ZMP
si:ch211-200p22.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to phosphatidylinositol binding clathrin assembly protein (Picalm) [Source:Uni
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14566 | Nonsense | Available for shipment | Available now |
sa26944 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14566
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 |
---|---|---|---|---|---|
ENSDART00000028566 | Nonsense | 622 | 648 | 22 | 22 |
ENSDART00000146104 | Nonsense | 561 | 587 | 17 | 18 |
The following transcripts of ENSDARG00000029170 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 24926205)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23487957 |
GRCz11 | 7 | 23759114 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGTTCCTCCTCAGCTGGGACAGATGGGAGGGGTTCCAGTCATGACCCAA[C/T]AACCCATGTTGTACAACCAGCCWGTTCTCAGACCCACTAACCCTTTCACA
Long Flanking Sequence:
ATCAGTTATTTATATATTTTCTTGCTCTAGTGTTGTGCAGTGTTGCATATACTGAGTGGACCAACCCACACATCTGTGCAGGCGAATTTACGTCCACCTGCCCTATAATTGTTGGAAATGAGTGTAATTAAAGATGATCTTTAAATGAAGCAAACATGATTAGTGAACCCAGTGGTGTTGAATTAGTACAGGAGTGTTTGATCAGAGTCTCATTGTTCACTTGATCAGTGCAGGGTTGTTTGATCAGTCAGCGTGACGAGGGTTGATTTTGTTGTGTGTTTTTTTTTTTTCTTTGCAGGCTCCTGCTCCCATGGCGTTTCCCATGACAACACCTCAAGTGCCTGTGTATGGAATGGTGAGCTTACAGTCACTACATGAATGTTGTGTACTCGAATTGCATAGTCAATAGCACCTCATAAAAAGACTGACTGTGGTTTTTCCAACGGGTTTAGGTTCCTCCTCAGCTGGGACAGATGGGAGGGGTTCCAGTCATGACCCAA[C/T]AACCCATGTTGTACAACCAGCCTGTTCTCAGACCCACTAACCCTTTCACACCCATCCCTGGAGCCCAGGTACTCATACAAACACACACCACCTGTGTCACACTCAAATACACTATGCTACATTATTTAATCTATTACTTAACAGTCTGAAAACGATGTAATATTTTAATTAAATGTGTTGCTGTCATGTTCCACATAAAAACATACTATAGTAATTTATAGTAAATAATATATATTTTTACCAGGCTTTTGTAAAGTTATATTATAGTATTTATGACACAGTTAATACAATGCTGATGCCTTCATTAACAGTAAACTGATAAACTGTAATAAGTAGTGTAGTATACTTTAGTTTTTACTACAATAGTAAAATATACCCTATAGTTGTAGAAAACTACATAGCAACCATTTTACCATAGAAACTGTAAAATTACTACAACAGATTAATTCAAGGATTTTATTATAGTATTGTTCAATAACACTATTGTATTTACTTTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26944
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 > C
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028566 | Missense | 645 | 648 | 22 | 22 |
ENSDART00000146104 | Essential Splice Site | 583 | 587 | None | 18 |
The following transcripts of ENSDARG00000029170 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 24926135)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23487887 |
GRCz11 | 7 | 23759044 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTGTTCTCAGACCCACTAACCCTTTCACACCCATCCCTGGAGCCCAGG[T/C]ACTCATACAAACACACACCACCTGTGTCACACTCAAATACACTATGCTAC
Long Flanking Sequence:
CATCTGTGCAGGCGAATTTACGTCCACCTGCCCTATAATTGTTGGAAATGAGTGTAATTAAAGATGATCTTTAAATGAAGCAAACATGATTAGTGAACCCAGTGGTGTTGAATTAGTACAGGAGTGTTTGATCAGAGTCTCATTGTTCACTTGATCAGTGCAGGGTTGTTTGATCAGTCAGCGTGACGAGGGTTGATTTTGTTGTGTGTTTTTTTTTTTTCTTTGCAGGCTCCTGCTCCCATGGCGTTTCCCATGACAACACCTCAAGTGCCTGTGTATGGAATGGTGAGCTTACAGTCACTACATGAATGTTGTGTACTCGAATTGCATAGTCAATAGCACCTCATAAAAAGACTGACTGTGGTTTTTCCAACGGGTTTAGGTTCCTCCTCAGCTGGGACAGATGGGAGGGGTTCCAGTCATGACCCAACAACCCATGTTGTACAACCAGCCTGTTCTCAGACCCACTAACCCTTTCACACCCATCCCTGGAGCCCAGG[T/C]ACTCATACAAACACACACCACCTGTGTCACACTCAAATACACTATGCTACATTATTTAATCTATTACTTAACAGTCTGAAAACGATGTAATATTTTAATTAAATGTGTTGCTGTCATGTTCCACATAAAAACATACTATAGTAATTTATAGTAAATAATATATATTTTTACCAGGCTTTTGTAAAGTTATATTATAGTATTTATGACACAGTTAATACAATGCTGATGCCTTCATTAACAGTAAACTGATAAACTGTAATAAGTAGTGTAGTATACTTTAGTTTTTACTACAATAGTAAAATATACCCTATAGTTGTAGAAAACTACATAGCAACCATTTTACCATAGAAACTGTAAAATTACTACAACAGATTAATTCAAGGATTTTATTATAGTATTGTTCAATAACACTATTGTATTTACTTTAAATTACTATAATATTTTTTCGTTTGGGTTCCCTAAGTAGTTAATGTATGTAACATATTTAATTATGTTAATAA
Associated Phenotype:
Not determined