ZMP
LOC565513
Ensembl ID:
Human Orthologue:
SNX29
Human Description:
sorting nexin 29 [Source:HGNC Symbol;Acc:30542]
Mouse Orthologue:
Snx29
Mouse Description:
sorting nexin 29 Gene [Source:MGI Symbol;Acc:MGI:1921728]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12737 | Nonsense | Available for shipment | Available now |
sa15604 | Nonsense | Available for shipment | Available now |
sa38885 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35267 | Essential Splice Site | Available for shipment | Available now |
sa22080 | Nonsense | Available for shipment | Available now |
sa35268 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9437 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12737
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114248 | Nonsense | 80 | 823 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 12 (position 20509204)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19291048 |
GRCz11 | 12 | 19412922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTAGCCCTCACAGCAGCTGCCATTAAACATGTTGCAGGATTTAGCAGT[A/T]AAACCGAAGCAGGYAMTGTAACTGGCTCCAGCAAMWAATGCACATCCAGA
Long Flanking Sequence:
ACTTAGCTGAAAAGAAAATGAATATACATTAACAGCGATTAAATAAATTCTGTAATAAATGTATTGTTTATTGTTTGTTCATGTAATTAAAAACATGAACTAATGGATCGTTATTTTAAAACATTACCCTGAATTGTATGTAATATGATAATTTCCATGTTAGCTTAAGGTTGAACTTGCTCTAAATGTGATTATTATCTCCTCAGTGCCAAATTCGCTTTGGTGGCAGGAAGGAGATCGCTTCAGATTCTGATAGCAGGTGAGAAGAATATTTCATCAGTGTATTACATATTAATTTTAGAAATCTGGAAAATCTGATATTTATTTATCTGGTATTTATATGTAGTTAACTGCTTTATTGCATAAATTATATTATTTTTTTTCGTAGGGTCATATGCCTGTGTGCCCAGTTTGAAGCGGTACTTCAGCACGGCTTGAGGAAGAGTCGAGGTTTAGCCCTCACAGCAGCTGCCATTAAACATGTTGCAGGATTTAGCAGT[A/T]AAACCGAAGCAGGTACTGTAACTGGCTCCAGCAAATAATGCACATCCAGAAATCCAGACTTTATTTTCTGTCAGTCATGTTTTGGCCAGCTAGTTTAATCCATGTGCTTTTCAGAAAAAGGATGCTTAAAATAAGCGCTTTACTAAGCAATTACCCTGTGAAATTCTTGGCCTTTTAAATGGTTTGTTTTAAGCTGGGTACACAAGAAAGGATTTTATTATTATCATCAAATTTATTAGAGACCACAAACATGGAGAAAAAATAGTTAAAAAAAAACAAAAAACAAATTAGCCCTTAAATCTAGTTTGGTAGCCTCTTTGCCAGATGTTATAGTCCAATAAAACAACAAAAATCCGAAATTCAAACAAAAAAACACAACAACAAACAACTACTAATGTTCAAAATGTTAATTATTAAGGAGCCTTTTCTTAAAATGATACTTAAACGGATTAAAGGTTGCACTTTCTCTAATAGATTGTGGTATTAAACTCCCATAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15604
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114248 | Nonsense | 80 | 823 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 12 (position 20509204)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19291048 |
GRCz11 | 12 | 19412922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTAGCCCTCACAGCAGCTGCCATTAAACATGTTGCAGGATTTAGCAGT[A/T]AAACYGAAGCAGGYAMTGTAACTGGCTCCAGCAAMWAATGCACATCCAGA
Long Flanking Sequence:
ACTTAGCTGAAAAGAAAATGAATATACATTAACAGCGATTAAATAAATTCTGTAATAAATGTATTGTTTATTGTTTGTTCATGTAATTAAAAACATGAACTAATGGATCGTTATTTTAAAACATTACCCTGAATTGTATGTAATATGATAATTTCCATGTTAGCTTAAGGTTGAACTTGCTCTAAATGTGATTATTATCTCCTCAGTGCCAAATTCGCTTTGGTGGCAGGAAGGAGATCGCTTCAGATTCTGATAGCAGGTGAGAAGAATATTTCATCAGTGTATTACATATTAATTTTAGAAATCTGGAAAATCTGATATTTATTTATCTGGTATTTATATGTAGTTAACTGCTTTATTGCATAAATTATATTATTTTTTTTCGTAGGGTCATATGCCTGTGTGCCCAGTTTGAAGCGGTACTTCAGCACGGCTTGAGGAAGAGTCGAGGTTTAGCCCTCACAGCAGCTGCCATTAAACATGTTGCAGGATTTAGCAGT[A/T]AAACCGAAGCAGGTACTGTAACTGGCTCCAGCAAATAATGCACATCCAGAAATCCAGACTTTATTTTCTGTCAGTCATGTTTTGGCCAGCTAGTTTAATCCATGTGCTTTTCAGAAAAAGGATGCTTAAAATAAGCGCTTTACTAAGCAATTACCCTGTGAAATTCTTGGCCTTTTAAATGGTTTGTTTTAAGCTGGGTACACAAGAAAGGATTTTATTATTATCATCAAATTTATTAGAGACCACAAACATGGAGAAAAAATAGTTAAAAAAAAACAAAAAACAAATTAGCCCTTAAATCTAGTTTGGTAGCCTCTTTGCCAGATGTTATAGTCCAATAAAACAACAAAAATCCGAAATTCAAACAAAAAAACACAACAACAAACAACTACTAATGTTCAAAATGTTAATTATTAAGGAGCCTTTTCTTAAAATGATACTTAAACGGATTAAAGGTTGCACTTTCTCTAATAGATTGTGGTATTAAACTCCCATAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38885
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114248 | Nonsense | 492 | 823 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 12 (position 20540418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19322262 |
GRCz11 | 12 | 19444136 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGCGGCAAGCCATTGTGGCCATGATGAACCGAAAAGATGAACTCACT[G/T]AGCAGAACACGTAGGAATTTCTAAATTACCTTTACTGATGGCATACCGGA
Long Flanking Sequence:
CTGTACCGAGTGTTGCCATTTCTTGTGTTTTGAAATGCTTTAATAATGCTTCCCAGTTAGAGCTTTATGTTTCTCTCAGATTATTCCCAGACTAATTTGTTTTGAGACTAAATCTTCCAAGGCTTCCCTTACGGCTGTGTTATAAATGCCTTACCCTTTCACGTCACCTTCATTTTAAAGAAATTAATGTCTGGTTGGTATTTTAAGCCTCGTGTAGTTCTCTTTATTAGTTCTGTGGTGCCACACAAATGAAAATGTCAGTGGTATAAAACAGTAACCCTTATTGAAGGAATGAAGATGGGTGTGGGACATGAAATCCCACCAAGATATTGAGTCTTATTGTTCAGAAGTCAAGTTTTTTTCATAGCTGGCTGAGAGAAAAAAGCCATTGTTCATTTTGAGTAGGTTTTTATACCTTTATAATGTACTGTACATTTCTTTCCTCAGCTGAACTGCGGCAAGCCATTGTGGCCATGATGAACCGAAAAGATGAACTCACT[G/T]AGCAGAACACGTAGGAATTTCTAAATTACCTTTACTGATGGCATACCGGAAAGTAGGGCTGCACAATGTTTAGTTTCAGCATCGATATTGTGATGTGATCATTCAAGATCTGCAATTTTGCTTCGGGATTATAACTTATAATTTGCAAGGATTCAGGCCTAAGAAATTGTACCATTTGTAACTTTTATTTTTTCAAATGTGTTTTTATTGACCATTTTTAGTGCAAAAATAATAACAATAATAATAATAATATCCATCAGTCAGGTAATTTGAATCCTAAACCCCACATGAAAAATTATAATAAAAAAATTAAGCAAACAAAAATAAAATTAAATAAAAAATAAGGACATTAAATACAAAATTATTTTACAAAAAGGCAGATTAAATTTTATTTATTACAGACAAGTTTTTAGTCTTCGAGGTTCCTAGATAATCAAAGAATGGACCCCAGGTCTGATAAAATAGAAAAGATTTGTTCTATTTAGCTGTGGAGAAAGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35267
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 |
---|---|---|---|---|---|
ENSDART00000114248 | Essential Splice Site | 538 | 823 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 12 (position 20543364)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19325208 |
GRCz11 | 12 | 19447082 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCCGAGCTTGAGGAGAGACATGCTGCCAAAGTCCAAGCTCTCATGAGG[T/C]AATATCGCAATAGACTGACTGAAAAGTATTCTTACATAGACAAACTAACC
Long Flanking Sequence:
TGAGCACAAATTTTTTAAAGAAGCATCAAATATTTAAACAGTAATGCAACTATACATCAAGTTTTGCAAGAATCGCAGACCACATAAATAACTGCTGAGACTGCTGAAGTTGAAGCACCTTCTTTCACTAAAAAAAGAAATGACTTGATTGTTAGTGAGTGTCAGGCCTTATTTTGTAGCCTGTTTGTGAAAATGTGCCCAGTCAATAAAGTGCTGCTGGGAAATTATCTTGTGCACCGGTAGTTATTAAAGACAGCTAAGGAAAAGTAGGTCAGGTGTGTGTGTGTGTTTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGATTTTGTGTGTGACTTACTGTTGTTAAACTGCTTTGGCACAGGTCTCTGCGTGGTCTCCTGGATGGGGAGATGGAGCACTCTGCTGGACTCAGACAGGAGGTGGACGGCTTGAAGAAGAGACTGGCCGAGCTTGAGGAGAGACATGCTGCCAAAGTCCAAGCTCTCATGAGG[T/C]AATATCGCAATAGACTGACTGAAAAGTATTCTTACATAGACAAACTAACCCAACCTAAAGTCTAGGCCGCACACCTTACACTTAAAGGGTCATGAAACCCTAAAACATATTTTTTTGAGATGTTGATAGACAGATTTTTTTCCCCTATTTCTGTTTAACAGAGAGAAATTTTTTTAACACATTTCTAAACATAATAGTTTTAATAATTCATTTCTAATAACTGATTTATCTTACCTTTGCTATGATGACAGTAAATAATATTCTACTAGATATTTCTCAAGACACTTCTATACAGCTTAAAATGACATTTAAAGGCTTATAGAAGTATAGACGCTGTATAGAAGTATCTTGAAAAATATCTAGTAAAATATTATTTACAGTCATCATGACAAAGATAAAATAATTCAGTTTTTAGAAATGAGTTATTAAAACTATTATGTTTAGAAATGTGCTGAATTTTTTCTCTCTCCGTTAAATAGAAATTGGGGAAAAAATAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22080
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 |
---|---|---|---|---|---|
ENSDART00000114248 | Nonsense | 550 | 823 | 14 | 21 |
Genomic Location (Zv9):
Chromosome 12 (position 20557054)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19338898 |
GRCz11 | 12 | 19460772 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACATTTTTGCAGAGAGAATGAAGTTCTGAAGGTTCAGCTAAAGAAGTA[T/A]GTTGGGGCTGTCCAAATGCTGAAAAGGGAAGGCAGCCAAGGCGGTGATGG
Long Flanking Sequence:
TGGTTACCTAACATGTTTAGGAAAAGAAAGATAATGGATTTAAATTCAAATAAAAATATTTCCACTGGATTTTACATTTTTCTTAAATAAAATGTCATATTTTCCCCCAACATATTAATTTGGGTGTACTTATTTCTGGACTGTGATGTTAAGGTTTTCGTTGGATTATTTGCAGTTTTAGCTTTGGTACTGCATAATCTGATGTATATGATCAAATATATTATTGGAAAGCCTACTAAAGACTACTAAATGTTTATCATATTAAAGTTGATCATTTCCTACTGTTTGCACTTATAGAACATGATCAGTCTTAACTTCATTTAAAATCCTATTTAGGAATATTTTAATAGCTTCACCCTTATTTAGCATGAAAAACATTATGCAGCACAGTTTTTACAATTTTTAAAAAAGTTAATTTTTGTGCATGTTTTGTTTTATTTATTATTTATTTGACATTTTTGCAGAGAGAATGAAGTTCTGAAGGTTCAGCTAAAGAAGTA[T/A]GTTGGGGCTGTCCAAATGCTGAAAAGGGAAGGCAGCCAAGGCGGTGATGGTAAGACAGTGTTCTCTTACCTTTGCATGTTTGGCAAACATGTAGCAACCTCTTGGCAGTTCTTGGTAGTTACAATTGGTTGTAATTTTGAACCAGTAGTTCATCCAATCTCATACTCTCCTCTGTGGTGTTGCTCTGATGACATATATTTTTTTAAAAACTTGACTGTGATTGGCCATAAAGGTCATCAGTTCGCCGAATCCACCGCTGTTGACTGAGTGTAACCACAGATATAGGGACATTTGGAGAGTTTTAAAGTCGCAAAGATCAGACGATTTATCAGCAGATCGTTTGTATGTCAGCTTATGAACAGACCAGCTGATCTTTGCGGCTTTAAATGCTCCAGTTTCGCTGTATTTGTAGTTAGATTCAGTAAACAGCGAATAGTTCGGTGAACTGATGACCTTCACTGCTAAAAGATGCTCTTCCATATAATGGTAGTAAATAGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35268
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114248 | Essential Splice Site | 567 | 823 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 12 (position 20611417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19393261 |
GRCz11 | 12 | 19515135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTTATGGAAAATATAAATGCTTTGTCTAATGTGTTACATTCTATTTCC[A/T]GCATTAACCAATCAGAGGAATTGTGAAGGTCTGCCTCCTGCCCCCCAAAG
Long Flanking Sequence:
CATCTTTAGAAAAGCATATGAAAAGCATAAAATTTCTCAATTTTTTTTTGTATTTGAATTTAAACTGAAGAATTGAAGCTATACTTTCGGATAGTTAATTAATAATTTAATAATAAAGGCATGGCAAGTTTATTTATATACTGTAGCACATTTTATACACAAAGATAATTCAAAGTGCTTTACAAAAACAAGAATAAAAGAAACAAGTATAAGAAATAAAAACAACAAAATATAAAATGGTTAAAAACCGACTAAAATGTGTTTTAACAGGTTTATTTTTTAACAGTTGATCATTTTAAGGTGACTGGTCACTTAAAAAAAAGTCAAATCAACCAATTACTTTAAAAGCTACAGGCTTGTTCACTTTTTTTCTTTTCAAAAGTCAGCTAATCACTTTCTACAGGTCACTTACAGTTAACTGGTTAAAAGGTTTTAAATGTATATTTGTAAAACTTATGGAAAATATAAATGCTTTGTCTAATGTGTTACATTCTATTTCC[A/T]GCATTAACCAATCAGAGGAATTGTGAAGGTCTGCCTCCTGCCCCCCAAAGCCGGTCTATGGCTGATATAGAAGAACTGGCGTCTAACTATGAGCGGAAACTCATTGAGGTTAGTTCTGGAGATTTCATAGCAAGTAACTCTTGCCCTCACCCGCCATAACCCCACTGTCCTTTAATGTGAAGCAATTAAGGGTGCCTGCCTTTGAGTAGAGATTGAATCAATCTGATTATTCATTGATAGGCTTTTGGTTCAATTAAAGATTTTCTTACAAGTTTGGATTTGATTGAAAACTTTTTTTCATTTATCTGATCCCTGATTCCAGACATTTACATAATGTGTTTTGCTCAGTCTCTTCAAAATTGGTGTGTTCTTGAATAAGCATAATTTTACGTAAATTAAAGCGGAAGTAATTTTTTTAACCTAAAGTATAATTTTTTTACCAAAAAATGAAGGAAAAAGCACTATAAAAAGAAGCTTTACTGGTAAATGTTGAGGTGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9437
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 |
---|---|---|---|---|---|
ENSDART00000114248 | Nonsense | 571 | 823 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 12 (position 20611430)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19393274 |
GRCz11 | 12 | 19515148 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATAAATGCTTTGTCTAATGTGTTAYATTCTATTTCCAGCATTAACCAAT[C/T]ARAGGAATTGTGAAGGTCTGCCTCCTGCCCCCCAAAGCCGGTCTATGGCT
Long Flanking Sequence:
GCATATGAAAAGCATAAAATTTCTCAATTTTTTTTTGTATTTGAATTTAAACTGAAGAATTGAAGCTATACTTTCGGATAGTTAATTAATAATTTAATAATAAAGGCATGGCAAGTTTATTTATATACTGTAGCACATTTTATACACAAAGATAATTCAAAGTGCTTTACAAAAACAAGAATAAAAGAAACAAGTATAAGAAATAAAAACAACAAAATATAAAATGGTTAAAAACCGACTAAAATGTGTTTTAACAGGTTTATTTTTTAACAGTTGATCATTTTAAGGTGACTGGTCACTTAAAAAAAAGTCAAATCAACCAATTACTTTAAAAGCTACAGGCTTGTTCACTTTTTTTCTTTTCAAAAGTCAGCTAATCACTTTCTACAGGTCACTTACAGTTAACTGGTTAAAAGGTTTTAAATGTATATTTGTAAAACTTATGGAAAATATAAATGCTTTGTCTAATGTGTTACATTCTATTTCCAGCATTAACCAAT[C/T]AGAGGAATTGTGAAGGTCTGCCTCCTGCCCCCCAAAGCCGGTCTATGGCTGATATAGAAGAACTGGCGTCTAACTATGAGCGGAAACTCATTGAGGTTAGTTCTGGAGATTTCATAGCAAGTAACTCTTGCCCTCACCCGCCATAACCCCACTGTCCTTTAATGTGAAGCAATTAAGGGTGCCTGCCTTTGAGTAGAGATTGAATCAATCTGATTATTCATTGATAGGCTTTTGGTTCAATTAAAGATTTTCTTACAAGTTTGGATTTGATTGAAAACTTTTTTTCATTTATCTGATCCCTGATTCCAGACATTTACATAATGTGTTTTGCTCAGTCTCTTCAAAATTGGTGTGTTCTTGAATAAGCATAATTTTACGTAAATTAAAGCGGAAGTAATTTTTTTAACCTAAAGTATAATTTTTTTACCAAAAAATGAAGGAAAAAGCACTATAAAAAGAAGCTTTACTGGTAAATGTTGAGGTGTGAACCAACCAACCCA
Associated Phenotype:
Not determined