ZMP
si:ch211-1e14.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LY95]
Human Orthologue:
KIAA1549
Human Description:
KIAA1549 [Source:HGNC Symbol;Acc:22219]
Mouse Orthologue:
D630045J12Rik
Mouse Description:
RIKEN cDNA D630045J12 gene Gene [Source:MGI Symbol;Acc:MGI:2669829]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18360 | Nonsense | Available for shipment | Available now |
sa11060 | Nonsense | Available for shipment | Available now |
sa43062 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43061 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16982 | Nonsense | Available for shipment | Available now |
sa36589 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16764 | Nonsense | Available for shipment | Available now |
sa36588 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18360
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 |
---|---|---|---|---|---|
ENSDART00000092522 | Nonsense | 119 | 1726 | 2 | 20 |
ENSDART00000144799 | None | None | 966 | None | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 11866707)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12449436 |
GRCz11 | 18 | 12418154 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATGTGCATTTATCTTGGTCCGCTATCAGCCCAGATCCTCAAATCTCAT[C/A]AGCTACAGATTCATCTGTTTCTTCTCACTTGCCTTTACTTGGACAAGATT
Long Flanking Sequence:
GTAATACTTTTATTTCTATTATTACTTTTATTGTTATTTTTACTCTTAGAGTGTGTGCTATGGTTTTGTTCAGCACTTTAGTCAGTGCCAAACTGAAGTAAATGTGCTTTATAAATAAACTTTACTTACCTACTATTATTGCCCATAGTTTCCTTATTGGTGTATGTCTAGTTTTTAGTAATTGGCGTTATAAAATTATTTCATTAAAATGTAATTTTATTGTTGTTTGTCTCCCTCAGTGCGGCCTTTGGACACTCCAATCATGCCAAATGAGTTTTCAACGGAAGTGCTGTATAATGTATCCACTGCCTTGCCTGGATCTTCTCTCTCAAATAGTTTGGATCCATCCAAAGCCACAGAGAATCCCAATCCCAATGTTAACACTAGATCTACCAATAAGGGTTCCATCAGACATCCTCGACAGCTAAATAATCCAGTGCCTACCTCCATTGATGTGCATTTATCTTGGTCCGCTATCAGCCCAGATCCTCAAATCTCAT[C/A]AGCTACAGATTCATCTGTTTCTTCTCACTTGCCTTTACTTGGACAAGATTTTCCTGTTCCCGAGCCTCCAGTTCCTTCCCCTCAAGTGCAGTATGAGACAGGGGGAATCAATGACACTAAAGTTCCTATTGGAGACAATTTGGAACCGTCCAGCAATATCCAGGACCTTCATTTACAACCCAGCCATGACCCAAACATCCAAGCACAATATCAGCAGTTGGAGCCAAGTCATGTGGTTTTTGTACACCATCAATTGACTTCAGCATCTGTTGAGCCAACTATGGGTCCACCTGAAGACTTTTTCCCAACCAATACAATGGATGTGGACTATGGTTCTGGAGATTACTTGGAAACTATGTCCTTTATGGGATCTGAAGGCAATGACTATTCACTAGTTACCAGCCTCCCCTCTGATGCGTATGACTTTGAAGACTCAAACTCTGAAACCTATGACACTGCATTCCCCTCAAGAATTGTGATGTCGTTTTCCAGTAAACACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11060
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 |
---|---|---|---|---|---|
ENSDART00000092522 | Nonsense | 369 | 1726 | 2 | 20 |
ENSDART00000144799 | None | None | 966 | None | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 11865956)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12448685 |
GRCz11 | 18 | 12417403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGYAACAGCAGTTCTTTATCTATTTCAACCATCCAACTAACTAGAGTCYA[T/A]TCAGAGTCTACGACAGTTGTGCCCTTTACKAYGTCACCACCTCCAGTATT
Long Flanking Sequence:
CAATTGACTTCAGCATCTGTTGAGCCAACTATGGGTCCACCTGAAGACTTTTTCCCAACCAATACAATGGATGTGGACTATGGTTCTGGAGATTACTTGGAAACTATGTCCTTTATGGGATCTGAAGGCAATGACTATTCACTAGTTACCAGCCTCCCCTCTGATGCGTATGACTTTGAAGACTCAAACTCTGAAACCTATGACACTGCATTCCCCTCAAGAATTGTGATGTCGTTTTCCAGTAAACACTTGTACACCCCCTCCACCAGTGTTAGAAGTCCCTTCTCCATTAAACTTGTCGGCAGTTCCAGTTTTAATAGTATTTCAACCTCGATTGCAGCCACCACTGATTCAATCATTCACACAACAACCTTTCAAAGTTTTACAACCGTTGTGCCCTTTACCACGTCAAGACCTGAAGTTTTCAGCAGTGTTTTGGCATCAGATCTTGGTAACAGCAGTTCTTTATCTATTTCAACCATCCAACTAACTAGAGTCTA[T/A]TCAGAGTCTACGACAGTTGTGCCCTTTACTACGTCACCACCTCCAGTATTCACTAGTATTTTGACGTCAGATCTTGGCCCCTCCATTTCTCCATCACTTTCAGCCATCCAACCAACAAGAGTCCATTCATTGCCTCTTCTTCCATCAACTTCAGATGTCTTGAACCAGAACCAGTCTGTGAACGAGAGCTCCGAGTTGGCATCTGATTGGCCAGGCACTGTTACAGTCCAGCCCACGGATGTCCTTTTACCAGACATGAACAGTTTAGAGTACTACACCATTCAGTTGACCAAGGACAATGATAGCTTGCCAGAGCACGCTGCCAATCAGACGACCTCTAGTGTTTTCTCTTTCATTCCGGTTGGCAACACACATATTGTCAGCACTAGAACCTACACCGTTGACCCAAGTTACATGCTAACAGCTCTGTTTGATGAAGATCTACAGCCTGCAGAAGGTAACAGCTCCTGGCCTGAAGAATCCTCAACAGACACCTCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43062
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 |
---|---|---|---|---|---|
ENSDART00000092522 | Nonsense | 642 | 1726 | 2 | 20 |
ENSDART00000144799 | None | None | 966 | None | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 11865138)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12447867 |
GRCz11 | 18 | 12416585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCACTCCCAATGGAGACTGTATTACCTAGCAGTGTACTTCCCAGTGTTT[T/A]AGCAACCACCTCTATCAGTGTTTCTGAATACCCAGATAACTCAACCTTCA
Long Flanking Sequence:
CGCTGCCAATCAGACGACCTCTAGTGTTTTCTCTTTCATTCCGGTTGGCAACACACATATTGTCAGCACTAGAACCTACACCGTTGACCCAAGTTACATGCTAACAGCTCTGTTTGATGAAGATCTACAGCCTGCAGAAGGTAACAGCTCCTGGCCTGAAGAATCCTCAACAGACACCTCTGGATTTGAGCCTTTTAACACCACTATCCTGGATCCTTCTGAAGTTACACCAAGTGTAGTAAATATAACTGTGTCATACATGGAGCCGTCATTCACATTGACACCCTCAGTAGATCCTTCAACTTCATTAGGAGATAAGAACTCAACCACTATTTGGCCTACCACACCATTTATAGCTGACAACACTTCCTTACTGGAGACTACGCCACCTTTGGCGACCAAGGAGCCAGATAGTGTATCTTCAGTTAATGTCAGCCAATGGATTACCACTTCACTCCCAATGGAGACTGTATTACCTAGCAGTGTACTTCCCAGTGTTT[T/A]AGCAACCACCTCTATCAGTGTTTCTGAATACCCAGATAACTCAACCTTCAACATCACCTCCACCCCTCCTGCAACAGAGATGGCAGACGAAGGATTCGTGTCTGGAACGGCATCTGACACCATGGCTACTGATAACACCACACCGTTCGATAGCCTTACAACCACGTTCTCTACTGTATTGCGTAATGACACTACTGAAACGCCTTTCACCGTCACAAGCTCTGACAACAACACCACAGTTACCATCCTAAGCACAACCCCTCCAACAACCACTGCCCGGAAGTATCTCTGCAGCATCACTAAACCTGACACCTACTTAACCAGAGTTGGTAAGACATACAAATCAATTTGCTTTATAGTAATTTGCACCAGCAAGGTTTGCCTGTCAGTTTTTAAAGATCAGTGTGCAGCTTTATCCATAAGGCACTGATCCGTCTTTAGAAATAATTGGATTACTAACCATGCTTGCTTTATTTTGTTGGTATTTTATATTTAAGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43061
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092522 | Essential Splice Site | 782 | 1726 | 4 | 20 |
ENSDART00000144799 | Essential Splice Site | 22 | 966 | 2 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 11863594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12446323 |
GRCz11 | 18 | 12415041 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATACATTTCCTTCACATCATGTGTTTACAATACGCTTTTTGTGTTTACT[A/G]GGTAGTGAAAGCTCCTCCAGACTTTGTGTTTCGCGCTGTGTCTGGAACAG
Long Flanking Sequence:
TTGATTGTGGTCTTGAATCAAATTGTCATGCTTATTTTTATCCACATTACTTTCCAGCAAATTCTCAAAAAATCTCTATTTAAACTAGAGAACTAAAGTAGTTTCTACTCTTCAGACTGAAGGAGCTATAAAGACATAAGGCAGCATTTGTTTTTTGTTTCTTCTAAACGTGTAGCATAGCAATGTTTATTTAATTCTGCTTTCTCTTGTTTTGAGTCGAAGAAACTTTAAGCATGTTTGTTAATCCAGTGAACATACAGATCAAGTCCTCCCTTCCTGTTTTATCTCTTGGGCCCTCCTCACGAACAAACAACACCTAATTTAGCTCAATGGAAACATATTCTCTGCATCTGAAAACGATACAGAATCAGCTTTGTTTTTTACAAGCTCATTAAACGACAAAATTTATGAGATATTTTCCAATGTGCCTCAAAAAAAAGCAAGATGTATTATACATTTCCTTCACATCATGTGTTTACAATACGCTTTTTGTGTTTACT[A/G]GGTAGTGAAAGCTCCTCCAGACTTTGTGTTTCGCGCTGTGTCTGGAACAGCAGTTTACACGGCCGCATCAGTCATTAATGCCTTGAAAAACTCTGCTCGGACTATCAACTCATTTATTAGCGTGTCTCCTATCAGTCCAGAACCAGACCGGCAGTACCATGTACACACAGGTACACTGCAGTTTATATTTGATTGCAAAATATCAAACATGTTGCTTTTGACTATATTCATGTTATCCTTTGATGGTATCATTTTCTTTTGTTGTGATTCATTGCTGAAGATTTTATCATCACATTCGGTATTATCAAAATATTGAGCTTCCCAATAGGTTACTTTAACAGGTATAATAGTGAAACATACTGTGTGTATTGCTTTGTTGTATACACAAGTTTAGAAAAAAGAAATTATCCTGTCTCCCTTTCTACTGTCCTATAAATTAAAGGTGAAAAACTTCTAAAATATAAATATAAAAAAAGTAACAGAGTTATAAAGTACAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16982
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 |
---|---|---|---|---|---|
ENSDART00000092522 | Nonsense | 851 | 1726 | 5 | 20 |
ENSDART00000144799 | Nonsense | 91 | 966 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 11860583)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12443312 |
GRCz11 | 18 | 12412030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTCTGCAGTGCTTCAGTTTGTGCCAAGCCAWGTAGATGTGCGTATGTG[T/A]ACCTTCAGTGAGCARGCAGARAAAGGTCTWATTGCTGCATTAGCTGAAGT
Long Flanking Sequence:
GGCTGAATGAAGGAAGTTCGTTCTTTATCCTCTCGCTGCAGATGGTTTAACTGTTTTTTCACTAGTGAAGCTTACAAAGTCCGCCATGTAAATAGTAAATGTGCCATAGCGACACAACTGACTCTTTAAGGGAATAGGAAATGAGACTCTGATTGGTTTAATACAAGTTATGCTTAAAACACACTTATAACTCATTAAGAGAATAAGCACAACCCTGTTAAACCATGTGCAGGGGCGCAGAGTGTATTTTTCTGTCCTTAAGATAGCAAAAGTGGATTCAGACATGCCCTTAATTATTTTGCGCCATGCACTTTTACTTTGCGCCTATATTGTTAAAATAGAGCTCTAAAAGTTTGAAGTATTTTGAAATGGCCACAATATTAGTATTGTGCATGTTCAATATCACAATATATGGAATTATCGACATTTGTCTATATGCATGTGTTTTGTTTGTCTGCAGTGCTTCAGTTTGTGCCAAGCCATGTAGATGTGCGTATGTG[T/A]ACCTTCAGTGAGCAAGCAGAAAAAGGTCTAATTGCTGCATTAGCTGAAGTCCGGCGGAACTCAGAGGAGTCCACAAACTTCACTGTGAATGTAAGTTGACTTCTTTATCCAGCTTATGGTATTAAAAGCTCAAACACTGATAACCTGACACTGAACCCCTTCAAATCCTCTTAATTAGTTCTTGTTTCATTGTCATTTGCTTAAATGACTTCTTTAGCATTACACACAAGTGCTGTTTAATGTAAATGAGCCAAATGTGAACTAATTCTCTGTTTAATACGGTGTTTTGATGTTAGAAAGATGGTTTTAAATTGTGTTGTGTGATGTGAATTCAAGGCTTTATTGCCTTCAGTGCAGAGGGGTGACGTCATCTGCATCTCTGTGCTCTGATTGGATAAGAAAAGAGCAGGACTGCTCAATTCAACCGTTGTCAAGGAAACTAAACTAATGGGTCTTATTCATTTCATTCAACGTTCAGAAAGTGTACAAGCTTTTTGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36589
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 |
---|---|---|---|---|---|
ENSDART00000092522 | Essential Splice Site | 965 | 1726 | 7 | 20 |
ENSDART00000144799 | Essential Splice Site | 205 | 966 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 11857788)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12440517 |
GRCz11 | 18 | 12409235 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGAGCTGAACACAACCCAGCTGCTTCGTTCCTCATGGGTCAGAACAG[G/A]TAATATTTCTTAACACTTTTTTATTCCAAAATAAACTAGCATTAAAGATG
Long Flanking Sequence:
AGACTGAATTGTTTTGTAGATATTGAATATTACAGTAAATCAGGACGTGGACGTGAAGGCACAACAGCAGAAGTTTCCAGTGGAGATCACCTTTGCTGTGCATGATATGCGCGGGTATGTGCCCGGTACAGAGGTCAGTGCTCTGCTCCGCCAGCTCAGTGTGGTTGAGTTCAGCTATTACCTTGGCTATCCTGTACGGCAGATCGCAGAACGTGAGTATGCACTCTCACTTTGATGGACCACATTTAAATACTCACAAAACAACTGTGCTTGTGTGTACAAGTGGTTATGCTGTATGTAGATTAAACTGTGACAAAGTAGGCTATCAGTATTGACCCATCTACTGGTATCCTAGCCTGTAAACTTCTCAACCATATTTAAACACTTAGAAATCAAGTTTTTGCTCATATTTGACATCTTGTTTTTCTTTTCATCATTAGCTTTCCACTACCCAGAGCTGAACACAACCCAGCTGCTTCGTTCCTCATGGGTCAGAACAG[G/A]TAATATTTCTTAACACTTTTTTATTCCAAAATAAACTAGCATTAAAGATGTTGATTTTGAAAACTGTTATTTTGGAATTGCAACAATTTAACAAATGGTATCACTATTTTTGCTTATTGTAAAATAAGCTATTGTAAGGAGAACCTTGGTCAGACTAAAAAAAATAAATAAATAAGTTCTAGAGAATAAATACATTTATTCTGAAAAAGAAATACATTTCAAATATATTTTGTATACTTATATTTAATATAATTAACTTATTAATTAATATTTATTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATAAATAATATATTTATTTAAATAATAATAGACACATATGTAATAATATTATCATACCACTTCACAATGTTGTTGTTTTTTTGTGCTTTTTGTCCAAATATGAGGCTTTGGTTTTTATTTTAAAAATAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16764
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 |
---|---|---|---|---|---|
ENSDART00000092522 | Nonsense | 1017 | 1726 | 9 | 20 |
ENSDART00000144799 | Nonsense | 257 | 966 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 11848349)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12431078 |
GRCz11 | 18 | 12399796 |
KASP Assay ID:
2261-1917.1 (used for ordering genotyping assays)
KASP Sequence:
ATTTTGTGTGAACAAGCCATTTTTTTTNCTWCCCACTTCATTTAGATCGTA[C/T]AGACRACCCATCTTGTAGGGCCAGACAACCCTCTGGAGATCATCTACTTT
Long Flanking Sequence:
CCTAGAGTGTGTATGTGAAGTTTCAGCTCAAAATACCTCATAAATAATATTTTATAACCCTTCGAAGCTGCCTATTTAAGGCTTTGATCCTAATTGTTCTGTTTTCGTCACTGTCGCTTTAAATTCAAATGAGATTGTGTTCCCAGTCCTATTTTAGAAACAGGGCGGAGCTATAAATTCCTGTGCATAAGTATATCAACAGATTCAAAACTCTAATGGCGGATGACTGCTTCTAACTCGAGGCTGTTTATGCTAATGAGGAAGAGAGTGTCACGAATGGGCGGGGCTTTCCTTCTCTGATGACATGTACAAAGGGAGAATGTCAATCAAAGTGTTTCTGCAGACTGTTTTTATCATGTGTGATTATAAAAAAGATAAGTAATTCTTACCATTAGAGGCTGAATATATTCACTCACTGTTGCCACACAACTGTGTTTAAACCCCTTATAAATTTTGTGTGAACAAGCCATTTTTTTTCTACCCACTTCATTTAGATCGTA[C/T]AGACGACCCATCTTGTAGGGCCAGACAACCCTCTGGAGATCATCTACTTTGTGGAAGGAGCTAACGGACAGAGGCTTCCTGCCACCACCACAGCCAACATGCTGAACAGTCTTGACGTGCAGCACGCAGCGATCATCATGGGATACCGCATCCAGGGAATATTAGCACAGCGTGAGCATTCATTCTTTTACTACAAAATAACCAGTGGGAGAGAAACCGTAATTGCAATAAACTATACAATAATGGTAAGACAAGATGAGGGAGTTATCATTGTAATGTTTTTGATTTGATGCTAACATAGCAGGCAGAGGTTTTTGTTGTAGCTTTCTTTATTTCTGCTGCTGGAAACCTCAAAGAGGAGAGTTCAGATAACATGACATCTCAAGAGAGCTCTGCCTTTTTATGTAACATTTATATGTGGCGGGCTTGCAACTGCATCACCCACAGCATAAACACTAGATTCATTAGACTAAATTTAGGAGCTTCCTGTTGTATAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36588
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 |
---|---|---|---|---|---|
ENSDART00000092522 | Nonsense | 1571 | 1726 | 18 | 20 |
ENSDART00000144799 | Nonsense | 811 | 966 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 11815461)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12398190 |
GRCz11 | 18 | 12366908 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTGTTGGAGTGCAGTGTGGGTATCTGATGTTTTTGTGTCTCTACAGA[C/T]AGGGATTGGGGTCCAGCTATATGCCATCAGGAGAATCTCTGCCTGCTGAA
Long Flanking Sequence:
CGACTCTAAATCAAATATTTAGCTAAAAAAAAATTGTTTTTTGCTCCAATTTTAGATTTAAACCTCTGCTGGATGTTTTTATCCACTTAGAGCCGTGTTACACACCGCATGGATGCTCATTTTCAAAAACCCATAATAGGGGCTCTTTAGTACATCAGCCTTATCAATATATTCGACAAGCACTAGTGTAAATTTCGTCCTCTAAAGATATTTTAGGGGATGTTTTGGAAAGTAACAGTGCTTCCGATCACTTTGCATGAGTGTATCCATTATTGTTGTTGTTCCTTTTTAACACATTTTTCAATCATTTTAATTTTTCTTACTTTTTATACTTATTGTGTTTCGTTTCTTTTATTATTCTTTATGTAAATCACTTTATATTACCATTGTGTCTAGAATGTGGTGTATAAATAAACTTGCCTTGATTGTAGTGAGATTGGTGAAGTCTTGTTTTTGTTGGAGTGCAGTGTGGGTATCTGATGTTTTTGTGTCTCTACAGA[C/T]AGGGATTGGGGTCCAGCTATATGCCATCAGGAGAATCTCTGCCTGCTGAACATCTACAGCCAGAGTCACTTTACCCTGGTCGAGGGACACACACTGATGAGCTGCCCTCCTCTGCCAGACCACGACCAGTAGGGGGCACTACAGGTACGAGAAAAACTCTGGATTGTGATTGGGGTTATTATAAGATTATTGAACTTTCATGACTTAACAAAGGGTTTTTAAGTTTTAATCAATGATGAGGAAGTTAACATTAGGCATGGGACGAAAACCGGTTTCAAGAAATACCACGGTTTGGAAAAGTCAAGTTTTGTTTGTTTTATTTTTTAGGATAACAGTATCTCCAGCAGAAAAGATATCCAAAGATGCCTTTTTCAAGTTGTAAAAAAACTGTGTTTTTGAAACTAATAAAGAGAGCAGAAGTCAATGATTTATTTAAATTATTCAACCTGACATGTTTACTGTCTCAAAATAGAATTGTTCAAAATGTATTGTGTTGAAAG
Associated Phenotype:
Not determined