ZMP
aspm
Ensembl ID:
ZFIN ID:
Description:
asp (abnormal spindle)-like, microcephaly associated [Source:RefSeq peptide;Acc:NP_001116845]
Human Orthologue:
ASPM
Human Description:
asp (abnormal spindle) homolog, microcephaly associated (Drosophila) [Source:HGNC Symbol;Acc:19048]
Mouse Orthologue:
Aspm
Mouse Description:
asp (abnormal spindle)-like, microcephaly associated (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:13
Alleles
There are 22 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24172 | Nonsense | Available for shipment | Available now |
sa12763 | Nonsense | Available for shipment | Available now |
sa37518 | Nonsense | Available for shipment | Available now |
sa17838 | Nonsense | Available for shipment | Available now |
sa24171 | Essential Splice Site | Available for shipment | Available now |
sa1008 | Nonsense | Available for shipment | Available now |
sa24170 | Nonsense | Available for shipment | Available now |
sa24169 | Nonsense | Available for shipment | Available now |
sa11648 | Nonsense | Available for shipment | Available now |
sa13529 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24172
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 |
---|---|---|---|---|---|
ENSDART00000105628 | Nonsense | 91 | 3411 | 1 | 30 |
ENSDART00000126795 | Nonsense | 91 | 3391 | 1 | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 24352033)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23520711 |
GRCz11 | 22 | 23547275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACAGTCATTGTGGATAAAATCTCAGCATCCAAGGGCTTTTCGGTGGAT[C/T]AAATGTCGTTCACAATACAGGTAATAGCAAATATACAAATGATTATGTGT
Long Flanking Sequence:
GATTTTTAAAGAAATCCTAGAGCTGCGATTGGCTCGATTTTACGCTTCTATGCAGTGATTGGACAATTCTATGAGCAGCAAAGAGCTGATTGGCCGCCTGGCCTGCACGCAAAATTCAAACGTACGAATGCGTGCTCTGTTTTGAAACGGTATTTGTAGTTCAGCTCAGCAGCACTGACACATGGATTTACCAACTTCGTTGTTCGCTTAGATGAGCCATAAACATAAACATGTCGTTTAAAGTAGCGAAATCGGAGTGTTTGGACTTCAGTCCACCGCTTGATTCTCACTGTAGTCGCGATAAATCCGGTAAGGAAAACAGCAGTTCGATTCCTGTGCTGAGTTTACTTCAGTTTTCCAGAGCTCCTTTCGTGTCGTTCGGGACGATCAAGTTGGGATCTTCGAAATCTTTACCTTTACGAATTGAAAATCCCACTGATGATGCCACAGCTACAGTCATTGTGGATAAAATCTCAGCATCCAAGGGCTTTTCGGTGGAT[C/T]AAATGTCGTTCACAATACAGGTAATAGCAAATATACAAATGATTATGTGTCATAAATGTGTAAATATGTTAATAGAAAGCATATTAAACAAATTTAAATGTCCATTTGTAGCCACGTATATACACAGTGAATGTTCACAACTGCATAGAAAAAAATTAATTTTTAGTAACTACAGTATAACTACTACAGTAGATTAAAGTGAAGGACTTCAGTTTATGAGGTAACTAAAACAATAACTATAGTAACCTATTTTATGTAACGTCACCAATACCAAGCTTTTTACAACTAGGCATGTTATACCACTTTAATTGAGTTTTACTATAGTAAATTGTGGTGTATACCACAGTAGTTATTGCAGTAACGTTATGCCAGTTCACTGTAGCTAATACTGCCTACATCATGCTGAAGTATTCACATTGACTAAATGTTGTAAATACAATGCAGTATAAAACTATTAATTGCAACATTATTTTTCACATGTGGTCATGCTTGATGCACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12763
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 |
---|---|---|---|---|---|
ENSDART00000105628 | Nonsense | 509 | 3411 | 3 | 30 |
ENSDART00000126795 | Nonsense | 509 | 3391 | 3 | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 24348535)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23524209 |
GRCz11 | 22 | 23550773 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTGGAATCGAAAATTTGTCCAGTTGCAAAAAAGAAGYCAACTTYAAATT[T/A]ATCCCCTCATGACCAACTTTTGTCCTCTATTTCTCCCATACGACCTMAAG
Long Flanking Sequence:
TTCTGATTCTCTGGAATCTGACAAACCGGACCCAGGAGCGTCCTTTAGAGCAAGAAGAGTCATTTCACCACCAGTTGAAACTGCTGACCCGAGGTTGACTTTCTGTGTGAAACCCAACAAAGCCATAGGCATTGCATCAAATCAAGATGAATTTAGGCTCAAGGCTTTACCTTTTAGCACCGCCACAGTGACAAAGTCAATTAAAGTAGATGACACCCATGTCCCAGATGACCCCAAGACGTTTCCTGTTAATTCTGCCACAGTGGTCAAAAGCAAAGCAGATGCTTCTGTTGAGAGTCCAGGACTGCGTAAGAAGAAAACCTCAAGGCGCAGACTCTTGGAGAAGACATTGGAGCTTTCAGAGCCTAGTAATGCAGAATCCAACACAAGTTCTCCTGACAGCTTCTCTGCTCTACCAGTCATCAACTCCGATTCAAGTCCAGATCTGCCACTGGAATCGAAAATTTGTCCAGTTGCAAAAAAGAAGCCAACTTTAAATT[T/A]ATCCCCTCATGACCAACTTTTGTCCTCTATTTCTCCCATACGACCTCAAGTTTTCCCCTCTGTTAGTAATAGTCCGTCAAGCAGCTTAGAGCTGTCAGCCAGTCATTTCTCTGAAAAAGTAAAACCAAATCTTTTGGAGAATCAGTTTCCCGTGCAAAGCAGGACATTAGTGCAAAGTAAAAAAAGAAAAAGCGATGAGTTTTTGAGAGGTCACTCAGAAGACAAGTCAAACATCCAAGCAAAAAAATGCCGAGCTCCTGCGCAGGCAACTGAGAAACCAAGTCAAGAAAGAACACTTACTTCAAGGTCTACATCTGGACCACAACGAAAAGCTGTTGGTGAGTCAAGTATGCGCAATAGAGCTGTGGCAAAAAATCATTTGAGACATTGATTCTGAGATTTTCAAAATGCATTATTCCAATGCTTCCCAATTCCAGTCCTCGGGAACAGCAGGTGGCACTCTAAGCTAGTTTTAACACCAGATGGCACTCTATGCTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37518
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 |
---|---|---|---|---|---|
ENSDART00000105628 | Nonsense | 657 | 3411 | 5 | 30 |
ENSDART00000126795 | Nonsense | 637 | 3391 | 4 | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 24347509)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23525235 |
GRCz11 | 22 | 23551799 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCACTGATGTAGATGCTCGGTCTGTGAAGTCAGCCAATAGCTCAACT[C/T]GAAAGACTGCGAGGATAGTAGCTGTGGCACAGGCCAGACTGACCTTTATG
Long Flanking Sequence:
CGAGTAAGAGTGCTTGTGCATTCATGAAGGTTGGCTTTTATGTCATAAGATTAATGTAAAAACAACTCACTTTGAACACTTAATGCGCTTGAATCAATTTCAAGCTTTAAGTATATTTTTAGGTATGAGTGGTATTTGTAAGGAATTAGTTTCAAACAGAATAAAGCTGATTGTAAAGCATACAACGCTATCAGAATCAATTCAAGAGAGAATAGCGAAAAACTCAGAATCTACACAAGATTTCTCGAGCGATTTACTGTAAGAGGTGTTTGGATGTTGTTTAATTTGAGACTTTTTTTCTTAAAGCACCCCCAAGCTCAAGAAAATTCACAAGGTTTCCACCAAAGAAAATCTCTCCAAAAACAGCTCAAAAAGGTACAATCCTTCTTAAGAATATCCTGAAATACACTTGCTATTAGTATGACCAGTCAGCTATATGATTTAAAACATGTTTCACTGATGTAGATGCTCGGTCTGTGAAGTCAGCCAATAGCTCAACT[C/T]GAAAGACTGCGAGGATAGTAGCTGTGGCACAGGCCAGACTGACCTTTATGAAGCCGACACAGACGGGTATGCTTTTACAGCTTTATTCATACAATTTTATGTATTTGTAAGATGCATAGTTACTTATGTTGTAAAATCCTGACAGCCATTCCAAGGCATCCATTGCCATTTGCGGCAAAAAACATGTTTTATGATGAGCGATGGATCGAAAAGCAAGAGCGAGGCTTTACTTGGTGGATGAACTACATTCTCACTCCTGATGACTTCAAAGTTGCTACTGAAGTTACCAAAGGTAGGCACTTAGTTGGAGTGATTGTATCCTAAAGTAATTGGATATCAACAAAGTTCTCATCTCACTTTAATGTTGTTCCAAACGTGTAAGTTATTTTGTTCAACTTTGGAGCACAAATGAAGATATTTCAGGTGAAACCCTAGAGCTCTCTTACCTTTTATAAACAACAAGGGTCCCAAGACCTTTAAAGTCCAGAAAGGTACCAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17838
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 |
---|---|---|---|---|---|
ENSDART00000105628 | Nonsense | 697 | 3411 | 6 | 30 |
ENSDART00000126795 | Nonsense | 677 | 3391 | 5 | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 24347310)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23525434 |
GRCz11 | 22 | 23551998 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCAAGGCATCCATTGCCATTTGCGGCAAAAAACATGTTTTATGATGAG[C/T]GATGGATCGAAAAGCAAGAGCGAGGCTTTACTTGGTGGATGAACTACATT
Long Flanking Sequence:
ATTCAAGAGAGAATAGCGAAAAACTCAGAATCTACACAAGATTTCTCGAGCGATTTACTGTAAGAGGTGTTTGGATGTTGTTTAATTTGAGACTTTTTTTCTTAAAGCACCCCCAAGCTCAAGAAAATTCACAAGGTTTCCACCAAAGAAAATCTCTCCAAAAACAGCTCAAAAAGGTACAATCCTTCTTAAGAATATCCTGAAATACACTTGCTATTAGTATGACCAGTCAGCTATATGATTTAAAACATGTTTCACTGATGTAGATGCTCGGTCTGTGAAGTCAGCCAATAGCTCAACTCGAAAGACTGCGAGGATAGTAGCTGTGGCACAGGCCAGACTGACCTTTATGAAGCCGACACAGACGGGTATGCTTTTACAGCTTTATTCATACAATTTTATGTATTTGTAAGATGCATAGTTACTTATGTTGTAAAATCCTGACAGCCATTCCAAGGCATCCATTGCCATTTGCGGCAAAAAACATGTTTTATGATGAG[C/T]GATGGATCGAAAAGCAAGAGCGAGGCTTTACTTGGTGGATGAACTACATTCTCACTCCTGATGACTTCAAAGTTGCTACTGAAGTTACCAAAGGTAGGCACTTAGTTGGAGTGATTGTATCCTAAAGTAATTGGATATCAACAAAGTTCTCATCTCACTTTAATGTTGTTCCAAACGTGTAAGTTATTTTGTTCAACTTTGGAGCACAAATGAAGATATTTCAGGTGAAACCCTAGAGCTCTCTTACCTTTTATAAACAACAAGGGTCCCAAGACCTTTAAAGTCCAGAAAGGTACCAAGAAGAGTCAAAGGTCCAATCCCAATTCTACCCCTTAGCTCTTCCCCTTACCTACCTTTCGTTTAGCATGATCACGTGAAGGGAAAGGGCTAGATAGCCTTTAAACTGAGATTTTCCCAGACCAAACTCGAAACCAAGGGGTACACAAAATAGAATAGGGCCAAAGTATTTCACAGTGGTTCAACCTTAATTTCATGAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24171
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105628 | Essential Splice Site | 829 | 3411 | 8 | 30 |
ENSDART00000126795 | Essential Splice Site | 809 | 3391 | 7 | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 24345208)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23527536 |
GRCz11 | 22 | 23554100 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAACTGGCTCATATCGTACAATCCACTTTGGCTGCGAATTGGACTTGAG[G/A]TATTTACTTTTCATTGTAAAAGCATACTGTTTGTCTCATCACTTGCTGAA
Long Flanking Sequence:
ACTATGAGGATTTTAAAAGCATTCAGGAATAAAAAATTGTACCGTTTGTAACTTAAATCATGATTAATTTTCTTGAATTATTTTTATTGTTTAATTACTGTATCGGATTACTGTTTACACTGTTTATATAATGTATTTCTATTGTATCTTTTTTATTGATCTATGCTTGTATACAATATGAATAACAAAATTTGTTAGATTTTTCCAATATCGTTCAGCCCTTATTTGGAATTATAATTGTTAAAATCACAACGATCCTTTTGAATAATACTATTCAAATTATAGTTCTTATTATCAGCAATGTTATTTTATTGTTCATATCATTTCTAGCTGGTTTTTGCCTGAGGATGTTAAGTTTTTAGCATTTTAATGAATGAATTAGATTTTCTTAAGCTACTGCTTTTTCTTATTTTCTCAATTTTTATTTCTCAGGTGAGCGCCAGAAAGTTCTCAACTGGCTCATATCGTACAATCCACTTTGGCTGCGAATTGGACTTGAG[G/A]TATTTACTTTTCATTGTAAAAGCATACTGTTTGTCTCATCACTTGCTGAAAATTCAATCAGCCACATTTTGATCCAATGCATGACACGTCTCTAACTCGTTCTGTGTTTCAGACAATTTATGGAGAGCTAATATCACTGGAAAGCAACAATGATGTCATGGGACTGGCCATGTTTATTCTTGGGCGTCTGCTGTGGAACCCAGATTTAGCCGCTGAGTTCAGACACTCTAAAGTGCCGCATTTGTATAGAGATGGTAACTTAATTTACTGTATTTTCAATATCTACTGTATTTTACTCTTAATTTTGCCCACAAGAAATGTTTAGCAACCTTTACTCCAACGTGACACGCATTCCTCATTTAATGTAAAGAAAGCCAAAAAATACAAAGCTTATATACCTCATAAATATAAAAATAATTGAAAAAAATTTTTTTTTTATTGCTCATTACACAGGAATCAGATGTTGCGACCTTTTTATTTTTCGATTTATGATGCAGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1008
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 |
---|---|---|---|---|---|
ENSDART00000105628 | Nonsense | 1834 | 3411 | 19 | 30 |
ENSDART00000126795 | Nonsense | 1814 | 3391 | 18 | 29 |
ENSDART00000105628 | Nonsense | 1834 | 3411 | 19 | 30 |
ENSDART00000126795 | Nonsense | 1814 | 3391 | 18 | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 24332755)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23539989 |
GRCz11 | 22 | 23566553 |
KASP Assay ID:
554-0912.1 (used for ordering genotyping assays)
KASP Sequence:
AACTCAAAAAGTACCGGAGACAACAGTGGGCCGCATCAGTTTTACAGCAA[C/T]GATTCAGAGCAACGGTGACCAAAAATGCTGTCATGAAGCAATATGCAGCC
Long Flanking Sequence:
GAGCACATATGTGCCATCAGCAGTTTTTAGCTCAAAAACATGCTGCTATTGTCATTCAGCAGCAGTTTCGGGCTTTTACATTTGGACGAATGGAAAGAAGCCACTATATGCGATTGAGAAAGGCAACTATAACCATGCAGGCCATATATCGGGGTTCCAAAGTGAGGCAGAATTTAAAAAGAGAACATCAAGCTGCTACTGTCATTCAAGCCCAATTCCGAATGCATAAGGTCCGCATTCCTTTTGTTGCCGCAAAGTGTGCAGCTATCCTTATACAGCAGCATTATAGAGCCTATAAGGTTGGCAAAACTGTGCAAGCTACTTATTTACAAATGAAAAATGCGGCCGTAGTTATTCAGTCAGCTTTCAGGGGGATGAAAGTTCGCAACTACTTACGAAAATCTCACCAAGCTGCAAAAGTGATTCAGGCACATTTCCGTGGACATTCCCAACTCAAAAAGTACCGGAGACAACAGTGGGCCGCATCAGTTTTACAGCAA[C/T]GATTCAGAGCAACGGTGACCAAAAATGCTGTCATGAAGCAATATGCAGCCATAAAAACTGCAACAATATGTATTCAGTCTGCTTTCCGCGGAATGGTGGCGAGAAAGCAGATCGCAGAAAAGCAAAAATGTGCTAAAATTATCCAAAAGATGTATAGAGCATACAAACAACGTCATGATTACCTTGCTCTTAGGAATGCCACAATTCGTATTCAGCAACAATACAGAGCAGTTGTAAGTGCAAGGCAACAGCATCAAAGGTATTGCTCCTTGCGAGCAGCTGCCATCACTTTGCAGTCTTCTTACAGAGGGTTGAGGGCAAGAAAAGAAATCAATAGAAGACAAAAAGCAGCCACTGTGATTCAGGCTGCTTACAAAATGTACAGAACAAGAGTACCTTTCCAAGCCATGAAACTGGCTTCATTGGTAATACAGAGGCAGTACAGGTGCCATTTACTGAGAAAAAAGGCAAGAGAGAACTTCTTAAAACTAAAGCAGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24170
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 |
---|---|---|---|---|---|
ENSDART00000105628 | Nonsense | 2161 | 3411 | 19 | 30 |
ENSDART00000126795 | Nonsense | 2141 | 3391 | 18 | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 24331774)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23540970 |
GRCz11 | 22 | 23567534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGTGCAGCTTTGATTCTGCAAGCAGCCTATCGTGGCAAGAAGACCAGA[C/T]AGGCTTTGAAGCAAATGCACCAAGCTGCAACAATCATTCAGTCCCATGTG
Long Flanking Sequence:
TCTTAAAACTAAAGCAGAGTGCAGTAGCAATTCAAGCTATATACAGAGGAAAACTTGCACGCCGTGATCTTGCTAGAAGGCATTTTGCAGCCACAATCATTCAAAGAAAGTACCTTGCCTACAAACAAAGGAAGTGTTTTTTGACCCTTCAAGCTGCTGTTATATTCTGTCAACAACACTATCGATCCATTTTGCTTACAAGGCATGACCGAAAAGATTATTTGACTAAACGCAGAGCTGTGGTAGCAATCCAGGCAAGTTTCAGAGGGATGAATGTCCGGCGCCAGATCCGAAGAGAGCACAAAGCTGCAACAATCATTCAGTCCCATGTGAGAATGCGCATCCTCAACTTGCGCTTCCAGCGACTTCGATGGGCAGTCTGTACTGTTCAGCAACGTTTCAGAGCTAACAAAATCATGAGGCAAGAGATGGCAGCACTACAGGAAAAGAAAAGTGCAGCTTTGATTCTGCAAGCAGCCTATCGTGGCAAGAAGACCAGA[C/T]AGGCTTTGAAGCAAATGCACCAAGCTGCAACAATCATTCAGTCCCATGTGAGAATGCGGATCCTTAACTTGCGCTTCCAGCGACTTCGATGGGCAGTCTGTACTGTTCAGGAGCGTTTCAGAGCTAACAGAATCATGAGGCAGGAGATGGCAGCACTACAGGAAAAGAAAAGTGCAGCTTTGATTCTGCAAGCAGCCTATCGTGGCAAGAAGACCAGACAGGCTTTGAAGCAAATGCACCAAGCTGCAACAATCATTCAGTCCCATGTGAGAATGCGGATCCTTAACTTGCGCTTCCAGCGACTTCGATGGGCAGTCTGTACTCTTCAGCGACATTTCAGAGCTAACAAAATCATGAGGCAAGAGATGGCAGCACTACAGGAAAAGAAAAGTGCAGCTTTAATTCTGCAAGCAGCCTATCGTGGCATGAAGACCAGGCACACGTTGAAGCAAATGCACCAAGCTGCAACAATCATTCAGTCCCATGTGAGAATGCGGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24169
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 |
---|---|---|---|---|---|
ENSDART00000105628 | Nonsense | 2314 | 3411 | 19 | 30 |
ENSDART00000126795 | Nonsense | 2294 | 3391 | 18 | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 24331315)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23541429 |
GRCz11 | 22 | 23567993 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCAGCCTATCGTGGCATGAAGACCAGGCACACGTTGAAGCAAATGCAC[C/T]AAGCTGCAACAATCATTCAGTCCCATGTGAGAATGCGGATCCTTAATTTG
Long Flanking Sequence:
CTTTGATTCTGCAAGCAGCCTATCGTGGCAAGAAGACCAGACAGGCTTTGAAGCAAATGCACCAAGCTGCAACAATCATTCAGTCCCATGTGAGAATGCGGATCCTTAACTTGCGCTTCCAGCGACTTCGATGGGCAGTCTGTACTGTTCAGGAGCGTTTCAGAGCTAACAGAATCATGAGGCAGGAGATGGCAGCACTACAGGAAAAGAAAAGTGCAGCTTTGATTCTGCAAGCAGCCTATCGTGGCAAGAAGACCAGACAGGCTTTGAAGCAAATGCACCAAGCTGCAACAATCATTCAGTCCCATGTGAGAATGCGGATCCTTAACTTGCGCTTCCAGCGACTTCGATGGGCAGTCTGTACTCTTCAGCGACATTTCAGAGCTAACAAAATCATGAGGCAAGAGATGGCAGCACTACAGGAAAAGAAAAGTGCAGCTTTAATTCTGCAAGCAGCCTATCGTGGCATGAAGACCAGGCACACGTTGAAGCAAATGCAC[C/T]AAGCTGCAACAATCATTCAGTCCCATGTGAGAATGCGGATCCTTAATTTGCGCTTCCAGCGACTTCGTTGGGCAGTCTGTACTGTTCAGCAACGTTTTAGAGCTAACAGAATCATGAGGCAGGAGATGGCAGCACTACAGGAAAAGAAAAGTGCAGCTTTGATTCTGCAAGCAGCCTATCGTGGCATGAAGACCAGACAAACTTTAAAACAAATGCACCAGGCTGCCACCATTGTACAGGCAACTTACCGAGCTTATAGTGGACGTAAGCGGTATTTAGAAATGAAATGTGCTGCCATTGATATTCAGCAAAGATATCGGGCTGTAAATGCAGCAAAGCAGCAGAGAAAGAGTTATCTTAAAGTGCGTCAAGGTGCACTTGTTCTACAAGCGTGCTATAGAGGTCGTAAAGTTAGGAGGAACCTGCAACTACAGTGCCAAGCCGCTGTCTTGATTCAATCATATTTTAGAAGACACAAAGAGATGGTTAAGTACCAGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11648
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105628 | Nonsense | 2382 | 3411 | 19 | 30 |
ENSDART00000126795 | Nonsense | 2362 | 3391 | 18 | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 24331110)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23541634 |
GRCz11 | 22 | 23568198 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTTTGAWTCTGCAAGCAGCCTATCGTGGCATGAAGACCAGACAAACTT[T/G]AAAACAAATGCACCAGGCTGCCACCATTGTWCAGGCAACTTACCGAKCTT
Long Flanking Sequence:
AAAGAAAAGTGCAGCTTTGATTCTGCAAGCAGCCTATCGTGGCAAGAAGACCAGACAGGCTTTGAAGCAAATGCACCAAGCTGCAACAATCATTCAGTCCCATGTGAGAATGCGGATCCTTAACTTGCGCTTCCAGCGACTTCGATGGGCAGTCTGTACTCTTCAGCGACATTTCAGAGCTAACAAAATCATGAGGCAAGAGATGGCAGCACTACAGGAAAAGAAAAGTGCAGCTTTAATTCTGCAAGCAGCCTATCGTGGCATGAAGACCAGGCACACGTTGAAGCAAATGCACCAAGCTGCAACAATCATTCAGTCCCATGTGAGAATGCGGATCCTTAATTTGCGCTTCCAGCGACTTCGTTGGGCAGTCTGTACTGTTCAGCAACGTTTTAGAGCTAACAGAATCATGAGGCAGGAGATGGCAGCACTACAGGAAAAGAAAAGTGCAGCTTTGATTCTGCAAGCAGCCTATCGTGGCATGAAGACCAGACAAACTT[T/G]AAAACAAATGCACCAGGCTGCCACCATTGTACAGGCAACTTACCGAGCTTATAGTGGACGTAAGCGGTATTTAGAAATGAAATGTGCTGCCATTGATATTCAGCAAAGATATCGGGCTGTAAATGCAGCAAAGCAGCAGAGAAAGAGTTATCTTAAAGTGCGTCAAGGTGCACTTGTTCTACAAGCGTGCTATAGAGGTCGTAAAGTTAGGAGGAACCTGCAACTACAGTGCCAAGCCGCTGTCTTGATTCAATCATATTTTAGAAGACACAAAGAGATGGTTAAGTACCAGGCCATGAAGCTGTCTGCTGTCATTATCCAGAGCCATTTCAGGTCATACATCCAGGCTAGAGCAGATCGGAAGAACTATCAACATTTGAGAAAATCTGCCATAGTCATTCAAGCTGCTTTTAGAGGACACTCTCTCAGGAGACATTTAGCAAGAAAGCAAGAAGCTTCTGTTATCATACAGGCCAGCTTCCGCATGTATCAGCAAAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13529
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 |
---|---|---|---|---|---|
ENSDART00000105628 | Nonsense | 2806 | 3411 | 20 | 30 |
ENSDART00000126795 | Nonsense | 2786 | 3391 | 19 | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 24329729)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23543015 |
GRCz11 | 22 | 23569579 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGGGAAGGCCAAACTTTTTTCCCCCTTGCTATCAAACAGGCAAATTAT[C/T]GAGGGATGRTTGAGAGACGCAGGTTTCACCAACTCAAGGAGTGTGCWTTG
Long Flanking Sequence:
GTTAGACAAGCTACGCTTACCTTGCAGTCTGCCTTGAGGGGAATGCTGGTGAGGAGGCTTGCAAAAAGAAGAAGGGCTGCAATAAAGATTCAGTCTGTGATGCGCATGCACATACAACGCAAGCGCTATGTAACTCTCCGTGCAAGTGCCCTGAAGTTTCAAGCTCATTACAGAATGTTAGTGGCCCAAAGAAAATACCGTCGATTGCAGGCTGCAACTGTTACTCTTCAAAAGCATTACAGATCTCATAGGGCTACATTGGAGCAGAGGTGCAGTTATCTGAAGACTCTCCAAAACATAAAAAAACTTCAGGCCAGAGTACGTGGACACATTGCGTACAAACGATTTCAGAGATTGAGAACATGTGCCATCACCATTCAGGTAATCACTATGCATTCTCTCTTGTCAACATGATTTTCTTTGGAAATTCAAAAGACGTGATTGAGCTCAATTGGGAAGGCCAAACTTTTTTCCCCCTTGCTATCAAACAGGCAAATTAT[C/T]GAGGGATGATTGAGAGACGCAGGTTTCACCAACTCAAGGAGTGTGCATTGGTTATACAGAAGCATTACAGAGCTTTCATTCTTTGCCAGAAAGAGCGTTCAAAGTTTCTTCAGCTGCGACAATCTGCTGTTGTGATACAAGTAAGATTGTGATATCTGTTTTATCTTTAGACTTTTAGTTTTCTGTTTATAACCCTATTTGAGATATTACAACTTTAACTATGTATTGAATGTTCATGTTTGGGTTGTCTTTATGTAATCTCAGAGAGCATATCGAGCTTATCAAAAAAGACAAAATGCAATGAAAGCACAGGCTGCACTGAAAATTCAGGCTTGGTTCAGAGGACGCCTTGCTAGACGCAACTACATCTTAAAACAAGCCGCTAGTGCCACCATTCGAAGATGTATCCAAGCGAGACGCCAACGCTCTAAGTAAGAAATTAAAGATATTATTTTGTTTATTCATTTTTTTGCTTTGTGTAACAAGGAGTCGCAACCTGA
Associated Phenotype:
Not determined