ZMP
SOLH
Ensembl ID:
Description:
small optic lobes homolog (Drosophila) [Source:HGNC Symbol;Acc:11182]
Human Orthologue:
SOLH
Human Description:
small optic lobes homolog (Drosophila) [Source:HGNC Symbol;Acc:11182]
Mouse Orthologue:
Solh
Mouse Description:
small optic lobes homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1355075]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8803 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19352 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14132 | Nonsense | Available for shipment | Available now |
sa44189 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37958 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19353 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8803
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085565 | Nonsense | 49 | 1122 | 2 | 12 |
ENSDART00000085565 | Nonsense | 49 | 1122 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 24 (position 40631008)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39163240 |
GRCz11 | 24 | 39051003 |
KASP Assay ID:
554-6219.1 (used for ordering genotyping assays)
KASP Sequence:
CATTCTCATTCACCTGGTTCGATGGAAGCAGTTGTGAGGAATTCTGATTG[G/A]TCCTGCGGGCGCTGCACGTTCCTCAACTCCAGCGGCTCYATGCGCTGCTC
Long Flanking Sequence:
CAGAACAGAAATTGGGGGGAAAAAATAAACGGGCTAATAATTCTGACTTCAACTGTACATTTCGCATTCTTTTAATTAATTTCAATTATTATTATTATTATAATACACCAAATATTTGATTTAAATTTTTTTATTAGGTGTAATCATACAAATAATTATGTATAATATATAAATAATTAACAATATTAATAACTATTAATTTATCTATTTACCTGTATTTTTTCTCCTTTTAGTTGTCGTGATATAACTTTATAAATGACATAAAACAATCCAATAATTTTTCAAATGTAAATTATAATTAAAATATAAAAAATTATTCATATTAATCTTCCTTAATCCCATGTATTTTCCTCCTCTCTCTTTGTGACCTCTGTTTTGTGTACATGTTTAAGTCTTAATATCCAGTCTGAAATCCATATCTAATTGTCTCCTCTTTCTCTCTCTCTCAGTCATTCTCATTCACCTGGTTCGATGGAAGCAGTTGTGAGGAATTCTGATTG[G/A]TCCTGCGGGCGCTGCACGTTCCTCAACTCCAGCGGCTCTATGCGCTGCTCCATTTGTGAAGCTCCCCGACAGAAGCCGGATCTGAACCACATTCTGCGCCTCAGCAGTGCAGAGGAACCCCGCTGGTCCTGCCCACGCTGCACTCTCACCAACCACCACGGGTTAGGCTCCTGTTCTGTGTGTGGAGCTGCTCCGGTAACACCCAACGGACCCCTCCCACCCAAACAAACCCCGCCCACTCCGATTGACCTCGCCTCTAGCCCTGAACCTAAAGGTCAGGTGGCGAATGGGGAATCCCAGTGCATAGAGTCCAATGGGGAGGTGCCTATGAGTGGGCAGGGCTCCTCAGAGTGGGCGTGTCCTCGTTGTACTTTAGTGAATACTCCAGTTGCGTTGTCGTGTTCAGCGTGTGGTGGTCCGAGGAAACTTTCCTTACCGAAAATCCCTCCGGAGGCTCTAGTGGTACCAGAAGTGCGCACACCTGTGGCAGGGTTTCCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19352
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085565 | Nonsense | 49 | 1122 | 2 | 12 |
ENSDART00000085565 | Nonsense | 49 | 1122 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 24 (position 40631008)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39163240 |
GRCz11 | 24 | 39051003 |
KASP Assay ID:
554-6219.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTCTCATTCACCTGGTTCGATGGAAGCAGTTGTGAGGAATTCTGATTG[G/A]TCCTGCGGGCGCTGCACGTTCCTCAACTCCAGCGGCTCTATGCGCTGCTC
Long Flanking Sequence:
CAGAACAGAAATTGGGGGGAAAAAATAAACGGGCTAATAATTCTGACTTCAACTGTACATTTCGCATTCTTTTAATTAATTTCAATTATTATTATTATTATAATACACCAAATATTTGATTTAAATTTTTTTATTAGGTGTAATCATACAAATAATTATGTATAATATATAAATAATTAACAATATTAATAACTATTAATTTATCTATTTACCTGTATTTTTTCTCCTTTTAGTTGTCGTGATATAACTTTATAAATGACATAAAACAATCCAATAATTTTTCAAATGTAAATTATAATTAAAATATAAAAAATTATTCATATTAATCTTCCTTAATCCCATGTATTTTCCTCCTCTCTCTTTGTGACCTCTGTTTTGTGTACATGTTTAAGTCTTAATATCCAGTCTGAAATCCATATCTAATTGTCTCCTCTTTCTCTCTCTCTCAGTCATTCTCATTCACCTGGTTCGATGGAAGCAGTTGTGAGGAATTCTGATTG[G/A]TCCTGCGGGCGCTGCACGTTCCTCAACTCCAGCGGCTCTATGCGCTGCTCCATTTGTGAAGCTCCCCGACAGAAGCCGGATCTGAACCACATTCTGCGCCTCAGCAGTGCAGAGGAACCCCGCTGGTCCTGCCCACGCTGCACTCTCACCAACCACCACGGGTTAGGCTCCTGTTCTGTGTGTGGAGCTGCTCCGGTAACACCCAACGGACCCCTCCCACCCAAACAAACCCCGCCCACTCCGATTGACCTCGCCTCTAGCCCTGAACCTAAAGGTCAGGTGGCGAATGGGGAATCCCAGTGCATAGAGTCCAATGGGGAGGTGCCTATGAGTGGGCAGGGCTCCTCAGAGTGGGCGTGTCCTCGTTGTACTTTAGTGAATACTCCAGTTGCGTTGTCGTGTTCAGCGTGTGGTGGTCCGAGGAAACTTTCCTTACCGAAAATCCCTCCGGAGGCTCTAGTGGTACCAGAAGTGCGCACACCTGTGGCAGGGTTTCCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14132
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 |
---|---|---|---|---|---|
ENSDART00000085565 | Nonsense | 253 | 1122 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 24 (position 40631619)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39163851 |
GRCz11 | 24 | 39051614 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCACCRTCTGAAACCCCATCTCCACCCCCTGTCCCRTTTCTGCCCCCYT[C/A]GTTGTCCKCACTTCAAAATAATCCTGTGCCTCGCAGCCGAAGAGAAGTYC
Long Flanking Sequence:
AGAGGAACCCCGCTGGTCCTGCCCACGCTGCACTCTCACCAACCACCACGGGTTAGGCTCCTGTTCTGTGTGTGGAGCTGCTCCGGTAACACCCAACGGACCCCTCCCACCCAAACAAACCCCGCCCACTCCGATTGACCTCGCCTCTAGCCCTGAACCTAAAGGTCAGGTGGCGAATGGGGAATCCCAGTGCATAGAGTCCAATGGGGAGGTGCCTATGAGTGGGCAGGGCTCCTCAGAGTGGGCGTGTCCTCGTTGTACTTTAGTGAATACTCCAGTTGCGTTGTCGTGTTCAGCGTGTGGTGGTCCGAGGAAACTTTCCTTACCGAAAATCCCTCCGGAGGCTCTAGTGGTACCAGAAGTGCGCACACCTGTGGCAGGGTTTCCTACGCAAACGGCAGGAGCATCTGCACCTCTTCTTATCGATCTAACCGAAGATTCTCCACCGCAGGCACCGTCTGAAACCCCATCTCCACCCCCTGTCCCGTTTCTGCCCCCTT[C/A]GTTGTCCTCACTTCAAAATAATCCTGTGCCTCGCAGCCGAAGAGAAGTCCCGCCCCCTGGGCGGCCTCCAAACCCTGGCCCCTCACCAACCTCACCTTCATCCTGCCCACCAACCAAGCCTAAACCCCTCCCACCATCAGGTAATTACCCAGTCAAGCGCCTCAGCGTGCTGGAGGAGGAGGAGCCTAATAACCCCACCCCTCCAGTCACATCTCCGCCTTCCTGGAAGTGCCCCGGATGCTCCGCCCCAACAGCTCCTCCTTCATCGTCTGCCGGGCGCTGCGATGCATGCAGAGGGTCGAGGCCGGGTTCGGGTGGTGATGTCATCGATGTGCTCGGCGAATCAGTGCGTTTCACGCCAGCGTCGCCATCCAGCCCAGACTTCAGCTCCTGGGCGTGCTCCAAATGTACGCTGCGCAACCCGACGGGCGCGGGTCACTGTACGGCCTGCGGATCCTCCAAACTGCATGGTTTCTCGGAGCCGTCCAGCTGCTCATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44189
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085565 | Nonsense | 453 | 1122 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 24 (position 40632218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39164450 |
GRCz11 | 24 | 39052213 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCTCGTCCTCCATTTCGTCCCCGTCGGCGCAGGACAAGAGTGTGTGC[C/T]AGTGGACGTGTCCTGCCTGCACGCTGCTGAACGAGGGAAGGATGAAGCAC
Long Flanking Sequence:
CATCCTGCCCACCAACCAAGCCTAAACCCCTCCCACCATCAGGTAATTACCCAGTCAAGCGCCTCAGCGTGCTGGAGGAGGAGGAGCCTAATAACCCCACCCCTCCAGTCACATCTCCGCCTTCCTGGAAGTGCCCCGGATGCTCCGCCCCAACAGCTCCTCCTTCATCGTCTGCCGGGCGCTGCGATGCATGCAGAGGGTCGAGGCCGGGTTCGGGTGGTGATGTCATCGATGTGCTCGGCGAATCAGTGCGTTTCACGCCAGCGTCGCCATCCAGCCCAGACTTCAGCTCCTGGGCGTGCTCCAAATGTACGCTGCGCAACCCGACGGGCGCGGGTCACTGTACGGCCTGCGGATCCTCCAAACTGCATGGTTTCTCGGAGCCGTCCAGCTGCTCATCATGCTCTCGGAAACAACCGCACTCCCACCCGCGTGCCTTTACCTCCACCTCCTCCTCGTCCTCCATTTCGTCCCCGTCGGCGCAGGACAAGAGTGTGTGC[C/T]AGTGGACGTGTCCTGCCTGCACGCTGCTGAACGAGGGAAGGATGAAGCACTGCGCCGCATGTCACACGCCGCAGCAGTACCTGAATCTGAGGAAAACCGGGAAGCCGCTCAAGCGCAGGGAGAGCATGCATGTGGAGGCCCGCAGGCGCACGGATGAGGGAGAGGCCAAGGAATTGTGGGAAAATATCGTCAGCTTCTGTAGGGAGGTAAGATTCTGTCACTTTCATTGACACAAAAAGGAATGTACGGTAACACTTTATAATAACTACACACTATCAATCATTTATTAAGCATTAGCAAATAGTGAATTCATTATCCGTTAAGCATTAACTCTACATTAATAAACGTTAGTAAGCAGTTTATAACTGCAGCTACAAATGCTCCATTCTTGACTTATAACCACATTTAAAATGTGCTTAATTATTGTATTTTCATACTTGGTAAATAATTTATTTTTCATTACTAAATTAAGTATCGCATTATTTACAAACCAGTTGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37958
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085565 | Nonsense | 571 | 1122 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 24 (position 40641819)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39174051 |
GRCz11 | 24 | 39061814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCCTCATGAGATCAACTGCAATAACTTTAAGGATCGCGGTGTGAAGTG[G/A]TCTGTGTTCAGGACACCCCGTCCCTCAGATATTCTGCAAGGCCTTCTGGG
Long Flanking Sequence:
GAAACCCACGCCAACACGGGGAGAACATGCAAACGCCAAACAGAAATGCCAGCTGACCTAGCTGAGGCTCGAACCAATCTTCTTGCTGTGATGGGACAGTGCTAACCACTGAGCCACCATGTCACCCATTATTTTGCAGCATATTTATTCAAAATATTTCACGATTTCATATATTCACGTGTGCATGTGATATCTTAATGGGCAAATAAGATCTATTTAATACAGATAAAACTTTTGCAACCGATTCCTATTTAAAAATATACCATTTTAGATTAAAATGATGCACACATTATTTTTAAATTTACATCTGTGTGTGAGATATCTTACAGTGCTGTGGTGTGTTTGTTGCAGAACGCAGTGAATTTCGTGGATGACAGTTTTCCTCCTGGTCCTCGATCGGTCGGTTTCCCGGAAAACGACAGCGTCCAGCAGCGGATCAAGAAGTGGCTCCGTCCTCATGAGATCAACTGCAATAACTTTAAGGATCGCGGTGTGAAGTG[G/A]TCTGTGTTCAGGACACCCCGTCCCTCAGATATTCTGCAAGGCCTTCTGGGAAACTGCTGGTAAGAGAAGAGCTCCATATAAAGCACTGCACCGTATATTACATACAGTAGCATATACAGTAATATGAACAGTATGCGAGTCAGCATGTTTAAAGGGACAGTTCACCCTAAAATGAGAATTCTGTCCTCATTTACTTGCTCTTTATTTGTTTCAAAGTCAAACCTGTATGAGTTTTGAACACAAAAGAAGATATTTCGAAGAATGCTGAAAATAGAGAAAGTTGGATGTTTTAATCGTCATTTATAAATGACACTAAGAAAATTTCATTTTTAAAAACACTAATGACATTTAACCTGTACAATAAAATTTTAGTAATGTCACATGACATCTTTAGCCAACTGAACTAAAAGATAGTGGCCATTAGCTTTACATAATTAGAAAACACAAACTAAATGAGACACCAGCACACATTAGGTGACATGCTCTCACAGCAAGATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19353
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085565 | Nonsense | 645 | 1122 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 24 (position 40644770)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39177002 |
GRCz11 | 24 | 39064765 |
KASP Assay ID:
554-6220.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCATGTGGACCACCGTTTTAGTGGACGACATGCTGCCCTGTGACGAATA[C/A]GGCTTTCTGCTCTTCTCGCAGGTTTGTTCTGCTGTAGTTTCTTAAAGGTC
Long Flanking Sequence:
GCATTTTCCCATTAGCTAAGAAACTTTCCATAGTCGTCTGTTTCTCTCTCATTTTGCTGCATGTGGGTTTAATTTGGGAGACCAACTGACCGAGATGTAAGCAAGTGAATATGCTCATTTTTTAAAATAAAAGATTTTTCAATATAAAAGATTGTTTAGACTTTAAAGATTATAAATAAAACGGAAATAATTAATGCTTTCTTGTGCGGCCAGATACCAATTGATCCACCTGATGGTTGAGGACCACTGGTTTAGACAATCTCTAGCATTGAGTTGATCTGTATTGTTGTTCACAGAGTCTTGATTTGTTTTTGAATTGTTCATGCTGTATTTTTCAGGTTTCTGAGTGCGCTGGCGGTGTTGGCGGAGCGGCCGGAGTTGGTGGAGCGAGTGATGATCACCAGAAGCATCTGTCAGGAAGGAGCCTATCAGGTCCGGCTCTGTAAAGACGGCATGTGGACCACCGTTTTAGTGGACGACATGCTGCCCTGTGACGAATA[C/A]GGCTTTCTGCTCTTCTCGCAGGTTTGTTCTGCTGTAGTTTCTTAAAGGTCTCGTGAAGTGCTTTGAAAGGTGCACTTTTTATTACCTTTAAAGAGATTGTGATTTAGTTTGATGCCTAATCTGCTTTTGATTGTTTAAATTAAACTGAACTGAATGATATTAAAGTGATGTTTGCACCACATCTGCACTTTGAAATCTCAGCAACAGCTGGAGGTTTGTAGTCCACAGCATGTTACTGCAATGTTTACAGTGCTGATCCTATACTCCTGGGTTTCTTCCCACCACAGTTTTGTTTTAAAATGGCGGCCACGTGAAATAAGCATATAGATGTCCCTAAAACTAACAGACTGAAACTAACTGAAAAACTTTAGTTTAATTTCACAGGACATTTAAAGTTTGTGTGAATCAAAAGTTGCTAAGACTTTATATGTCATAATATGAAAGGTATTTCTTTCTAATGTTAGGATCATTTTAGAAAAAGTCACCAAACGTCAAGATAA
Associated Phenotype:
Not determined