Busch Lab

ZMP

MAP1A (1 of 2)

Ensembl ID:
ENSDARG00000022045
Description:
microtubule-associated protein 1A [Source:HGNC Symbol;Acc:6835]
Human Orthologue:
MAP1A
Human Description:
microtubule-associated protein 1A [Source:HGNC Symbol;Acc:6835]
Mouse Orthologue:
Mtap1a
Mouse Description:
microtubule-associated protein 1 A Gene [Source:MGI Symbol;Acc:MGI:1306776]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa24659 Nonsense Available for shipment Available now
sa44280 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa19362 Nonsense Mutation detected in F1 DNA Not yet available
sa10906 Nonsense Available for shipment Available now
sa45851 Nonsense Mutation detected in F1 DNA Not yet available
sa1846 Nonsense Available for shipment Available now
sa6130 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38058 Nonsense Mutation detected in F1 DNA Not yet available
sa31110 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24659
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
ENSDART00000067321 Nonsense 475 2253 3 22
Genomic Location (Zv9):
Chromosome 25 (position 19863104)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 19275081
GRCz11 25 19373032
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAGCCTTCTAAGAAAGAAACAGACGAGCATGAGGATGTATCTGTAGTC[G/T]AAACAAAGAGTGACTCTGTCAAAGAGAACAAGGTTGAGAAAAAAGAAGAA
Long Flanking Sequence:
CCATCGAGCCCATCACTCTTTTCCACAAGATGGGTGTGGGAAGGTTAGACATGTTTGTCTTGAACCCTGTGAAGGACAGTAAGGAAATGCAGTTCCTCATGCAAAAGTGGGCAGGTAACAGCAAGGCCAAGACAGGGATAATTCTTCCCAATGGAAAAGAAGGAGAAATATCTGTACCATATTTGACATCTATTACTGCTCTCGTTGTATGGCTCCCTGCCAGTCCCACAGAGAAAATCGTAAGGGTTTTATTTCCTGGAAATGCACCACAAAACAAAATACTTGAAGGGCTCGAAAAGTTAAAGCACCTTGATTTCTTGCGGTATCCAGTAGCCACACAAAAAGACATAAATTCTGGTGTTTCACCTTCAGCAGTAAAACAAACAAAACTAAAGCAAAGGACTGACAGCAAAGAAAGTCTAAAGTCATCTCCCAAGACTCACACACCAGCCAAGCCTTCTAAGAAAGAAACAGACGAGCATGAGGATGTATCTGTAGTC[G/T]AAACAAAGAGTGACTCTGTCAAAGAGAACAAGGTTGAGAAAAAAGAAGAAAAGAAACACACCAAGTCATTGAAACCAAAAGCAGAAGTAACAGAAAAGAAAAAGTTATTGAAGGAAAAACCACTAAAAAAACACCCGAAGGAAAGGTTGTCCAAAATGGATGAAAAGAAAGACAAAGAAAAGAGGGAGATTAAGAAAGAAAAACGTGTAATTAAACAAGATGATTCAGTGAAAAAAGATGAGAAAAAAATGAAAGCCAAGGACAGTTCTAAACCTGAATTGAGGAAAATAACTAAACCTGAACTGAAACCTTTCACACCAGAGGTCAGAAAGACCCTCCATAAGGCCAAAACCCAAGGGAAACCCAAATCAATAAAGAAAAAACCTACAACTGCCAAGGCAGAGATTGCAGAGATTACAGCAGAACCTGTGGCCGAAAAGACTGAACCTGAGAAGCAGGAGAATGGGACTGTAGAAGATATATCTGCTCCGGAAGATTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44280
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000067321 Essential Splice Site 504 2253 3 22
Genomic Location (Zv9):
Chromosome 25 (position 19863013)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 19274990
GRCz11 25 19372941
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGAAGAAAAGAAACACACCAAGTCATTGAAACCAAAAGCAGAAGTAA[C/T]AGAAAAGAAAAAGTTATTGAAGGAAAAACCACTAAAAAAACACCCGAAGG
Long Flanking Sequence:
GTTCCTCATGCAAAAGTGGGCAGGTAACAGCAAGGCCAAGACAGGGATAATTCTTCCCAATGGAAAAGAAGGAGAAATATCTGTACCATATTTGACATCTATTACTGCTCTCGTTGTATGGCTCCCTGCCAGTCCCACAGAGAAAATCGTAAGGGTTTTATTTCCTGGAAATGCACCACAAAACAAAATACTTGAAGGGCTCGAAAAGTTAAAGCACCTTGATTTCTTGCGGTATCCAGTAGCCACACAAAAAGACATAAATTCTGGTGTTTCACCTTCAGCAGTAAAACAAACAAAACTAAAGCAAAGGACTGACAGCAAAGAAAGTCTAAAGTCATCTCCCAAGACTCACACACCAGCCAAGCCTTCTAAGAAAGAAACAGACGAGCATGAGGATGTATCTGTAGTCGAAACAAAGAGTGACTCTGTCAAAGAGAACAAGGTTGAGAAAAAAGAAGAAAAGAAACACACCAAGTCATTGAAACCAAAAGCAGAAGTAA[C/T]AGAAAAGAAAAAGTTATTGAAGGAAAAACCACTAAAAAAACACCCGAAGGAAAGGTTGTCCAAAATGGATGAAAAGAAAGACAAAGAAAAGAGGGAGATTAAGAAAGAAAAACGTGTAATTAAACAAGATGATTCAGTGAAAAAAGATGAGAAAAAAATGAAAGCCAAGGACAGTTCTAAACCTGAATTGAGGAAAATAACTAAACCTGAACTGAAACCTTTCACACCAGAGGTCAGAAAGACCCTCCATAAGGCCAAAACCCAAGGGAAACCCAAATCAATAAAGAAAAAACCTACAACTGCCAAGGCAGAGATTGCAGAGATTACAGCAGAACCTGTGGCCGAAAAGACTGAACCTGAGAAGCAGGAGAATGGGACTGTAGAAGATATATCTGCTCCGGAAGATTTAACAAAAGACTTAAATAAAATCAAACCCACTGAAGTGACATATCAGTCAGAATCCCCCAAAAGTGACCTTACTGTCTCTGAATTACCAGCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19362
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
ENSDART00000067321 Nonsense 774 2253 5 22
ENSDART00000067321 Nonsense 774 2253 5 22
Genomic Location (Zv9):
Chromosome 25 (position 19862063)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 19274040
GRCz11 25 19371991
KASP Assay ID:
554-6229.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGTTTGAAGAAGAGGACGTGATTGAAAAAGCTGAGCTGGAGGAGGCT[G/T]AAGATTTAGATGCCATTGCAGATGAAGAAATTAAAGAGCTCTCTCCTGAG
Long Flanking Sequence:
ATCAGTCAGAATCCCCCAAAAGTGACCTTACTGTCTCTGAATTACCAGCTGAGAAAGATATTGAACCCTCAAAGTCTGCAGAGGACAAAGTTGGAGAAACCGATATGGTGGAACAGAAAACTAAAGTGGAAGAAGTATCTGCATCAGCAGGAATTAAAGAAGTGTCATCAGCTGCTGTGAAAGAAAAAGATGAGTCCCAAACTTCAGAAATTGAGAAATTTGAGGATGAGGGTGCTGCAATTGAAGATGAAGATGAGGAAGAGATTGATATACAGCCTGTTAAGAAAAAGACTGACGATGAGGAGGAGGAAGATATGGGAATTGGAGATGAAGAGGATGAAGGGCCAGCAAAAGAAACTAAAGACCTGGAGGGAGTGGACAGAAAACATGAAGTTGAGGAAATGGAGAAGCAAAAACAAGTGGAGGAAAGAAGGATTGAAGCTGAAGACGAGCAGTTTGAAGAAGAGGACGTGATTGAAAAAGCTGAGCTGGAGGAGGCT[G/T]AAGATTTAGATGCCATTGCAGATGAAGAAATTAAAGAGCTCTCTCCTGAGAAAGTCAAAGACGAAGAGGATGCATACATGTCAAATGTTGGAGGTGTCACAGCTGGCATTACCTCTACAGCGCAAGGCGCTGCTGCAGCAGAAAACCTATCATACATCCAGGATGAAACCATCCCAGGTTACTCTGAGACTGAGCAGACAATTTCAGATGAGGAGATCCATGAAGAAGCAGAGGACAGGATACCACACCTTCAGTATGAAGTTGGAAGCTATGACGTCTCTGTCCCAGACCAACCAGGCTCATTTGATGCCATGCATGGAATGAGAGAAATGCAAGCTGCTGCAATGGGCAATGGAACCAGCAAAGTATTCATGGGTGCACAGGAACCAGCGATTTCTATCTACACCAGCATTCTTGCAGCTCCATTAGCTGAAGAAGAACATGTTTCTTCAGCGACATCCATAACAGAGTATGACAAACTGTCTTCTCTACCCACTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10906
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000067321 Nonsense 774 2253 5 22
ENSDART00000067321 Nonsense 774 2253 5 22
Genomic Location (Zv9):
Chromosome 25 (position 19862063)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 19274040
GRCz11 25 19371991
KASP Assay ID:
554-6229.1 (used for ordering genotyping assays)
KASP Sequence:
AGCAGTTTGAAGAAGAGGACGTGATTGAAAAAGCTGAGCTGGAGGAGGCT[G/T]AAGATTTAGATGCCATTGCAGATGAAGAAATTAAAGAGCTCTCTCCTGAG
Long Flanking Sequence:
ATCAGTCAGAATCCCCCAAAAGTGACCTTACTGTCTCTGAATTACCAGCTGAGAAAGATATTGAACCCTCAAAGTCTGCAGAGGACAAAGTTGGAGAAACCGATATGGTGGAACAGAAAACTAAAGTGGAAGAAGTATCTGCATCAGCAGGAATTAAAGAAGTGTCATCAGCTGCTGTGAAAGAAAAAGATGAGTCCCAAACTTCAGAAATTGAGAAATTTGAGGATGAGGGTGCTGCAATTGAAGATGAAGATGAGGAAGAGATTGATATACAGCCTGTTAAGAAAAAGACTGACGATGAGGAGGAGGAAGATATGGGAATTGGAGATGAAGAGGATGAAGGGCCAGCAAAAGAAACTAAAGACCTGGAGGGAGTGGACAGAAAACATGAAGTTGAGGAAATGGAGAAGCAAAAACAAGTGGAGGAAAGAAGGATTGAAGCTGAAGACGAGCAGTTTGAAGAAGAGGACGTGATTGAAAAAGCTGAGCTGGAGGAGGCT[G/T]AAGATTTAGATGCCATTGCAGATGAAGAAATTAAAGAGCTCTCTCCTGAGAAAGTCAAAGACGAAGAGGATGCATACATGTCAAATGTTGGAGGTGTCACAGCTGGCATTACCTCTACAGCGCAAGGCGCTGCTGCAGCAGAAAACCTATCATACATCCAGGATGAAACCATCCCAGGTTACTCTGAGACTGAGCAGACAATTTCAGATGAGGAGATCCATGAAGAAGCAGAGGACAGGATACCACACCTTCAGTATGAAGTTGGAAGCTATGACGTCTCTGTCCCAGACCAACCAGGCTCATTTGATGCCATGCATGGAATGAGAGAAATGCAAGCTGCTGCAATGGGCAATGGAACCAGCAAAGTATTCATGGGTGCACAGGAACCAGCGATTTCTATCTACACCAGCATTCTTGCAGCTCCATTAGCTGAAGAAGAACATGTTTCTTCAGCGACATCCATAACAGAGTATGACAAACTGTCTTCTCTACCCACTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45851
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
ENSDART00000067321 Nonsense 1065 2253 6 22
Genomic Location (Zv9):
Chromosome 25 (position 19861076)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 19273053
GRCz11 25 19371004
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAAAGGCATCGGTAGCATCTCCTAAGGAGGATATGTCTTTTAAAGAA[C/T]AAGCAATTCTCTCTTCCTCATCTCACAGTGTTTCTAAGCTTCCTGTTTCT
Long Flanking Sequence:
CTCTACCCACTTCCATTGCAGAAGATCAGTCAGTGGCATCAGTCACAGCACCTCAGACTGAAGACACAGGAAAAAGCTCCCTGGTCTTGGACACTGTTCAACCAATTACACAGACTGAGGCAACCCAAGGGAAAGACTACTTACATTCAGCTGGAACCATCTCACCAACATCCTCCTTGGAGGAAGACAAGTGCTTCAAGTCCTCTCCCTCTGATGAATCCCCTCCACTTCCCTTAGAAGGCAAAACTGAGGGAATTGAGATGGCTGCCCATTACGATGATGAAGAAGAGGATGAATATGATCAAACGCCAAATGTTGACATTTCACTTGAAAAGTTACAAGAAGGATATGCCTCACCAGATAAACTTGAACACAAGGACAAAGAAATGGACAAACCCAAAAGTCCTGTGCCCTTAGCTCCTGATATGTCAAAATCCTCTATTCCTGAGTCAGAAAAGGCATCGGTAGCATCTCCTAAGGAGGATATGTCTTTTAAAGAA[C/T]AAGCAATTCTCTCTTCCTCATCTCACAGTGTTTCTAAGCTTCCTGTTTCTGAAGCTAGTGTTTATCCAGAGGTAGAAGACCGGTGCGTTAGCCCTGATGACAGCACTGTAAAAATGGCATCTCCTACACATTCTGGACCACCTAGTGCTTCTCACTCTCCCCTTAGAATGTCACCGGTGGAAGGAAAGGATAAAGTGCTCCTTAAAGACACTCATCAAGAACAAGGAGTGCCAATTAGCCCTACTGAATTTAAATTTGAAAAGAAAAATGAAAAACAAGAATCTGACATTTTAGATGAGAAGGAAAAACCTCAAGCAGAGAAAGAAGAAAAAATTATTATTCAGAAAGCAGTCACTGCACCATCCCCACTAGTTGATGACTTCTTGGCTAAAAAGGAAAGTGAGTCAGTTCCACCACCAAAAGATGTAAGTGATACGAAGGAAATACCAGATCCAAGTGTTGAAAAGAAAGTTGAAGTTAAAGAGGGCTTAAAAGAAGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1846
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
ENSDART00000067321 Nonsense 1780 2253 15 22
Genomic Location (Zv9):
Chromosome 25 (position 19855936)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 19267913
GRCz11 25 19365864
KASP Assay ID:
554-1837.1 (used for ordering genotyping assays)
KASP Sequence:
TCTTCAAGATCAAATATCTTCGGCAGAGGAAAAATCWGAGGAAGATATGT[C/A]AAGCATTAAATCTGACAAAGATCATGTCTCTGATCCTAAGCATGTAGAAC
Long Flanking Sequence:
GAAAGAAGATACTAGTTCAGTCCAATCTGAGACATCCAAACCCAGCGATGACAAACATGAACCACAGAGAACTGATAAAAAGCCTGAAGTGTCTGAATCCCTAACTGCCACTCAAGCGCCCATGTCTGATGGAACTTACTCATCATCTTCATCTATTAGTTACTCTTCTTCAACATCTGCATCATATTCTACTGGCCAACATATAGGAGATGGGCTAGATACACATATTAATGTTCCTAGTTTTCAACTAAGGTCAGATGGGGACACTGTATCATATGAATACTCTTCCCTAAAAGAGGAAGAGTCACCCACTATGGATTTACCATGTTTAAAAAAGGACGAATACATGGAAGTCTCGGATCGAATGACACATGCTACGACAACAGCTGAATCAATATCTAGTCTTGCTAGGTTTTCTCCTCTCAGTCCCCTGGAGGAATCCAAATCATTTCTTCAAGATCAAATATCTTCGGCAGAGGAAAAATCAGAGGAAGATATGT[C/A]AAGCATTAAATCTGACAAAGATCATGTCTCTGATCCTAAGCATGTAGAACCACCTTTCTCAAAAATGCCAGAATCGGAAACTTCTAAGCATGCAGCTCAAACAACTGAGGTGGCATCTACAACATCTCTCAAGTTTGAGATAGCGCCTTTGGAGAAAGCTGACTCCAAGGAAAAACACTCAGAAGAAAAGTCCTCTGATGATGAGCCTGAGAATAATAAAAGCGATTTTGAGGAAGGAACACTGCCTTGCAGAATTGAGTGTGACAAATCATCTTCATCTGAGCAACACACTGATGCAAATGTACTCTCAACCAAAACATTGCATTCATTTGAGCTGAAATGCAGCTCTGAACCAACAGAAATGGCAAGTTCTCAAAACGTGCCAGTCATGGCATGTGGGACTCTGAGTACAAGCACACTAAGTGAACAAATCGTGAAGCAAGAATGGGAAGAGATGTCTGAAAAAATTAAAGACTTGCCTGAGAAAGTAGAAGAGAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6130
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000067321 Essential Splice Site 1817 2253 16 22
Genomic Location (Zv9):
Chromosome 25 (position 19855152)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 19267129
GRCz11 25 19365080
KASP Assay ID:
554-3709.1 (used for ordering genotyping assays)
KASP Sequence:
GAAAGCAAAGAAAARGACAAAGAGAGTAAAAAACAAACTGAAGAAATTAT[T/A]ATGGAAAAATATAGCAAAAAYGTACCYGAGTCTAGCCAGCATACTGCCAT
Long Flanking Sequence:
CAACACACTGATGCAAATGTACTCTCAACCAAAACATTGCATTCATTTGAGCTGAAATGCAGCTCTGAACCAACAGAAATGGCAAGTTCTCAAAACGTGCCAGTCATGGCATGTGGGACTCTGAGTACAAGCACACTAAGTGAACAAATCGTGAAGCAAGAATGGGAAGAGATGTCTGAAAAAATTAAAGACTTGCCTGAGAAAGTAGAAGAGAGATTTGACATGAAAGAAGAAACGTTGAGCCAGGCAAAATGTGAAGAAGTGATAGTAAAGCATAAAGAAATAGAGGATGAACAGATACATCCTGAAAAGAAGTGTGATGTGAGGTCAGAAAAGATGGGAGAGATCCTAGATGGCAAGAAATCAGAGAATAAGAGTGAAAGTGAAGGAAAACCCAAAGAGTCAGAAGAAAAAGAAGAGGTAAAACAAGCTGAAATCGTAGTAGAAAAGGAAAGCAAAGAAAAAGACAAAGAGAGTAAAAAACAAACTGAAGAAATTAT[T/A]ATGGAAAAATATAGCAAAAACGTACCCGAGTCTAGCCAGCATACTGCCATTTCTTCCACAATGGAACATGAAGATATTGTATGTCTAAAGGCTCCCCCTGGCTATGGGGAAGATGTTTATGAAGATATAGACAGGGAAGAATCGGATGAAGAGAGGGAAGTGAAGTATGATTCTAAAGAACGTCCATCAAGTCCACCATCAGGAGCGCAGGCTTGTTACGCTGAAGTCTCCAAGAAAGCAGATGAGGGATTCACTCGACCTTCTGACCTCAGTATGGAGGCCACGTCCTCTCATTCACCTTCACTTTTTAAACATCGTAAAGGGGATATTTCCCCATCCTTTATTAATCCAAGCCCACATGATCTGTCAAGTGAGGAGGGAGACGATGATGCCAGAAGTGATCATTCAAGAGATGATGATGGTGATGAGCGTGAGCAGCACTCTGTCAAAAGGAGATCCCACAAGCAACAACATCATCATCAGCAAAGTCGTCAGGAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38058
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
ENSDART00000067321 Nonsense 1820 2253 16 22
Genomic Location (Zv9):
Chromosome 25 (position 19855140)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 19267117
GRCz11 25 19365068
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGACAAAGAGAGTAAAAAACAAACTGAAGAAATTATTATGGAAAAATA[T/A]AGCAAAAACGTACCCGAGTCTAGCCAGCATACTGCCATTTCTTCCACAAT
Long Flanking Sequence:
GCAAATGTACTCTCAACCAAAACATTGCATTCATTTGAGCTGAAATGCAGCTCTGAACCAACAGAAATGGCAAGTTCTCAAAACGTGCCAGTCATGGCATGTGGGACTCTGAGTACAAGCACACTAAGTGAACAAATCGTGAAGCAAGAATGGGAAGAGATGTCTGAAAAAATTAAAGACTTGCCTGAGAAAGTAGAAGAGAGATTTGACATGAAAGAAGAAACGTTGAGCCAGGCAAAATGTGAAGAAGTGATAGTAAAGCATAAAGAAATAGAGGATGAACAGATACATCCTGAAAAGAAGTGTGATGTGAGGTCAGAAAAGATGGGAGAGATCCTAGATGGCAAGAAATCAGAGAATAAGAGTGAAAGTGAAGGAAAACCCAAAGAGTCAGAAGAAAAAGAAGAGGTAAAACAAGCTGAAATCGTAGTAGAAAAGGAAAGCAAAGAAAAAGACAAAGAGAGTAAAAAACAAACTGAAGAAATTATTATGGAAAAATA[T/A]AGCAAAAACGTACCCGAGTCTAGCCAGCATACTGCCATTTCTTCCACAATGGAACATGAAGATATTGTATGTCTAAAGGCTCCCCCTGGCTATGGGGAAGATGTTTATGAAGATATAGACAGGGAAGAATCGGATGAAGAGAGGGAAGTGAAGTATGATTCTAAAGAACGTCCATCAAGTCCACCATCAGGAGCGCAGGCTTGTTACGCTGAAGTCTCCAAGAAAGCAGATGAGGGATTCACTCGACCTTCTGACCTCAGTATGGAGGCCACGTCCTCTCATTCACCTTCACTTTTTAAACATCGTAAAGGGGATATTTCCCCATCCTTTATTAATCCAAGCCCACATGATCTGTCAAGTGAGGAGGGAGACGATGATGCCAGAAGTGATCATTCAAGAGATGATGATGGTGATGAGCGTGAGCAGCACTCTGTCAAAAGGAGATCCCACAAGCAACAACATCATCATCAGCAAAGTCGTCAGGAGGAAGGCAAAGAGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31110
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000067321 Missense 2114 2253 19 22
Genomic Location (Zv9):
Chromosome 25 (position 19854016)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 19265993
GRCz11 25 19363944
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGGGAGACTCAGGAAGAGGGCTGGTCAATGGCGTTAAGAGTAATGCAG[G/A]TACAAATTAAGTTATCAGATTTTATAGAGATGATAGAGCCTTGTCTTTGC
Long Flanking Sequence:
GACTGAGGAATGTCCATCAATTACAGCAGAAGGAAACCTTGACTCTGATGAAGATGCAGAACATCTTCCAGTGGACAAAATGTCTGCAGCTGGCGGCAGTGGAGGAAGCCATCATTCCTCCTCCCCGAGGAGCCACGATCCCCCTCCCATTCCAATGAAAGACCCACTTCCACATCCACCACACCCTGATGTGTGCATGATTGACCCAGAAGCACTTCTTAATGGTCAGATCCAAACAGAAAGACCAGTCAAGAAAGACCATAAAACAAATAGAGGTTTGAGGAAGACACTAGGAAAATCTGCTTCGCCAGCACGTAAGGGAGATGCAAAAACCAGAAGATCTACTACCCCAGTGAAACAGACATCCAAAGACTCCTCACCTCATACTCTCAAAAGAAAAGATTCAGAAAAGACATTTCGTTTGACAAAAATGTCTGAGACAGAGGGATCCAGGGGAGACTCAGGAAGAGGGCTGGTCAATGGCGTTAAGAGTAATGCAG[G/A]TACAAATTAAGTTATCAGATTTTATAGAGATGATAGAGCCTTGTCTTTGCTGACAAGTAAACCTTTTAATTTGAATTCATGCCGTACATTAAGTTATAATTCCTAAGTTCACTTGTAGCACTGATTTTAGTTTTTAATTTATTCATTTACTACTGCAATTTGATCCATTTAACAGTGAATAACAATAACAAACAAATAATATCTTGACTGCACAGCAATGGTATTGCATACTGTTGATATTAATCAATGTTATTTAACCAATGTTATTATTTTAGCTTCCAACCTGAAATCCAATGCTGGGACTCCACCAGGACCACCCATCTATGTCGACCTAGCTTACATTCCCAACCACTGCAGTGCTAAAAATGTAGATCAAGAGTTCTTCAAGCGAGTGCGAGCAGCATACTACGTTGTCAGTGGAAATGATCCAGGGAGTGGTGAACCCAGCCGTGCAGTTCTAGATGCACTCCTAGAAGGGAAAGCACAATGGGGCACTAATC
Associated Phenotype:
Not determined