ZMP
si:dkeyp-114g9.1
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC555399 [Source:RefSeq peptide;Acc:NP_001037797]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11088 | Nonsense | Available for shipment | Available now |
sa17018 | Nonsense | Available for shipment | Available now |
sa17559 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11088
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 |
---|---|---|---|---|---|
ENSDART00000100967 | Nonsense | 271 | 529 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 42011725)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 42082884 |
GRCz11 | 20 | 41979994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGGCTCTTCACATACTGGTTGTTTCGCCAGCCCACTCCATACAACAAG[C/T]AGCTGCGCTCTATTTTCCTACAGTGGAAGAAGCACAGCAAGAGAAAGGTG
Long Flanking Sequence:
CTCATCTGCATTTTGGCTGATCCAAAAAAAGAGATTTGTGATCCATTACACTAGTAGTAATAATACTCCTGCAAATATTATGTTTGGGTTTCTTTGTTACAGAGCTTGAGTAGTTGTCTGCATATAAATTAGATTGATTTTCATAACCTAAGGTAACTAAAACCGGGAAAACGAGTATTGAATTGGGATTTGATATTTATTACTGGTACTCGATTTCAAATAATTGAAATCGCATGTTGGTTAAATACAGTGCATTATTTTACGAATTCTTAATATTTTACTGACGTGAATTTTTATTTATTTACTTATTTATTTACTGGTTTTTGTTTTCTACAGTAAGACAATTTTGAATTGTCTACTGTATTATTGAAATGGACTGATTTCTTGTGCTGATTTTAGATCACACAGAGCTGGAATCCATGTACCATCAGTACGTCCAGTGCAGGTTCCAGTGGCTCTTCACATACTGGTTGTTTCGCCAGCCCACTCCATACAACAAG[C/T]AGCTGCGCTCTATTTTCCTACAGTGGAAGAAGCACAGCAAGAGAAAGGTGTCCACCTGGGGAGAGACCCTGTGTGACGTGAGGTATCTGGCCTCCCTGCATCCCATCACCAAAGACTACTGGAGAGGACGATTGGCTCGGGGAGATGAGAGTCTGGGTGAGTTGTCTGCTGAAAATTAAATCAATTTTTAAATGCATTGTGATTTATTCTTAATTTTAATCTTCAAATATTACCAAATAACTTAGCCCAGTCCTGACACTACTGCCATTTAATAATAATAGTAATTAAAAAATAATGATTATAAATAATACTTATATCCTTATCAACAAACTATAAAATCAGCATTGTTTTGGTGTGTATTTTATTAGCAACGAAAATAACACAATGACAGTATTCTTATAGATGTAATAGATGCTATTATGCTATTAAATAAAACTATCATTATATTTGATAGCAAATATTCTTGCTCTCTGATTTTTTTTTCTTTTTATTTAATTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17018
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 |
---|---|---|---|---|---|
ENSDART00000100967 | Nonsense | 413 | 529 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 42007731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 42078890 |
GRCz11 | 20 | 41976000 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACYGCAGCAAACTRCGTCAACTGGAAGATGATCGAGACGCTCCCTTACTA[C/A]AAGTCAGTACTCATTCATCTGATATAACAACACTATCTCACATCAATTST
Long Flanking Sequence:
AATTATTACATTTTATTTTTTATGTTTAAATTATTTTTTATATTTTATTTAATAGTTTTTTTATGTATTTATTTTTCAATGTATTTTTTATTTATTAAATATAAATATAGTTTATGTATTTTATTTAAGAAAGTTTATGTGTGTGTATACATGTATTATTATTATATATTTTATTATTATATAAAGATAGTTTTTACAATACCGTATTTTTTTTATGATGTTCCCATTTTACATTTGGGCCTGTTCCCTTATTCTTTTAGGCTCTGATTGTGAATGAAGGTCAGTTCAGTTGTAATATTTGGTTTGCTGTGACATTGCCAGGTTTATGAAGACACGCTGGAGGGAGTGTATCTTCTGCTCAGGCGAGAGATGCAGGAGACTCTGATCGAGCACGAGCGCTTCTGGCAGGTGGCTAAAGTCCAGATGAGCCGCGTCTGCACACTGGAGGAGACCGCAGCAAACTACGTCAACTGGAAGATGATCGAGACGCTCCCTTACTA[C/A]AAGTCAGTACTCATTCATCTGATATAACAACACTATCTCACATCAATTCTGAACTTTTTGGTGGCTCCTTTTGAAAACCGTAAATTTTTGTTTAACTGAACTTGTATGAATTTATATGAATTAGCCACGAAACTGACAAAGCGAAATAGTTCTGTTTCCTCGGGAGATTGGGCTGAACATTATGCTCACTTTTTGCTCTTTTTCGTTCACTTTCTTTTTGCATCCTAAGTATACAGAATTAGGACTGTTTAAAATGTCCATTAAGCAAATGGCCACATACACACTCACAGGCCACTTCATAGGTTTTCCCGTCCAACGACTTGTTAACTCAAATTTGTAATCAGCCAATCACATGGCAGCATCTCATTGCATTTAGGCATGTTGACATGGTCAAGACGATCTGCTGCAGTTCAAAGAGAATGAAGAGAGCAGTTCAAACGATCTACTGCAATTCATCAGAATGGAGAAGAAAAGTGATTTAAGTGACTTTGAACGTGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17559
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100967 | Nonsense | 512 | 529 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 41999540)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 42070699 |
GRCz11 | 20 | 41967809 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTATCTGGAGGAGCTGAAGGCTATGGTGCTGCACTGTGCTCGGGTCTG[T/A]CTCGGGCAGATCTCAGTCAGCTGGAACTCWGCAGACTCACCACACACACG
Long Flanking Sequence:
AAGGTAATGCATAGAGTGAAATACATGTTGGATCATTGAAAGTTTTAAAATTACCCATGTACAACATGGACATGTACATAAATTAAAAATCTTAATGTAATTAACAAATGCTTATCTTTTTATTGTTTCATTTCAGACTCCTAGTTCATATGCAAAAACATCACAAATTACAAAAAACAAATACAATACACTTGGTTAAATTCAGTCTGTGGTTTAAAAGAAACTACTCTTTCTCACTGTTGAACACAAGATTTTTTTTGAGAAATGTTGATTTTAGAACAGTAGTTTCTAGATGTCAAACCTGCAATAATGCAGCACCTCAGCCTTTGTTAACAGTGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGCAGAGAGTTTGCATGGGGACTCAGTGTGTGCTCAGCTGAGTCGAGTGATGTGGCTGTATCTAAACTCAGGTCAGCAGGAGTATCTGGAGGAGCTGAAGGCTATGGTGCTGCACTGTGCTCGGGTCTG[T/A]CTCGGGCAGATCTCAGTCAGCTGGAACTCAGCAGACTCACCACACACACGCTGATCTGTTTTTACTTTAATATTTTTACATTTTTAATCGTGTTTTTTGGCCTCAAATATCTACATCTTAATTGTTTTTGAACACAGAGTAGTTTTCCCCCACAATTTCTTTTCATTCAGGCTTTTTTTAGTGCACAACTTCTCTCATCTTCTGTCTGAGTAAATGCAGAAATGCACATGTTTTTTTTATATATATATATAAGTGCAATATGATAGTTTTAATCATGTTTTCTTTAGCATGTTGATTGTGGATTCCTTTCGATGTAGTTTTTAAACAATGGTTGTTGGTTTTATAAGTGCAATACAGTGGTTTTAATCTTGTTTTTAGCATTCCGAAATGTGAACTCCTTTCTGTGTTACTGACTTTTTAAATTATTTTTTTAAACATGGGTTAATGGTATTATGATCTGCAAGGTTGCTGATTGATAAAAGCAACTTCACACCTGTCTG
Associated Phenotype:
Not determined