ZMP
si:ch211-222n4.5
Ensembl ID:
ZFIN ID:
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37275 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25153 | Essential Splice Site, Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44964 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa708 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37275
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065699 | Nonsense | 132 | 290 | 3 | 6 |
ENSDART00000146743 | Nonsense | 132 | 265 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 21 (position 17786679)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 18934931 |
GRCz11 | 21 | 18971567 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACACGGCACATCATGTGGCAGGTAGTGCAGGCTGCCCACATGTGCTG[T/A]CAGCGAGGGGTCCTCCATCGGGACATTAAATTAGAAAACCTCCTGATAAA
Long Flanking Sequence:
CTGTTCAAGTCTGGTTATTGTGTCACATGACATTGAAAAAGTTGAATGACTGTGATGATTTGAGCTCAGAGCAAGAATTACTAATGTTTTTTTTTGTTGTTGATCAGGTGGCAATGAAGGTGGTTGTGAAGAGCAGTGACATGGATTACCTCAGCATTGTAAGCAGCTCTCTTGGTTTTTACTTCAAAATTTGTTAATTAGAGCCAAAAAGGATTTTAAACATCACTGACAACAAATGTCTTTCCTCTACAGCCTGGTCATCCTACACCCCTTCCGTTAGAGGTTGCTCTAACCATTCTTGCCAACAATGGTCCGACCGTTCCTCAGATAATCCGGATGCTGGAGTGGCAGGAGAGGTCTGACTCCTACATAATGATCTTGGAGCGTCCCTCACCCTGCGAAGACCTGTTTGATTTCCTGGAGCGGCACAGAGGAACCCTCAGTGAGAACATGACACGGCACATCATGTGGCAGGTAGTGCAGGCTGCCCACATGTGCTG[T/A]CAGCGAGGGGTCCTCCATCGGGACATTAAATTAGAAAACCTCCTGATAAACAAGGAAACTCTGGAAGTGAAGCTCATCGACTTTGGCTGCGGTGACCTTCTGAAGACCTCAGCATATACAACATTCTGTGGTATGTATTGTCCTTCAAGTCTGCAGTTTGAGATTTTAATTCTTCAACTCCATATTTTGAACAGCATCAGCTTTCTTACTGTCACTAATGAAGAAAATCTTCTTTTTTTTTTAGGGACAGAAGATTACTGTCCACCTGAATTTAGATCCAGTGGCAGGTACCATGGAAAGGCGGCAACCGTTTGGTCACTGGGGGTTCTCCTGTATGAGCTGCTGTGTGGAGAACCTCCAAAACACAGTGACCTGGACTTGACAGACGAAAGAACTTGGATCAAATCTGGATTGTCAACAGGTGAGCTGGCCATTTATTACAGCAGAGAAAGCCAACTGTAAATCTAAATGACACAGAGGAATAATTCAGTGATGTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25153
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:
T > C
Consequence:
Essential Splice Site, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065699 | Essential Splice Site | 176 | 290 | 4 | 6 |
ENSDART00000146743 | Splice Site | None | 265 | None | 5 |
Genomic Location (Zv9):
Chromosome 21 (position 17786438)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 18934690 |
GRCz11 | 21 | 18971326 |
KASP Assay ID:
554-7609.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGCATCAGCTTTCTTACTGTCACTAATGAAGAAAATCTTCTTTTTTTT[T/C]TAGGGACAGAAGATTACTGTCCACCTGAATTTAGATCCAGTGGCAGGTAC
Long Flanking Sequence:
TTCCTCTACAGCCTGGTCATCCTACACCCCTTCCGTTAGAGGTTGCTCTAACCATTCTTGCCAACAATGGTCCGACCGTTCCTCAGATAATCCGGATGCTGGAGTGGCAGGAGAGGTCTGACTCCTACATAATGATCTTGGAGCGTCCCTCACCCTGCGAAGACCTGTTTGATTTCCTGGAGCGGCACAGAGGAACCCTCAGTGAGAACATGACACGGCACATCATGTGGCAGGTAGTGCAGGCTGCCCACATGTGCTGTCAGCGAGGGGTCCTCCATCGGGACATTAAATTAGAAAACCTCCTGATAAACAAGGAAACTCTGGAAGTGAAGCTCATCGACTTTGGCTGCGGTGACCTTCTGAAGACCTCAGCATATACAACATTCTGTGGTATGTATTGTCCTTCAAGTCTGCAGTTTGAGATTTTAATTCTTCAACTCCATATTTTGAACAGCATCAGCTTTCTTACTGTCACTAATGAAGAAAATCTTCTTTTTTTT[T/C]TAGGGACAGAAGATTACTGTCCACCTGAATTTAGATCCAGTGGCAGGTACCATGGAAAGGCGGCAACCGTTTGGTCACTGGGGGTTCTCCTGTATGAGCTGCTGTGTGGAGAACCTCCAAAACACAGTGACCTGGACTTGACAGACGAAAGAACTTGGATCAAATCTGGATTGTCAACAGGTGAGCTGGCCATTTATTACAGCAGAGAAAGCCAACTGTAAATCTAAATGACACAGAGGAATAATTCAGTGATGTTCATCAGTTTTGGGCTTCATGTTTCAGCATCATCAAATCTTATTGTTAAGATTTTGATTATTAAAGCAAGTAGATGTAGTTTAGGTAATAATAATCAGACTCCTCCATCTTTTTCCACAGAGTGCTGCCAACTGGTCCAGTCCTGCCTGCAGAGGAGCCCCAGGAAGAGGATCGCTTTGGGGAAACTCAGCAGCCATCGCTGGTTCAAGGTATTCAATTCTACATTTTCTTCCTTGAACATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44964
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065699 | Nonsense | 232 | 290 | 4 | 6 |
ENSDART00000146743 | Nonsense | 231 | 265 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 21 (position 17786270)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 18934522 |
GRCz11 | 21 | 18971158 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAACACAGTGACCTGGACTTGACAGACGAAAGAACTTGGATCAAATCT[G/T]GATTGTCAACAGGTGAGCTGGCCATTTATTACAGCAGAGAAAGCCAACTG
Long Flanking Sequence:
TTGATTTCCTGGAGCGGCACAGAGGAACCCTCAGTGAGAACATGACACGGCACATCATGTGGCAGGTAGTGCAGGCTGCCCACATGTGCTGTCAGCGAGGGGTCCTCCATCGGGACATTAAATTAGAAAACCTCCTGATAAACAAGGAAACTCTGGAAGTGAAGCTCATCGACTTTGGCTGCGGTGACCTTCTGAAGACCTCAGCATATACAACATTCTGTGGTATGTATTGTCCTTCAAGTCTGCAGTTTGAGATTTTAATTCTTCAACTCCATATTTTGAACAGCATCAGCTTTCTTACTGTCACTAATGAAGAAAATCTTCTTTTTTTTTTAGGGACAGAAGATTACTGTCCACCTGAATTTAGATCCAGTGGCAGGTACCATGGAAAGGCGGCAACCGTTTGGTCACTGGGGGTTCTCCTGTATGAGCTGCTGTGTGGAGAACCTCCAAAACACAGTGACCTGGACTTGACAGACGAAAGAACTTGGATCAAATCT[G/T]GATTGTCAACAGGTGAGCTGGCCATTTATTACAGCAGAGAAAGCCAACTGTAAATCTAAATGACACAGAGGAATAATTCAGTGATGTTCATCAGTTTTGGGCTTCATGTTTCAGCATCATCAAATCTTATTGTTAAGATTTTGATTATTAAAGCAAGTAGATGTAGTTTAGGTAATAATAATCAGACTCCTCCATCTTTTTCCACAGAGTGCTGCCAACTGGTCCAGTCCTGCCTGCAGAGGAGCCCCAGGAAGAGGATCGCTTTGGGGAAACTCAGCAGCCATCGCTGGTTCAAGGTATTCAATTCTACATTTTCTTCCTTGAACATTTTTATACAGGAGGTGTGTACTAGTGTAACATGGAGACCAACATATGTGTGTGTTGCTTGTTTCAGGTCACCAGATAAAGAACAACAAGAAGTTCCAGAGCCCTCCATCAAGACGATTATATCATCTGATCTTCTACATCTTCTTGTCATGAGACTCAAATAAATTATTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa708
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 |
---|---|---|---|---|---|
ENSDART00000065699 | Nonsense | 277 | 290 | 6 | 6 |
ENSDART00000146743 | None | None | 265 | None | 5 |
Genomic Location (Zv9):
Chromosome 21 (position 17785657)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 18933909 |
GRCz11 | 21 | 18970545 |
KASP Assay ID:
554-0616.1 (used for ordering genotyping assays)
KASP Sequence:
AGCAAACCAGAGCTGATTCTCAACACTTACCCAGTGCCAGTGCTGTGTGC[C/T]AACACTGTCCTCATCTGTCAACACTTACAGATCCTGACAAAGCTGTAGCT
Long Flanking Sequence:
AGCATCATCAAATCTTATTGTTAAGATTTTGATTATTAAAGCAAGTAGATGTAGTTTAGGTAATAATAATCAGACTCCTCCATCTTTTTCCACAGAGTGCTGCCAACTGGTCCAGTCCTGCCTGCAGAGGAGCCCCAGGAAGAGGATCGCTTTGGGGAAACTCAGCAGCCATCGCTGGTTCAAGGTATTCAATTCTACATTTTCTTCCTTGAACATTTTTATACAGGAGGTGTGTACTAGTGTAACATGGAGACCAACATATGTGTGTGTTGCTTGTTTCAGGTCACCAGATAAAGAACAACAAGAAGTTCCAGAGCCCTCCATCAAGACGATTATATCATCTGATCTTCTACATCTTCTTGTCATGAGACTCAAATAAATTATTGCTTTATAAACACCGTTGTGCCTGAACTTCCTGTGATGGATTGAGGAGAAAATGTGCCTGCAAGAAGCAAACCAGAGCTGATTCTCAACACTTACCCAGTGCCAGTGCTGTGTGC[C/T]AACACTGTCCTCATCTGTCAACACTTACAGATCCTGACAAAGCTGTAGCTGTCTTAACTTTAGCTTTAATCTCTCCATCCCGAACATGCTTTATAGAGGGACCCTCAAGAGCACAGGTGTCAAATCCAGTTTGTGTAGGGCCGCAGCTCTGCTCAGTTTAGTTCCAACCCTGCTTCAACACACTTACCTGTGGGTTTCTCACAAGCCCGAGGGACTCAATGAGTTTGATCAGGTGAGTTTAATCAGGGTTAAAGCTAAACTGTGCAGAGCTGCGGCCCTCAAGGAACTGGATTTGACACCTGTGCTCAAGAGCATCCCGAGCAGCTGCATCAACTGAACTACCTCCAAACACATGCACTTATTCAGAGGAACTGTGTTTACTGATAAATGTAATGTTTCTGCTTCTGTTTCTGCTTCTGAATTGTTTAATGCACTTTAATGTCTGTCTTGCACTGTTTGCACCAGGTTGCACTTTACATCGTCAGGTAGTTTACTCTTTA
Associated Phenotype:
Data not yet available