ZMP
si:dkey-24l11.3
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100034462 [Source:RefSeq peptide;Acc:NP_001076531]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36666 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29046 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12363 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36666
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 |
---|---|---|---|---|---|
ENSDART00000098350 | Nonsense | 10 | 696 | 1 | 12 |
ENSDART00000147735 | Nonsense | 10 | 240 | 1 | 2 |
The following transcripts of ENSDARG00000068140 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 26838969)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26912224 |
GRCz11 | 18 | 26894602 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTACAGGGTGTTTGTCGATCTAATGGAGTCAGAAAGTGCGGGTGTGGCG[C/T]AGGTTAGTGGCTAACCTCAGTTAAACAACATCCACCAGTGGTTTTGATAT
Long Flanking Sequence:
TAGGGTACAGAAGTGTTTTGATGGAGGTGTCACGTGGATTGTGTTACTTTCCTCAGCGCTGGTCAGCACCAACCAATTAGACTAGCTTGTGATTACGTGGAAAATTTACTTTGACAATCGCTTAGTATGAATTACGGTTGCAGAGTTGGCATTTAATTATGTAGTACGTTTGGTACTAATTGATAAATTCGAATGATTACCGTTTTAAGTTCGCTAATTTCTCAGCCAATACAAAAAATGTATTGCTATTTGAATGCTTTTCTACAGAGGATTGGGCTTTTTGAGCCGTTATGACGACCCCTGGAGGAAGACGACGTTTAAATTCGCTTTTTCATGTAACACACACCTTCCAATCTTAGAAACTGGTATGTTATGCTAACGCAAAGGTAAACGTAGTCATTGACAGACAGCAACAGCTATAAGCACTGAAGTATTGGACAGTTTACATTGACTACAGGGTGTTTGTCGATCTAATGGAGTCAGAAAGTGCGGGTGTGGCG[C/T]AGGTTAGTGGCTAACCTCAGTTAAACAACATCCACCAGTGGTTTTGATATGTTACAATTCAGAACATTGTTAGTGGCAATTCATACAATCACCAGCACGACTAATCCGAAACTACACAGTGTTTTAAACAGTTACATTTCAAGTTTAACAGCACTTCCTGATCCCAAATTGCGTATTGCGATGTTTGATTCTTCAGTGAGTTGTGAATCGAATCTTTTAGATGAATTGTTTGAATGCGTTCATTTCGATCTGCGTTAGAAACACGGGATGCTTAAGACAGTTAATAAAAATGTTAAGTAGTATAAACGGGAACACATTGAAAGGAAAATGTATGCTTTAAAACTCTGAAAGAATTGTTTTGCAATATGTTTCACTTTCGAAACACTCGAAACACCACCTGCTGGACAAAAGCGCGTGACTGCAAGACTGCCTTAAGGTTTATGGTAGCCCAGACTTGTATAAAAGTTATTCAATTAAATGTAATCTAAAACATAACTACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29046
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 |
---|---|---|---|---|---|
ENSDART00000098350 | Nonsense | 62 | 696 | 2 | 12 |
ENSDART00000147735 | Nonsense | 62 | 240 | 2 | 2 |
The following transcripts of ENSDARG00000068140 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 26836084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26909339 |
GRCz11 | 18 | 26891717 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGGCTGAACGGGTGCAGCAATTGTGTCGCTTCTACTCTCAGGGCAGG[C/T]GATGCTATTATGGAAAAAGGTGCCACTTTCTTCATCAGAGAGCTTCAGGT
Long Flanking Sequence:
TCCCAATGCTCTATTCATTGCAGTTGAATGCAGAGCACGTTTTACCCCTCATTAGAGCTTTACAGTTACGCATTGCTGCTTAAAAATGTTATACAATATTACAATTAAGCACTGTAGGTGTTTTGTGCTTCAACTCGCTTGCTTCAGTGGCCGGTTGAACTTTAGTTACCCATAATTATGTAAAGTTAATTGCTCATTATTGTGGGAATGCGGTTTTAAGATCCAAAAGCCTCTTTCGTTAATTCATAGCTACGACCTCAAAAACAATTCTGCATCTCCCATTAAAACTGTGCTGCATTTACAGTTAATGATATGCTAAGACACAATATATGTTTTGTGTTTTACAGTCACTAGATCCTAAGGATGAACCAACAACTTCACCAGTGTCAGTTGACACTAAAAAGGAAAACTCAGGCCGTGATACTGAGATAAGCAGCAAAGATGTTTCCCAAAAGGCTGAACGGGTGCAGCAATTGTGTCGCTTCTACTCTCAGGGCAGG[C/T]GATGCTATTATGGAAAAAGGTGCCACTTTCTTCATCAGAGAGCTTCAGGTGCACCAAAAGATGGAGAAAATGGTACATCTCATAAGGAGAAAGAAGCAAAAGAGCCACAGCAACAGCTAAGTGAAAACAGCCAACCCACTACAGAAGATCTTCCACCTCCATCTAACCATAAACCTGCTCCTGTGAGGCAACAGAGAGCCAGAAGACCATGTCGCTACTTCCTCTCAGGGTTTTGTGCTATGGAGGATCGATGTCGTTTTTTGCATCCACAAGAGTTTCCGCCGGTGGAGGACAAACATCAAGGTCCGAAAGAGAGGAGCAGCTTCAGGCCTAACGCTCCAGCTATGCGTCCCGCTAAAAGTCACGAGCAGGTCAAACTGGCTGAGCTCACAGAAGAAGTCTGCAAGCAGCTGCGAGAAACGGAGATCGCTCAGCTGATGAAGAGATTCCCCAAAGACAAGCTCATCATCCAGGAGCGAGAAGATGGACAGCTCACTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12363
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098350 | Essential Splice Site | 636 | 696 | None | 12 |
ENSDART00000147735 | None | None | 240 | None | 2 |
The following transcripts of ENSDARG00000068140 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 26814478)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26887733 |
GRCz11 | 18 | 26870111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RATGGAGCTGGCCACCAGAATGATYTGCGGTTACTGTGCCAAAGAGCAGG[T/G]CAGCGACAGAAACTCCCTCAGACCGACTGAAGCAGGATTAYATTCACCYC
Long Flanking Sequence:
TATAAGCAGGATAATTGACTCTGGTCCATTAAATTATTCCTCTCTTCATGTCGTGGCATCATCAACACTTCAGTTGTGTGTTATTTTCTGATAATGTAATGGCTTGTCATCAGTTATTCCTTATGTACTGAATTTACAGGTGCAGCTGGTCAATATCCTCGACGTTACAGGGACCCTGCAGTTCAGCAAGGAAAACCTCTTCCTGATAAAGGTGCCTGCAAGCATTTTAAACAAAGTCACCGGTGGCTAAGGTAAATATCAGAACAATGCGCTGGCTATAAGAGGTTTATTTTCTTGCTGTGTGTACCACATGTTGAATTTGACCTACAAAATGCCCTTGGCTCAGATTTAAGGCTTCCATCTTGCATTAACGGTCTGTTCCGCCAGATTTCCATGCTGTGGTCGGGCATACCCGTGCGACGCATGCCATGATGAAGACCAGGACCATTTAATGGAGCTGGCCACCAGAATGATCTGCGGTTACTGTGCCAAAGAGCAGG[T/G]CAGCGACAGAAACTCCCTCAGACCGACTGAAGCAGGATTACATTCACCCCAATCCCCCTTGAGCCAGATATTCTATTGAAATTAGATGCCAGTTAGGCAGGTTTTCCCGTTTGTTAAACCTTTGGAAATATTACAACACTCAGGTGCAACACTTGGAATTTGACCCACATTTTGCATAGACAAAAACATGAGACATTTGTTGCAAAAGAAAGGACAAAGAATCTCATGTGGTTTTGGGGCAAAGCAGTGAAATCCAGATTTTAAGTTGACCACAAATCAGTCCAACAGTTTATCATAGAAAAGTATTGGTAACATTTTAAAACATGCTTCCACAAGTCCACATTATGAAACAAACTAAAGACACAGTTCACCAAACACTGATTTGCACCACTGACAAAATGTTTTCCCCATTCTATGGAAGTCAGTAGGGGACCAGTAACAGTTTGGTAACCCAGTTTTCACAATATCTTCTTTTGTGTACAGCAGAAGAATGAAACTCT
Associated Phenotype:
Not determined