Busch Lab

ZMP

A2ML1 (4 of 15)

Ensembl ID:
ENSDARG00000041685
Description:
alpha-2-macroglobulin-like 1 [Source:HGNC Symbol;Acc:23336]
Human Orthologue:
A2ML1
Human Description:
alpha-2-macroglobulin-like 1 [Source:HGNC Symbol;Acc:23336]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa16120 Essential Splice Site Available for shipment Available now
sa32029 Nonsense Available for shipment Available now
sa42533 Nonsense Mutation detected in F1 DNA Not yet available
sa45535 Nonsense Mutation detected in F1 DNA Not yet available
sa42532 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa2817 Nonsense F2 line generated Not yet available
sa35872 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa24980 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa16992 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16120
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
ENSDART00000061098 Essential Splice Site 29 1452 2 35
Genomic Location (Zv9):
Chromosome 15 (position 20200239)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 21302865
GRCz11 15 21238597
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACATTAGAACATGRAAATTTAACAATACTGYAYGATTATTTCTTTCAAC[A/T]GATCTTTCATGGTGATATTTCCTGCTGTGATTGAGTCTGGATCTGAGGCC
Long Flanking Sequence:
TTAAGCAGACAGTCTACTAATACACAAATGGACCATCAAAAAAGTGTTACCAATAAATGTATTATTATTTATAACTTACAGAACAGGCAATTTACAATAATTAAAATGTATCCATTTAGCTTTTTTTCTATGGGTATTTGATATAAGAATTGTTTATTAAAGAATATTTCAATTATAACTTACGTTACAAGTGTCGATTGAACATTTATTTTCACCTAACTTTAATTTACACTATTATATTTTATATTTATATATTTTTTTAAATTATTACAAAATATAACACAAACATTTAATTTTAATTTCCAGTAAGAATTGAATTTCTGATGACATGAGTTTTGGACATCTGGAAAAGAGACCTTTCAGTATACTAGTCACTGTGTCGGACAGCTATCTCTTGCATTTATTTAGCCCCCCTGTGTTGCAATATAAGCCTTTGCGGAGTGAACTATTTACATTAGAACATGAAAATTTAACAATACTGCATGATTATTTCTTTCAAC[A/T]GATCTTTCATGGTGATATTTCCTGCTGTGATTGAGTCTGGATCTGAGGCCAAATTGTGTGCAAGTCTTCTGAATCCCAATGAAAGCCTCGTCATGAACATTTATCTGGTTCATGGGAACCAGAGCACATTACTGCTGCAGGAGAAAGCTGAGCAAGAGTTTCATCGCTGCTTTAACTTTAAGGTCTTTTACACAACAAAATGTATTAAATACAATTATTAAATGGTACAAATATAATAACTATGTATGTACATTTGCAATGCGTTTTGTTTTTGAGATGTAGAAGTTGTAAATACAGGACTTTATTTCTCATCAGGCTCCTCTAGCTGTAGCAGAATCAGTGCAGATAATGAAGGTTGAACTTCAGGGAGAATCCTTCAAGAGGACTGAGGAGAGAAAAGTCATGTTCAAATCTTACCACCCTTTGACCTTTATCCAGACAGATAAACCCATCTATATTCCTGGACAGACTGGTGAGTTGTGAATGTTTCAAAGAATAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32029
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061098 Nonsense 681 1452 16 35
Genomic Location (Zv9):
Chromosome 15 (position 20195136)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 21297762
GRCz11 15 21233494
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTGGGGCTGAAAATGGCTTCAAATTTGTTTGTGCGAGTCCCTGAGTG[T/A]CTGTCATACAGAGGCCTGACTTATCACAGAAAAATAGGTACCTGTACTGC
Long Flanking Sequence:
CAGTATAAAAAAAACTTTGTATCGTAGTAATCTACACTCGAGTGAAAAAAGATTATAATTGAATATGTCTGTTATAATCCATTTTCTGATATTCAGATTTTGGAAAATTAATGAATGAATTAGAAACAGTGTGTAAATGTGGTCTCATTGCAGATCTTCAACCTGCTGCCAGTTCAGTCGGTGTCATATTATCCATACAGTGTTGAAGATGAGCAGCCGTGTCTACATGTGAGACCCCGTCGATCTGTGCTAACAGACAACGTCTATGAAAACTTAAAGGTAACAGGTCGAATCCATGTGTGACAGTACAGATTAGAATCCTAGATTTGGTTTGGGTGAGTGAATACCAAACATACTTTAAGCGCACAAAAAGCCCTCTTGATATTTCAGACGTGATTATTCTGTATTTCAATTCAATTTGACAGATTTTATTTAATTTTGTTTTCACAGAGAGTGGGGCTGAAAATGGCTTCAAATTTGTTTGTGCGAGTCCCTGAGTG[T/A]CTGTCATACAGAGGCCTGACTTATCACAGAAAAATAGGTACCTGTACTGCTATTTATGTTCGTGCTGTTTGTTTTTGTTTGTTTTGAAACACACCTATTATTATATACACCATGAATCCAAAAGATACGGAGACCAGGAAGGGACGTGATGGTGAGGAAACAAATTGGTGGAAAAAAAATAATAATTGGTGAAAGAAAAAAAAAAACTGGGTGATAGGAAAACATATTTTAAAGTTTTTTTGCCTTCCCTCGCACAGACGTTTTGCATTATCTTGCAAAACTGTTTCTCCACAAACACTTCCTGTTCACTTCATTCATGTAAACCCTCACATTTTTGCCAAAATTCTCCCATATTTTAAATTTCTATCCCACTATCATCCTATAATTTAGTATTTTCCCATATTTCTGATATATTTTTAATCTTAAAAGCATGCTGAAAGTAATAATAAAATGTCTGCATTCACTTTCTTTACATTAAAGCTGTGCGTCGATCGTCGCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42533
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061098 Nonsense 1021 1452 25 35
Genomic Location (Zv9):
Chromosome 15 (position 20185845)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 21288471
GRCz11 15 21224203
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCATTAACCATTATGTCACTTAACAGGATACCAGAGACAACTGAACTAC[A/T]AGCATTTTGATGGGGCTTACAGCACATTTGGTTATGGTGATGGGAATACG
Long Flanking Sequence:
TTGACCTTTCTCTTGGTCCCTATGTAGCACCCGTCTAATCGGTCCGGAGGTCGAGCTAGGGGGACAAGCAATCTCGATCCTGACCTCCAAAGCAGCCCGGGTCATCAGTTGCACAACAGTCATGCCCTCACTGCTTGGGAAAACAGCTTGGCAGAAGTCTCTTCAGCCTCATGTAAGGGTCTTAAGTAAAAAAGATTAAAAAGTGCTTGCATTGTGTGTGTTGGCTATATACTCTACTAATGATTAATTGGCGGCACTTGCGAATCCAAGCTCTGCCACCTCATTGGCATTCATCGGGCCATTTACCTACTCGGATCTTACTTGATTGGTCGTATAGCTTACTCTCAAAGTATCTTTCCAGACACATTTCAGAGTTGCCTCTGAAGGGGAACTACTGAGACTGTTTGCTGAAAAATTTATTTATTATTAATGTCAGACACAAACTGTTGAAGCATTAACCATTATGTCACTTAACAGGATACCAGAGACAACTGAACTAC[A/T]AGCATTTTGATGGGGCTTACAGCACATTTGGTTATGGTGATGGGAATACGTGGTATATATATTTTCACTCTTTTGTTAAAAAGAAATAATGTCAAGGAGTTATTCTTAATAGTTTAAACTTTAACACAACCAGGTTGACTGCCTTTGTCCTGAAGTCTTTTGGCAAAGCTCAAAAATACACATTTATTGATCCACAAATTATTCAGAGTGCAAAGGATTGGTTAATAAGCAGACGGAATTCAGACGGCTGTTTTATCCAACAGGGAAGACTGTTTAACAACAGAATGAAGGTCTGTCTGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCACTATAGCAATATCTAGAAAGAAATCTAGTAACTAGGAAACTTAGCTTTTACTTTTAAACTTTTCTCTTTCAAACATTTAGGATTTGTCAAGCCAAGATAAATGTCTGTCTAAATTAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45535
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
ENSDART00000061098 Nonsense 1051 1452 26 35
Genomic Location (Zv9):
Chromosome 15 (position 20185674)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 21288300
GRCz11 15 21224032
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAACACAACCAGGTTGACTGCCTTTGTCCTGAAGTCTTTTGGCAAAGCT[C/T]AAAAATACACATTTATTGATCCACAAATTATTCAGAGTGCAAAGGATTGG
Long Flanking Sequence:
TGTAAGGGTCTTAAGTAAAAAAGATTAAAAAGTGCTTGCATTGTGTGTGTTGGCTATATACTCTACTAATGATTAATTGGCGGCACTTGCGAATCCAAGCTCTGCCACCTCATTGGCATTCATCGGGCCATTTACCTACTCGGATCTTACTTGATTGGTCGTATAGCTTACTCTCAAAGTATCTTTCCAGACACATTTCAGAGTTGCCTCTGAAGGGGAACTACTGAGACTGTTTGCTGAAAAATTTATTTATTATTAATGTCAGACACAAACTGTTGAAGCATTAACCATTATGTCACTTAACAGGATACCAGAGACAACTGAACTACAAGCATTTTGATGGGGCTTACAGCACATTTGGTTATGGTGATGGGAATACGTGGTATATATATTTTCACTCTTTTGTTAAAAAGAAATAATGTCAAGGAGTTATTCTTAATAGTTTAAACTTTAACACAACCAGGTTGACTGCCTTTGTCCTGAAGTCTTTTGGCAAAGCT[C/T]AAAAATACACATTTATTGATCCACAAATTATTCAGAGTGCAAAGGATTGGTTAATAAGCAGACGGAATTCAGACGGCTGTTTTATCCAACAGGGAAGACTGTTTAACAACAGAATGAAGGTCTGTCTGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCACTATAGCAATATCTAGAAAGAAATCTAGTAACTAGGAAACTTAGCTTTTACTTTTAAACTTTTCTCTTTCAAACATTTAGGATTTGTCAAGCCAAGATAAATGTCTGTCTAAATTAACATAAATGTATTGTGTTGCCTTACCCCAAATTCTCCTCTATCATAGGGTGGAGTGAATAATAATGTGACCATGACGGCCTACATTACTGCATCACTGCTTGAACTGGAAACTCCAGTCACAGTAAGTTCATCATCAGGAAACTCAGTATAAACTCTTAGTAAAATGATACTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42532
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061098 Essential Splice Site 1115 1452 27 35
Genomic Location (Zv9):
Chromosome 15 (position 20185223)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 21287849
GRCz11 15 21223581
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGGCCTACATTACTGCATCACTGCTTGAACTGGAAACTCCAGTCACAG[T/G]AAGTTCATCATCAGGAAACTCAGTATAAACTCTTAGTAAAATGATACTCG
Long Flanking Sequence:
TAACACAACCAGGTTGACTGCCTTTGTCCTGAAGTCTTTTGGCAAAGCTCAAAAATACACATTTATTGATCCACAAATTATTCAGAGTGCAAAGGATTGGTTAATAAGCAGACGGAATTCAGACGGCTGTTTTATCCAACAGGGAAGACTGTTTAACAACAGAATGAAGGTCTGTCTGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCACTATAGCAATATCTAGAAAGAAATCTAGTAACTAGGAAACTTAGCTTTTACTTTTAAACTTTTCTCTTTCAAACATTTAGGATTTGTCAAGCCAAGATAAATGTCTGTCTAAATTAACATAAATGTATTGTGTTGCCTTACCCCAAATTCTCCTCTATCATAGGGTGGAGTGAATAATAATGTGACCATGACGGCCTACATTACTGCATCACTGCTTGAACTGGAAACTCCAGTCACAG[T/G]AAGTTCATCATCAGGAAACTCAGTATAAACTCTTAGTAAAATGATACTCGCAGCATCTGTTTGTCTGTTTGTGTTTCAGGATCCTGTCATCACTAAAGGTTTGTCATGCTTGAGGTCTGTCATCGAGGATGTCAAAAACACTTACACCACTGCTCTGCTGGCCTACACTTTCAGTCTGGCCAGAGACACCAACACTCGACAGCAGCTTTTCAACAAACTGGAGGATCTTGCTATTTCAGATGGTAAGAGATTGCTTTCTGATGACTTTCTGCACTGCACTGTTGCTTTTGTCCTGCTGGTTGAGTTTGTCTTTTGTGTCCTAAAGGTCCTCTTGTCCACTGGTCTCAGTCTGCATCTGCTGATGACTCTGCTTCTCTGGATGTGGAGATCAGCTCATATGTGCTGCTAGCTGTTCTCACTGCAGATTCACTCACTACAGCTGATCTGGGCTTTGCTAACAGGATTGTCAGCTGGCTTGTGAAGCAGCAAAATGCCTATGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2817
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061098 Nonsense 1150 1452 28 35
Genomic Location (Zv9):
Chromosome 15 (position 20185041)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 21287667
GRCz11 15 21223399
KASP Assay ID:
554-3224.1 (used for ordering genotyping assays)
KASP Sequence:
TCAAAAACACTTACACCACTGCTCTGCTGGCCTACACTTTCAGTCTGGCC[A/T]GAGACACCAACACTCGACAGCAGCTTTTCAACAAACTGGAGGATCTTGCT
Long Flanking Sequence:
TCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCACTATAGCAATATCTAGAAAGAAATCTAGTAACTAGGAAACTTAGCTTTTACTTTTAAACTTTTCTCTTTCAAACATTTAGGATTTGTCAAGCCAAGATAAATGTCTGTCTAAATTAACATAAATGTATTGTGTTGCCTTACCCCAAATTCTCCTCTATCATAGGGTGGAGTGAATAATAATGTGACCATGACGGCCTACATTACTGCATCACTGCTTGAACTGGAAACTCCAGTCACAGTAAGTTCATCATCAGGAAACTCAGTATAAACTCTTAGTAAAATGATACTCGCAGCATCTGTTTGTCTGTTTGTGTTTCAGGATCCTGTCATCACTAAAGGTTTGTCATGCTTGAGGTCTGTCATCGAGGATGTCAAAAACACTTACACCACTGCTCTGCTGGCCTACACTTTCAGTCTGGCC[A/T]GAGACACCAACACTCGACAGCAGCTTTTCAACAAACTGGAGGATCTTGCTATTTCAGATGGTAAGAGATTGCTTTCTGATGACTTTCTGCACTGCACTGTTGCTTTTGTCCTGCTGGTTGAGTTTGTCTTTTGTGTCCTAAAGGTCCTCTTGTCCACTGGTCTCAGTCTGCATCTGCTGATGACTCTGCTTCTCTGGATGTGGAGATCAGCTCATATGTGCTGCTAGCTGTTCTCACTGCAGATTCACTCACTACAGCTGATCTGGGCTTTGCTAACAGGATTGTCAGCTGGCTTGTGAAGCAGCAAAATGCCTATGGAGGATTCTCCTCCACACAGGTTCCTCAAATCAGACACATTATTGCTGAATGGCTAAAATTGTCACATGATTGAACTTATTTCTTTCCCAGGACACAGTGGTGGCTCTTCAGGCTCTGTCTTTGTACGCCACCAAAGTGTTCAGCTCTGACGGCTCCAGCACAGTGACTGTACAGTCAGCAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35872
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
ENSDART00000061098 Essential Splice Site 1234 1452 29 35
Genomic Location (Zv9):
Chromosome 15 (position 20184703)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 21287329
GRCz11 15 21223061
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGCTTGTGAAGCAGCAAAATGCCTATGGAGGATTCTCCTCCACACAG[G/A]TTCCTCAAATCAGACACATTATTGCTGAATGGCTAAAATTGTCACATGAT
Long Flanking Sequence:
TCAGTATAAACTCTTAGTAAAATGATACTCGCAGCATCTGTTTGTCTGTTTGTGTTTCAGGATCCTGTCATCACTAAAGGTTTGTCATGCTTGAGGTCTGTCATCGAGGATGTCAAAAACACTTACACCACTGCTCTGCTGGCCTACACTTTCAGTCTGGCCAGAGACACCAACACTCGACAGCAGCTTTTCAACAAACTGGAGGATCTTGCTATTTCAGATGGTAAGAGATTGCTTTCTGATGACTTTCTGCACTGCACTGTTGCTTTTGTCCTGCTGGTTGAGTTTGTCTTTTGTGTCCTAAAGGTCCTCTTGTCCACTGGTCTCAGTCTGCATCTGCTGATGACTCTGCTTCTCTGGATGTGGAGATCAGCTCATATGTGCTGCTAGCTGTTCTCACTGCAGATTCACTCACTACAGCTGATCTGGGCTTTGCTAACAGGATTGTCAGCTGGCTTGTGAAGCAGCAAAATGCCTATGGAGGATTCTCCTCCACACAG[G/A]TTCCTCAAATCAGACACATTATTGCTGAATGGCTAAAATTGTCACATGATTGAACTTATTTCTTTCCCAGGACACAGTGGTGGCTCTTCAGGCTCTGTCTTTGTACGCCACCAAAGTGTTCAGCTCTGACGGCTCCAGCACAGTGACTGTACAGTCAGCAGGAGACTCTCACCACTTTGATGTCAATCAGGACAACAAGTTACTGTACCAGGAGAAGCAGCTGGCCAATGTGCCGGGCAAATACAGCATTGAAGTCAAGGGTTCAGCCTGTGTGTCTGTGCAGGTCTGTAGTTTCAGCTTTGTTCACTCACTTTTTTTTTTTTGCCATTTTGTGGTTATTCTACTTTGAGATGCTTTGATGATGGTTAAGAATGTGTTTGTTTTGACTCTCTCAGATGGCTCAGTTCTACAACATTCTCACTCCTACTGAAGCTAAAACATTAAGTATTGATGCTGAGGTTGAGGGAGATTGCAAGAAAACCTTTGGAAAAAGTCTATTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24980
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061098 Essential Splice Site 1306 1452 31 35
Genomic Location (Zv9):
Chromosome 15 (position 20184309)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 21286935
GRCz11 15 21222667
KASP Assay ID:
554-7531.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTGAGATGCTTTGATGATGGTTAAGAATGTGTTTGTTTTGACTCTCTC[A/T]GATGGCTCAGTTCTACAACATTCTCACTCCTACTGAAGCTAAAACATTAA
Long Flanking Sequence:
TCTCACTGCAGATTCACTCACTACAGCTGATCTGGGCTTTGCTAACAGGATTGTCAGCTGGCTTGTGAAGCAGCAAAATGCCTATGGAGGATTCTCCTCCACACAGGTTCCTCAAATCAGACACATTATTGCTGAATGGCTAAAATTGTCACATGATTGAACTTATTTCTTTCCCAGGACACAGTGGTGGCTCTTCAGGCTCTGTCTTTGTACGCCACCAAAGTGTTCAGCTCTGACGGCTCCAGCACAGTGACTGTACAGTCAGCAGGAGACTCTCACCACTTTGATGTCAATCAGGACAACAAGTTACTGTACCAGGAGAAGCAGCTGGCCAATGTGCCGGGCAAATACAGCATTGAAGTCAAGGGTTCAGCCTGTGTGTCTGTGCAGGTCTGTAGTTTCAGCTTTGTTCACTCACTTTTTTTTTTTTGCCATTTTGTGGTTATTCTACTTTGAGATGCTTTGATGATGGTTAAGAATGTGTTTGTTTTGACTCTCTC[A/T]GATGGCTCAGTTCTACAACATTCTCACTCCTACTGAAGCTAAAACATTAAGTATTGATGCTGAGGTTGAGGGAGATTGCAAGAAAACCTTTGGAAAAAGTCTATTGTTAAATTTCACTGTGACGTAAGAAGTGTAACTTTACACTATAAAACCTGATTATGGTTGTGGCTTTAGTTTATTCATCATTAACTCTGATGATTCTTGTGTTTGTGTTTTACAGATATGATGGTCCACAGGCCAAAACTAACATGGTTATTGTGGACATTAAACTCTTATCAGGATTCACAGCTGATACGTCAATGGTGTGTTTGACTGTTAAGGGATTTATTCGATGTATTGATTTACTGTGAACCGAGGCGTAGCGCAAAAAGGCAGAGGATGGTGGTGGGGGTGTGTCATGGTTCGGGAAGGATGAGGGAGCAAGGACTTAAATGCAACATAAGATGGCTTTTATTTATTAAAAACAAAACAAAAAGTCAACAAAAACCACCCTGATGGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16992
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
ENSDART00000061098 Nonsense 1347 1452 32 35
Genomic Location (Zv9):
Chromosome 15 (position 20184085)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 21286711
GRCz11 15 21222443
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTATTCATCATTAACTCTGATGATTCTTGTGTTTGTGTTTTMCAGATA[T/G]GATGGTCCACAGGCCAARACTAACATGGTTATTGTGGACATTAAACTCTT
Long Flanking Sequence:
GTTCAGCTCTGACGGCTCCAGCACAGTGACTGTACAGTCAGCAGGAGACTCTCACCACTTTGATGTCAATCAGGACAACAAGTTACTGTACCAGGAGAAGCAGCTGGCCAATGTGCCGGGCAAATACAGCATTGAAGTCAAGGGTTCAGCCTGTGTGTCTGTGCAGGTCTGTAGTTTCAGCTTTGTTCACTCACTTTTTTTTTTTTGCCATTTTGTGGTTATTCTACTTTGAGATGCTTTGATGATGGTTAAGAATGTGTTTGTTTTGACTCTCTCAGATGGCTCAGTTCTACAACATTCTCACTCCTACTGAAGCTAAAACATTAAGTATTGATGCTGAGGTTGAGGGAGATTGCAAGAAAACCTTTGGAAAAAGTCTATTGTTAAATTTCACTGTGACGTAAGAAGTGTAACTTTACACTATAAAACCTGATTATGGTTGTGGCTTTAGTTTATTCATCATTAACTCTGATGATTCTTGTGTTTGTGTTTTACAGATA[T/G]GATGGTCCACAGGCCAAAACTAACATGGTTATTGTGGACATTAAACTCTTATCAGGATTCACAGCTGATACGTCAATGGTGTGTTTGACTGTTAAGGGATTTATTCGATGTATTGATTTACTGTGAACCGAGGCGTAGCGCAAAAAGGCAGAGGATGGTGGTGGGGGTGTGTCATGGTTCGGGAAGGATGAGGGAGCAAGGACTTAAATGCAACATAAGATGGCTTTTATTTATTAAAAACAAAACAAAAAGTCAACAAAAACCACCCTGATGGGGACCAACATAACTATAACACAAAAGGGTAAACAAACTTGGCTGGGCTGGCAAGACAGGACTGGAGCAGGAACACAGGGGAGTGTAGAAAACAAACAGGCACAGGACAGCAGACATGAGGAGACTTTAAGCAGAAGTAAATGAACACACAAACAGATGAACATAATTAACTAATGATGGGTTAACAAGGAGGCTGGGACTAGACAATAGACAGGAGAGCACATGAC
Associated Phenotype:
Not determined