ZMP
thbs3b
Ensembl ID:
ZFIN ID:
Description:
Thrombospondin-3b [Source:UniProtKB/Swiss-Prot;Acc:Q1L8P7]
Human Orthologue:
THBS3
Human Description:
thrombospondin 3 [Source:HGNC Symbol;Acc:11787]
Mouse Orthologue:
Thbs3
Mouse Description:
thrombospondin 3 Gene [Source:MGI Symbol;Acc:MGI:98739]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43283 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17980 | Nonsense | Available for shipment | Available now |
sa13482 | Nonsense | Available for shipment | Available now |
sa23526 | Nonsense | Available for shipment | Available now |
sa29208 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43283
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043133 | Nonsense | 434 | 906 | 12 | 22 |
ENSDART00000090825 | Nonsense | 457 | 929 | 13 | 23 |
Genomic Location (Zv9):
Chromosome 19 (position 24915467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 24845579 |
GRCz11 | 19 | 24429802 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTTAATATCTGTTGTTAATTCTAACTCTTCCATGTGCAGGATAATTG[T/A]GCAAACACTCCAAACTCTGGGCAGGAGGATACAGATGGAGATGGCATTGG
Long Flanking Sequence:
CGGTACATTACATTACATCCTCTTGACTTCAAGCATGGAATTTACAAAGAATGCGTGGTCAATTTATCTGCACAAAAATTGCCTAATGTATCCTCCATTCCACTGTCTGCTTCAGTATTATTCAATCAAAAATGTACTGGTTATAATATTCCTTTATCATCTGATGAAATAATGAAATCTTAATTGATACAATATGTGCAAATGTTTTCTTTAATTGTGCATTTGCTTAAGTGTGCATTTGCTTAATTTAATCTGCATGTAACAGCACTGCACCAGACCAAACAACATTTTGTTTGAGTTGGACTGCAAGTAGTTAGAAAATAGGACACAGAATTTGACTCTAAAAAGTGAAACAGTTGATTATTTGATTTTTCTAATTTGATTGTATTCAATATATACAAACCTTTCAGCTTAGCTGATGACAGCATGGTGTTTCTTTATAAAAACATGTATTTTAATATCTGTTGTTAATTCTAACTCTTCCATGTGCAGGATAATTG[T/A]GCAAACACTCCAAACTCTGGGCAGGAGGATACAGATGGAGATGGCATTGGTGATCAGTGTGACGAGGATGCAGATGGAGATGGAATTAAAAACGTTGAGGTATCTGATCAAGTAGCAATGATTTGTTAAATGATTTGAAAAATTATAAGATATACCAGTATTTTCAAATCGGCTGATGTATTTGAAAAATTAGTTTTCAGTATTTTCCTATGCAGAAAAATATGAACATAAAGTTAACAATTAAAAACATATGTACAATATTCTAATTCTAACAGCTGAAAAGTACTTATAAATGTAAAAGATATGTAAATGGCTATTTTTACAATATTTTGAAATTTATGTTGCAAATATGCACATATACAGTATATGACATCTTTACACACTACCTGACAAAGTCTTGTCGTCAATTACAGTTGTAAGAGCAACAATTAATAACTTGATTTCTAGTAGATCATTTGGAAAAGTGGCAGATGGTAGATTTTTGATGAATCATCTGTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17980
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 |
---|---|---|---|---|---|
ENSDART00000043133 | Nonsense | 501 | 906 | 13 | 22 |
ENSDART00000090825 | Nonsense | 524 | 929 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 19 (position 24913924)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 24844036 |
GRCz11 | 19 | 24428259 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCCTATGGTGATGCTTGCGACAACTGCCCCAACGTACCCAACGGCGAT[C/T]AGCTTGATACTGATGGCAATGGCAAGGGAGACATCTGTGACACTGATATT
Long Flanking Sequence:
TGAACCATGACTTTATATTCTATACTGTACGTTATTTCTGTTAAGTGACAAGACTTTTTTCTAAGCAAAGTCAGACCTTACTTAATGCCTAAATAAATAATTAAAAATCAAGGCATAATCATATTTTATTTTGGTAAAATAAGCTTAAGCTTGCCTTTCATATAAGCCACTTCTGATCAACTAGAAGTAAAGTTATCATTTAATGTTCCTAAAACTTGGATAGGTGACAAGACTTTTGTCAGGTAGTGTATATGTGAAATCTATACATTAACTTGTATGTGAGATGAGATGTGAGACTTGTATGTGAGATTAATATGTGATATGATTTTCACCTATTGTCATAAATCAGACTTTTATATTGGTTTAAATGAATTGCCCTTAGCTTATATATCATTTTCCAGGACAACTGTCGTCTGGTGCCCAACAAGGACCAGCAGAACTCTGACACAGACTCCTATGGTGATGCTTGCGACAACTGCCCCAACGTACCCAACGGCGAT[C/T]AGCTTGATACTGATGGCAATGGCAAGGGAGACATCTGTGACACTGATATTGATGGAGATGGTACAGTCCCATTTAACTGTTCTGTGGTTTTACAGCATTGTTCTGCTGCATCATCTGTCTTTACCACTGATTTTCTTTACAGGGATCCCTAACGTTTTGGATAACTGTCCTAAAATACCCAACCCCATGCAGACAGACCGAGATGGAGATGGTGTGGGGGATGCATGTGACAGCTGTCCTGAGGTCAACGACCCACTGCAGGTTAGACAAAGATAACAAGTTAAAACTATAGGGAAGAGAAGAACGGGGACTATCTAGTGATACAACCAAAGCTCCATCATCAAGATTTAGATTTCTAAAAAGGCAAGCTGAGATAGTGGGGTCATCCAAAACAATAAAACTGCTGCCATCTGTGTAGAAGCTACAGGAGAAGTGTGTTTTTATGATTCACTAATATAGAAAAGAGAAGAGGTCTAAGCACCAAACCTTGATGCACCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13482
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043133 | Nonsense | 526 | 906 | 14 | 22 |
ENSDART00000090825 | Nonsense | 549 | 929 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 19 (position 24913766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 24843878 |
GRCz11 | 19 | 24428101 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATCATCTGTCTTTACCACTGATTTTCTTTACAGGGATCCCTAACGTTT[T/A]RGATAACTGTCCTAAAATACCCAACCCCATGCAGACAGACCGAGATGGAG
Long Flanking Sequence:
CATATAAGCCACTTCTGATCAACTAGAAGTAAAGTTATCATTTAATGTTCCTAAAACTTGGATAGGTGACAAGACTTTTGTCAGGTAGTGTATATGTGAAATCTATACATTAACTTGTATGTGAGATGAGATGTGAGACTTGTATGTGAGATTAATATGTGATATGATTTTCACCTATTGTCATAAATCAGACTTTTATATTGGTTTAAATGAATTGCCCTTAGCTTATATATCATTTTCCAGGACAACTGTCGTCTGGTGCCCAACAAGGACCAGCAGAACTCTGACACAGACTCCTATGGTGATGCTTGCGACAACTGCCCCAACGTACCCAACGGCGATCAGCTTGATACTGATGGCAATGGCAAGGGAGACATCTGTGACACTGATATTGATGGAGATGGTACAGTCCCATTTAACTGTTCTGTGGTTTTACAGCATTGTTCTGCTGCATCATCTGTCTTTACCACTGATTTTCTTTACAGGGATCCCTAACGTTT[T/A]GGATAACTGTCCTAAAATACCCAACCCCATGCAGACAGACCGAGATGGAGATGGTGTGGGGGATGCATGTGACAGCTGTCCTGAGGTCAACGACCCACTGCAGGTTAGACAAAGATAACAAGTTAAAACTATAGGGAAGAGAAGAACGGGGACTATCTAGTGATACAACCAAAGCTCCATCATCAAGATTTAGATTTCTAAAAAGGCAAGCTGAGATAGTGGGGTCATCCAAAACAATAAAACTGCTGCCATCTGTGTAGAAGCTACAGGAGAAGTGTGTTTTTATGATTCACTAATATAGAAAAGAGAAGAGGTCTAAGCACCAAACCTTGATGCACCCAATAATCGATTTTACATCACACACTTATTTTTCAGATTACCTTACAAAATATGTTGTGTGTGTACATTTATACAAAATAGTGATAGGAAGATAATATAGCTAGCTTCTTTGAAACGGTAGAAAATCTTGGTTAATTTCCTTTAGTTTAGCCAAGTTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23526
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043133 | Nonsense | 583 | 906 | 16 | 22 |
ENSDART00000090825 | Nonsense | 606 | 929 | 17 | 23 |
Genomic Location (Zv9):
Chromosome 19 (position 24911309)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 24841421 |
GRCz11 | 19 | 24425644 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAAAGCTCTAATGAAAATGACTGTCTGTGTGTAGTGATGGTGATGGATA[T/A]CAGGACACCAGGGATAACTGTCCTGAAGTGCCCAACAGTTCTCAGCTGGA
Long Flanking Sequence:
CGATTTCCAACCAGCTCACAGTAAATCATTACATCCCTATTGTGAACAAATAGTGGCACCTAAGCCAATAAAGGATCTTGCCTCTCAAGTAATAACACAGTAATTCATTTTTAAAATTTTGCTTATTTGCAGTCAGACATGGACAATGATCTGGTGGGAGATGTATGTGATACAAACAAGGACATGTAAGTATATGTTTAAATAAAAGCTTATTTTATGCAACAACAGACAAAAGGACCTTTATAGTTCTATAATCGCAGTAACGGAAGTCCACTGTCAATAGCTATTCATGAAGCTCTAATTACTCAGAGATCATCTGCAAACCAAGTTGTTTTTTAATGGTAAATCTGACAGCTTCACATTTTTGAAAGATAAAGTTAGTTTTGATTTAGCATATATCACTTTTTTCATATCTGCTCTGGTTTGTGGTTTCTGCTAGTACAATGTTGTGTAAAGCTCTAATGAAAATGACTGTCTGTGTGTAGTGATGGTGATGGATA[T/A]CAGGACACCAGGGATAACTGTCCTGAAGTGCCCAACAGTTCTCAGCTGGACTCTGATAATGACGGCATCGGGGACGAATGTGACGATGATGATGATAATGATGGCATCCCGGATATTCTCCCTCCAGGCCCAGATAACTGCAGACTCGTTCCCAACCCCAGTCAAATAGACACTGATGGTGTGCTCTTTCATTTTACATTTCAAATATATTTGAATACTACTAATATACATATAATGTGTGTATTAGTGTAATATTTACAGACTGTGGTCATGCATTTACAATAATTAGCATAGTGAATCTAGCTGTTGGTTATTTGTAAATGTATTTTAGTTTTAAGAATCATTTTCAATTTTAACATTATACCTTCACAGTCTAGAGGTTAACATCTTTGTTTTTGACTTTCTCTCCTGTCAGCCAATGGAGTTGGTGACGTGTGTGAAACTGACTTCGACAATGATAAAGTGACTGACCTGTTAGATGCGTGTCCTGAAAGCGCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29208
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 |
---|---|---|---|---|---|
ENSDART00000043133 | Nonsense | 762 | 906 | 19 | 22 |
ENSDART00000090825 | Nonsense | 785 | 929 | 20 | 23 |
Genomic Location (Zv9):
Chromosome 19 (position 24908533)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 24838645 |
GRCz11 | 19 | 24422868 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCTTTGGCTATCAGGACTCATCCAGCTTCTATGTGGTGATGTGGAAA[C/T]AGACAGAACAGACGTACTGGCAGAATTTACCATTCAAAGCCTTGGCTCAG
Long Flanking Sequence:
ACGTACATCACACAAAATGCAGATCTACTTTGCATGTACGTATGTAAAAAACAATAATTACAAAGAATTGGCAAGTAAAATTGAACTAAACCAAAACATTTTAAGATGTAAAAGTATTTTTGTGTAAAACATACAAATAATAACAAAACTAGTGAAAATAAACTGTATATAGTACATATTTTTTATCTTTTTCATTTCACATGTGATGCATGGAGATTTTAAATTGATTTTATGTAGTTTTGTAGGCAAAACTGTTGCTTTTAAATGTGCTATAGAAAGTCATTTTGACTTGACTCTGTAGTGTACTAAAAGGTTTTTTATAAGTACACCTTAAACTTCTTTTTAACGTCATTTTTCTTGTTTATTATTTAGGCTACACAGCATTTAATGGTGTTGATTTTGAGGGCACGATCCATGTGAACACAGCCACTGATGATGATTACGTGGGCTTCATCTTTGGCTATCAGGACTCATCCAGCTTCTATGTGGTGATGTGGAAA[C/T]AGACAGAACAGACGTACTGGCAGAATTTACCATTCAAAGCCTTGGCTCAGCCTGGAATACAGCTGAAGGTGAGAGTACAGGAATAAAGTAAAAATAAAGTGCTACAGCCATGATGTCAACAAAACAAAGGCTGATTTGTCACTAGTTCCATTGGGATTTTTACATGTATGAGTAAAGAACTGGTTAATGTAACTATGATACTTGGACATTTCCATTGCAGTGGAAACTGTATGCACTCAAAACATTCTCACGTAGTAAAACAGGCATTTATAAAATAAACTTAAAAGCTTTAAATGTGTGTTATAGACATAAATTGGTGTAATTTATGTTGTAAAGCAACACATCTGGTTATTATTGAAACGTTGTTTACCACAAAATAAATTAAATTCATAGAATATTCTGAGGGAACCACTGGTGATTTCCTTTAAAGTCAATGTTGCAGCTCTCAAAGTAAAGTTAGAGCTGTTGATTTAAGGGTGCTATGCAAATTATTCAGTCAA
Associated Phenotype:
Not determined