ZMP
zgc:113183
Ensembl ID:
ZFIN ID:
Description:
SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing D
Human Orthologue:
SMARCAD1
Human Description:
SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing D
Mouse Orthologue:
Smarcad1
Mouse Description:
SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing D
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38698 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1299 | Essential Splice Site, Missense | Available for shipment | Available now |
sa18922 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12057 | Nonsense | Available for shipment | Available now |
sa11941 | Nonsense | Available for shipment | Available now |
sa41231 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18923 | Nonsense | Available for shipment | Available now |
sa16448 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38698
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 |
---|---|---|---|---|---|
ENSDART00000091409 | Essential Splice Site | 104 | 972 | 3 | 23 |
ENSDART00000133047 | Essential Splice Site | 38 | 154 | 3 | 8 |
ENSDART00000139029 | Essential Splice Site | 104 | 385 | 3 | 8 |
The following transcripts of ENSDARG00000014041 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 30485081)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 29627807 |
GRCz11 | 8 | 29637039 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGCTGTTAGAGATATTCCCACAGAAGAGCAAGAAAGATCTACTAGAGG[T/C]AATGAGAATGTCAAGAAATGGAGGTTCTTGAAAAATTAGGTGAACGTTGT
Long Flanking Sequence:
CACTCCATTTTTATTAACCATTAGCGTACTAGACGTAGAATTACATAGCGTTCTCATATCACATCTGTATCGTAATTTTTGTAACGTGACAAAGTATGTTGTTTGACAAAATGTCTTGAATCTTCTCTCTGTAGCTCATCAAAGAAAGGCGGATGGTCAGTTTCCATCAGGCAAGACATCAAGACAAGTACTAGAAGATGTTTCTTCAGATGACGAAGTTGTCAGGATGGGCAAGTAAGCGAGATTAGGATTTTGTCAAAAATGATACAATGACACATCTTTCAGCTGTTTCTGTGGATTTAGTTACATTGTTACAAATTGCTATATCTTTTTTGTTTGTTGTTAAAACGCAGCATCAATGCACTAACGCATGATAATGCAATTACTTAACAGGGATTCAGCATCAGATTTGCAGCAGCATATAAACAAGGACATGGAGGACAAAATCATTAAGCTGTTAGAGATATTCCCACAGAAGAGCAAGAAAGATCTACTAGAGG[T/C]AATGAGAATGTCAAGAAATGGAGGTTCTTGAAAAATTAGGTGAACGTTGTAGTTTGTTTGCTGTTATCTAACTTGATGTTGTGACAGGTCATCGAGAACACCAGCACCCTGGATGGAGCTGTAGCACATTGTTTGATGATTTATGGGGATGAAGGTAAACTGTTTTTATTAGAATTTATTCAATGCTTTGAAGGTTGATTGCTGAATATTTTAGTCATGTATTTTTACACATTTGCACATCATTCCTCATTTTACTCATTTACTCATTTTTATGTCATTCCAAACCTGTGACACTTTTGTTCATATTTAAAGGGCAAATAAAGATATTTTTTAACAAGTTTGAAAGATTTCTGCCCGTCTATTAAAGGCTGCTCTGATAAACCACTTGTGCTTCAAAACCTGTTCTAGAATATTTATAATAAAAAAATATATATGAATCAAGTCATATTTCAAATTTATTTGACTTACAGATTAAATTTTTTATTTTATTCACATATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1299
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 > G
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091409 | Essential Splice Site | 379 | 972 | 8 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | Missense | 380 | 385 | 8 | 8 |
The following transcripts of ENSDARG00000014041 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 30489020)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 29631746 |
GRCz11 | 8 | 29640978 |
KASP Assay ID:
554-1214.1 (used for ordering genotyping assays)
KASP Sequence:
AGCCCAGAAGATCATTTCACTGAGGCCTTTCAACACTTGGAAAGATGTGG[T/G]AAGGATCTGCTGTCTGTAACTTTYTTGTTAATCTTTACTGGCARTTATTT
Long Flanking Sequence:
CTTTTCTGTTATAAATTCAGATACAAGTTCACCAGAAAATCAGAAGTCAAAACAAAAGTCAAAATCCTCGCACTCTAAGGAAAAAACTGACAAAATCACACAAAGGCCCAGCGGCTCGTCTAGTCTGTCTCGATGGCTGACAGCAGCATCATCTCATGTGCCTGAAGTATCAAGCATGTCTGCTTTAAAAACACAAAAATCTGCACTTAGCAAAAGCACAAGCAAGAACTCATCCTTTAAAAGGAAGAGGGGCGATGAAATGCCACTAAATGATGTCAGCGCCTCTGAGGATGAAGATGAGATTGACAGTGATGTTGATAGTATGTCTGATGATCAGGATTCGGAGGACGAGGACAGCATCTCTGGCACTCTTCAGGACAAGATCATTCAGTTCCTTCAAGATGCTTCCCTAGATGAGCTCGCCCTGATATCTGGCTGCTCGATCAAAAAAGCCCAGAAGATCATTTCACTGAGGCCTTTCAACACTTGGAAAGATGTGG[T/G]AAGGATCTGCTGTCTGTAACTTTCTTGTTAATCTTTACTGGCAGTTATTTTGTTTGGAATTATGAAGTGCTCCAATGGTATTATTTATTCTTTAGCTTCAAAAGAAGATTCAGGTTTGACAGTTTTGTATTTTCCTGCCGACAGATTTAACATATTTAATCTACAAGAATGTCAGTCTCTAGTTTCAGTTTTGCTATAAATTCACAAGGCTTTGTTTATAGTGAAGGTATGCATGTCGTACATGCCTGTACATGTATGCATGTTGAGTGAGGGGATCTACAGTGCATTTTATTATACATTATTATTGCTGAAATAGGGCTACCAGTAGCCTGTTTTTCATTATTATTTTCTTTTCTATGAACAATGCAATTGTGGCAGTGTGAATGGAGGTAGGATTACACAATTTATATACTAAAAGCTAATTTTTTTTCTAAGTTTTATTTATCCATTTACTTTTTAATTAAGTTTTGCAGACAGATGAATATTGTGTCAGAACAATA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa18922
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 |
---|---|---|---|---|---|
ENSDART00000091409 | Nonsense | 575 | 972 | 14 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
ENSDART00000091409 | Nonsense | 575 | 972 | 14 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
ENSDART00000091409 | Nonsense | 575 | 972 | 14 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
The following transcripts of ENSDARG00000014041 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 30491966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 29634692 |
GRCz11 | 8 | 29643924 |
KASP Assay ID:
2260-0748.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGGAAATGACCATGATCGCAGTCTCTTCCGCAAGCTGAAGCTGAAATA[T/A]GCAGTGTTTGATGAGGGCCACATGCTTAAAAACATGAACTCGCTACGCTA
Long Flanking Sequence:
CCCAGTCTCAAAGTTCTTATTTACTATGGTGAGAGAGTTTGCAGGCATCACTAGCGCCACATTTAAACCCTGATCTTTGTATTTGTTTAACAGTTTTGATTTTTTAAAGAGATCACATTATACATTTTAATGTTCATGAAATGAACTTGATGTTTTCGTTTATTACATTTTCAAAATAGTCCACTTTTTTTTTTTTACTCTCTCCATCATTCTGTTTATACTTTTAGGGTCTGTGGAAGACCGCAAATACTTGCGACAAGACATCCTCACTGGCTTAATTGATTTCAACATCATTGTATCCACGTAAGTTTAAATGGCTAATATGCTGCGATCCTTATTTTTTGTGAATTAATTTTAAGAGGCTAGGCTTTGTTATGAAAGTCAGTTTTTTTTTTTATTTATCGGTGCCTGTCTATTTCTTCTTTCATCTATATTAGGTACAATCTCACAATAGGAAATGACCATGATCGCAGTCTCTTCCGCAAGCTGAAGCTGAAATA[T/A]GCAGTGTTTGATGAGGGCCACATGCTTAAAAACATGAACTCGCTACGCTACCGCCACCTTATGACTATCAATGTTAGTACAAGCACTTTTCTGCACCACAAACATTGTAAATGAAGTGTAAACAGATGCTTTGTACAGCAATTCTCATTGTTGTTGTTTTTTCATATCTACAGGCTGAGCACAGATTACTATTGACCGGAACGCCTTTACAAAACAACCTGTTGGAACTCATGTCCTTGCTGAACTTCATAATGCCATCCATGTTCTCCAGCAGCACCTCACAGATCTCCAAAATGTTCTCTACGGTATAGACAGTACATGGGTTCTGTTGAAATAATAATTTGTGCCACCAAAATAGAACCTAATTAAAAAATCAAATTAGCCAGAGATCAGTCATCAAGATTTAAAGATTAATCATCTGCCAAATCATCTTAGATTAAGCTGGAACTGCATTAATCGCTATATATTCATAAAGAATACTCTTACTTGTTACCCATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12057
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 |
---|---|---|---|---|---|
ENSDART00000091409 | Nonsense | 575 | 972 | 14 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
ENSDART00000091409 | Nonsense | 575 | 972 | 14 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
ENSDART00000091409 | Nonsense | 575 | 972 | 14 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
The following transcripts of ENSDARG00000014041 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 30491966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 29634692 |
GRCz11 | 8 | 29643924 |
KASP Assay ID:
2260-0748.1 (used for ordering genotyping assays)
KASP Sequence:
ATAGGAAATGACCATGATCGCAGTCTCTTCCGCAAGCTGAAGCTGAAATA[T/A]GCAGTGTTTGATGAGGGCCACATGCTTAAAAACATGAACTCKCTACGCTA
Long Flanking Sequence:
CCCAGTCTCAAAGTTCTTATTTACTATGGTGAGAGAGTTTGCAGGCATCACTAGCGCCACATTTAAACCCTGATCTTTGTATTTGTTTAACAGTTTTGATTTTTTAAAGAGATCACATTATACATTTTAATGTTCATGAAATGAACTTGATGTTTTCGTTTATTACATTTTCAAAATAGTCCACTTTTTTTTTTTTACTCTCTCCATCATTCTGTTTATACTTTTAGGGTCTGTGGAAGACCGCAAATACTTGCGACAAGACATCCTCACTGGCTTAATTGATTTCAACATCATTGTATCCACGTAAGTTTAAATGGCTAATATGCTGCGATCCTTATTTTTTGTGAATTAATTTTAAGAGGCTAGGCTTTGTTATGAAAGTCAGTTTTTTTTTTTATTTATCGGTGCCTGTCTATTTCTTCTTTCATCTATATTAGGTACAATCTCACAATAGGAAATGACCATGATCGCAGTCTCTTCCGCAAGCTGAAGCTGAAATA[T/A]GCAGTGTTTGATGAGGGCCACATGCTTAAAAACATGAACTCGCTACGCTACCGCCACCTTATGACTATCAATGTTAGTACAAGCACTTTTCTGCACCACAAACATTGTAAATGAAGTGTAAACAGATGCTTTGTACAGCAATTCTCATTGTTGTTGTTTTTTCATATCTACAGGCTGAGCACAGATTACTATTGACCGGAACGCCTTTACAAAACAACCTGTTGGAACTCATGTCCTTGCTGAACTTCATAATGCCATCCATGTTCTCCAGCAGCACCTCACAGATCTCCAAAATGTTCTCTACGGTATAGACAGTACATGGGTTCTGTTGAAATAATAATTTGTGCCACCAAAATAGAACCTAATTAAAAAATCAAATTAGCCAGAGATCAGTCATCAAGATTTAAAGATTAATCATCTGCCAAATCATCTTAGATTAAGCTGGAACTGCATTAATCGCTATATATTCATAAAGAATACTCTTACTTGTTACCCATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11941
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 |
---|---|---|---|---|---|
ENSDART00000091409 | Nonsense | 575 | 972 | 14 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
ENSDART00000091409 | Nonsense | 575 | 972 | 14 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
ENSDART00000091409 | Nonsense | 575 | 972 | 14 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
The following transcripts of ENSDARG00000014041 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 30491966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 29634692 |
GRCz11 | 8 | 29643924 |
KASP Assay ID:
2260-0748.1 (used for ordering genotyping assays)
KASP Sequence:
ATAGGAAATGACCATGATCGCAGTCTCTTCCGCAAGCTGAAGCTGAAATA[T/A]GCAGTGTTTGATGAGGGCCACATGCTTAAAAACATGAACTCKCTACGCTA
Long Flanking Sequence:
CCCAGTCTCAAAGTTCTTATTTACTATGGTGAGAGAGTTTGCAGGCATCACTAGCGCCACATTTAAACCCTGATCTTTGTATTTGTTTAACAGTTTTGATTTTTTAAAGAGATCACATTATACATTTTAATGTTCATGAAATGAACTTGATGTTTTCGTTTATTACATTTTCAAAATAGTCCACTTTTTTTTTTTTACTCTCTCCATCATTCTGTTTATACTTTTAGGGTCTGTGGAAGACCGCAAATACTTGCGACAAGACATCCTCACTGGCTTAATTGATTTCAACATCATTGTATCCACGTAAGTTTAAATGGCTAATATGCTGCGATCCTTATTTTTTGTGAATTAATTTTAAGAGGCTAGGCTTTGTTATGAAAGTCAGTTTTTTTTTTTATTTATCGGTGCCTGTCTATTTCTTCTTTCATCTATATTAGGTACAATCTCACAATAGGAAATGACCATGATCGCAGTCTCTTCCGCAAGCTGAAGCTGAAATA[T/A]GCAGTGTTTGATGAGGGCCACATGCTTAAAAACATGAACTCGCTACGCTACCGCCACCTTATGACTATCAATGTTAGTACAAGCACTTTTCTGCACCACAAACATTGTAAATGAAGTGTAAACAGATGCTTTGTACAGCAATTCTCATTGTTGTTGTTTTTTCATATCTACAGGCTGAGCACAGATTACTATTGACCGGAACGCCTTTACAAAACAACCTGTTGGAACTCATGTCCTTGCTGAACTTCATAATGCCATCCATGTTCTCCAGCAGCACCTCACAGATCTCCAAAATGTTCTCTACGGTATAGACAGTACATGGGTTCTGTTGAAATAATAATTTGTGCCACCAAAATAGAACCTAATTAAAAAATCAAATTAGCCAGAGATCAGTCATCAAGATTTAAAGATTAATCATCTGCCAAATCATCTTAGATTAAGCTGGAACTGCATTAATCGCTATATATTCATAAAGAATACTCTTACTTGTTACCCATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41231
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091409 | Nonsense | 661 | 972 | 16 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
The following transcripts of ENSDARG00000014041 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 30492526)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 29635252 |
GRCz11 | 8 | 29644484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCCTCAGAAGAGGAAAGCAGTTTTCACAAGGACAGAATCGCTCAGGCC[A/T]GACTTATCATGAAGCCATTTATCTTGAGACGAGTCAAGAGTGAGGTAGAC
Long Flanking Sequence:
TATGACTATCAATGTTAGTACAAGCACTTTTCTGCACCACAAACATTGTAAATGAAGTGTAAACAGATGCTTTGTACAGCAATTCTCATTGTTGTTGTTTTTTCATATCTACAGGCTGAGCACAGATTACTATTGACCGGAACGCCTTTACAAAACAACCTGTTGGAACTCATGTCCTTGCTGAACTTCATAATGCCATCCATGTTCTCCAGCAGCACCTCACAGATCTCCAAAATGTTCTCTACGGTATAGACAGTACATGGGTTCTGTTGAAATAATAATTTGTGCCACCAAAATAGAACCTAATTAAAAAATCAAATTAGCCAGAGATCAGTCATCAAGATTTAAAGATTAATCATCTGCCAAATCATCTTAGATTAAGCTGGAACTGCATTAATCGCTATATATTCATAAAGAATACTCTTACTTGTTACCCATCTTTGTTTCAGAGGTCCTCAGAAGAGGAAAGCAGTTTTCACAAGGACAGAATCGCTCAGGCC[A/T]GACTTATCATGAAGCCATTTATCTTGAGACGAGTCAAGAGTGAGGTAGACAGTTTTAAAAAAAAAATGTATTAATATTATTTATTTTTTATTTTTTTCATTGTGATTATCAAGTCTTTGATATTTATTACTTAGTTACTAAATTATGACACTGGAGAGACACTACTGAACTGATTAACTACTCTGCAAGTCTTACAGAATATGCCATATGCCTGTATTGTATCTTCTATTGTGAACAATTTGGTTTTAAAAATGTCCTTCATATATCATTCTAGGTGTTGAAAGAACTTCCACCAAAAATGGAAAAGATTGAAATGTGTCCAATGAGTGATGCCCAGCATAAGCTGTATGACATACTTTTCAAAAGACTCAAGAAGACTCCAAATGGAGACAGTAAGTACTATTCCGTTTTTATGCCAACCATTTCATCTAGAAGTAAAGCATGCTGAAAATGTATGCATAGGCTGTCAGGAAAATTCAGGGTTTCCTCTCACCGTGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18923
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 |
---|---|---|---|---|---|
ENSDART00000091409 | Nonsense | 671 | 972 | 16 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
ENSDART00000091409 | Nonsense | 671 | 972 | 16 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
The following transcripts of ENSDARG00000014041 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 30492556)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 29635282 |
GRCz11 | 8 | 29644514 |
KASP Assay ID:
2260-0749.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGACAGAATCGCTCAGGCCAGACTTATCATGAAGCCATTTATCTTGAGA[C/T]GAGTCAAGAGTGAGGTAGACAGTTTTAAAAAAAAAATGTATTAATATTAT
Long Flanking Sequence:
TCTGCACCACAAACATTGTAAATGAAGTGTAAACAGATGCTTTGTACAGCAATTCTCATTGTTGTTGTTTTTTCATATCTACAGGCTGAGCACAGATTACTATTGACCGGAACGCCTTTACAAAACAACCTGTTGGAACTCATGTCCTTGCTGAACTTCATAATGCCATCCATGTTCTCCAGCAGCACCTCACAGATCTCCAAAATGTTCTCTACGGTATAGACAGTACATGGGTTCTGTTGAAATAATAATTTGTGCCACCAAAATAGAACCTAATTAAAAAATCAAATTAGCCAGAGATCAGTCATCAAGATTTAAAGATTAATCATCTGCCAAATCATCTTAGATTAAGCTGGAACTGCATTAATCGCTATATATTCATAAAGAATACTCTTACTTGTTACCCATCTTTGTTTCAGAGGTCCTCAGAAGAGGAAAGCAGTTTTCACAAGGACAGAATCGCTCAGGCCAGACTTATCATGAAGCCATTTATCTTGAGA[C/T]GAGTCAAGAGTGAGGTAGACAGTTTTAAAAAAAAAATGTATTAATATTATTTATTTTTTATTTTTTTCATTGTGATTATCAAGTCTTTGATATTTATTACTTAGTTACTAAATTATGACACTGGAGAGACACTACTGAACTGATTAACTACTCTGCAAGTCTTACAGAATATGCCATATGCCTGTATTGTATCTTCTATTGTGAACAATTTGGTTTTAAAAATGTCCTTCATATATCATTCTAGGTGTTGAAAGAACTTCCACCAAAAATGGAAAAGATTGAAATGTGTCCAATGAGTGATGCCCAGCATAAGCTGTATGACATACTTTTCAAAAGACTCAAGAAGACTCCAAATGGAGACAGTAAGTACTATTCCGTTTTTATGCCAACCATTTCATCTAGAAGTAAAGCATGCTGAAAATGTATGCATAGGCTGTCAGGAAAATTCAGGGTTTCCTCTCACCGTGAGAATCTGTATAAAAAGTGTGACTGTTTAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16448
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 |
---|---|---|---|---|---|
ENSDART00000091409 | Nonsense | 671 | 972 | 16 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
ENSDART00000091409 | Nonsense | 671 | 972 | 16 | 23 |
ENSDART00000133047 | None | None | 154 | None | 8 |
ENSDART00000139029 | None | None | 385 | None | 8 |
The following transcripts of ENSDARG00000014041 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 30492556)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 29635282 |
GRCz11 | 8 | 29644514 |
KASP Assay ID:
2260-0749.1 (used for ordering genotyping assays)
KASP Sequence:
AGGACAGAATCGCTCAGGCCAGACTTATCATGAAGCCATTTATCTTGAGA[C/T]GAGTCAAGAGTGAGGTAGACAKTTTTAAAAAAAAAATGTNNNNNNATTAATATTAT
Long Flanking Sequence:
TCTGCACCACAAACATTGTAAATGAAGTGTAAACAGATGCTTTGTACAGCAATTCTCATTGTTGTTGTTTTTTCATATCTACAGGCTGAGCACAGATTACTATTGACCGGAACGCCTTTACAAAACAACCTGTTGGAACTCATGTCCTTGCTGAACTTCATAATGCCATCCATGTTCTCCAGCAGCACCTCACAGATCTCCAAAATGTTCTCTACGGTATAGACAGTACATGGGTTCTGTTGAAATAATAATTTGTGCCACCAAAATAGAACCTAATTAAAAAATCAAATTAGCCAGAGATCAGTCATCAAGATTTAAAGATTAATCATCTGCCAAATCATCTTAGATTAAGCTGGAACTGCATTAATCGCTATATATTCATAAAGAATACTCTTACTTGTTACCCATCTTTGTTTCAGAGGTCCTCAGAAGAGGAAAGCAGTTTTCACAAGGACAGAATCGCTCAGGCCAGACTTATCATGAAGCCATTTATCTTGAGA[C/T]GAGTCAAGAGTGAGGTAGACAGTTTTAAAAAAAAAATGTATTAATATTATTTATTTTTTATTTTTTTCATTGTGATTATCAAGTCTTTGATATTTATTACTTAGTTACTAAATTATGACACTGGAGAGACACTACTGAACTGATTAACTACTCTGCAAGTCTTACAGAATATGCCATATGCCTGTATTGTATCTTCTATTGTGAACAATTTGGTTTTAAAAATGTCCTTCATATATCATTCTAGGTGTTGAAAGAACTTCCACCAAAAATGGAAAAGATTGAAATGTGTCCAATGAGTGATGCCCAGCATAAGCTGTATGACATACTTTTCAAAAGACTCAAGAAGACTCCAAATGGAGACAGTAAGTACTATTCCGTTTTTATGCCAACCATTTCATCTAGAAGTAAAGCATGCTGAAAATGTATGCATAGGCTGTCAGGAAAATTCAGGGTTTCCTCTCACCGTGAGAATCTGTATAAAAAGTGTGACTGTTTAAAAA
Associated Phenotype:
Not determined