ZMP
si:ch211-223m11.2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC558615 [Source:RefSeq peptide;Acc:NP_001038334]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23652 | Essential Splice Site | Available for shipment | Available now |
sa10977 | Nonsense | Available for shipment | Available now |
sa43399 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18263 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23652
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 |
---|---|---|---|---|---|
ENSDART00000104032 | Essential Splice Site | 7 | 890 | 1 | 21 |
Genomic Location (Zv9):
Chromosome 20 (position 14028831)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 14218077 |
GRCz11 | 20 | 14114057 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTATATACACTTTAAAAGAATCCAAGAATGAGGTGCTTTGAAACAGGG[T/A]ATGTGTGGGGATGTTTAAATATTAAGGTTTGGACCACGAGGTGTTTTGAT
Long Flanking Sequence:
TTTTAAATATTTTAAATATAGGCTATGTTAACATTTTATATGTGTGATACGAGTCAAAGCATGTTATTGAGAAGCAGTCTTAATAAAAATTTATATTTACAAAAATATCCGCATTATCTTCTTACACATAATAACTAGAATAAACGATCAAACAGAACTGTCAAAAAGTGAGACAACTTGTGCAAATAAAACCAAAAGATCACATACCCACGAGTCCTCAGCTCTTTCGCTTCTTTCAGCACGTCTGTTTTAACAAACACAAAAGAAACGTTCACTTCATCAATAATACATGATCGGTTTGAGTTAACCCTCAAAACTCCACACCTAGTTGGACGGAGCTGTTGGACCTGCTCACCTGTTTGCAATTTCGCGCAATCAGACGGAACGCGCGTGCGCACTAATTACCTCTCTCATCCCTCTCGCGTTTGTGTAGAAAACATAACTTTGACGGTTTATATACACTTTAAAAGAATCCAAGAATGAGGTGCTTTGAAACAGGG[T/A]ATGTGTGGGGATGTTTAAATATTAAGGTTTGGACCACGAGGTGTTTTGATTATTATTTTTTTCATGTTTGTAGAGCTTTATGGCTTATGACCACACTAATAAGTACGTTTGCGGATACCTTTGAAGGTAAGCCTTACTATCGGTGTAAAATAGCTTGAGTCAAGTGTGTGTAATAAACTTAATGGATGCATTTCTTTGATTGCAGAAATTCAAGCTGAATGTCTTGGAAACCGGGTGCAGTTTACCCTCCCTGGTTCTTTGAGTCTTCTTGAGGTTTATGCAGTCAGTAAGTTGATTGACCTTTTGCCTGCGTGCCAGTGAGTTTAATACACCCAGCACTCAATTCAGACCTGCTCTGGTTGTTTCAGATAACACCCAGACAGTCCTTCTCACACCTTTCCTGGCGGCTCAGTGTGGATACACACAGAAATCTGATCCCTGGGGCAATATGATAGTGTCAGCTTCCCTACAGAGCTGTTTTGCAGAGAAACAGGTTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10977
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 |
---|---|---|---|---|---|
ENSDART00000104032 | Nonsense | 327 | 890 | 10 | 21 |
Genomic Location (Zv9):
Chromosome 20 (position 14020635)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 14209881 |
GRCz11 | 20 | 14105861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATTGACTAACCTGWTTTAATTACAGAGCCATACTCTTAAGGATCAGTA[T/A]CATMTCAGTTACACCATAGAGCCCATGCTTGAGTTACTGTGGCRGGAGGG
Long Flanking Sequence:
GTCATATGGGGATATCAAAGTTGGTGTTGACCAATCTAATGGATCCAGATCCATTTTTATTTTTTTGCCATTCTCAATCCGAAATTCTTAGCAACATTGCTCTAAAAGTTGTACTGTTCATCACCTTTAGGTCATTTAAGCAAGACAAAGAATTGACTCCCAAATTTCTGTTTGACTGATTAAATTTCAGGTGGAGCTTCTGTTGAGGGGGACACTATTTTTTGGCGCCTTCCTCTGCGCATAACTCCATTGGTGTCCTCTGAATTTGAAATCCTGGAGGTGCATATGGGTGTTAATGGCAGAAGGCTAACACCCAATGAAATGGCCAGCCACAGCTATAACATGAGATTAACAGAATCCCATGTAGTTGTTGGGATTCCCATCGGGGCACCTGATGGATATTTCAAGGTTGAGTTTTTTTAACTTGTCATTTTTGTGTTTTGCTTGATTAAATTGACTAACCTGTTTTAATTACAGAGCCATACTCTTAAGGATCAGTA[T/A]CATATCAGTTACACCATAGAGCCCATGCTTGAGTTACTGTGGCGGGAGGGAGTCGACAAGACCAAATATACAGTCTTGTTCCCCATGACCACTCCTTTGACACCATGGCCACCTCAAATCGCAGACAGTGAGTGTTGTTTTTTGACCAGAACAGATTGTTTTACTTTATTTGTCAGTATGCTTGTTTTTATGCGATCAGAAACTGAACCCGATCAGAAGATGTTTGATGTGTTTTTGGGGTACTTCCTACCTGATGTGGAGCTGCTGAGTGTCACCATTGGCTCTGAATTGATCACTGTTCCGGAGCTCATTTTTAAAGGAATTGTGCTACAAGAGCACAGCTTCCCCAATGATACAAAGGCCTTTTCTCTTCAGATTCCCTTCTCTGAACCACATGTCCAAATAAAGGTATGTATTTTAGTTTTGGTTCAGGAAGCCTTTTTTAATTTGGCATGGGTTAATATACTGTAGTTGTTTCAATGCAGAAAGTTCACCTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43399
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104032 | Essential Splice Site | 440 | 890 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 20 (position 14020151)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 14209397 |
GRCz11 | 20 | 14105377 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCTTTTTTAATTTGGCATGGGTTAATATACTGTAGTTGTTTCAATGC[A/T]GAAAGTTCACCTTGATAAAACAACCTACACTCTTCCTGTTGTCTTTGGAT
Long Flanking Sequence:
CTCTTAAGGATCAGTATCATATCAGTTACACCATAGAGCCCATGCTTGAGTTACTGTGGCGGGAGGGAGTCGACAAGACCAAATATACAGTCTTGTTCCCCATGACCACTCCTTTGACACCATGGCCACCTCAAATCGCAGACAGTGAGTGTTGTTTTTTGACCAGAACAGATTGTTTTACTTTATTTGTCAGTATGCTTGTTTTTATGCGATCAGAAACTGAACCCGATCAGAAGATGTTTGATGTGTTTTTGGGGTACTTCCTACCTGATGTGGAGCTGCTGAGTGTCACCATTGGCTCTGAATTGATCACTGTTCCGGAGCTCATTTTTAAAGGAATTGTGCTACAAGAGCACAGCTTCCCCAATGATACAAAGGCCTTTTCTCTTCAGATTCCCTTCTCTGAACCACATGTCCAAATAAAGGTATGTATTTTAGTTTTGGTTCAGGAAGCCTTTTTTAATTTGGCATGGGTTAATATACTGTAGTTGTTTCAATGC[A/T]GAAAGTTCACCTTGATAAAACAACCTACACTCTTCCTGTTGTCTTTGGATTCACTGTCTTGCCTGATCATTCATCATTTTCACACTCGGCAGAACTAGAAACGTCTGTAACTGACACTGGTAAGACCTCTTGACTGATGTGAGAACTATAAAGATGTGCCATGTCTTGCTCCTGAATATTTTCGTTTGTGTCAAGGGGTCACATTATGGCAGGTTGGAATGATCCATATAATGGAGTTATGCATGTCACATTTCAGGATTGTTTCTAGTAAAGGGTTTAACAATCGTTCACCCACAAATAGAAATGTTCTTGTAATTTTCTCATCAAGTGGTTCTAAACCTTAAAGTGATTTTTTTTCTTCTTCTGTTGAACAGAAAATAAACTTTGATATGCTGATTCTTTTTTCTTCTTCTTATTTCCTTGTTTCTTTTTCACTTTTCTTCAACTTCTTTAACATCTTCAATTTTTTTTTTCCCCTTGCAGTACTTCCAAAAGCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18263
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 |
---|---|---|---|---|---|
ENSDART00000104032 | Nonsense | 639 | 890 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 20 (position 14018671)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 14207917 |
GRCz11 | 20 | 14103897 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AARACCACTTTGCTTATTTTCGCTATAATGTCAMCAGTTGTGGAACCACW[C/T]GAAAGGTACATTTGTGGTACAAGGGGACTTGTCAAGTACTTGTAAAGCWG
Long Flanking Sequence:
TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTGCGCAACGCATAAATGCATATTTGTTTACTATAAAATTTTGTCTTAAGACTTTTGATTTGATTTTTTTTCCTGTTTTTGAAGTCAGTTCAGTTGACTGGAATTGAAGGAAGAATTGATGTGAAAATGTACAATTCCATGAATAACTGGAAATTTAATGATGTCTCCCTTACATGCACCTTTTTGGTAAAATTATCAGGTAGGTTCATATCTTGTCTGTCTTCCCTGATGATTTCTTGTTGCTAGTTTGCAATAGTGAGTTTCTCAATCTGTTATTGTACCAGAGTGTTTTCCTAATGGAACGGTTACTGTGGTGCTTCCCAAACTGGAATCGGTGCAGTATCTTCCCGGTGAACTTTCTTTAAGGGACCCCACTTGCAAACCCTACTACAATGAAGACCACTTTGCTTATTTTCGCTATAATGTCACCAGTTGTGGAACCACA[C/T]GAAAGGTACATTTGTGGTACAAGGGGACTTGTCAAGTACTTGTAAAGCTGTGGTTACTAACTCTGTCTTATTCAGTTTGTTGAGGACACCATGATATACGAGAATGAAATCACCTCGAAGACTGATCCTTTGCCTCAGACTTCTGAATTGGAACCTGAGCCAGAATACAGGTTAGGAGCTTGAAATTGAGTTTGATTTATTTACAAAGGACATTAAAAAAGCAGGTTTTGAGGTCATTATTATCAAGTGTTTAACCCAGAACAGAAACTAATCTACTTTACATAGAGTCCATCAAGTTGATCATTGTCGCCTGTGAAATCTTGGTTTACTCTTTAATGGTTGTTCGAAGTTGCTAGATATTGGCAGAAACTAGAACACACTGTTGTATATGTAAATCCCAAACATGCTCAATGGTTGACATGTCCGGTGAGTTTGCTGGCCATTCAAGAACTGAGATGTTTTCAACTTTCAGGAATTGTGTACCAATCCTTGCAACTGGG
Associated Phenotype:
Not determined