Busch Lab

ZMP

abca5

Ensembl ID:
ENSDARG00000074041
ZFIN ID:
ZDB-GENE-050517-5
Description:
ATP-binding cassette sub-family A member 5 [Source:RefSeq peptide;Acc:NP_001092716]
Human Orthologues:
ABCA10, ABCA5, ABCA6, ABCA8, ABCA9
Human Descriptions:
ATP-binding cassette, sub-family A (ABC1), member 10 [Source:HGNC Symbol;Acc:30]
ATP-binding cassette, sub-family A (ABC1), member 5 [Source:HGNC Symbol;Acc:35]
ATP-binding cassette, sub-family A (ABC1), member 6 [Source:HGNC Symbol;Acc:36]
ATP-binding cassette, sub-family A (ABC1), member 8 [Source:HGNC Symbol;Acc:38]
ATP-binding cassette, sub-family A (ABC1), member 9 [Source:HGNC Symbol;Acc:39]
Mouse Orthologues:
Abca5, Abca6, Abca8a, Abca8b, Abca9
Mouse Descriptions:
ATP-binding cassette, sub-family A (ABC1), member 5 Gene [Source:MGI Symbol;Acc:MGI:2386607]
ATP-binding cassette, sub-family A (ABC1), member 6 Gene [Source:MGI Symbol;Acc:MGI:1923434]
ATP-binding cassette, sub-family A (ABC1), member 8a Gene [Source:MGI Symbol;Acc:MGI:2386846]
ATP-binding cassette, sub-family A (ABC1), member 8b Gene [Source:MGI Symbol;Acc:MGI:1351668]
ATP-binding cassette, sub-family A (ABC1), member 9 Gene [Source:MGI Symbol;Acc:MGI:2386796]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa12201 Nonsense Available for shipment Available now
sa30964 Nonsense Mutation detected in F1 DNA Not yet available
sa44774 Nonsense Mutation detected in F1 DNA Not yet available
sa15733 Nonsense Available for shipment Available now
sa22162 Essential Splice Site Available for shipment Available now
sa42088 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa22163 Essential Splice Site Available for shipment Available now
sa35362 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa12201
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
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112302 Nonsense 2 1673 1 39
ENSDART00000127464 Nonsense 2 1673 1 40
Genomic Location (Zv9):
Chromosome 12 (position 40351448)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 38633191
GRCz11 12 38807692
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAAACAACAACGCRAATCTGGAGGACAGGAAAGACATGTCTTAATGTA[T/A]TTCATACGTAAGTGCGCTTCTTTGTTTARGCATGAGGGAAAGCTRTTAGC
Long Flanking Sequence:
GTATATTTTATATTTCAATTGAAATGTTTTTATACATTTATATACATCACATTTTAGATTATTCATTCAAACCCTTGTAATATTATTTGCACAATATAACCCGCTTTAATATTTAATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACTACGTACACAGTACAGTTCATAGCAGCTGCCGCCAGATGTGTTGTGATGACGTCAATCACAAACTAAAAGACCAATCCGCGCAGTCTTACAAGTTCTGAGTCTCGGGATTGGCTCCCTCGGTACCGACGAATCCCGAGTCTAGTAACTTGTAGGGCTGCACTGATTGGCTGACTGACTGGTCGGTCCAGCTGATGGCAGAGGCGCAAGTAGTGTTGACAACGCCGCCCTGGATCTCTTCTGTTTTTATTTATTTCCCAAAGGTTTTTTATTTGGAAACAACAACGCAAATCTGGAGGACAGGAAAGACATGTCTTAATGTA[T/A]TTCATACGTAAGTGCGCTTCTTTGTTTAGGCATGAGGGAAAGCTGTTAGCCAGTTAGCGTTAGCTGTCAGTGTTTACACAATGATAGCAGGGAACAAAACTCACACTTGCATCGACAATTTGCACGTTTGGCTCGAATATTGTATATTAACTAGAAGAACACATTGGTTATCTACATTTAAGAAAATAGGAAGGGGCGAAAGCCCAACCCAGTCGTTATTGACCTGCACCGCGCGCGCTTGCGAGCACGCGCAACACGTCGGGTGCACGCGACCTCCTGCACGCGCAGAAATATATAAATATATTCTGCATAGAAATTGCAGTTTGACTGACTGTACATCGTAGTATTTAGCAGCATTTGAGGTAAAGTTGGTTTAATATTCGCACATTCGTTTAGTGACAACTTGTGACATGCTCCCTATATTGTTTGCCATGGTTCTTTGAATATTCGGTCTAAAATATGTAAGGATGACTTTAAAACAACATCAGCACTATTTATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30964
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112302 Nonsense 51 1673 2 39
ENSDART00000127464 Nonsense 51 1673 2 40
Genomic Location (Zv9):
Chromosome 12 (position 40353118)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 38634861
GRCz11 12 38809362
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAGGAGCCTGCTCTACAAAAACCTGCTGATCAAATGGAGGACCAAACAA[C/T]AGAGTCTCCAGGTGCCTTTCATCTACCAATCACTTGCTTTCTTTTTCCCT
Long Flanking Sequence:
TCGATTGCTAAACTTTAGTCTCATTACACTAAGTAATGCTATAAATGTAAAATCACTTATTTTGCTGCTAAATCTAAATATGTATTTTCTGTGTAAAAAAAAAAATGTTGTTTTCATTGTTAAGTTAAACACAAAGTTTAAAAAAAATCCTGAATGAGCTGTATTGTAAGGTCAATTGTCAAACGAAAAACAAATTAGAAAGTCTGGGCTTTGCAGCATCTTTTTTGACACGCTGTCATGTGCATTGCTGACTAAACAGTATAAATAATGATTTGTGAGGAACCATAAATATAAAAAGAACAGATTTAAAGCAAATAAATCTGCTCCTGGTTTGGATTGAGAAGGTTTTGATGTGTTTTGCAGCGGTGTCTGATCCATGTGGCAGTCAGCTGAAGCATGCTGGAAGAATGCAGCCCTTAACCAGAAGAGATGCCGGAGTCTGGCATCAGACGAGGAGCCTGCTCTACAAAAACCTGCTGATCAAATGGAGGACCAAACAA[C/T]AGAGTCTCCAGGTGCCTTTCATCTACCAATCACTTGCTTTCTTTTTCCCTCTTGTAGGTGCAAATCTGTTGCACGATTAAAGCTTTTGCAAGTTTCGTCAATGCGCTGGTATTCTACACCCTGTGAAGGTTGAACAGTGAAGCATACACTTCTCAGGAAAGGCTTGAATGATTTTTATTCTATTAAAATTCAATCTTTCGTGTCACATTACTCAGTGGGGATTTTTCCTGTTGTATACAGCGTTCCAGTTGTTATTTAATCCAAAAAGAAGTTGTATAGCAAAACTAGTATATGTGTAGTACATGCCAAATTTCACCTGATATTTAGAGCTAAATGAATGTATTATCATTATTTTACTTTCACATAATCTCTCAGAAAAAAATGGTATAATGTTTTACCAAAGAAGGTGCCAACTCTTGTCACTGGGGCAGTACCTTTTTATGGAACAGAATTATACCTTAGAACAAAGGCCCCGTTTGCACTAGTGCGTTTTGTTTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44774
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112302 Nonsense 519 1673 11 39
ENSDART00000127464 Nonsense 519 1673 11 40
Genomic Location (Zv9):
Chromosome 12 (position 40373876)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 38655619
GRCz11 12 38830120
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCAATATCCGAAAAATTTATCGGGAGAAGGATACCAAAGTGGAGGCTT[T/A]AAGAGGTGAGACTACCCACCTTTAATCTATCTTCATGACCAAGCATTATG
Long Flanking Sequence:
ACTCCTCTACAAGATTATTACAATCACTTTGGAATCACTCAATTCCAAATAGAGCTAATAAAGTCATCTGCTGAAATCGTATCCAATATCACAATATAAATCGGAGAAAAATGAAATGTCGTTTTTGAAATTTCCAAATGTGTGCAGGCTTAGTTAAGATATTTCTTTTTTCAGTATATGAAGTATATGTAAACTCAATGGCGTTTTAGTTGGTGTCTTCTTTTAAATCACTGTTCACATTTGACCAAATGTATTTTGTATATTTGATGTTGTGCAGTGATTTAGGGAGCAGTTTGGGAAAGGGACCAGTGTTTTTTTAGATTTGATGTGTTAAAATCCTTCAAAGCCCTGGGTAGATTTGGGCTTCGAAGAGAGCTGGCATGCAGCCAGAATGACCATTTAATATCCATCACAAGCTTTCTGTGTTTATATTTTTATTCCTGTTAGGATTTGCAATATCCGAAAAATTTATCGGGAGAAGGATACCAAAGTGGAGGCTT[T/A]AAGAGGTGAGACTACCCACCTTTAATCTATCTTCATGACCAAGCATTATGCAGCTCTTGAGCAGTATTGATGTCTAAAATGATTCCTGTGTATTGCTGATTAAATGTTTATTAAATAGATAGTTCACCCAAAAAATTAAAATTTTACTCTCCCTCAAGTACACTAGGTTGACTCCTAGTATTTATTATGTATTTATTATTATGTATTTATTGAATAATGATTCACCACAAACTTGTAATTACTTTCAAGTGGCTCTCATGATGAAAACATATTTTATTAAAATGTCAGTTTACGTACAATTAGACCTTAAGATTTTTATAGTCAAAGTATTTTGGATTATTTTAGAAAAGGTATCACCAGGAAGAACTTTAAGTTATCAAATATTGAAATGAAAAAAAAAAAAACTTTTAATATACAACTTTTATAATATACTTTTGATATATTTTTATTTAACTTTTAATATACATTTTTTGTGAATTTTATTTATTTCTATGTATGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15733
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112302 Nonsense 694 1673 15 39
ENSDART00000127464 Nonsense 694 1673 15 40
Genomic Location (Zv9):
Chromosome 12 (position 40378304)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 38660047
GRCz11 12 38834548
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTACTGAAGAGCCGTAGAGCAGGCAGAGTTACWGTTCTCAGCACTCACTA[T/A]ATGGATGAGGCTGATATACTTGCAGGTGCTTCTCTCATTTTTCTCTTCCA
Long Flanking Sequence:
ATCATTCCAATGCGTTTTTTAATGGTTATGAAATCTTTATTTATTTAATATTTTATTATATAAAATTTCATTTCAAACATTATTATACATTTATTATTCAATAATTCAATAAATGATTTTCCAGGCATCTTTTTTTTGTGTGTGTTTTCTGCTTTAAAATATCTCTCTTTTTAAGGTAAGGAAAGTTCTAAAGGATCTGGATTTGGAAAAGATTATGGATGCTCTGGCAAAAAACCTCAGTGGAGGCCAGAAGAGGAAGCTCTCTGTGGGCATAGCCATTCTTGGAGATCCCAAGGTAAACGTCTGACAGCTTATAACTCTGACTTGTTGATCCGTTATCTTATTTATCCATCTACTTCAAATTTTTTTTTTTCGTTTATGAATCAGATCCTCCTTTTGGATGAGCCTACAGCTGGTATGGACCCAGTGTCTCGGCACCAGGTTTGGTCTTTACTGAAGAGCCGTAGAGCAGGCAGAGTTACAGTTCTCAGCACTCACTA[T/A]ATGGATGAGGCTGATATACTTGCAGGTGCTTCTCTCATTTTTCTCTTCCATCAGTCATTTTCTCAGTCTCTTTTCTCATGCACCTCTCTGTGTTTTCTGTAACACAGATCGTAAAGCTGTCATCTCGCAAGGACAGCTCAAGTGTGTTGGCTCTTCTTTGTACCTGAAGACCAAGTGTGGAGTTGGGTATCATCTTAGGTTAGTTTGGTATTTGTTCTAATGTAAAATACTATTGTGTTGTATTATAAAGTCATGGTTTGGCATGTGTTTAGGGCAGCAGGCTGGAAAAACTCTTATGTCCTAAAGGGATAGTTCACCCAATATTGAAACTCAAGTGGCTCCAAACATTATTTCTTACTTCTGTTGAACACATAAGAAGATATTTTGAAGAAAGTTGAAAACCGGTAACCATTGACTTCTATAGTAGAAACAATACTATGGAAGTCAATGGTTACAGGCTTCCAACATCTTTCGAAGTATCTTTTTTGTGTTTAAAAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22162
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112302 Essential Splice Site 1031 1673 22 39
ENSDART00000127464 Essential Splice Site 1031 1673 22 40
Genomic Location (Zv9):
Chromosome 12 (position 40387218)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 38668961
GRCz11 12 38843462
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATAATGGCACTGGACACATTAGAACATGGTCCAAACCCTTTGATTATG[T/G]AAGTGCAGTGCTCTAAAACATCAAAGTCAACACATTAATTTTGCGGTTTT
Long Flanking Sequence:
ATGTTATTTTCTTTTGTTGTTTTTTTTTTGTAGCAAATAAAACTAAGAGAGCTAAACTACAAGTGTAAACACTCTTAAAATAACTGCTAATAATTGGATTGTTTATTTGTTTATTTATTTATTTTATTTTATTATATTATTTATTTTATTTTAATATATATGAGAGTAGTAAGATTTATTTACAGATAAGTAACATATCTTAATTAATTTTTTTATTTATCTCATTTATTTTGTTCATATTTATTTCATATTTATTTATTTATTTACTAATATTTTTTATTATATATTTTTTCTTTGGCATTTTAAAATGTTTGTTGTCCCATCTCTAATCCTTTCTTTGTTCTCTTTGTGTGACTTACAGGATTTTACCTACATTTTAGCGTTTAACAGCACCACTGTGCACTCTTTGCCCATGGCTGTGAATGTGCTCAGTAATGCTCTCCTGAGAGGTTATAATGGCACTGGACACATTAGAACATGGTCCAAACCCTTTGATTATG[T/G]AAGTGCAGTGCTCTAAAACATCAAAGTCAACACATTAATTTTGCGGTTTTCTGTTTCTAGAAACATTTTGTTTGTGTTTTTAGCAAATTCCAGATAAAACATCTTATGCACTGGTTTACATTGAAGCTGTGATTCTTGGGATGCTGGCTGCTGGGATGCCAGCTTACTTCGCAATGGACCACACAAGAGACAGAGAAGTATGTCGTTTGGGTTGTAATTTATTTCAATTGACCATTTAAATTTAACTAATAAAACACATTCTTAGTTATGCATATACAGATCTACAGTACTTTTTACTATAAACTCTAAAGAGTTAGAGTTAATAATCTTTCTTTGTATTATAAATTAATTCTATTATTTATATGAAATATAAATTGGACAAAATTAAAATTAAGCAAAACAACTTTTTTTACACTTTCATTTTTTTCTATAAATTATATGAATTGTCCTATATATATAAAAAAAAACAATCCTCAAAAATATTAGGCTATGCAGCACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42088
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
ENSDART00000112302 Essential Splice Site 1491 1673 34 39
ENSDART00000127464 Essential Splice Site 1491 1673 34 40
Genomic Location (Zv9):
Chromosome 12 (position 40394276)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 38676019
GRCz11 12 38850520
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGATGAACCATCTACAGGGATGGATCCTAAATCAAAACAACGCATGTG[G/A]TAAATTTCCCTTCACATGCTCTTTATACAAAATAAATCATAACTTAATAT
Long Flanking Sequence:
CACATCCTGCAAATATCAAGGGGTAAATGCTGAATAATTGCATCGTCATGGTAACCAAACTATAATTTGGTCATTAACAATGTGCTTTCATAGCTAATTAAGAATGATTTATGGCCAGTAATGTTTTTCTAACCTTTGGCCAATCTGTTTGGTTTTGCTAATTATTTTGATTATGTATCGCCCACATTAAACATTATATAATATGACCAACACTGTAATGTTTGATGTTTTTGTGTGTTAACAGTGTTGTGAGTGCTCTTGAGCTTAAGGATCATCTTTACAAACAGTCAAAAAACTTGTCTGCAGGGCTAAAGAGGAAGGTGAGTCCTACATTTAAATAAATATAAAATATAAAAAAGCTGACTTTGTCTAACGTTTTTTTAAATATATATTTTTCCATACCAGTTGTGCTTTGCACTAAGCATGCTGGGAAATCCTCAGATAGTTTTGTTGGATGAACCATCTACAGGGATGGATCCTAAATCAAAACAACGCATGTG[G/A]TAAATTTCCCTTCACATGCTCTTTATACAAAATAAATCATAACTTAATATATGGTCAGAAATGTACATTTAAACTGCAAGACTGCTAAAATTTACTGTTTTTTTTTCCTAATAGGAGAGCAATCCGTGCTGCTTTTAAGAACAAACAGCGAGGGGCACTGTTGACCACCCATTACATGGAAGAGGCAGAGGCTGTGTGTGACCGTGTGGCGATCATGGTATCTGGTCAGCTGAGGTAAACACTGACTACAACTAAAGATCTCAATTTTTAAAAAATGTTATGCAAATGAATTTGAAGCAAGTCCATAATTTGGAATAGAAAGCCCTTTTTTGTTGCCCCCCCTGCAGGTGTATTGGCTCAATCCAGCACCTGAAGGGGAAGTTTGGCCGAGGATACAGCCTAGAGATTAACCTCAGGGAGGAGCTCACAGGTCTCCAGCAGGTAGCGCTGTTGCACAAAGAGATACTGAAGATATTTCCCCATGCTGTTCGTCAGGACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22163
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112302 Essential Splice Site 1608 1673 37 39
ENSDART00000127464 Essential Splice Site 1608 1673 37 40
Genomic Location (Zv9):
Chromosome 12 (position 40394979)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 38676722
GRCz11 12 38851223
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGGAAGATGTGAAGTCTTTAGCCAAGTCTTTTGCCCAGTTAGAAAGTG[G/A]TAAGAGATGGACACCATAACAATGAGAAGAATTTGAGAAGAATTGAAAGT
Long Flanking Sequence:
CGTGTGGCGATCATGGTATCTGGTCAGCTGAGGTAAACACTGACTACAACTAAAGATCTCAATTTTTAAAAAATGTTATGCAAATGAATTTGAAGCAAGTCCATAATTTGGAATAGAAAGCCCTTTTTTGTTGCCCCCCCTGCAGGTGTATTGGCTCAATCCAGCACCTGAAGGGGAAGTTTGGCCGAGGATACAGCCTAGAGATTAACCTCAGGGAGGAGCTCACAGGTCTCCAGCAGGTAGCGCTGTTGCACAAAGAGATACTGAAGATATTTCCCCATGCTGTTCGTCAGGACAGGTGAGATGGGTTTAATTAAATGAGAAAAGGTTTAATCAAATGCACCAAAACAGAAATGTCTTTTTAAAAATGAGAATGTAAAATATTCAGTCGTTTTTTTTCCGATATGTTTTGGGTTGTAGTTTTGCCACTATGATGGTGTATAAAATCCCAATGGAAGATGTGAAGTCTTTAGCCAAGTCTTTTGCCCAGTTAGAAAGTG[G/A]TAAGAGATGGACACCATAACAATGAGAAGAATTTGAGAAGAATTGAAAGTACTATTTTAATCTTTAACCATTGTTTTTTTTTTCCTCCACAGCTAAACAGAACTTCAACTTTGAAGAGTACAACTTTTCCCAGTCAACTCTTGAACAAGTATGTCAAAATGTTCTTATTTAAAAAGTATTATTTTTGTCAACATTTTAAAATAGGCAAGGCAAACTTTATTTATAGAGCACAATTTTATACAACCGTAGTTGATCCAAAGTGCTTTACAATGAAATAAAATATTTAAGAAAATAAAATAAAACTTGTATTAAAAATATAAGGAAATCAAATAAATATGTATATATGTAATACTAAAATACAGATAAGAAATTACATGTATGAGTCACTCAAAAGCAAGGGAGTAAAAATAAGTCTTTAAATTAGATTTAAAAGTATCCAAGGATGGAGAAATCCTCATGTTCAATGGGAGACTGTTGCAGAGCCTTGGGGCCACAACACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35362
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112302 Nonsense 1644 1673 39 39
ENSDART00000127464 Nonsense 1644 1673 39 40
Genomic Location (Zv9):
Chromosome 12 (position 40398344)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 38680087
GRCz11 12 38854588
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTTTTCATGGAGTTTGCCAAGGAGCAGGAGAACGAGGAAGAAGAGGTC[G/T]GATCACTAAGCACGACTTTTCAATGGCAGAGACTGAGACAGGACGGCCCT
Long Flanking Sequence:
AATGCGGTCTCCTTTAGGTCGCTTTATAAATGAATAGAAAAAAAAATGGATGTCTTTGGAAAGATGACTGTAATTTAAAATTCAATGTAATAACGTTTTTGTTTTGTTTTTATTATTATTTTTATATACGCACACACATTGGTCAATTTGAATGTATTTTATTTTATGATTTATTTTAAATGTCTTTTCTGTTTAGCAAATGTTGCGGTGGGAAAGTTAATATTCTGTATTGTTTGCTGGGTTTTATAATATAATTCAAATCAATAAAAACAACCTTGGGAAAAAAAAAACATATAAAGTGTAAAAAAAAAAAAAAAAAGAATTAAATAAATAAATAAATAAAATAGTTGACAAGATCAGTTTACTGAAAATAATTAGGATTATTGCTTTATTTATCTCTGTCTACATAACCTGAACAAGAGAATTTAATTAACCATACACCCGTTCTGCAGGTTTTCATGGAGTTTGCCAAGGAGCAGGAGAACGAGGAAGAAGAGGTC[G/T]GATCACTAAGCACGACTTTTCAATGGCAGAGACTGAGACAGGACGGCCCTGTATCTATTAATCACGCTGACAGCATAGTACACCAGCTATGAACCAATCCTGTTCCCTGAAGCGTTCTGCCCTTGCCTCTTTCTCCTTTTCCTTCGTTCTGCATGTGCCGTCTTTTGCCTTAAGAGCCTTAAACCCATGGGACTCACAGGACAATCGACTCCAGAGACTCCAATGGCCACTAACGCACACTAATAACGTGTGTATGTGTGTGTGTGTTTATGTGGCTCTGGCACTGGCACTTGCTCAGAAGGAATCAGACACACGACTTGAGTGTCATCCGTTAAACACAGAGCTAGACTCGTCGTCATCTGTTTTTACAACGACAAAAAAAAAAAGATTTTATTTTTTAAACTCTCACTTCTACTTGTATCTATCAAGCTCACTGTTTTCTTGTGTCCATATAACACACGTCTATCACTGGGAAATGAATTTGCATGAAGCGGGTTCCA
Associated Phenotype:
Not determined