Busch Lab

ZMP

zgc:175142

Ensembl ID:
ENSDARG00000077623
ZFIN ID:
ZDB-GENE-081205-4
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
sa43713 Essential Splice Site Mutation detected in F1 DNA Not yet available
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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:
sa43713
Status:
Mutation detected in F1 DNA
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
ENSDART00000113436 Essential Splice Site 386 1165 13 16
ENSDART00000137444 Essential Splice Site 386 1016 13 15

The following transcripts of ENSDARG00000077623 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 21 (position 39301327)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 40441392
GRCz11 21 40464945
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATTAGCACTATGTCCATCTTTTAACACAAGACTAATCTGATTCCTCCA[G/T]AAAAGCCGGAGCGAAGTGTCTTGTGCACTGCAAGATGGGTGTTAGTCGTT
Long Flanking Sequence:
AATATTTAGGCGAATTGATTGATTGATTAATTTACTTTTATTGCCTTCAGAAGGGCAACAAAGCTCCAGCCTATCGAGCAACGACTAATCTAGACACCTCTGATTGGTTACGGCATTCATATGCTCACATTTGATTGGCTACAGAGGCTCAGCGCTGCTGCAAAAGCAAGAAATTGGTGTTAAATTGAAATCGAACGCAGTGTTTGCAAATGTAAATGTCCCAAATTTCACAATTCACTTCAGTCTTGACAACCATATAGGTTTTATTTAATTGTACAGTGCATTTTTTGAAAGTGTGAACATTTTTCAGTCAGAAATAATAACATAATATATAAACAAAATGTAATTTCAGTCTCTCTTTATCTCTTTCTCTTAATTTCAGATAAAGTCTTAATTCAGATTGTTTACCTATCTTTTTCTTGTGCTTCTTCAACAAATACCATGTTGAAACTATTAGCACTATGTCCATCTTTTAACACAAGACTAATCTGATTCCTCCA[G/T]AAAAGCCGGAGCGAAGTGTCTTGTGCACTGCAAGATGGGTGTTAGTCGTTCGGCCTCCACTGTTATCGCATACGCCATGAAGGAGTACGGCTGGGACATGGAGCAGGCCTTTGAGTACGTAAAAGAGCGGCGAGCCGTCACCAAACCCAACCCATCATTCATGAGACAGCTTGTGGAGTACCAGGGAATACTGATAGCAAGGTAAACACTGCATTTGAATGTGTGCAGTCATGTGATTGGCTGGAAGCATATGTGTGTGTGCATTCAGGGCTGAAGTGGGACTCCTTTTCAGCCCTGGAGTTTCAAGCCTCAGACCGGCCCACCTCAGTTCTCGACTGACTATATTAAAATAAGGTCATTTCCAATTCAGTTTCTAATGACACTATCACGTCTTTTTTTGAGAAAACAGCTGCTTTAGAACTTCAAATGTTCAACAACCCAAACAGTATTATACGTCTCAACAATAAAAATGAAAATAATAACATACTCAGACGAGGATC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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