Busch Lab

ZMP

sbf1

Ensembl ID:
ENSDARG00000062968
ZFIN ID:
ZDB-GENE-040718-139
Description:
myotubularin-related protein 5 [Source:RefSeq peptide;Acc:NP_001038623]
Human Orthologue:
SBF1
Human Description:
SET binding factor 1 [Source:HGNC Symbol;Acc:10542]
Mouse Orthologue:
Sbf1
Mouse Description:
SET binding factor 1 Gene [Source:MGI Symbol;Acc:MGI:1925230]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa26228 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38424 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33397 Nonsense Mutation detected in F1 DNA Not yet available
sa20215 Nonsense Available for shipment Available now
sa45166 Nonsense Mutation detected in F1 DNA Not yet available
sa1459 Essential Splice Site Available for shipment Available now
sa11843 Essential Splice Site Available for shipment Available now
sa33398 Nonsense Mutation detected in F1 DNA Not yet available
sa25276 Nonsense Mutation detected in F1 DNA Not yet available
sa1433 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa26228
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
ENSDART00000091599 Essential Splice Site 19 1850 1 40
ENSDART00000091601 None None 1885 None 41
ENSDART00000109452 Essential Splice Site 19 1849 1 40

The following transcripts of ENSDARG00000062968 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 8973963)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9910811
GRCz11 4 9911727
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCTCGCCGATTACTTCGTTGTAGTCGGCTACGATCTGGATAAGAGAGG[T/C]AAGAGTGAGACACAGCCAGCGATTCTTCCTCCTCCTCTTCCCCTCCTCCT
Long Flanking Sequence:
GTAGAAAAAATTAATGTATTTATTCAATTTGTTTTTTTAATTGTAAGCAGTTTAATTTATATTTCAATTTTAATTTATATTTTTTAATTGCATTATTGCATAACTATTGAGTCTCTATGTAAAGTTACTTAAATGTAACGAATGGATATGTTTTATTGACGCATTTTTTAGGGTATTTTTATTTTTTACAGCATATCTTCGTGCACGCGCTGTAATGAATGACCACGCAACATTCCCCGGCCGCGCGCCCCTCCCTGTCGTCGTTGAGCTCAGTGCGCATGCGCAGAATGCTGTCAGGGCACGGCTCACTCACAGCGACAGTATGGCGGCGGGCTGGTGCTGTAGGGATGCTGCTTACGCCGCTTTCTTCACAATGTAATAAGGATATCGTCTACTTGTGGAAAGACAGTCATCCCCGAGGCCTGACGCCGTGATCCCGAAAAGATGGCGAGGCTCGCCGATTACTTCGTTGTAGTCGGCTACGATCTGGATAAGAGAGG[T/C]AAGAGTGAGACACAGCCAGCGATTCTTCCTCCTCCTCTTCCCCTCCTCCTCCTCCTGATCTCTTAGATTGGAGTGTATTAGTCGCGGTTTATTCACGGTAAACACGGCAGAAGGCGGAGGGAGCTGGACGCGGTGCCGACACAACTGATTCCGGGCCGGGATGGGCGAGCTACTATCAGCCGCGGATGTCCCAGGCCTCTGGATGTGTACCGCCGAACTCGAAAAGCCGAACCCGAACGAAGTTGCACGAAGCGCGAATTCGACTGTACTTTCTGTCCGGCCTTTCACACGAATCCTTTACAGTTGATAAGAAGTTTGCCAGAGGGTACGGTTTTGTTGTTTTGCCAGGGTGTGACTGTACTTACAGGGATTTATTAGTGCAACCTTTGCCACCCAGTGTTTGACATGTAGCTGTTTGTTATTTTGACCCAACATTCGTGCATTCAGTTGAGTTGAAATGCAAAAAATGGATTGTTTACACATGTCAACAACCCTCAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38424
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
ENSDART00000091599 Essential Splice Site 390 1850 11 40
ENSDART00000091601 Essential Splice Site 392 1885 11 41
ENSDART00000109452 Essential Splice Site 390 1849 11 40

The following transcripts of ENSDARG00000062968 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 9024363)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9961211
GRCz11 4 9962127
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGCACATCATTCGCATCCACCCTGAACCCGTCATCCGCTTCCATAAG[G/A]TAATTAATACAGCCCTGAATACGATTTAACAGTAGAACCTATGATATTTA
Long Flanking Sequence:
TTAGTATCATTTTAATATGCATTTAATGATTAAACTCCAACAAATCAAAATAAATGGAATATTAATATACAACAACAATTTAGCTGCATTATTGTACTGTGATCTCAATATGCATGTTTTGTGTAATAAAGGTTCTGGATCCAGAGCTGGAAGTGGCTGATCACGCTTTTCCTCCACCTTCCATTCAACCCTCCGCTCTTAAGATTCAGGTACTTTTCCTTTGTGAATCTATAAATATGTTGTTCCTCCTTCCTTGTGTATAACAATCAGCATCTTACATAACGTATAAAATGCAAATTTTTCTAGCTGAATCTCTTCGGGTTGATGTGACATTGCAGGATGTGCTTTGTTTTAATGAAAGTTGAATTGTTTTATGTGCTCTGCAGGATAAAGAGATCCGCGCTGTCTTCCTGTGGCTGTTCTCGCAGCTCTTTCAGGGCTATCGGTGGTGTTTGCACATCATTCGCATCCACCCTGAACCCGTCATCCGCTTCCATAAG[G/A]TAATTAATACAGCCCTGAATACGATTTAACAGTAGAACCTATGATATTTACAGTGTTGGACAAAATAATTGACAGATCTAAAAATATTGGCCTTTTTTATATATCCAAAACATGATTCCATTTCAAAAGCAAGCAAATTTCTGATGAACTATTTGTTGTGTGAGAGACGTGTTATTTTTTATCCACCTTTAACTGAAATACTTGGTAACTATTATACATTTGAACGGTAAAACAGATCATAAAAGCTTGTTGTTTTCTCTCCAGGCTGCTTTTTTGGGGCAGCGAGCACTATCTGAGGATGACTTCCTGATGAAGGTGCTGGATGGCATGGCCTTCGCCGGGTTTGTGTCTGAACGCGGTCCTCCGTATCGAGCCACTGACCTGTTTGACGATGTAAGTCATGGTTCAGTTTTAGATTTCTCAATCTTAGAGTCTTAAGATTCTCTCTGACTTCTTTATTTTCCTTTTAGCTCATAGCCAATCAGGTGGAGCGCATTCGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33397
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
ENSDART00000091599 Nonsense 443 1850 13 40
ENSDART00000091601 Nonsense 445 1885 13 41
ENSDART00000109452 Nonsense 443 1849 13 40

The following transcripts of ENSDARG00000062968 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 9024861)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9961709
GRCz11 4 9962625
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACTTCTTTATTTTCCTTTTAGCTCATAGCCAATCAGGTGGAGCGCATT[C/T]GAAAGGAGACTGGAGATCCTCATAAAGTCATGAAGCACATTAAGGAGCTG
Long Flanking Sequence:
AGGTAATTAATACAGCCCTGAATACGATTTAACAGTAGAACCTATGATATTTACAGTGTTGGACAAAATAATTGACAGATCTAAAAATATTGGCCTTTTTTATATATCCAAAACATGATTCCATTTCAAAAGCAAGCAAATTTCTGATGAACTATTTGTTGTGTGAGAGACGTGTTATTTTTTATCCACCTTTAACTGAAATACTTGGTAACTATTATACATTTGAACGGTAAAACAGATCATAAAAGCTTGTTGTTTTCTCTCCAGGCTGCTTTTTTGGGGCAGCGAGCACTATCTGAGGATGACTTCCTGATGAAGGTGCTGGATGGCATGGCCTTCGCCGGGTTTGTGTCTGAACGCGGTCCTCCGTATCGAGCCACTGACCTGTTTGACGATGTAAGTCATGGTTCAGTTTTAGATTTCTCAATCTTAGAGTCTTAAGATTCTCTCTGACTTCTTTATTTTCCTTTTAGCTCATAGCCAATCAGGTGGAGCGCATT[C/T]GAAAGGAGACTGGAGATCCTCATAAAGTCATGAAGCACATTAAGGAGCTGGCGGAGCAGCTTTTCAAAAATGTATGTCCGATTTGTGGGTCTTATATGAATATATATTTTTGTCCAGTTTTTTTTCACAACCTTTTATTTTTAAGCTAACTGTATATATACATACAGTTGAAGTCAGACTTATTGCCCCCCTGTTTATTTTCCCCCCAATTTCTGTTTAACGGAAAGAAGAATTTTTCAAAATATTTCTAAACATTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTGACTAGATATTTTTCAAGACACTTCTATACAGCTTAACGTGTCACTTAAAGGATTAACTAGGTTGACTAGGCTGGTCAGGGTAATTATCGTATAACAATGGTTTGTTCTGTAGACTATTGAAAAAAGTATATAGCTTAAAGGGGCTAATAATTTTTACCTTAAAATGGTTTTTAAAAAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20215
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
ENSDART00000091599 Nonsense 462 1850 13 40
ENSDART00000091601 Nonsense 464 1885 13 41
ENSDART00000109452 Nonsense 462 1849 13 40

The following transcripts of ENSDARG00000062968 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 9024918)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9961766
GRCz11 4 9962682
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACTGGAGATCCTCATAAAGTCATGAAGCACATTAAGGAGCTGGCGGAG[C/T]AGCTTTTCAAAAATGTATGTCCGATTTGTGGGTCTTATATGAATATATAT
Long Flanking Sequence:
GTTGGACAAAATAATTGACAGATCTAAAAATATTGGCCTTTTTTATATATCCAAAACATGATTCCATTTCAAAAGCAAGCAAATTTCTGATGAACTATTTGTTGTGTGAGAGACGTGTTATTTTTTATCCACCTTTAACTGAAATACTTGGTAACTATTATACATTTGAACGGTAAAACAGATCATAAAAGCTTGTTGTTTTCTCTCCAGGCTGCTTTTTTGGGGCAGCGAGCACTATCTGAGGATGACTTCCTGATGAAGGTGCTGGATGGCATGGCCTTCGCCGGGTTTGTGTCTGAACGCGGTCCTCCGTATCGAGCCACTGACCTGTTTGACGATGTAAGTCATGGTTCAGTTTTAGATTTCTCAATCTTAGAGTCTTAAGATTCTCTCTGACTTCTTTATTTTCCTTTTAGCTCATAGCCAATCAGGTGGAGCGCATTCGAAAGGAGACTGGAGATCCTCATAAAGTCATGAAGCACATTAAGGAGCTGGCGGAG[C/T]AGCTTTTCAAAAATGTATGTCCGATTTGTGGGTCTTATATGAATATATATTTTTGTCCAGTTTTTTTTCACAACCTTTTATTTTTAAGCTAACTGTATATATACATACAGTTGAAGTCAGACTTATTGCCCCCCTGTTTATTTTCCCCCCAATTTCTGTTTAACGGAAAGAAGAATTTTTCAAAATATTTCTAAACATTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTGACTAGATATTTTTCAAGACACTTCTATACAGCTTAACGTGTCACTTAAAGGATTAACTAGGTTGACTAGGCTGGTCAGGGTAATTATCGTATAACAATGGTTTGTTCTGTAGACTATTGAAAAAAGTATATAGCTTAAAGGGGCTAATAATTTTTACCTTAAAATGGTTTTTAAAAAATTTAAAACTGCTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAGAAGGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45166
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
ENSDART00000091599 Nonsense 733 1850 19 40
ENSDART00000091601 Nonsense 737 1885 19 41
ENSDART00000109452 Nonsense 733 1849 19 40

The following transcripts of ENSDARG00000062968 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 9031564)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9968412
GRCz11 4 9969328
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAACAGAGTCGTCTGTGGCCCACGCTGAGTAAAGAGCAGCAGCAGGAG[C/T]GAGTCCAGAAAGAGGAGAGCACAGTGTTCAGTCAGGCCATCCACTACGCA
Long Flanking Sequence:
AATTCATTATGGTCTTAAAAGGGTCTTAAAAACTCTTAAATTTGACTTGATAAACCTGTAGAAACCGTTTTTTTTTTATTTATTTATTTTTTTTAAGATTTTAATAATATTTTAAGTTATTAAATCATTTGTTACATAGTTGTTTGATAAGAATTTCAATAGTTTAGTTAATTTATTTTAGGTATGAAAGTTATATACATGTTTTTAATTTAAACCCGCTTAAGAATTTTAGTTTTTTTGATTTATTCAAAGTTTTTGTTTCATTTTATTGGTTTTTAATAAAATTTGTAAAAATTATTTAAACTTTTTATTAATCAATTAATGCACACAAATATTAAGCAAAAATGCCGCCTTTTTTAGTGCTGCATTTGAGGGCTGATCTGTGTTTATTTCAGGAGGTGGAGGGTCTTGGTGTGTCTCAGAATCAGCTCAGCGCTCTTGAGCTGGCATCAGAACAGAGTCGTCTGTGGCCCACGCTGAGTAAAGAGCAGCAGCAGGAG[C/T]GAGTCCAGAAAGAGGAGAGCACAGTGTTCAGTCAGGCCATCCACTACGCAAACCGAATGAGTTACCTGCTTCTGCCCCTCGACACCAGCAAAAACCGCCTGCTCCGCAACACCGGCCTTGGGGACGTCGAGAGCGTCAGCAACAGCTACGTCACCAACAGGTTTGTGCGGGCTCGGACTGGGAGACAATAAAAAAAGCAAACATTTTATTCAAATACAGGGTATCCGCGGGGTCTTAAAGTCCTAATATGACATAAATTTCAAAAACAAAATTTTAGGCCTTAAAAATAAAAACTTATAACAAAAATATATTTATAAATAATATTATAACTTTCTGCTGTGCATACTTTTAGTTTTTAAAGAGTTTTTTTAAGTTATGTTGAAACAATGCATGTATACAACTAGAGTCTGCTTTTTTGACACATTGTTTAAAATACGTAGCTCAGAAATAACTAATTAGAAATATAGCCGCAAGCGGCGATTGACGGGGGTCAAGCAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1459
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091599 Essential Splice Site 786 1850 19 40
ENSDART00000091601 Essential Splice Site 790 1885 19 41
ENSDART00000109452 Essential Splice Site 786 1849 19 40

The following transcripts of ENSDARG00000062968 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 9031725)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9968573
GRCz11 4 9969489
KASP Assay ID:
554-1384.1 (used for ordering genotyping assays)
KASP Sequence:
ACCGGCCTYGGGGACGTCGAGAGCGTCAGCAACAGCTACGTCACCAACAG[G/A]TTTGTGCGGGCTCGGACTGGGAGACAATAAAAAAAGCAAACATTTTATTC
Long Flanking Sequence:
GTTTAGTTAATTTATTTTAGGTATGAAAGTTATATACATGTTTTTAATTTAAACCCGCTTAAGAATTTTAGTTTTTTTGATTTATTCAAAGTTTTTGTTTCATTTTATTGGTTTTTAATAAAATTTGTAAAAATTATTTAAACTTTTTATTAATCAATTAATGCACACAAATATTAAGCAAAAATGCCGCCTTTTTTAGTGCTGCATTTGAGGGCTGATCTGTGTTTATTTCAGGAGGTGGAGGGTCTTGGTGTGTCTCAGAATCAGCTCAGCGCTCTTGAGCTGGCATCAGAACAGAGTCGTCTGTGGCCCACGCTGAGTAAAGAGCAGCAGCAGGAGCGAGTCCAGAAAGAGGAGAGCACAGTGTTCAGTCAGGCCATCCACTACGCAAACCGAATGAGTTACCTGCTTCTGCCCCTCGACACCAGCAAAAACCGCCTGCTCCGCAACACCGGCCTTGGGGACGTCGAGAGCGTCAGCAACAGCTACGTCACCAACAG[G/A]TTTGTGCGGGCTCGGACTGGGAGACAATAAAAAAAGCAAACATTTTATTCAAATACAGGGTATCCGCGGGGTCTTAAAGTCCTAATATGACATAAATTTCAAAAACAAAATTTTAGGCCTTAAAAATAAAAACTTATAACAAAAATATATTTATAAATAATATTATAACTTTCTGCTGTGCATACTTTTAGTTTTTAAAGAGTTTTTTTAAGTTATGTTGAAACAATGCATGTATACAACTAGAGTCTGCTTTTTTGACACATTGTTTAAAATACGTAGCTCAGAAATAACTAATTAGAAATATAGCCGCAAGCGGCGATTGACGGGGGTCAAGCAGTTTAGCAGGGTAAGGTTATATAGCAGTCATGAAGCCTGTGAATTTACAATGCATAGCGCCACCATGTGGCCAATGTCTACGAGTTTCATGCTATGGCCAATTACTTTACATTCTTTTCTAAAGAGCAGTAAAATAAACTATAAACTATCAGTGGTGTGTTACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11843
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091599 Essential Splice Site 868 1850 21 40
ENSDART00000091601 Essential Splice Site 872 1885 21 41
ENSDART00000109452 Essential Splice Site 868 1849 21 40

The following transcripts of ENSDARG00000062968 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 9037556)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9974404
GRCz11 4 9975320
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGGACGCGGTTCACAGGGAGAGCAAACGTCTGCCGCCCATCCAAAAGG[T/C]AACMAACTCATTGTTTTACGTTCCTCTGGGCAGGAAAGGCAGTGTAGAAA
Long Flanking Sequence:
GGCGTCACCAACGAACACCTAAAAGCCCTCCACACAATGATACCAGGTAAAACTCCTTTCTTATTTTTTTAATTATTAGCCCTTATATAAAATTATATATTTTTTGGTGCTGTATAAGAGAGAAGATTTTTTAAAATACACATTTAAAAAAAAAAGTTTTAATATGTGACATATCTGTACAATAGTGTTTTTTCTGTAGCCAATTACAAAAAAAAGTTTTTTAGTTAAAATGTATTATTAAAACTGTCTTTATTTTGGCCAAAATAAAATAAGTAAAATAATTAAATAAAGTAAATATAATTTAATTATATCTATTTAAAAATAAAAAAAAAGAATTACAATTTATTTGGCGGACTCATAATTTGGACTTCAACTGTACATTAAGTTTTTTCTTAACTTTTTTAATGTTCCCGTTTGTCTTTCAGACATCGTTCAGATGCACATCGAGACGCTGGACGCGGTTCACAGGGAGAGCAAACGTCTGCCGCCCATCCAAAAGG[T/C]AACCAACTCATTGTTTTACGTTCCTCTGGGCAGGAAAGGCAGTGTAGAAACGCAGGCAGATTCCTCTTCGCCCCACTTCATCTCCTCCACCATTGAGTCCCAGAGTCACAACAGGTACGTTCAGCTCTCAGAGCGGCGCCTGACTCTGATGCATGATGGGATTTCTGGCCTGCTGTTTTGAGCGCACTTCAGTTTGATGTTCTGCTGTGCTTCCTTTTAACATGTAGGTGTGATTTCCTTTCTTTTTGTATCGGAGATCTTGGTTGCAAGGTGACCAAAGCAAACGCCCTCACAAAACCTTCATGGTTTTTTTGTGTGTGTGGAGGTTGTCAGAGACATTTCTGATGGATTGTGCAATCAGATTATTTTCTCCTGCATTTAAGATCTCAGTCTACTAATTAGGAGATCTTCAATGCTTTTGTTGTTCCAAACCCATATTTTTATATGCACCTTAATGATTATGGCAAATTAGCTTTATTTTCTCTTTCATATGTCTTTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33398
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
ENSDART00000091599 Nonsense 1117 1850 26 40
ENSDART00000091601 Nonsense 1120 1885 26 41
ENSDART00000109452 Nonsense 1116 1849 26 40

The following transcripts of ENSDARG00000062968 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 9045578)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9982426
GRCz11 4 9983342
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGTCAAACCATGAGTAATGTGGTGGAGCGGGCCTGCTGTCGGGACTAC[C/T]AACGGTTGGGACTGGGCACGCTCAGTAACAGCCTGACCCGCTCCAAAAAC
Long Flanking Sequence:
TCTCCACCGACCTGGGAGAACCGCAGCAGTATGCAGTCAGAAATGGACGAGGATGAGATCTCTGGTGAGAATTTTTTTTAATTGGCAATCACTAACACATGATTATTAAATTCAGTTTTTATTACATTTTCTTTATTTGTCACATATAGAGTAATACACAGTATGATATGCAGTGAAGTGCATACACAAACACTTAAAACAATAACCCAAAAAAATAGAAATAAGAATCTAAATATGCAGAAATAGAAGTTATTGAAAGACTTTTGATATAGAGTATGTGGTTGTAGAAAAGGAAAAAGTATAAAAATATAAAAGAAACATATAAGGTTTTCTAACAAAGTGTATTTAAGCATAATTATGATATTACAATTTTTCACAATTTTCATGCAATAGTTTCTGAAGAGCCCGAGCCCAGTTCATTGACGCTCTCGTCCACCATCCGCTCATCTGACCGTCAAACCATGAGTAATGTGGTGGAGCGGGCCTGCTGTCGGGACTAC[C/T]AACGGTTGGGACTGGGCACGCTCAGTAACAGCCTGACCCGCTCCAAAAACGAGCCCTTCCGCATCTCCACCGTCAACCGGATGTACACTGTATGCCGAAGGTGAGCCCCATTAAAGCGACAGTTCACCCAGAAATAAAGATTTACTCCATCTCGCATGGTTGCAGCCTTATGACTACTATGACTATTTTCTGTCAAGCACAAAAGATGTTTTGAAAAATGCTGGAAACCACTAACCATTGACTTTCATAGGAAGAGAAAATGCTTATGCAAGTCAGTGGTTACCGATTTCCAACATTCTTGCAAACCTTTATGTGTTTTATTTTTTTGTTGAGCACAAAAGAAGATATTTTGAAGAATGTTTGAAACTGGTAACTATTGACTTATATTGTAAGAATAAAATGCTTTGGAAGCCAATAGCTGTCAACTTTATTCAAAATAAAAGTCACTAAAAATGCTGTGGAAAAAAAAGCATTGAAATGTTATTTACAGCTGTGTTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25276
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
ENSDART00000091599 Nonsense 1699 1850 37 40
ENSDART00000091601 Nonsense 1734 1885 38 41
ENSDART00000109452 Nonsense 1698 1849 37 40

The following transcripts of ENSDARG00000062968 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 9056049)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9992897
GRCz11 4 9993813
KASP Assay ID:
554-7485.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCTGATGTCCTCTAATCTGAGCCACCAGCGGCGCTCTCAGGGAGTCTA[T/A]CTGCAGGAGAGCGGCGTTGGCTCCTCCATCAATCTGGCTCTAGACTGTGA
Long Flanking Sequence:
TACATGTAACTATTAAAATGACCAAACAATTTAAGTTAAAACTAAGTAAAGCATTTTTAAAATACCTGAAATTAATGAAAACACTTATACTTATTAAAGATATCAATAAATCCTGTAATAGTATGTAAATATTACCAAAAAGCACCTATAGCCTTGACCAGACTTTTGTTTCATCACGTGAGGAACAAAAATTTAATATATGTTTAAAAAAATCCTCCTAATGTTCAACTTACTGTGTTTATGAACAGGATGTGCAGAACCTGGAAACTGAGCTGGGACAGCCTACAGAGAAGTGGAAGGACACATGGGACAAGATTAAAACGACCCAGCGGGTGGAGTCCAGACTAGAGAGCAGGGTATGAAAACTAACACTACGTCTAACCTGCATCTACTAATGTGCGACGTACTGATGCTCAGTTTGTGTGTGTGCAGCATTCGTTCTCCAGCTCTCTGCTGATGTCCTCTAATCTGAGCCACCAGCGGCGCTCTCAGGGAGTCTA[T/A]CTGCAGGAGAGCGGCGTTGGCTCCTCCATCAATCTGGCTCTAGACTGTGAAGTCAGCGCTACATCTACACCCGCTGCGGGACGGCCCAGTACCAGCACTCTCTACAGCCAGTTCCAGAGCACTGAGAGCGAGAACAGGTCTGTCTACACTTCCTACACAAGGCTGCTGGGGGGATTTTCTGAATGGATAGTGGAATTTCAGGGCAGATATATATAGAGGAAAGTCTGCAGTATACCTGCTTTTTTCATTACATTTAATACAATAAGAACAATATATAAACTCAAAATAACTTAATACACTTTGAAATAAAGACATAAAAATTGATTATAATATTAAATAATACAGGAATAACATATTTTAATGTCCATCAGTTCAACAAAAGAGTCAAAGTATACCGACTTAGTTCAAATAAAAAACAATGCTTTAGGAAAATAACTGACATAAGTTTTGAGTAGTAAAATTAAAGTAGTTAGCAGTGTCACCTCACAGCAAGGTCGCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1433
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
ENSDART00000091599 Nonsense 1829 1850 40 40
ENSDART00000091601 Nonsense 1864 1885 41 41
ENSDART00000109452 Nonsense 1828 1849 40 40

The following transcripts of ENSDARG00000062968 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 9060465)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9997313
GRCz11 4 9998229
KASP Assay ID:
554-1361.1 (used for ordering genotyping assays)
KASP Sequence:
CTTTTTCTTCTCTTCCAGCTCAAGACGACCAAAAGAGTGTACAACTTCTG[T/A]GCCCAGGACAGCTCAAATGCGCAGTCATGGATGGACAGTATTCAGGGTTG
Long Flanking Sequence:
GCATTAACATTTTCACACTTTTCTCCGGTTTAAACACTCTTAAAGTTCAAACTTTCATACACAAAGTAAGTTCAGTATTACAAAATTAAACCTAAGATCAAAACCTGTTGTCAGGTGCAAGAGTCGTAGCTGGGAACTGCATACAGCCACCAACTTGTGGTGCCGGTGCTTACCCATATATAAACCTATGTTTGAATGCTGCTTCACGGCGCATCCGGTGTGCAACCCCCTTTACGATGGTCTTGCTGCGGACAGTTACCAGCCTTTTTGCATTCTTGTTGAAACTCACACTGCTAGCGATCAAAAATGTATGTTAATTCGGCAAGCTGAACGCATTCTGTACTGTCCAGGAGACACGGAGGAGATTTATTGACAAACAGCCAATCAGGACGCAGAACACAAGTGTAAAAAAAGGGAGTAAAAAATTATTTCCTAGTAAAAAAAATATTCCTTTTTCTTCTCTTCCAGCTCAAGACGACCAAAAGAGTGTACAACTTCTG[T/A]GCCCAGGACAGCTCAAATGCGCAGTCATGGATGGACAGTATTCAGGGTTGCCTATCTGATGCGTAGGTGTCGGATCCTAGCAGACAACATAACTGTGACGCATAGTAAAGAGGAGGGGCGGAGCCAGTGACGGACAGAGGCCTCATAGCCAATGGGGAGCCACTCCCCGGGCGTTTACAGAGGAAACAGGGCTTCCCTATTGGTGTTATTGAACTTTGCGATGTCGCATCTCATTTCAAAGACTGATATCCGTGCTCGGCTTCAAAACACTTCCTTCACTTGTTTGAAAAAAAGGCATGACCTGCGAGTCTTCTTCAGTTATCGCTCGCATCCCATAATTATCGCTCCAATACTGCCACCTTTCAGCTATGCAGGGGCTCAAAAATGCCCACTAACTAGCCACACAGCTACTAACTACTCACTATTCCATGGTTCGGAGGCAAGTCTAGACTATTGCATCGATTTCCTGCCTTCTCATTGGCCGGTTAAGTTCTCACACT
Associated Phenotype:
Not determined