ZMP
agtpbp1
Ensembl ID:
ZFIN ID:
Description:
Cytosolic carboxypeptidase 1 [Source:UniProtKB/Swiss-Prot;Acc:Q4U2V3]
Human Orthologue:
AGTPBP1
Human Description:
ATP/GTP binding protein 1 [Source:HGNC Symbol;Acc:17258]
Mouse Orthologue:
Agtpbp1
Mouse Description:
ATP/GTP binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:2159437]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17482 | Nonsense | Available for shipment | Available now |
sa8921 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2426 | Nonsense | Available for shipment | Available now |
sa8379 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17482
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 |
---|---|---|---|---|---|
ENSDART00000026050 | Nonsense | 115 | 1153 | 6 | 26 |
ENSDART00000134147 | None | None | 722 | None | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 52180162)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49929115 |
GRCz11 | 8 | 49917884 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCGCAGGACTGGCTTGTTCGTGTCTAAAGGAGGAMCAGCCATTYTGCTG[C/T]AGCTGCTRGTGAGCTCCAGCAAAGACCCTCCGGCCAACGAGGAACTRATG
Long Flanking Sequence:
AATTGCATCGCGCCATATTGCGCCGGGTGTATTGTAGAGCCCTAATTGTTTTACGTTTAATGCACTTTAATGTGTAAAAACTAATAAGCTAACTTAATTCCTTCATGTTGTCCCACAATTCGATTGTGTGGAACCCAGCATCTTTTACAGTGTTTTCCTTCTATGGAAGTCAATGGTTACAATTGCTTAGCTTTCTTCATGATATCTTCTTTTGCGTTCAACAGAAGAAAGAAACTCGTATGAGGTTAAAATGTTTATTTTTAGATGAGCTATCTGTTTAATGAACTGGTAATTGCTTTGTTGTTTGTTTTAAATGGCTCTAAGCCTTAAAAAAGACAGCAGAGTCAGCTGAGAAAGGCTGTAATCAGTGAACTTCAGTCATAACAGTGTGTTTCTGAAGGTCAGAATCTAGCGTAATCTTTCTTTGGCTGTGTTGTGGTATAGGTGGAGGCCGCAGGACTGGCTTGTTCGTGTCTAAAGGAGGAACAGCCATTTTGCTG[C/T]AGCTGCTGGTGAGCTCCAGCAAAGACCCTCCGGCCAACGAGGAACTGATGCTTCACATTCATTCTCTACTTGTCAAAGTCGGACCCAAAGGTACAACAAACCCATGCTCACTATAGCTTTCACTAGTGGTGTTATAAATCAGATCATGTTATGGTTTTTGGGTCACGGATCAAACCATTTTTGGATCAGGCTAAAAGGGGAGGAGACAAATGTCATTGGCTTTCCCTTTATTACAATCACCGTAATGCTTGTGTAAACCTGCTGGTCCTATGCCACCCAACCCACTCTGAGCTGGTATTGATCTGGCAACCTTCCGCATGGGAGTTGGATGCTCTAACAAGGGGGCTAAAGACCATGGCCTCTAGCGTCTGTTGCTAGAGCACCTTTAGAGGTCAGAGGAGTGAGGTTTACCTGCACAGCACTTACTAACTAACCTCCGTTACACTAACCCCCTAAACCTCACTCGCATCCGGGTCACGGCACCAATGTAACCCCGCCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8921
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026050 | Essential Splice Site | 434 | 1153 | 13 | 26 |
ENSDART00000134147 | None | None | 722 | None | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 52170780)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49920861 |
GRCz11 | 8 | 49909630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ARCTCCGAGTCTACGAGCATTTCTGTCGGGAATTCACTGAAACTTTTCAG[G/A]TGAGGACTCTTCTGATTCACAATGTGAAATGAAACTAAGAATTTGAAAAA
Long Flanking Sequence:
AAGTCATTTATTTGCTGTATTTTTAACTAGCCTTAATTTCTATATTCTAAATTACATGATATTATATTTATTTTAGATTTTAGTCAACATTTTAGTCATGCACATCTTTTATATGCTTTTATTTCAGTTTTAACTTAAACTGAAGCTTAGTTTCATCCAAAATTACTTCAAGTATTTATTTCAATCAGTTTTTAAGTCGAATCTTTTATTTTAGTGTATCTTTTATTTGATGGGACAGTAGTGAACAGACCTGTTCTCTGTCAGTGAACACAATCCTATTCAATGACTCTTGTCTCTACTCAATGACATGCCTAATATTAGTAAAAGAGCGATCAGAGTTCTGGAAAACTGAGTTTGTATCTGAGGTTTGTTTTGCGCTGCAGAATGATGACATAGAGACGGATATCAACAAACTAAGACCCAAGCAGATGAACACACGACCCTTTGAAGAACTCCGAGTCTACGAGCATTTCTGTCGGGAATTCACTGAAACTTTTCAG[G/A]TGAGGACTCTTCTGATTCACAATGTGAAATGAAACTAAGAATTTGAAAAATAAAGACTGTAAAATATAAAAAATATATATACTGTAATATAATAAGATACTGAAAAAATATACTTTAAAAAATATATACTCAATATTCTGTTGACGTCAAAATTATTAGCACTCCTGCGAAATTTTAATTCGTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGAATTCACTGAAACTTTTCAGGTGAGGACTCTTCTGATTCACAATGTGAAATGAAACTAAGAATTTGAAAAATAAAGACTGTAAAATATAAAAAATATATATACTGTAATATAATAAGATACTGAAAAAATATACTTTAAAAAATATATACTCAATATTCTGTTGACGTCAAAATTATTAGCACTCCTGCGAAATTTTAATTCGTTTTCAAATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2426
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 |
---|---|---|---|---|---|
ENSDART00000026050 | Nonsense | 486 | 1153 | 14 | 26 |
ENSDART00000134147 | Nonsense | 55 | 722 | 1 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 52169662)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49920049 |
GRCz11 | 8 | 49908818 |
KASP Assay ID:
554-2807.1 (used for ordering genotyping assays)
KASP Sequence:
TTCAAAACAGACGTCCGCTCCGGGAAARCGCCCTGCCCCTAAAGCCTGAA[C/T]AATCTCCTCTGGAGCTGGACAGCATCTCCATAGCCAAGAGGCCGGACGGC
Long Flanking Sequence:
TTTTTTAAACCATTTCATGGTGAAAATTATAAGCCCCCTTAAGCAATAATTTTTTTCCATAGTCTACAGAACAAACCATCGCTATACAACGACTTGCCTAATTACCCTAACCTGTCTAGTTAAAGGTGCAGTATGTGATCTGTGGACATGATTATACACGTTAATACAGAGACATGATAAAACGTCAAGCCTGTCAAACAATAGCGGTGGGTGAGGATTACTGCACTGTTACGTCACCTGTCATTTCAATATGCGCATTAAACCGTGAAGGTCATACCGAACATGGTTCGATATTATGTTGAGTATTGCGACATCCCAAGTGATCCCCATTACGCTTTTGTTCTCAGGATATTGACTTTGAAGACTCCATTTCTGCCATTCCTCCATCAAGAGTCAACTCAGAGCATCACCGTCCCATCATCATTCCCACCACACAGTCCTCACCAGGACTTCAAAACAGACGTCCGCTCCGGGAAAGCGCCCTGCCCCTAAAGCCTGAA[C/T]AATCTCCTCTGGAGCTGGACAGCATCTCCATAGCCAAGAGGCCGGACGGCAGAGCAGACGCTGATCTGGTGTGCAGTTTAGGTCATCTGATTCTGGACGCTGCTGTGAATGGAGGCTCTGTGGACGGATGTCAGGATGACGGCGGTGAACAGTCGGTGCTGGAAGTGCCGGATACCGCAGCACTGTTGCCACTACATGACCCGGAGCTTTATTTGGAGATGGTGAAGAGCACGCGATCAGTTCCTGGGTACACAGAGGTGGCATATCCAGATTACTTTGGCCATGTGGCGCTCAACCTCCGGGAGCCAATTCTGGAGAGGGTTTATGGTGTGCAGAGGTAATACACGTGTGTTTTTATTGCCTGTTCGATGTGAAATGCTGTACCTAAGAAATTAAATTTTCTGATCCACGCCAAAACAATTAGTCTGAGATCACTAGAGTGACTAGAGTGGTTGAAACGCCTAAATGGATCAACAATTTAACCGACTTTACCTCATACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8379
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026050 | Essential Splice Site | 734 | 1153 | 18 | 26 |
ENSDART00000134147 | Essential Splice Site | 303 | 722 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 52163593)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49913980 |
GRCz11 | 8 | 49902749 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACGGCAGCCCTCATTGGGTTAGAACTGGATCAGACATCWGCTATTACAA[G/A]TAAAGAGCAAGTSGYACAGTGATTTATGGGTTGGTKTNNGCKMTGAAAAGTT
Long Flanking Sequence:
AGTTTGCTCTTGCAATCTTGAATTGAAGTCTGATGCACTCCCTGTTTGTTTTCAGTTAAATTCTCAGATAAGGTCTGTCTGAGGTTATGGGCGTGGCTAACATACCTAATCACGCCCCTCCTACTGTCAGTTTTAACAACAAACAGAAATAGTGAGCTGGAGGAGGAGTCTGTTAAGTTGTAATAATTCTCCCCAGACCCTTTTCACAATTTTTCTGAACGAAATGCCATCTTTACTACATCCAATCAGCTCATAGTAGAAAAAACAAGCCACGCCCACTGTTCTCTCATTTAATATTCCCTTTCTCCGCATCACAATCCGGAAAATTTGGCTTCCGGTTCATATGGACTTTAAGTTAGTCAGCTATTTACATACATTTGGCTAACCTATCTATACCTTTCTTGTCTGACAGGTATGCAGGTGATCATGTACTCGGTACAGGAGGCCATCAACGGCAGCCCTCATTGGGTTAGAACTGGATCAGACATCTGCTATTACAA[G/A]TAAAGAGCAAGTGGTACAGTGATTTATGGGTTGGTGTGCGCTGAAAAGTTACAGTTTTGCAGAAATCCTGTCTGTTTTTGTCCACCCAGGAATCATTTTGCACGAAGCTCCATTGCAGCCGGAGGTCAAAAGGGAAAATCGTACTTCACCATGACCTTTACTGTGACCTTTCAGCATAAAGATGACGTTTGCTACTTTGCCTATCATTACCCTTACACCTACTCAATGCTGAAGGTACTGTTCAAAATACATATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTATATCTATCTATCTATCTATCCATCCATCCATCCATCCATTCATCCATTCATCCATCCATCCGATGTCTGTCTGTCTATCCGTCCATCTG
Associated Phenotype:
Not determined