ZMP
tspan15
Ensembl ID:
ZFIN ID:
Description:
tetraspanin-15 [Source:RefSeq peptide;Acc:NP_001017773]
Human Orthologue:
TSPAN15
Human Description:
tetraspanin 15 [Source:HGNC Symbol;Acc:23298]
Mouse Orthologue:
Tspan15
Mouse Description:
tetraspanin 15 Gene [Source:MGI Symbol;Acc:MGI:1917673]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15593 | Nonsense | Available for shipment | Available now |
sa35477 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28103 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15593
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 |
---|---|---|---|---|---|
ENSDART00000057641 | Nonsense | 40 | 296 | 2 | 8 |
ENSDART00000143112 | Nonsense | 40 | 250 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 23093444)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22822782 |
GRCz11 | 13 | 22953232 |
KASP Assay ID:
2260-6348.1 (used for ordering genotyping assays)
KASP Sequence:
TTCGTTTTGTTTTAGTTGATCGGGGGCTTTATATTGGCCATCRGTATTTA[T/A]GCCGAGGTGGAGAGGCAACGATACAAAACATTGGAAGGAGYGTTTCTGGC
Long Flanking Sequence:
CTCTGGGTTACAGAGCTGCGTTTGCGGTGCGTTCCTGTGTGCTGTACTTATCCGACGTTGAATTCTTCTGCTTTTACTTTCTTCTACTCCAATTGTGACACAGAAATGCTTTGGGGTTCACACCACATACTTAAACGTTTTAATTAGACAAGTACAGCTCCAATTGGTAGAGTATGATAATCATGTAGAATATTTCCAAATGGAAATCACACTCAGCACAGAAGGGAGCCATTAAGATTCAAGGTTAGAATACATTATCTCAGGAAGTCACAGAAGTTCTTCTTAGCTTTATGTATTTAAATATTATGAAAAATATACCCTTAAATTCAATAATATCCATCTTTCTTAGGCCTTTTGAGACTCTTAAGCATAATTCACATGCTGTGTTATGTTGTTGATCTATTCTTATGCAATCAAATTTGACATTAAATGCAAATTATCTGATGTATTTTCGTTTTGTTTTAGTTGATCGGGGGCTTTATATTGGCCATCGGTATTTA[T/A]GCCGAGGTGGAGAGGCAACGATACAAAACATTGGAAGGAGTGTTTCTGGCTCCTGCCATCATCCTCATTGTGCTTGGTATCATCATGTTTATTGTTTCCTTCATCGGGGTTCTGGCATCTCTCAGAGACAACTTGTGCCTTCTCAAAGTGGTAAGTTTTCTTTTCCATCAGACTCTTGCACAGTAGTGTCCTCTATATAACAAATGCTCTACTTTAGCAAATTATTTATTATATAAACAGTTTTGTGTTTTGCTGCAAATACAGTTCACATATTATTGTTAAAAAGTATACTCTTTGAAAGTAGCAAACAGGCCAATGTGGTTCTTTCTTTGACAAAACGCAAAATAATATTTTAGTTTTTTCTATACAGTGAAAGTCAATGTCCAGTGTTGTTTTAGTCTTCCCTGAAAATATTTATATGATAAAAAAATTCTACATATTTTCATTTGTATTGAAGGAGGGGCAGTACTAGAAACTATACAGTATTATTAAGACTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35477
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 |
---|---|---|---|---|---|
ENSDART00000057641 | Essential Splice Site | 91 | 296 | 3 | 8 |
ENSDART00000143112 | Essential Splice Site | 91 | 250 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 23089052)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22818390 |
GRCz11 | 13 | 22948840 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTAATATGTCTGTTTCACTTGAGAACCACTGTTTACTCTTGTCTTGCA[G/T]TTTCTTTACATGCTGGCTCTCTGTCTCGTTTTGGAGCTCGTCGGTGGGAT
Long Flanking Sequence:
GTTTCACGGATGGTTTGTCAAGCCCACTCACCTGTGTGAGACACACTCAGAAATGCACAATGTTTTCAAATAGATATAGAGTGTTTTTTTTTAGAAAGTGTCTGGTGCAGATGTCTGTTAAAGTGTATCAGACACTTGCTATACTATTCAGTATGGCTGAGAAAAACACTAAAAGTACATCCTGTTTCAAACAGAAAGTGAAAAGTTTGTCTCGTGGAGAAAACTTCTTGTTTTCCAATCTCTGTTGACGTGCCTTCCAAAACCGCACACTAGCAAGAAAACAAGATGATAGGAATTGAATCATATTATGAGCTATTTGTATTCAGTGGTTCGTCTGCCTTTGTGAAAATGTCAGCGAGTGCTATACACACACACACACACACGCACACACACATAGATGGGCTCGCTGCCCATGTAGGGCAGAAATGGAGGTGTGTGACTGTTGTGTTTCATTAATATGTCTGTTTCACTTGAGAACCACTGTTTACTCTTGTCTTGCA[G/T]TTTCTTTACATGCTGGCTCTCTGTCTCGTTTTGGAGCTCGTCGGTGGGATCGTTGCTCTGATTTTTAAGAACCAGGTACAATCATTGTACTTCTTTTATTTAATTTTAATTTAACTTTATAAACTTCATCCTTTTGTTTGATTGTTTCAAATACATTTACACCGTAATCTCAGTGTTTTATAATTATTAGCTGTGAAATGCAAGAATAATTGTTGTCAGTTTCTTTGTGATGTCAGTTGGTTAATGTGTGATCCATGCTAATGTAAAAAGGATAATTGGGTGAGCGGTGTTATATGATTTGGGTCAAGACTGTTTTGTGATGAAATGAGGCTGTGTCTAGTCGTCTGCTGGAAGTGGCAATTTGTTTGGCTTCTTGACACTTCAGCAATCATTAACAAAATAATTTTGATGCCAGAGCATAATTAGCATCATCATTGTGAGCTTCATTTTAATAATATTTCTTGAGAACCTAATTGTACCATTGCTTAGACACTGCAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28103
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057641 | Essential Splice Site | 147 | 296 | 4 | 8 |
ENSDART00000143112 | Essential Splice Site | 147 | 250 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 23088332)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22817670 |
GRCz11 | 13 | 22948120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATGATGACCTTGATTTCAAAAACATCATGGACTTTGTTCAGAAAACGG[T/G]AAGCGATTTCTATCAGGGTGCACATGAAAGTTGCAGAATTGATATGCTGT
Long Flanking Sequence:
TTTCTTTGTGATGTCAGTTGGTTAATGTGTGATCCATGCTAATGTAAAAAGGATAATTGGGTGAGCGGTGTTATATGATTTGGGTCAAGACTGTTTTGTGATGAAATGAGGCTGTGTCTAGTCGTCTGCTGGAAGTGGCAATTTGTTTGGCTTCTTGACACTTCAGCAATCATTAACAAAATAATTTTGATGCCAGAGCATAATTAGCATCATCATTGTGAGCTTCATTTTAATAATATTTCTTGAGAACCTAATTGTACCATTGCTTAGACACTGCAGTCTTTTCAAAAAGGCAGATCAAAAGGAATAAAAGCTTCAAATCCCATCTTATGAAATTGTGCATATGATGTTTTGTTGCAAAAAAATCTACCTGTAATAATACTGACATCCCTTTGTCTAACAGACAGTGGACATTCTCAACAAAAACATCCGTAAAGGCATGGTGAATTACTATGATGACCTTGATTTCAAAAACATCATGGACTTTGTTCAGAAAACGG[T/G]AAGCGATTTCTATCAGGGTGCACATGAAAGTTGCAGAATTGATATGCTGTGCTTTGAAGATTATTCTGAAGGCATTTGTGATTTTGATCTGTCTACATATTTTTCACAGAAGTTAAGTGAGACTAAATGAAATATTTTCTCTGTATTCTTTTTTATTTGTTCATAATTTTTTTCTGGATTAATTCAATCCATCTTCTGAAAACAAAAACATTTATTTTTTAACAAAACCAACTAACAAATTAAGTAATCGAATAAAGGGCTACATTTTTTATTTTATTTTTATTTTTTTGTAATAAATGATACTATGCTGTCATAAGTTTGTCATTTATTTGGTTAGATTTTATTAAATGAAATCTAAGTTCAAGATTTCCTTGTCAAATATGCAGACACCGATTTAAAAAAAATGTGTTTAATTTGTCATATAGATACATTTTTTATTTCTAAATGCAAAATCTGTAAACTTTTATTTATATATATTTTGTTTAAAATCCAACTCTAAT
Associated Phenotype:
Not determined