ZMP
cmn
Ensembl ID:
ZFIN ID:
Description:
calymmin [Source:RefSeq peptide;Acc:NP_571089]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22049 | Essential Splice Site | Available for shipment | Available now |
sa22050 | Nonsense | Available for shipment | Available now |
sa12588 | Nonsense | Available for shipment | Available now |
sa22051 | Essential Splice Site | Available for shipment | Available now |
sa3334 | Essential Splice Site | F2 line generated | Not yet available |
sa41981 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2627 | Essential Splice Site | F2 line generated | Not yet available |
sa35227 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22049
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077840 | Essential Splice Site | 348 | 1207 | 21 | 54 |
ENSDART00000124453 | Essential Splice Site | 348 | 1249 | 21 | 56 |
ENSDART00000127870 | None | None | 136 | None | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 14239177)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13094830 |
GRCz11 | 12 | 13133133 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATAGCTAACTGAAGCACCTCTAAATGGATTTGGGATTGTTTGTTGTTC[A/G]GGAAATGGAGGATATCCTAATGGAGGCGCAACTAGTCAACATAATGGAGG
Long Flanking Sequence:
CTGAATCACCTCTGAACTGCTTTTTGTTCAGGATATGGAGGATATCCCAATGCAGGTGCAACTAACCAGCCAAATGGGGGTAATATGAACGTCACCAGCTCTTTCATATAGATTTAATTTTACAGTGTTACTATTATAGTGCAGATGATACTACATTAAAGAACTGGGTAAAGCATAACTGGTCTAAATGAGACTTTCTTGAAATTATTTTTGTCTTAATAGGGCCATTTCAAAATATGGGTTACCCCAATGGTGGAACCAAGGGCCCTAAACCAGGTAAACATTTTTGTTTGAGTGCAGTGTGTATGGCACCTATTTCTTTTTTTTATACATAAATGATATGAATATTATTTGTGATATCTGTTTCAAAGGATATGGTGCTAAAGCTGGACCCTCGGCTGGACATGTAGCCAAGCCTAATGGTACATAAAATTTAATTATTTATTGTAAAGATAGCTAACTGAAGCACCTCTAAATGGATTTGGGATTGTTTGTTGTTC[A/G]GGAAATGGAGGATATCCTAATGGAGGCGCAACTAGTCAACATAATGGAGGTAATGGGAATTTCACCATCTCTTTTTTTTAAATAGACTTTTACAGTGTAATTTTCACAGTGCAGATGAAACTAAATTAAGGAACTTGGGAAACTACAAACCCATTTCCAAAAAAGTTGGGACACTGTACAAATTGTGAATAAAAAAGTAATGCGCTAATTTACAAATCTCATACACTTATATTTTGTTTACAATAGAATATAGATAACCGAATCTAGATGCCGACAGCTAGCTCTCTGCAACAGTATGGTGACAGGGACTCTATACTGCTCAATGAGCACTGTCTTTCGGATGAGAAGTTAAACCGAGGTCCTGACTCTCTGTGGTCTTTAAAAATCCAAGAATGGCCTTCGCAAAAGAGTAGGGGGTTTAACCCTGGTATCCTGGCCATATTTGCCCACTGGCCTTTGTCCATCATGGCCTCCTAACCATCCCCATATCATAATTGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22050
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 |
---|---|---|---|---|---|
ENSDART00000077840 | Nonsense | 437 | 1207 | 26 | 54 |
ENSDART00000124453 | Nonsense | 437 | 1249 | 26 | 56 |
ENSDART00000127870 | None | None | 136 | None | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 14242095)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13097748 |
GRCz11 | 12 | 13136051 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGCATTTAAACTGATTTGGGATTTTTTTTGTTCAGGATATGGAGGATA[T/A]CCTAATGGAGGCGCAGCTAACCAGCCTAATGGGGGTAATATGAATGTCAC
Long Flanking Sequence:
GTCTGCTTTTGAAGGATATGGTGCTAAAGCCGGATCTTTAGCTGGACAAGTAGCCAAGCCTAATAGTAAATAGCATTAATTTGTTAATTTATTTATTTAAATAAATATATTTTGCAAAAGATGTATGGATGCAGTCCTCCAAGCTCATGCCAGTCATACCCAATATTAATTCTTTCTTCACTGCACCGTGACTTTATATTCTGTACTGTACATTATTTCTGTTAAGTGACTTGTATAAGTCAGACCTTACTGTCCTATTTAAACATTTAAAAATCAAATCATTATCAGATTTTATTTTGGTAAAAGAAGCGTAATTTAGAGGCCTTTGCATTTTATATAAGCCACTTCTGATATCAAATGATCAACTAGAAGTCAAGTTATTATTTCTTGTTCTTACAACTTGGATAGGTGTCAAGACTTTTGTCAGGTAGTGTAAATAGAAGGAACTGACATGCATTTAAACTGATTTGGGATTTTTTTTGTTCAGGATATGGAGGATA[T/A]CCTAATGGAGGCGCAGCTAACCAGCCTAATGGGGGTAATATGAATGTCACCAGTTATTTTATAGAGATTTAATTTTACAGTTTAACTATTACAGTGCAGATGACTCTCGGGGAAACTACATGAGAATTCAACTTTCTCGAAATTATACTTGTCTTATTAGGATCCACTCAAAATATGGGTTATTCCAATGGTGGAACCAAGGGACCTAAACAAGGTAATTTGTTTTTTTCTGCAGTGTGTATGTTGTGTATTTTAAGATTTATAATTTGAATCTTATTTGTGATCTCTGCTTCAAAGGATATGGTGCTAATGCTGGACCTTCAGCTGGACAAGTAGCCAAGCCTAATGGTAAACTGTATTAAATTAGTTAACTATTAATTGTTACAGTTCTAAACTGATCTGTGATTGGTTTTGTTCAGGATATGGAGGATATCCTAATGGTGGTGCAACTAACCAGCCTAATGGGGGTAATATGAATGTCACGAACACTTTTTACATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12588
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077840 | Nonsense | 572 | 1207 | 34 | 54 |
ENSDART00000124453 | Nonsense | 614 | 1249 | 36 | 56 |
ENSDART00000127870 | None | None | 136 | None | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 14245389)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13101042 |
GRCz11 | 12 | 13139345 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATGTAAACTTTTAACTGTCATATTAACTTTCTTGTGACCTACAGGTTA[C/A]GGTGTTCCTGGATATAYGTCAAAAGGACCTAAAGCAGCWAATTCAGGTAA
Long Flanking Sequence:
TACAGATGTTTTTACAGATTTTTGCCAAACTACATAGGCATCTTGGTTAAAACAAGGCTAAGTTTGGGCTGTTTGTAAAAATTTAATAGAACTTAAACGCATATTAAAATTAAATACACATATTAGAAAGACTTTGCATGTGTAGTTATTCATTCTAGTCTATTTGACTTGGGGATGACAGGCTGATGTTTGGCTATCCTTAGACATCTATTAGATTTTTACTGACTGTCCAAATTTAGTCTAGTTTTAGCCAAGATATCTATTTTTAATTGTCTCTACATAGTCTTTTAAATAGATAAAGTGCTTATTGGGAAGCCACTGTGTTGACTGCATATTATTTTAATTTCTTATTTATGCAAATTCTAATCCCATTCAGAATAATATAATAATAAAATTGTTTCATTTTATGAATCTACTTTTAGATCCGGTTTTACTCAAATAAGCATGATCTAATGTAAACTTTTAACTGTCATATTAACTTTCTTGTGACCTACAGGTTA[C/A]GGTGTTCCTGGATATACGTCAAAAGGACCTAAAGCAGCTAATTCAGGTAAAATTATAAGTGCATTTACTTCCTCCACATGACATGATTAGTGACATTTTGTAATCTGTCTTTGAGAAATGCATGTATTTCCCTGCGTTTACGTTTGTCATGTTGACTTCTCAGTTTTGTAATAAAATGGGTTTGTTTTCTAGGGTATATGCCTGTAATAACTGGAAATAAGGGTGCTTCAATTGGAAAGGGGCCAAAGGGGGAGATTTTAAGTGCTGAAGCACCAAGTCAAGCACCACTGTCCAACACAAAGGGTGTTCTACCAGTTGCTCAACAAGAACCAGTTACAGGATTACTTCCAAATCAGGGAACTAAAGGCCTTCCAGTTCTGCAACAAACAAAGGGACAAATTCTTCAAGCATCATTACCACAGAGTAAAACCCAAAACTCTATGGTACCTCAGTTTGCTTCAAACCCATTTATGCAGGGCCCTAGCTCTTACAAACCTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22051
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077840 | Essential Splice Site | 790 | 1207 | 35 | 54 |
ENSDART00000124453 | Essential Splice Site | 832 | 1249 | 37 | 56 |
ENSDART00000127870 | None | None | 136 | None | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 14246189)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13101842 |
GRCz11 | 12 | 13140145 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAACCCTGCTTTGCCTCAGTTGAAGAATCCAACCACAACAAATCCTGG[T/C]AAATCTCTAAAGTTTCAGATTAAAATGTTACATGATCTCCTCTAACTGTA
Long Flanking Sequence:
AAGGGTGTTCTACCAGTTGCTCAACAAGAACCAGTTACAGGATTACTTCCAAATCAGGGAACTAAAGGCCTTCCAGTTCTGCAACAAACAAAGGGACAAATTCTTCAAGCATCATTACCACAGAGTAAAACCCAAAACTCTATGGTACCTCAGTTTGCTTCAAACCCATTTATGCAGGGCCCTAGCTCTTACAAACCTAGTAAAATGTATAAACCACCAACATCTACAATTCCAATTGAAAAGCCAGAGATTCCAGTAATTCCTCAGTCAGTGCCTGCACCAGAATCTGCGTTCATTCCTCAAACATCACAGACAACTCCACTAGAGCAGGAGCAAGTCCTTTCATTGGAACAGAAAAGTCAAGTGACCGCACAACCAGTTACACAACAAGGCAGCATTTCTTCTCAGGCGGCTCAATCAACTCCAGTTTTGCAGCAAGCAGAAATACAGTCAAACCCTGCTTTGCCTCAGTTGAAGAATCCAACCACAACAAATCCTGG[T/C]AAATCTCTAAAGTTTCAGATTAAAATGTTACATGATCTCCTCTAACTGTATAGCAACTTGAAGTTGTTACAGCGTTTAACTTTCACTTTGTGCACAATCATTAAAAACAAAAAGGAAAAGTGAACCACCAGTAATGACTGCTTGTATGTGTCTGTAAATGCCCACTCAAATTATTCTAAAAACCTGGCCTTTTGTTTCACAACTATCATTTCAAAATTTGGAAGAGGTGGCTAATATCTGGATTTACTTATCTTTTGCTGTCAACTAGCATTAAACTCGGCTTCTTTTAACTGATCTCTTTTTGTGTTCCACAGAACTCACTGGTCTAGAACAACCTAATGGTCAGGTGCAGGGTGCTGTGCCGGCAAAGCCTGGTAAATCATAAATAGTACTCCAATTAGTTACATTAAAATACATCCCAGAGTAATTAGCAGTTCATCCATTTATCTGCTCTCTTGTAACTCTCTTGTTAATATTTTCTTAGACTGTGGACCTGAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3334
Status:
F2 line generated
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077840 | Essential Splice Site | 875 | 1207 | 41 | 54 |
ENSDART00000124453 | Essential Splice Site | 917 | 1249 | 43 | 56 |
ENSDART00000127870 | None | None | 136 | None | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 14248811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13104464 |
GRCz11 | 12 | 13142767 |
KASP Assay ID:
554-2450.1 (used for ordering genotyping assays)
KASP Sequence:
GTGACCAGGTTTTCTTTRAGACAACTAAATGTCTTTTCTGTTACTTTGAT[A/G]GCTGGACTACAAGGTGGACCACCAGCACGATTGGGAACAAAGGGAAAATC
Long Flanking Sequence:
TATAATTCCAGGGCCTTATTTTGCAATATGTTACCTACAAAAATAAGAATAACACTTTATATAAATAAATAAATAATATTTATTTATTTATTTTTTATATATAAAGGTTTACAAAATATTTGTCCATGTTTTTTCTGCTTGTGCCTCAGACTGTATATGTTGTAAACTGCTTTAAATAGTGTGTGTAGTTTTTTGTGTGCTGTAAGTTTTTCGATAACACTTTATTTTGATGGTCCATTTCAGTATTAGTAGACAATCTGCTTTATATCTGTTGATATTGCTCTATCAACAGACATTTAACTGAATATTAGAGACTTTGCAAGTACTGTACATGTCAACTTACACTAACCCTAACCCCAATTTAACAGTCTATTTATAATCTAATGATAATTAGTTGGCAAGTACATGCAATGTAACTTAAATTCAACAAATGGACCATCAAAATAAAGTGTGACCAGGTTTTCTTTAAGACAACTAAATGTCTTTTCTGTTACTTTGAT[A/G]GCTGGACTACAAGGTGGACCACCAGCACGATTGGGAACAAAGGGAAAATCTCAAACAAAATATGGTTAGTCTTAGGAGGAAAATGTAAAAATTTTAAAACTAATTATGTTGTTAACAATTGTTTGTCAACAATAACTTTTTTTATTTTTCTAATTTTGTCAGGAATTGGTGGACTTCCCTTTGGTGGTTCCCCCAGTGGATATCAGTCCAACCCCTACGGACAATATGGTATGTTATCAGTTTCTTACAATATTGCACTATGTAATGTAAGCATTGTCCCTGACAGTAGTTCTGACTGGATTAGTGGTGTGTTATTTTTCATAGGTAATGATGGTCAGCGATATGGAGCTAAACCCTACAATCCTAAAGCACCAGGAAAATACGGTGATGATTAGATGTTTTAATGTTCCTTTGCGCTTTTTAATAATTGTTCGAGTGCCTTCATAGAATATCAGGCAGTGTATAGCATTGCTTATGGTAAATGAAGTTAGCAGATTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41981
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 |
---|---|---|---|---|---|
ENSDART00000077840 | Nonsense | 886 | 1207 | 41 | 54 |
ENSDART00000124453 | Nonsense | 928 | 1249 | 43 | 56 |
ENSDART00000127870 | None | None | 136 | None | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 14248845)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13104498 |
GRCz11 | 12 | 13142801 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTGTTACTTTGATAGCTGGACTACAAGGTGGACCACCAGCACGATTG[G/T]GAACAAAGGGAAAATCTCAAACAAAATATGGTTAGTCTTAGGAGGAAAAT
Long Flanking Sequence:
CTACAAAAATAAGAATAACACTTTATATAAATAAATAAATAATATTTATTTATTTATTTTTTATATATAAAGGTTTACAAAATATTTGTCCATGTTTTTTCTGCTTGTGCCTCAGACTGTATATGTTGTAAACTGCTTTAAATAGTGTGTGTAGTTTTTTGTGTGCTGTAAGTTTTTCGATAACACTTTATTTTGATGGTCCATTTCAGTATTAGTAGACAATCTGCTTTATATCTGTTGATATTGCTCTATCAACAGACATTTAACTGAATATTAGAGACTTTGCAAGTACTGTACATGTCAACTTACACTAACCCTAACCCCAATTTAACAGTCTATTTATAATCTAATGATAATTAGTTGGCAAGTACATGCAATGTAACTTAAATTCAACAAATGGACCATCAAAATAAAGTGTGACCAGGTTTTCTTTAAGACAACTAAATGTCTTTTCTGTTACTTTGATAGCTGGACTACAAGGTGGACCACCAGCACGATTG[G/T]GAACAAAGGGAAAATCTCAAACAAAATATGGTTAGTCTTAGGAGGAAAATGTAAAAATTTTAAAACTAATTATGTTGTTAACAATTGTTTGTCAACAATAACTTTTTTTATTTTTCTAATTTTGTCAGGAATTGGTGGACTTCCCTTTGGTGGTTCCCCCAGTGGATATCAGTCCAACCCCTACGGACAATATGGTATGTTATCAGTTTCTTACAATATTGCACTATGTAATGTAAGCATTGTCCCTGACAGTAGTTCTGACTGGATTAGTGGTGTGTTATTTTTCATAGGTAATGATGGTCAGCGATATGGAGCTAAACCCTACAATCCTAAAGCACCAGGAAAATACGGTGATGATTAGATGTTTTAATGTTCCTTTGCGCTTTTTAATAATTGTTCGAGTGCCTTCATAGAATATCAGGCAGTGTATAGCATTGCTTATGGTAAATGAAGTTAGCAGATTGTTATGAAATAATTTGTTTTGCTGTCATGTACACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2627
Status:
F2 line generated
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077840 | Essential Splice Site | 896 | 1207 | 41 | 54 |
ENSDART00000124453 | Essential Splice Site | 938 | 1249 | 43 | 56 |
ENSDART00000127870 | None | None | 136 | None | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 14248877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13104530 |
GRCz11 | 12 | 13142833 |
KASP Assay ID:
554-2508.1 (used for ordering genotyping assays)
KASP Sequence:
GGACCACCAGCACGATTGGGAACAAAGGGAAAATCTCAAACAAAATATGG[T/C]TAGTCTTAGGAGGAAAATKTAAAAATTTTAAAACTAATTATGTTGTTAAC
Long Flanking Sequence:
AAATAAATAATATTTATTTATTTATTTTTTATATATAAAGGTTTACAAAATATTTGTCCATGTTTTTTCTGCTTGTGCCTCAGACTGTATATGTTGTAAACTGCTTTAAATAGTGTGTGTAGTTTTTTGTGTGCTGTAAGTTTTTCGATAACACTTTATTTTGATGGTCCATTTCAGTATTAGTAGACAATCTGCTTTATATCTGTTGATATTGCTCTATCAACAGACATTTAACTGAATATTAGAGACTTTGCAAGTACTGTACATGTCAACTTACACTAACCCTAACCCCAATTTAACAGTCTATTTATAATCTAATGATAATTAGTTGGCAAGTACATGCAATGTAACTTAAATTCAACAAATGGACCATCAAAATAAAGTGTGACCAGGTTTTCTTTAAGACAACTAAATGTCTTTTCTGTTACTTTGATAGCTGGACTACAAGGTGGACCACCAGCACGATTGGGAACAAAGGGAAAATCTCAAACAAAATATGG[T/C]TAGTCTTAGGAGGAAAATGTAAAAATTTTAAAACTAATTATGTTGTTAACAATTGTTTGTCAACAATAACTTTTTTTATTTTTCTAATTTTGTCAGGAATTGGTGGACTTCCCTTTGGTGGTTCCCCCAGTGGATATCAGTCCAACCCCTACGGACAATATGGTATGTTATCAGTTTCTTACAATATTGCACTATGTAATGTAAGCATTGTCCCTGACAGTAGTTCTGACTGGATTAGTGGTGTGTTATTTTTCATAGGTAATGATGGTCAGCGATATGGAGCTAAACCCTACAATCCTAAAGCACCAGGAAAATACGGTGATGATTAGATGTTTTAATGTTCCTTTGCGCTTTTTAATAATTGTTCGAGTGCCTTCATAGAATATCAGGCAGTGTATAGCATTGCTTATGGTAAATGAAGTTAGCAGATTGTTATGAAATAATTTGTTTTGCTGTCATGTACACTTTGTACAGTGGGTAGGGAAAATATCCAGACCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35227
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 |
---|---|---|---|---|---|
ENSDART00000077840 | Nonsense | 990 | 1207 | 46 | 54 |
ENSDART00000124453 | Nonsense | 1032 | 1249 | 48 | 56 |
ENSDART00000127870 | None | None | 136 | None | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 14251316)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 13106969 |
GRCz11 | 12 | 13145272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTTTACTGTCATTTTTTTCAGGACAAAAGGGTCCTCAATATGGTGGT[C/T]AGTCCCTTGGTCACGGGCCTGATGCAATTTCTGGAAAATACGGTGACAAC
Long Flanking Sequence:
TTGGCTCATGACTGAAAAGACAAAATCTTGGATACTTGGCCGAAATGACTTTCCTTCGCTTATAGATAGGATAAGGAGCTCTGTCACACGGGAGGAACTTGGAGTAGAGCCGCTGCTCCTCCACATTGAGAGAAGCCAGCTGAGGTGGCTTGGGCATCTGTTTCAAATGCCTTCTGGATGCCCACCTAGGGAGGTGTTTCAGGCAGGTTCTCCTGGGAGGAGGCCTTGGGGAAGACCCAGGACACTCTGGAGTGACTAGAGTACGTCTCTAGGCTGGCCTGGGAACGACTCGGGATTCCCCCGGAGGAGCTGGAGGAAGTGTCTGGGATGAGGGTAGTCTGGGGTTCTCTCCTGAGACTGCTGCCCCTACGACGCAGCCCTGGAAAAGCAGATGAAAATTAAAGAATGAAAGCATGAATGAATTAATAACTTTTTTGATTTAAAGTGAATGTCTTTTACTGTCATTTTTTTCAGGACAAAAGGGTCCTCAATATGGTGGT[C/T]AGTCCCTTGGTCACGGGCCTGATGCAATTTCTGGAAAATACGGTGACAACAAATGCTTTTTATAGATGATCATATGACAATGATATTATAATATTATTGTACTAATACTTATTCTCATACTCTCCACACCTTTCAGGGTCTCCTGAATCCTTGTACACACCAGAAACGGTCAATCTTGGAGGCAATGCCAAATCAACTAAATATGGTATGACAGTTTCTTTTTCATATCTTTTCTTTTAATTTATTTAGGTTTTGGTTTAAATTACAATTCCTCTGTATGTGAATTGTGGCTAACATCATACAGTTAGGCTAATGAAACAGTCAAACTGAGTTACTGGAGAGGCTGAGGCTCTGCACAGTTTAGTTCCAACCCTAATTAAACACACCTGATCAAACTGATTGAGTCCTTCTAGCTTGTTTGAATCCTACAGGTAATGCCGCAGTCACACTAAAGTTTGAGCTTGCGAAATTCTGTCTTACGGTGCTGCAAAAAGGGGCAG
Associated Phenotype:
Not determined