ZMP
dcdc2b
Ensembl ID:
ZFIN ID:
Description:
doublecortin domain-containing protein 2 [Source:RefSeq peptide;Acc:NP_001032778]
Human Orthologue:
DCDC2B
Human Description:
doublecortin domain containing 2B [Source:HGNC Symbol;Acc:32576]
Mouse Orthologue:
Dcdc2b
Mouse Description:
doublecortin domain containing 2b Gene [Source:MGI Symbol;Acc:MGI:2686212]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42243 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1463 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42243
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075826 | Essential Splice Site | 108 | 447 | 4 | 14 |
ENSDART00000145295 | Essential Splice Site | 108 | 153 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 33530907)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33176855 |
GRCz11 | 13 | 33307305 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTAGTTATCTGAGCGCAGGACTGAAGAAAGCTGTTGAACCAACCCAG[G/A]TATATCCGTGACAATTCAGTGCTCGTTACTTTTTTATTTGTGACTTTTTT
Long Flanking Sequence:
GTGATAAGTTGGCGGTTCATTCCGCAGTGTCGACCCTAGAATTATAAAGGGACTAAGCTGAAATAAAAATGAATGAATGAATAGCTGATATTGATATGACTGCCGATATATCGTGCATCCCTAACGGTGAGGTTACATATTTTGTTACCTTAACAAAACATCAAATCAAGTAGTAATACTATACAGTAAGGTTTCAATTGTTAACATTAGGAAATGCATCAGCTTGCATGAATGTAGATTTAAGTATAAATTATTCAAAGAGAACTGTATTATTTCATTACTGTAGTTATTTAAAGAAAACACCTAAACACTTAAATTCACAGAAAAAGATCTTAAAACTTACCTGATAATCAAATGGAAAAGCAGATCCCAAAGTGAAGCCCTTCATGTGATCTGTCATGCCATTGTGAGTGAGTGTCATTGATTTATTCATGTGTTTTTTTGTGTGTATGTTTAGTTATCTGAGCGCAGGACTGAAGAAAGCTGTTGAACCAACCCAG[G/A]TATATCCGTGACAATTCAGTGCTCGTTACTTTTTTATTTGTGACTTTTTTTTAATTCACAAAGCATACAGCTCTATGAATGTATATATTTTGTGTTTGTGTTTTGATGTTGCTGTGGATGCTTAGCTGAAGTGCCATAAAGAGGAGGAGAGGGGAGTTATTGTCCTTTCCAACAATAAAAGGCCAGGGGAGACGCACTTATTAGTGTTATCATGCCAGAAAGCTTGTTGGGGCATGTTTTAGTGCCTGACCCTTTAATGCTGCACACAGAGCTGCTAAAACCACTGTTGATAATAGCCCTGAGAGCAGGGGACACTGACTCAGCATCGACACACACACGCACTTCTTTCATTTACAATGACGGAAAATCACTGGCTTTGCATTATCCTGCTTATTACACAGCTAACGCATGAGTTAAGGGCCAAGACATTCTGATTTGCAGTCATTTTATAATAAAGGGGCTGCAAAGTTAAATGAGAGATGCATTCTGCTGTGTGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1463
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075826 | Essential Splice Site | 396 | 447 | 12 | 14 |
ENSDART00000145295 | None | None | 153 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 33536470)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33182418 |
GRCz11 | 13 | 33312868 |
KASP Assay ID:
554-1388.1 (used for ordering genotyping assays)
KASP Sequence:
AAACACCACAGGAACACACACCTCCGCATGAGACAAACAAATATGAGAGC[G/A]TAAGATTATGCACGTTGGACAACAGCTTTTATATTCTAATCTAATACAAT
Long Flanking Sequence:
TGGACCTGCATCTGTTTGACCCTTAATATTTTTGTAAGAATTATATAGAAACTCTTATTGAATTAATAATTATTACATTTGTTGGATGCTAATTAAACATTAAATGAATGATTAATTGAAATATATAAACTTTGTGCTTGCAGAATGATTGGTTGGTTTTACCTCCACGTTTGTTATAGTGAAATATATTGCTTTAATAAGGGAAAAAATGTATTAAAAGTGTCCTTCTGCAAATAAATGTATAATGCAGATCCACCATTTGATATAATAAGTGAAATAAATAACAATAAACATCATTGAATCATAGTGTTTTATTGAAAAGAGAAAGAAACACACTTTGTTTATTATGTCAGAGAGAAGCAGAAATTGTGGAGGATGAGGAGCTCCCTGAAAGAGAATTTGCTGCATCTGAGATACAGACATGGGATGACACGTCAGCTCCACAGAGAGAAACACCACAGGAACACACACCTCCGCATGAGACAAACAAATATGAGAGC[G/A]TAAGATTATGCACGTTGGACAACAGCTTTTATATTCTAATCTAATACAATAATAGCTCTGTTTTTAAGTATATTAGTAAAGTGTGGTCTGCCTTTTTTAAAACTTAAATCCAACAATTATTTGAAATATTTTTATTCTGTTTACAATCAGGAGTCACACCATTCCAGATCATCATCGTCATCATCTCTCCGTCTTTCCCCACGACATGAAGAAACACAGCAGGAGCCTGTCGGTTAATCAGTTTAATACTTTTTATTTAATGTTTTTAACCATGTATTCTGCAGCATTTACCATTTCAGTTATGTAACTACTGATGGTATATTCTCAGATAAAATGTTACCAATCTGTCACTGGGTGATACCCTTTTAGAAGGTACTAACGTGTTTCTTTAACCAAATGGTGCTGTCTTTATCATATAATTCCCTACAGAAATATTGTGTTTATAGGAAATTGTATGGCACTCAATCATTATTATGCAAGTTATAATCTACTAAATTCCT
Associated Phenotype:
Not determined