ZMP
spock3
Ensembl ID:
ZFIN ID:
Description:
Im:7139568 protein [Source:UniProtKB/TrEMBL;Acc:A8KB02]
Human Orthologue:
SPOCK3
Human Description:
sparc/osteonectin, cwcv and kazal-like domains proteoglycan (testican) 3 [Source:HGNC Symbol;Acc:135
Mouse Orthologue:
Spock3
Mouse Description:
sparc/osteonectin, cwcv and kazal-like domains proteoglycan 3 Gene [Source:MGI Symbol;Acc:MGI:192015
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39600 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11967 | Essential Splice Site | Available for shipment | Available now |
sa17392 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39600
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078295 | Nonsense | 86 | 393 | 6 | 13 |
ENSDART00000102969 | Nonsense | 105 | 412 | 4 | 11 |
ENSDART00000139461 | Nonsense | 82 | 308 | 4 | 10 |
ENSDART00000145418 | Nonsense | 95 | 253 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 19455136)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 19980895 |
GRCz11 | 1 | 20673832 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTGAAGATAAAATGTGGCCGTCATAAAGTGTGTGTAGCTGAAGATTA[C/A]CAAACACCCACCTGTGTCAGTCAGCGCAGGATGAGGTAAGCTGACTCACA
Long Flanking Sequence:
ATGCATTATTAACAAAGTCAAAATTTAGATGTAATATGAATTACAGTAAAGGGGCAGATATCTCTCTGTTGAATTATATAAAGTTTCAATTTTAAGCGGCAGAAAATACTGTGGGTTTGGATCCACACTAGCATAAATAACTGATGAAATTTTTACTTTTTTTTTTTTTTAGTTAATTAACCTTTCAAATCTGGGCTTTTTTGTGCAAACACACCACGCTTATATGCAGATTAGGCTTATTAAAGATTTACTTTATTCAAAAAACACCATTTTAATTGCATCTTGTGCAAATGAGCACTATCACAACTGTCATATTATCAGCATTCCACCATGTGAGCTGAATATGAGGGTACTGACATATTCAATATTTGCTTTTCATATGTTTTCAATGTTTATGTTTATACATGTTTATTTTTGCGTGTTTCAGCTCTGGACCCTGCCAAAGATCCATGTCTGAAGATAAAATGTGGCCGTCATAAAGTGTGTGTAGCTGAAGATTA[C/A]CAAACACCCACCTGTGTCAGTCAGCGCAGGATGAGGTAAGCTGACTCACAGTACCTGCTTATTAATGAAATTATAGTAAAAACAATGTACAAGAGAATGGCACATTTGGCACCTTATATCTGTGTAATGAATATATCATGTATTTCAGCTCTGTCAAACATCAAACACTTTACAAAATAGCCCAAAAACCTATAGAGTCCAGAACTTGCTTCTACTGAATATCATTAAATAAGTCTATTAAATATAGAAACTTGTTCTTGTCACGGAATAGAAGAATGTTATTGTAAAAATAAATTATGATGATCTTTCTTGAATGAACTTTCTTTTTAACTCCCAATCTTGAGTATCTCACAAGTCACAATACAATCTTTTCTTTTTGCAATGACAGTTTGTTTTCTCAAAATTTTGACTGCATTTTTTAGATTTGATTTGCAGTTGTGAGTTTATTGTTGTGTATAAAAAAAGCCAGAAATTACGAGAAAATAAAGTCAGAAGCGCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11967
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 |
---|---|---|---|---|---|
ENSDART00000078295 | Essential Splice Site | 98 | 393 | 6 | 13 |
ENSDART00000102969 | Essential Splice Site | 117 | 412 | 4 | 11 |
ENSDART00000139461 | Essential Splice Site | 94 | 308 | 4 | 10 |
ENSDART00000145418 | Essential Splice Site | 107 | 253 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 19455172)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 19980931 |
GRCz11 | 1 | 20673868 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTRGCTGAAGATTACCAAACACCCACCTGTGTCAGTCAGCGCAGGATGAG[G/A]TAAGCTGACTCACAGTACCTGNNTATTAMTGAAWTTATAGTAAAAACAAT
Long Flanking Sequence:
TGAATTACAGTAAAGGGGCAGATATCTCTCTGTTGAATTATATAAAGTTTCAATTTTAAGCGGCAGAAAATACTGTGGGTTTGGATCCACACTAGCATAAATAACTGATGAAATTTTTACTTTTTTTTTTTTTTAGTTAATTAACCTTTCAAATCTGGGCTTTTTTGTGCAAACACACCACGCTTATATGCAGATTAGGCTTATTAAAGATTTACTTTATTCAAAAAACACCATTTTAATTGCATCTTGTGCAAATGAGCACTATCACAACTGTCATATTATCAGCATTCCACCATGTGAGCTGAATATGAGGGTACTGACATATTCAATATTTGCTTTTCATATGTTTTCAATGTTTATGTTTATACATGTTTATTTTTGCGTGTTTCAGCTCTGGACCCTGCCAAAGATCCATGTCTGAAGATAAAATGTGGCCGTCATAAAGTGTGTGTAGCTGAAGATTACCAAACACCCACCTGTGTCAGTCAGCGCAGGATGAG[G/A]TAAGCTGACTCACAGTACCTGCTTATTAATGAAATTATAGTAAAAACAATGTACAAGAGAATGGCACATTTGGCACCTTATATCTGTGTAATGAATATATCATGTATTTCAGCTCTGTCAAACATCAAACACTTTACAAAATAGCCCAAAAACCTATAGAGTCCAGAACTTGCTTCTACTGAATATCATTAAATAAGTCTATTAAATATAGAAACTTGTTCTTGTCACGGAATAGAAGAATGTTATTGTAAAAATAAATTATGATGATCTTTCTTGAATGAACTTTCTTTTTAACTCCCAATCTTGAGTATCTCACAAGTCACAATACAATCTTTTCTTTTTGCAATGACAGTTTGTTTTCTCAAAATTTTGACTGCATTTTTTAGATTTGATTTGCAGTTGTGAGTTTATTGTTGTGTATAAAAAAAGCCAGAAATTACGAGAAAATAAAGTCAGAAGCGCGGTAAAGCTTATCAGCTTGCAATTGCAATATATGACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17392
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 |
---|---|---|---|---|---|
ENSDART00000078295 | Essential Splice Site | 300 | 393 | 11 | 13 |
ENSDART00000102969 | Essential Splice Site | 319 | 412 | 9 | 11 |
ENSDART00000139461 | Essential Splice Site | 296 | 308 | 9 | 10 |
ENSDART00000145418 | None | None | 253 | None | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 19479349)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 20005108 |
GRCz11 | 1 | 20698045 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGAGATCACCATYATCCACAAACAGCAGGCTGGCAAGAAGCTACTGGG[T/C]GAGTCTAGTGTCTTGTGTATTTACAWATGGACTTTTCTGGTACATGTTTG
Long Flanking Sequence:
ATTGTTTGGGTTTTTACCAAAATCCAGTTCAATTCCATGTCAGCAGCACCTTTTGAAATATTATTCCCAGTAAAAACATGATGTTAAAGTGTATACTCAATACTTCTTTTCCCTCCTGTACATTGATTTATAATTACATTACATATATTTACAGTATCCATGTACTACATGACATTTTTAGATAAAAAAATGTTAGTATTTGCAAATGCAATTTTATTTTATGGAGGAAGTTCAACCAGTGTAGGTTTTGATGCTCATTAGGCCATAAACACAAAATCATCTTAGCGCTTATTCTCCTCTTTGCATTGTGGGATAATGCAGTTCTGTGTTTTTTTATATACTAAACAACATAATGCCTGCAGTTCAAATCTCTCTCACAGAGAAGTAATGGCGATGGTTTCTTTCTCACTGCTGATCTGAAATCAATGTGTTTCAGAGGCTCCCTGTCAATCAGAGATCACCATCATCCACAAACAGCAGGCTGGCAAGAAGCTACTGGG[T/C]GAGTCTAGTGTCTTGTGTATTTACAAATGGACTTTTCTGGTACATGTTTGTAATACAAGATCATGTTTAGTGACAAATTGGTACGTATATACTGGTATACAGGCTTTATGCATGTGGCCATTTTGAGATATTCAGAATTGGTGTATGATAAAACACCAATTTGTTTTTACAATTTATTTTACAATTTCAGGTGAAATTCCAAATTAGTAGAAACAAAAATGCCAGAATTTATAAACAGTATGTATAAATATAAGCAGGTGAAGGCAAAATGATTAGCCCTTTCATGTAATTAAAAATCTTATACATATTTATATATTTTACAAGTAATGTTTAACAGAGCAAGGATATTCTTCTCAGAATTTTCTATTATATATATATTTTTTTTAATAAATTCATTTTTTTGTTGTTGAAATAAACACATTTTTACATGTAAAAATGTTTTAAACATATTTTAGCCACCTTAAGAAATGTATTTCTTATATTTCTTATAATATTTTTAT
Associated Phenotype:
Not determined