ZMP
zgc:66419
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC394086 [Source:RefSeq peptide;Acc:NP_957405]
Human Orthologue:
HOOK2
Human Description:
hook homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:19885]
Mouse Orthologue:
Hook2
Mouse Description:
hook homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2181664]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45132 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa39997 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33094 | Essential Splice Site | Available for shipment | Available now |
sa39998 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45132
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057434 | Essential Splice Site | 15 | 268 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 8299904)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 7877320 |
GRCz11 | 3 | 7763160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCATGAGCCTGAATAAACATCAGCTGAGCGACTCTTTATTTATCTGGG[T/G]AAGATATAAACCCATCCCGCTGACAAGCAGCTATATTTAGAGGGTGTTTG
Long Flanking Sequence:
ACGTTAAGAAATGAAGGGGTAAAAACATTGTGGTAAATGTGAGTGCTTGGCTGTTGTTGGCTTGCGTCACCTAGTGGTCACATTGTAGAAATAGTAAAGTGATTTTTAGTTTATCTTTATATATATANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATATATATATATATATATATATATATATATATATATATATATATATATATTATTGAAAGTTATTCCTATACATCATCAAATTCCTAAATACTTTAAGAGCGCGCGTCTCTCTATTGCTATGGCGACGACGCTGCCAGTGCAAATATGTGCGTCGGTGACGCGTCCAGCTCTTGAGTGCGCGCATTTAGCAGCGCAGCTAGTGTGCGTTTCAGCACGAAGCGGCACCATGAGCCTGAATAAACATCAGCTGAGCGACTCTTTATTTATCTGGG[T/G]AAGATATAAACCCATCCCGCTGACAAGCAGCTATATTTAGAGGGTGTTTGTTTGTGTTGAAAAAAGAACGAAGTAGTTTGTTTGTGTTTAGCGCGCTAGCCTGTTAGCAGCAGCAGGTGGAATCCACACAGATTTGACACACTTTTAATTATATTGAAATAAATCGCTGTTTTCTGGGGATTATACACGTGTAGATCAATCAGCCGGTTTTATTAGTGCTTTGTACGAATATCCAGCACGTGTGAGAGTGTGTTTGTTTGCTGTGTCAAAGTCATTACGTAACTGATCAAAGGTCTTAAGAGTTTAGCATATGTTACAAGCTATACTACTAAGGTTTTTATTTATTCATTTATTTATTTATTTTGTTTATAAAGGTTTATTTCTGAAGATTTTGATGTAAATTGTTCCTTCTGTGATAACCAAACTGAAGATCCGTCTCACCTTTTTTTGGGAGTTGTGAATACTCCAAAAGTTTTTGCAAAAATGTATTAGAGGTATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39997
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 |
---|---|---|---|---|---|
ENSDART00000057434 | Nonsense | 64 | 268 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 8312099)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 7889515 |
GRCz11 | 3 | 7775355 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAATGAGACTTGGCTCAGCAGGATAAAAGAGGATGGAGGCACAAACTG[G/A]AGGCTGAAGGTATTTTACTGGAGTTGTAGTCTTTCTGTACTGTATACTGT
Long Flanking Sequence:
GTGTTTTACAGCCGTGGAGATCAGCGGGTCTGTTTATAAGCAGACACATGAGCGATCTGTTGATGAATCGACTGCTGTTCGCGGCTTTAATACACGACAGTGTCTCGTTTTCTGTTAGCGGTGAACTGATGAGCTTTACAGCCAATCACAGTAATTTCTGTTGAACTTGTGAGCACAGTGGCAAATCATCTGTGTTTAAGGACGCGCTCAACAGTGCTCAAATCTTAGCTGGAAATTGACGTTTTTAAAATTACAGTATCGTAATTCAGTATCGTGACACTTCTCTCTTTCTCGAGTACTTTTAAGGGCTACTTTTTGCTCATTCTTGGAGTAGTGTTTACAACAGATTCGTTTACCCGCACTACATTTGTTGGGAAAGTAATTGTGCTTTTACTTGAGTATTAGTAGTTTGGAAAGTGTTTTTTTTTGTCCTTCAGAGATTCTACATGGTTTAATGAGACTTGGCTCAGCAGGATAAAAGAGGATGGAGGCACAAACTG[G/A]AGGCTGAAGGTATTTTACTGGAGTTGTAGTCTTTCTGTACTGTATACTGTATGTTGATGTGTTTTAGTGAACATGTGTATATATACTCTGACAGGTCAGCAACCTCAAGAAGATCCTCCAGAGCATGATGGAGTATTATCATGACGTAAGTGTGGTTTATTTCAGCATTAACCCTATTGTATACTGTATTTTTTCCCTCAAAAAATGGCAGTTGAACAGAATAATAAACACACAAACACATGAATGAACAAAATATTTGTAAATGCTGAATGTTGGCAGTCAGTTTATTTTTTATATTTTATGTATGTACAGTGTATCTGGAAAGTATTCATAGCGCTTCTCTTTTTCCACATGTTTTTAATGTTACAGTCTTACTCCAAAATGGATTCACTCCATTTGTTTCCTCAATTTTACACACAATGCCCCATAATGACAATGTGAAAAAAAGAGTTTTTGATACTTCATACTTGATACTTCAGAGTGCTCTTGACCTCAGACCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33094
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 |
---|---|---|---|---|---|
ENSDART00000057434 | Essential Splice Site | 67 | 268 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 8312110)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 7889526 |
GRCz11 | 3 | 7775366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGCTCAGCAGGATAAAAGAGGATGGAGGCACAAACTGGAGGCTGAAGG[T/A]ATTTTACTGGAGTTGTAGTCTTTCTGTACTGTATACTGTATGTTGATGTG
Long Flanking Sequence:
CCGTGGAGATCAGCGGGTCTGTTTATAAGCAGACACATGAGCGATCTGTTGATGAATCGACTGCTGTTCGCGGCTTTAATACACGACAGTGTCTCGTTTTCTGTTAGCGGTGAACTGATGAGCTTTACAGCCAATCACAGTAATTTCTGTTGAACTTGTGAGCACAGTGGCAAATCATCTGTGTTTAAGGACGCGCTCAACAGTGCTCAAATCTTAGCTGGAAATTGACGTTTTTAAAATTACAGTATCGTAATTCAGTATCGTGACACTTCTCTCTTTCTCGAGTACTTTTAAGGGCTACTTTTTGCTCATTCTTGGAGTAGTGTTTACAACAGATTCGTTTACCCGCACTACATTTGTTGGGAAAGTAATTGTGCTTTTACTTGAGTATTAGTAGTTTGGAAAGTGTTTTTTTTTGTCCTTCAGAGATTCTACATGGTTTAATGAGACTTGGCTCAGCAGGATAAAAGAGGATGGAGGCACAAACTGGAGGCTGAAGG[T/A]ATTTTACTGGAGTTGTAGTCTTTCTGTACTGTATACTGTATGTTGATGTGTTTTAGTGAACATGTGTATATATACTCTGACAGGTCAGCAACCTCAAGAAGATCCTCCAGAGCATGATGGAGTATTATCATGACGTAAGTGTGGTTTATTTCAGCATTAACCCTATTGTATACTGTATTTTTTCCCTCAAAAAATGGCAGTTGAACAGAATAATAAACACACAAACACATGAATGAACAAAATATTTGTAAATGCTGAATGTTGGCAGTCAGTTTATTTTTTATATTTTATGTATGTACAGTGTATCTGGAAAGTATTCATAGCGCTTCTCTTTTTCCACATGTTTTTAATGTTACAGTCTTACTCCAAAATGGATTCACTCCATTTGTTTCCTCAATTTTACACACAATGCCCCATAATGACAATGTGAAAAAAAGAGTTTTTGATACTTCATACTTGATACTTCAGAGTGCTCTTGACCTCAGACCGGGGTAACAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39998
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 |
---|---|---|---|---|---|
ENSDART00000057434 | Nonsense | 178 | 268 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 8336356)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 7913772 |
GRCz11 | 3 | 7799612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAACACTCTCTGACAGTACTGTGTGTGTTACAGAAGCTCATTTCTGAA[C/T]GAGACACACTGAGAGAGACGACTGAAGAGCTGAGGTGTGCTCAAGTCCAG
Long Flanking Sequence:
CTTATGATTTGTCTGAATGATTTATAATGATAATAATAGTGTTTAATATTATTTTAAAGGAAATACTTAAATATTCATAATGGAATACAAGTTTCACCGGAGGATGAATAAGTCTGGCTTCAACTTCATGTGCTAAATTTAAAGTATGATTATGATTATTTTTGTGAGATTTACTTGAATGTTTTTAATGCATGTTTGCAGCAATGAAAATTGAGTGTAATTTATGATATAGTTGTTCAGAGAGCATCTTCAGTCGAATCCAATAAGCAAATAAATGATGAGTGCGGTTGTGTGTGCACCTCAGGCTCATGAGATGAGCGCTAAACACTCAGCGGAGGCCATGAAGGCGGAAAAATGGCAGTTTGAGTACAAGAACCTCAACGACAAATACGAGACCCTGCTGAAGGAGCGAGAGGTACGAAACCAACACTTACTGTGATAAGAACTGTGCTGAACACTCTCTGACAGTACTGTGTGTGTTACAGAAGCTCATTTCTGAA[C/T]GAGACACACTGAGAGAGACGACTGAAGAGCTGAGGTGTGCTCAAGTCCAGCAGCAGTGTTTAACAGGTCTCTCACACACACAAGCTACACCCCTCGCTCCTCCTCCAATCAGCTGTCTCCCTAAGAATCACAAGCCCCGCCTCCTCTTTTCTCTTCTCCAGTCAGCTCTCTGGTTAGAAAACACAAGCAACATCCTCTTTCACTCCTCCAATCAGCTTTCTCCCTAAGAAATATTGGTCCCACCCCCACACTCCTATTCCAATCAGCTTTTCCCTTAAGAAACACAAACCCCACCTTCTTTTACAATCAGCTTTCTCCCTATAAAAACTCAAGCCCCACCTTCTTTCACTCCTTCAATCAGCTCTCTCGCGCTAACACAAGCCCCGCCTCCTCTCACTTTGTCTCCTGTCAGCTCTCCCCCTAAGAAACACAAGCCCTACCTTTTTTACACCTCCTCCTGTCAGCTCTCTCCCCAAGATAAACTAACCCCGCCCCCTTTT
Associated Phenotype:
Not determined