ZMP
zgc:92458
Ensembl ID:
ZFIN ID:
Description:
sorting nexin-7 [Source:RefSeq peptide;Acc:NP_001002229]
Human Orthologue:
SNX7
Human Description:
sorting nexin 7 [Source:HGNC Symbol;Acc:14971]
Mouse Orthologue:
Snx7
Mouse Description:
sorting nexin 7 Gene [Source:MGI Symbol;Acc:MGI:1923811]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16486 | Nonsense | Available for shipment | Available now |
| sa37919 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16486
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 |
|---|---|---|---|---|---|
| ENSDART00000045724 | Nonsense | 153 | 413 | 4 | 9 |
| ENSDART00000123598 | Nonsense | 175 | 469 | 4 | 10 |
| ENSDART00000132597 | None | None | 257 | None | 6 |
| ENSDART00000145658 | Nonsense | 248 | 508 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 32599421)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 30261144 |
| GRCz11 | 24 | 30267408 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGAAGATTTCATAGARACCAGAAGAARGGCTCTGCACAGGTTTCTTAAC[A/T]GAATAGCAGAACATCCCATTTTCTCCAGCACTGAAGACTTTAAGATCTTT
Long Flanking Sequence:
TGACCAGGTTAAATTTAGGAATAGGACGATAACTGGTTTCAAGTTTTACCACGGTTTGGAAAAGTCATGGTCTTAAAACCACAAAAATTTAGTTATCCCGTTCTGTGTTATATTTAAGGTTTTTTCCTCATGTTGTGTAGATTATCTTTATCAGACCCTTTGATATTTACTTAACACTTAGTGAACTGTTTATTAGTAATAAATCAAAAATTTTGATTTCTGTCATGTGTACAATTTAGTGTTGTCAAAAGTATCAGGTTCAGTACAAATCGGTACTGATATTTTAAAAACGTCCATTTTCTGCTTACATTAGAGCAGTGGTTGTCAACCATGTTCCTGGAGGATGATGAGTAGTGCTTTTACTTGCGCATTTAAAACCCTAACGTGTGATTGTGTCCCATCAGCCTCTGCCAGAGAAGTTTGTGATGAAGGGAATGGTGGAGAGGTTTAATGAAGATTTCATAGAGACCAGAAGAAGGGCTCTGCACAGGTTTCTTAAC[A/T]GAATAGCAGAACATCCCATTTTCTCCAGCACTGAAGACTTTAAGATCTTTCTCACAGCTGCATCTGAGGTAAGGCTTTTGTTTTTTCTTTTTATCCATTCATCTCTCCCTCCGTCCATCCGCCCACCCGTCTGTCTATCTGTCTATCTATCAGTCTATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCTATCTATCTATCTATCCGTGTCTCCGTCCATCCATCCATCTGTCTGTCTGTCTTTGTCTGGCTATTCGTCTATCCGTCTCTCCGTCTATCCATCCGTCTCTGTCTATTTGTCTATCTATAACTATTCATCTATCCATCTCTCCATCCATCCATCCATCCATCCGTCTGTCTGTCCCTCTATCTGTCTGTCCGTCTATCTGTCCGTCTATCCATCTTTCTATATCTATCCGTCTCTCCGTCCATCTATCTATCTATCTATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37919
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 |
|---|---|---|---|---|---|
| ENSDART00000045724 | Nonsense | 288 | 413 | 6 | 9 |
| ENSDART00000123598 | Nonsense | 310 | 469 | 6 | 10 |
| ENSDART00000132597 | Nonsense | 98 | 257 | 2 | 6 |
| ENSDART00000145658 | Nonsense | 383 | 508 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 24 (position 32605778)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 30254787 |
| GRCz11 | 24 | 30261051 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCCGACTGTCTGGACAGATGCTATAAGGAGACAGACGAGCAGGTCAAA[C/T]AGCTGAACGATCAGCTCAGTCCAGCTCTTCATGAGTACGTGCTCTGCACA
Long Flanking Sequence:
GGTTTTGTTTTGCACGCTGCTTATGCGTGCTGCATGCCTCACGTTTTAATTTGTACATTTTATTAATTTATTTACATATTTTTAATTTAGTAGACTTGTTTTTATATTTTTGTTTTTTGTGCACTTATTTTATTTATAAGTTCTGTAATTAATTCACATTTTACTTTTATGCATTTTATTTATCTACACATTGTTTTTTTTCATAATTTTTATGCATTTCTTATTACCATTGATTTTTTTTATGCAAAAATACATTTGCTCCTTTAATTGACTGACACTTTAAGATAGAAGTATTTGTACATAGCTCTGCAGCTTTTATAACAGTAGTTTCACTGAATTGTTGTTGTTGTATTGTGATGTCAGAGTACCTGGAGGAGCTGAAGGAGTGCGGGCCGACGTACACACTGTGGTCAAACTCCGAGCAGGAACTGGCTGAACCCCTGAAGAACATGGCCGACTGTCTGGACAGATGCTATAAGGAGACAGACGAGCAGGTCAAA[C/T]AGCTGAACGATCAGCTCAGTCCAGCTCTTCATGAGTACGTGCTCTGCACAGAGACGCTCAAGGTAAACCAGCTCAAAACACACTCCTGCATTCTCTCTCAAACTCAACATTCAGCCTAAAAATAAATGGTTATTTTAAATTGGCAGTAAAGTGGCAACAATGGTGGCATTAAAGACAATTGGTAATGTTACAAAATGTTTTTATCATCTATTTTTTTTTACTTTTTTTGTTTTTTACCAGAGGGCATTTTGAATCTAAGTGAGAAAGTTCTTTAGGTTTAAACACCCACAGTTCCACAACAATATTAAGCAGTGCTGTTTAACATTTGTAATAAATATCAAATATTAATTTGAGCTCCAGTTTAACACATTTTAATAATTTCTAAAGGATCGTGTGACAATGAAAATTGGAATGACACAAAGTTCAGAATCGCAGGCATACACATAATAATACTTATAATAATAGTATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined