ZMP
herc2
Ensembl ID:
ZFIN ID:
Human Orthologue:
HERC2
Human Description:
hect domain and RLD 2 [Source:HGNC Symbol;Acc:4868]
Mouse Orthologue:
Herc2
Mouse Description:
hect (homologous to the E6-AP (UBE3A) carboxyl terminus) domain and RCC1 (CHC1)-like domain (RLD) 2
Alleles
There are 20 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40738 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15868 | Nonsense | Available for shipment | Available now |
sa44640 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13507 | Nonsense | Available for shipment | Available now |
sa30874 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13593 | Nonsense | Available for shipment | Available now |
sa13641 | Nonsense | Available for shipment | Available now |
sa40739 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33904 | Nonsense | Available for shipment | Available now |
sa33905 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33906 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38562 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20751 | Essential Splice Site | Available for shipment | Available now |
sa10421 | Essential Splice Site | Available for shipment | Available now |
sa20752 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20753 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40738
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000110770 | Nonsense | 273 | 4832 | 7 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37720324)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37794082 |
GRCz11 | 6 | 37771976 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTGACATCCATGGAAGTGCCAGTGGAAAAGCACCCAGTAACATTCCCT[T/A]GCAGGATCAGCACTTGGCCCTTGCCATCCTGCTGGAGCTCGCAGTGCAAC
Long Flanking Sequence:
TTTGTGCCCTGTCAGGAGATGATGCAGACCTGTGCAGTGAGTTACTGCAGGAGTCTCTGGATGCTCTGCGGGCTCTTCCAGAAGCTACTCTGTTTGATGAGGGCACTGTATCTCCTGTTTGGCTGGAGGTGGTTGAGAGGGCTACTAAATTTCTAAGGTTGTCTTGTCATTTACACTATTCTCAAAGCATACATATTATGATTTTGCATAAATTCTCAAAGTTTAAAGAAGTCTAAAAATATTTTTTACTCATCAATGTTTATTTATTTGATTACAAAATGAAGTGGAAAAATGTTTAATTAATGTTACAATTAAAAACAGCTTTATTTTAATATATTTAAAATATTTATAGTTAAGAAATTAATTCCTGTTATGCCATCACTTAATAAGAGAAACACAATTTGAATGATTGCTGACATTTTTAAGCTTATTTTTCTATATTTTGTTTTTTAGTGACATCCATGGAAGTGCCAGTGGAAAAGCACCCAGTAACATTCCCT[T/A]GCAGGATCAGCACTTGGCCCTTGCCATCCTGCTGGAGCTCGCAGTGCAACGAGGAACTCTCAGGTATTCAGCATGCTCTTACATGAATTTTCCAAGAAATATTGACTGTGACCAAAAGCCATTTTCACTCCTAAATTTTTATTTTAAACCTTGCGTGTACCATTAAAAAAAAAAACTTTTTTTATTTATTTATTATATATATATATATATTTTTTTTTTTTCAAGACTGAAGCATTTTCATTCATAAATCCAGTCTCTAAACTGCTTGTTCATGTTTTTGTACTGTAGTCAGCTGCTGTCTGCAGTTCTGCTGCTTCTGAGGCTCTGGGACAGTGGAACTAGAGAGATGGATAATGAGCGCTCCACCCAAGGCACCAGCGCCCCGTTACTGCCCCTCCTGCAGCGCTTCCAGAACATCCACAGCAGTAAAGAGGAGCCTGTTCCTGAAGAGGAGATTGAGGTAAGCTCACCAAACAATAGTTAGAACTTTATCTTTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15868
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110770 | Nonsense | 667 | 4832 | 14 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37727770)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37801528 |
GRCz11 | 6 | 37779422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGGTGTGCTGTGGGAGCCAGTTCTCCGTAGCGCTCACTAAAGATGGA[C/T]ARGTTTACACCTGGGGCAAAGGAGACAATCAACGACTTGGACATGGCACT
Long Flanking Sequence:
AGCAGATGGAGAGCTTCACACATGGGGCCGAGGAAACTACGGCAGACTGGGCCATGGTAAATGCAGTAGAATCCTGTTTATACCATGACATGCAGTATTTGACTTTAGGACGAAGTAAAATGACACATATGTGTTTATTGATCCTGAAGGCTCCAGTGAGGACCAGACCACTCCCATGCTAGTAACTGCACTGAAGGGGCTGAAGGTGATCGATGTGGCCTGTGGAAGCGGAGATGCTCAGACGCTTGCTGTGACTGAGAATGGTGTGATATCTGACATTTGACTGCTTTTATTGTAATGATTGAGTGAAACAATCACTTTTCTCTTGATTGCTCTTTACAGGTCAGGTATGGTCATGGGGTGATGGAGATTATGGGAAACTGGGCCGAGGGGGCAGTGATGGATGCAAAACACCAAAACTAGTGGAGAAGCTCCAGGATCTGGATATTGTGAAGGTGTGCTGTGGGAGCCAGTTCTCCGTAGCGCTCACTAAAGATGGA[C/T]AAGTTTACACCTGGGGCAAAGGAGACAATCAACGACTTGGACATGGCACTGATGAACATGTCCGCTATCCAAAACTACTTGACAGTCTGCAAGGTTCAGTGTTTTCCTTTATTTTCAAACCATTGTTTTTTTTATTTACTGGAATTACTTGTACTGAAATTACATGTTTGGTTTACTGAGGCAAACCAAACATGACAATGTCTTGACACATTTCTTAGTTTGTATCTTATGAGTATCAGATAGGTCTTTCCCTGCACTGAATAGTACTGTATATACTTTTGAAGGTAAAATTGTTAGCCCTCCTATGAAATTATTGTTTTTAAGTTATTTGCCAAGTGCTTTTTCAGGGTCTTTTATCAACACATTTTTAAAATAATAATTTGTTAGTTTTAATAACTAATTTGTCATAAATAGTTTCTTCTGCCTTTGCCATGATAAGAGTAAACTAGTGTTAAAGTGCCATCTAAGGGGTTAACTAGGGTAATTAGGCAAGTCATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44640
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000110770 | Nonsense | 894 | 4832 | 17 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37732757)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37806117 |
GRCz11 | 6 | 37784011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACCGTGCTCCAGAGTGGCTGGTCAGTGCTACTCCCCACTGCAGAGGAA[C/T]GAGCAAGAGCCCTGTCCTCGCTGCTGCCCAATGCAGGTCAGTGCATGAAA
Long Flanking Sequence:
TTTTAGATTACAAGTGCAAAACAATCAATGTAAGGTAACAAAATCATTTAATTAGTTTTGATTTCATTTGCACTATAATTCATAAGAAATTATTATTTTTTTATTTTAATAATATTTAACCTTTGTGCTATTTTTCTACTGTTTTTTTTTATCAAACAAATGCAGTCTTGTTGAACCGAGTAGTTTAAATTTCACATTCAAACCTCTTGATGAGTTTTGTAGGCTTATTGCTTCAAAAATATCAGTTTGATTGGTAGGGAATGTCTTGGAACAGTGCTTTAAAATGGGGATTTTTGTTTTGTGTCCAGCTTCATGCAGCCATCAGTAATCAGGTGGATCCCGAGGAGCTGGGTCTGGGTCTGGGCAGTGTGCTGCTTAATAACCTCAAGCAGACGGTGGTGACTCTGGCCAGCAACGGCGGGGTGCTAAACACTGTGCAGGCTGCCGCCCAGACCGTGCTCCAGAGTGGCTGGTCAGTGCTACTCCCCACTGCAGAGGAA[C/T]GAGCAAGAGCCCTGTCCTCGCTGCTGCCCAATGCAGGTCAGTGCATGAAATCTGTGCTTGGAAAAACAGCTTGAATTAATGCTTAATACTATTGGTATCTGTTTTCCTTTATTTTTATTAAGTGTTCCATTTATTTTATCATTTGTGGATAAGTGTCATCTTGGCACCATTGTATAAAGTCAAAAAATAAGTCGAGGTCTGTTTCCAGCAGAGTGTTGTTGGTCAAAAGCATTTCTGTGTTTTTTAGCATCTGCTAATGAGATGAGTGTAAGTCCTGGCCGTCGCTTCATGATCGACCTCTTGGTTAGTAGTCTGATGGCAGATGGAGGGTTGGAGTCTGCTTTGAATGCTGCCATCACGGCCGAGATCCAGGTCAGCATGTTTTATTTAATAGTCATTTCATCATTTATTCACCCTCCATGCCTTATATCTGCAACATCCCACAGAACCCTGCCAAAAACAGACAGAGGAGGAAACAGATTCATGACCCCTCAGGGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13507
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110770 | Nonsense | 1088 | 4832 | 21 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37736814)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37810174 |
GRCz11 | 6 | 37788068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACTCAGARATTCWGGGAGTTGGCTCTCTCYTGAAGAAGTATATGGCTT[T/A]GCKTTGCACACACATCGGTGATATCCTTCCTGTGGCCACCAGCATTGCCC
Long Flanking Sequence:
GCCACAGTCTTAGCCAATTCAACTAGCTCGGATGCTATTGAATGAAGCTGACCAGCGCTTAACGATGACCCAAATTTGGGTGGAGACTGGTGACTTGGTGTCTCAGGGTTTTTTTTTTCTAACTAACTGAATTTGCCTGTAGTAACACTTTTTGTGTGTGTTTGTTCTGAAGGAACATTGCTTCACAGACTATAGCCCGTCTTAAGGATGTGGCCCGACGCATCTCAAATTGTCAAGACACCGAGCAGGTCAGCAAGGAGCGCTCAGCCTCTCTGGACCTGCTGCTGCGCTTTCAGAGGCTTTTGGTCTGCAAATTGTATGTCGGAGTCAATGGCACTGTGGGTGTGGGAGGATACAGTAAGTAAAAGAACTTAATTTAGTGAATTTATTATGGAAGTTATACCATCTGTACATCTAATGAGAAGCATCTCTCATTGTCACAGCTTTGAGTCACTCAGAAATTCTGGGAGTTGGCTCTCTCCTGAAGAAGTATATGGCTT[T/A]GCTTTGCACACACATCGGTGATATCCTTCCTGTGGCCACCAGCATTGCCCTCAACAGCCATCGTCACTTTGCAGAGGTGGCTCGTGTCCTTGAGGGAGATCTTACAGGTGAAATGCAGTGCTATGTCATCAGACAATAATGACTTCTGTGAAAATCCACAGAAGAATCTTGCTCTAGAAAACTTGAAAGACTTTTTATTTATTTTTTTAAATGTATTTATGTATTTATTTTAAACTTTTTAAAATGTATTATTGTTGGTATGATTTTTTTTGGAGCAAGATCCTTATAGTCTAATCCAATTAAATTATTTAAACTAAGCTAAGCTAAAAGTGCTTCCGTAACTTCTAAGCTAAGCTAAAATTTCTGAAAATGTAAAAATGTTAAAACTCAACTTTTGAACTGTTTACAAATGATCTTCCTTTAAAAGACTTGGGGTTGAACATCTTTTTTTTTTTTTTTTTTTTTTCACATATTTCTTAAAAATAATAGGTGGTGCATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30874
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000110770 | Nonsense | 1166 | 4832 | 22 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37737471)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37810831 |
GRCz11 | 6 | 37788725 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCATTCCTCTGCTCGCTGCTCTTCTGGAGCACTTGGACCGTTTTAACTA[T/G]CTTGCACCTGGTACAGAAAGAGATGACAATGAGGATCTTGCCTGGCCTGG
Long Flanking Sequence:
CACAGAAGAATCTTGCTCTAGAAAACTTGAAAGACTTTTTATTTATTTTTTTAAATGTATTTATGTATTTATTTTAAACTTTTTAAAATGTATTATTGTTGGTATGATTTTTTTTGGAGCAAGATCCTTATAGTCTAATCCAATTAAATTATTTAAACTAAGCTAAGCTAAAAGTGCTTCCGTAACTTCTAAGCTAAGCTAAAATTTCTGAAAATGTAAAAATGTTAAAACTCAACTTTTGAACTGTTTACAAATGATCTTCCTTTAAAAGACTTGGGGTTGAACATCTTTTTTTTTTTTTTTTTTTTTTCACATATTTCTTAAAAATAATAGGTGGTGCATTTTCAGACTGTCTGGTTTCTTCACCCACCAGGTGTTCTGCTACCAGAGCTCATTGTGTCCATTGTGCTGCTGCTGACCCATGATGCTGGACTAATGCAAGAGACTGGATCCATTCCTCTGCTCGCTGCTCTTCTGGAGCACTTGGACCGTTTTAACTA[T/G]CTTGCACCTGGTACAGAAAGAGATGACAATGAGGATCTTGCCTGGCCTGGACTCATGGGTATGTGAGAAATCCCTCTAAACTATTGTTTAATGTATATGAGTTATGCTTAAATCCAATCCTATTTAACATGAATGAAATTATAGCAAATGAGATGAATTGCTATATTTATGAATTTAGTGTAAGAGAATGTGGTAGGATGGCAAATAGATAACATCTTAGTGGTAAGATGACAAAGCAAAAATGCACAATGGAGTGAAGAAACAACAGTGATTTATTAGAGAAAAGAATTCGAATTTTGAAAGAACATGACCATGTGTGCACCACATGTGGATAACGGTAATAAGCTGTAAATATATATAACATAGANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCCGTTGCAGTTGCTACTCTATGTTATATATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13593
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110770 | Nonsense | 1331 | 4832 | 26 | 93 |
ENSDART00000110770 | Nonsense | 1331 | 4832 | 26 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37740398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37813758 |
GRCz11 | 6 | 37791700 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGCATGTNAAAAAAAAAGTCACTTGCTYCTATACCTYCCAGAATGGCTC[C/T]AGTCATCYATTTTCTTYGGTGGACTTCAGACCAGTCAGATCCACTATAAT
Long Flanking Sequence:
AAATAAGAGTGGCGGAAAACTGCTTTAGGAGGATGTTTGATGGGGAAATCACCCCCCTCCCTTACGAAAAAAAAAACAACAGGAAAAAAAATAACAAGACATGATAATCAATTTATAAGAAATTTTAATTACCAACTTCAAATAAATAAAATAGCAGATAATGTAACTAGTAAAATTATTTCTAACTATTTATTGATCAGTAAATTATGTCTGGCTGAACTGTATTACATATTATCATAATAGTATTTTAGTAATGGCACAGCCAGTTGGAAGAATGAATCTAAAGTCAAAAACAATAGTATGTTGATTTGACTGGCATTCAGTTCAAAATTAATAAATTTACAATTCATTTTTTTCCCTTGATAGTTTAGTAAAGTAATGAAAAATTCAACTCATTCTGTTCTGTACTGTACTGTACTGTAGAATGACCTGTTTTTGCAAAAAGATTTTAATGCATGTAAAAAAAAAGTCACTTGCTCCTATACCTTCCAGAATGGCTC[C/T]AGTCATCTATTTTCTTCGGTGGACTTCAGACCAGTCAGATCCACTATAATTATAACGAGGAGAAGGATGAGGACCACTGCAGCTCTCCAGGGACCACCACACCAGACAAAGCCAAACTGTACTGCCGCAGAATCACCCTGAGTGATCACGCCCAGCCCTTCCTGCAGGCCATCGCTGACAACACCACCCAGGATCACACTGTGAAGGTCACAGCATTTATTTGTCTCCTCATTTAATATTATGTATAATACAGATTTCTCTTTATAAATCTAAATATTTAGTTGTTACTCTGTTAATCAAAGTCAATTCAGGATAATGTGGCATGTACTGATTTATTAATGACTGAATTGTTTTTTTTTATTTGCTACAGGACTTTTTATGCCAAATCGAGCGGTGCTGTAAACAGTACCATCTCATCACTCCCATCACTTTTCCACCTGAACATCCTGTGGAGGAAGTGGGTCGCCTGCTGCTCTGCTGCCTTCTGAAGCATCAGGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13641
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110770 | Nonsense | 1331 | 4832 | 26 | 93 |
ENSDART00000110770 | Nonsense | 1331 | 4832 | 26 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37740398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37813758 |
GRCz11 | 6 | 37791700 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGCATGTNAAAAAAAAAGTCACTTGCTYCTATACCTYCCAGAATGGCTC[C/T]AGTCATCYATTTTCTTYGGTGGACTTCAGACCAGTCAGATCCACTATAAT
Long Flanking Sequence:
AAATAAGAGTGGCGGAAAACTGCTTTAGGAGGATGTTTGATGGGGAAATCACCCCCCTCCCTTACGAAAAAAAAAACAACAGGAAAAAAAATAACAAGACATGATAATCAATTTATAAGAAATTTTAATTACCAACTTCAAATAAATAAAATAGCAGATAATGTAACTAGTAAAATTATTTCTAACTATTTATTGATCAGTAAATTATGTCTGGCTGAACTGTATTACATATTATCATAATAGTATTTTAGTAATGGCACAGCCAGTTGGAAGAATGAATCTAAAGTCAAAAACAATAGTATGTTGATTTGACTGGCATTCAGTTCAAAATTAATAAATTTACAATTCATTTTTTTCCCTTGATAGTTTAGTAAAGTAATGAAAAATTCAACTCATTCTGTTCTGTACTGTACTGTACTGTAGAATGACCTGTTTTTGCAAAAAGATTTTAATGCATGTAAAAAAAAAGTCACTTGCTCCTATACCTTCCAGAATGGCTC[C/T]AGTCATCTATTTTCTTCGGTGGACTTCAGACCAGTCAGATCCACTATAATTATAACGAGGAGAAGGATGAGGACCACTGCAGCTCTCCAGGGACCACCACACCAGACAAAGCCAAACTGTACTGCCGCAGAATCACCCTGAGTGATCACGCCCAGCCCTTCCTGCAGGCCATCGCTGACAACACCACCCAGGATCACACTGTGAAGGTCACAGCATTTATTTGTCTCCTCATTTAATATTATGTATAATACAGATTTCTCTTTATAAATCTAAATATTTAGTTGTTACTCTGTTAATCAAAGTCAATTCAGGATAATGTGGCATGTACTGATTTATTAATGACTGAATTGTTTTTTTTTATTTGCTACAGGACTTTTTATGCCAAATCGAGCGGTGCTGTAAACAGTACCATCTCATCACTCCCATCACTTTTCCACCTGAACATCCTGTGGAGGAAGTGGGTCGCCTGCTGCTCTGCTGCCTTCTGAAGCATCAGGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40739
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000110770 | Essential Splice Site | 1399 | 4832 | 26 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37740606)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37813966 |
GRCz11 | 6 | 37791908 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCCTGCAGGCCATCGCTGACAACACCACCCAGGATCACACTGTGAAGG[T/G]CACAGCATTTATTTGTCTCCTCATTTAATATTATGTATAATACAGATTTC
Long Flanking Sequence:
GTCTGGCTGAACTGTATTACATATTATCATAATAGTATTTTAGTAATGGCACAGCCAGTTGGAAGAATGAATCTAAAGTCAAAAACAATAGTATGTTGATTTGACTGGCATTCAGTTCAAAATTAATAAATTTACAATTCATTTTTTTCCCTTGATAGTTTAGTAAAGTAATGAAAAATTCAACTCATTCTGTTCTGTACTGTACTGTACTGTAGAATGACCTGTTTTTGCAAAAAGATTTTAATGCATGTAAAAAAAAAGTCACTTGCTCCTATACCTTCCAGAATGGCTCCAGTCATCTATTTTCTTCGGTGGACTTCAGACCAGTCAGATCCACTATAATTATAACGAGGAGAAGGATGAGGACCACTGCAGCTCTCCAGGGACCACCACACCAGACAAAGCCAAACTGTACTGCCGCAGAATCACCCTGAGTGATCACGCCCAGCCCTTCCTGCAGGCCATCGCTGACAACACCACCCAGGATCACACTGTGAAGG[T/G]CACAGCATTTATTTGTCTCCTCATTTAATATTATGTATAATACAGATTTCTCTTTATAAATCTAAATATTTAGTTGTTACTCTGTTAATCAAAGTCAATTCAGGATAATGTGGCATGTACTGATTTATTAATGACTGAATTGTTTTTTTTTATTTGCTACAGGACTTTTTATGCCAAATCGAGCGGTGCTGTAAACAGTACCATCTCATCACTCCCATCACTTTTCCACCTGAACATCCTGTGGAGGAAGTGGGTCGCCTGCTGCTCTGCTGCCTTCTGAAGCATCAGGATCTTGGTAAGCTAGAAATAGTTTGTTGTTTGAATGGCAGAAGCTAAAATCTATGTATAGTTTCCAGATTTTTACTCTTTGAACTAACCAAAAACAGTGCTGTGCATTTCACATCTCGATTTAATAGTATTTTTGTTGTCATTTATTTATTTCTTTATTGGAGGTCAGGTTTTTCTTTCATTGTTTTATGTTATTATTTGAATGTTGCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33904
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110770 | Nonsense | 1463 | 4832 | 28 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37741232)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37814592 |
GRCz11 | 6 | 37792534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGCCCTCTCCCTAGTTGATCAATGTGCCTTGGGTATGGACCAGGGGAAA[C/T]AGAGGTCCCTCCCGAAATCTGTGATTGATGTGTGTCGAATGGTGTATCAG
Long Flanking Sequence:
TATTAATGACTGAATTGTTTTTTTTTATTTGCTACAGGACTTTTTATGCCAAATCGAGCGGTGCTGTAAACAGTACCATCTCATCACTCCCATCACTTTTCCACCTGAACATCCTGTGGAGGAAGTGGGTCGCCTGCTGCTCTGCTGCCTTCTGAAGCATCAGGATCTTGGTAAGCTAGAAATAGTTTGTTGTTTGAATGGCAGAAGCTAAAATCTATGTATAGTTTCCAGATTTTTACTCTTTGAACTAACCAAAAACAGTGCTGTGCATTTCACATCTCGATTTAATAGTATTTTTGTTGTCATTTATTTATTTCTTTATTGGAGGTCAGGTTTTTCTTTCATTGTTTTATGTTATTATTTGAATGTTGCATTTTGTTGCTTAATTAAAAAAAAAAAAAAATCTGTTTTTTATTTGAGGGAGACATTTGTGTTCTTGTGCAGGTCATGTCGCCCTCTCCCTAGTTGATCAATGTGCCTTGGGTATGGACCAGGGGAAA[C/T]AGAGGTCCCTCCCGAAATCTGTGATTGATGTGTGTCGAATGGTGTATCAGGCCAAGTGTTCGTTGATAAAAGTGAGCATTTAAATAAGATTACTCCTGGATTATTATTTTATTGTAGTGTTCTCTTATTTTAGTGGTAATTTTTGGGAATTCATTTTTAAATTAAATCTTACAATTTGTTCAAAAACTACAACAAAACCATACGGAATCTGCAAACGTTTTTTGCTAAATCTGCGAAGAATTTTGGTAAAAATCTGCGAATTTCTGTGGAATTATTTTGGGAGTATTATAACTAAAACCTTAATATGTGACTTATTTAATGTTTAAAATGCAAATCCAATTAGATTCCTATTATTTGGTAAACAAAGCAACAAAGCAATCTCATATAATATATCTACTAAAATACAATTTATTACTGTACAAACTGCATTTTCATATTAATCAATAATATTATTGTCATTAATTTATAAACTGAATAAATAAAGATTTACAGAATTAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33905
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110770 | Essential Splice Site | 1595 | 4832 | 30 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37742438)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37815798 |
GRCz11 | 6 | 37793734 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGCCCCGCTCCTGTTGACAAGAAGCAAACAACTGTCAAATCTGCAAAG[G/T]TTTGCCACTTTCTATTTACGTTAATTTTTTAAGTCACTGTCCTTTTAGAA
Long Flanking Sequence:
TACACAGATATATTGGGTTTAGGTGAAGCATATCATGTCTTTCTGGTTATTTACATCATAATGATTGATTATGATTTCTGTCCCTTCTATAGACACACCAGGAACAGGGTCGTTCTTATAAAGAGGTGTGCGCTCCTGTTATTGAGAGGTTGCGTTTCCTGTTTAATGAGCTACGACCTGCCGTCAGTAATGACTTGTCCATTGTGTCCAAACTCAAACTGCTGAGCTCTCAGCCTCGCTGGAAGAGGATCACACAGAAACTGATCAGAGACCGCCGCAAAAAGAGAGGTGATGAGTCTAACCAATGATTTTAAATGTGTGTAAGGATGTAGAGTCTATAATTATAGCACGTTTTGCTTGATCTTTCAGTGCCTAAAAAGTCGGAGTCAGCTGATCTGGAGGAGTGCAAGATGGAGAGGGAAGGGACCAATGAGGAACCACCTGCTCCTCTAAGCCCCGCTCCTGTTGACAAGAAGCAAACAACTGTCAAATCTGCAAAG[G/T]TTTGCCACTTTCTATTTACGTTAATTTTTTAAGTCACTGTCCTTTTAGAACTATTTAAAGGTGCAGCATGTATGATTTACACCTACCCAGTGGTTGAGGTTTTGCAGTCCAAATACAAAATATTGGATATATATTTTATATATTTTTTTTTTTCCCCACCCGGTCCTCCTGCCAACCACTTAATTCGCATGCAGGCTACCAGATTGATGACACAAACATGAGTAAGCGTGTCTGATAATTGGGTCGCACACCAGACACGCTGCTCTGTGCCACACTGTGACGCACTATGCACATCGAAGCTGTTATTAATCTCCTGTTCGCATTGCTTAGTACACAACCCTTACACAACTATGTATCGACAGGGCATCTGGTGTGCGACCCACTTTATAATGCAAGCTGTTTAGCTAATGTTTACATCTGTAATATTTGCATGATTTGCTAATTAAAGACCACCTAATGAACTTGTATCTCGTTTTGGAGGCTGCTACTGCCCTCTGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33906
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000110770 | Nonsense | 2185 | 4832 | 41 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37751571)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37824931 |
GRCz11 | 6 | 37802867 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTAGTTCTCCTATGCTGTTTTTTCTGTCAGGCTTTGCTTGAAGACTA[T/A]CTCCCCAATGCGGAAGCAGCAGCGGTGGGCAGTCTGATGGCTGTTTTGGC
Long Flanking Sequence:
AGCTTGCTCAGCACTTGTTCTTCAGATCTGCCTCTTCTTAGGGGTATATTACTTTTGTTATTTCTTTGCTCAATGTGTTACTCCGTTCTTTTATTATAGGTCGAGCAAACTCTGATATCAGGATTTCACCTTAACATCTTTGTGACTTACAGAAGGTTCAATGCGTAGGAGGAAGTCCCGCCCCCAGGCCTCACTGACAGCCACTCATAGCAGTACTTTGGCAGAGGAAATAGTGACAGTATTGCGCACGCTTCACTCCCTCAGCCAATGGAATGCCCTGATTAATGAATACATTAACTCTCAGCTCAGTGGAATCGGGGATGTCATGGCAGGCCGACACACTGAAGTGGTAAAAGTCACATTTTTATATGTTTTTGAATTTTTGATATATTAAAGTTGACAAAATTATATTTAGGTGCTCAGTATTGATAATGAGGTATGACTAGAGGATGGTTAGTTCTCCTATGCTGTTTTTTCTGTCAGGCTTTGCTTGAAGACTA[T/A]CTCCCCAATGCGGAAGCAGCAGCGGTGGGCAGTCTGATGGCTGTTTTGGCAGTCATCGGGGGGATTGATGGACGTCTGCGTCTGGGTGGACGTGTGGTCCATGAGGAGTATGGAGAAGGCACAGTGACTCGCATCACACCTAAAGGACGAATCACTGTTCAGTTTCATGAGATGAGGAACTGCAAAGTGTGCCTGCTCAGTCAGCTCAAACCGGTACATATGCACTTACATGCAGTATTGCTTTTTGTTCATTCGTTACCCTGGAGATTCATGTTAAGAATAGTGTAGGGATGAGACAAATTTTTTCTTTCATGAAAAAATTAAAAATGACCCCAAACCTGCAAGTATAGGTGTTGACAAGTCCCTGACAAGCTATTTATTTAAAACGGCTGATACATTTAGCCAAAACTTGCATACCTAAACATTTTAATGGCAATATGTATTATAAATAATATTCATAAAGCACTTCTGCAGATATATATTAAAAATTTAAAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38562
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000110770 | Essential Splice Site | 2303 | 4832 | 42 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37752254)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37825614 |
GRCz11 | 6 | 37803550 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTGGAGAAACAACGCATGAAGAAATCTCTTAGTAGAGGACTTACAGG[T/C]ACAGCACATGCACAGATCCATAGAAAAACACATATTTGTTCACTTGATCA
Long Flanking Sequence:
CAAAGTGTGCCTGCTCAGTCAGCTCAAACCGGTACATATGCACTTACATGCAGTATTGCTTTTTGTTCATTCGTTACCCTGGAGATTCATGTTAAGAATAGTGTAGGGATGAGACAAATTTTTTCTTTCATGAAAAAATTAAAAATGACCCCAAACCTGCAAGTATAGGTGTTGACAAGTCCCTGACAAGCTATTTATTTAAAACGGCTGATACATTTAGCCAAAACTTGCATACCTAAACATTTTAATGGCAATATGTATTATAAATAATATTCATAAAGCACTTCTGCAGATATATATTAAAAATTTAAAAATAAAGGTTTGTGTGATGTGAATTTTGTTTTATGGATGTCTTTGCAGCTTCACATGATTCCATTCAGCGTTCAGAATCTGCCCTTCGCTGAGCCCATGCTAATGGTGTGGGCCCAGCTAGTCAACTTGGCTGGGAGCAAGCTGGAGAAACAACGCATGAAGAAATCTCTTAGTAGAGGACTTACAGG[T/C]ACAGCACATGCACAGATCCATAGAAAAACACATATTTGTTCACTTGATCAGTCCATATTTGGCCTACTTGACCTCTGCATGGTACAGGGTTCCCACACTTCCTGAAAGAACAGTACTTGAATGTCAGACATATGGTTAAGGACTGAAAAGTACTTTAGTAAAAAAAAAAACACAGGTCTTTCAAAGTGTGTGAATTACACTTTAAATTAATTTTGTTAATGCTGTTATTTGAGCAAGTGTACTGTGCTGCCATAAAAAAAGATAAATTCTTAATTTTAAAAATAATAAATTTTGTACAAGAACTGTGGGAAATAATGGACATTTGAACATTGCCAGTATCAAGTTCAACACATTTTATCACATTTTATAAACATAAAAATAAAAACGTTTCACATTTTTTGAAAATGAAACATTCTAAACATCATAATATCTCTACTATTTTAATGTAAATATTAAGTATAAGCAAACTGTTAAGAACAGTAAGGAGTTTCATGGCACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20751
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110770 | Essential Splice Site | 2535 | 4832 | 46 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37757566)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37830926 |
GRCz11 | 6 | 37808862 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGAGGTGCTGGAAGAGCTTGAGGAGCCTGAGCCTGCCTTTCCTGTGG[T/A]ACATACAAATACACTGATCACACAATCCAGATGTGAGGTGCTGATTCACT
Long Flanking Sequence:
CCCCCTGCTCCCATCGTCCTGCAGCTGATGGAGATGGGCTTTCAAAGGAAAAACATCGAGTTTGCTCTTAAATCACTGTCTGGAACCACAGGTGCTTCTGGAGTGCCAGGTAAAAACATAATTGCTTACGTTGGAGCATGGTATTATCATTGTCTTAAAGAAAATATCCTTTATCCTAATTTATTCATACCCTAAACATGAATAAATTAGACATGATGTATGCCGTATGTTTCAATATAGATATTTATTGTCATTTTGTCATTAAAAAATGTGTCCTAGTGATTGTTAAAAAAAACCTGTAAGAATACATAGAGCAATTTTTGCAAGCAACTGATTCTTTATTGCTTTGGTTTTAGGTGTCGAGGCATTGGTGGGCTGGTTGTTGGACCATCCAGATGTTCTCATTACAGATCTGTCGGATGCAGAGACTGTATCAGATGAATACTCTGATGAAGAGGTGCTGGAAGAGCTTGAGGAGCCTGAGCCTGCCTTTCCTGTGG[T/A]ACATACAAATACACTGATCACACAATCCAGATGTGAGGTGCTGATTCACTTGTTGTCATCAAATGTGTGGCTGACTAATGCTCTTTCATTCGCATGTCAGCCTCCTGGGGTTGTGGTGACTGAGAGTCAGACGTTTAAAAAGAGGTCGGACTTTCAGAGCAATGACGATTATGCTGTTTACGTGAGAGAGAACATTCAGGTGAGGTGTTATTCATATTCCTTAATTTTCTGGAAAATAAATAATGTGAAATCAGCTACTGGTAGCCCTGAATAAACTGAAACATTTACAATTATGTATTTTAGTTCCTGCCACTTCTCCATAGTATTCAACAGAATTCAAAACAGAAATGTAAGCGATGAATAGTATACATTAAAGCAAAATGTCACCATGTGGTAAATGAACTTCATATTCCAAATGCTTACGTTTTTTTTTCTTACATTGTTTGTTTTGTAATGTGCTTTGAAATATAAGTGAATTTACATCAGATTTTGTCATTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10421
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110770 | Essential Splice Site | 2625 | 4832 | 48 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37758769)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37832129 |
GRCz11 | 6 | 37810065 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAAAGGAGGAACYTACTGGGTCCGTTACATCCACACTGAGCTGCTGGG[T/C]AATACTCTTTMTGTTCTCTTAMACATTTTTATAGGTATTTGTTAATTGAA
Long Flanking Sequence:
TATTTTTCATGTGTAATAAACCTTTAGGTTTGTTGTCTGAACAATCTCAAAATGAGCCCAAATTTATACATAAAATGAGGAAAAAGCTATAAGTCAATTATGTAAAAAAAAAAAAAAAAAGCCTTTTTTCTTGTAAATGTTTGTCGTTTTAAATGACATTTACTGGAAAAACAAGAAAAATAATAAAGAAATAATAATGAAATCAATAGTAAATTATATTATAATAACATATTTTTTCTTTTTTTTAAAGTGTTCTTTCATGATTTTTAATATTCAGATTGTGTTCTAAAGTTTGGGTGGTAACTGATCTGAGCTCCGTGTGTGTTGCAGGTGGGCATGATGGTACGGTGTTGCAGGACATATGAGGAAGTGTATGAAGGAGATGTGGGGAAAGTGATCAAGCTTGACAGAGACGGCCTGCATGACCTGAATGTTCAGTGTGACTGGCAGCAGAAAGGAGGAACTTACTGGGTCCGTTACATCCACACTGAGCTGCTGGG[T/C]AATACTCTTTCTGTTCTCTTACACATTTTTATAGGTATTTGTTAATTGAAGCTGGAATTGTGTCATTATAGAAATGTACGGTTGTATAGTTATTGAAAAAAAAATTATATAAACTTCTATTTTCCAGGGTTTCCCCCTCAGAGTTCTCCATCTCATATAAAGATTGGTGATAAAGTGCGAGTGAAGCCCTCGGTCACAACACCAAAATACAAGTGGGGGTCAGTCACTCATAGGAGTGTGGGTGTGGTCAAAGGTAACACGATTGTGTTTAAATTCAGTTCATCTTTATTTCTATAGCACTTTTACAATGTTGATTGTGTCAAAGAAGCTTAGCATGGACGAAGTTCTGGTAAATTTAAACTGCTGATCTGCTTCAGTCCAGTTTGCACAGTTTAGTACTGCTCAGTGTTATGTAAATGTCACTGTTGAAAGCTAAAACACTGAAGAGCAAATCCAAAGATACGCAGGACATTTTAATGATATGGTAATGTTAAACAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20752
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000110770 | Nonsense | 3466 | 4832 | 66 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37771813)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37845173 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCAGAGAGTGAGGAGAGGGTCAGTCCGCACCCCTGGATGGACAGCAAA[C/T]GAGGAGAGGTGAGGAGTTCTGCCAATTCTTGACTGTGTGTGTGTATGTAT
Long Flanking Sequence:
TTGCCATCAGAGTCTCAATAGACAGCCTTTCTATGAATATTTGCTGTATTACAACTAATGAGGTGGACTCAAAATGAACTTAAAATGCCTGTGTACTATGTAACGATTTTATTAGATAGTTTTCCAAATATTATTATGCAGTAATAGTTTTTAATATCTATGAAAGTTAGTACATATATTAATGGTTTTAGTGTATATAGGCATTTTGTTTCTGTCCATTTCAGTAATAAAACAAATATTTTAAAAAGAATTATAAAAACAGTTAAAGCAATGCAAAGCTTTGGCATCCTTTAAACACTCTCACATCTTTCACACCCCATAGAGATGCAGTGGTGGGTGCATTAATGCCATCCTGTATGATGCCTCTGGAGTGTCCCTCCAGCTCTCCGGTGCCCCCATCAGACTGTTCATCAGCTTCCAGCCCCTGTGAGGCTGAGGGTCCTGCCCTGCCCTCAGAGAGTGAGGAGAGGGTCAGTCCGCACCCCTGGATGGACAGCAAA[C/T]GAGGAGAGGTGAGGAGTTCTGCCAATTCTTGACTGTGTGTGTGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTGTGTGTGTGTGTATATATGCATGTATGCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCCAGTGATTCATTTGTTCCCAAACCCCTCCTTAGCGCGAAGCTAATCTGCGCTGATTGGACCGATGACAGTCTGTTGCGATTGGTCGACTGCCTTCAGTCAGAGAATGAAATGCCAAACAGCTAATCAGCAATATAAAAGTAATCACAGTTCATACACGCTCGATAGTGTAAGGCGTGGATTTTAGCTGCCAGTGGGTCAATGTAAATACAGACTATGGACTTGAAAATACAGACGACTAACTATTTTATTGAGCAAAAACTCCAAAAACAGTTGAGGAGATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20753
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110770 | Nonsense | 4262 | 4832 | 82 | 93 |
Genomic Location (Zv9):
Chromosome 6 (position 37784148)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37857508 |
GRCz11 | 6 | 37834714 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAAAAAGGTCATCGCAATAGCAACTGGTTCCCTTCACTGCGTTTGCTG[C/A]ACGGAGGACGGTAGGTCATTAGTATGTTTGAATTATGCTGGCCTTTGTCA
Long Flanking Sequence:
TTTAACATTTCCTATGACAAAAGCTATCCCTTTATCGTTTACAGATGGAAGCTCAAACCATTTGCGAGACAACCTATCAAAATAGTTTCAGTTTGTTTTGGTTTAATTTGAAAAATGTAATATTTCAAAGTGTTCCAAATGTTTTTTATTTTTCATAATTTGATGTTAAACTGAGTTTTTTTGTTGTATTTAATTCTACATTTTTTGATGAATAAACTAAAATGAAAAAATCTGAAAAAATAGAATTTGAGGAAAAAAGTAATAAAAATTTTGGAAAAAATAAATAATTTCATAGGACTGTACATAATGCATTGTAACATAAGCTGATGTTATATTTAGTGTGGGTAATTGTACATGTTTGTGTTTTTTAGGGGGAAGGGTGACTATCACAGACTGGGACACGGCTCAGATGATCATGTTCGCAGACCCCGGCAGGTCCAGGGTTTACAAGGCAAAAAGGTCATCGCAATAGCAACTGGTTCCCTTCACTGCGTTTGCTG[C/A]ACGGAGGACGGTAGGTCATTAGTATGTTTGAATTATGCTGGCCTTTGTCACTTTTTAGGTATTCTGTCTTCTGTTGAACCCAAAACAACATATTCTGGAGAATGTTGGAAACCAGCAGACGTTGACATCCATAGTAGGAAGAAAAAAATACTATGGAAGTCAATGGCTGCTGCTTCCCAACATACTTCAATATATTCTTTATGTTCAACAGAAGAAGGGAAAAAACAACATATTTGGAATAAATGGATGAGTAAATAACAGAATTTACATTTTTGTGTGAAGTGTCCCTTTAATGAGCTACCTTTTTTTTGTTCTCTGAGGTCCACTAATAACATTACATAGTACATTTATACATTACACAATTACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTGTATTTGTATATATATTGTATTTGTATAATGTGTGTATATATATATATATATATACACACACACACACACACAC
Associated Phenotype:
Not determined