Busch Lab

ZMP

im:7149048

Ensembl ID:
ENSDARG00000076870
ZFIN ID:
ZDB-GENE-041111-255
Human Orthologue:
FAM38A
Human Description:
family with sequence similarity 38, member A [Source:HGNC Symbol;Acc:28993]
Mouse Orthologue:
Fam38a
Mouse Description:
family with sequence similarity 38, member A Gene [Source:MGI Symbol;Acc:MGI:3603204]

Alleles

There are 14 alleles of this gene:

Allele Name Consequence Status Availability
sa30895 Nonsense Mutation detected in F1 DNA Not yet available
sa30894 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa12608 Essential Splice Site Available for shipment Available now
sa34199 Nonsense Mutation detected in F1 DNA Not yet available
sa27065 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa17785 Essential Splice Site Available for shipment Available now
sa10147 Essential Splice Site Available for shipment Available now
sa34198 Nonsense Mutation detected in F1 DNA Not yet available
sa7089 Nonsense Mutation detected in F1 DNA Not yet available
sa34197 Nonsense Mutation detected in F1 DNA Not yet available
sa34196 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa2346 Nonsense F2 line generated Not yet available
sa21090 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa30895
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
ENSDART00000108646 Nonsense 78 2538 3 51
Genomic Location (Zv9):
Chromosome 7 (position 56692231)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55127557
GRCz11 7 55428968
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCACTCTTCAGCACCAGTCTGATTTTTATCTTGGGACACGTTACCTTT[C/T]AGATCTGCCTGTATACCATCCCAAGCCTTGATGACGCACTGGGACACAAC
Long Flanking Sequence:
TTTTGACGGTCCTGCCATGATTAGAATAACTGGGCCTGCGTTGCATTTTCCCAATTCTCACAAAAGTTAAACACTCGCACATGTGCTTTCTTTGCTCTTATACTGCTGCGTTGTTGGAAAAAAGTTAGAAATCCCATTTTTGGGTGGCAACAATGTAAATGTTGCAATTAAATATTACGAGAGTTTCTGCAAGGCCTGTTATTAAACTATTGTTATGGCAACAGAGTTTAGCTGACACTAACTGTGTCCATGGACTTTTAATATTAGGATTTTTATTATTAAAAATATCAGGTTAAAACTAATTTAATGTTAAAATAGGGTAGTTTATGAATGAAAATGGCAGTTTCTGTAAACATTGATCATTGTGTTTTTTATGATCTATACAAAATCCTTCAACTTTGACCATTCTCTGTGTTTTTCTTTCCACAGGACACACTGGATGTTACATCAAGGCACTCTTCAGCACCAGTCTGATTTTTATCTTGGGACACGTTACCTTT[C/T]AGATCTGCCTGTATACCATCCCAAGCCTTGATGACGCACTGGGACACAACTGTAAGTTTGACCCATACACAATCAAGAATTATGCAACATAAAAATCGGGTGCATGGAAACAAAGCTAATGACAAACAGAGTCATATGTGCGTTTGTGTCTGCATGCCATTATGTTTTAGAAAGCTTGCACTCCAGGCAGTCGTAAACATGTTCAGCACTGTTTATAGAAGCTGTGGTTTTGAGATGATTTTGTTGTAAACAATGTCCCGTTTCGTTGCACAGATGGTCAGTTCATTTCATAAGACCTCAGTGTGTTGTCAGGTACCACAGGTATTTATTTAGTTTCGTCTGTATGTGTTTTTTTGTTTTTGTTTTTTTGACTCTCAAATGGTCAGATACAGTTTATAATTCTTCAAGGAATATTGTATAAGCTGATAAGATCTTCTTTAGTATTGTACTGCTAAAGAAAAAAAGGGGGAAATAGACATTTGCATACATTACCTGACAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30894
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000108646 Essential Splice Site 160 2538 5 51
Genomic Location (Zv9):
Chromosome 7 (position 56684238)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55119564
GRCz11 7 55420975
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAGAGACGAGGGCTCCGTTCCTCACATGTCTGCTCTTCTGCATGAGG[T/C]GAGCTGAACTGAACTTTGGGAATTTGTTGAGTAATGCTGTTAGTCTGGGC
Long Flanking Sequence:
AAAATAAACAAATTATATATTTAAAGTCTCACAAAAGAGCCTCCACACACACACAAAAACACACTGTTCTATTGGAGACATGCTGCTTAAATGCCCACAACTTTACTCATCCTCCAATCACTGAGTGGTTCATGAGTGGCAGCAGGTGACGTTCATCATCTCCTATTAGGGTGTAGCAGAGAAAGAAAGAAAATACAAAACAGAAACAAATACATCCTGGGACGTAACAAAGCAAAATACATATTTTCTTAATAATCACTAACAGTCTTTTGACTTGTTTGTTTGCAACACTTTATAGTTTAGATATGACGCTGTGTAACAGCTGAATTTTGTTTGCTCCTTCAGGCTCCCGCTGGAAGATCCTCAGGGTGTGCTGTGGCTCCTGACCCCAGATTTGGGCGTCTTCATCATGTCGCTGATCACCCTGATCTTGTGTAGCCGTCTGTTGAAGAAGAGAGACGAGGGCTCCGTTCCTCACATGTCTGCTCTTCTGCATGAGG[T/C]GAGCTGAACTGAACTTTGGGAATTTGTTGAGTAATGCTGTTAGTCTGGGCCTCAGATGCTCCACCCATAAATGCTGTGGTGGTTAGTGCTGATGCAATCCACCAAGTGCAGTCTCATTAGCTTAGTTTCCATCCAAAGAGGTGAATTAGATTTATGCGCAAAACTGGAATATCACATAAAAACTTTGTGAAGCCACTGTGGGCCTTTTTCATGATAAACTACTTGTGCCTTAGAAAAAAAGGATGTAACAATGAACGCACGGTTGTTTTTAAGGGAGCAAGACTACTCTTTGGGAGCTCAGATCAGTTCTGAGAGGTAATAATATTAATTTTAGAATGACCAAAACAACATGTTAGGTGTTATACGATGGTTTTGATCTGCTGTTGTATCCATAATTTTTTGTTATCGCATGATCAGTTCAAACAAAACTCAAAATCTAGACATCAAATATATATTTTATGGGACGTCTATTTCTTGTTTTCTTCATGCCATCAAAACTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12608
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000108646 Essential Splice Site 390 2538 9 51
Genomic Location (Zv9):
Chromosome 7 (position 56657533)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55092859
GRCz11 7 55394270
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTCAGATTGTGGGAGGCAAGGAGACAAAGCAGTGAAGAYGACACTAAG[G/A]TAAAGAATAAAACTTGACATTTTACATTTAYATATTATGGAACCTTAGAG
Long Flanking Sequence:
GTAATGTCTAAAGTGATTGCAAAACAGGTAATTTTACTAACTTTTTTTGCAAGATTATAAGGCTGAACCACATGAAATGCCATCAGTCTACAGAGATTTCCTAAAATTATTCTGCTGTAGAATTCTGGTAATTCTTGTGTTAGAAAAGGACAATAAAATAAGCATTAAAATTATGCATATCAACTGTGCATTTTATTCTCAAGCAATACATTGAATTTTAATACATTTATTTAGCTTACCTATTCCTTTGAGAGCCCTTTGTAAGGTCAAAAATCCAACATTTGTACAATCGTAAGCCAGTCAATCACATTGTTTGTGTATAATAAATTAGTTTGGGCTAGTGTCTGATTCACACAGTATATACACTGATGCGTAATGTCTTTATGTTTGTCTAGGCCCGTGAGGGTGAAGCTGTGAAAACAGTGCAGGGTGAAGCTGGAGAAGAAGTAGAGCTCAGATTGTGGGAGGCAAGGAGACAAAGCAGTGAAGATGACACTAAG[G/A]TAAAGAATAAAACTTGACATTTTACATTTATATATTATGGAACCTTAGAGAAAAAAATGTCTTTTGGGTTTTGAGGGGGTACAGAAGCACATATGCATGTCTGATGAAATATTTAAGGAGGTTTTATTAGTCTCTATGTTGTCATTGCTGTATCCACATGCTGTAATTAAAAAGTATTACATTTTAGTTGCTTTATGTGCATGCTGATGCCTCTATTATGATATATTAAATAATTTTATTAGGATCTCTTATGAAAAGTCTATTCAATATTTTAAAAAATAGAGCAAAAGCTTTTCTCCTTCTGTAACCGTTCATTCAAGGACTCAAGCTTCAAACAGCTATTTCACACTGCCTGAAAGATAAAATCTGTAAATGCAAAATAGGGGACGCCACTGGTAAACATTCCCTGCCTCTGGCATACAGCACCAAATGCACACATTTGTATCAGTATTTTAAAACCTGGCATCAGAAAAAGTATCACCATTGCATGTTTGTGTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34199
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
ENSDART00000108646 Nonsense 568 2538 13 51
Genomic Location (Zv9):
Chromosome 7 (position 56649904)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55085230
GRCz11 7 55386641
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGTCAGTGAAGGACACATTCAGCAGGAAGAAGAGTTTGACTGTGCCAT[T/A]GCAGGAGGTCACAACTGGAGGTGAGCGAGAACACTGGGGGCTCTATTTTG
Long Flanking Sequence:
GTGTAGTATATGTATGTATATTTATTTTTATTTATTCATTCATTCATTCATTTTCAAAATCTTTCAGGTCAAACCCACCTGTTTTACCTTATCAACTTGTTAGCGCAGACTTTAAAACCTAAAATGGATGATCCAGCAAAAGGAAACATCGAAAATGTGCATCGCTGGTATGCCTCCAGGATCAGGATTGAGTAACACACTTAAAGCAAACTCTTAGAGAAACTCATTCCTAAGCATTGGGATAAAGATGACTGCAGTTAACAGTCTGAGAAATCTAAATAGAAAAGGCTTGTAGTCACTTGCTACACTTTTACACAATAAGCCCACATGATTGGTCATAATTCAGTCATGATGATGTTGCTCAATGCGCTGTGAGTAAAGTGTAAACATTGCTTCATTCTCGCTTTGTTTTCAGCTGCTGTTCACATTGACTTTCTGGCTTCTGCTGAGGCAGTCAGTGAAGGACACATTCAGCAGGAAGAAGAGTTTGACTGTGCCAT[T/A]GCAGGAGGTCACAACTGGAGGTGAGCGAGAACACTGGGGGCTCTATTTTGACGGTCCATGCACAAAGTGCAAAGCGCAGGGTGCAAACGCAATAAGGGCATGTGGGAAACCAGTTTTGCTTTTTTAAAGATGAAAAAATCCACTTTGCACCATGGCGCATGGTCTAAAAGGGTTGAGCTTATTTTCTTAATGAGTTATGGGTGTGTTTTGAGAATAAGCCAATAAGAATCTCATCTCCCATTCCCTTTAAGAGTCAGTTGCGTCGCGCCATAGCGGATTTGCTATTTAAATGATGGACTTTGTAAGTGGAAAAACTGAGTGCTTCACTAGTGAGAAAACAGTTAAGAGCATCTACAGCGCAAGAATAAGAGATAAGCCTCCTCATTATTTACTTTTGCTTTCACTCTCGTGGAAAAGGAAATGTGTTGTACGCACAGACATCCATTAGCCTATAAATATATATATATATATATTTTTGTTAAGCGCAAAGATTTGTTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27065
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
ENSDART00000108646 Essential Splice Site 774 2538 17 51
Genomic Location (Zv9):
Chromosome 7 (position 56641555)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55076881
GRCz11 7 55378292
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAAGAGCTGATCGTGGATCAGGATGATTATCCATCAGAGGCTGACGG[T/A]GAGAGTAATGAAGGCTGCTTCTGTGCCATTGTTGTTCAATCAAAACAAGT
Long Flanking Sequence:
TATTATTTGTTGTTCCTAAAACTTGGAAATGCAACAAGACTTTTGTCAGGTATTGTACATTCCTGTGCAGTCTGTCTCTGATGTCAGTACATTTTTCTATCCACGATTTGATTGGACGAGAACCACAGGACTGATTAGTCTAACATTTTAAAAACAGTAAAAAGTTTTATGAGAAGTCTTATATGAAAATAAATAGTAATAATAAATAGTAATAATTATATATATATATATATATATATATATATATACATACACACACACACACACACACACATTTTTATATATAGTGCACATTTTTTATCTGAAGATCTAATTCAAATTTAAAATAGGTAGTTGTCATATTAAGTTGAAAATATGTAATCAGGATGTATTTTTGTGATTTTTCCTGACAGGAAGAGAGGTATAGATAATCCAGATTTGGTTCAATCCACAGAAGAAGTGAGGCCTGAGGAGGAAGAGCTGATCGTGGATCAGGATGATTATCCATCAGAGGCTGACGG[T/A]GAGAGTAATGAAGGCTGCTTCTGTGCCATTGTTGTTCAATCAAAACAAGTTTAATATTAGTCAGTAATGCTATATGATCACCCCCAACTTTAGTGTGCATTCTTGCTCTGTTCTCAGAGGTGATACCCAGCAAGTGGGGTCTAGTGATGGACAGGCTAATGGTGTTGTCCAGGAAGTTCTCTGACACCTTGACCCATGTCCAGAGTTTCATTTGGAGAGTCCTGGAGCTGCACATCGTCAAAATTGTTGCCTTTTTTGTTGTTTGGGTGGCACTTTTGGAGGTTTGTACCTTGCATACTCTTAGGAGCCGTTCACATACTGTAGAATGTTTTTTCTCTTTAATTTGCTACTATTCTATTGTTTTTCAATGTGAACTGCTTGACATACGTGTGTGACCAGTACGCTAACTTGACTTTTAAATCAGCACACTTTGACTCCTGCATTTTTTTAAGATTCCATGTGAAGTTAAAAAGAACCATGTGCAGAACAGCTCATCACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17785
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000108646 Essential Splice Site 1065 2538 22 51
Genomic Location (Zv9):
Chromosome 7 (position 56631928)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55067254
GRCz11 7 55368665
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATAYCAGTATGTTCTGTGTGTGGGGATTCCTCCTGCCCTCTGTAYAGG[T/A]AAGTCAAACACTATAATYAATRMACTAGTTGTTGTTGTTGACATTATTCA
Long Flanking Sequence:
ACTTAATGTTCAATCTACCTAAGTTTGTTACATTAACTTAATTGGTTTGTGTTGGGAAAACATGAATGAATTGTGTGGAACCCTGCATTATTTCCCATGTGATCTATAGTGTTACCATCAGCTAGATGCAATGCTTTAAATATAAATTGCCTGGGAAGGTTTCCAAATTATCTTTTTTTTTTTTTTTTGAGCATGTTTTGAAGTTGATAATCAAAAGCACTTCCCAACATTGGTTTCTCAAATGTTAAATCTAATGATCATTTGTGGCTAATGATCATTTGGTCTTGCCTCTAGATCTGCTTTCTAATGACCGTGAATGTTATCGGTCAGCGCATGAATTTCCTGGTTATTATCCACGGCTGTTGGTTGGTGGCCATTATGGTGCGGCGGCGCAGAGCAAATATAGCCACGATTTGGTCAAAGTACTGCCTGTTTCTGGTTGTCTTCATGATATACCAGTATGTTCTGTGTGTGGGGATTCCTCCTGCCCTCTGTATAGG[T/A]AAGTCAAACACTATAATCAATGCACTAGTTGTTGTTGTTGACATTATTCAAGTCATTTGTTTTCACAACGTTATTTGTAGCATTAAAGAACACATTTTAATTACATTTAATGTACATTTATTTGTAAAAAAAATTTTATTTGTAAAACATTTTTACATGCTGCAAAAACCTTTTTCTAGTTTTCTTTCTAGTCCAAATGTAAAAAAAAAAAAAAACTTAAATCAAGAAGTATTTTCTAGACAAGTAAAATATTGTTTTGCTTTTAGAAATAATAAGTCAAAATTAACTGTTTTTTTTTTCCTTAAACAAGCAAAATAATCTGCTAATGTTATACGTATTATAATAATCTTATTTCAAACATAAAACACGGTTGTTTTATGTATCCCATTGGTAGATTAATTAGCTTTTTTTAATGGAAAAACAAACTTAATTTTGAGATTATTTCTGAAAACAAAATAAAATTTACTTGTCCATATAAAAAGCTTCTTTATGTAGGAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10147
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000108646 Essential Splice Site 1152 2538 24 51
Genomic Location (Zv9):
Chromosome 7 (position 56630207)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55065533
GRCz11 7 55366944
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGGAGAACATGCTTTTCAAWCCTGCCCCAAACTTCATCAACTGCAGG[T/A]ACGTACATCACRGTATTTGTACATGATGTAAGTTTCATTATCCCCACAGT
Long Flanking Sequence:
AAACATTCTTTGTTAATGATTCATTTTCCATTACTAATTTAAGTATTGCATTATTTACGAACCAGTTATTTAAAAATAATTGGTGTTTTTTTTTAAGATCATTCAGAATACGTAAGTAAATTATTAATTAACTATTCAAATTAACATTTATATAACTTATTATTCAGGCATATACTAATAGTTTCTTTGCATGTTAATAAATGCTTTTATAACTCAACTTCCTCCAGTTTTGTGACCTAATCTAAAGTGAGGGCTATTCATGCTTTGTAAATCTGCAATGATGACTGTCATCACACTTAAATTCTGAAACCTTGCCTAAATTTACAAACTGATCTTTTGCAGCGGACTTCCTTTTGCTGATGTGTGCCTCTCAGCAGTGGACGGTGTTTGACAATGAGAAAAAGGAAGAGTGGATGGTCATGGGAGGAGAAAACCGAGACAATCCAGACCCCATGGAGAACATGCTTTTCAATCCTGCCCCAAACTTCATCAACTGCAGG[T/A]ACGTACATCACGGTATTTGTACATGATGTAAGTTTCATTATCCCCACAGTAAATTCCTCTGAGTAAAATTTACTCAGTTTAAATAGTATTTGGTCCCTCTCTAAATTGAGTTTAAGTTATTCAAGTTTATTAGACAATGAAAGGAATAATTAGGTGATGATTAAGCATTGATATTGAACACCTGCTGTTAATAAACAGAAACACACAAGAGAAACACATAAGTCACTTCAGTCACAGCCTTAGATGAAATCAGCTGCAATATAATACATTTATTCTTTCAAAATCTCAGCAGAGGATCATTAAGCAACTCTACAAACAGCAGCTTTACTGATTACTAACCTTTTTGCCCTTGTTTAAAGAGGGACCAAATACTCTGTGAAGTAAGTCAATTTTACTCAGAGGAATTTGCTGTGTACATGCGTACCCCTGCAGCCTAACCTTTCTAAACTCAAATTCTTGAAATGTCTGAAGAAAAAATCAAAATAAGCAGCTCAGCTCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34198
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
ENSDART00000108646 Nonsense 1410 2538 31 51
Genomic Location (Zv9):
Chromosome 7 (position 56619705)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55055031
GRCz11 7 55356442
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATATAAATCTATGTTGTCGTTTTAGTGTTGCATTCTGGGGAATACTA[T/A]ATGTTTGAGTCTGACAGTGGAGAGGAGGATGAAACCTTTCAGGAAGAACA
Long Flanking Sequence:
GGGTAAGCTAAAATTGTCAGTAGTGTATGTGTGCGAATGAAAGAGTATGGGTGTTCCCCAGTGATGGGTTGCAGCTGGAAGGACATTTGCTGCTTAAAACACATACTGGATAAATTGGCTGTACATTCCGCTGTGACGACCCCAGATTAATAAAGGGACTAAGCTGAAAATAAAATAAATGAATGAGTGAATGTTCAAACTATTCACTTGCTTGAGCTCATGCACACTTCACATACTAGAGACTGAACGCGATTCAAAAACCAGTCTCTATTTTTTTATGCATTTCATTACAAGCTGTTCACACACCGCCAATGTAATATTGATTCATATGAACTCTTGCATGTAGCCTCTTTAATGTTTTCTTTCTTTAATTATTTACTTTACAGTTTTAATTTTATGTTATGAACATGTTTTTAGAAGAGAGAGCAAGGGAATCAGAATGCTAGAGTTTAAATATAAATCTATGTTGTCGTTTTAGTGTTGCATTCTGGGGAATACTA[T/A]ATGTTTGAGTCTGACAGTGGAGAGGAGGATGAAACCTTTCAGGAAGAACAGAAACCTCGCAGACAGACTGCCTTTCAGGTGAGAACACTTATATTTGTACTCTGTTTTAGATTTGTCAGTTTTGTTGTTGACCGTAGAAGTGTGAAAAGCTTTTATTTTGAACTGATTTCCACAGCTGGCATATCAGGCTTGGGTCACCAGTGCAAAAGATGCCCTGAAAGAGCGTCAGCAGAGGCAGAGAAAGCAGAGAGCAGAAGCAGAGAAACAACAAAACGCTCAGGCTACAGGTTTAAAGAAGGATATAAATACACATATGACACGTTCAGACATAAAAATTCACACAGTGTTCCACAGAGTTACATGTTATTTTTGTTCTGGTTATCAGACGACGCTGAGGAGGGTGAAACAGTCTTTGATGGGGAAAATTCCCAGCATGCGGAGGAGATGCAGGAGGAAGGAGAGGATGCGGGTGGGTTATCTCTGCATTAGGAGGGATGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7089
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
ENSDART00000108646 Nonsense 1439 2538 32 51
Genomic Location (Zv9):
Chromosome 7 (position 56619521)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55054847
GRCz11 7 55356258
KASP Assay ID:
554-4890.1 (used for ordering genotyping assays)
KASP Sequence:
GTAGAAGTGTGWAAAGCTTTTNATTTTGAACTGATTTCCACAGCTGGCATA[T/A]CAGGCTTGGGTCACCAGTGCAAAAGATGCCCTGAAAGAGCGTCAGCAGAG
Long Flanking Sequence:
GAGTGAATGTTCAAACTATTCACTTGCTTGAGCTCATGCACACTTCACATACTAGAGACTGAACGCGATTCAAAAACCAGTCTCTATTTTTTTATGCATTTCATTACAAGCTGTTCACACACCGCCAATGTAATATTGATTCATATGAACTCTTGCATGTAGCCTCTTTAATGTTTTCTTTCTTTAATTATTTACTTTACAGTTTTAATTTTATGTTATGAACATGTTTTTAGAAGAGAGAGCAAGGGAATCAGAATGCTAGAGTTTAAATATAAATCTATGTTGTCGTTTTAGTGTTGCATTCTGGGGAATACTATATGTTTGAGTCTGACAGTGGAGAGGAGGATGAAACCTTTCAGGAAGAACAGAAACCTCGCAGACAGACTGCCTTTCAGGTGAGAACACTTATATTTGTACTCTGTTTTAGATTTGTCAGTTTTGTTGTTGACCGTAGAAGTGTGAAAAGCTTTTATTTTGAACTGATTTCCACAGCTGGCATA[T/A]CAGGCTTGGGTCACCAGTGCAAAAGATGCCCTGAAAGAGCGTCAGCAGAGGCAGAGAAAGCAGAGAGCAGAAGCAGAGAAACAACAAAACGCTCAGGCTACAGGTTTAAAGAAGGATATAAATACACATATGACACGTTCAGACATAAAAATTCACACAGTGTTCCACAGAGTTACATGTTATTTTTGTTCTGGTTATCAGACGACGCTGAGGAGGGTGAAACAGTCTTTGATGGGGAAAATTCCCAGCATGCGGAGGAGATGCAGGAGGAAGGAGAGGATGCGGGTGGGTTATCTCTGCATTAGGAGGGATGAGAGACCAGGGGCCTCATGTACGAAGACTTGCGTGGAAATCTTACTAAAACATTGCGTACGCACAAAGCTGTAAATGTGCGTACGCAGAAAAAAATTCAGATGTATGAAACACTGCGTACGCCGAATCTCACGCATATTCTTTTGTACATCTGAATGAACGTGAAACTGAGCGCAACATGCACGAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34197
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
ENSDART00000108646 Nonsense 1543 2538 34 51
Genomic Location (Zv9):
Chromosome 7 (position 56615998)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55051324
GRCz11 7 55352735
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCATGGTGGACGGATTCACCATGTGGCTCAACCTTCTCACCAAGCAGTA[T/A]GTTGACACCTCAATGGTCCTTAGTGAGGAGCGTTACCTGTTTATTCACAA
Long Flanking Sequence:
TAATTGAAGTTATTTTTAAAAGATAGATATAATGTGTAAAACTATATATTATTTATATTACTTCATAATACCCATACATCTGATAAGCGTTTTATATTAATGGATATTGCACAGATATTGATGTGTCACAATGTTTGTATGCTACAAGAGGATTTTGTCTCTGAACTCTTCAAATATTTTTAATAGCTGTATATGGTGTATATCTAGCTAACTATAAAACATTTAAAAATACTGAATAATGGTACAACCATGGACAAAACTCCATAAAAAATATAAACATTAACCAATGCCAGAATGTAAGCAACTGCTGACAGCAAAAGCACTTAAAGGTGCCATGAATTTCCTGAAATCTCAGTGCGTTCTTCTTGTTTTCCAGCTTCTCAAGCCACCGGCAGTGATATGGTGCAGAGGATTCTGGACATACTGAAGTTTCTTTGGGTGCTTTTCCTAGCCATGGTGGACGGATTCACCATGTGGCTCAACCTTCTCACCAAGCAGTA[T/A]GTTGACACCTCAATGGTCCTTAGTGAGGAGCGTTACCTGTTTATTCACAACGTCAGCCAGGTGGATCACCCGCTCAAACACACATTACGCAGGGCTGCGATTCTGCAACTGTTCTCATGAAGCATATGTGTGTGTGTGTGATTCACAGAGAGCCTCCAGAGAGAACATGGATGATCAGATTTCACACGACAGTGAGGATCTGACTCTGGAGACCTGTCTTGATGAAACTGACACTGACAACATTTGCGACACTAAGTAAGTCTAAGCTGACCAAAAGAACTAGTTGCCTATAGAGATTAATGTGTTTTCAAAAGGGTGCATTTTCATTTGGATGTCTTTTTTTTCTTCATGTTTTAACAGTGTTATTTTCATAAGCTTGGTTTAGCAGTTCAACCAGTGCCATGAAACTAGATTTATATTTTCAACTAAATGTATATTGCAGTGATTTTCTTTCAAATTGTAACCAAAGGTTTAAACAAATAATTAACGTTTTAATTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34196
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
ENSDART00000108646 Essential Splice Site 1803 2538 38 51
Genomic Location (Zv9):
Chromosome 7 (position 56607857)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55043183
GRCz11 7 55344594
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATCTGCTTCAACTGCTGGTGCTCTTCTTTCACCGCTCACTTCTCCAGG[T/A]AGTAAAAAAAAACAAAAAACAAAAAAACAAACCTAGACTAACATAGCTGT
Long Flanking Sequence:
TATAGAGCTCAGATTTAAGAAGCATTAAGGCGCCTTCTATTCAGAGACCCAAACTAGTAACATAAGCAGATGTTGTTTTACATGGTCAAAGTAAAATTAAATTCCAAAAGTATATAGGTATTTAAAACAATACAATACAATACAATACAATACAATACAATACAATACAATACAATACAATACAATACAATATAATAGAAGTTAGTATAAGTTAAGTTAGTAAGTATAGTTGAGAAAATTCTAAATAAATATTTTGGAATATGAACAATAATGACTTATTTTTATCTCTGGCCTGATGTGTTTTCCTCAGGTAATGGTGGTGGTCAAATACCTCTTTCAGTTCGGCTTTTTCCCATGGAATACTGAGTATGAGCTGAAGTTGAATGAGGACAAGCCCTTCTTCCCTCCACGCATCCTGGGCCTGGAAAAAACTGACAACTACATCCGATATGATCTGCTTCAACTGCTGGTGCTCTTCTTTCACCGCTCACTTCTCCAGG[T/A]AGTAAAAAAAAACAAAAAACAAAAAAACAAACCTAGACTAACATAGCTGTTTTAGAGGGTCAACAATACCTGACATCTTGTCATCGATCCCAGTTGTAAGAGCAACAAATAATAACGTAACTTCTAGTTGATCATTTGAAAAAGTGTCAGAAGGTAGATTTTTCCATTGAATCATCTGTTGAACTGCATCCCAATTTTCACAAATACTGCAGAGGACCAATTAAAACTCGCATGGACCCAACATTCTCACAGAAATCTGTCAAGTTTAGTGAAAAAAAAAATTATGGTTTGGAGTCACAATCAGTAAGGGGGCATGTAAGAGTTCTGCTTCTTATTTTTAAAAGCAAGACAATAATTTTAATTCATCTAAAAATACTTCTTGAAATACGACTTTGTATTATTAGACTTGAAATAAGACCTAAACATGTAATTAAAAAATTGCATGTCAGTATCCTTAACTAAGCCCATCTTAGCATTAGTTTGCTATTAGGGAATGAGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2346
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000108646 Nonsense 2043 2538 42 51
Genomic Location (Zv9):
Chromosome 7 (position 56604050)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55039376
GRCz11 7 55340787
KASP Assay ID:
554-2478.1 (used for ordering genotyping assays)
KASP Sequence:
GTTYAGCACCATGATCATCGATCGAGCATTATACCTGCGGAAGAGCATCT[T/A]GGGAAAGCTCATCTTCCAGGTTATCCTGGTTTTTGGCATCCACCTTTGGA
Long Flanking Sequence:
GTCACTTAAACGTGGTCTTCTCTACTTGTTCATAGGTACCTGCATATTTTATTGAATCAATGTGATATTTGGGTTTAATTGTCATTTATTTAATCATGGTGTGTTTTTGGTCTGTGCAGAGTGAAGAATGTGTACAGGCCAACCTGGGATTTCTTCCAGAACATCCTGCATGCGGAGTACAGGGCCTCAACTGATGTCTATGCTCTTATGTTCCTCACTGACGTAGTGGATTTTATCATCATTATCTTTGGTTTCTGGGCTTTTGGGGTGAGTACAGAAAATAGACAGATATCATTAGATAAAAAAATGTAGAGGAATGTCAATATCCAGTGAGGATTTTTAATATTAAATGTTTGCTCTTTCTCAGAAACACTCGGCGGCGGCAGATATAGCCTCCTCTCTGTCCGAGGACCAGGTCCCTGAGGCATTTCTGGTCATGCTCCTCATTCAGTTCAGCACCATGATCATCGATCGAGCATTATACCTGCGGAAGAGCATCT[T/A]GGGAAAGCTCATCTTCCAGGTTATCCTGGTTTTTGGCATCCACCTTTGGATGTTTTTTATCCTTCCTGCTGTCACTGAAAGGTAAGAAAGACTCCAGGAGTGCATTTATTTATTATTATTATTTTTTTTTCAAAGAGTGAGTCATCTCCTTTTTTTTCACAGGATGTTCAATCATAACTCGGTGGCTCAGCTCTGGTATTTTTTCAAGTGCATCTACTTCACTTTGTCAGCGTATCAGATCCGCTGTGGATACCCTACAAGAATCCTTGGAAACTTCCTCACTAAAAAATTCAATCATCTTAACCTGTTCCTCTTCCAAGGGTGAGCACTTCTTGTCTCTTAATGTTCATCTTATTTTTTTTAAATACGATTGTTTGATAGCCACTATTTGTTCATTTACTGTGTGTTTCTCCATAGATTCCGTCTGGTTCCATTTTTAGTGGAGCTTCGAGCTGTGATGGACTGGGTTTGGACAGACACCACACTCTCTCTCTCTAACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21090
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
ENSDART00000108646 Nonsense 2134 2538 44 51
Genomic Location (Zv9):
Chromosome 7 (position 56603601)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55038927
GRCz11 7 55340338
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGTGTGTTTCTCCATAGATTCCGTCTGGTTCCATTTTTAGTGGAGCTT[C/T]GAGCTGTGATGGACTGGGTTTGGACAGACACCACACTCTCTCTCTCTAAC
Long Flanking Sequence:
AGTTCAGCACCATGATCATCGATCGAGCATTATACCTGCGGAAGAGCATCTTGGGAAAGCTCATCTTCCAGGTTATCCTGGTTTTTGGCATCCACCTTTGGATGTTTTTTATCCTTCCTGCTGTCACTGAAAGGTAAGAAAGACTCCAGGAGTGCATTTATTTATTATTATTATTTTTTTTTCAAAGAGTGAGTCATCTCCTTTTTTTTCACAGGATGTTCAATCATAACTCGGTGGCTCAGCTCTGGTATTTTTTCAAGTGCATCTACTTCACTTTGTCAGCGTATCAGATCCGCTGTGGATACCCTACAAGAATCCTTGGAAACTTCCTCACTAAAAAATTCAATCATCTTAACCTGTTCCTCTTCCAAGGGTGAGCACTTCTTGTCTCTTAATGTTCATCTTATTTTTTTTAAATACGATTGTTTGATAGCCACTATTTGTTCATTTACTGTGTGTTTCTCCATAGATTCCGTCTGGTTCCATTTTTAGTGGAGCTT[C/T]GAGCTGTGATGGACTGGGTTTGGACAGACACCACACTCTCTCTCTCTAACTGGATGTGTGTGGAGGACATCTATGCTAACATCTTCATCATCAAGTGTAGCCGGGAAACAGAAAAAGTAGGTCTTTAGCTTGTTTTTCAATTATACTTCTAAATAATAAATAAAACTGTTTATAATTTTTCATTCAGATTAAATTGAACTGTTGTGATATTTTACACACACCAATATACAGAGTTGGGTGTAATGTGTTCCACAGTAACGCGTTACTATATTCTAATGACATTTTTGGGGAACGCAGTAATGTATTGAATTACATTTTAAATTTGTGTAATTTGATTACAGTTACTAAAGTTAATGTAATTGCATTACTTATGTTACTAATATAGTTTTTAGAAGGAAAAATACTTCTTTCAAATCACGTTTTCTGCTGCAACGTCAGTTAATAAGCATGTGCTTTTAAATTCCTGGAGAACGCGAGCTGAAATGGCTGCTGACGAGAGT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27064
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000108646 Nonsense 2392 2538 49 51
Genomic Location (Zv9):
Chromosome 7 (position 56594891)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 55030217
GRCz11 7 55331628
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGAGCACCCAGTGGAGCTGAAGCTAAACCTGTCATGCAGCTGTTTGAT[G/T]GTACTAAACAACGCCTTTTTCTACTTGTGGTGACAATTTCTTCTCAACTA
Long Flanking Sequence:
TAATAACTAGAAAATTAATAACTGAATTTAATTTTAATCCAATAATTTGCACCTTTTGTAAAGGTATTTTGAAACAACAATTATTGTGAAAAGAACCATAAACTTAAAATAAACTTAATTGAATAAATGTAAATGAATTATGAAGTATAATTGAAACTACAGTATTAGTAACAATATTTTAGCAAATGTTAAAGCAGATATCTTAATGCGGTCAGTTGCATCCTATATAAAATACTATCTATATCTATAATAGATGCATATAAATGACACCTCTACTGTAAATACTCTTTAAGGATCAGTGCTTGTCTGTGTATTATGTTTCGTAATTAACGTATATTATTTATTGTGTTGTATTGTAGATTTTATATATTTATTGTATTGTTAAATTATATTCTGATTTTGTTTATAATCTCTGTTGTAGACATGTGCCGCATATGTTTCCTAACTACATCAGAGCACCCAGTGGAGCTGAAGCTAAACCTGTCATGCAGCTGTTTGAT[G/T]GTACTAAACAACGCCTTTTTCTACTTGTGGTGACAATTTCTTCTCAACTACGGCATATATGTTCCCGGTTTACCTTAAAATTTAAGAGAAAATTATCAGCCCCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTGTGTGTGTGTGTGTACAGTATGTCACAAAAGTGAGCACACCCCTCCTACTTCTGTAAATATTTATTTATAACTTTTTATAGGACAACAGTGCAGAAATGACTCTTTGACACAATGAATAGTAGTCAGTGTAAAGTGTTTATAGCAGTGTAAATTTATTGTCCTCTCAAAATAACTATCCACTACTAATAACTACTCATAATCACTGGCCACTTTTTTAGGTACATCACTCTAACTACTCATTAACGGAAATTACAAATCAGCCAATCGCATGGCAGCAAGCCAATGGATTTAGGCATGTAGACATGGTCAAGATGATCTGACT
Associated Phenotype:
Not determined