ZMP
si:dkey-108c13.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A5WV09]
Human Orthologue:
RP4-788L13.1
Human Description:
Lipid phosphate phosphatase-related protein type 4 [Source:UniProtKB/Swiss-Prot;Acc:Q7Z2D5]
Mouse Orthologue:
D3Bwg0562e
Mouse Description:
DNA segment, Chr 3, Brigham & Women's Genetics 0562 expressed Gene [Source:MGI Symbol;Acc:MGI:106530
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7490 | Missense | Mutation detected in F1 DNA | Not yet available |
sa13790 | Essential Splice Site | Available for shipment | Available now |
sa31271 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7490
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112131 | Missense | 126 | 775 | 3 | 7 |
ENSDART00000144624 | Missense | 126 | 765 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 18871732)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 20700463 |
GRCz11 | 2 | 20358435 |
KASP Assay ID:
554-4006.1 (used for ordering genotyping assays)
KASP Sequence:
CAGAGGCTAACATAAATGCTGCTGGCTGCAATTTCAACTCTTACATCCGA[C/T]GGGCTGTGAGGTTTGTTGGTGGGTGTATATTTTTCCTGCACTTGTGACCA
Long Flanking Sequence:
GCAGCAAGTGTGATCTCAGGGGGGTACAGTACCAATGCTTTTTCATCTCTTTCTCTCTGTCTTCTCGTCTGCAGCAGATGCCCTCTTGCAGAAGAATTTACATTTAAATCTATGGGTTCCTGCTTTTCATTTACATGAAATTAACAGTTTAGTCAATGCTAGCGGAGGCCTGGATTACTACCAAGATACTCGCCTAATCGGTTTTTACAGTTTTGGATGGAATCCCTCGCATATGGCCATGAATGAATGGGTGGACGGATGGGAGTGATTACTTTAATTACTGTAATGAACTTGATGTGTCAGTGATTCTATTTGTAGTGACCTCTGGAATCTAGAAAAGGAAAGTGTGGTGCTGTATTTTTGGGTAAATACAGATGATCTTCCCACAGATCATGATTGGGGAGGGAATCCTGTACTGCTGTGTGGCCAGGAGAAATATTGCCATCAAGACAGAGGCTAACATAAATGCTGCTGGCTGCAATTTCAACTCTTACATCCGA[C/T]GGGCTGTGAGGTTTGTTGGTGGGTGTATATTTTTCCTGCACTTGTGACCATAAAAAGCTATATGGCATGTATAAATATTGTATAGATTTCACCATTTATCTTAACTCTGTTTTATAATCTATAGTGGGGAAAGTTCAGCCCAGAAAAGCAGTAAACATGGTCTTTGGTGATTCATAAAATACATGGTTATGACTAGGAAGACGTTGAGAGCACATACAAAATAAAACTATTTCCTGTGGTGTCTGATGATACATGATCTGTGCAAGTAAATTCACATTATTTACACCATTATAACCTTTCAACAACATATCTGCAAACAGTTAACAAGTCTGGAGTGGAAGCGTCCTGATTCAAAATAACATGTTCAAGTTTGTGTAATGCCGAGTTCAGACTGCATGATTTTCAAAGTAGTGTGTCACAGATGTTTTTACACAGCATGACTATCTGGGGCAGCGTTCTGTTGGTGCTGTGTTTACACTGTAGGATGGATCCACGTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13790
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112131 | Essential Splice Site | 275 | 775 | 7 | 7 |
ENSDART00000144624 | Essential Splice Site | 275 | 765 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 18880951)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 20709682 |
GRCz11 | 2 | 20367654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGTGCTCACTATCCTTACCAAGAGATTTCWGCCTTTTGCACTACTTTA[G/A]GGTCTGTATGCAGTTGGGAACTTTAAACCTAGTGAAGACACATCTCTGAG
Long Flanking Sequence:
TTCCACCTGGTATACTTTACAGGTGGTCAGACCAGCAGAACTTCTAGTTACTCAGCTAAATCAGCCAAATACAGCTTGGCCAGGCTGGCATACCAACTTAAAACTGCTAGCATACTCTTCAGCGGGGAATATATTGGCTAACACTTTATTTTGATGGTCCATTTGAGGATTAGTAAACTGTCTGCTTGATATCTGTTGATACAGACATTCAACAGACATTTAACTGATTATAAGAAACTTTGCCAGTACATGTCAACTTACACTAACCCTAACCCTAACCCCAACCTAACAGTCTACTCATAATCTAATGAGAATTAGTTGGCATGTAGTTGCAATGTAATGTAAATGCAACAAACAGACCATCACAATAAGGTGTGACCATGTATTTTCTTGAATTATTTGCAAAATATCCCTATAAAACCCTCATTTTAAATATATATGTATTTTTTTCAAGTGCTCACTATCCTTACCAAGAGATTTCTGCCTTTTGCACTACTTTA[G/A]GGTCTGTATGCAGTTGGGAACTTTAAACCTAGTGAAGACACATCTCTGAGGATACATGTGCATCCTCCTATCCGACAACCCCTACCACCGCAACCTCTACCACAACCCCAGCCGGTGGGGCCTCCACCTGCCTTGCGGGAACCTCTGAGACCTCTCCCTAACCTGAACACAGATCCACCACGCTTACTTCCACCTAAAAGCCTAAGCATGCGTGAACGTCCAACCTCAGCCCGCTCTGAGAGTATCCTGCTACGTGGCCCATCCCACAGAGAGAACAGCTTGTCCAGCTTGAAGAGGGCAAGCACAGAGGTAGAGTGCATTACACCACCCAGTCCCCTCTGCAAGGAAAGCTTTGTGACCTTCAGCAACACCCTTCCTCGTGTGCATTCAACTGGAGTTGAAGAACCAGTGCCACGACGCCACGCTGCTATCCATGCCTCCATGGATTCCACACGTTCTAAGCAGCTGCTCTCACAGTGGAAGATCAAGAATGAGAACCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31271
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 |
---|---|---|---|---|---|
ENSDART00000112131 | Nonsense | 710 | 775 | 7 | 7 |
ENSDART00000144624 | Nonsense | 710 | 765 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 18882257)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 20710988 |
GRCz11 | 2 | 20368960 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCATCCCCACTTCCATCATCACCACCACCAACAGAGTATCACCACTATT[C/T]GAGTCACACCAGTGGAAGTCAGCAGTGAAGCCACCTCGGAGACTCTCTCC
Long Flanking Sequence:
AGATGAATGATAGTGGGGGAGGGGGTGGGTCGGCACGATCAAAATGGCTAAAGGTGGCAGAGAAAAGCACTGTCTGCAGGACTAACAGTCAACCACGTATCATGCAGGTAATTGCAATGTCCAAGCAGCAGGGCATGCTACATGGTAGTCCTAAAAGTGAGGCTAGCACCGTGAGTTGTACCGGATCTATCCGTTATAAAGCCCTGATGGATCAGGAACCTAACAGTGGCATTGTTCGAGTGGAGGCCCACCCTGAGAACAAGCCTGTGGTGAAACCACCATCCACAGATGGAAGTGGATCTTGGAGGTGGAAACCACAGGAGCGGGTCAGTATCCGACAGTCCCTCGAGTTGAATGATCTAAACCGAGATTCTGAAAGCTGTGAGTCATTAAGAGATGGCTACGGGTCCGTAGATGGAAACCGAAGCCTACCTGACATGAGCAACCCTCACCATCCCCACTTCCATCATCACCACCACCAACAGAGTATCACCACTATT[C/T]GAGTCACACCAGTGGAAGTCAGCAGTGAAGCCACCTCGGAGACTCTCTCCACCACCTCCAGCCGAGACTCCACCTTGCGCAGGAAAGGCAACATCATTCTGTTGCCCGAAAGAGGACCTAGTCCTGACAACGCCAGGAACCTGCCTCACTTTTTCAAACCCTCCCCAACACCTCCCCCCATTTTGACTTTCAAAGAGTGAAAGAAACATCTTTCCATGTCAACCCTAAGAGTTGCTTTGCTCTCTGAACTATGAAGACTAGAGCTCCTGTTAGGGAACTTAGTAGACATGGTGAGTCTGGATACATCGACATTTCCTGACCGTTAGACACCACTGCACTCTTCAGAACACATAAGACAACGTTGTGCTTTTTCTGTCTACGTTCTGTAGGCCTCATTACAAAAACATAAGCACAAAATATGAAAATTGGGGCTGTTTGATAAAGGTATTTGTTTGATTTCATCTAATTAGCTTTGTTATCGAGTCCATTGTCTGTTGTCT
Associated Phenotype:
Not determined