ZMP
snx14
Ensembl ID:
ZFIN ID:
Description:
sorting nexin-14 [Source:RefSeq peptide;Acc:NP_001038258]
Human Orthologue:
SNX14
Human Description:
sorting nexin 14 [Source:HGNC Symbol;Acc:14977]
Mouse Orthologue:
Snx14
Mouse Description:
sorting nexin 14 Gene [Source:MGI Symbol;Acc:MGI:2155664]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23619 | Nonsense | Available for shipment | Available now |
sa18413 | Nonsense | Available for shipment | Available now |
sa29287 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa914 | Essential Splice Site | Available for shipment | Available now |
sa16606 | Nonsense | Available for shipment | Available now |
sa23618 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23619
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 |
---|---|---|---|---|---|
ENSDART00000020506 | Nonsense | 27 | 934 | 2 | 29 |
ENSDART00000104725 | Nonsense | 27 | 936 | 2 | 30 |
ENSDART00000141333 | None | None | 179 | None | 6 |
ENSDART00000142361 | Nonsense | 27 | 936 | 2 | 29 |
Genomic Location (Zv9):
Chromosome 20 (position 915323)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 871188 |
GRCz11 | 20 | 892014 |
KASP Assay ID:
2261-3840.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAGGAGGGGTCTGCGCTTCGACATGTTTAAGGATGTTGCTCGTCAATA[T/G]CCGGTCATCTTCTGCATCTTCACGGTTATGATCTCCTCCACCATCATACT
Long Flanking Sequence:
GCTTTCAACCACAACCCAGTACTGGGAAACACCCATTCACACTCAGACACATTCATACACCTGTACTGCATGTGTTTTGACTGTGGAGGCAACCGGAGCACCCGGAGGAAACCCACACCAACACGGGGAGAACATTCAAACTCCACACAGAAACACCAACTGACCTAGCCGAGGCTCAAACCAGCGACCTTCTTGCTGTGAGGCCACAGTGCTAACCACTGAGCCACCATGCAGCCTTGTCTGCTAATATGATTTTCCTATTTAGAATTTGCAAACATTACTTTTCAGAAATTATATTATTACGTAGAAAGTCTGAATGTGCAAATATGAAACCAAGTTTACCCCAGTAATATCATCAGGATTGAAAGAGAGGGTGTGTTCTGTTGACGTCATGGTTGTGTATGCTCTTGTTTAGGAATAATGTCGGACCCTCACTCATTTCTGGGCTGTGTGAGGAGGGGTCTGCGCTTCGACATGTTTAAGGATGTTGCTCGTCAATA[T/G]CCGGTCATCTTCTGCATCTTCACGGTTATGATCTCCTCCACCATCATACTGAACCAGTGAGTGTTCTCTCACACATACACACACAGATAGAGAGAGAGAGAGACACACTTATTCTTTCGGCACGTTTCTGCACATAATAGCGTTAATATCTCATCTCTAATATCTGATTTATTTTCTCTTTGTCATGATGATGGTAAATAATATTAGACTAGATATTCTTCAAGACACTTCTATACAGCTTAAAGTGACATGTAAAGGCTACACTAGGGTAATTAGGGTAAAGTTAGGGTAATTAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGGAGACAATCCAACACTAATATTGCTGAAGGGGCGAATAATATTGAGCTTAAAATGGCTTAAAAACAATTAAAAACTGCATTTATTCTAGCCGAAAATAAAACAAATAAGACTTTCTCCAGAAGAACAAATATTAAAGGAAATACTGTGAACAACTCCTGAATCTGTTCAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18413
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 |
---|---|---|---|---|---|
ENSDART00000020506 | Nonsense | 55 | 934 | 3 | 29 |
ENSDART00000104725 | Nonsense | 55 | 936 | 3 | 30 |
ENSDART00000141333 | None | None | 179 | None | 6 |
ENSDART00000142361 | Nonsense | 55 | 936 | 3 | 29 |
Genomic Location (Zv9):
Chromosome 20 (position 914680)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 870545 |
GRCz11 | 20 | 891371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATATCCTCMCRCTTTCTGCAGGTATCTCCATAKTCTRATGGTTTTYTG[G/A]TCATTTCTGGCTGGAGTGATCACGTTTTACTGCTCCCTCAGCCCAGAATA
Long Flanking Sequence:
TTAATATCTCATCTCTAATATCTGATTTATTTTCTCTTTGTCATGATGATGGTAAATAATATTAGACTAGATATTCTTCAAGACACTTCTATACAGCTTAAAGTGACATGTAAAGGCTACACTAGGGTAATTAGGGTAAAGTTAGGGTAATTAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGGAGACAATCCAACACTAATATTGCTGAAGGGGCGAATAATATTGAGCTTAAAATGGCTTAAAAACAATTAAAAACTGCATTTATTCTAGCCGAAAATAAAACAAATAAGACTTTCTCCAGAAGAACAAATATTAAAGGAAATACTGTGAACAACTCCTGAATCTGTTCAACATCATTAGGGAAATATGGCAATTGTTTCCTGGTGATAGTTTTAAAAAGAAATTAGTGTATATTCACCTGCTTGGATTAATGTATCTTTCTCTTTTTATATCCTCACGCTTTCTGCAGGTATCTCCATATTCTGATGGTTTTCTG[G/A]TCATTTCTGGCTGGAGTGATCACGTTTTACTGCTCCCTCAGCCCAGAATACCTGCTGCCCAATATTCTCATCTCAATAAAGACCAAGAGGAAAGTGAGTATAAAACAAAACAAAAACAAAACAGTCCTGACTTTAAAACCACTGTCGTATCTACTAGAGGAATGTCTATTCAAGAGTACAAATCGAGTAATACTACTACTACTAATAATAATAATAATAAGTGTAATAATAAAAAGAGTAATAATAATTATAATAATAGGTGTAATAATAATAATAAAAAGAGTAATAATAATAATAATAATAATAATAAGTGTAATAATAATAATAATAATAATAATAATAATAATCATAATAAGTGTAGTAATAATAATAATAAGTGTAATAATAATAATAATATTAATAATAATAAGTGTAATAAAAATAATAATAATAATAATAATAAGAGTAATAATAATAATAATAATAATAATAATAATAATAATAAGTGTAATAATAGTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29287
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020506 | Essential Splice Site | 153 | 934 | 6 | 29 |
ENSDART00000104725 | Essential Splice Site | 153 | 936 | 6 | 30 |
ENSDART00000141333 | Essential Splice Site | 34 | 179 | 2 | 6 |
ENSDART00000142361 | Essential Splice Site | 153 | 936 | 6 | 29 |
Genomic Location (Zv9):
Chromosome 20 (position 907978)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 863843 |
GRCz11 | 20 | 884669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGGTGTTGGAGTTAGTCCTAGAGAACTTTGTGTATCCGTGGTACAGG[T/A]ATGGCGGATTTAAAACGTTCACTATTGTTGACTATCAGCTGGAAAAAATC
Long Flanking Sequence:
ATGAGCAATATTACACGAGTAGCAGTGGTGGGAGGCGTACGTTAGTGCCCCAACCAGTGCCGATATACAGCATATCGCACTGCCAAGAGTGTGATATTACGTTTATACAACAGTTTGACGGCATAATTGTGTATATAAAAACAAAATCAAACATGGAGAGTCTCAAAAACCCTTTTGCATGAGGAACTACTTTCTTCCGCGTTGGATTCAAATCATAAGCTGATAGTTAAACCGCTGAGCGTGCATCTTTTACACTTCAGATCTGTAGTGTCTGCTTTCTGCTGGCTGTATGTGGGCGGAGTAATACACAAAGGGTAAAGAGGCTGTACGGGTGCTGATATTACTCACGGCTATCAGCCAATCAGATTCGAGAACCAGACAGAACTGTTGTATAAAAGTATATAAGTGATAGATTCAAATCAAACTAATCAACGCTTTGCTTGACTGATCTTCAGGTGTTGGAGTTAGTCCTAGAGAACTTTGTGTATCCGTGGTACAGG[T/A]ATGGCGGATTTAAAACGTTCACTATTGTTGACTATCAGCTGGAAAAAATCTTGAATGTTCAAATCTTTTCTGATGTTTTTCCGTCAGGGATATTACAGATGACGAGGCGTGTGTGGATGAGCTGAGGCAAACCATCCGCTTCTTTGCTGCAGTCCTGGCTCACCGAGCACAAAGAGTACAAACACACTTCAGTTCTGATACATGCTTCGTAATGCTTCCTGTGGATTTATTATCTGATTACGTTTGCTTGTAGGTGGACGTTCCTTCTGTGGTGATGGACAAGATGATGAAAGCGGCTATGAAGCACATTGAGATCATCGCCAAAGCGCAGCAGAAAGGTGCGTCCTGAAAACGCTGAACACGAGAAGAGCTCATACACAGATTTATTCATAACACTTTACTTAAAGGAGTGTTCATAAGACGGGCATGAATACGGATGAGATTTAATGCATGCTTATAACAACTGCTCAGTTATGACATTTTAAATCAAAGATGACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa914
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 |
---|---|---|---|---|---|
ENSDART00000020506 | Essential Splice Site | 482 | 934 | 16 | 29 |
ENSDART00000104725 | Essential Splice Site | 482 | 936 | 16 | 30 |
ENSDART00000141333 | None | None | 179 | None | 6 |
ENSDART00000142361 | Essential Splice Site | 482 | 936 | 16 | 29 |
Genomic Location (Zv9):
Chromosome 20 (position 898080)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 853945 |
GRCz11 | 20 | 874771 |
KASP Assay ID:
554-0820.1 (used for ordering genotyping assays)
KASP Sequence:
ATCTGCTCTGCGGCGCCGAGTCTCCAGCTAGAAATTCAAAGCTCAACAGG[T/C]GAGCCTCTTCCACWTGTATGTAGAGTCGGGGGGAAAAGCTGCAACACAAC
Long Flanking Sequence:
GTCCTGATCTGAGCGACGACGAGAAGCAGCGTCTGCACGAGGAGGTGAAGAAGATCTACGAGACGTACTGTCTGGAGGAGAGCATCGACAAGATCAGCTTCGACCCCTTCATCATCGAGGAGATCCACAGCAGTGAGTTTGAGCCCTGCAGCAGCAGCTGTTCTCTCTCTCTCTCTGACCTCTGACCTCTGTGTGCTCCTGTCTCCTGCAGTCGCTGAGGGCCCGTACACCGGCGTGGTGAAGCTCCAGACCATGCGCTGCCTGTTCGAGGCCTACGAGCATGTGCTGTGTCTGCTGGAGAAAGTCTTCACCCCCATGTTCTGCCACAGTGATGAGGTGAGATCCTCTGCTGCACTCTAATAAATCATCATGCAGTTATTATTATTTTTTGCTGATATATTGCACATGGCGAATCGTCTCTCTCTCTGTTTCTTCTTCAGTATTTTCGCCATCTGCTCTGCGGCGCCGAGTCTCCAGCTAGAAATTCAAAGCTCAACAGG[T/C]GAGCCTCTTCCACTTGTATGTAGAGTCGGGGGGAAAAGCTGCAACACAACAGCATTACACTCATTATTAGTGTAACAGTCAGGGTAATGGGTGTGGAGCCAATTAAACACAAACATGCAAAACTAATGATTAAAAGTGGCAAAGAATAAAGACATCAAACTACATATATTGAATATTTTGGGGCCAAAGTTGCCATCAAATGATGCAAATATGCCTCAGGAGATTTCTGGCTCCCATTATGAGCCAGATCAGTCTCAATAATAATACATTTGCATTCATAAAATTCACAAATGCAAAGCACAATTCATAAATGCACAACACAATTCATCAATTCAAAAGTAAAATGCCTTAATATTTCCCAATATGCATCTTGCATAAACACATTTAACATGTTTACACAGTCATGTGAAGTTCTTGCATGACTTTCCTCATGCATTTATCAATTTTGTTAGATATGTGGAGTCTTCTGAATTATTGTGCGATATTTTCCAGACCTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16606
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 |
---|---|---|---|---|---|
ENSDART00000020506 | Nonsense | 585 | 934 | 18 | 29 |
ENSDART00000104725 | Nonsense | 585 | 936 | 18 | 30 |
ENSDART00000141333 | None | None | 179 | None | 6 |
ENSDART00000142361 | Nonsense | 585 | 936 | 18 | 29 |
Genomic Location (Zv9):
Chromosome 20 (position 887248)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 843113 |
GRCz11 | 20 | 863939 |
KASP Assay ID:
2261-3837.1 (used for ordering genotyping assays)
KASP Sequence:
ATKATGAGGTTAAGAAAGAGCGTATTCCAGTCTTCTGCATCGACGTGGAG[C/T]GAAACGATAGGAAAAACGGTGAGTTTCTGAAACGTACATYCACTCCAARC
Long Flanking Sequence:
CCAGCCTAAGGCACACCTGTGCAATAATCATGTCTTCTAATCAGCAATGGTCAATGCATTATCTCTGCAAAGAAGCGCTCACTAACCTACATTTAGACAGGTGTGTATCCTCTATTTGAATAAAATATATCCTTGTGTGTACATGTAGATCTACAGATCTAAAAAAGTACAGCTCATGAAAAAGAGGAGCAAAAACAAAAGTGTGTTGTTAATATTTTTGTTGAGTGCAGAAATCTTTGATGCACTCTACAGGTTACATTTTATGTGCACTGGAAGATCTGAAAACACAGAAATGAGGCGTAACATTCATTGTTCTGTCCTCTCAGGTGGAGGAGGCCGTGATGGTGTTTGAGGACGACTCTCCAGGGCCCATGGATGCGGTCGGTACTCCGGGAACTCTGCGCAACCTCTCCGCTTGGACCATCTCTATCCCGTATGTGGACTTTTATGATGATGAGGTTAAGAAAGAGCGTATTCCAGTCTTCTGCATCGACGTGGAG[C/T]GAAACGATAGGAAAAACGGTGAGTTTCTGAAACGTACATTCACTCCAAACTCTATTTGATTATTAAGGTCCTGTGAGATCTTTGTGAACGTGTTCATTGCTTCACAGTGGGACACGAGACTGAGAGCTGGTCTGTGTACAGAAAATATGTGGAGTTTTATGTGCTGGAATCTAAACTCACCGAGTTTCACGGTAAAGTTGATTATCGTCTCTCTTGTTTGGACAGAGCCTTCATGTGTTTGGGTCTATTGATCTCTCTGGTTTGATTTTGTATTACAGGCCCATTCCAGGACGCTCAGCTCCCCTCCAAAAGAATCATTGGACCAAAGAATTATGAGTTCCTGTCCTCTAAACGAGGAGAATTTGAGGAATATTTACAGGTAATTAATCTGACCCTGTACAAATCATAATAAAAGTGCTGTATTGACTCTTCTGAAGCATAAACACACCACAGTATGTGTGCAGATAGTTCATACACATGCTAAGTGACCATTCTTCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23618
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 |
---|---|---|---|---|---|
ENSDART00000020506 | Essential Splice Site | 703 | 934 | 22 | 29 |
ENSDART00000104725 | Essential Splice Site | 703 | 936 | 22 | 30 |
ENSDART00000141333 | None | None | 179 | None | 6 |
ENSDART00000142361 | Essential Splice Site | 703 | 936 | 22 | 29 |
Genomic Location (Zv9):
Chromosome 20 (position 881444)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 837309 |
GRCz11 | 20 | 858135 |
KASP Assay ID:
2261-3836.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGCTACAGGAAAAATATTCAAGTCAGTGCCAGGAAAACTAATCAAAGAG[G/A]TAAGAGTTAGAATTGCATTGTTCGTGTGTATTTCACCTCTGTGCTCTTTG
Long Flanking Sequence:
AGCTCTAAAATAATAACACATGTTAACCCCAAAATCTAAAGTTCAGAGCAAACCAAGAATTCCACATACCAGACCTACCTCAAAACTAGTGCTTGAAACAGCCTTCATGCTGCAGTGGGTGTAGGGAGGATGGAGAAACATGCTGTTCGAGAGGAGTTTCTGCCGTGCTCGACACAAAACACACAGATGGCCAGGCTAGTTTTTCTGGTGTCCGTGAGAAACCCTGTTACACAACCTTAATGACAATCGCACGTGTTTTCCCTATCCAGAACATTTGCTAGCATTGAAGAAAATCCCAAATACGTAACACTTTAAAGACTTTATTTATTTATTTATTTAAAAAAAAGAGAGAAGCTAAAAAATCTCTTCAGTCCATTTTGAAGTGTGTAACACAGCCAAACAAAAATGCGTGCTCTGATTACGTTGATGACTGGTTTTATTTGTTGTTTTTCGCTACAGGAAAAATATTCAAGTCAGTGCCAGGAAAACTAATCAAAGAG[G/A]TAAGAGTTAGAATTGCATTGTTCGTGTGTATTTCACCTCTGTGCTCTTTGAAATCAGAGTTATTTTGAAGAAGTCTTGATTTGGTTTTTAAGACTTTTTAATGGTGCCATGAAAATCTGCCATAGGCCATTTTGAGGGATGTAAACAACAACAACGGCCCCAGCGTATTTCCTGTTTTACATTTATAATGTCTAAAGCTTTAGAGTATCCAAAAAGAGCCACATATTGATAAATGTTATGATAGCTGTTTTAACATTAAGGTATGATTAAATTGCATCTTATTACAGTTATGAAATACAGTAGTTTGATAACAATGAAATGTCCAGGGGCCAGTGACATGAACACATTGAAATGGTCTACATCTAGGCAGAGCTGAAAAGTAAGACTGGGAATTACACACCGTGGCTCAAACACCATTGCTGCCACATTTTTATGTAAATCCTGTTAAAGATTCTGGTAAAAAAAAACAGGCCAATCAGAACAGAACACCACCACATTAA
Associated Phenotype:
Not determined