGATATGAACAACAAAATTAAATGAGCCAAAATTCATGTCAATCATGCTTCTTTTTCATTTTTTAATATTGCTTCTATAAGTCTGAAATTTGTGAAAATGTTGCTTTATTGAATGAAATTCATGTGAATTACTGTCAAAAAAGTAGTGAAAAAATTTAGGGTATAAAGTCACTCACTTTATAGTGGATAGAGAGTGGTTTCAGACACCACTTGAGAAATTGCTATCAGATTTGCTCAATTAGTCATGTTTGGAAGCTTGATTGGATCTTTGTCTTTGTCAGCGAGGCCCAGAATCTTCCACCCAGGCCCTGCACCTCCTCGCAGGAAGAGCACAACACCGCCAGCGCAGGACAGGACCACACACACACCCAACATCCGAAACTCCACCATGCCTCCACACTCCCATGACG[G/T]TAAGATATTCTGCATTCACTACAGCAACATTACATCACTACAAGCTCTGTTATAAGCCTGCCTCCGTCCTTCATACAGAGTCTGTTCTTATGTTTAAAAATGCAGGCCAGTGGAATAAATAAATAAAATCAACTAGAAGAAACATTTTCAAAGTTGAACTTCTTTCAATTTAAGTTGCCGGTTCTTTGGATGTTGTGTCGAGAGCCTTGCAACTTGTAATTTCTGAAAACAGCAGAAAATACAGTTGAAAACAGGGAATTTTCCAGATATCCTAGAATTTTGCCAAATGGGTTAATAATCAGAACTGACATTGTACACCAAATCTATCTATTATATGGATTAATGTCTGTGAATTTAAAAGCGTAAACCACTATATGGTCTTACTCATCTACACAAGTGGATTCACGACATCTTGTTGAAATAAAAATTCTGTTTAGTTTAAAGAAATTCTGATACACATGGCAGCATGATGGCTCAGTGGTTAACACTGTTGCCTTACA
Associated Phenotype:
Not determined