Busch Lab

ZMP

mink1

Ensembl ID:
ENSDARG00000035360
ZFIN ID:
ZDB-GENE-060526-45
Description:
misshapen-like kinase 1 [Source:RefSeq peptide;Acc:NP_001083048]
Human Orthologue:
MINK1
Human Description:
misshapen-like kinase 1 [Source:HGNC Symbol;Acc:17565]
Mouse Orthologue:
Mink1
Mouse Description:
misshapen-like kinase 1 (zebrafish) Gene [Source:MGI Symbol;Acc:MGI:1355329]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa40516 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa20489 Nonsense Available for shipment Available now
sa20488 Nonsense Available for shipment Available now
sa40515 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa45216 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa20487 Essential Splice Site Available for shipment Available now
sa40514 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa11333 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa40516
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
ENSDART00000051233 None None 149 None 5
ENSDART00000051236 Essential Splice Site 213 1287 7 31
ENSDART00000082408 None None 156 None 4
ENSDART00000135260 Essential Splice Site 213 1270 6 31
ENSDART00000140337 None None 208 None 5
Genomic Location (Zv9):
Chromosome 5 (position 39958669)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 37758059
GRCz11 5 38358212
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAGTCATTGCCTGTGATGAAAATCCCGACTCCACCTATGATTACAGG[G/A]TAAAATGAGCTTCTGACTGTTGATGCACACTAAACTGTTCAAAAGTTTGG
Long Flanking Sequence:
CATTACCTTCAGTTTAGCTCTTATCTGATATGGAGATATCTGATTTGTGTAGCTGTATTTTGTGTGTGTTGTCTAGCCTATATCCTATATCCTTCATTTCGTTTAACAACTAGAGCAAAGCACCGAAGCTCATTAATGTAGGCCTGACACCATGACAAAAATATCTTCACATCACAACCTGAGGGAGAGTGTGGCGGAAGTGGAAGAGTCTGCGTGTGTGAGGTGGAAGAGATTAGCATAGATGAATATAAACATCTTGGCTGCGCAACAGGTTTCATAAGAGCGCTTGAAAGCAGAAATGGCCCTGTAATATTACAGACTCTGATTGCTTCCGCTTTTTCTTTTTTTTTCTTCTCACTCTCTGTGTAGTGGATTTTGGGGTGAGCGCACAGTTGGATCGTACTGTCGGCAGAAGAAACACTTTCATTGGCACTCCATACTGGATGGCCCCAGAAGTCATTGCCTGTGATGAAAATCCCGACTCCACCTATGATTACAGG[G/A]TAAAATGAGCTTCTGACTGTTGATGCACACTAAACTGTTCAAAAGTTTGGGGTCAAGAGTTTTTTTGAAAGAAGTCTTTTATGTTGAACAACATTGTTTATTTGATGTAAAGTACAGTGCAGGGTGTCCCCAGACTCTTCAAAATCTTAAATAAAAAAATAATAATAATGGTGTAGGCCTTAAAAAGTCAAAGAAATATTGTCCTAAATCATTTTAAACAGGTCTTATAATGTATTTTGAACAGATCTTATAATAGCTTTATAACTAATATGGTTTGATTATATTCTTTGCAATGTCCCCATCCCATATGGTCTATAAATAAACAGAGAACATTTAAACAAAAGTTCTCTGTGTATTTATAGACCATATAGGATGGAAACACTGACCTGGACAGACTGTTGTCCATAAATTTGGGATAATATATTTTTAGGAGTTATTTTATATGTTTCTGGATTATTTAGAAAAGTTATGTTGAAATAAATTGTGTATAAAACTAGGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20489
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051233 None None 149 None 5
ENSDART00000051236 Nonsense 451 1287 14 31
ENSDART00000082408 None None 156 None 4
ENSDART00000135260 Nonsense 449 1270 13 31
ENSDART00000140337 Nonsense 88 208 4 5
Genomic Location (Zv9):
Chromosome 5 (position 39931523)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 37730913
GRCz11 5 38331066
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCGCTGCTTAATGACTTATTAATTGTTTGTTCATGTGTGTGTAGGAGTA[T/G]AAGCGTAAACAGCTGGAGGAGCAGAGACAGTCAGAGAGGCTTCAGAGGCA
Long Flanking Sequence:
TTACTGTATACCCACTACACTGAAGAAGAATCGTACAGCTAAGACAAATGTTTTGCTTTTGTCGTTCAGTTGTACAATAAACACTGCTCAGACTCTTCAGTAAATGTGAGCTATGATCTTATATATATATAATGTAAAACTCAAATAATTACGTTTTCTGTGTGTGTAATAATTCACTAAAGGGATAGTTCACCCAAAAATGACAATTTCCTCATTTACTCACTCTCAAGCAATTCTAAAAACTTAAGATATTCTAAAGATTTTGGAAAAAAATAATATTATGGATGACAATGGCTTCAGTCTATCTTCCTTTGTGAACTATTCCTTTAATACACAATTGTTCGATTGCATGTTGTGAAGGGGTACGTTCTACGTTTATGTGTATATATGTGTATGCATGTTGACTGTGCAGTCCTTTTTTCCACCTGCAAACAACACAGTGCAGTGTATCTCGCTGCTTAATGACTTATTAATTGTTTGTTCATGTGTGTGTAGGAGTA[T/G]AAGCGTAAACAGCTGGAGGAGCAGAGACAGTCAGAGAGGCTTCAGAGGCAGTTACAGCAGGAACATGCGTATCTGGTCTCTCTACAGCAACAGCAGCAGCAGCAAGACAAGAAACCACAGATGTATCACTACAGCAAGAACCTAGAGAACAACAAACCAGCCTGGGCTAGAGAGGTACGCTCTCACCCCACTGAGGGTAAAAGCGCTCTAATAGTCCATTTCCACTAAGTGGTATAGTACAGTACGGGTGACCTTTATTAGGCTTGCATATCCACTGCCAAAATGGTACCAATGGTATGATTTTAATTGCAGATCAATGATAAATAGCTAAATAGCCTACTGCAATATCAGCAATTATATGAACAAAAATAAGTAAATGCAACATATACAGACCCTTACAGTCTGCGATATGTTACCAATTACAGTAAACTACACACATTTATTTCGTTTTTATTTGGGTTCAAAAACAAGACGAAATATAGCACAGTCAGTGCAAACCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20488
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051233 None None 149 None 5
ENSDART00000051236 Nonsense 461 1287 14 31
ENSDART00000082408 None None 156 None 4
ENSDART00000135260 Nonsense 459 1270 13 31
ENSDART00000140337 Nonsense 98 208 4 5
Genomic Location (Zv9):
Chromosome 5 (position 39931495)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 37730885
GRCz11 5 38331038
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTCATGTGTGTGTAGGAGTATAAGCGTAAACAGCTGGAGGAGCAGAGA[C/T]AGTCAGAGAGGCTTCAGAGGCAGTTACAGCAGGAACATGCGTATCTGGTC
Long Flanking Sequence:
AATCGTACAGCTAAGACAAATGTTTTGCTTTTGTCGTTCAGTTGTACAATAAACACTGCTCAGACTCTTCAGTAAATGTGAGCTATGATCTTATATATATATAATGTAAAACTCAAATAATTACGTTTTCTGTGTGTGTAATAATTCACTAAAGGGATAGTTCACCCAAAAATGACAATTTCCTCATTTACTCACTCTCAAGCAATTCTAAAAACTTAAGATATTCTAAAGATTTTGGAAAAAAATAATATTATGGATGACAATGGCTTCAGTCTATCTTCCTTTGTGAACTATTCCTTTAATACACAATTGTTCGATTGCATGTTGTGAAGGGGTACGTTCTACGTTTATGTGTATATATGTGTATGCATGTTGACTGTGCAGTCCTTTTTTCCACCTGCAAACAACACAGTGCAGTGTATCTCGCTGCTTAATGACTTATTAATTGTTTGTTCATGTGTGTGTAGGAGTATAAGCGTAAACAGCTGGAGGAGCAGAGA[C/T]AGTCAGAGAGGCTTCAGAGGCAGTTACAGCAGGAACATGCGTATCTGGTCTCTCTACAGCAACAGCAGCAGCAGCAAGACAAGAAACCACAGATGTATCACTACAGCAAGAACCTAGAGAACAACAAACCAGCCTGGGCTAGAGAGGTACGCTCTCACCCCACTGAGGGTAAAAGCGCTCTAATAGTCCATTTCCACTAAGTGGTATAGTACAGTACGGGTGACCTTTATTAGGCTTGCATATCCACTGCCAAAATGGTACCAATGGTATGATTTTAATTGCAGATCAATGATAAATAGCTAAATAGCCTACTGCAATATCAGCAATTATATGAACAAAAATAAGTAAATGCAACATATACAGACCCTTACAGTCTGCGATATGTTACCAATTACAGTAAACTACACACATTTATTTCGTTTTTATTTGGGTTCAAAAACAAGACGAAATATAGCACAGTCAGTGCAAACCTCTCATCTGTGTCTTTAATCTTCACCAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40515
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051233 None None 149 None 5
ENSDART00000051236 Essential Splice Site 653 1287 None 31
ENSDART00000082408 None None 156 None 4
ENSDART00000135260 Essential Splice Site 649 1270 None 31
ENSDART00000140337 None None 208 None 5
Genomic Location (Zv9):
Chromosome 5 (position 39924920)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 37724310
GRCz11 5 38324463
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGCACGACTGATGCATGATTTTTCTATAATTCCTAATTTCTCTCTCTT[A/C]GATTCCTCAGAGAACAGCCTCTATAGCCACTGCACTGAACACAAATCTCT
Long Flanking Sequence:
ATGACATAAATTTTTTCCCCACACACTCTTTAAAGGAAGGAAGAAGTACATGAGTTAGACACGGCTTTGTATATTTTGGATATTAGTCCTTTGGATCACTTGGCATTGTAATGTAGCATTTGTATTAGAAGCATCACTTTGGCCACCTCCAGATGATTTTCTTTTTGTATTCCCTACAGTAAGACAGTTTCGAGTTCTTCTTTCAGTTATTGATGTTATTTGTGAAAGTTTTCTCATTGCACCCTAATTTTTTTATTTCTTTTTAAAGCACTTATTGTTTAGTTTAGCAGAAGTTTCTCCCTCCACAAAGCATTATTGGGTGTGGGAAAAAAAATGTTGATGCAGGCTTTGTTAATCTAACTAAAAATCTTGTGCAAATAAACTGTGTATAGTCGCTAAATTAAGATACAACAGTAGATGTGTGCTAATTTGTCCTTGTAATGATTAACATCAGCACGACTGATGCATGATTTTTCTATAATTCCTAATTTCTCTCTCTT[A/C]GATTCCTCAGAGAACAGCCTCTATAGCCACTGCACTGAACACAAATCTCTCCTCTGGTATCAGACACCCAGTCCGAGCAAGGTAAAGTGTGTACCGTATATATATATATATATATATATATATATATATACACCCACGTTCATCTGAAGTGACACGACTCGTGTGACTGGCCTGACTCCTGCACCGTGTTTTCTTTCTGTGTCAGTAATCCAGATCTGAGTCGCAATGAGCGCTGGGAGAGAGGAGACAGCATGAGCATCATGTCCAACCTGCCACAGACCGGCTCTCTGGAGAGACACCGCATACTCAGTGAGTGTTGTATGCGACATGTTTTGCAAATATTGTGATAGCACATCTGCCCTCAAGCACAGTAAAACTTCAGATTGCCTAACTGTAAGGACAGCACATAACATAACCACAATAAAAAAATGTCTTGATAAAGTCCTCAAGGATTTCGCGAATTGAGTGATAACAGAATTTTATACAAGTAATGCCTGATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45216
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
ENSDART00000051233 None None 149 None 5
ENSDART00000051236 Essential Splice Site 677 1287 18 31
ENSDART00000082408 None None 156 None 4
ENSDART00000135260 None None 1270 None 31
ENSDART00000140337 None None 207 None 5
Genomic Location (Zv9):
Chromosome 5 (position 39924764)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 37724154
GRCz11 5 38324307
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATATATATATATATATATATATACACCCACGTTCATCTGAAGTGACAC[G/A]ACTCGTGTGACTGGCCTGACTCCTGCACCGTGTTTTCTTTCTGTGTCAGT
Long Flanking Sequence:
TTTTCTTTTTGTATTCCCTACAGTAAGACAGTTTCGAGTTCTTCTTTCAGTTATTGATGTTATTTGTGAAAGTTTTCTCATTGCACCCTAATTTTTTTATTTCTTTTTAAAGCACTTATTGTTTAGTTTAGCAGAAGTTTCTCCCTCCACAAAGCATTATTGGGTGTGGGAAAAAAAATGTTGATGCAGGCTTTGTTAATCTAACTAAAAATCTTGTGCAAATAAACTGTGTATAGTCGCTAAATTAAGATACAACAGTAGATGTGTGCTAATTTGTCCTTGTAATGATTAACATCAGCACGACTGATGCATGATTTTTCTATAATTCCTAATTTCTCTCTCTTAGATTCCTCAGAGAACAGCCTCTATAGCCACTGCACTGAACACAAATCTCTCCTCTGGTATCAGACACCCAGTCCGAGCAAGGTAAAGTGTGTACCGTATATATATATATATATATATATATATATATATACACCCACGTTCATCTGAAGTGACAC[G/A]ACTCGTGTGACTGGCCTGACTCCTGCACCGTGTTTTCTTTCTGTGTCAGTAATCCAGATCTGAGTCGCAATGAGCGCTGGGAGAGAGGAGACAGCATGAGCATCATGTCCAACCTGCCACAGACCGGCTCTCTGGAGAGACACCGCATACTCAGTGAGTGTTGTATGCGACATGTTTTGCAAATATTGTGATAGCACATCTGCCCTCAAGCACAGTAAAACTTCAGATTGCCTAACTGTAAGGACAGCACATAACATAACCACAATAAAAAAATGTCTTGATAAAGTCCTCAAGGATTTCGCGAATTGAGTGATAACAGAATTTTATACAAGTAATGCCTGATTTGGCATTGGTGTTTGGCATGACACAAGCATTTCAGTAGTCACTGCCAGTTTAACACAATAGCAAAACTCAATTTAGCTTAAACGTTTTTTAAAAAATTTACTCATTAATGCTTTTAATAATTGCATACAAGAATTAAAACATTAGCTTGATAATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20487
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051233 None None 149 None 5
ENSDART00000051236 None 926 1287 23 31
ENSDART00000082408 None None 156 None 4
ENSDART00000135260 Essential Splice Site 916 1270 None 31
ENSDART00000140337 None None 208 None 5
Genomic Location (Zv9):
Chromosome 5 (position 39915693)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 37715083
GRCz11 5 38315236
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAATGTACCAGCCATCAGGGGGTAGTGGAGATAACATTTCTGTTGGAGG[T/C]AAAGTGGTTAGTTTGGGTACGGAGATTTTAAGGGGATTTTTAACACAAAA
Long Flanking Sequence:
ATTAGTGTCCCACTATGCCTCAGAAGGATAAAGCCTTTATGTGCATGCTAGAAGCCAATATCATAGCACCAGTGTCAGCCCGAGTTTGTTTGTGTGTTTGTTTCTGTCAGACTCCAGAGAAGCGCAGTCATAATGGATACACCAACCTGCCTGATGTGGTTCAGCCTTCTCACTCTCCCACAGACTCGGCCTCCCACTCCTCCCCCGGGAAAGACTCTACTTATGATGTGAGTCTCTGCCCACTTCTGGAGCTTCAGTTACTCCACCGTTTATCATTTCATCAGCATGCCATCCAGCTTTTTTTTTTTGTAATTGATTCTTTATCTGATGTACTGGACAACAAGTGTGTGTTCAATTGGCTGACCGTGATCATGCTATTCATTTCAGTATCAGTCCAGGGGATTGGTCAAGGCCTCTGGAAAATCCTCTTTTACTACCTTTGTGGACCTTGGAATGTACCAGCCATCAGGGGGTAGTGGAGATAACATTTCTGTTGGAGG[T/C]AAAGTGGTTAGTTTGGGTACGGAGATTTTAAGGGGATTTTTAACACAAAAATGTAAATTCCTGTTTAAGTTTCTGTTTTGTTGAACCTAAATGAAGATATTTTGAAGCTTGTTGGAAATGGGTAACCATTGTCTTCCATAGTATTTGTTTTTCATACAACACATGTTAATGTTTACTAGTTTCCAACATTCTTTAGAATCTCTTTTTATGTGTTCAAAACAACAAAAAACTCCCAACTGGTTTAAAAACAAGTCAAAGATGAGTAATAGATGACAGAATTTTTGTTGAATTTTTTAGAATCATTTGTGGGTGAACTACCCCTTTAAGATACACTATTGTTCAACAACACAGGGTGTACTCTGTTCACTGCATTTACAATTACAGGAAAAACAAAAATATTAGCAAACATTAATTTTTAAGATAAATTTTATGATGTAAACTAATGTGAAAGATTTTTAAGTATAATTATTGTCTCATTAAGTAATTAGTGTCATTCAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40514
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
ENSDART00000051233 None None 149 None 5
ENSDART00000051236 Essential Splice Site 1031 1287 25 31
ENSDART00000082408 None None 156 None 4
ENSDART00000135260 Essential Splice Site 1015 1270 25 31
ENSDART00000140337 None None 208 None 5
Genomic Location (Zv9):
Chromosome 5 (position 39912318)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 37711708
GRCz11 5 38311861
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGCAGATGGATGTCCTGGAGGGACTGAACCTCCTCATCACTATATCAG[G/A]TTATAAAATGCTCTGTTCCTTATTTCACACACCCGTCTATCTTTGCCGGG
Long Flanking Sequence:
TTTAATGTGTTGACATGAACTTTGTTATCTTTGCACCAATTCCCTGAGCGTTCAGGAGGACTAGTTTGATGGCAGTGCCACCCACTGGCCAAAATGCATAAAATATGACCACAAAGCATGGTGGAATAAAGTGGCACAAGGTCAAATTTCTCCATAATACCCTTTTGAGCAGTGTACCGTTTTTTTCATCCACTCCTACAGAGAGTTTATTATATACAGTCAAAACTTTTCTACTTTAAATTCAGTACACCCCTAAAGCATGATAAACAGTTTTCTCAGAATAGCTCCATAGCACAGTCTGTGAGCATTTTAGGTCTTGAAGGGTGTGTGTGTTTTAACTGTGTATGTTCTGTCAGGTGTGAATCTGCTGGTCGGGACAGAGAATGGTCTGAAGCTGCTGGACAGAAGCGGTCAGGGTAAAGTGTATCCACTGATCAACTCGCGCAGATTTCAGCAGATGGATGTCCTGGAGGGACTGAACCTCCTCATCACTATATCAG[G/A]TTATAAAATGCTCTGTTCCTTATTTCACACACCCGTCTATCTTTGCCGGGACACATAGATATAGACCAGACCACCTATTTTAGGATCTTCATGTGTAGTTTCTCTCTTTTCTTAGGCAAGAAGAATAAGGTACGCGTGTATTATCTGGCCTGGCTGAGGAATAAGATCCTCCATAATGACCCAGAGGTGGAGAAGAAACAGGGCTGGACCACTGTAGGGGAAATGGAGGGCTGTGTGCACTATAAAGTGGGTAAGTGTGCATGTATGAGGTGCTTAATTATGCGCAAACCAAAAGAAAGTGATGAAAGATTGTGCTCAGCTGCTGCTTGGCGAATAAGCAAAAGTGAAACCGAATAGGTCAGAAGACATGAGGAAAGCTACTTTTATCTTAGAATTTTCCTCTCAACTCTTTTAAAGTGCTTTGTGCCTTGTAATAAAAGTGCTGTGAATGTCGTGTTTATTTTCCCAGTGAAATATGAAAGGATTAAGTTTCTGGTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11333
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
ENSDART00000051233 None None 149 None 5
ENSDART00000051236 Nonsense 1191 1287 29 31
ENSDART00000082408 None None 156 None 4
ENSDART00000135260 Nonsense 1174 1270 29 31
ENSDART00000140337 None None 208 None 5
Genomic Location (Zv9):
Chromosome 5 (position 39910543)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 37709933
GRCz11 5 38310086
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTCAGATGGGATGGAGATGCTGTTGTGTTATGAGGACGAAGGTGTTWA[T/A]GTCAACACGTACGGACGYATCATTAAAGATGTGGTGCTGCAGTGGGGAGA
Long Flanking Sequence:
ATCGTGGATGAAATGTGCTACATAAACTTGCCTTGCCTTAAAATTCTTTTAATTTACAATCTTATTATGTTTTTGTTGTTGTTAAAAATAATTAATATCATGCTTTTATTGATGTTTCTTAGTCATTTGGAGACCTGCCGCACAGACCTGTGTTGGTTGACCTCACAGTGGAAGAGGGTCAGAGGTTAAAGGTCATCTATGGCTCCTTGGCTGGCTTCCATGCCATTGATGTTGACTCTGGAAACAACTACGACATCTACATTCCTGTACATGTGAGTTATGTTGTCATGTGACACACCAAGAATACACTGGGTCAGTCAATTGGAAAATGCAGAGGAGAGTTTGATAGTGATTTATTTCTCCTATAAATCCATGTTCCTCTCTCTTGCTCTCGGTCTGCTGCTGTAGATCCAGTCACAGATCACTCCTCACGCCATCGTGTTCCTGCCCAACTCAGATGGGATGGAGATGCTGTTGTGTTATGAGGACGAAGGTGTTTA[T/A]GTCAACACGTACGGACGCATCATTAAAGATGTGGTGCTGCAGTGGGGAGAAATGCCCACATCAGTAGGTGAGTGTGTATACTAGATTAGAATAGATTCAACTTTATTATCATTACAAGTACAAGGCAACGGAATGGAGTTTAGATCTAACCAGCAGTGCAATAGCAACAAGTGCAGGATATAGCTATAAGCTATAAAGTGCAATTATAGAAAAACTATGGTAACATTAGAGCTAAAAAGGGCTTCGTCGCTGCCTATTTTTAAGTCCAAATTAAAGACGCATTTATTTTCTAAGTCTTTTTGAAGCATAAGTCCTTCCCTTTCAGAAGGGGGGGGGTGTTGGGAGTGGGGAGGGGGATAAAAACGGTCATGTTCTCTATCGTGTTTAGTGTTGGTCAACTGTGGTAGCATATTTTAATTAGGAAAAATATTGTATTATTATTATTACGATTTTTTATTTTTATTTACATTTTTGCTCTTTTATTGATAATTTTTCTATGT
Associated Phenotype:
Not determined