ZMP
zgc:162582
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100037329 [Source:RefSeq peptide;Acc:NP_001082953]
Human Orthologue:
SCMH1
Human Description:
sex comb on midleg homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:19003]
Mouse Orthologue:
Scmh1
Mouse Description:
sex comb on midleg homolog 1 Gene [Source:MGI Symbol;Acc:MGI:1352762]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39122 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17669 | Essential Splice Site | Available for shipment | Available now |
sa11528 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39122
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102181 | None | None | 120 | None | 4 |
ENSDART00000115339 | Essential Splice Site | 330 | 733 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 39545565)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 35619688 |
GRCz11 | 16 | 35572563 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAATCTATTAAAATCCCCAAGAAACGAGGTCCCAAACCAGGAAGCAAGG[T/A]AAAAACGATATTGAAAGACATTACAGATTCAAGTATTTCAGTAGTTGCTG
Long Flanking Sequence:
AATTCTTACGTGCTGATCTCTTCCTCTTTTCTTGTTGTGTTTTCCCTCTTGCGTTTTTTCTTTTCGTCTCTGTTGCACTTCAGAAGCTCTAAAAATGTGTAACACAACACGTTTCTTTGTTAGGATGCCTTAGAGAAAAATGGGTCAGCTCTGCACAGCGCTTCTTTTCATCTTCAGCTTCTGTTTGTAGCTGCACGTTGTGTTGTAATACCCTGTTTGATTTGTATTTTCTTATCGTTTTTGATATTTTGCAGTTGGGTTACCGAAGACACTAGGTGCACTTAGTGCCCTGCCAGACAGTGGCACAGAGGGGACAGGCATGCCTCCTACGCCAGGCCGACCTCCATCACAGAAGAAACGTAAGCCTGGCCGCAAGAAAAACAAACTGTCTGGGCCCTGGGGTCAGAAGGGAACACTTGGTTCTCAGACAAGCCTACCTGACAAAGAAGTGGAATCTATTAAAATCCCCAAGAAACGAGGTCCCAAACCAGGAAGCAAGG[T/A]AAAAACGATATTGAAAGACATTACAGATTCAAGTATTTCAGTAGTTGCTGGGGTCTTCATGTTTTGCAACAAGAACAGCTCGAGAAAGCAGGTAAAACAAAAGCAAAAGGCAAAAAAAAAAAAACAAGTAAATAAAATGTGGTTAAAATTAGGCAGCTGCAAGGGCTTTTCTTTTTCTGGATTGCTTTTGAAAACACTGTCATTTGAATTTTGGGAAGGTGGCGGGTGGGGGGATCGGTTGGTAGGTCAGTCAGTCAGTTGCCAACAGCCTCTGGTGGATTTACGTGAGAAGAGAATGTGGTTGGTCTAGATCGGATACGTGGCTGACCGGAAGTGCGATATGCGCATCAATATAGCAGCATTTTTTTATGACACTGTATAACAATAATTTATATTTTTACAGTACTGTGACGATTGGGTTTAGGGTTGGGGTGGGGGTAGACGTTAATAAATAAAATAAATGGGAAATTGAATAAATAATTCTCGTTAACTTCCGGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17669
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102181 | None | None | 120 | None | 4 |
ENSDART00000115339 | Essential Splice Site | 430 | 733 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 39542123)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 35616246 |
GRCz11 | 16 | 35569121 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGATGGACAATGCCACAATTCCCAAAGCYGCCCTACAGGCCCCTACAGG[T/A]ACTACTGCAWGYGTATATTTTCAGGTTTACCCTTGCAAAGAAGTATTCCA
Long Flanking Sequence:
TTGCCACCAAAACAAGAATTTACAAGACCAGAGTGGTAGAACCCTGATAGTATCATTAGTTTTCAGAGTATCGACTTGTGTTTGAATGTGTTTTTTATGTTGTCTTCTAGTTGAGCTGGGCTAAAAAGACAGCATGGCTTGAGGAAACAATTGGAGGTCCCGGTAGACCTATCAGCAAACCCAGAGGAAAACTACCAGCCAGCTGGACCCAGAAAGTGCAACAAAATCCAACTGATCCCATTAAACTCCCAAAAAAGCGAGGCCCCAAACCTGGCGTAAAGGTTCACATTTTCAACGATTAATCTTAGAAACCAAACGGACCAGCATAAGGCAGTGCTATTTATGCAAACTCCTCCTTACTGTCTCACACAGAGAAAGCCTCGATTGATACCCAACCCAATGCCCACCTCCCCAAGCAGTAGCACTCCAGAGCCGGACACCAGCTCAGTCCCGATGGACAATGCCACAATTCCCAAAGCCGCCCTACAGGCCCCTACAGG[T/A]ACTACTGCATGTGTATATTTTCAGGTTTACCCTTGCAAAGAAGTATTCCACTGTTGCATACTTGCATAACTTACAATTTTTCTGTTTCAGTGTGTGTGTACCTGAATAAACATGGCAATGTGGGTCCCCATCTGGATGCACGGCGTGTCCAGTCTCTCCCAGATCACTTTGGGCCTGGCCGAGCCTCCTCAGTGCTGCAGCAGTGTGTTCAGGCTTGTGTGGACTGTGCACATAACCAGAACACAGTTTTTTCCTGCCTAAAACCAGGCCATGGAGGTGAACTCATATCAGGTCAGCTTGCACAAACTACTATTACTGTAATTAAATAAAGCTAAAATGATTTTATAAATGCCACCAGATTAATTTTACTGCAGTTTAATAATTTAGAATACACTGTTAGACATTTCAAAGGGTTTTTACAGTAACTTACTGGCAACACTGTTGCCAGTAAGTTACTGTATTTTAGATTTACAGTATACAACTGTAAATCCGTTTACAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11528
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 |
---|---|---|---|---|---|
ENSDART00000102181 | None | None | 120 | None | 4 |
ENSDART00000115339 | Nonsense | 656 | 733 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 39533122)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 35607245 |
GRCz11 | 16 | 35560120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGACTGCTTTCTAGGTTCAGAGCGCTTTCTGAGCTYCAGGGAAAGCCCA[C/T]GACCCAGTGGACAAGACCCCAACCTATGGACWGTAGAGGATGTTATGCAG
Long Flanking Sequence:
CAAATTGAATTGACCGTAAGCATCTCGCTCAATAATATAAAGAAATAAAATAAATTCAATAACTTTCCAGTTTAAAGTTGGACTCTTCTGTCGTTACACTGTACTAAGGTCTACAGACAATGTAAAGTTGCTGTTTTTAGGTCAATATATCTAGGAGCTTTTCTCTCATTCCCAATGTAACTAAATAGGAAAAAAATCGGAAATAGGAAAAGGATCGAATTGCTATGCTATTGAGATGCTAATGGTCTAATCCTATTCAATGAATTATGCTAAGCTAAGCTAAGGTAAAAGTGCTCCCACCAGACCCAGAGATTGGCTGAATGGATGTAAAATTGTTAAATGTGTGTTGCTTCAAAACCTGGGGGTTAGGGATATTTGAACCTTATTCTTTAATGCAATTATGTAAACACCTTATGGATTAAAAACTGACAAAATTTTAACTGATGCCTTTTGACTGCTTTCTAGGTTCAGAGCGCTTTCTGAGCTTCAGGGAAAGCCCA[C/T]GACCCAGTGGACAAGACCCCAACCTATGGACTGTAGAGGATGTTATGCAGTTCATCAGAGACATCGATCCTCAACTCGGACCACACGCAGACCTCTTCCGCAAACACGTAAGTGAGGAATACAAAACAGTTTTATTATCATCTTACATTTCAAACAGAAAACTGGAAGTGCTATATAGCCTGATGTTACTATTTTACTTCAAAAAATGTTCCATATAATTTTTTTGTTATTGTACAAATAGCCACTGGCCACCACTGACAGTCTTTAAGGAGTAGTTCAACCAAAAACGGAAATACACACACTATTTACTCACCCTCAAGTGGTTCCAAACACAAAATAAGATATTTTTAAGAAAGCTAAAAACCTGTAACTATTTGCTTTCATTCTAGAACGAACTACAGGGTTCAACGCTAAGGATTTTTTCTACTGGCCCGATCGGGCCAAAGGTTCTGATTTTTACTTGCCCTGCCAAAATTTTCACTGGCCCCACCTAAAAAAAA
Associated Phenotype:
Not determined