ZMP
si:dkey-50p8.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
SFRS15
Human Description:
splicing factor, arginine/serine-rich 15 [Source:HGNC Symbol;Acc:19304]
Mouse Orthologue:
Srsf15
Mouse Description:
serine/arginine-rich splicing factor 15 Gene [Source:MGI Symbol;Acc:MGI:2146350]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21738 | Nonsense | Available for shipment | Available now |
sa736 | Essential Splice Site, Missense | Available for shipment | Available now |
sa13563 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21738
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 |
---|---|---|---|---|---|
ENSDART00000108981 | Nonsense | 382 | 1104 | 11 | 26 |
ENSDART00000125665 | Nonsense | 373 | 1023 | 10 | 22 |
ENSDART00000140483 | Nonsense | 347 | 1056 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 10 (position 26343721)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 25747578 |
GRCz11 | 10 | 25709291 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATGGGGCAGCCGAACGCAGCTTTCCCTCCTCAAAATGAGGCCTTCAAT[C/T]AACTCATGTCTGGACATGCGGTAAAAGGATTGTGACTGATGTATAACAGG
Long Flanking Sequence:
CTTTGACTATGACGATGAGCCAGATGCAGGAGAGGATGCCAAGAAGGAGGAAGCGCAGTCTGTCCAACCTTCTATGTATACAGAATCTCCTTTTCTAAATGTTGAAGTGCACAACATGCTTACTTTTGAGCAAGTTTTATAATTTGGTTAATCTTTGTCTCCACAGGGGTTTTCCTGAGCAAACTGTCCCAGGATTTCCTCCAGCCAATCAGATGCAGCACTTTCAACAGCATATGATGGCTGTATCACAGCGCCAACAGGTAGATTATCACAGCCTCCTTTTTTGGAAGGCATTTTTTGCCTAATATTTAATCAGATGACATTTATCTGTGATTTATTATTCCCTAGTCATGTTTTGGTTTTGATGTGCTCAGGTTGTTCTACCTTCAAATGGACAGGTCCAAGGCTTTGGTCTCATGACCTCTCAGCCCTATCCAGGCATGATGCCTCCAATGGGGCAGCCGAACGCAGCTTTCCCTCCTCAAAATGAGGCCTTCAAT[C/T]AACTCATGTCTGGACATGCGGTAAAAGGATTGTGACTGATGTATAACAGGGAAAAACTGCCATTAAATCTTACACTAATCATTATTCGATTCTGTCACAGGAAAGTCTGATGAATTCAGATGCATCTGCGAGGTCTGCCCATGAAGACAAGAGGTCAAGGTCACGCTCGGGGTCGAGGTGTGTACACAAAAATCCTTATGAACAACAATAACCATTCATCTAAAGCTCACAGTTTTTATTTTGAGTCCTTGCGGCAAGGTTAGAGGGTCATGAACCAGTACAATAACATTTTAGACTTTTATTTCACTTCGCCTGCCTTAAAGAGATAATTCACCCCAAAAGATCAATTCTTTCATAATTTAATCACCTTTTACTTGTTCAAATATACAGAATTTTTTTCCTACTATGGAGATCGATGGGTCCCAGCAATACTTTCTTTTGTGTTCCAACAGTAGAAAGAAACTCATAAAGGTTTAAAACCACATGAGAGAGAGTAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa736
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108981 | Essential Splice Site | 688 | 1104 | 19 | 26 |
ENSDART00000125665 | Missense | 636 | 1023 | 16 | 22 |
ENSDART00000140483 | None | None | 1056 | None | 20 |
Genomic Location (Zv9):
Chromosome 10 (position 26338692)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 25742549 |
GRCz11 | 10 | 25704262 |
KASP Assay ID:
554-0643.1 (used for ordering genotyping assays)
KASP Sequence:
TGTCATACCTATGCAGGTAAAGCAACATTGCCTGATTCATATGYATTCAA[G/A]TTTGGGTTTGTACTATTTATTTATTCTTTTTTTAATTATTCATCWTCAGG
Long Flanking Sequence:
CTAATACCATTGTTTACTGCAATTTGTGTAGGTTTGATTTGAAAAAAATGCTTTAAAGCAGGGGTGTCCAAACTCGGTCTTGGAGAACCAGTGTCCTGCTGAGTTTAGCTCCAACTTGCTTCAACAAACCAGCCAGGAAGTTTATAGTTTATCTAGTAAGAGCTTGATTAACTTGTTCATGTGTGTTTGATTAGGGTTGGAGTTAAACTGTTCAGGACACCGGCCCTCTAGGACTGAGTTTGAACACCCCTATTTTAAAGCATTGTTTTTTATTTGATACTCTTCTTCTGAAGACATAGAATATTAGTCAGCTTGATTTGTCAGCTTTGAGGACACACAGTTATACGTGATTTATCCTTATACAGAATGGCGAAACTCTCAGATTGAACAGAAGACTGATGAGTCTCAGAACGGCCGGCCAGAGGTGGGAAAAGTGGAAGAGACCCAAACTGTCATACCTATGCAGGTAAAGCAACATTGCCTGATTCATATGCATTCAA[G/A]TTTGGGTTTGTACTATTTATTTATTCTTTTTTTAATTATTCATCATCAGGTTCCTCCTGTCCAGCCAATAGGAGCAGTCGGTGTCCCACCTCCGGGATTCCCAGCACACATGAACATCCCACCACCCTCATTCCCACCTGGTGTTCCTCCACCTCCAGGTCCCTTCATGCGGCCAGCCTTTAACCCCATGCAGATGCCACCAGGTATAGAAATAATACTCACACAGCATTAATTATAGATGTTTGTGTCCATTTTCCAACACGTATAGTTTTTTTCTTTCAGGATTTCTCCCACCGGGTGCCATGCCCCATATGGGTGCTGCTGGCCCTCCTCCACCTACAGCAGGCATCGGGATGCCTCCAGGTGGGCAGTCTTCAATTTATACACTTTAGCTTTAATTTAATGGTATGGATTTCAGCAGTAATTCTTCCTGTGTAATATTGAGACAGTCATACTAATCTCATTTTGCCTTTTTAATCGCTGTAGTTGGCAGCTCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13563
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108981 | Nonsense | 1042 | 1104 | 26 | 26 |
ENSDART00000125665 | Nonsense | 984 | 1023 | 22 | 22 |
ENSDART00000140483 | Nonsense | 909 | 1056 | 20 | 20 |
Genomic Location (Zv9):
Chromosome 10 (position 26336234)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 25740091 |
GRCz11 | 10 | 25701804 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGATGGTGGAGAGAGGGAACGAGGACGCGATGGTGGAGAGAGGGAAAGA[G/T]GACGCGATGGTGGAGAGAGGGARCGAGGACGTGATGGTGGAGAGAGGGAA
Long Flanking Sequence:
CACCTCCGCACATGCAGCGATTCCCCATTCCCCCACCTCGGGCAGGCATGCCACCCATGCCACCACAGATGATGCCACCCAGGGGTCCACCTCAGATGATGCACCGCGAACCTCCACCGGGTGGTTTCAGCATGCCTCCTCCACCTCATGGCATCCGGGGACCGTTCCCACCTCCCGGACCTCACTTTATGAGGCCGAGCTTACCAAGGCCTGAGGGGCCAAATGATCATGAGGCTCGACCTTTTAGAGGAGAACGTCCCGGATTAGGAAGAGGCCGAGAGCAGGACTGGTTTGGAGGACGACGGCCTTTTGGTGAGGGACGTGGTGGGGAAAGACCAGATGGACGTGAGCGGTTTGGAGGATGGCACGAGGAGCCAGAGAAACCAGGTGGGTGGGAAAGAGAACGCAGGGAGGAACGCTGGAGGAGAAGTCCAGATGGAGAACGAGGACGTGATGGTGGAGAGAGGGAACGAGGACGCGATGGTGGAGAGAGGGAAAGA[G/T]GACGCGATGGTGGAGAGAGGGAACGAGGACGTGATGGTGGAGAGAGGGAACGAGGACGCGATGGTGGAGAGCGGGAACGAGGACGCGATGGTGGAGAGCGGGAACGAGGACGCGAAGGTGGAGAGAGGGAACGAGGACGCGATACTGGAGAGCGGGAACGAGGCCGCGATGGTGAAGAACGGACCAAGCGGCCCGCAGGGAGCAGAGAGAGGAGCACACGCTGGGACCGCGACGATAGACTCGATCGATTGGGTCTGGCCGGCGAGGAACCCAATGAGAGACTCTCAGCAAATACCAACGAGCCCAGTGCAAACCCTACTAAAGAACTTGCTGAAGCCAAGCCAGATGTTCCAGCACCTTCTGCTGCAGCTACAGCAGACTCGGAAGCTTCAGAACCCATAGCAGAGAACAAATCTGAAGAACAAACACAAAAAGAGGAGTCGTAGAGGCTTCTTTACTCATTAAGACCACATGAGCTTCTTCTGTGTCAGTGCTAATCT
Associated Phenotype:
Not determined