Busch Lab

ZMP

shank3a

Ensembl ID:
ENSDARG00000063332
ZFIN ID:
ZDB-GENE-060503-369
Description:
Novel protein similar to vertebrate SH3 and multiple ankyrin repeat domains 3 (SHANK3) [Source:UniPr
Human Orthologue:
SHANK3
Human Description:
SH3 and multiple ankyrin repeat domains 3 [Source:HGNC Symbol;Acc:14294]
Mouse Orthologue:
Shank3
Mouse Description:
SH3/ankyrin domain gene 3 Gene [Source:MGI Symbol;Acc:MGI:1930016]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa16683 Essential Splice Site Available for shipment Available now
sa17971 Nonsense Available for shipment Available now
sa8445 Nonsense Mutation detected in F1 DNA Not yet available
sa8619 Nonsense Mutation detected in F1 DNA Not yet available
sa25052 Nonsense Mutation detected in F1 DNA Not yet available
sa16870 Nonsense Available for shipment Available now
sa43043 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa23228 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16683
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092456 Essential Splice Site 214 1467 4 12
ENSDART00000139188 Essential Splice Site 101 185 3 4
ENSDART00000139505 Essential Splice Site 101 1353 3 11
Genomic Location (Zv9):
Chromosome 18 (position 7168902)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7746592
GRCz11 18 7705527
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTATTACGACGATGCATGTTAATGTGTGTGATGTTGTGTTTTTTCTKTC[A/T]GAGACRAGAGAGGATCGAAACAAGAGGCTRTTCAGACATTACACTGTGGG
Long Flanking Sequence:
CAAATTAATGTATTTTACGTTTCTCCCATATTTTAATGGTTACATTCCAGCAACCATATCTTACGCTTATTTTACCATCAATTTTACAGATTTTTCTTTTTTTTTTTTACAGTGTAGGTGTGTGAATGTGTGTGTGTACGTGTGTCAGCAGATCGGCTTTCTGTAGGGGAAGCAGTGCATTGATTTCCAGCTGAAAGTCCAATCACATAAATCTGGTCTGGCTTGAGACACCAGGCCTATTAGCCAGACCTTCTCACTGGATTAACAACACACACACACACACACACACACACACACACACAAATATATACAATTGACCTTGCCTCTGCATTTAATTAAGCCTGTCTTAGTTTCTGCACACACATTTCTGCATAAGGCTGATGAGAGACATGCGGTCGGCTCGGAAATGTAATGCAAATATGATAAGCAGCTTGAAAATGATAAATGTGGTCTATTACGACGATGCATGTTAATGTGTGTGATGTTGTGTTTTTTCTTTC[A/T]GAGACGAGAGAGGATCGAAACAAGAGGCTGTTCAGACATTACACTGTGGGCTCCTACGACAACTTTACCTCATATAGGTAAGGTATACATATTTATGGATGCATGCATTGATAAATATAAGGGCATTTTTGTTATCAGCAGCTCAAGGTTAGCCTGAAGACATCGCAGGTTGTTCTGACTCATTTATCAAAGCTGGTGTTTGTAGTGTTGAGTCTCTACTGCCATCTAGAGGATAGATGTTGTCAGCACACATTCGCAGACGTCACACACATGCTTTCTTTTTTTATCGTTCACCTTTTTTATTGCATCCTACAATCTATTTTGTTTGTTAAAAAAAACAGTTACATGATTTACTTGAATCCTCAGCATTTAATTTAATAAGATTTTAGAGCCTGTATAATATTAAAATGCATTCTTCTCAATGTTGCAGTGTAATTTGCATATGTAAATTTACTTATGTATGATAGCCACTGTGTCCGCTTACACTAGATTGGCTATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17971
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092456 Nonsense 553 1467 11 12
ENSDART00000139188 None None 185 None 4
ENSDART00000139505 Nonsense 439 1353 10 11
Genomic Location (Zv9):
Chromosome 18 (position 7138269)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7715959
GRCz11 18 7674894
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGAGCCGAGACTACATGCATTGCCTCAGACAATGTCTGCTGAGCTGTA[T/G]GAGCCGCCTCGCCATGCCTCCCACATGGAGAGGCAGAAGAAAGCCCGCTC
Long Flanking Sequence:
AAACAAGCTCCACAGTTTGAAACAGCTGAAAAATATTATTCTCTGGTTTCTTCTATCTGTCTGTGCTTTCTTAAATATCAGCGTATTGAAATGCAGGACTTTGACACACAATAACGATCAGAATTTAAAGGAAAGTTTAGATGTGAATTATGTGAATTATTGTTATCATTCAAGCTCCACCAAACCCAAATACATTTCTATCTGTCTAAATGTGCAGGAGCCACCGAAGAGGATCGACTGTCTGCCCTGGCAGCGGAGCACAGATTTCCACGAAGCTCCTCCATGACGGACAGCCTGAGAGACAGCCATAGTATCCCTCCACCTCCTCAGATGGCTCCCCCACCTCCTCCATCGCTTTACTATCTAGATACTGGACCCCCTCCTTCATTCTGCCCACCCCCTCCCCCTGGCCGCCTTCACGACCCCAGCCGTTCCAGTTTTAAACCAGGCTCTGAGCCGAGACTACATGCATTGCCTCAGACAATGTCTGCTGAGCTGTA[T/G]GAGCCGCCTCGCCATGCCTCCCACATGGAGAGGCAGAAGAAAGCCCGCTCCATGATCATCCTGCAGGATTCCTCCCACCTCCCTGTGGAGCCTACTGACATCCCCAGGCCAGGTCCTGTCTCAACTCCGCCTGAGAGAATCAAGCGGAAAGGCAGAATCATAGATAACCCCTACGCCAATGTGGGTCAGTTCAGCGTGGGTATGTTCACGCCAACTCCCAGCAAGCCACAACGGAGGAAGAGCCCACTTGTTAAGCAACTGCAGGTGGAAGATGCTCAGGAAAGAGCCTCACTAGCATTGGCATCCATCCATGCGAGGGAGCACTCTCCTTCTGGGCGCCTTGCTGCCCAGCACACCAGCAGGTCTGACTTCTTTCATCAGCAGCAGCAGCTGTTGCATGAACGCAGTCAAGCTCATGCTGAAGGACTGTTGCAAGGAAAAGGACCTTTTGCTGCTGCCATTGCTGATGCTGTGAAGGACAGAGAACGTCGTCTGGAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8445
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092456 Nonsense 611 1467 11 12
ENSDART00000139188 None None 185 None 4
ENSDART00000139505 Nonsense 497 1353 10 11
ENSDART00000092456 Nonsense 611 1467 11 12
ENSDART00000139188 None None 185 None 4
ENSDART00000139505 Nonsense 497 1353 10 11
Genomic Location (Zv9):
Chromosome 18 (position 7138095)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7715785
GRCz11 18 7674720
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCCRCCTGAGAGAATCAAGCGGAAAGGCAGAATCATAGATAACCCCTA[C/A]GCCAATGTGGGTCAGTTCAGCGTGGGTATGTTCACGCCAACTCCCAGCAA
Long Flanking Sequence:
CTCCACCAAACCCAAATACATTTCTATCTGTCTAAATGTGCAGGAGCCACCGAAGAGGATCGACTGTCTGCCCTGGCAGCGGAGCACAGATTTCCACGAAGCTCCTCCATGACGGACAGCCTGAGAGACAGCCATAGTATCCCTCCACCTCCTCAGATGGCTCCCCCACCTCCTCCATCGCTTTACTATCTAGATACTGGACCCCCTCCTTCATTCTGCCCACCCCCTCCCCCTGGCCGCCTTCACGACCCCAGCCGTTCCAGTTTTAAACCAGGCTCTGAGCCGAGACTACATGCATTGCCTCAGACAATGTCTGCTGAGCTGTATGAGCCGCCTCGCCATGCCTCCCACATGGAGAGGCAGAAGAAAGCCCGCTCCATGATCATCCTGCAGGATTCCTCCCACCTCCCTGTGGAGCCTACTGACATCCCCAGGCCAGGTCCTGTCTCAACTCCGCCTGAGAGAATCAAGCGGAAAGGCAGAATCATAGATAACCCCTA[C/A]GCCAATGTGGGTCAGTTCAGCGTGGGTATGTTCACGCCAACTCCCAGCAAGCCACAACGGAGGAAGAGCCCACTTGTTAAGCAACTGCAGGTGGAAGATGCTCAGGAAAGAGCCTCACTAGCATTGGCATCCATCCATGCGAGGGAGCACTCTCCTTCTGGGCGCCTTGCTGCCCAGCACACCAGCAGGTCTGACTTCTTTCATCAGCAGCAGCAGCTGTTGCATGAACGCAGTCAAGCTCATGCTGAAGGACTGTTGCAAGGAAAAGGACCTTTTGCTGCTGCCATTGCTGATGCTGTGAAGGACAGAGAACGTCGTCTGGAGGAGAGGCGGAAATCTACAGTCTTCCTATCAGTGGGAACTATGGAGGGCAGTTCAGCACCACCCCCCGAGGCCCCCTCGCTCACACCATCCCGTTCTGTTGATGAACGAATGCTCACTCGTGAACTCGGTCAATTGCCTCCTCCCGCCTTGGCGTTACGTCCCTCACCTGGGGGCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8619
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092456 Nonsense 611 1467 11 12
ENSDART00000139188 None None 185 None 4
ENSDART00000139505 Nonsense 497 1353 10 11
ENSDART00000092456 Nonsense 611 1467 11 12
ENSDART00000139188 None None 185 None 4
ENSDART00000139505 Nonsense 497 1353 10 11
Genomic Location (Zv9):
Chromosome 18 (position 7138095)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7715785
GRCz11 18 7674720
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCCRCCTGAGAGAATCAAGCGGAAAGGCAGAATCATAGATAACCCCTA[C/A]GCCAATGTGGGTCAGTTCAGCGTGGGTATGTTCACGCCAACTCCCAGCAA
Long Flanking Sequence:
CTCCACCAAACCCAAATACATTTCTATCTGTCTAAATGTGCAGGAGCCACCGAAGAGGATCGACTGTCTGCCCTGGCAGCGGAGCACAGATTTCCACGAAGCTCCTCCATGACGGACAGCCTGAGAGACAGCCATAGTATCCCTCCACCTCCTCAGATGGCTCCCCCACCTCCTCCATCGCTTTACTATCTAGATACTGGACCCCCTCCTTCATTCTGCCCACCCCCTCCCCCTGGCCGCCTTCACGACCCCAGCCGTTCCAGTTTTAAACCAGGCTCTGAGCCGAGACTACATGCATTGCCTCAGACAATGTCTGCTGAGCTGTATGAGCCGCCTCGCCATGCCTCCCACATGGAGAGGCAGAAGAAAGCCCGCTCCATGATCATCCTGCAGGATTCCTCCCACCTCCCTGTGGAGCCTACTGACATCCCCAGGCCAGGTCCTGTCTCAACTCCGCCTGAGAGAATCAAGCGGAAAGGCAGAATCATAGATAACCCCTA[C/A]GCCAATGTGGGTCAGTTCAGCGTGGGTATGTTCACGCCAACTCCCAGCAAGCCACAACGGAGGAAGAGCCCACTTGTTAAGCAACTGCAGGTGGAAGATGCTCAGGAAAGAGCCTCACTAGCATTGGCATCCATCCATGCGAGGGAGCACTCTCCTTCTGGGCGCCTTGCTGCCCAGCACACCAGCAGGTCTGACTTCTTTCATCAGCAGCAGCAGCTGTTGCATGAACGCAGTCAAGCTCATGCTGAAGGACTGTTGCAAGGAAAAGGACCTTTTGCTGCTGCCATTGCTGATGCTGTGAAGGACAGAGAACGTCGTCTGGAGGAGAGGCGGAAATCTACAGTCTTCCTATCAGTGGGAACTATGGAGGGCAGTTCAGCACCACCCCCCGAGGCCCCCTCGCTCACACCATCCCGTTCTGTTGATGAACGAATGCTCACTCGTGAACTCGGTCAATTGCCTCCTCCCGCCTTGGCGTTACGTCCCTCACCTGGGGGCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25052
Status:
Mutation detected in F1 DNA
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
ENSDART00000092456 Nonsense 952 1467 11 12
ENSDART00000139188 None None 185 None 4
ENSDART00000139505 Nonsense 838 1353 10 11
Genomic Location (Zv9):
Chromosome 18 (position 7137074)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7714764
GRCz11 18 7673699
KASP Assay ID:
554-7631.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCTTCCCCTAAGGGGATATTGTCAGAAAGCCCCAAACCCATGTTGGCC[G/T]AAATTAAACGTGCAAAGTCCCCTGGTCCCGAAGCTCCTTCGATATCCACC
Long Flanking Sequence:
CAGGTAAGCCCCTGGACCCCAACTCTCCATTGGCACTTGCGCTGGCCGCAAGAGAACGGGCATTAACTTCCCAGAGTCAGTCCCCCTCAAGCAGCCCTGAGCCCAGAACTAAACATGAAACTGCTGGAGGGGTACTGTATATGGAGACCCAGACCAAAGAGGCTGAGCGGTCAGAGGGTGAGGGTGGGTTTGCTTCACCTCCCTTTTCTCCTGCAACAAAAAGAATTTACGAGACCTCCGTCCCCACTAGCAAGATTCAGTGGGGAAGTCCCATATCTACCAGGAAAGAGTTAGAAACAAGGACAGAAAGGAAGGAGGAGAGGAAAATTGAGGACAAAAAGAGTATGATCATCAGCATCATGGACACGTCTCAGCAGAAAACTGCTGGGCTTATCATGGTTCATGCAACGAGTAATGGGCAGGCTGTAGGGCCCAGTCCAGAGCGCAGTGTCCCTTCCCCTAAGGGGATATTGTCAGAAAGCCCCAAACCCATGTTGGCC[G/T]AAATTAAACGTGCAAAGTCCCCTGGTCCCGAAGCTCCTTCGATATCCACCCCACCACCCACCGCAGCTCCAACTTCCCAGCCCCCTCCCAGCCCATCCTCAGACAAAACCTTGGCTCAGGGTAGTTCTGAGGAGGATGCCGAACCCTATACAGTCACCTTGCCACCTGCCATGCTATCCTCCAGTGACGAGGAGACAAGAGAGGAGCTTCGTAAAATCGGTGTGGTTCCTCCGCCGGACGAATTTTCAAATGGCCTTCTTGCTAAGACTCCTGAAACTGCAGTACCTCCTGCTCCCACGTTGACGCAGACAACTCCTTCTACCTTGCCCTCAGCTCCACCCGCTCCACCACCCCCTGCTCCTTCAGCAGCGGTCGCTGCAGCAGCACAGGTCCCTGCTAGCAGTGGCCTGCAAGCAGCCTCAGGGAAGCCATCTGAGTCCCACCTGGGCCCAGAGTCTGCTGCTGACTCCGGGGTGGAAGAGGTAGACACTCGTAGCTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16870
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092456 Nonsense 1189 1467 11 12
ENSDART00000139188 None None 185 None 4
ENSDART00000139505 Nonsense 1075 1353 10 11
Genomic Location (Zv9):
Chromosome 18 (position 7136363)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7714053
GRCz11 18 7672988
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCCCAGCTCAGCAAGGGCCCGGTGACGTTCAGGGACCCCCTGCTCAAG[C/T]AGTCATCTGATAGCGAACTGCTCTCAMAGCAGCATGCGGCTGCACTGGCT
Long Flanking Sequence:
GTAAAATCGGTGTGGTTCCTCCGCCGGACGAATTTTCAAATGGCCTTCTTGCTAAGACTCCTGAAACTGCAGTACCTCCTGCTCCCACGTTGACGCAGACAACTCCTTCTACCTTGCCCTCAGCTCCACCCGCTCCACCACCCCCTGCTCCTTCAGCAGCGGTCGCTGCAGCAGCACAGGTCCCTGCTAGCAGTGGCCTGCAAGCAGCCTCAGGGAAGCCATCTGAGTCCCACCTGGGCCCAGAGTCTGCTGCTGACTCCGGGGTGGAAGAGGTAGACACTCGTAGCTCCAGCGATCACCACCTGGAGACCACGAGCACCATCTCTACTGTCTCCAGCATGTCCACACTGTCCTCGGAAAGCGGCGAGCCAACAGACACTTACACCACCCACGCAGATGGCCAGACGTTCATTCTTGATAAGCCGCCAGTGCCTCCAAAGCCAAAGCTCAAGTCCCAGCTCAGCAAGGGCCCGGTGACGTTCAGGGACCCCCTGCTCAAG[C/T]AGTCATCTGATAGCGAACTGCTCTCACAGCAGCATGCGGCTGCACTGGCTGCTGCTGCGGGAGCCTCAGGCCCGGCCAGACCCCGCTACCTCTTCCAGAGACGCTCTAAGTTGTGGGGGGACACAGTAGAACCCCGTCCGCTTTCGGGGGCAGAGGAAGGCAAGCCCACTGTGATCAGCGAGCTCAGCTCCCGGCTGCAGCAGCTGAACAAGGACACACGCTCACTTGGGGAAGAGCCACTTGGAGCTTCACTTGACCCCGGACGAAAATCCCCCGTGGTCGGTCCAAGGTAAAGTGCGAATCTTACAGGAGAGCATTCAATCAGCAATTTTTCAAAATTTCTATGAAAAATGCTGATTTTGTCTGTTTATGATCCAAATGCAGTTTTCTATTGGTTAAATGGCACTGAGAATATTTACCCTGTGCAGTTATTTTTATCAAATATGATTAACAGTGATTAATTGAAACTAATAAATCTGTAATCGTTAATATGGAATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43043
Status:
Mutation detected in F1 DNA
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
ENSDART00000092456 Essential Splice Site 1285 1467 11 12
ENSDART00000139188 None None 185 None 4
ENSDART00000139505 Essential Splice Site 1171 1353 10 11
Genomic Location (Zv9):
Chromosome 18 (position 7136073)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7713763
GRCz11 18 7672698
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGGAGCTTCACTTGACCCCGGACGAAAATCCCCCGTGGTCGGTCCAAG[G/A]TAAAGTGCGAATCTTACAGGAGAGCATTCAATCAGCAATTTTTCAAAATT
Long Flanking Sequence:
AGCGATCACCACCTGGAGACCACGAGCACCATCTCTACTGTCTCCAGCATGTCCACACTGTCCTCGGAAAGCGGCGAGCCAACAGACACTTACACCACCCACGCAGATGGCCAGACGTTCATTCTTGATAAGCCGCCAGTGCCTCCAAAGCCAAAGCTCAAGTCCCAGCTCAGCAAGGGCCCGGTGACGTTCAGGGACCCCCTGCTCAAGCAGTCATCTGATAGCGAACTGCTCTCACAGCAGCATGCGGCTGCACTGGCTGCTGCTGCGGGAGCCTCAGGCCCGGCCAGACCCCGCTACCTCTTCCAGAGACGCTCTAAGTTGTGGGGGGACACAGTAGAACCCCGTCCGCTTTCGGGGGCAGAGGAAGGCAAGCCCACTGTGATCAGCGAGCTCAGCTCCCGGCTGCAGCAGCTGAACAAGGACACACGCTCACTTGGGGAAGAGCCACTTGGAGCTTCACTTGACCCCGGACGAAAATCCCCCGTGGTCGGTCCAAG[G/A]TAAAGTGCGAATCTTACAGGAGAGCATTCAATCAGCAATTTTTCAAAATTTCTATGAAAAATGCTGATTTTGTCTGTTTATGATCCAAATGCAGTTTTCTATTGGTTAAATGGCACTGAGAATATTTACCCTGTGCAGTTATTTTTATCAAATATGATTAACAGTGATTAATTGAAACTAATAAATCTGTAATCGTTAATATGGAATAAAAAGAACATAAACAAGATCCATTAAACATTCTCATAAACATCATAAAGAATGCCAAAGAATGTAATGCAGACATGATTAAATGGGCAGACTTTTATCTTAAATAAAGCAAATTAACATCTTTAACCTTTGGAACGTGTTTAGAAGAAATGAAGTGGTAATGTCTAACATGCTTTCTTCATTGAGATGTTTGGAGCCCAAGAACAATCTCAGCATTCGATTTCCAATGGTAAGTAACATAGGATACCCTGATTTTACCAACCAACCATAGACTATGCGGATGCAAAAATACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23228
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092456 Nonsense 1407 1467 12 12
ENSDART00000139188 None None 185 None 4
ENSDART00000139505 Nonsense 1293 1353 11 11
Genomic Location (Zv9):
Chromosome 18 (position 7127360)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7705050
GRCz11 18 7663985
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACCCTGCGGCCGTTCCACCAGAAACCCCTTCATCTGTGGAACAAGTA[C/A]GACGTGGGAGACTGGCTGGCCAGCATTAACCTGGCCGAACACCGGGATCG
Long Flanking Sequence:
GTAGACTCCTAACATAGCTGATGCTATTACTAAAATTGGGTTACAGAGAGACCATTTCTCTAAAAACATTTTAATTTGACTTTCACTCTCTGCCCCCTTCCATTTCTCTTTCTCCCCATGTTTTCAACTTTTAGACTCTTCAGCAGTTTGGGAGAGCTCCATACTATCTCTCAGAGAGGCTACGGCACCACCTACACCATCAGACCAGGCAGCCGCTACCCAGTAACCCGCAGGACTCCCAGTCCCGGATCCCCGGACCGCTCAGATCCTCTAGGACCCATCCGGGGTTTCGGCCTGGCCACGTCACCGATCACACCGCCCACCATCCTTAAGTCGTCCAGCCTCAGTCTCCCTCACGAACCGAAAGAAGTGCGTTTCGTCATGAGGAGCTCCAGTGCACGGAGTCGCTCACCCTCGCCGGCCCCTTCGCCAGGCATGACCTCCCCGCTTCTCACCCTGCGGCCGTTCCACCAGAAACCCCTTCATCTGTGGAACAAGTA[C/A]GACGTGGGAGACTGGCTGGCCAGCATTAACCTGGCCGAACACCGGGATCGTTTCCAGGAGCACGAGATCGAGGGCTCCCATCTGCCTGCTCTGACCAAGGAGGACTACGCTGAGCTGGGTGTGACACGTGTCGGTCACCGCATGAACATTGAGCGCGCCCTTAAACAGCTGCTGGAGAGTTGACCACGCGCCTCCCTCTGCCTGTAGCTAGTCTCAACACGGTTTACTTTTAAATTCCTACTTTATTTCATTTGGGGGGGGGGTTCTTGTGATTTCAGAGCTTTCAAGAAACACTCTATGTTTTTTTTTTGGAAGTGACCTGAAGTTAACAGTTGGGGTTTACCATTTTTGAAGCCTTTTAGCTGATCTCTGGGTCTGGCAGGAGCACTTTTAGTTTAGCTTAGCATAGATCATTGAATTGGATTAGACCATTACCATCTTACTCAATAAAAAAAACTGAAAATTATTTTTAATAAGCTTAATATTTTAAGCTTCTCGCT
Associated Phenotype:
Not determined