ZMP
si:ch211-279i17.1
Ensembl ID:
ZFIN ID:
Description:
Novel glutamate receptor interacting protein family [Source:UniProtKB/TrEMBL;Acc:A5WUM3]
Mouse Orthologue:
Grip2
Mouse Description:
glutamate receptor interacting protein 2 Gene [Source:MGI Symbol;Acc:MGI:2681173]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37555 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13297 | Nonsense | Available for shipment | Available now |
sa13477 | Essential Splice Site | Available for shipment | Available now |
sa32411 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37555
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092447 | Nonsense | 231 | 1118 | 7 | 24 |
ENSDART00000133267 | Nonsense | 118 | 923 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 22 (position 34178027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 31434232 |
GRCz11 | 22 | 31383427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCGTGTTATTGTGCAGAGAAGGGACTCTAAAATCGGGTGACCGGATCT[T/A]AAGCGTGGATGGTGTGGTTTTACACAGCGCCACTCACAGTGATGCCCTTG
Long Flanking Sequence:
TGCTACAAGTGTGATATTGCTTATATATATATATATATATATATATATATATATATATATATATATAAATTAATTAACTACTTAATTAATTAATTAATTAATTTATTTATTTATTTATTATTTTTGCTGTTCTAACTACATATTTAAAATGACCTCAGTAAACAGCTTAATAGTTTTATGTTAAATCAACTTAAAATGATTGTAATTACTATTGAGCTAACCTAATTGATTTGTGTTTGATGACATTAAGACTTTGTGTGGAACCCATCATTTTTTATATAATTTTATTTTTTAAATAAAATACACTGTGAAAAGCGTTTAGTAACCGTTATTTAAAATGTGAGTAAATGTGTTGCTGTGAAATAGAATTGATATTATTTAAAATAACAATGTTAGTGTTTAGTGGCACATGATTTTTCCTAAATCATTCTAATGTTATGTGTATTATCTTTGCGTGTTATTGTGCAGAGAAGGGACTCTAAAATCGGGTGACCGGATCT[T/A]AAGCGTGGATGGTGTGGTTTTACACAGCGCCACTCACAGTGATGCCCTTGTTGTGCTGACCCAGTGTGGACAAGAAGCCCTTTTCCAAATCGAATATGATGTCTCCATCATGGGTGAGTTACTTTGGTTGTGCTTGTTTTATACAGTATGCAGATAGGATGAACATTTCACATATTCCAGTGGACTAGTTTTGTGTACAGCGGTCCCTTGTTAATCGCGGGAGTTATGTTCTAAAAATAGCCAGCGATAGGCTAAATCCACGAAGTAGCAGCTTTATTTTTTATGATTATTATAGATGTTTTAAGGCTGTGAAACCCCTCACTGCACACTTTATACACTTTTTTCAGACAGCCATTACATTTTCACACTTTTCTCACTTTTCTTTTGTTTTAACACTCTCAAAGTTCAAAATTTCGTAGCTTTCATGTCCATAAAATTAGGCCCAGTATTATAGAACGAAACCAGAGATCAAAACCTATTAGGCGCAAACATTTATCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13297
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 |
---|---|---|---|---|---|
ENSDART00000092447 | Nonsense | 404 | 1118 | 10 | 24 |
ENSDART00000133267 | Nonsense | 291 | 923 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 22 (position 34200125)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 31455249 |
GRCz11 | 22 | 31404444 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCCTGTGTGAACTACTGCCATTCTCAACATCCTGGTCAYTGTAAGACAT[C/A]GACGTGGACATCTGCTTCCAGYAACCCTTCCAGCTCTCAGGATTACTGCA
Long Flanking Sequence:
GATACTGCTGCGGTCCTGCAGAACAAATGAGAACAAGCACATGCACGTTCACAGAGGCACTCAATTACACGGCCCGCCGCTAGCAGCAGGACTTCATTAGCCTGTTTGCTAATGAGCTTCTTCATTGTTTTTGCATGCACATTCATTTCCCACAGATCAGTATTAGAGGCACAAATGCATCTTCAACAGATCCTCAAGACTTCATATGATGTCCAAACATGTATTAATGAAAATAATATTGAAAGTGTATACATTTTTATGATATTTTGTGTCATTAAATATGTTAGAAACATTAATGTCATCAACATGCTAATTCCTTTTAGCAGCATGTGGTGGGAGCAATATTGAGTGTTCATATTGCTTTTGAATATCATTTTGTCATTTTCTGATATATTTTTATGTCATGTGTTCAGTGAAAGTTCAGAAAAGTGACCACCCTCACTGCTGGGACCCCTGTGTGAACTACTGCCATTCTCAACATCCTGGTCATTGTAAGACAT[C/A]GACGTGGACATCTGCTTCCAGCAACCCTTCCAGCTCTCAGGATTACTGCAAATGTAACTACAGTGTAAAATGCTGTTTTTATTTCATTATAAGTAGTGGTGTGTACTGTGTATATTTTTTTGTGCATTTAAATATATGCATGAGCATATTGTATAAAATATTTATGTATGCATATATTATGTAAATACAAACTTGCACATAATTTTAAGATGTGAAGTTAATTTGGCTAATTTGTACTGGCAATAACCACTGAAACTTTGCGGTCACACTTATATTTTCCAGGCACTATTCAACTATTCAACTACTTACTGTATAGTTACATATCCAGGACTTTAGGATCCAGCACTTTAAGGTCTTTTAGGCACATTTTTGCAAAGATTTTGTAGGAAAAAAAAAAAAAAAACAGTCACTGAACATACTAAAATCATAATTTACAAATAATAATAATAATAATAATAATAATTTCTAATTGCTTCTCCTCCTACAACTTTCAGCCTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13477
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 |
---|---|---|---|---|---|
ENSDART00000092447 | Essential Splice Site | 421 | 1118 | 10 | 24 |
ENSDART00000133267 | Essential Splice Site | 308 | 923 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 22 (position 34200179)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 31455303 |
GRCz11 | 22 | 31404498 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGACATCTGCTTCCAGYAACCCTTCCAGCTCTCAGGATTACTGCAAAT[G/A]TAACTACAGTGTAMMATGCTGTTTTTATTWCWTTATAAGTAGTGSTGTGT
Long Flanking Sequence:
AGGCACTCAATTACACGGCCCGCCGCTAGCAGCAGGACTTCATTAGCCTGTTTGCTAATGAGCTTCTTCATTGTTTTTGCATGCACATTCATTTCCCACAGATCAGTATTAGAGGCACAAATGCATCTTCAACAGATCCTCAAGACTTCATATGATGTCCAAACATGTATTAATGAAAATAATATTGAAAGTGTATACATTTTTATGATATTTTGTGTCATTAAATATGTTAGAAACATTAATGTCATCAACATGCTAATTCCTTTTAGCAGCATGTGGTGGGAGCAATATTGAGTGTTCATATTGCTTTTGAATATCATTTTGTCATTTTCTGATATATTTTTATGTCATGTGTTCAGTGAAAGTTCAGAAAAGTGACCACCCTCACTGCTGGGACCCCTGTGTGAACTACTGCCATTCTCAACATCCTGGTCATTGTAAGACATCGACGTGGACATCTGCTTCCAGCAACCCTTCCAGCTCTCAGGATTACTGCAAAT[G/A]TAACTACAGTGTAAAATGCTGTTTTTATTTCATTATAAGTAGTGGTGTGTACTGTGTATATTTTTTTGTGCATTTAAATATATGCATGAGCATATTGTATAAAATATTTATGTATGCATATATTATGTAAATACAAACTTGCACATAATTTTAAGATGTGAAGTTAATTTGGCTAATTTGTACTGGCAATAACCACTGAAACTTTGCGGTCACACTTATATTTTCCAGGCACTATTCAACTATTCAACTACTTACTGTATAGTTACATATCCAGGACTTTAGGATCCAGCACTTTAAGGTCTTTTAGGCACATTTTTGCAAAGATTTTGTAGGAAAAAAAAAAAAAAAACAGTCACTGAACATACTAAAATCATAATTTACAAATAATAATAATAATAATAATAATAATTTCTAATTGCTTCTCCTCCTACAACTTTCAGCCTACAGCCACCAACCATGGCTCAGACCTTCAGATAGTGCTGAAGATTTTGGCTATATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32411
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 |
---|---|---|---|---|---|
ENSDART00000092447 | Nonsense | 1048 | 1118 | 23 | 24 |
ENSDART00000133267 | Nonsense | 881 | 923 | 19 | 20 |
Genomic Location (Zv9):
Chromosome 22 (position 34253496)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 31508620 |
GRCz11 | 22 | 31457815 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACATGATCAGACCTGAGGGTCCGGCAGACCGCGCTGGGCTCAAACCCTA[C/A]GACAGGATCCTTCAGGTGCCTCTTCTCAGATCTCCAGCTATACGATCTGC
Long Flanking Sequence:
AGTTTCACTTTGCTGTTTTGTTTCACTTTTTTAAATCTGATTTTCCTCCTTTCGATTTCTTTGCTTTGCAATTGCTTACTGTTCCCTTTTGAGCTTTGCTTACCCGTTTACCTTACCTTTTTGTTTGTGCTTTGCTTAAATGTGTTTCGCATTTTGTTTTGTATTTATGTTTTGTTTTGCACTTGGCTTGAATACGTTTCAAAGGAATTTATTCCATTATTTACTTTTTTCATTTGAAATTCCATAAATAAACACCATATTGTTTTATATTTTTTTGAACTATTACTTTAAGACTTACACATAATCTACCAAACACTTTCAGAGGAAATGAACTCATGGTTAAATATCTAAATAATTCCATGTTACCAGGTGACGGTGATGAAAGACCCGGAGAGTGACGACTTCGGCTTCAGCGTATCGGACGGTTTCTTGGAAAAGGGTGTTTACGTGAACATGATCAGACCTGAGGGTCCGGCAGACCGCGCTGGGCTCAAACCCTA[C/A]GACAGGATCCTTCAGGTGCCTCTTCTCAGATCTCCAGCTATACGATCTGCCCAGTGCAGTTAAATATAAACCCAAAGACGTGAGAGCGTCAGTAAGGCGTTTGGCTCTGGGAGGACATGTCGGGTTAAACAATGATTTCACTGGATCTTCACAGCATCTATGGTCAATTCTTAAAGAAAGTCCCCTTCTTGGTAATCTCACACGCGTCACTGGCCCTGGAAATGACTCAGGCTATGTTAATATTATACTGAAAGTTAAATAATATAATATGTTAAAATTATACTCCAAAAATCAAAATTATATTTAGGGTTTTTTGACTGTTAGTATCAATTTGCATTTAGAAGACTTAAAGGTCCCATTAAATTAAAATAAAGTTTTTCAGATGTTAGTATCAGTATGTTAGGTTTTAGAATATCTATAAGCTAATGCGCACCAAAACAGTGACAAAATTTGCGTCTATAAGATATAAAACTTTCACTTTCACCTAAATGGATCAATGT
Associated Phenotype:
Not determined