ZMP
LOC100331540
Ensembl ID:
Human Orthologue:
SPOCK1
Human Description:
sparc/osteonectin, cwcv and kazal-like domains proteoglycan (testican) 1 [Source:HGNC Symbol;Acc:112
Mouse Orthologue:
Spock1
Mouse Description:
sparc/osteonectin, cwcv and kazal-like domains proteoglycan 1 Gene [Source:MGI Symbol;Acc:MGI:105371
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa28231 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19073 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa9838 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa28231
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109378 | Essential Splice Site | 151 | 355 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 14 (position 2051995)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 1767076 |
| GRCz11 | 14 | 2666766 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACGCAAACCGAGACCTGAAGACCAGCACCAGTGAAGCTGCACAAGGAC[G/T]TGAGTGTGTGTTTATTAATCACACAAATGAGTTCACAGCCAATGCTTGTC
Long Flanking Sequence:
AACAGCTTTATAGTTCAAGGAAACGTTCACCGCTATGAACTCTATTAAATCTCCTGAGCCGTGAAAGACAATCTGTATGTTCTTCGTCTGATCTCTGACCTCTTTAAACTCGCTTTAGTCTCTAATATGCTTTTTTGTAGATGCATTTATAAATGAGGATAAAGGCTGTTGTTTGAAGAGCTGAGTTTAATCAGTTTCTCCAGCACTATTGTGGTAATGTTTAAAGGGATACAGCTATGGAGTCCCCATCAATATAGCTGTATCACTTTTAGCAACAAACCACTATTGTGAAGACAGAAGGATATGTTTCATCAGGACACACATACACACACACACACACACACACACATGCTTATTAAATCTGTGTTTGTGTGTTGGTTTAGGGTGCACTGATGCTGATCTGAGAAGTTTAGCCTCCAGACTCAAAGACTGGTTTGGGGTGTTACACACAGACGCAAACCGAGACCTGAAGACCAGCACCAGTGAAGCTGCACAAGGAC[G/T]TGAGTGTGTGTTTATTAATCACACAAATGAGTTCACAGCCAATGCTTGTCTTTTCAATACAATTTATTAATATTGCTGCTGTATTATTTATTTGACCTATTAAAATAAGTTTATATGACACTCATTTTATTAGGATTTATTTTATTTTTATATATATTTATTTATTTTGCCTATCAAAACACAAAAAAATATAGCACAATGACAAAATAACACTCAGTTATACTGTCAGTTCTGTGTAAATCAGAAAAAAACATATTTTACATATTTTACAACAGAATATGTCCAGTATTATGTACAATTAAACACTCATTTAATAATTTTTATTATTATTTTTATTATTATTGTTGAATTTTTCTTCTTTTTGTTCTTTTTCTATGATTTACATGAGCTCCTAAGTCAGCATTTCTTTTATTATTCGTTTATTTTCTTTAACAAAATTATTTCACCTAGCAAAACCCAATAAATATAGCACAATTATTATTATTTTTATTATTTTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19073
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109378 | Essential Splice Site | 226 | 355 | 5 | 9 |
| ENSDART00000109378 | Essential Splice Site | 226 | 355 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 14 (position 2053509)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 1765562 |
| GRCz11 | 14 | 2665252 |
KASP Assay ID:
2260-7135.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAACTGTCCAACAACGAGTGGTGCTACTGCTTCCAGAAACCCGATGG[T/C]GAGTTTGCAAAAAAGAGGTATAATAAATCACATAAGCTTATTGGGATGAT
Long Flanking Sequence:
AAATTAAAAATAATCACTATTATTATTGTTTTTATTAGTAGTAGCAGTAGTCATAGTAGTAGTAGTAGTAGTAGTGAATAAGTTTACAAATAATAATATAAATTATAATTTGACTTAATTGGAATTAATAATATATTATACATTAAGAATTTTAAATAATTATTTTATTACATCATTATAATTAGGATAAATTATGTAATTATTTGTTATTTGTAATTGCATTGTTTTAAACTAATGTTAAAATGAAAGTGCTTTTAAATCTCTTTCTCTCCTTTAGGTTTCGACACAAGCATTTTACCCATCTGTAAAGATTCTCTCGGCTGGATGTTCAACAAGCTGGACATGAACTATGACCTCCTCCTCGACCAATCAGAGCTCAGTGCTATTTACCTGGACAAATACGAGCTGTGCATGAGGCCGCTGTTCAACTCCTGCGACTCCTTTAAAGATGGAAAACTGTCCAACAACGAGTGGTGCTACTGCTTCCAGAAACCCGATGG[T/C]GAGTTTGCAAAAAAGAGGTATAATAAATCACATAAGCTTATTGGGATGATCTTGTTTATCTCTGCTGTTAAATTAAATGAAACTGTATGTTTCTTCAGGCATGCCATGTCAGAACGAGATGAACAAGATTCACTCTCAGAGCCGAAGGAAGACTCTGTTAGGTAGGTGGATTTGATGGACAGGTGTTAACCCCGCTCCTGAGACCCTGTATACAGTTGAAGTCAGAACTATTAGCCCTCCTGTTCACTTTGAATTCTTTTATATTTATTTCCAAGAAGATTTCTGAACATCATAGTTTTACTAACTCATTTCTAATAACTGGTTTCTTTTATCTTTGCCATGATGACAGTACAGAATATTTGACTAGATTTTTTTTTGGGGTGCTTTCACACCTGTGAATCGATTCAGTTGTTCTGAAACAGAGATTACAATTGTTAAATTGTTGCTGTTTGCTCTTGGAGCGGTTCGCTTTACCAATCCAAAGTTTCTAATCGGACTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9838
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 |
|---|---|---|---|---|---|
| ENSDART00000109378 | Essential Splice Site | 226 | 355 | 5 | 9 |
| ENSDART00000109378 | Essential Splice Site | 226 | 355 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 14 (position 2053509)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 1765562 |
| GRCz11 | 14 | 2665252 |
KASP Assay ID:
2260-7135.1 (used for ordering genotyping assays)
KASP Sequence:
GGAAAACTGTCCAACAACGAGTGGTGCTACTGCTTCCAGAAACCCGATGG[T/C]GAGTTTGCAAAAMAGAGRTATAATAAATCACATAAGCTTATTGGGRTGAT
Long Flanking Sequence:
AAATTAAAAATAATCACTATTATTATTGTTTTTATTAGTAGTAGCAGTAGTCATAGTAGTAGTAGTAGTAGTAGTGAATAAGTTTACAAATAATAATATAAATTATAATTTGACTTAATTGGAATTAATAATATATTATACATTAAGAATTTTAAATAATTATTTTATTACATCATTATAATTAGGATAAATTATGTAATTATTTGTTATTTGTAATTGCATTGTTTTAAACTAATGTTAAAATGAAAGTGCTTTTAAATCTCTTTCTCTCCTTTAGGTTTCGACACAAGCATTTTACCCATCTGTAAAGATTCTCTCGGCTGGATGTTCAACAAGCTGGACATGAACTATGACCTCCTCCTCGACCAATCAGAGCTCAGTGCTATTTACCTGGACAAATACGAGCTGTGCATGAGGCCGCTGTTCAACTCCTGCGACTCCTTTAAAGATGGAAAACTGTCCAACAACGAGTGGTGCTACTGCTTCCAGAAACCCGATGG[T/C]GAGTTTGCAAAAAAGAGGTATAATAAATCACATAAGCTTATTGGGATGATCTTGTTTATCTCTGCTGTTAAATTAAATGAAACTGTATGTTTCTTCAGGCATGCCATGTCAGAACGAGATGAACAAGATTCACTCTCAGAGCCGAAGGAAGACTCTGTTAGGTAGGTGGATTTGATGGACAGGTGTTAACCCCGCTCCTGAGACCCTGTATACAGTTGAAGTCAGAACTATTAGCCCTCCTGTTCACTTTGAATTCTTTTATATTTATTTCCAAGAAGATTTCTGAACATCATAGTTTTACTAACTCATTTCTAATAACTGGTTTCTTTTATCTTTGCCATGATGACAGTACAGAATATTTGACTAGATTTTTTTTTGGGGTGCTTTCACACCTGTGAATCGATTCAGTTGTTCTGAAACAGAGATTACAATTGTTAAATTGTTGCTGTTTGCTCTTGGAGCGGTTCGCTTTACCAATCCAAAGTTTCTAATCGGACTAA
Associated Phenotype:
Not determined