ZMP
si:dkey-7o6.7
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate ATP/GTP binding protein-like 4 (AGBL4) [Source:UniProtKB/TrEMBL;
Human Orthologue:
AGBL4
Human Description:
ATP/GTP binding protein-like 4 [Source:HGNC Symbol;Acc:25892]
Mouse Orthologue:
Agbl4
Mouse Description:
ATP/GTP binding protein-like 4 Gene [Source:MGI Symbol;Acc:MGI:1918244]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41158 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12099 | Nonsense | Available for shipment | Available now |
sa21233 | Nonsense | Available for shipment | Available now |
sa34357 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41158
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063707 | Essential Splice Site | 127 | 486 | 4 | 13 |
ENSDART00000132908 | None | None | 226 | None | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 16273735)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 15718623 |
GRCz11 | 8 | 15754396 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGAGATGGGATGTCCCCCGTGGTGAAGTCGACCAGCCGGCCTAAATGG[T/A]ATTCATACCCTCTGCAAATATCACATCTCCACCTACACACTGCGCTTTCC
Long Flanking Sequence:
TTGTCTGTCTGTCTGCCATTCTATCATTTTATCGATCTGTCTATCACTCTTTCTAGCCTTCTATATATTGTTTTATTGTTTTGTTTTTACATTCTATCCGTCTGTCCGTCTATCCGTCTGTCCGTCTATCCGTCCATCTGTTTGTTTGTCTGTCTGTATATCTATTGTGCTATTTATTGTTCGATCATGCTATAATGCTATCAATCTATCATTTAATCATGCCATCTATCATTCTATCAATCTATTGTATATCTATCTATCATCCATCGATCTGTTTAACATTTACAGTGTCTGTTGCTCAGTTTGTTTGCAAACTCCCACTTTCACTTTCCAGTTTTTCTTCTTAAATAATTAAATAATCTCTGTTCCACCTCACTAAAAATCTCTGTTTCTCCTCGTTTCAGAGAGTGATTTTCAACATTGTGAACTTCAGCAAGACCAAGAGCCTGTACAGAGATGGGATGTCCCCCGTGGTGAAGTCGACCAGCCGGCCTAAATGG[T/A]ATTCATACCCTCTGCAAATATCACATCTCCACCTACACACTGCGCTTTCCACGCTTCAGTTCTGAATAACAAATCCACAACTTATCTTCCATGTGTAGTTTCCCCATTTGTGTAGCTTAGGCCTTAGCATGGTTTCCACACAAGCCCTGCAGACAGAGTGAATATTGTGTACACTGTCATCATATCTGACGGTCTCATCTCTCTCGCACACAAACAACAGGATTTTTCGTTACCACCTTTTGGAGTTTTCACACTGCCGGTGTTCCTTAAGCATTCAACGCTTTCTCACTTTCTCTTCCTTCTCCAAGTTGACAATAGTGTGTTTGATGTTCCAGATGAGAGCTTGTGTTGCCGGGGATGTTTGGTCTTTGTAGAAAATAAGAGAGAGACACTGACAGGACTGTTGATAGAAGAATTATGAAAAATGCAAGAGAAGGAAGCAACTCCGTATACGCCACTGTTTACATCACATCACATTGGAGCCATTTTTTTCTAAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12099
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063707 | Nonsense | 178 | 486 | 5 | 13 |
ENSDART00000132908 | None | None | 226 | None | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 16150549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 15595893 |
GRCz11 | 8 | 15633598 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATCAGTTTGCATACTGCTACCCCTACACCTATTCGCGTCTGCAACATTA[C/A]CTGGCCAGCCTGGAGCGCAGAAACCTCGATTACCTGCAGCGAGAACAGCT
Long Flanking Sequence:
ATACGTCACCTTTTTCACGATCTTTGTTTTATTTTCGCTTGACTTTTGCATTTGCAGCTCATTGAACTTCAGTCATCAGTCATGTAAGAAATTTCCAAGTAAAACAGAACATTAAACAGAAGATAATGCAGTTGTTGATTGAATTGTGATGTTGATGCTATGGCTGATTAATATTATTTTCCTACATATGCAGCCTTGCTTACATAAAACGAGAACTGATGATTAAAGATTATGAACTCAAACTTTTGATTTCTCATATCAACATCACATTAACCAATGGATATTTGTTGAGAAAGCAAATAGAGCACATCTTATTACCATTGTTTTTCTTTATTTCTTTCTCACAGGCAAAGACTTCCAGCCAAGAATGTGTATTACTACCGCTGCCCTGATCATCGGAGGAACTACGTGATGTCTTTCGCCTTCTGTTTCGACCGAGAGGATGATGTTTATCAGTTTGCATACTGCTACCCCTACACCTATTCGCGTCTGCAACATTA[C/A]CTGGCCAGCCTGGAGCGCAGAAACCTCGATTACCTGCAGCGAGAACAGCTGGGCCTCAGTGTGGTTAGTCAATGCATGTTTCTACACCACATGTGTTTTAGCGCCTGTTTTTTCAGGTGTTTCTGTCATTTTTTATTATGTTAGCATCTTCCTCTATCTGCTGTGCACGGCAATCTTATTTTCTATAAGGGGGCGCACACATGTAAGTGTCTTTGAGGATGCATGACGGTGTGTGAACACACAGGTACTGGATCATTCACACTGCCTACAGTCCCGTCTGCGCTCTTATCAAATAATTGTAGAGGAAAACTCATTAGGAATGCTCAAGAGATTAAAGCCCTCTTTTAGGGCCTTCATCACTTTTACGTTCGTCAAGGAGAGCCAGGCACGGGAAGCCACTGATGAAAGGACATTTATTGATAAGAAATATGGTGTCAATGGAAAAAAAAAAAAATCTGTTTCACATGAAATGGGATTTGAAAGGGCAAATATATCAGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21233
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 |
---|---|---|---|---|---|
ENSDART00000063707 | Nonsense | 219 | 486 | 7 | 13 |
ENSDART00000132908 | None | None | 226 | None | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 15928369)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 15373713 |
GRCz11 | 8 | 15411418 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTTTCTGCATTTATGTGTGTGTGTGTTTCAGCCCATCTGAACCAAGAG[C/T]GAGAAAAGCGGGTGGTATTTCTCACAGCCCGCGTTCACCCCGGAGAATCA
Long Flanking Sequence:
CTTAAAAGTGGCTATTCTTTATTTTATGTAAGTGTTTGAATGTAAAAATGTAATTTTATAATATTATGAAGACTTAAAAGTGGCTCTTTCTTCATTTTTAGGGGGTGTTTGGATGTTAAAATGTAGCTTTAGAATATTATGAAGACTTGAAAGTGGCTATTTTCTTCATTTTATTTGTGTGTTTTGATTTTAAAGTCATAATTGTGAACAGATAGGAGCTGGAGAATCCCTCACCATCCACAAGGTGTTTTTCTCCTGTTTCTGTGATCAGTAGCTCGTAGTGTTTTGTCCTCCTGTGGAGTCTTCATTAGCTCTGACATTTCCTATCATTCCTTTTCTGTCATACTGGGTTTCCTGCAGCACGTCTGAGGTCCGAAAATCCAGGGTCCAGACATATGGCTCCTGACCACACACATACCATCCTGCCAGGACCCCTACCTGCTGAGACTAACCTTTCTGCATTTATGTGTGTGTGTGTTTCAGCCCATCTGAACCAAGAG[C/T]GAGAAAAGCGGGTGGTATTTCTCACAGCCCGCGTTCACCCCGGAGAATCACCTGCTTCCTTCATCTGTCAGGGTAAGACCTTGTCTCGTCTCGACACACAAACACAAGGCAGATGATGTCCTGAGATCCTGTAATCTGCTGAAACACAAAACACTGACCAACGGCCTCTGTGGCCTCACAGAACGCATCTTCTCTTGTACTTTAAAGCAGGTCATGAACTAAGAAATCAAAATCCCTTTCATCTTTTCACTTATGAGAGGTTATTGTACTATAAAACATCCCACAAGTTTCAGATCTCAAAACTTTCATGTTAGTTAAAAAACTGTCATTGAAGGTCTGTCAAAATGGCGGTTTCTGAATGGCCCTTGTTATTATATAATAGCAAAGACTATAGAATACACAAGACGTGTTACTCATATAGTTTTTGGATAGGGAAAAGAATGCAACGATCAATATGGAGGTTCTAGTGAAGAAAACTCTGCCTTCTAATAAAGAAGCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34357
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063707 | Essential Splice Site | 243 | 486 | None | 13 |
ENSDART00000132908 | Essential Splice Site | 24 | 226 | None | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 15928295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 15373639 |
GRCz11 | 8 | 15411344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGCCCGCGTTCACCCCGGAGAATCACCTGCTTCCTTCATCTGTCAGGG[T/C]AAGACCTTGTCTCGTCTCGACACACAAACACAAGGCAGATGATGTCCTGA
Long Flanking Sequence:
TAAAAGTGGCTCTTTCTTCATTTTTAGGGGGTGTTTGGATGTTAAAATGTAGCTTTAGAATATTATGAAGACTTGAAAGTGGCTATTTTCTTCATTTTATTTGTGTGTTTTGATTTTAAAGTCATAATTGTGAACAGATAGGAGCTGGAGAATCCCTCACCATCCACAAGGTGTTTTTCTCCTGTTTCTGTGATCAGTAGCTCGTAGTGTTTTGTCCTCCTGTGGAGTCTTCATTAGCTCTGACATTTCCTATCATTCCTTTTCTGTCATACTGGGTTTCCTGCAGCACGTCTGAGGTCCGAAAATCCAGGGTCCAGACATATGGCTCCTGACCACACACATACCATCCTGCCAGGACCCCTACCTGCTGAGACTAACCTTTCTGCATTTATGTGTGTGTGTGTTTCAGCCCATCTGAACCAAGAGCGAGAAAAGCGGGTGGTATTTCTCACAGCCCGCGTTCACCCCGGAGAATCACCTGCTTCCTTCATCTGTCAGGG[T/C]AAGACCTTGTCTCGTCTCGACACACAAACACAAGGCAGATGATGTCCTGAGATCCTGTAATCTGCTGAAACACAAAACACTGACCAACGGCCTCTGTGGCCTCACAGAACGCATCTTCTCTTGTACTTTAAAGCAGGTCATGAACTAAGAAATCAAAATCCCTTTCATCTTTTCACTTATGAGAGGTTATTGTACTATAAAACATCCCACAAGTTTCAGATCTCAAAACTTTCATGTTAGTTAAAAAACTGTCATTGAAGGTCTGTCAAAATGGCGGTTTCTGAATGGCCCTTGTTATTATATAATAGCAAAGACTATAGAATACACAAGACGTGTTACTCATATAGTTTTTGGATAGGGAAAAGAATGCAACGATCAATATGGAGGTTCTAGTGAAGAAAACTCTGCCTTCTAATAAAGAAGCCAATCATTGATCGCTATAGACTGATGATTCTCTGGAGGAGGGGCTCGGTCCAGACATGCTGTTTTTTATTCTGTAG
Associated Phenotype:
Not determined