ZMP
THBS1 (2 of 2)
Ensembl ID:
Description:
thrombospondin 1 [Source:HGNC Symbol;Acc:11785]
Human Orthologue:
THBS1
Human Description:
thrombospondin 1 [Source:HGNC Symbol;Acc:11785]
Mouse Orthologue:
Thbs1
Mouse Description:
thrombospondin 1 Gene [Source:MGI Symbol;Acc:MGI:98737]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22971 | Essential Splice Site | Available for shipment | Available now |
| sa32115 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22971
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 |
|---|---|---|---|---|---|
| ENSDART00000092683 | Essential Splice Site | 350 | 804 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 513412)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150104.1 | 6723 |
| GRCz11 | KN150104.1 | 6723 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCCGCAGCATGTGAAAATCTTCAAAACTATGAACACACGTCCTCTTTC[A/T]GGATAACTGCCCTGACCTTCCCAACTCTGGACAAGAAGACTACGACAAAG
Long Flanking Sequence:
ATTAGATTAGGATTGAATTGCTATATAGTGAAGTCAACGTTTAATGGTTAAGGGGTTCAAATCTATCTTAAGTGTCTGCTAAGAATGACTGACTAATGTAAATGGGGTTAAATTGTTTTCTCGGCAGGTTTGCACACCAAGAAACCCATGTGCTGACGGCAGCCATGACTGCAATAAAAACGCCAACTGCATCTACCTGGGCATCTTCTCAGACATCATGTTCCGCTGTGAATGTAAACCTGGATACGCCGGGAACGGCCACATCTGTGGGGAGGATCCAGATCTGGACGGCTGGCCCAACACAGACCTACACTGTGTGGAAAACGCCACTTACCACTGCAAGAAGGTATGTTTGACTGTGTTCATTTAACCTTTAGGACGTCACTGATGCAAATTGGGATGCACTATTACTGTTTTCCAATACGGTTTAGCACAGAGAGAGTGTGAATTGTGCCGCAGCATGTGAAAATCTTCAAAACTATGAACACACGTCCTCTTTC[A/T]GGATAACTGCCCTGACCTTCCCAACTCTGGACAAGAAGACTACGACAAAGACGGCATTGGAGACGCTTGTGACCATGATGATGACAATGATGGGATCCCTGATGACGGGGTGAGTCTTAAAAACACATTCCTCTTCTCAAACAGCATTTAGCATTGCTACTGCACTGCAAAACAATGCCTTTCTTACTTAGAGCTTCTGTCCTGTTTCTAGTCCAAATATCCACAAACCCTTCAATAAGTCAGCATTTACTAGAGTAAACGATATAGTGCTGTTTTCAGAATAATGAGTCAAAATGAAGAGAGTTTATCAGTAAAACAAGCAGAATAATCTGACTATGGGGTGGGTGAAATAATGTTGTTTTGGCCTTGAAAGAAGACTATTTGTATGGAGCCATATAAGTCTCAAAAATAACACATCTGCAGAATAAATTCATGCATGCACATTTTATTAATTGCATTTGCATTAACAAATTAGATTTGTGTATTTATAAATAGCATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32115
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 |
|---|---|---|---|---|---|
| ENSDART00000092683 | Essential Splice Site | 439 | 804 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 517640)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150104.1 | 10951 |
| GRCz11 | KN150104.1 | 10951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAATTGATGGATGGAAACACAGCCAGTGACGTTGTTATTTGTTTGTCC[A/T]GGCATTCTGAATGAGAAGGACAACTGTCCATATGTGTACAACACCGACCA
Long Flanking Sequence:
TCCAGGCTAGGATCGAACCAGCGACCTTCCGCATGAGAGTCAGTTTCTCTACCAAGGAGGCTAAAGACCATGGCAAGTGAATTATACTATAAAGTCATGGTGTACACAACTGTCTCTGGGCTTGCTGCATTACAAATACCAAAAACATTAATCACTTTCTGGCCATCAGATATTAGGCATGGATATATATATATATATATATTGCTGTTGTGATTTTCGAAAGTATTACAGCGCTTAGTAAATGTTTATTATTACCACTTGATGAGTCTCCACATACAGTTTGATAGAGCGTTTGGACCCGGAAGCTGCTACGCTCGACATCACACTTAACAAGCGGACATAAACAAACATTAAAATCATAGAAGCGTTTCTAAGAAAGTGCCTGATGCATATAGAGGAAAGAGAGTGTTTTACAGGTGTTGTTTCAATGCGATAATCCAAAATGTGCAGTACAATTGATGGATGGAAACACAGCCAGTGACGTTGTTATTTGTTTGTCC[A/T]GGCATTCTGAATGAGAAGGACAACTGTCCATATGTGTACAACACCGACCAGAGAGACACTGACCGGGACGGAGTCGGGGACCACTGTGATAACTGCCCACTGGAGCACAACCCTGACCAGGTCTGATCTTATTATTATTATAGTCACACCCACATATATTATATAGAGCCACTGCATAAATAAACCATCATAAAAAACAGAAACAATATTATAGAAAGGAGGAATTTAAGGTTGAAGAAAACAAGTAGTGTAACACGATTTGTTGTACATTCACAAGTACACATCGTTTACCTTACTGAGTCTGTAAGTTTAAGCCAAGTGTCTGGTGCATATGGAGAGACGAGTGTTACTGCAGGTGGGGTTTACAGTAAATACCATCATGCAGTCAAACATGGCACTCTACCAACCTTAAACCACTTTAAAAGTATTGTAGGTGCCGGTATCACAAGGATGTGATATGTGATTCTACAATGTTTGCTTTAAAATAAATCACTGAAATG
Associated Phenotype:
Not determined