ZMP
zgc:111944
Ensembl ID:
ZFIN ID:
Description:
PERQ amino acid-rich with GYF domain-containing protein 2 [Source:UniProtKB/Swiss-Prot;Acc:Q4KME6]
Human Orthologue:
GIGYF2
Human Description:
GRB10 interacting GYF protein 2 [Source:HGNC Symbol;Acc:11960]
Mouse Orthologue:
Gigyf2
Mouse Description:
GRB10 interacting GYF protein 2 Gene [Source:MGI Symbol;Acc:MGI:2138584]
Alleles
There are 16 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19882 | Nonsense | Available for shipment | Available now |
sa18439 | Essential Splice Site | Available for shipment | Available now |
sa11852 | Nonsense | Available for shipment | Available now |
sa19881 | Nonsense | Available for shipment | Available now |
sa19880 | Nonsense | Available for shipment | Available now |
sa10322 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19882
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056277 | Nonsense | 38 | 1329 | 3 | 29 |
ENSDART00000146705 | Nonsense | 38 | 1329 | 2 | 28 |
Genomic Location (Zv9):
Chromosome 2 (position 48359422)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 48391086 |
GRCz11 | 2 | 48245250 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAGCAGCATTGTGGCCTCCCCTCCGCTCTCGCCTGCATTGCCAAAGTA[T/A]AAACTTGCAGACTATCGCTACGGGAGAGAAGAGATGCTAGCACTTTATGT
Long Flanking Sequence:
TATTGTGATATGTTGAATGGCAATGAAATATAAAAGCCCACAACTTGCATTTAATAAGCTTTAAATCACTTCTGTTAATTTATTTTAATCTGGATGGCTTAAATGTGACATCTTCTTTTCGAGTCTGTTATGTAAATACAGTAGCTTTTGTTTCATTGTATTTTTGATTTACTGATCTGTACATAGAATGCATCACCACACTTTAATTCACTAAACCATTCATTCATTTAGCAGGCGTAAAAGCTTTAACAAAAATTTTAAAACTTCTTAATTTGAATTCATATAACATTTTTAATGAATAGTTTAAAATTTTATTTATTTAAATACTATTTATATTATTTTATTTTTTAAAAGAAAAGTATTTGTTTTACTGTCGCCTTGTATGATTTGGTGACGTAGCATGTTCTCTCTTCTCTGTGTGTCAGGCTCCGTGCTCTGGCTGGTGGGGTGGGCAGCAGCATTGTGGCCTCCCCTCCGCTCTCGCCTGCATTGCCAAAGTA[T/A]AAACTTGCAGACTATCGCTACGGGAGAGAAGAGATGCTAGCACTTTATGTAAAGGATAACATGGTAAGGATGCTGGTTTTAATTTTATTTTCACATTTAGAAGCCTTGTTAATCTTCTAGTTCTGCAAATTTTTAAAGCATATAGTGTTATTTACATTTACAACAAGTTTAAAATGTTTTCGATCATTTTTAGATTCCGGTAGATCTTCATGATAAGGAATTCCTACCTATTTTACAAGAGGAGCCCCTGCCACCTTTGGCATTAGTCCCTTTTACAGAGGAGGAACAGGTAAGAATGGACCTGTTTATGAACTGAACATGTTTTTTTATCAGGGCTTTATAGTAGGGCTGAACAATATATTGTTTGAGCATCATTATTTGCAATAGTCACATCGCAGGATTAGATTATTTTTTAAAGGATATTTAATATTATATATAATATAACGATATTATTAAATTGTAGATATTTTTTTATTTTTTATACAATGATGATCATGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18439
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056277 | Essential Splice Site | 319 | 1329 | 10 | 29 |
ENSDART00000146705 | Essential Splice Site | 319 | 1329 | 9 | 28 |
Genomic Location (Zv9):
Chromosome 2 (position 48354256)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 48385920 |
GRCz11 | 2 | 48240084 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTGACTCCTCAGGGGCCTTCCTCTCACTTAAGGTGAGGGCGCTGGAAG[T/C]GAGTGGTKGAGCTTTGATTAATCATTTTACAWTTTTGAATGYTYGATAAG
Long Flanking Sequence:
ACATTTGGTAACCTTATGTATTACGTACTAACATGAACTAACAATGAACAATACTTGTACATCATTTATTAATCATAGTTCACCATATGCTAATTCATTAATAAAATCTAAATTCATGCTTGTTAATATTAGTTGCGCAACTTTTTTCCAATAGCATAAACAAAGATGAACAACTATAATAAATTTCATTTGTTAATTTTTTATGTTAGTAAATACGTTAACATTTACTACTACAGCCTTATTATGAAGTGTTACTGCAATTTCTTTATTTCCAGATGGTCCACGATCAGCAGGGTGGCGGGAACACCCAGATCAACGTCGACGCTTTGGTTTTGGGGATGAGGAACGCAGTGGTTACCGTAGGCCTCGGTCGGGCAGCGGGAGCGCAGAGGAGGAGAGGGACAGTTTACCAGAATGGTGTCTGGAAGATGCAGAGGAGGAGACAGGGACGTTTGACTCCTCAGGGGCCTTCCTCTCACTTAAGGTGAGGGCGCTGGAAG[T/C]GAGTGGTTGAGCTTTGATTAATCATTTTACATTTTTGAATGCTCGATAAGGAAGCCTGTTTGAATTAATGTGGGTTTTGATGATTGTTCAATTAGAAAGCTCCTAAGGAGCCAATCCTGGAAGAGGCGGAGCTGGACTTCCGGCCATTGGAGGAGAATGACGAATATGCAGAAAAGGATGACAGTGAAACTGAACAAACCAAAGATACTGACACAAATACTAGGCACGAAAGTGATCGAAATGAAGGTGAGAAGAAAATATGGTTTCCTATAGGCTACTTAAAATCTCCAAATAAACACTTATCAGTTGTTTAGTAGCTTACTGGTCAGTATAAATTTTTAAAATGTCTTTGAAAGAAGTTTTTATATATCATATACTCACTTGCAAATAGTTGAAGCCATAGTGGGTGGAGTTGCTCACTATAAATAGTAGAGGTGTGAACCTACACTAGTCTCACGGTTCGGTTACGATTATCATGCCATCGATTCGGTTCAATTCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11852
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 |
---|---|---|---|---|---|
ENSDART00000056277 | Nonsense | 636 | 1329 | 16 | 29 |
ENSDART00000146705 | Nonsense | 636 | 1329 | 15 | 28 |
Genomic Location (Zv9):
Chromosome 2 (position 48346592)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 48378256 |
GRCz11 | 2 | 48232420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGTTTGACTCAATATAGGGAGATGCAGATCAAGAAAGGATGRAGAGA[C/T]AACAGGAGATTAATGCTCTAAATATGTATCAGCTACAGCAGATGCAATAT
Long Flanking Sequence:
GAATTCTTCTGCTAATGAGTTGTTTTGTGTTTGATTACTCGACTTTAAATTGGTCAATGCATTACAACTTGATTTGTGGCATGTGGCTTCGGCCTTTTCCAGTGATGACTTTATCTAAGCTTCAGAAAATGTAAAAAATTACCATGCAACTCAATATAGTTGCGTTCAGTGACCCCAGTCTGTCTGTCTGTCTTTTTAAAGGACCATTTAATAATCAGGAGATGTCTGAGTGGTTTCAGGCGGGCTATTTCACCATGACCTTGCAGGTAAAGCGAGGATGCGACGAGATGTTCCAGCCTCTGGGCGAGATGATTAAGTTGTGGGGACGAGTGCCCTTTACACCGGGCCCGACACTACCTCCCATACTGGTAATATAAAGACGCTCACTTTTCAAATCTCTGACCCAAGATGACTTAACACTACTGTTCGGCATCTGAAAAGTTTTGATTTGTGTGTTTGACTCAATATAGGGAGATGCAGATCAAGAAAGGATGAAGAGA[C/T]AACAGGAGATTAATGCTCTAAATATGTATCAGCTACAGCAGATGCAATATCAGTATTTACTCAGGTATGAGAGAAGATTATGAAGCGACATGTTTTTTTTATAGCAGTAAAAAATAATAGTTAAAAATACACGACTCTGTTTAATTTATTTGACAATTTTGCACCATATTATGATATGCAGCAAATTATTTGAAACACTTCGCTCCAGTTGGCTACATAATACAGCATTTGCACTATTAATGTGACTTGTAATGCAGAAATGAACTTTTTTTTTTCTCAAATATATTTTTATTAATTTTATTTTAGTGTAAAAACATGTCGGTAATTTATATTGAATAATAAGATAATATACATCTTTCATGTAATTTGAATCCTGCTCCCCACATGAAAAATCTAATAAAAAAAATAATAATAATAACAACAACAACAAATAATTCAATTTGTATTTAATAAATAAACAAATAAATAAATAAGGACATAAATTGCATACATTTTGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19881
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 |
---|---|---|---|---|---|
ENSDART00000056277 | Nonsense | 651 | 1329 | 16 | 29 |
ENSDART00000146705 | Nonsense | 651 | 1329 | 15 | 28 |
Genomic Location (Zv9):
Chromosome 2 (position 48346547)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 48378211 |
GRCz11 | 2 | 48232375 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGACAACAGGAGATTAATGCTCTAAATATGTATCAGCTACAGCAGATG[C/T]AATATCAGTATTTACTCAGGTATGAGAGAAGATTATGAAGCGACATGTTT
Long Flanking Sequence:
TAAATTGGTCAATGCATTACAACTTGATTTGTGGCATGTGGCTTCGGCCTTTTCCAGTGATGACTTTATCTAAGCTTCAGAAAATGTAAAAAATTACCATGCAACTCAATATAGTTGCGTTCAGTGACCCCAGTCTGTCTGTCTGTCTTTTTAAAGGACCATTTAATAATCAGGAGATGTCTGAGTGGTTTCAGGCGGGCTATTTCACCATGACCTTGCAGGTAAAGCGAGGATGCGACGAGATGTTCCAGCCTCTGGGCGAGATGATTAAGTTGTGGGGACGAGTGCCCTTTACACCGGGCCCGACACTACCTCCCATACTGGTAATATAAAGACGCTCACTTTTCAAATCTCTGACCCAAGATGACTTAACACTACTGTTCGGCATCTGAAAAGTTTTGATTTGTGTGTTTGACTCAATATAGGGAGATGCAGATCAAGAAAGGATGAAGAGACAACAGGAGATTAATGCTCTAAATATGTATCAGCTACAGCAGATG[C/T]AATATCAGTATTTACTCAGGTATGAGAGAAGATTATGAAGCGACATGTTTTTTTTATAGCAGTAAAAAATAATAGTTAAAAATACACGACTCTGTTTAATTTATTTGACAATTTTGCACCATATTATGATATGCAGCAAATTATTTGAAACACTTCGCTCCAGTTGGCTACATAATACAGCATTTGCACTATTAATGTGACTTGTAATGCAGAAATGAACTTTTTTTTTTCTCAAATATATTTTTATTAATTTTATTTTAGTGTAAAAACATGTCGGTAATTTATATTGAATAATAAGATAATATACATCTTTCATGTAATTTGAATCCTGCTCCCCACATGAAAAATCTAATAAAAAAAATAATAATAATAACAACAACAACAAATAATTCAATTTGTATTTAATAAATAAACAAATAAATAAATAAGGACATAAATTGCATACATTTTGTTTTTGAGCTGTAGTTATATTTAGCAAAGTGTCAAGTTTTTTTTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19880
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 |
---|---|---|---|---|---|
ENSDART00000056277 | Nonsense | 923 | 1329 | 22 | 29 |
ENSDART00000146705 | Nonsense | 923 | 1329 | 21 | 28 |
Genomic Location (Zv9):
Chromosome 2 (position 48335581)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 48367245 |
GRCz11 | 2 | 48221409 |
KASP Assay ID:
2259-2653.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGACAACAGCAGGAGGAGCAGAAGAAGAGAGAGCAGGAGGCGCAGAGA[C/T]AGCAGGAGCTGCAGAGACAGAGACAGCAGCAACAGGAGGCACTCCGACGA
Long Flanking Sequence:
ATCTACCTGCTTGCACAGCAGACACAAGAACACAGATCTGATTCATATTAGATAAATTTCCACATATGAACAAGGTCTGAATATGATTTGAGTTAATCGGAATCCATGTGATTTGTTCCTGCTTACATGTACTTGGGCCATATCCGATCTGTGCCACATGGGAGAAAAAAATCAGAATTGAGTCACTCGAACAGTGCAGTGTTAATGCAGCCATAAAGTGTATTATTTGAAAGCAAAACAATGGCTTTATTAATAATATTTTCATTATACTTTGTGTCATTAATAACCATAGTCCTTCATACAATTGGCAGCATTTAATATTTTTAAATTGATGTTATTAAATTCAGCAGGAAGAGGAGCGGAGGAAGCAGGAAGAACTGGAAGCTCAGAGGCGGCGTGAGGAAGAGAAGAGGCTGGAGGAGGAGGCTGCGGCCGCTGCAGCAGCACTGCTCAGACAACAGCAGGAGGAGCAGAAGAAGAGAGAGCAGGAGGCGCAGAGA[C/T]AGCAGGAGCTGCAGAGACAGAGACAGCAGCAACAGGAGGCACTCCGACGACTCCAGCAGCAGCAGCAACAACAGCAGCTCGCACAAATGAAGGTGAACATCCTGCACACCATATATTTTCTTGCCATGTCATCTTGTAGCCTAATAATAATTATTTATTTTATTAGATTCCATCTTTAGATGGACTTTAGTACAAAATCTTTCTCGTTTCTCTTTCGGTTTCTTGTTAAACTGTTTTCCATTAAGGAGAGTACATTATAAGTCTACCTTTTTAAATTACCAAAATGAGAGCTCTTTAATATTTGTTTTTTACTCTGCTTTATGACATGACTGGATTCAAGGCCTTGAAAGCACTTAAAAACACAGATGCTTGAAAGTGCTTAAATTAAATTTGAAATCAAATTAGATTTTAGTGTTATTTCAACAGATGTCATGCTGCTGTCAAAAACAGAATGAAAATAAATAATTCTTAATTCCGCAATCTTAAATTAAAATCTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10322
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056277 | Nonsense | 1296 | 1329 | 28 | 29 |
ENSDART00000146705 | Nonsense | 1296 | 1329 | 27 | 28 |
Genomic Location (Zv9):
Chromosome 2 (position 48321466)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 48353130 |
GRCz11 | 2 | 48207294 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGCANNNNNNACAGCAGCGGTTTGAAACRGTCACTTCCGGCAAGAAGAAGAAR[A/T]AACAGAAGATGGTACGAGCCGACCCAAGCCTTCTAGGTGAGTCATACATC
Long Flanking Sequence:
GGAAAGCTCTATTTGAAGAGTTATCGTTATCGTATATTGCATCAAAATTGCCAAAAACTACTGGAACTTTGTACGATTTTTTTCTGATGTAAGTACTTGTATTTTCAAATGATTTGAGGAATGTTCAAATCCAGAGAAATAAGCAGTTTTAACATGAGACGAGCGTACGCTGTCAATTTCCAATTTAGTTTTATAGATATAAGGGAAACACAGAAGACTTTAATATGCTTTGTGTGTGTTTTATTAGACTGCACAGAGCAGCATTATAACAGAAGCCTAAGATGTATTAAAAAATGAATAAAAGCTCTGCTGCTTTTGTGCCACATTATGTGCATGTTTGAGTGGTTTGTGCTGATCTGTCTGCAATTTTGTGTCAGGAGTCGGTGTGGGGAATAAGAGAAGTGCCACAGTCAGTCCTGCTTCAACAACAACAACAACAACAATTACAGCAGCAGCAACAGCAGCGGTTTGAAACGGTCACTTCCGGCAAGAAGAAGAAG[A/T]AACAGAAGATGGTACGAGCCGACCCAAGCCTTCTAGGTGAGTCATACATCAAGTTTAGAGGTTAAAACGTATTAGACAAATGACTCAACTGAGACTTTGAAATACTGTGACGTGAAGAGAAACTGATGAGTAAGCATGACTTCAGTCAAAACCAGACTAACAGATTGATGGGAAAAACCACATGAGCGTCTGGACCACCAACATCAATTAAAATACTCAAAAGGAAATAAAAAATCATATGAATATACAGTGCTCAGCATATATAAGTAAACCCCCCACAAATCTCTCATTTAAATTCATATTTTTTATAGAAAGCTATACAAAATTATATTTGTGCATATACATTAGATTAGTCCAGTGGTTCTCAAATTTTTTTCATCAAGTACCACCTCAGAAAAAAATTGTCTCTCCAAGTACCACCAAAATGAGCAGTATTGAAATACAGTAGCTAAGTAGGCCCAGTAAAGCAGCTACAACTCTGCACAGTTAAAAAATGTGGC
Associated Phenotype:
Not determined