ZMP
dkk1b
Ensembl ID:
ZFIN ID:
Description:
dickkopf-related protein 1 [Source:RefSeq peptide;Acc:NP_571078]
Human Orthologue:
DKK1
Human Description:
dickkopf homolog 1 (Xenopus laevis) [Source:HGNC Symbol;Acc:2891]
Mouse Orthologue:
Dkk1
Mouse Description:
dickkopf homolog 1 (Xenopus laevis) Gene [Source:MGI Symbol;Acc:MGI:1329040]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27882 | Essential Splice Site, Splice Site | Mutation detected in F1 DNA | Not yet available |
sa27883 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16096 | Nonsense | Available for shipment | Available now |
sa19025 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9337 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27882
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:
A > G
Consequence:
Essential Splice Site, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066477 | Essential Splice Site | 65 | 241 | 2 | 4 |
ENSDART00000122271 | Splice Site | None | 240 | None | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 7149648)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 6432379 |
GRCz11 | 12 | 6465882 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTCAGACAGCTGGTGGTTTTTAGACTAATAGTGTATTTCCAAACCTCC[A/G]GCAGCCTTTAATCTGTGAGAGTGATGAGGAATGCGGTGGAGAGGAGTTTT
Long Flanking Sequence:
CACTATTACTGTGGTGTCTGTTTGATGCCAGCTCATAAAGACGTGCATTCACTGATAGACAGACAGCTCATGACACAACGCTTTGAAATTTCATCCAGCCCTTTGTTGCTCACAGCAAGGGGCGGGAGCGCAAACAACCCCGCGCGCGTATAAATGAAGCGGCTTGCGCTCATGAGGAACCACAGAAGAGCTCCGCTCACCCAGGGAATACATCCTACAATTCAAGGAATAACATGATGCACATCGCCATGCTCTCTACTGCATGCCTCATTTTTATGGGCTGCATCAAAGTGGCCGGTTCTACGATGCTCAACTCCAACGCTATTAAAGTCGGTTCAGGTGCGGCGGGTGCCAGTCATCCGGTTAGCCCGAGTCCGGACGTGTCACTTTTGGACAGTCTGAACTTCGCCCTCGATACACCGCAGGTAAGCATAGAAATATGCATATGCTATGTCAGACAGCTGGTGGTTTTTAGACTAATAGTGTATTTCCAAACCTCC[A/G]GCAGCCTTTAATCTGTGAGAGTGATGAGGAATGCGGTGGAGAGGAGTTTTGCTTCCAGTCTCGCGGTGTCTGTCTCCAGTGCAAGAAGCGCAGGAAGCGCTGCATCCGGGATGCGATGTGCTGCCCTGGCAACCACTGCAGCAATGGTAAGATCAGACTCGTGTAACGCGGAGAATGCACATATTTTTTATTTACTATCATGTAGTTTGAGGTTTATAGCGTTGGATAATATTGACGAAACCTTTCGTTATAGGTGTTTGCATTCCAAATGACCCTGACATGATTCAGCAGCTTGGCATGGAAGAGTTCGTGTCCATCGCCCATGAAAACTCTACTGCTCTAATGCCGAAAGTTTCGACTCAAGGATCACCACAAAACCAGATGCTGAAAGGTATGCAATGTTATGTTTATATGTTTGCATTTGACCTAATAATGTATGTGTGGATTAGATTCGAATATGTTTCCGCTCTGTAATAGCAACTTTGCAGATTTTTATTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27883
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066477 | Nonsense | 145 | 241 | 3 | 4 |
ENSDART00000122271 | Nonsense | 144 | 240 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 7149997)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 6432728 |
GRCz11 | 12 | 6466231 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAAGAGTTCGTGTCCATCGCCCATGAAAACTCTACTGCTCTAATGCCG[A/T]AAGTTTCGACTCAAGGATCACCACAAAACCAGATGCTGAAAGGTATGCAA
Long Flanking Sequence:
TGCCAGTCATCCGGTTAGCCCGAGTCCGGACGTGTCACTTTTGGACAGTCTGAACTTCGCCCTCGATACACCGCAGGTAAGCATAGAAATATGCATATGCTATGTCAGACAGCTGGTGGTTTTTAGACTAATAGTGTATTTCCAAACCTCCAGCAGCCTTTAATCTGTGAGAGTGATGAGGAATGCGGTGGAGAGGAGTTTTGCTTCCAGTCTCGCGGTGTCTGTCTCCAGTGCAAGAAGCGCAGGAAGCGCTGCATCCGGGATGCGATGTGCTGCCCTGGCAACCACTGCAGCAATGGTAAGATCAGACTCGTGTAACGCGGAGAATGCACATATTTTTTATTTACTATCATGTAGTTTGAGGTTTATAGCGTTGGATAATATTGACGAAACCTTTCGTTATAGGTGTTTGCATTCCAAATGACCCTGACATGATTCAGCAGCTTGGCATGGAAGAGTTCGTGTCCATCGCCCATGAAAACTCTACTGCTCTAATGCCG[A/T]AAGTTTCGACTCAAGGATCACCACAAAACCAGATGCTGAAAGGTATGCAATGTTATGTTTATATGTTTGCATTTGACCTAATAATGTATGTGTGGATTAGATTCGAATATGTTTCCGCTCTGTAATAGCAACTTTGCAGATTTTTATTGCTTGTTTAAAATCAGAAAGTATGTATAGGTGTTTCGAAAAAGAATATTGAATATGGTCAAATTAGTCTTATAAGCATTCAAAAGGAGTGTTTACAAAAAAATGCATATCTTGTCATAATTGATTTATTCTCTCTTCATTTGTTCCAAATCTGTTTGAGTTATTATTGAACCCAAAGAAAGATATTTTGAAGAAGGATGAAAACTGGTAGCATCGACTTCCATAGTATTTGTCTTTCAGGCATTGGTTACCAGTTTTCAGCTTTCTTCAAAATATATTTTGTGTTCAACAGAAGAAAGAAATGCATACGGGTTTGAAACCATTCGTGAATAGCAAGTAAATTCCATTATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16096
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066477 | Nonsense | 202 | 241 | 4 | 4 |
ENSDART00000122271 | Nonsense | 201 | 240 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 7150953)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 6433684 |
GRCz11 | 12 | 6467187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGCAAGCCTGTCCTAAAAGAGGGCCAGGTCTGCACCAAGCACAAGAGG[A/T]AAGGCACTCATGGCTTGGAGATATTCCAGCGCTGCGACTGCGGGGAAGGC
Long Flanking Sequence:
CGGGTTTGAAACCATTCGTGAATAGCAAGTAAATTCCATTATTTTATAGTGAAGTCTTTCTTTAAGACCGCATTTTCAATGTAATGCAATGCCTTTTAAAGACCAGGTTAATATAACAATTCACTCCAAAATGTACATTCTGTCATTATTTATTAGATATTTTGAGAGAAATCATAAGACATTGACATTCATAGTACTTTTGTTCTACTTCGGAGGCGATTACCTAACAGTATACAACATTCTTCAAAGTATCTTCTTTTGCGTTCAACAAGTAAAAAAGGCATTTAGGGTGAATCCCCCCTTTAAAAGATCAACTTTATTTTAATGTGTGGTGTGTGCATGATATTAATGAATGTTGTTGTGTTTTTGAAGGTCTGGAGGGAGAGAACTGTCTGAGATCATCAGATTGTGCAGAGGGACTTTGCTGCGCTCGTCACTTTTGGTCCAAAATCTGCAAGCCTGTCCTAAAAGAGGGCCAGGTCTGCACCAAGCACAAGAGG[A/T]AAGGCACTCATGGCTTGGAGATATTCCAGCGCTGCGACTGCGGGGAAGGCCTGTCCTGCAGAACGCAGCGAGGAGACGGCGGCAAGGCTTCACGGAGTCTGCACACATGCCAGAGACACTAAATGAAAATTCAAGGAATTTTCTTTCACCAGCTCCCAGAGAAGCAGACTTGAGTCGAGGGAAGCAGGACTTGGAATGGGATACTCTGTTTTTCAACTGGTTTCCTTCATATTCTCGAGTCAACATTGAAGAGTAGATTTAATTGTTTCTCAACGGAACTTAAATAATTGCAGTAAATTACTGTATTATACTGTAAATAATATAAGGCAGTTGGCACTTAAATATTTTTGTCAACCCTGTTATGAAAGAAGGTGCATCAGTCTTTTCTAGTCTACCTTAAATGTATATACATTCATTCTACAGTCATATAGAGCTGATTTAAATGTCTATTTTATTCTAAATAAAGAGTGTACAGATGATATACAGCATACAATGTCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19025
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066477 | Nonsense | 222 | 241 | 4 | 4 |
ENSDART00000122271 | Nonsense | 221 | 240 | 4 | 4 |
ENSDART00000066477 | Nonsense | 222 | 241 | 4 | 4 |
ENSDART00000122271 | Nonsense | 221 | 240 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 7151013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 6433744 |
GRCz11 | 12 | 6467247 |
KASP Assay ID:
2260-4949.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGCTTGGAGATATTCCAGCGCTGCGACTGCGGGGAAGGCCTGTCCTGC[A/T]GAACGCAGCGAGGAGACGGCGGCAAGGCTTCACGGAGTCTGCACACATGC
Long Flanking Sequence:
TTTAAGACCGCATTTTCAATGTAATGCAATGCCTTTTAAAGACCAGGTTAATATAACAATTCACTCCAAAATGTACATTCTGTCATTATTTATTAGATATTTTGAGAGAAATCATAAGACATTGACATTCATAGTACTTTTGTTCTACTTCGGAGGCGATTACCTAACAGTATACAACATTCTTCAAAGTATCTTCTTTTGCGTTCAACAAGTAAAAAAGGCATTTAGGGTGAATCCCCCCTTTAAAAGATCAACTTTATTTTAATGTGTGGTGTGTGCATGATATTAATGAATGTTGTTGTGTTTTTGAAGGTCTGGAGGGAGAGAACTGTCTGAGATCATCAGATTGTGCAGAGGGACTTTGCTGCGCTCGTCACTTTTGGTCCAAAATCTGCAAGCCTGTCCTAAAAGAGGGCCAGGTCTGCACCAAGCACAAGAGGAAAGGCACTCATGGCTTGGAGATATTCCAGCGCTGCGACTGCGGGGAAGGCCTGTCCTGC[A/T]GAACGCAGCGAGGAGACGGCGGCAAGGCTTCACGGAGTCTGCACACATGCCAGAGACACTAAATGAAAATTCAAGGAATTTTCTTTCACCAGCTCCCAGAGAAGCAGACTTGAGTCGAGGGAAGCAGGACTTGGAATGGGATACTCTGTTTTTCAACTGGTTTCCTTCATATTCTCGAGTCAACATTGAAGAGTAGATTTAATTGTTTCTCAACGGAACTTAAATAATTGCAGTAAATTACTGTATTATACTGTAAATAATATAAGGCAGTTGGCACTTAAATATTTTTGTCAACCCTGTTATGAAAGAAGGTGCATCAGTCTTTTCTAGTCTACCTTAAATGTATATACATTCATTCTACAGTCATATAGAGCTGATTTAAATGTCTATTTTATTCTAAATAAAGAGTGTACAGATGATATACAGCATACAATGTCTGAAGTCATGCTTCAATTAAGAGTGTGTACATGTTTCGAATGGCCATTTTTGTTGGCGCATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9337
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066477 | Nonsense | 222 | 241 | 4 | 4 |
ENSDART00000122271 | Nonsense | 221 | 240 | 4 | 4 |
ENSDART00000066477 | Nonsense | 222 | 241 | 4 | 4 |
ENSDART00000122271 | Nonsense | 221 | 240 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 7151013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 6433744 |
GRCz11 | 12 | 6467247 |
KASP Assay ID:
2260-4949.1 (used for ordering genotyping assays)
KASP Sequence:
ATGGCTTGGAGATATTCCAGCGCTGCGACTGCGGGGAAGGCCTGTCCTGC[A/T]GAACGCAGCGAGGAGACGGCGGCAAGGCTTCACGGAGTCTGCACACRTGC
Long Flanking Sequence:
TTTAAGACCGCATTTTCAATGTAATGCAATGCCTTTTAAAGACCAGGTTAATATAACAATTCACTCCAAAATGTACATTCTGTCATTATTTATTAGATATTTTGAGAGAAATCATAAGACATTGACATTCATAGTACTTTTGTTCTACTTCGGAGGCGATTACCTAACAGTATACAACATTCTTCAAAGTATCTTCTTTTGCGTTCAACAAGTAAAAAAGGCATTTAGGGTGAATCCCCCCTTTAAAAGATCAACTTTATTTTAATGTGTGGTGTGTGCATGATATTAATGAATGTTGTTGTGTTTTTGAAGGTCTGGAGGGAGAGAACTGTCTGAGATCATCAGATTGTGCAGAGGGACTTTGCTGCGCTCGTCACTTTTGGTCCAAAATCTGCAAGCCTGTCCTAAAAGAGGGCCAGGTCTGCACCAAGCACAAGAGGAAAGGCACTCATGGCTTGGAGATATTCCAGCGCTGCGACTGCGGGGAAGGCCTGTCCTGC[A/T]GAACGCAGCGAGGAGACGGCGGCAAGGCTTCACGGAGTCTGCACACATGCCAGAGACACTAAATGAAAATTCAAGGAATTTTCTTTCACCAGCTCCCAGAGAAGCAGACTTGAGTCGAGGGAAGCAGGACTTGGAATGGGATACTCTGTTTTTCAACTGGTTTCCTTCATATTCTCGAGTCAACATTGAAGAGTAGATTTAATTGTTTCTCAACGGAACTTAAATAATTGCAGTAAATTACTGTATTATACTGTAAATAATATAAGGCAGTTGGCACTTAAATATTTTTGTCAACCCTGTTATGAAAGAAGGTGCATCAGTCTTTTCTAGTCTACCTTAAATGTATATACATTCATTCTACAGTCATATAGAGCTGATTTAAATGTCTATTTTATTCTAAATAAAGAGTGTACAGATGATATACAGCATACAATGTCTGAAGTCATGCTTCAATTAAGAGTGTGTACATGTTTCGAATGGCCATTTTTGTTGGCGCATGT
Associated Phenotype:
Not determined