Busch Lab

ZMP

LOC569603

Ensembl ID:
ENSDARG00000077901
Human Orthologue:
HERC1
Human Description:
hect (homologous to the E6-AP (UBE3A) carboxyl terminus) domain and RCC1 (CHC1)-like domain (RLD) 1
Mouse Orthologue:
Herc1
Mouse Description:
hect (homologous to the E6-AP (UBE3A) carboxyl terminus) domain and RCC1 (CHC1)-like domain (RLD) 1

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa34085 Nonsense Mutation detected in F1 DNA Not yet available
sa26964 Nonsense Mutation detected in F1 DNA Not yet available
sa14578 Essential Splice Site Available for shipment Available now
sa38615 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa20959 Nonsense Available for shipment Available now
sa25364 Nonsense Mutation detected in F1 DNA Not yet available
sa7596 Missense Mutation detected in F1 DNA Not yet available
sa14254 Essential Splice Site Available for shipment Available now
sa40906 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa34085
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
ENSDART00000109030 Nonsense 115 4852 1 77
Genomic Location (Zv9):
Chromosome 7 (position 30607873)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 29000215
GRCz11 7 29271365
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGCCACTGCCCTTCGCAAGCGGCTGCTGGTCCTGCAGCGGGTTTTTTA[T/A]GCACTTTCTAACAAATACCATGACAAGGGCAAAGTCAAACAGCAGCAGCA
Long Flanking Sequence:
GAACCTGTTGAGTAGTTTAGTCCGAGCAGGTTTTAATACTTTCATACACCTCTAGATTCACTTGGCAAGCAGTGATCATTTATATATCACATTTATTGTGTATTCACTGTTCCTCTTTATCTCTCAGATGTGACGTGGAGGGTGTAAGGTGGCACCATGGCTGCGATGATACCTCCAGTAAAACTCAAATGGCTGGAGCACCTCAACAGCTCCTGGATCTCCGAGGACAGTGAGTCCATCTCCACCCGTGAGGGCGTGGCGCTGCTCTATGGGAAATTGCTGACCAATAAGGAGGTGGTGGTCCTCCCTCAGCAAGTGCTCTGTCTGAAGGGCCCTCAGCTGCCGGACTTTGAGCGAGAGTGTCTGTCTAGTGATGAACAGGAGCATTATCTGGACGCCCTGCTGGCCAGTCAACTCGCTCTGGCCAAGACGGTGTGCTCAGACTCGCCGTTTGCCACTGCCCTTCGCAAGCGGCTGCTGGTCCTGCAGCGGGTTTTTTA[T/A]GCACTTTCTAACAAATACCATGACAAGGGCAAAGTCAAACAGCAGCAGCACTCGACCGAAAATACTATGGGTTCTGCGGACTTGCAAGCGGTAAGCGAGCGGCCGCGATCTAGCACAGATGCTCTTATTGAAATGGGTGTTCGGACGGGTCTAAGCTTGCTTTTTGCTTTGCTCCGGCAAAGCTGGACGCTTCCTCCGGCCGGTCCTGGGATCAACCTTTGCAATGATGTCATCACCACAGCCATCGAAGTAGTGGGTTCGCTTCCGCCGCTGTCTTTGGCCAACGAGAGTAAGATCCCTCCCATGGGTTTGGACTGCTTGGCTCAGGTCACTTCGTTTCTGAAAGGAGTGACCATGCGGAACTCTGGGGCTGATGTGGTGGGACGAAGGTTAGCGTGTGAGCTTCTGTTAGGCTTGGCGGCGCAACGAGGGTCTCTGAGGTACCTGCTGGAGTGGGTTGAGATGGCCCTCGCCGCATCAGCGGGAGTCAGCAGTCTGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26964
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
ENSDART00000109030 Nonsense 143 4852 1 77
Genomic Location (Zv9):
Chromosome 7 (position 30607790)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 29000132
GRCz11 7 29271282
KASP Assay ID:
2259-8928.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCAAACAGCAGCAGCACTCGACCGAAAATACTATGGGTTCTGCGGACT[T/A]GCAAGCGGTAAGCGAGCGGCCGCGATCTAGCACAGATGCTCTTATTGAAA
Long Flanking Sequence:
ATATCACATTTATTGTGTATTCACTGTTCCTCTTTATCTCTCAGATGTGACGTGGAGGGTGTAAGGTGGCACCATGGCTGCGATGATACCTCCAGTAAAACTCAAATGGCTGGAGCACCTCAACAGCTCCTGGATCTCCGAGGACAGTGAGTCCATCTCCACCCGTGAGGGCGTGGCGCTGCTCTATGGGAAATTGCTGACCAATAAGGAGGTGGTGGTCCTCCCTCAGCAAGTGCTCTGTCTGAAGGGCCCTCAGCTGCCGGACTTTGAGCGAGAGTGTCTGTCTAGTGATGAACAGGAGCATTATCTGGACGCCCTGCTGGCCAGTCAACTCGCTCTGGCCAAGACGGTGTGCTCAGACTCGCCGTTTGCCACTGCCCTTCGCAAGCGGCTGCTGGTCCTGCAGCGGGTTTTTTATGCACTTTCTAACAAATACCATGACAAGGGCAAAGTCAAACAGCAGCAGCACTCGACCGAAAATACTATGGGTTCTGCGGACT[T/A]GCAAGCGGTAAGCGAGCGGCCGCGATCTAGCACAGATGCTCTTATTGAAATGGGTGTTCGGACGGGTCTAAGCTTGCTTTTTGCTTTGCTCCGGCAAAGCTGGACGCTTCCTCCGGCCGGTCCTGGGATCAACCTTTGCAATGATGTCATCACCACAGCCATCGAAGTAGTGGGTTCGCTTCCGCCGCTGTCTTTGGCCAACGAGAGTAAGATCCCTCCCATGGGTTTGGACTGCTTGGCTCAGGTCACTTCGTTTCTGAAAGGAGTGACCATGCGGAACTCTGGGGCTGATGTGGTGGGACGAAGGTTAGCGTGTGAGCTTCTGTTAGGCTTGGCGGCGCAACGAGGGTCTCTGAGGTACCTGCTGGAGTGGGTTGAGATGGCCCTCGCCGCATCAGCGGGAGTCAGCAGTCTGGAGCAGAGCCAGGAGGGGCTGATGGGATACGACTGCTTCATGAACATTCTGATGCAGATGAGACGATCACTGGTATGGTGCTGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14578
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109030 Essential Splice Site 337 4852 2 77
Genomic Location (Zv9):
Chromosome 7 (position 30607116)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 28999458
GRCz11 7 29270608
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATGGCCTTTGTTCCTTATATGAAGCTGCACTTTGCCTGTTTGAGGAGG[T/G]AACATGGTTATAAATATGTAAAACAACTGTATAAAAACANNATTTTATTTTT
Long Flanking Sequence:
GTTCGCTTCCGCCGCTGTCTTTGGCCAACGAGAGTAAGATCCCTCCCATGGGTTTGGACTGCTTGGCTCAGGTCACTTCGTTTCTGAAAGGAGTGACCATGCGGAACTCTGGGGCTGATGTGGTGGGACGAAGGTTAGCGTGTGAGCTTCTGTTAGGCTTGGCGGCGCAACGAGGGTCTCTGAGGTACCTGCTGGAGTGGGTTGAGATGGCCCTCGCCGCATCAGCGGGAGTCAGCAGTCTGGAGCAGAGCCAGGAGGGGCTGATGGGATACGACTGCTTCATGAACATTCTGATGCAGATGAGACGATCACTGGTATGGTGCTGATTGAAACTCTCAAACACAGAAACCAATCTGCTTTCACAAATGATATTGTTAAACGACTGGTTGTGTGGTGATTTTAGGGTTCTTCTGCTGACCGGAGCCAGTGGAGAGAACCGACCCGCACTGCTGATGGCCTTTGTTCCTTATATGAAGCTGCACTTTGCCTGTTTGAGGAGG[T/G]AACATGGTTATAAATATGTAAAACAACTGTATAAAAACAATTTTATTTTTACTGTAAAAAGTACCATTTAAAGTGAAAGAAACAGAAACTAACATTCTGTATATCCTGAAAAAACATTAGGATATAAAGTAAAATGAACATTTACATTTTGCTGAAACCCACTTCTTAATTAATCTAGCAAATCTAAATAATGAGAGAATTTTAAAGTTATCTTAATTATTTTCAAATTTTCTGAATTCTTAACTTTTTCTTTAAAATTTGCCTTGCATTCTAAAACAATTGTCAGATGTTTTCCTTTCACTTCATTATCTTTTTATTACTGTTGTGAGCAATTCTTTTGTTCTCCTGAATCCAGTTTTCCAGTCTATTTTGCTGTATCAAAAAAATAGATTGTTTGAATGATAAATCATACCAGTTTTTATTTTAATTAATCAGTTGTCCTGATGTCACAGGTGTGCCGCATGGCCTCAGACTACTCAAGAACATGTGCGAGTCCGGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38615
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
ENSDART00000109030 Essential Splice Site 402 4852 3 77
Genomic Location (Zv9):
Chromosome 7 (position 30606467)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 28998809
GRCz11 7 29269959
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGATCCTCCAGCCCAAACTTGCTCCCAGCTTCAGTGATGCACAAACGG[T/A]AGAAAGCATCCTCAGATTATTCTTATTTTTTTCATTCTTCCTTTGATTTT
Long Flanking Sequence:
TTGCTGAAACCCACTTCTTAATTAATCTAGCAAATCTAAATAATGAGAGAATTTTAAAGTTATCTTAATTATTTTCAAATTTTCTGAATTCTTAACTTTTTCTTTAAAATTTGCCTTGCATTCTAAAACAATTGTCAGATGTTTTCCTTTCACTTCATTATCTTTTTATTACTGTTGTGAGCAATTCTTTTGTTCTCCTGAATCCAGTTTTCCAGTCTATTTTGCTGTATCAAAAAAATAGATTGTTTGAATGATAAATCATACCAGTTTTTATTTTAATTAATCAGTTGTCCTGATGTCACAGGTGTGCCGCATGGCCTCAGACTACTCAAGAACATGTGCGAGTCCGGATAGCATCCAGGCAGGTGAAGCAGCCATGGTATCTGAGACCTGCGAGGTCTATGTGTGGGGCAGCAACAGCAGCCATCAGCTTGTAGAGGGAACTCAAGAGAAGATCCTCCAGCCCAAACTTGCTCCCAGCTTCAGTGATGCACAAACGG[T/A]AGAAAGCATCCTCAGATTATTCTTATTTTTTTCATTCTTCCTTTGATTTTTACGTTAGTTGAATTCGGTTTTATGCTTTTTATGTCTTGCATAGCATAGTCAGAATTGCATTATAGCTGTAAACGGGCCATAAAAGCTAGGCCTGAGCCCAACAAGTACATTTTGATTGACAGCTTTTTAAAAGCCTGAACCCGTTTACAGCCAGACATTATTAAGATGTGAACATGCACACAGCTCTTTCACCTTTTTTCAAGAATAAGTCGTTTATATGTGTTTTAACATAATTTATTCATAACAAATGTATATGCCACTTAGAAGTTGGAACAAAGAAATAAAATAAGTCTTCTGTAACATGATAACGTCTCAGCACTCTAAATAGGCCAAGGTACATACACTTAGCAGTTAAATTGGCCAACACACCAATAAAAATAAGGCTTTCTTACCAAATTAAAATAAATTCTAAATTATGACTGTATTTGGCAATAACGAAATTAAGATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20959
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
ENSDART00000109030 Nonsense 984 4852 14 77
Genomic Location (Zv9):
Chromosome 7 (position 30592669)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 28985011
GRCz11 7 29256161
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATCTGATAGCAGCCAACCAGCACACCTCCATGAACTGCTCTGCTCTT[T/A]GCAGAAACAACTGCTGGCCTATTGCCACATCAACAGTGTTACAGAGGTAC
Long Flanking Sequence:
TCATTATTGTAGACTGAAGTAATTGACAGCTATGTTTTGTTCTATTGTTGGTAAGGGTTATAGGATTTGTGAATGGATATATCTGAAAAATAATAATAAAAATATAAAATCAAAAATTATCAAATGATTTAAATTTTAATATTTTTTTTTGATAAGTAAAAATCTTTTTTTAACTGGGATATTTGAAGAAATCCTTTGCATTTAGCCCTGTTAAAGTCAAAAATTTCATTCATAATGGTCTTAAAATTGTCTTTAAAAGTCTTAAATGTAACTTGGTGACACCTGTGGAAACTCTGCCTTTCAATCTTATGACCCAGTCTTAACATTGTAGCTATGTTGATGCCCAAGATCATCATCCTGCTCTTCAATATTTCTCTGTGTGTTAACTGGAAAGGACCAGGCGTTTGGAGAGCTGGAGAAGAACAGTGATAAGATCTTGCAGGGAACATCTTCATCTGATAGCAGCCAACCAGCACACCTCCATGAACTGCTCTGCTCTT[T/A]GCAGAAACAACTGCTGGCCTATTGCCACATCAACAGTGTTACAGAGGTACACACACACACACAAGCAAACACGCATTACCACATGTTCATTTGATTGAGTCTGAGAAGTCTGTGTGTTTTTCAGGGCTCCAGTAGTGTGGCACTTCTTCATAAACACCTGCAGTTGTTACTTCCTCACGCAACTGATATTTTCAATCGCTCTGCAACCCTTCTTAGAGAAAGCTCTGGGAATGGCAGCGTGCGTGAGAAGCTGCGGGGTATGCGAGTGCACACGTTCAAGCTTCACCCATTTAAATGTTAATGAACCTGCTAAATTTGCTTCTGTCTGGATGGTGTAGATGTGATCTACATGTCAGCAGCGGGCAGTATGCTGTGTCAGATTGTGACGTCGTTGCTGTTGTTGCCTGTTTGGGTGGCACGACCTCTGCTCAGCTTCCTCTTGGACCTGCTTCCCCCGCTGGACCGTCTCAACAAACTCCTGCCTGCAGCCACACCTCTAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25364
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109030 Nonsense 1125 4852 17 77
Genomic Location (Zv9):
Chromosome 7 (position 30588916)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 28981258
GRCz11 7 29252408
KASP Assay ID:
554-7418.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCGGATCTGGTTGATCCAGTGTGTGTGTCAGGACCGGCACAGAGCTG[G/A]GTGTGGTTGGTGGATCTGGAGCGCACCGCAGCTCTGCTGGTGGGACGTTG
Long Flanking Sequence:
TGCTTATTGGTTAAATCCGCCCCTGCATATACCTCAACTTTTTTATAATAACTTTTTTATTTTATAATCACCCATAAGAACTGCATATCAACTGGTGGTCATGTTTGATACTGCGGCCAAATAAAGTCTTACTGTAAGCAAATTTTTTAGATAACAGCTTCAAATATGGAATATAATGTGTTCATGTATTTAGCTTTGTTTTTTCTGTCAAATTTAGGCAAAGAAAATCTCATAAGATAAACATTACTACCTTTAGGAAAATAGCCTAAAAACAGCTGGATAACCTTGTGGTGCGTGCTTAGCATTATTGGTCACTCTGCACACAAAAATGACTGATTTGTGTTAAACTTCTTTAACTTTACGGTAATATTCAATTGAATGATTTTTTCTTTGAATCACAACTCATACATTTAGAATTTTTTTTTTTCCTGCCGTTTTCTCCCTGTAGGCTCTCCGGATCTGGTTGATCCAGTGTGTGTGTCAGGACCGGCACAGAGCTG[G/A]GTGTGGTTGGTGGATCTGGAGCGCACCGCAGCTCTGCTGGTGGGACGTTGTCTTGGAGGAATGTTGCAGGGAGCAGCACCCTCCGCAGAGGAACAGCACACCACCCACTGGCTCAAAACACCACTCTTTAGTAACGGCCTAGAGACTGAAATACCACAGCTTGGTATGCACACACATACATACTTCTCAGTCTTATGGTCATCTGTATTGTTGCTCTTTGAAATGTACATTTAGTTAATTGTCCAAAACGACATTGTGCTGGTGAAATCCAAACATTTCTATGGAAATTGTATGACTGGTTGTTGCTTATGAAGATGAAAAGCTGCTTGGTTTAAATGTGACATCTATAACGTGACCACACTTTTATAGAAGTATAAACAGATGTATGCGCCACTGGTAATGTTCAAGCTAAAAGAAATTGTGTATGTGTGTTTCAGATGCGTGCATTAGCTCTCTGCTGGAGGTGGCTCTGTGTGGAAATGAGGAGCAAAGACCGTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7596
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109030 Missense 1412 4852 22 77
Genomic Location (Zv9):
Chromosome 7 (position 30582312)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 28974654
GRCz11 7 29245804
KASP Assay ID:
554-4306.1 (used for ordering genotyping assays)
KASP Sequence:
CCGGAAGCATGAGCGTGCAGGAAGAGCCTCCTCAGCCTGGTCCAGAGCGA[C/T]GCAACAGCWCGACCCCTCAGGAGGGACAGGATCTTTACACCACCTCCTGC
Long Flanking Sequence:
ATGCTGGATTCCCAAGAGCCCCCATGTGGTTTCCAAAAAGTAGTTGGTCCATTTGAATGACTAAAAGCTAAAGGTCATGTTTTTAGCTGTAATCATGCCAACCATTAGGGCTTGCTGTTGAGTGTTCATTATAGGTGTTCATTATATTTAAATATCCAAAAATAGCCAAATTGTCGTCAAGTTGGATATTGGTTCCATAATTACTGTAAAACAATTAAAACCAAAACTCATAAAGAACAGGACAAAACCAAAATAAACATACCAGAGTCTCTTCTGCGCCACCACATCTGTCACATTTAGGAGATACAGAGGGAACAATTTTGTTTTAACATGCTTTTTGGCTGCTTCCCTAACCCAGCCGCTCTGTGTCTCATGTCTCGGTGGACACAGAAATCTTTCAATGTTTCCTATCAGCACGAGAAGCAGCACGAGGAAGGGACCGGGACCGAACCGGAAGCATGAGCGTGCAGGAAGAGCCTCCTCAGCCTGGTCCAGAGCGA[C/T]GCAACAGCTCGACCCCTCAGGAGGGACAGGATCTTTACACCACCTCCTGCAATGCCGTCATCCACCGCTGTGCCATGCTCCTCTTGGCACTCAGCACACCGCTGGCTCAGCACATAAATCAGCAGCCTCTGACAGGTGGGGTCAACCAGGACGGAGTCGGGTTTATGACAAGGTGAGTGACGTCACCCTTATAAAGCGCAGTTAGCTGATATTAAACAAGCGTTAGCATGACTTTCAAGTTTGAGTCGTAACCCTTATCATTGGAGCCTTAAGGTCTCAGTGAACTCGCTTACCTCTGCCATCGGCTCCAGCACGCCCTCGTATCGCACAGGAATGCCTGACCTACTTTTCCAGATTGCACATTATCCAGTTGCACCTTACGTACTGCCCTAATTTTGAAATGCCTTCATAAGCTGACCCAAATATTTTGTCTTTTTTTTACTGTTTTCAAATCTAGTTATGAACATATTGTTCTACAAGTTTGGTTTTAGGTTGTACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14254
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
ENSDART00000109030 Essential Splice Site 1730 4852 27 77
Genomic Location (Zv9):
Chromosome 7 (position 30575957)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 28968299
GRCz11 7 29239449
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTCAGTCACATTAGAAAGAGCCCTGCAAGCAAACAAACACCACATAGG[T/C]AATGGACTCAAACTCATACACTGYTTTGATTCAGGTACCATTTGCTATTA
Long Flanking Sequence:
ATGTTTCTTCAGATGACTTTCTTTGCTTTTAGCTGCAGCTTTTTCTGTTTTATGCATTTCTCTAGTTGCGTCTGGAAGCCCTTCATCAGATTGTGGTGTTGATTTCTGGGATGGAGGAGAAGAGCAGTCAGGCAGGCTCTGGAGCTGGACGCACAGGCCTCAGTTTTCACTCTGCATCTTTGCTAACTTCAGTCAGACTTCAGTTCCTGTCTGGATGTTTCGGCCTGGGGGCTGTCAGTTATGGAGGTCCAAAGGGGGAGAATGTCCAGCTACATCATTACCAGGTAAACTGTTGCACTGGTCTGACCTTTGAGATTAGAGCTACTCCTAAAACATTTTTTTAATAAACTGTATGCACATGCTTTATTTTTTTTGTAGGATGGAGTCAGAGCAGCCAAGAAGAGTTTACAGATGGAAATTCAGACCGCTGTGCATAAGATCTATCAGCAGCTGTCAGTCACATTAGAAAGAGCCCTGCAAGCAAACAAACACCACATAGG[T/C]AATGGACTCAAACTCATACACTGCTTTGATTCAGGTACCATTTGCTATTATTTTATTATGCTATATATACTGTAAAAATGATTTGGATTGCTGTGTGTGTGTGTGTCCAGAGGCCCAGCAGAGACTTCTATTGGTGACGGTGTTCGCATTAAGCGTGCGATACCAGCCGGTTGATGTTTCATTAGCTATTTCTAGTGGCCTTTTGGATGTTCTTTCTCAGCTTTGTGGAACAGAAACCCTTCTTGGACAAACTCTGCAACTCCTGCAAAAGCCTGCTGGTTCTCAGCTCAGCACTGCCCTTAAAGTGGCCAGCACCAGACTGTTACAGATACTGGCCATCAGCACTGGGTACAACACAACGTTTTATTTCATTATACGTCTGTTCATTTCAGAGGCAATGTGAAAGTCAGCTGCTTTGTTTTATATTCTGATTCTAGACATGAATCTTCTTTTTAAAACTTGTGGGTGTGGGGGTCCTTTTCCACAAAAAATATAAAGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40906
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109030 Nonsense 4550 4852 73 77
Genomic Location (Zv9):
Chromosome 7 (position 30532154)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 28924496
GRCz11 7 29195646
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAGTGGATCTTCTCATCCCTTCTCCAAATGCCGCAGCAGAGGTGGGCTA[T/G]AACAGAGACAGGTGAGTGCAGACCAACACCACTCTGAATGCTAGACTCCT
Long Flanking Sequence:
TACTGAAATATATATCAACAACTTCTAGTTCATTCAGACTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTGTGGCAATAAATTAAAAAAACAAACAAAACTATTTAGTGTTTTCCCTATACAGAGTTTATTTTCAGCTGCAAATTTTTTTTTTAAATAAAATCTCGTTTGCTGCCTGTGAATATAGTTCACAAACTTTACCTAAGCAACCTCAAGGTGAAAATACCTACTTGCAGCTTCAGTCTCCACCCAGAGTGAAAGGCAACTACAAAATCTCTGTTAGTGTGAATGAAGCTGAACTTAGTGTAGTCTAGTCAGTAGCTAATGATATAAATTTAGTCACTTTGTGTAAAATCAAATATCATTACATAGTAAAGTGATTTACGGATCTGGTGAATGTGTGCAGGAGCTAGAGACAGGAGTAGTGGATCTTCTCATCCCTTCTCCAAATGCCGCAGCAGAGGTGGGCTA[T/G]AACAGAGACAGGTGAGTGCAGACCAACACCACTCTGAATGCTAGACTCCTCTGGTCTTCTTAACTCATTGTTGCTTTTGTTTTTCGTCAGGTTCTTGCTGAATCCTTCGGCCTGTCTGGAGGAGCACCTGCTGCAGTTCAAGTTTTTAGGCATCCTGATGGGAGTCGCAATCCGCACAAAGAAGCCTCTGGATCTGCACCTGGCACCGATGGTGTGGAAGCAGCTGTGTTGTATCCCGCTCAGCCTGGAGGATCTGGAGGAGGTGGACCTGCTGTATGTACAGACCCTCAACAGCATCCTGCACCTGGAGGACAGCGGCATCACGGAGCAGAACTTCCATGAGGTGCAGTGGTCAACAATACTCACTTACTGAGCAAAGCATGACGAGTCGTTCAGTCCAACTCGCAATTGACTGGTTAAATTTTTGTTTAAGGACCAAAATTCCCACAATCACAGTGAACATTATTGGCTAAATGTTTTATCTCTTGATCTAAAAAAGT
Associated Phenotype:
Not determined