ZMP
sparc
Ensembl ID:
ZFIN ID:
Description:
SPARC [Source:RefSeq peptide;Acc:NP_001001942]
Human Orthologue:
SPARC
Human Description:
secreted protein, acidic, cysteine-rich (osteonectin) [Source:HGNC Symbol;Acc:11219]
Mouse Orthologue:
Sparc
Mouse Description:
secreted acidic cysteine rich glycoprotein Gene [Source:MGI Symbol;Acc:MGI:98373]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22481 | Essential Splice Site | Available for shipment | Available now |
sa22480 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22481
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 |
---|---|---|---|---|---|
ENSDART00000039660 | Essential Splice Site | None | 291 | 1 | 10 |
ENSDART00000135627 | Essential Splice Site | None | 237 | 1 | 9 |
ENSDART00000141304 | None | None | 157 | None | 7 |
ENSDART00000146022 | Essential Splice Site | None | 109 | 1 | 7 |
The following transcripts of ENSDARG00000019353 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 26966309)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25659511 |
GRCz11 | 14 | 25956756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTTCACCAGCTGACTTCTCCTCTGGCTTCTCTGTAAGACGGACAGAAG[G/A]TAAGAGCTTTCATTTGCCTCACCTTGTCATTCTCCAAAAACTTGACTAAC
Long Flanking Sequence:
TTTTCTGTTGAACACAAAAGAAGGAATATTGAAGAATATTGGGGGGAAAGCAGCTATTGACCTCCACAGTATTCTGGCTTTTTTTTAATACTAACATACATTTGAAAAAAGTCATAAAAAGTAAATAGTGAGGACATTTAGATTTTTGGGTGAGCTATCCCTTTCACTAAAAATCTTCTTTTAAGTGTTTAAAAAAAGAATAAATAAATAAAATAAAAAATAGATATTTGTAGTTTTCTAAAGCTATCAAGCTTAGCACAATAGGATGATGTTAATATTCACATACCTAAATGTTAAAAGTTTGAACTTTTAGAAGTTCGACAAGGTCCACGTGAGTTGGATACACAGAGTTAACTGTGGGACGTCCCAAGTGAAGGGGGTTGAGTGGACCTGCCCACAGCAAATGTCTTCTGTGTGAACTTGTGCTGCTTTCAGAAAGTTCTCTCAGAAAGTTTCACCAGCTGACTTCTCCTCTGGCTTCTCTGTAAGACGGACAGAAG[G/A]TAAGAGCTTTCATTTGCCTCACCTTGTCATTCTCCAAAAACTTGACTAACAAACTAACAAGCGTTGATTTACTAACACTGTTAAAACTATTGTCAAAGCAAACAGTAGCTTCATTTTTGTCCTACATGCTCAAAAGTACAGATACAAAAGAAGTCATTGTCAACGTTTTGTACTTTTTAGGTACTAATATGCACACGTAAGGCACCAAAATCTAGCTTTAGGGTACCAGCTTGAATCCTATTATGATCTTTTGAAAATGTTTGAATTGCTGCAGTTCTGAAAGTGAATTTGCCTCCAAACTATCTCAAAGTTGTAAGCATCATTTTCTCCTGAAAGCACAGATTTTACAGAGAGCACTAAAGTATTTATACAACATCCACACTAAGCAGGTGTCTGTTATTTTGTGTAAACTTTCTGCACTTATTGATCACAAAGTCTTTGTGAATTAAATGTGAACTGGCTTTTTATCAAACTGGCTTCCTTACTGTGCTGTTTACTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22480
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039660 | Essential Splice Site | 58 | 291 | None | 10 |
ENSDART00000135627 | Essential Splice Site | 58 | 237 | None | 9 |
ENSDART00000141304 | Essential Splice Site | 63 | 157 | None | 7 |
ENSDART00000146022 | Essential Splice Site | 70 | 109 | None | 7 |
The following transcripts of ENSDARG00000019353 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 26954415)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 25647617 |
GRCz11 | 14 | 25944862 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTAATAATTCTGACTTCAAGTATGCCATTAAAGAATTTTTTTTTCTGCT[A/T]GACCCCTGCCTAAACCATCACTGCAAGAAGGGCAAAGTGTGTGAGGTAGA
Long Flanking Sequence:
GCAAGGAAATTTTCACAGTATGTCTGATAATATGTGTTCTTCTGGAGAAAATCGTATTTATTTTCTTTCGGCTAGAATAAAAGCGTTTTTTAACTTTTGTAAAAACCAATTTAAGGTCAAAATTATTTGCCCCTTTCAACTTTATTTTTTTTGATAGTCTACAGAACAAACCATCGTTATACAATAACTTGCCCAATTCCCCTAACCTGCCTAGTTAAACTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTACAGAAGTGTCTTGATAAATATCTAGTCAAATATTATTTACTGTCATCATGGCAAAGATAAAATAAATCAGTTATTATAAATGAGTTATTAAAACTAATATGTTAAAAAATGTGTTTAAAAAAATCTCTCTGTTAAACAGAAATTGGGGGGAAAATAAACGGGGGCGGTGGATTAATAATTCATGGGGGGCTAATAATTCTGACTTCAAGTATGCCATTAAAGAATTTTTTTTTCTGCT[A/T]GACCCCTGCCTAAACCATCACTGCAAGAAGGGCAAAGTGTGTGAGGTAGATGACAGCAACCAGCCCATGTGTGTGTGCCAGGACCCTTTGACCTGCCCCGCTCCAATCGGAGACTTCGAGCATGTGCGTGTCTTTTCTCATTCCCTTCATTTCACTTCCGTATGGTGACAGCAATGCCTAGAAGAATACATGCACACAGTTTCAGCAGCTTGATTGAAACGTTGCCTTATGTATTGGGCAAATAACGTCAGAAAACATTAGTATAATACTGTGGGGGAACTCAAACCTGTCAGTCTCCTGACATCCGTGGCATTTCTGGCTGCTCGCATTTACGCTGTTTATTTCACAGGTCTGCGGCACTAACAACAAGACCTACGAGTCCTCCTGCCACTTCTTTGCCACCAAATGCTCTCTGGAGGGCACCAAGAAGGGCCACAAGCTGCACATGGATTACATCGGACCCTGCAAATGTGAGCACATACCTGTGGAAAAAGAAGTGG
Associated Phenotype:
Not determined