ZMP
sh3pxd2a
Ensembl ID:
ZFIN ID:
Description:
SH3 and PX domain-containing protein 2A [Source:UniProtKB/Swiss-Prot;Acc:Q1LYG0]
Human Orthologue:
SH3PXD2A
Human Description:
SH3 and PX domains 2A [Source:HGNC Symbol;Acc:23664]
Mouse Orthologue:
Sh3pxd2a
Mouse Description:
SH3 and PX domains 2A Gene [Source:MGI Symbol;Acc:MGI:1298393]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39678 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa32757 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa19571 | Nonsense | Available for shipment | Available now |
| sa19572 | Nonsense | Available for shipment | Available now |
| sa19573 | Nonsense | Available for shipment | Available now |
| sa31233 | Nonsense | Available for shipment | Available now |
| sa19574 | Nonsense | Available for shipment | Available now |
| sa10307 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39678
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 |
|---|---|---|---|---|---|
| ENSDART00000084457 | Nonsense | 197 | 1068 | 7 | 12 |
| ENSDART00000109244 | Nonsense | 264 | 1140 | 10 | 16 |
Genomic Location (Zv9):
Chromosome 1 (position 48164667)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46976328 |
| GRCz11 | 1 | 47667560 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGAGGCTCGACCGGAGATGGACACTAGGGGGAATAGTCAACCGCCAA[C/T]AGAGCCGAGGTGAAACATACATACAGTCACGCCTGCATAGACTGATCACA
Long Flanking Sequence:
TTAGTGTTATACAAAGTTTACCTAAATATTTTACTCAGTTTGATTGATGTAAGTTGAGATGATTTGACAGTTATTTTGATTCAACTAAAATTAAAGGCAGCAGATTGTTTATTAACAGTGTACATTTGCATCTTTGGAGCACTACGAGCAGATGACGTTTCCATTCTGCAGCACAATAGAATATCAAAACACTACATTTTCCACAGTATAACAAGCTCCACTAAAATCCAATAACACATGTATTAATCCAAGTCCTCTATTGCTTTCTTTGTCATCGTTCGAGCGTCGCTAACCGATCACGACTCTCTCTTCCTCCATGTAATCATTTATCTTCATTACACTAATCCCAGTGTTGCTTCTCAGTTGTTTACGTTGAGTTTGTCATGTCTCTGTTCTCTTTCTGCTGCCCTCATTCATCCATGTCAGTTACTAAAAGGCGTAAGGCTCATCTGAAGAGGCTCGACCGGAGATGGACACTAGGGGGAATAGTCAACCGCCAA[C/T]AGAGCCGAGGTGAAACATACATACAGTCACGCCTGCATAGACTGATCACATGCAAGCACTCACGTGTGTGTGACCAATCTGCATGCTGCGTTTGTGTGTGAGTGTGTGTACACGGTGGTTAGCGTAAATATGCACACAGAAACTCACTTTATGGAGCCAGCTACTGGATCAGGCTCCCAAAGCATGCTGGGTGGCCTGTTTCATCCGCGCTCCATCATAAAACCTTTATGATACTTTGCTTGCTTAATGTCTGTGTTTGTGTTTACATGTGTATGGATGTAAAATGTTTGCTTGCTGACCAAGAAAATGCTGTTTTACAGTGTTTCTCTGGAGGAAGATTGGTTTCGAAGTACATAGTTCTGAAAAAAATAAAAGTTTTGTCTTCTCAAATTTAGGATTAGCGCCCAAAGATTTGATCGTAAAGAGATAAAAATATTTAAAAAAAAGAGTTAACCCCTCAAAAATGAAAGCGTACTCACCCTAAAGTTCAATCCTGCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32757
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084457 | Nonsense | 431 | 1068 | 12 | 12 |
| ENSDART00000109244 | Nonsense | 503 | 1140 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 1 (position 48178449)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46990110 |
| GRCz11 | 1 | 47681342 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATTATGTAATATGTGGTCTTCAGGTCATAGAAAAGAACTCTGGAGGAT[G/A]GTGGTATGTCCAGATTGGGGATACGGAGGGCTGGGCACCCAGCTCATACA
Long Flanking Sequence:
TTGATAAGAGAGACAGCGTATAAACATGTTTTATGTTCAACTGACAGGATCTCCAAACCTCAGACAGAAACCTCCTCCTCGGAGAGATGCAAACCTGGTAAGTTAGGCAGTCCAAAGTAGGTTATTATTATTTAAAATAGCGCAGCATCTATTAATTAGGCCTTTTCTCTATTACTCAAGGCATTCCAGTTGCCCAAACCTCCAGAGGCCCCTACTGTGGAAGCGGAGTATTACACCATAGCAGAGTTTCAATCCAGTATCTCAGATGGCATCAGCTTCCGTGGAGGACAAAAGGCTGATGTAAGGCCGATATATTCTGACTAAAATCTGTGATTTTTAAATATTTAATTTTTAACACATATTTATTAGCAGTCTTTTTAAATATCACTATACAGGGAATTTAATATATGTCAGTGTATTGTGTAAACATATGTGGTGTGATAAAAGTTATAATTATGTAATATGTGGTCTTCAGGTCATAGAAAAGAACTCTGGAGGAT[G/A]GTGGTATGTCCAGATTGGGGATACGGAGGGCTGGGCACCCAGCTCATACATTGATAAACGTAAGAAGCCCAACCTGAGCCGGCGAACCAGCACACTCACACGTCCTAAAGTTCCACCCCCTGCTCCACCAGTCAAGAAACAGGACTCAGAGGAAGGCCCCTCTCTGGGTGGCTCTGCCTCCAAAGCTCCCGAGTCTCCTCAGCGTGTCTATGAGGAGCCAGAATATGATGTTCCTGCCCTTGGTTTTGACTCTGAGCTGGATTGCAATCCTCCAAAACCGAAAACACATAACTCCCCAAAACCAGAGCCCCGTAAGTTTGAAATTAAAAGCAATCCAGCGGCTGCTGAAAGGATTGCACAAGCTGGCAAAGCGTCGCCTTTATTAAAAGTGATGACCTCACCCCTGAGGAAAAGAAACTCTTTAGAGAATATCAACAAGGAGGAGGTGATTTATGAAAATGAAGGCTTCAGGTTCTCCTCTGATGACTTCGCCAGTGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19571
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 |
|---|---|---|---|---|---|
| ENSDART00000084457 | Nonsense | 762 | 1068 | 12 | 12 |
| ENSDART00000109244 | Nonsense | 834 | 1140 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 1 (position 48179441)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46991102 |
| GRCz11 | 1 | 47682334 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTCTCCAGTGTTTATTCAAAGGGTAGCCGAGGTGGAGAATCCGACCAC[G/T]AAAGTGTGCTCTTTAGGACCACAGATGCCTATGAACGAGCCCAGGAGTCA
Long Flanking Sequence:
CCAGTGGATGTGATTCACATACCCCAAGGAGTCTCACATTGGGTCGCAAACCTTTCGGATCCTCTTCTGGTGGAGGGAAGCCCCTTCGGAAGGTATCGCCGGATCTAAACCGAAGCCACTCTCTTGGCCGTGCTGAGAGACACAGCTCCAAGTTATTTTCCGATGAATCAGCACGCAATCCCAAAAGAGAGCCTGTCATGCGTAAAGATGTGGAGATCCGGATCGGTCAGAGTCCCTTAGCAAGGCCCAAACCAGTGGTGCGACCCAAACCTCTGCTTACAAAGTCAGAGCCACAAAGTCCTGAAAGAATGGACATCAGCAGCATACGCCGTCACCTTCGACCCACCGGAAGCCTTCGGCAAGGAGCAATTCGTGCAATGCGTGGTGAAGACTCCGAGACAGCTTCTGTTGTGTCCTCTGAGGACTCCACTTCCTCAAGAAGTACCTCTGATCTCTCCAGTGTTTATTCAAAGGGTAGCCGAGGTGGAGAATCCGACCAC[G/T]AAAGTGTGCTCTTTAGGACCACAGATGCCTATGAACGAGCCCAGGAGTCAGAGCTCAGCTTCCCAGCTGGTGTGGAGGTTGAGGTACTGGAGAAGCAGGAAAGTGGATGGTGGTTTGTTCGTTGGGGCAGTGATGAGGGTTGGGTACCTACTTTTTACTTGGAGCCGATTAAACATACCCACAACGTCGGTATTCAAGAATCCCGTGATAGCCCTCTTGTTGATCTAGGAAGCACCAACAAGTCCAATAGTCTTGAGAAAAATGAGCAGCGTGTTCAGGCCCTTAACAACCTCAACCAGCAAAACCTAAGAAGCATGAGCAACCCTAGCCCACCAATCCCATCCAAACCACCAGGGGGATTTAGCAAACCAACAGCAATGCTGAACGGCTCAAGTGTACGGATGCGCAACGGTGTCCGTCAAGCAGCAGTGCGACCACAGTCAGTGTTTGTGTCTCCACCACAGCCCCTAAAGGAAACCAATATCCATACAGGGTCTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19572
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084457 | Nonsense | 799 | 1068 | 12 | 12 |
| ENSDART00000109244 | Nonsense | 871 | 1140 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 1 (position 48179553)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46991214 |
| GRCz11 | 1 | 47682446 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGCTGGTGTGGAGGTTGAGGTACTGGAGAAGCAGGAAAGTGGATGGT[G/A]GTTTGTTCGTTGGGGCAGTGATGAGGGTTGGGTACCTACTTTTTACTTGG
Long Flanking Sequence:
AAGCCACTCTCTTGGCCGTGCTGAGAGACACAGCTCCAAGTTATTTTCCGATGAATCAGCACGCAATCCCAAAAGAGAGCCTGTCATGCGTAAAGATGTGGAGATCCGGATCGGTCAGAGTCCCTTAGCAAGGCCCAAACCAGTGGTGCGACCCAAACCTCTGCTTACAAAGTCAGAGCCACAAAGTCCTGAAAGAATGGACATCAGCAGCATACGCCGTCACCTTCGACCCACCGGAAGCCTTCGGCAAGGAGCAATTCGTGCAATGCGTGGTGAAGACTCCGAGACAGCTTCTGTTGTGTCCTCTGAGGACTCCACTTCCTCAAGAAGTACCTCTGATCTCTCCAGTGTTTATTCAAAGGGTAGCCGAGGTGGAGAATCCGACCACGAAAGTGTGCTCTTTAGGACCACAGATGCCTATGAACGAGCCCAGGAGTCAGAGCTCAGCTTCCCAGCTGGTGTGGAGGTTGAGGTACTGGAGAAGCAGGAAAGTGGATGGT[G/A]GTTTGTTCGTTGGGGCAGTGATGAGGGTTGGGTACCTACTTTTTACTTGGAGCCGATTAAACATACCCACAACGTCGGTATTCAAGAATCCCGTGATAGCCCTCTTGTTGATCTAGGAAGCACCAACAAGTCCAATAGTCTTGAGAAAAATGAGCAGCGTGTTCAGGCCCTTAACAACCTCAACCAGCAAAACCTAAGAAGCATGAGCAACCCTAGCCCACCAATCCCATCCAAACCACCAGGGGGATTTAGCAAACCAACAGCAATGCTGAACGGCTCAAGTGTACGGATGCGCAACGGTGTCCGTCAAGCAGCAGTGCGACCACAGTCAGTGTTTGTGTCTCCACCACAGCCCCTAAAGGAAACCAATATCCATACAGGGTCTTTGAGGAGAAATGAATCACTGGGTGCCGGCGACCACTTGAGGTCCACAGGTGGCGTTCGACGAAACTCCTCCTTCACCGCCGTACGACCACAGCCCGTGACCGATGTACGGGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19573
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 |
|---|---|---|---|---|---|
| ENSDART00000084457 | Nonsense | 814 | 1068 | 12 | 12 |
| ENSDART00000109244 | Nonsense | 886 | 1140 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 1 (position 48179599)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46991260 |
| GRCz11 | 1 | 47682492 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGGTTTGTTCGTTGGGGCAGTGATGAGGGTTGGGTACCTACTTTTTA[C/A]TTGGAGCCGATTAAACATACCCACAACGTCGGTATTCAAGAATCCCGTGA
Long Flanking Sequence:
TCCGATGAATCAGCACGCAATCCCAAAAGAGAGCCTGTCATGCGTAAAGATGTGGAGATCCGGATCGGTCAGAGTCCCTTAGCAAGGCCCAAACCAGTGGTGCGACCCAAACCTCTGCTTACAAAGTCAGAGCCACAAAGTCCTGAAAGAATGGACATCAGCAGCATACGCCGTCACCTTCGACCCACCGGAAGCCTTCGGCAAGGAGCAATTCGTGCAATGCGTGGTGAAGACTCCGAGACAGCTTCTGTTGTGTCCTCTGAGGACTCCACTTCCTCAAGAAGTACCTCTGATCTCTCCAGTGTTTATTCAAAGGGTAGCCGAGGTGGAGAATCCGACCACGAAAGTGTGCTCTTTAGGACCACAGATGCCTATGAACGAGCCCAGGAGTCAGAGCTCAGCTTCCCAGCTGGTGTGGAGGTTGAGGTACTGGAGAAGCAGGAAAGTGGATGGTGGTTTGTTCGTTGGGGCAGTGATGAGGGTTGGGTACCTACTTTTTA[C/A]TTGGAGCCGATTAAACATACCCACAACGTCGGTATTCAAGAATCCCGTGATAGCCCTCTTGTTGATCTAGGAAGCACCAACAAGTCCAATAGTCTTGAGAAAAATGAGCAGCGTGTTCAGGCCCTTAACAACCTCAACCAGCAAAACCTAAGAAGCATGAGCAACCCTAGCCCACCAATCCCATCCAAACCACCAGGGGGATTTAGCAAACCAACAGCAATGCTGAACGGCTCAAGTGTACGGATGCGCAACGGTGTCCGTCAAGCAGCAGTGCGACCACAGTCAGTGTTTGTGTCTCCACCACAGCCCCTAAAGGAAACCAATATCCATACAGGGTCTTTGAGGAGAAATGAATCACTGGGTGCCGGCGACCACTTGAGGTCCACAGGTGGCGTTCGACGAAACTCCTCCTTCACCGCCGTACGACCACAGCCCGTGACCGATGTACGGGTGAGGGCTGGGACCACCATTACAGCTCCCGCCGGAAGCTCAAGTCCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31233
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 |
|---|---|---|---|---|---|
| ENSDART00000084457 | Nonsense | 815 | 1068 | 12 | 12 |
| ENSDART00000109244 | Nonsense | 887 | 1140 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 1 (position 48179601)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46991262 |
| GRCz11 | 1 | 47682494 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGTTTGTTCGTTGGGGCAGTGATGAGGGTTGGGTACCTACTTTTTACT[T/A]GGAGCCGATTAAACATACCCACAACGTCGGTATTCAAGAATCCCGTGATA
Long Flanking Sequence:
CGATGAATCAGCACGCAATCCCAAAAGAGAGCCTGTCATGCGTAAAGATGTGGAGATCCGGATCGGTCAGAGTCCCTTAGCAAGGCCCAAACCAGTGGTGCGACCCAAACCTCTGCTTACAAAGTCAGAGCCACAAAGTCCTGAAAGAATGGACATCAGCAGCATACGCCGTCACCTTCGACCCACCGGAAGCCTTCGGCAAGGAGCAATTCGTGCAATGCGTGGTGAAGACTCCGAGACAGCTTCTGTTGTGTCCTCTGAGGACTCCACTTCCTCAAGAAGTACCTCTGATCTCTCCAGTGTTTATTCAAAGGGTAGCCGAGGTGGAGAATCCGACCACGAAAGTGTGCTCTTTAGGACCACAGATGCCTATGAACGAGCCCAGGAGTCAGAGCTCAGCTTCCCAGCTGGTGTGGAGGTTGAGGTACTGGAGAAGCAGGAAAGTGGATGGTGGTTTGTTCGTTGGGGCAGTGATGAGGGTTGGGTACCTACTTTTTACT[T/A]GGAGCCGATTAAACATACCCACAACGTCGGTATTCAAGAATCCCGTGATAGCCCTCTTGTTGATCTAGGAAGCACCAACAAGTCCAATAGTCTTGAGAAAAATGAGCAGCGTGTTCAGGCCCTTAACAACCTCAACCAGCAAAACCTAAGAAGCATGAGCAACCCTAGCCCACCAATCCCATCCAAACCACCAGGGGGATTTAGCAAACCAACAGCAATGCTGAACGGCTCAAGTGTACGGATGCGCAACGGTGTCCGTCAAGCAGCAGTGCGACCACAGTCAGTGTTTGTGTCTCCACCACAGCCCCTAAAGGAAACCAATATCCATACAGGGTCTTTGAGGAGAAATGAATCACTGGGTGCCGGCGACCACTTGAGGTCCACAGGTGGCGTTCGACGAAACTCCTCCTTCACCGCCGTACGACCACAGCCCGTGACCGATGTACGGGTGAGGGCTGGGACCACCATTACAGCTCCCGCCGGAAGCTCAAGTCCATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19574
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 |
|---|---|---|---|---|---|
| ENSDART00000084457 | Nonsense | 1018 | 1068 | 12 | 12 |
| ENSDART00000109244 | Nonsense | 1090 | 1140 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 1 (position 48180211)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46991872 |
| GRCz11 | 1 | 47683104 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTCATTCACAACAACCTTCGAGAGGTTTACGTATCCATCGCAGATTA[T/A]CGCGGAGATGAAGAGACCATGGGTTTTTCAGAGGGCACTTCTCTTGAAGT
Long Flanking Sequence:
CGTGTTCAGGCCCTTAACAACCTCAACCAGCAAAACCTAAGAAGCATGAGCAACCCTAGCCCACCAATCCCATCCAAACCACCAGGGGGATTTAGCAAACCAACAGCAATGCTGAACGGCTCAAGTGTACGGATGCGCAACGGTGTCCGTCAAGCAGCAGTGCGACCACAGTCAGTGTTTGTGTCTCCACCACAGCCCCTAAAGGAAACCAATATCCATACAGGGTCTTTGAGGAGAAATGAATCACTGGGTGCCGGCGACCACTTGAGGTCCACAGGTGGCGTTCGACGAAACTCCTCCTTCACCGCCGTACGACCACAGCCCGTGACCGATGTACGGGTGAGGGCTGGGACCACCATTACAGCTCCCGCCGGAAGCTCAAGTCCATTGATTGCTCAGAGAAACGGGATTCCAATCTCTACAGTAAGACCCAAGCCCATTGAGAAGATGCAGCTCATTCACAACAACCTTCGAGAGGTTTACGTATCCATCGCAGATTA[T/A]CGCGGAGATGAAGAGACCATGGGTTTTTCAGAGGGCACTTCTCTTGAAGTTTTGGAGAAGAATCCAAATGGATGGTGGTACTGCCAGGTTCTCGATGGTTTACAGGGACGTAAAGGCTGGGTACCTTCTAACTACCTGGAGAGAAAAAAGTAATTCCCCCAAAAATGTTTTAAACATGCACAATTGTAATCAACATGTAAAAAGATAAACTGACTGAAGGACTATTGGTTTGAGATGAGCGGGACAGAGCCTTTTAGAAAGGAGTTTACATTAAAACTACAGAAAAGCAGGTGAATGTTTAGCAAAATACCTGCCATAACTTTATACCAAATGGGTGCCTTCGAACATCTTTCACTGAATGTTAAGAGGAATCGGTCAAATACCAGTAAAGCATCAGAAAATACCAAACTTCAACTCAGTGCCATAGGCCTACAAGTACAGAAAGCAACAAACTTATTTTTGTTACAGTGTTAAAAAGAGAGAAAGAGAATTTCAGCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10307
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 |
|---|---|---|---|---|---|
| ENSDART00000084457 | Nonsense | 1034 | 1068 | 12 | 12 |
| ENSDART00000109244 | Nonsense | 1106 | 1140 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 1 (position 48180257)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46991918 |
| GRCz11 | 1 | 47683150 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTATCGCGGAGATGAAGAGAYCATGGGTTTTTCAGAGGGCACTTCTCTT[G/T]AAGTTTTGGRGAAGAATCCAAATGGATGGTGGTACTGCCAGGTTCTCGAT
Long Flanking Sequence:
TGAGCAACCCTAGCCCACCAATCCCATCCAAACCACCAGGGGGATTTAGCAAACCAACAGCAATGCTGAACGGCTCAAGTGTACGGATGCGCAACGGTGTCCGTCAAGCAGCAGTGCGACCACAGTCAGTGTTTGTGTCTCCACCACAGCCCCTAAAGGAAACCAATATCCATACAGGGTCTTTGAGGAGAAATGAATCACTGGGTGCCGGCGACCACTTGAGGTCCACAGGTGGCGTTCGACGAAACTCCTCCTTCACCGCCGTACGACCACAGCCCGTGACCGATGTACGGGTGAGGGCTGGGACCACCATTACAGCTCCCGCCGGAAGCTCAAGTCCATTGATTGCTCAGAGAAACGGGATTCCAATCTCTACAGTAAGACCCAAGCCCATTGAGAAGATGCAGCTCATTCACAACAACCTTCGAGAGGTTTACGTATCCATCGCAGATTATCGCGGAGATGAAGAGACCATGGGTTTTTCAGAGGGCACTTCTCTT[G/T]AAGTTTTGGAGAAGAATCCAAATGGATGGTGGTACTGCCAGGTTCTCGATGGTTTACAGGGACGTAAAGGCTGGGTACCTTCTAACTACCTGGAGAGAAAAAAGTAATTCCCCCAAAAATGTTTTAAACATGCACAATTGTAATCAACATGTAAAAAGATAAACTGACTGAAGGACTATTGGTTTGAGATGAGCGGGACAGAGCCTTTTAGAAAGGAGTTTACATTAAAACTACAGAAAAGCAGGTGAATGTTTAGCAAAATACCTGCCATAACTTTATACCAAATGGGTGCCTTCGAACATCTTTCACTGAATGTTAAGAGGAATCGGTCAAATACCAGTAAAGCATCAGAAAATACCAAACTTCAACTCAGTGCCATAGGCCTACAAGTACAGAAAGCAACAAACTTATTTTTGTTACAGTGTTAAAAAGAGAGAAAGAGAATTTCAGCATAGGTGCATAAAAAAGTGCTAGTTTAATCGTGGGCGCTCGAAAAACGA
Associated Phenotype:
Not determined