ZMP
zgc:175142
Ensembl ID:
ZFIN ID:
Description:
slingshot 2-like [Source:RefSeq peptide;Acc:NP_001128575]
Human Orthologue:
SSH2
Human Description:
slingshot homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:30580]
Mouse Orthologue:
Ssh2
Mouse Description:
slingshot homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2679255]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16355 | Essential Splice Site | Available for shipment | Available now |
sa9803 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16355
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113436 | Essential Splice Site | 321 | 1165 | 10 | 16 |
ENSDART00000137444 | Essential Splice Site | 321 | 1016 | 10 | 15 |
The following transcripts of ENSDARG00000077623 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 39298553)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 40438618 |
GRCz11 | 21 | 40462171 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YTTGGGGCAGATGGACAGGCCCACAAAGATTTTTGAGCATGTTTACCTGG[T/C]GAGAGCGACGTCTCCTTTACGTTTTAATCATACATATCAGTTATAAGATG
Long Flanking Sequence:
GAAGCATAAGAATCGCTATTCGGTAGCGGCCGATCACCATGCCAAGAATATATACTCTGTATCGGCTGCAAAATTCCTGATCGGAGCATCCCTACTTAAATTGCTTGGTGCGTATAGAGAATTAAGATACTGTATATGTGACTTTTAAAAACAAACGTCTACTTTATTTTTTCAGGCCAACTGAGCGGGAAAGAACAGAGAGATTCATCAAGACTCGATTAAGAGAGATCATGATGCTAAAGGATCTTGAAAATGTCACTTCAAAAGATGTAGGATGCTAATATTCATCCTAAAAATCACTTTCTGAATGACTACAGGTTTATTCTGTACAGACTTTCGTATTGTACATCACGCTGCACCTTCTGTTTAGATCCGCACAGAGCTGGAGATGCAGATGGTGTGTAACCTTCGGGAGTTCAAGGAGTACATCGATAACGAGATGATCGTCATCTTGGGGCAGATGGACAGGCCCACAAAGATTTTTGAGCATGTTTACCTGG[T/C]GAGAGCGACGTCTCCTTTACGTTTTAATCATACATATCAGTTATAAGATGCACCATCAGTCATTTTTCAATTGTATCTAATTACAGGGTTCTGAATGGAATGCATCAAATCTGGAAGAACTGCAAAACACCGGGTACATTTTGACATCCTTGTTTATGAAAAAAAGCACACACATACCAATAATACCTGCAGTTGAAGCCAGATTTCCAGACTGTTTCAGTCATAAACCTGTGTTATCTTTATGCTCTCTTTGAAGTCTGTTCTTGTTGTTAATGATTATTCTGGTTTTCGGTTATGTCTTTGTGTTTACCATCAGGGTGCAATATATCCTTAATGTGACGCGGGAGATCGATAACTTCTTTCCAGGGCTATTTGAATACCACAATATCCGGGTTTACGATGAAGAAGCCACAGACTTGCTGGCTTACTGGAATGACACTTACAAGTTCATTTCTAGGGCCAAGTGAGTAAAAATATGCTGTACTGAAATTTTCTGACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9803
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113436 | Nonsense | 919 | 1165 | 15 | 16 |
ENSDART00000137444 | Nonsense | 919 | 1016 | 15 | 15 |
The following transcripts of ENSDARG00000077623 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 39311368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 40451433 |
GRCz11 | 21 | 40474986 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACACCGGCCTCACACACTCGAGACAAAGCCATTCGCACTCGTCCAGTTG[C/A]TCTCCGCCTCTGGTTCTCCAGCTCGAGGGCATCACAGAGCAGGAGAGTTA
Long Flanking Sequence:
ATGTCCGGAGTGGAGTCCACATGGCACAATGTAACCCCTTCCCCCCCTCCAACCAGTCAACCTGTTTCCAGTAGCAGCAGTGAGGAAGAGGAGTTTGCTCAAGTCATGTCAGCAGAAGCTGAAATGGAGAAGGTGGAGCATGGGAAAGACTGGCCTAAGGGCACAGTGTGGCGAGCCACCCGGGAGCTGGAGCAAAAGATCAAGCAGGAGGTCTCGTCAGTAGCGCTGGTGTCCTCTGCTCCCGTGTGTCCCTCGCGACGCTCCCCCGTCAACACCAGCAGCATGGAGAAAACTGAGGAGACCTCATCCCACACACACCTCACACCTGATCCAAACACTGTGTCAACACGCCATCACCAGCCTCAGTACCACAAGGTGGAGAAAGACCGGAGTTTTTCATTTGAAGAGGGAAGTGAAAGCGAGAGACGACTCAGGGAAGGAGAGCACAGGAACACCGGCCTCACACACTCGAGACAAAGCCATTCGCACTCGTCCAGTTG[C/A]TCTCCGCCTCTGGTTCTCCAGCTCGAGGGCATCACAGAGCAGGAGAGTTACACGGATTCTCGCTGTCCGAAGGACATGAGGGAAACCTGGGAGACCCTAAAAGAGCTCGGGGCGTTTCTCTGGCAGGTGAGCAACTGCTCCGACAGGAGGCTCAGCCAACCGTGGTCTAGGAGGGAGCAAAGGAAAGGCCGGGCTGCTCGAGAGAGGACCAAAGAGGTGGAGGCTCGGATCCGGCAGGCTGGACTGACCCCACCCTCAAAGATGAAGCGTTCAGCCTCGTTGGCCAAGCTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAAGAGGTGGAGGCTCGGATCCGGCAGGCTGGACTGACCCCACCCTCAAAGATGAAGCGTTCAGCCTCGTTGGCCAAGCTTGGGTCGCTGGAGATCTCGCCTATTGACCT
Associated Phenotype:
Not determined