Busch Lab

ZMP

si:dkey-208b23.5

Ensembl ID:
ENSDARG00000058280
ZFIN ID:
ZDB-GENE-081104-362
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8JLM6]
Human Orthologue:
SPAG17
Human Description:
sperm associated antigen 17 [Source:HGNC Symbol;Acc:26620]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa21219 Nonsense Available for shipment Available now
sa41140 Nonsense Mutation detected in F1 DNA Not yet available
sa969 Splice Site, Nonsense Available for shipment Available now
sa9290 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa31634 Nonsense Available for shipment Available now
sa7123 Nonsense Mutation detected in F1 DNA Not yet available
sa18106 Nonsense Available for shipment Available now
sa27145 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa34341 Nonsense Mutation detected in F1 DNA Not yet available
sa21218 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa21219
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000081048 Nonsense 158 1612 5 42
ENSDART00000126551 Nonsense 166 1743 5 45
ENSDART00000129168 Nonsense 157 819 5 20
ENSDART00000137784 None None 413 None 11
Genomic Location (Zv9):
Chromosome 8 (position 13577832)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13023176
GRCz11 8 13060881
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTAACACAGAATATGAATATTTCAGGCCGTAGAGGAGAATGCTCATGTT[A/T]AAGTAGGACTGAATTCTGCCAATAAAGATCAGGGAGGTAAAGGAGCAGCA
Long Flanking Sequence:
TTATGAAGAAATTTACACTGGATTTCTGCTGTATAATACAAAACAACTTTCTACACAGTGATAACTGATAGTGTTTAAATTTTTGTGAATAATAGTGTATGCAACAAATATCAATAACAGGCATGTCCAAGCTCGGTCCTGGAGGGCCAGTGTCCTGCAAAGTTTAGTTCCAACCCCAATCAGACACACCTGGGCTAGCTAATCAAGTTCTTACCAGGCTTTCTAGAAACATCTTTGCAGGTGTGTTGAGGCAAGTTGAAGCTAAAATCTGCAGGACATCGGCCCTCCAGGACCGAGTTTGGACACCCCTGATCTATAACATGCCTGAGAAGTTATGTTTTTCTTTAATTGAGTTAAAGATTACATATTTATTTAGCAATAAATTAATTCTAATCTACAGTAGAAGAGTGTGCTTATGTTTTTTTTTTATTAACTATTTCTTAGATAAATAGTAACACAGAATATGAATATTTCAGGCCGTAGAGGAGAATGCTCATGTT[A/T]AAGTAGGACTGAATTCTGCCAATAAAGATCAGGGAGGTAAAGGAGCAGCAAAGGGGAAAAAAGTGGCTGACATTCCAGTTCCAACCAAAGACACCAAACTCAAACGCAGGGGGGAGGAGGAAAACACAATCAAATATATAGGTGAGGCATGACCACAGTTAACTAACCACCTTTATCAAAAAACAAGTCTGGTTTTGCACTGTTTATAGTGTTTTAATGTTCTCTTTAAACATGTCTGTCTAGATGATGAGCCTGATGATGGTCCACAGCAATACATTCTGATAGTGGGATTCTATGAACCCCTTCTGATTGCAGTGCTGGACTCAATGGGTATCCATGTGTCCAATGTTATTAAACTGGGTTTACAGAGAGATGAACATTCAGAGGCTCTAGAGGACACAGAGGCAGAGGAGGATCACCAGTCAAATGAAGACCAGGGCAAGATACTGTTTTTACATATATGTGTTCTGTTATAAATAACACAGTGCATGGAGAATGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41140
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
ENSDART00000081048 Nonsense 246 1612 6 42
ENSDART00000126551 Nonsense 254 1743 6 45
ENSDART00000129168 Nonsense 245 819 6 20
ENSDART00000137784 None None 413 None 11
Genomic Location (Zv9):
Chromosome 8 (position 13577466)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13022810
GRCz11 8 13060515
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGGACTCAATGGGTATCCATGTGTCCAATGTTATTAAACTGGGTTTA[C/T]AGAGAGATGAACATTCAGAGGCTCTAGAGGACACAGAGGCAGAGGAGGAT
Long Flanking Sequence:
ATTTATTTAGCAATAAATTAATTCTAATCTACAGTAGAAGAGTGTGCTTATGTTTTTTTTTTATTAACTATTTCTTAGATAAATAGTAACACAGAATATGAATATTTCAGGCCGTAGAGGAGAATGCTCATGTTAAAGTAGGACTGAATTCTGCCAATAAAGATCAGGGAGGTAAAGGAGCAGCAAAGGGGAAAAAAGTGGCTGACATTCCAGTTCCAACCAAAGACACCAAACTCAAACGCAGGGGGGAGGAGGAAAACACAATCAAATATATAGGTGAGGCATGACCACAGTTAACTAACCACCTTTATCAAAAAACAAGTCTGGTTTTGCACTGTTTATAGTGTTTTAATGTTCTCTTTAAACATGTCTGTCTAGATGATGAGCCTGATGATGGTCCACAGCAATACATTCTGATAGTGGGATTCTATGAACCCCTTCTGATTGCAGTGCTGGACTCAATGGGTATCCATGTGTCCAATGTTATTAAACTGGGTTTA[C/T]AGAGAGATGAACATTCAGAGGCTCTAGAGGACACAGAGGCAGAGGAGGATCACCAGTCAAATGAAGACCAGGGCAAGATACTGTTTTTACATATATGTGTTCTGTTATAAATAACACAGTGCATGGAGAATGGTGGATTTGGTATTGTGATGTAGTTGAGAAGGCTATTTTACATTTGTATGGATTTAAAAGATTCTCATTTTAACATTTCATCTGTATAGAAGTTGAGACTCTGAAGCAAAAAAGACAGCAGGAGCTAGATGTTTTCTGGAAGCAGTTGGATCAAGTCTTGAACAGTGAGAATATGGGATCCAGACTCAGTCATGTGGCCAGGTTGAACTATATTGTGAAGAGCCAGCTGCTACCCCAGGCTAAGTGTAACACTGAAGCAATGGAAAATAGAGATCAAGTACACATTTTTTGAACCACATACACTGTCAAAAAAGTTCTAAAAGCTGTTTTTTGCAGCAATGCCATGGAATCCATTTTGATTCCCAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa969
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000081048 Nonsense 722 1612 18 42
ENSDART00000126551 Nonsense 737 1743 18 45
ENSDART00000129168 Splice Site None 819 None 20
ENSDART00000137784 None None 413 None 11
Genomic Location (Zv9):
Chromosome 8 (position 13570678)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13016022
GRCz11 8 13053727
KASP Assay ID:
554-0874.1 (used for ordering genotyping assays)
KASP Sequence:
TGCACYATCATGAGMAATCAATTGATTTATAATATCCTATAAACTGATTA[T/G]AAAAAGGGTAAYGAAGTGACCCTGACAGACCTCCAGGAGACCCTAATTCG
Long Flanking Sequence:
TTTGGTTGCCTAGAAAATGTTTCTTGATTAAAGATTTTTTTAGATATTTGGACTAAAAAGAAGACAAAAAAATAAAAGAAAAGAATTTTTTTTTTGCAGTGTATGGTTTTGTTTCTTCATAGTCCTGCATTTTCCTCTTCTGTTATTTATCTAATGCACATGTAAATCTGTGGGCGGTGATAAACAGACTTTAACATGATCCTAAACATGATCCTCTGTGGAGGTGGAGTTTAGCCACATAATTACATAATAAATACGCACATTCCACAACCTGTTGTTTGTGACCCCTTTAAATACAAAACAAATATTTGACAAATCTTTAAAGCCTTTTGCCATTTTATATTTTATAGGATCAGCAAAACGCAGTGCTGAGAATGATGAACAAATGGTAGGATTAATGTTTTGAAACCAAAAGTTGACATTTCTATAAATACACTACACATTTATCTCTGCACCATCATGAGCAATCAATTGATTTATAATATCCTATAAACTGATTA[T/G]AAAAAGGGTAACGAAGTGACCCTGACAGACCTCCAGGAGACCCTAATTCGCCGACTGGAAGACTATAACTTTGTAGAGAAGCACAGTGCTGATGTTTTTCCCCAGGTAACAATCTTCAGAACACTATTTTCAATATTACTTTTAAAATCTATAAAACATTTAATTACAGATGAGTGTTTCTCTTTCAGGTCCTCCAATCTGCTTCCGAAATGTATAGATGTGTGGACACATTTCAGTGTAGAGACAATGCCGTGTATGTCATCTGCCACAATCCAATGAGCCAACAGAGGAGCTGCAAAGAATTCTGGGAAGGATCACTTCACACAGATGTGGGCTTCAGGTACTTTATCTCTTCTTTGAGATCACAAAATTATTTCAAAATTGATTTGCTATGTAATGACAATTTAGAATTAATTAGAATTTGAATAACTAATTTCTAATAACTAATTCATATTCTAAGAAATAATAATAGTACATACATTTTTAATATTTATTTTGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9290
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
ENSDART00000081048 Essential Splice Site 758 1612 19 42
ENSDART00000126551 Essential Splice Site 773 1743 19 45
ENSDART00000129168 Essential Splice Site 688 819 17 20
ENSDART00000137784 None None 413 None 11
Genomic Location (Zv9):
Chromosome 8 (position 13570491)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13015835
GRCz11 8 13053540
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACTTTTAAAATCTATAAAAMAWTTAATTACASATGARTGTTTCTCTTTC[A/C]GGTCCTCCAATCTGCTTCYGAAATRTATAGATGTGTGGACACATTTCAGT
Long Flanking Sequence:
ACTTTAACATGATCCTAAACATGATCCTCTGTGGAGGTGGAGTTTAGCCACATAATTACATAATAAATACGCACATTCCACAACCTGTTGTTTGTGACCCCTTTAAATACAAAACAAATATTTGACAAATCTTTAAAGCCTTTTGCCATTTTATATTTTATAGGATCAGCAAAACGCAGTGCTGAGAATGATGAACAAATGGTAGGATTAATGTTTTGAAACCAAAAGTTGACATTTCTATAAATACACTACACATTTATCTCTGCACCATCATGAGCAATCAATTGATTTATAATATCCTATAAACTGATTATAAAAAGGGTAACGAAGTGACCCTGACAGACCTCCAGGAGACCCTAATTCGCCGACTGGAAGACTATAACTTTGTAGAGAAGCACAGTGCTGATGTTTTTCCCCAGGTAACAATCTTCAGAACACTATTTTCAATATTACTTTTAAAATCTATAAAACATTTAATTACAGATGAGTGTTTCTCTTTC[A/C]GGTCCTCCAATCTGCTTCCGAAATGTATAGATGTGTGGACACATTTCAGTGTAGAGACAATGCCGTGTATGTCATCTGCCACAATCCAATGAGCCAACAGAGGAGCTGCAAAGAATTCTGGGAAGGATCACTTCACACAGATGTGGGCTTCAGGTACTTTATCTCTTCTTTGAGATCACAAAATTATTTCAAAATTGATTTGCTATGTAATGACAATTTAGAATTAATTAGAATTTGAATAACTAATTTCTAATAACTAATTCATATTCTAAGAAATAATAATAGTACATACATTTTTAATATTTATTTTGCAAGATACAAGTATTCCTGTTGAACAGCAATTTTTAAAGGCTTAAATAGGCAGGTTAGGTTTATTGGGAAGGTCAGTAGTTTGTTCAGCAGCCCCAAAAAAAAAAAATTCTTATGGAGCTAATTATCCATATCATATTGACATGGCAGTTAAAATAATATATTTATATATTTTTAATCCCAGCTAAACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31634
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000081048 Nonsense 794 1612 19 42
ENSDART00000126551 Nonsense 809 1743 19 45
ENSDART00000129168 Nonsense 724 819 17 20
ENSDART00000137784 None None 413 None 11
Genomic Location (Zv9):
Chromosome 8 (position 13570381)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13015725
GRCz11 8 13053430
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCCGTGTATGTCATCTGCCACAATCCAATGAGCCAACAGAGGAGCTGC[A/T]AAGAATTCTGGGAAGGATCACTTCACACAGATGTGGGCTTCAGGTACTTT
Long Flanking Sequence:
AAAACAAATATTTGACAAATCTTTAAAGCCTTTTGCCATTTTATATTTTATAGGATCAGCAAAACGCAGTGCTGAGAATGATGAACAAATGGTAGGATTAATGTTTTGAAACCAAAAGTTGACATTTCTATAAATACACTACACATTTATCTCTGCACCATCATGAGCAATCAATTGATTTATAATATCCTATAAACTGATTATAAAAAGGGTAACGAAGTGACCCTGACAGACCTCCAGGAGACCCTAATTCGCCGACTGGAAGACTATAACTTTGTAGAGAAGCACAGTGCTGATGTTTTTCCCCAGGTAACAATCTTCAGAACACTATTTTCAATATTACTTTTAAAATCTATAAAACATTTAATTACAGATGAGTGTTTCTCTTTCAGGTCCTCCAATCTGCTTCCGAAATGTATAGATGTGTGGACACATTTCAGTGTAGAGACAATGCCGTGTATGTCATCTGCCACAATCCAATGAGCCAACAGAGGAGCTGC[A/T]AAGAATTCTGGGAAGGATCACTTCACACAGATGTGGGCTTCAGGTACTTTATCTCTTCTTTGAGATCACAAAATTATTTCAAAATTGATTTGCTATGTAATGACAATTTAGAATTAATTAGAATTTGAATAACTAATTTCTAATAACTAATTCATATTCTAAGAAATAATAATAGTACATACATTTTTAATATTTATTTTGCAAGATACAAGTATTCCTGTTGAACAGCAATTTTTAAAGGCTTAAATAGGCAGGTTAGGTTTATTGGGAAGGTCAGTAGTTTGTTCAGCAGCCCCAAAAAAAAAAAATTCTTATGGAGCTAATTATCCATATCATATTGACATGGCAGTTAAAATAATATATTTATATATTTTTAATCCCAGCTAAACTAAAAGAAATAAGTCTTTCTCCAGAAGAAAAATATAATGCTATTTTTCTGTTCTGTTAAACATCACATTTGAGAAATCTTTGACAAAGAATAAAAATTTTAATCTAAAATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7123
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
ENSDART00000081048 Nonsense 939 1612 22 42
ENSDART00000126551 Nonsense 954 1743 22 45
ENSDART00000129168 None None 819 None 20
ENSDART00000137784 None None 413 None 11
Genomic Location (Zv9):
Chromosome 8 (position 13569096)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13014440
GRCz11 8 13052145
KASP Assay ID:
554-5303.1 (used for ordering genotyping assays)
KASP Sequence:
ACAACATGTCCAAAACACCCAGCTCAGCTACAATGTCTAAAGAAAAGGCC[A/T]GAGACTTTCAAGAGATGTCACAAGAACCAGCAAACAATGATGTATGAAAA
Long Flanking Sequence:
CCAATACAATCCCCTTTGGAAACCAACAGGATAAGAGGCAACATATTCATACCTAACACCTAATATGCTAGCCTGAGCCAGATCAAAAATAATATATATATTAGATATTTGAAAATGTTATTGTGAATTGGGTTGTGTTATAATTGTTTCCTTTTAGACTCTCCAGTTTCAGACACATGTGAACCATATATAAGAGAAGACTCTCTTAAAGTGAGCTGTTTACCTTAACATTTAAGTTTACACAGATTTTCAGTTTTCATGCCTTAACTTTAGGCCTTATTCTCATGTATTTACTGTAGGCATGGAAAATCGAGCAGGAAAGATTAAGGGAAGAGGAGCAATCCATAAAGGCAAAGAAAGAAAAAGGAGGAAAAGCAACACCAAAAGTAGAAGAGAGGATTGACTCTGTAAAGGAGAACAAGAAGGCGATATCAGCAAGAAAAAGCAGAGACAACATGTCCAAAACACCCAGCTCAGCTACAATGTCTAAAGAAAAGGCC[A/T]GAGACTTTCAAGAGATGTCACAAGAACCAGCAAACAATGATGTATGAAAAATATGTAAAACATTTCTAGTATCTCAATTTGAAATGGTTGAATCATTGTATACTTTCCACAGGTATTCACAGGCTACAGTTTAAATGGAAAACTGGTGCGGATCATTGGTAAGGTTGAGTCTCTGTATCCCCGTGATGGAGCCCAAATAGATGTGGAGAGCTTTGGCTTTACTCAAGGTTTGAGATCAGGAAAAACTAACATGTACAAACATAAATGTGTTTTTAGAGCTAGTAATTGAAAGCTTTTGTTTATATCTTTCTTACATGATTGTTTTCCTTCATTAGGGTTGACACAAATGAAAGTATGTGTGAAGAAAGATGGCCATCACTTCTACACACACATTTCAGAGAGAAAAATGGATAGTAAACTAAAAGAGGTTGACATGTTCAGTAAACAAGGTATTGATGTGACATTATTTAAAAATAATATATACATATAAGATGTATATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18106
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
ENSDART00000081048 None None 1612 None 42
ENSDART00000126551 Nonsense 1150 1743 28 45
ENSDART00000129168 None None 819 None 20
ENSDART00000137784 None None 413 None 11
Genomic Location (Zv9):
Chromosome 8 (position 13566246)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13011590
GRCz11 8 13049295
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTTTGAAAATCATTTGGACAAGGAATATTTTGTCAACAAAATCACCTA[T/A]ACTGGCGTCACGGTGGCGCAATGGGTAGCAAGATCGCCTCATAGCAAGAA
Long Flanking Sequence:
ACTAAATATTTTTCTCTCTGCGCTGGACCAGCTTTTTCTTGGTCAAAGGCGCAGTCTATTTCAGTTTCTCAAAATAGCAACACTCCAACATTGCGCCTTAACACGCCTCCTTTATAAACCGGCACACCCATGAGTCCTCAAAGTAGCACAAATGGATTTGCTATTTAAACAATGTGGCGCAAAATGTGACAACTAGGGTTTGAAAATAGCAAAAAAAAATCGGGCAAAATACACCTTGCGCCGGGTGTATGATAGGGCCCTTTATGTGTTTTAAAATACAAAATTTTGCAAAGTACTTACAGTTTTTTTTTTTTAAATGATAATGCAAATCACTTGTTTTGGCTAATACTTAATGACTGAAACAACAATAGTGTACTACTACAGCCCTATGAGTTTGCAAAGTGGTATAGACAACTACTAGCCTTACATAAATAATAGTTTTTTTCTTGTCATTTTGAAAATCATTTGGACAAGGAATATTTTGTCAACAAAATCACCTA[T/A]ACTGGCGTCACGGTGGCGCAATGGGTAGCAAGATCGCCTCATAGCAAGAAACTGGTTCGAGCCCCGGCTGGGCCATTTGGCAATTGTGTGTGGAGTTTGCATGTTCTCCCCATGTTGGCGTGGGTTTCCTCCGGGTGCTCTGGTTTCTCCCACAGTTCAAAGACATGCGCTACAGGTGAATTAAATAAGTTAAATTGGCCAAAGTGTATCTGTGTGAAAGAGTGTGTATGGGTGCTTCCCAGTGTTGGGTTGTGGCTGGAAGGGCATCCACTACGTAAAACATATGCTGGATATGTTGGCGGTCCATTCCACTGTGGCGACCCCTGATTAATAAAGAGACTAAGCTGAAAAGATGAATGAATTTATTAATTAATCACCTATACTAAAAAACTGTTTTAGCACATTTAGTGCATTGTTTCATGTGAGTTTTAACATATCTTGTTTAAAAAAATAAATAACACTACAAAATTCCGCAAAACATGTAATTTCTACATGCAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27145
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
ENSDART00000081048 Essential Splice Site 1370 1612 35 42
ENSDART00000126551 Essential Splice Site 1510 1743 38 45
ENSDART00000129168 None None 819 None 20
ENSDART00000137784 Essential Splice Site 83 413 2 11
Genomic Location (Zv9):
Chromosome 8 (position 13562709)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13008053
GRCz11 8 13045758
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGATGTTTTATGTCAAGTAACGGACTCAGAGTGGAATCACTTTCAGG[T/G]AGACTGAAGTAATATGTCTGAAAAAAAAAAAATATCTTGCACTAAAAAAT
Long Flanking Sequence:
TTAGGGGAGTTGTAAAATGAGCGTATTGTTCATGTAATGTAATTAATTAACCGGGTCAAAATTATTTTGACCATATCCTCCTGCAGTATCTTACGTAATGCTCAAATCTGATTACAGAAGAGAAAAGAGTGAGAGTGGAAAAAGCTGAATTTGCCACAGTGGTGATGGACTGTGAAGCACGAACGTGTGAAGTTTTTTTTAGTGATGGCACATCTATCAGTGCAACTGCCCAAGGATTTTATAAAGTAAGAGGATGGATGGACAAAATATATCAGATATATAGGAGGGAACTTCATATGTAATGCCTCTTTCTGTGTCTTTAATACAGATTTATCCTCATAGTGGAGGTGTTCTTCATATTGATAAGGATGGTGGAGCTGTGTACTCATCTAAAGCGTCAAAAGAGCAACCAGAAAGAGACCCGACAGGCCAATATGTGATGAACCACAGAGCAGATGTTTTATGTCAAGTAACGGACTCAGAGTGGAATCACTTTCAGG[T/G]AGACTGAAGTAATATGTCTGAAAAAAAAAAAATATCTTGCACTAAAAAATGATCATATTTACCTAGTTATGGACAGATCTAAAAAAATATTTAAAAAGTTTGTATGCAAATGAGGAGACAAAGCAAGGACATAGTTTTGAAAATTTAAAAAAAATTAATTAAATTCCTTATTTTCATGCCAAAAAATTATATACAAATGCAATTACTACATGTTAGAACATGTCGTGATTTAAGTTTAAATTATTATTTTTTATTTATTTTATTTAGTTTTATTTGAGTTTGTAAACTTGTGTGCAGATGTTGAATATATAATATAATAAAACTAATTTTGATGTAAAATATTATTTAAATATAAGTATTTTTAACTGTTTTAATAATAACAGCAACCCTGTATAATAAAAAAATTAAATATTTTCCGTTATTTGGATAAATGGGAAGATTAAGCTGGACTGTGATTATTGCAGTTATCCTGTATAGCTGTGATGAGACTGAATATCAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34341
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
ENSDART00000081048 Nonsense 1545 1612 41 42
ENSDART00000126551 Nonsense 1676 1743 44 45
ENSDART00000129168 None None 819 None 20
ENSDART00000137784 Nonsense 242 413 6 11
Genomic Location (Zv9):
Chromosome 8 (position 13557583)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 13002927
GRCz11 8 13040632
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAGAGAAGCCGTCAAAGTCTGATTCAGTCCACGTCCAACCAGTTTTA[G/T]AGTGTCCTGAAGTGCTGCTGGTGCGACAGATTACCCAGAATCCACCTGTC
Long Flanking Sequence:
TTAACATTGCAGCCTATTAAACACCTCAATCATTGTTCTCCTGACTGATTCCCGCTCAGAATCATTTGGCATCACTCTGCTAAGGCCTTTCCCAGACATCAAATCTCATTGGCTCTCATCCAAGCAAGATGATGACATCATTCCCACCAACCTCAAATCCAGGAAATGGGAGTCTTTCCCGGCTTCTGAGGTAATTTCTTATCTTTAGGTGAAACTTTCTTTTAGGATTACCTTTGGTCCAAATGTTTTATATTGCCAAAACAAATCCACATTAAACATCTCATTTATTTGCACCCTAAACATGTTTGGATATGTCTATATGTGATGTATAAGTGTGTGTTGTTTAGTGTGGATTACCTATAATTCCTTAATGGTTTGTTTCCATCTCTGCTGCTTAGAAGAAAACTCCAGGCCCTGTTTTTGGGACCACCCTTGGTTGTAGTCTCCAGTTCAAAGAGAAGCCGTCAAAGTCTGATTCAGTCCACGTCCAACCAGTTTTA[G/T]AGTGTCCTGAAGTGCTGCTGGTGCGACAGATTACCCAGAATCCACCTGTCACTGAATCAACACGAAGGAAACTGCAGAACAAAGTCAAGGTGATTTAATTCCTGCACACAAAATAAGCAACATGTGATTTGGTTCTTATTAACGTTAACCTTTTTTAACCTTCCGGTAATAATATAATGTGTCAGTAAAACCACAGCTTTACCACCCATATTATGCTTCCCTTTTCACTTCCTTTCAACATGTTCTGTAACTGAGCAGTTTGTGAATTTTTGAGCTTCAAAAATAAATTGTTTGTACACAGTAGTTTGGCAATAATCGTTACATGCGCACATGGATCATATTTTGGTGTCAGCATCTAATAAAGGGAACAAAAAGTGATTTGAACTGCATAGAAAGCATACACAGGATCTACTTTAAGGTTTTAAATGATGTTTGTTATTTTGGCCTTTACCTTATTATTAGCTAGGCCTCATATTCTAGTTCACTGGAAATCAAATAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21218
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
ENSDART00000081048 Nonsense 1591 1612 42 42
ENSDART00000126551 Nonsense 1722 1743 45 45
ENSDART00000129168 None None 819 None 20
ENSDART00000137784 Nonsense 288 413 7 11
Genomic Location (Zv9):
Chromosome 8 (position 13554393)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 12999737
GRCz11 8 13037442
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCATATCTGGAGCAGTTGCTTCAGAGAGAGGCTCAGTGGGAGAAAATG[C/T]AGCTAAAGGATCCACGAACAGCACAGGAGAAGAGTCATCAGAATGAGCTG
Long Flanking Sequence:
TCTTGCCTAAATACCCTAACCTGCCCTAGCTAACCTAATTAAGCTAGTTAAGCCTTTCAATGTCACTTTAAGCTGTACAGAAGTGTCTTGAAAAATATCTAGGAAACTATTATCTACTGTTATCATGGCAAAGATAAAATAAATCAGTTATTAGGAATGAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAAAAACACAGAAATTATGGAAAAAATAAACAGCTAATAATTCTGACTTTGACTGTATGTATGTGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATAATTTTTAGTGTTTACTTTATATTTCACTCATTTAAATATCCTTCTGTCTTCTTGTGTTGATGTATGTACTGTATATGTGCTCCTGAAAACCACAGAAAAACTTTAATAAAGCTCATTCTGATTCTGATATGGATTTAATCACGTAGGCATATCTGGAGCAGTTGCTTCAGAGAGAGGCTCAGTGGGAGAAAATG[C/T]AGCTAAAGGATCCACGAACAGCACAGGAGAAGAGTCATCAGAATGAGCTGCTGCGCCTTGTACTGGTCAGACAAGATCCTATGTTCTTAAACTATTCAGACGATTAAATAAATACAGATGGTGACTTATATAAATTGTTTTAGTCTCTGCCTGATGCTGTAGATCTTCCAGCTACCATAGATACAAGGCCTCAGTCAGGTGAGAAAATGTATTAACAAATTAAATAACAGTTCATTAAAATAAAAACTGTTTCTTAATATTGAATTTGATTTATTATTGAAGGTTATACATTGTTATATTTCCTAATGATAATAAATATAATAAATATATTATTGTTCATTAATTATAAGTTATTTAACCCTCTGATTCATCAATGTATTTGAGCATTAAATATGTTCAGTGTGATATTACATAGTGTCATAAACAATGGTTTTAAATAGGGAAAATGTTGTGGCAGCGCTGTAGCTAATGAATATTTTTAGCACTGTTAAGCTGTCATC
Associated Phenotype:
Not determined