ZMP
dnm2
Ensembl ID:
ZFIN ID:
Description:
dynamin-1 [Source:RefSeq peptide;Acc:NP_001025299]
Human Orthologue:
DNM2
Human Description:
dynamin 2 [Source:HGNC Symbol;Acc:2974]
Mouse Orthologue:
Dnm2
Mouse Description:
dynamin 2 Gene [Source:MGI Symbol;Acc:MGI:109547]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20128 | Nonsense | Available for shipment | Available now |
sa20129 | Essential Splice Site | Available for shipment | Available now |
sa13248 | Nonsense | Available for shipment | Available now |
sa13768 | Nonsense | Available for shipment | Available now |
sa17720 | Essential Splice Site | Available for shipment | Available now |
sa16501 | Essential Splice Site | Available for shipment | Available now |
sa20130 | Nonsense | Available for shipment | Available now |
sa15133 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20128
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 |
---|---|---|---|---|---|
ENSDART00000024031 | Nonsense | 25 | 755 | 1 | 18 |
ENSDART00000097146 | Nonsense | 25 | 872 | 1 | 22 |
The following transcripts of ENSDARG00000069937 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 48319404)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50320544 |
GRCz11 | 3 | 47131184 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTGATCCCCCTGATCAATAAACTCCAAGATGCTTTCAGCTCCATTGGC[C/T]AAAGTTGTAACCTGGATCTGCCGCAGATAGCAGTTGTCGGAGGACAGAGC
Long Flanking Sequence:
TTTCCTATTCTTTTCTTATTGAAATTAAATTGACGTCCAAGCCGTCCAATAGCACTCTTCCGCCGTTGGAGGCCGAAAGCCGATCAAAACGCAGAACACACCAGGAAGCGCTCCCTTGGACCAATCAGATATCACGTTGTCGGTTGACAGGAGGCGGGACTCGCGTCACCGGTGGAGGTCGGATGTCGCCTGACCGGATGATAGCGAGAAGTTTTGTTTTGTGACTTTACGAATGATTGATCCTCTGATCACAGCACGTATTACAACACATGCGCGTCTTCTGTCAGTCAGCGAGTGTTTTACGCGCCGTTTGCCTTTGACAGACCGTTCTGGAAGCGTTTGAAGGGTGGAAACTGAACACTTGAAAGTAACCCGAGCGCCCTGCTGCTGCGAGCCCGTTCCTGCGCGCTGAGAGACGGCCAGAAACCATGGGCAACCGGGGGATGGAGGAATTGATCCCCCTGATCAATAAACTCCAAGATGCTTTCAGCTCCATTGGC[C/T]AAAGTTGTAACCTGGATCTGCCGCAGATAGCAGTTGTCGGAGGACAGAGCGCCGGAAAAAGCTCCGTGCTGGAAAATTTCGTCGGCAGGTTGGTTACTGGTTTCTCTTTTGGTTTGACTTTAGTCGAATACGTCACCTCGGCTCGTTACATTCACGAACGTGCAATTTATAAGCGGCCACGAGTCTCGTTTGCTACTTTCCAGCTGCGTTTTTATAAAAGACACACGCAACGTTCATTCACAAACGCGAGTTACGCAGTTGACGTAAGCGGACGCTCGCCGTCATTCATTGAACTGAAATGGGCGTAAGTCAGAGCAGAGAGCAAAATGGGGAAGTTTCGCGGCACTGCACACACACAACACATTAAGTTATAGTCCTGGTGTCCTTGATAGTTGTAATATGGCAAACAGGGAAATCATAATCATATTCACAACTTACGTCGTTAAACTTAAAGTCGTTTCCTCGTTCACAGTGCGTGTGTGTCTGCTCGGACCTTACGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20129
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 |
---|---|---|---|---|---|
ENSDART00000024031 | Essential Splice Site | 129 | 755 | 3 | 18 |
ENSDART00000097146 | Essential Splice Site | 129 | 872 | 3 | 22 |
The following transcripts of ENSDARG00000069937 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 48352601)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50353741 |
GRCz11 | 3 | 47164381 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGGCATCTCTCCTATCCCCATCAACCTGAGAGTCTACTCTCCTAACGG[T/C]AATGCAAAACTAGACCCTGGAGGAGCGCAGTTTCCCGCAGTCAGTCTGCT
Long Flanking Sequence:
CCTTAAATTCACTGTAAATTACCGACTAATAATTGCATTATTTACAATTACATTTTGAGCTGAAACTTTACAGACACATCTTGTAAAAGTGGTAAAATAGGTGCCCTTTAAAACAATTTTAGCTGGTGAAAAAAACTGTTTTCTAATAGTTTTGGTCACCACTAAATATATTTTAATGTCGATGTTTTTACCTCATTTTCCATTCCCCACCAGTACATGTTATCAGTATGTAAATGAAAATGGTTTAGACTTTAGATGAAAACACCACTTTAAGATAAATTCTCATTTGCCTCCACTGAAATGTCACCCATATCAACCTAATCCTTGCTCTCCATCTCTCTGTGTGCAGAATATGCAGAGTTCCTACACTGCAAAGGGAGGAAGTTCGTGGACTTTGATGAAGTCCGGCAGGAGATTGAAGCAGAAACCGACAGGATTACAGGCTCCAATAAGGGCATCTCTCCTATCCCCATCAACCTGAGAGTCTACTCTCCTAACGG[T/C]AATGCAAAACTAGACCCTGGAGGAGCGCAGTTTCCCGCAGTCAGTCTGCTATTGGTGAAATGTCACTCTCCTCTGTCTTTGATCAACAGTATTGAATCTGACACTCATCGATTTGCCTGGGATGACGAAGGTGGCAGTGGGCGACCAGCCGCCTGACATCGAGCACCAGATTCGGGACATGATAATGCAGTTTATCACCAGGGAGAGCTGTCTAATCCTTGCCGTCACCCCAGCCAACATGGACTTGGCCAATTCGGATGCCCTCAAGGTGGCGAAAGAAGTGGACCCTCAAGGTGAGGGGATTCACAAGTCAAATAATGAGAGAAGCTGGATAGAGTTTAGGAAAACCTGAAAAATATACACCATGTAGTAAAGTTGTGCTGCTTTAGGAGAGAAAAGGCCATGATACTTAAATAAATGCAGTAAAAATGTGTAAATTATGGAGTCAATTATGGGACAAAATAAAGCAAATGCAGCTCATGAGCAAATTACGTTACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13248
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 |
---|---|---|---|---|---|
ENSDART00000024031 | Nonsense | 130 | 755 | 4 | 18 |
ENSDART00000097146 | Nonsense | 130 | 872 | 4 | 22 |
The following transcripts of ENSDARG00000069937 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 48352694)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50353834 |
GRCz11 | 3 | 47164474 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCTGCTATTGGTRAAAWGTCACTCTCCTCTGTCTTTGATCAMCAGTAT[T/A]GAATCTGACACTCATCGATTTGCCTGGGAYGACGAAGGTGGCAGTGGGCG
Long Flanking Sequence:
AAAATAGGTGCCCTTTAAAACAATTTTAGCTGGTGAAAAAAACTGTTTTCTAATAGTTTTGGTCACCACTAAATATATTTTAATGTCGATGTTTTTACCTCATTTTCCATTCCCCACCAGTACATGTTATCAGTATGTAAATGAAAATGGTTTAGACTTTAGATGAAAACACCACTTTAAGATAAATTCTCATTTGCCTCCACTGAAATGTCACCCATATCAACCTAATCCTTGCTCTCCATCTCTCTGTGTGCAGAATATGCAGAGTTCCTACACTGCAAAGGGAGGAAGTTCGTGGACTTTGATGAAGTCCGGCAGGAGATTGAAGCAGAAACCGACAGGATTACAGGCTCCAATAAGGGCATCTCTCCTATCCCCATCAACCTGAGAGTCTACTCTCCTAACGGTAATGCAAAACTAGACCCTGGAGGAGCGCAGTTTCCCGCAGTCAGTCTGCTATTGGTGAAATGTCACTCTCCTCTGTCTTTGATCAACAGTAT[T/A]GAATCTGACACTCATCGATTTGCCTGGGATGACGAAGGTGGCAGTGGGCGACCAGCCGCCTGACATCGAGCACCAGATTCGGGACATGATAATGCAGTTTATCACCAGGGAGAGCTGTCTAATCCTTGCCGTCACCCCAGCCAACATGGACTTGGCCAATTCGGATGCCCTCAAGGTGGCGAAAGAAGTGGACCCTCAAGGTGAGGGGATTCACAAGTCAAATAATGAGAGAAGCTGGATAGAGTTTAGGAAAACCTGAAAAATATACACCATGTAGTAAAGTTGTGCTGCTTTAGGAGAGAAAAGGCCATGATACTTAAATAAATGCAGTAAAAATGTGTAAATTATGGAGTCAATTATGGGACAAAATAAAGCAAATGCAGCTCATGAGCAAATTACGTTACTATACACCTGAAGGATGGGTCAATTAACAAACTCAAGCACAAAATATATTAAATTAATTACTATAATTGTAATTATTATTATTGCAGAAATTATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13768
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 |
---|---|---|---|---|---|
ENSDART00000024031 | Nonsense | 265 | 755 | 6 | 18 |
ENSDART00000097146 | Nonsense | 265 | 872 | 6 | 22 |
The following transcripts of ENSDARG00000069937 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 48355835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50356975 |
GRCz11 | 3 | 47167615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTGCTGCGMTGGCAGCAGAAAGGAAGTDTTTCCTGTCCCACCCTAGTTA[C/A]AGACATATGGCTGAAAGGATGGGAACGCCACACCTGCAAAAAGCCCTCAA
Long Flanking Sequence:
AATCATCACTGAGTAAACATGTTTGTTTATCTATCTGACTCAAATTGTAGTTAATGTGAACAGATTCAGTTTTAGAAAAAAATAAATAAATCATTATCATGTGCTATGAATTGGGATGTAAACACATTTTCCAAGACGTTTGTTGACATACTTTACAGTCTTTGGAAAGTTATTTCTTGTCCTAACTTGTTTTGCTCATTTCTTTCTCTGTATTTTCACATTCTCTCTTGTTTCTTTGCTGCTGTAAGATGCAGTTGATATTTTTGGTCTATGATATCAGTTAAATTATGATAAATAAACTGTACTGCACACATTTCTCCTATTGTATGATTTGAATGCCCAAACCATCCAGCACAGACAGGCACCCTCTAATGTGATTTTTCCCTTGTCGTAGGTTATATCGGTGTAGTGAACCGGAGTCAGAAAGACATTGATGGCCGTAAGGACATTCGTGCTGCGCTGGCAGCAGAAAGGAAGTTTTTCCTGTCCCACCCTAGTTA[C/A]AGACATATGGCTGAAAGGATGGGAACGCCACACCTGCAAAAAGCCCTCAACCAGGTACAACCACATCACCGTCTGAAGCTGTTGTACTGCTGCTTGCCACACTTCTCAATAGTTTAACTCTTATGGGCATTGCAGTAACTTTAAAATGATTTCTTATCAGAGTTTTTGCGGGGTCTTAAAGTCTAAACTTTAAAAAAAATGACATTTAAGGCCTTAAAAAGTCTAAATACACTCTTCTAGGTCTTAAATATTTTTGCACAGAAACTGGTCCATGAACTGTGCAATGTTACTTATAAAGTTTGTGTCTCTGACAAAGTCCCATACATCAATAGTCTTTTCCGGTCCCTCTTTTAACAAACGGACGACAAATCCTCTGCTGCAGGGTGGATTACTGCATTAATCACCAGAAAGCTCACTCATTAATGTTCACTTATCTTCAGTCATGATCAGTCCCACACACCCCTACACTCCACTAGTGTTTTAAGGGAAAGGAGCATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17720
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024031 | Essential Splice Site | 331 | 755 | 8 | 18 |
ENSDART00000097146 | Essential Splice Site | 331 | 872 | 8 | 22 |
The following transcripts of ENSDARG00000069937 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 48358454)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50359594 |
GRCz11 | 3 | 47170234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TYGCTCGTAACTAATTCTAGCAGTTTCTAACTCTGAGTTCTGCTTTTTTA[G/T]RATGGTCCAGCAATTTGGTGTGGACTTTGAGAAGTGCATTGAGGGRTCCG
Long Flanking Sequence:
GATTGGTTAATATCAGCTGTCAATCACTCTGTCAGTGCCTTCTGGCTTGGGATGACGGAGAGAGCAACTACCGTGAAAAATTGTAAAGCGCTGAAGAAGAGAATGAAAAAAGTTAAAGCCATAAAAATTAGGCCAAATAAAAATTACCATTGATTTTCTTTATTTTTTTTATTTGCAATTTCTTTACAAGTATGGATTTGCACAAATAGCTAACCATTTCAGAAAATGTTTGCATAGAGTCCCCGCCTATATCATGTTCTCACTTCTTGTTTTTGTATTTTTAGCAATTGACCAACCACATCCGGGACACACTTCCCGGCTTGCGGAGCAAACTCCAGTCTCAGCTTCTCTCTCTAGAAAAAGAAGTGGAAGAGTATAAGAACTTCCGCCCAGATGACCCTACTCGAAAGACCAAGGCCCTGCTGCAGTGAGTGACTATCATGACTAGCTTTGCTCGTAACTAATTCTAGCAGTTTCTAACTCTGAGTTCTGCTTTTTTA[G/T]GATGGTCCAGCAATTTGGTGTGGACTTTGAGAAGTGCATTGAGGGATCCGGAGATCAGGTGGACACTGCAGAGCTGTCTGGAGGTGCCAGGATTAACCGAATCTTTCATGAGCGCTTCCCCTTTGAGCTGGTCAAGGTGCATACTTGTTTCGCCTGTCTGTGAATTCATAATGTTGATCTGAGTCAGTGTTGTAAGTTACTAAAATTGAATAAATTCTAGATTACTTTGCTAATTAATGTAAGAAGTAATCAGATTACTAATTACTACATTTTCAAGTTACTTTGATAACCTGAAAAAATCTAAAAAGCACTGAAGTGAAAATTGTTGTTCTCTCACGAATTTAATGTTGACTGAAAAATGATACAAAGGCTTTTTTTGATTCATATTCTGCTTTAAGTCAGGGGTACCCAAACTTTTCAACCCACAACCCCCAAAATAGAAATCCCTGTGAAATGCAGAAGTTCGTTTCTTTCCATTTGTGTGGATTATTAAATGCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16501
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 |
---|---|---|---|---|---|
ENSDART00000024031 | None | None | 755 | None | 18 |
ENSDART00000097146 | Essential Splice Site | 518 | 872 | 14 | 22 |
The following transcripts of ENSDARG00000069937 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 48373125)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50374265 |
GRCz11 | 3 | 47184905 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCACCCCCTTCCCCCTCCCTCTTACTTATCACTACAGGGTGAAATCCTGG[T/A]AAGTACCATAAACTTACAAGYCACACCCAGTTAAAGGTCACCAGTGCTTA
Long Flanking Sequence:
TGTGCTTTCACTAGCATCACAGCAGCACTAGTCGCTAGTAACACTGACGCATGACAAATGAATAATCAATGCATTGTCTTGTTTTTTCCAGTCTTGCCCTAATGCAATGCAAACTTCCTCTTTATATTTGAAGTGTAATCCAGAATGTGCATGGATCCAGCCATGACAATGACAACCTATTATATAATTCTGATTTGTGGTACTGTCAATCTAATTGCATGTAACTTTGTTCTGTTGCTCTCTCTCTCCCTCTCTCTTTCTCTCTCTCTCTCTCTCTCTCTCTGTATGTCTGCCTCCAACCTTTTACTCATTTCTTTTTTAACTCATTCCATCACTTCTATATTCCCAATCTTTTTATATCAATTTCTCTCTAACGCGTGCTGTCCTGGTTTTCCCGCTTTTGCTTGTTTACTGTGTCTCCGTCTCATTTCTTCTACTCAAAACTCGCCCCCACCCCCTTCCCCCTCCCTCTTACTTATCACTACAGGGTGAAATCCTGG[T/A]AAGTACCATAAACTTACAAGCCACACCCAGTTAAAGGTCACCAGTGCTTATCCAGACAGGAGAACTGAGGCCGTAGCAGGTTCATCATTTTTTTATTGAAGCAGTGTGGACGGCATACCTCTGTGTAAACTTGATATTGGCAAGGATTATAAAGCTGATGGTTGTTCTTTCACCCTGCAGCTAGGTGGCCTGAGAGAAGGTGAAGCTGAGAAGGTATAGTCTGGTGGAATAACAAAAACAAAAAAGATATAGTGAAACCGGGAGTCAATTAAAATCATGGCTAGTTCAGTTATACACTGAAAAAACTTTAAGTTGTTGCACCTTGATTAACTTAGTTTTTTTTTCCCCTATTCATCAGAGTTTTGAGTTGTAAATAAAGTTTATAAAACTAATTAATTTAGGTACAGCAACTTGACAATTTATATTTATTTATTTGTTTTTGTTTGTTTGTTTGTTTTATTTATTTATTTATTTATTTATTTATTTATTATTTTTATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20130
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 |
---|---|---|---|---|---|
ENSDART00000024031 | Nonsense | 594 | 755 | 16 | 18 |
ENSDART00000097146 | Nonsense | 598 | 872 | 17 | 22 |
The following transcripts of ENSDARG00000069937 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 48386994)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50388134 |
GRCz11 | 3 | 47198774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGTGGCTTCATGTGTTCGATCCCCCTCGCAGGAATGTGTATAAGGACT[T/A]GCGTCAGATCGAGCTGGCCTGTGACTCGCAGGAGGACATGGATAGTTGGA
Long Flanking Sequence:
ACTTTAGACTTTGTGCCTATATCTTTAAAATAGAGCCCTGGATGTCAAACCTTGTTACGTAATCACATTTGTGCTGGACAAACTGACTTGTTTACAACACATCAGAGACAAGCGTGTTGTATTGTATTGCTCGCTTATGCTTCTCTGGAATACATAAAAAAGGTGCCAACAAATCTCAATTGATTCCAACAATATTGTCTATACTGTTAAATTTTTTACTTAATTTTTACCTTCATAGCCGTCATCTTTAGTGTAAACATGCTTTAAGACTCTGCCTTTTTCATTTCACTCTAATAGGAAAAAGAGAAGAAATACATGCTTCCTCTGGATAACCTGAAGCTCAGAGACGTGGAGAAAGGCTTCATGTCCACTAAGCACATTTTTGCAATCTTCAACACTGAGCAAAGGTTAGGGCTGACTGCAGATCTGTGTGTGTTTGTGTGTTTGTGTTTGGTGGCTTCATGTGTTCGATCCCCCTCGCAGGAATGTGTATAAGGACT[T/A]GCGTCAGATCGAGCTGGCCTGTGACTCGCAGGAGGACATGGATAGTTGGAAAGCCTCTTTTCTCAGAGCAGGCGTTTACCCTGAGAAAGATCAGGTACTGATCCAACACACGCACAGACAAACACATTTAACATGATATGAGTTAATAAATCATAAAACTGAGCATTACGAGCATTACTCACTTGAAAGCATATCCAAACAAATCACAAAATAACCGGGCTGGCCACACATCTTTTCTCCCACGCTAAACAGCTGAAAAGCATAATAGAAACTTTTTGGACGAGCCTCCAATTAATGTTACTGACAACATCAGGAACATTAAATGTAATTGACAACATCAAATGAGGGAGAACACAAACTGATCGGTCTGGGGGTTTTATTAACAGATCAACCTAATCAAACTGTGGGGAGAAAGCACAATAAACTAAGGCTGAACACTAAATGGAGCACAACTCCGCGTCTGGGCGGCCGCTTAAATCCCTGTTACTGAAGTTCTGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15133
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024031 | Nonsense | 648 | 755 | 17 | 18 |
ENSDART00000097146 | Nonsense | 656 | 872 | 18 | 22 |
The following transcripts of ENSDARG00000069937 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 48389670)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 50390810 |
GRCz11 | 3 | 47201450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCCCCAGCCGACAGCTTCTCCATGGACCCTCAGTTGGAAAGACAGGTC[G/T]AGACCATCCGTAACCTGGTGGACTCCTATATTGGAATCRTCAACAAAACC
Long Flanking Sequence:
AAACCTCAGTTTTTGAGCTATTTAATTTAAAAAAGTTAAAAGAGAGCCAGGATCTGATTTCTGTTAAGCAGACTGTAAGGGATGTAGGTGGAAAACAAGAAGAGGGTTTGCCAGAGAAATAGAGCTGGGTGTCATCCTCATAGCAATGATACTGTAAATCATAAAAGAAGTAAAAACATCATCAGCTCAGCAACTCACCACAAATAGATCTTCAGTTTCAACCATTGTTAAAATTGACCTGACGTATTTTTTTCAGTTTCACTGCTAAACCAAAAAAGCTGTTTCCCCAAATCTAAGGACAGTTTAAGGCGAAACCAGTTAGAGATTTCTTCAGTTTGTTTACATAATTCACTTAGAGTGTTTATTTATATTATAAGTCACTTTTTCAAGAATTGTATTTCTTGACAACTCATTTATTGTATGTGCGTGTGCAGGTGGAGTCAGAAGAGGCAGCCCCAGCCGACAGCTTCTCCATGGACCCTCAGTTGGAAAGACAGGTC[G/T]AGACCATCCGTAACCTGGTGGACTCCTATATTGGAATCGTCAACAAAACCATCAGAGACCTCATGCCCAAGACTATCATGCATCTCATGATCAACAGCGTAAGCGCACAACCATTCAGATTTAAAGGGGACCTATTATGCCACTTTTTACACGATGATGTAAAGTAAGTCTCAAGAGTGTGTAAAGTTTCAGCTCAAAATACTCCACAAATAATGTTTTATTACTCTTTGAAATACTTTTACGGTGTGTTCATTCCAGAGTCAGAGGGAGCATCTAGCACACAGGTGTCAAAGCCTGTTCCTGGAGGGCCAGAGCTTTGCACAGTTTAGTTTCTATCCTAATTAAACACACCTGGGGCCTGTTTCAGTAAGGAGGTTCAACCAACTCGGAGTTTAAACTCGAACTTGATTTATTGAGAGATTAAAAACTCATAGTTTTCAGTTTCAGAACAACCGATCTGAGTTAGGTCAATCAACTTTGAGTAGACCAACTTAAGTTAA
Associated Phenotype:
Not determined