ZMP
si:ch73-250d21.1
Ensembl ID:
ZFIN ID:
Description:
glutamate receptor interacting protein 2 [Source:RefSeq peptide;Acc:NP_001116760]
Human Orthologue:
GRIP1
Human Description:
glutamate receptor interacting protein 1 [Source:HGNC Symbol;Acc:18708]
Mouse Orthologue:
Grip1
Mouse Description:
glutamate receptor interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1921303]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21193 | Essential Splice Site | Available for shipment | Available now |
| sa41117 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa883 | Nonsense | F2 line generated | Not yet available |
| sa15003 | Essential Splice Site | Available for shipment | Available now |
| sa21192 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21193
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 |
|---|---|---|---|---|---|
| ENSDART00000092426 | Essential Splice Site | 176 | 736 | None | 16 |
The following transcripts of ENSDARG00000063337 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 7797421)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 7184224 |
| GRCz11 | 8 | 7227772 |
KASP Assay ID:
2260-0125.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCGCCGGCTGCCATCCGCTTTATAGAGCCTGACACACCTGCTGAACGG[T/C]GAGAGCAGAGCGCACCTCATGTGTGCTCAACACACTGTGCAATTTGATGT
Long Flanking Sequence:
AAATTATCCATGTTGCATAAATGTATTCTAGGATAAACCAATCATGCTGTTAATAATGACATTTAAGCAAAATTAACATGATTAAAATGATGAAGAAATTCAATGGACATGATTACAGTGCAAGGAAAGTGTTTTTGGAGTTATATTTTCACTATTCATGTTATTTTATATTCATTGTATTATCATCATCGGATATGTAGTTTTTTTTTTTTAAAGAGTGTCTTTTGTCATAATGTTTTTGAACAAATAAAATCTGAAGGTTGTGCATTAGTTGTAGTGTATTTGACAATGTTGTGTATTCTTGTGTGTCAGTGTCTCTGGCATCGAGTACGGTGGGCGCTGGAGGTCAGGTAGTGCATCTAGAAAGCGCGGAAGTGCTGCTGAGAGGAGATCCTCTGACTGGATTCGGGCTGCAGTTGCAGGGAGGAGTGTTTGCCACAGAGCCGCTGTCAGCGCCGGCTGCCATCCGCTTTATAGAGCCTGACACACCTGCTGAACGG[T/C]GAGAGCAGAGCGCACCTCATGTGTGCTCAACACACTGTGCAATTTGATGTCCCAGATTAGTTCTATCATTCGGTCTGTTTTATGGTTCTGTTGCTCTACAATCCTATGGTTAAATCCATCATTCTGGTGTTTGATATATTCTGTCCATCCATCTCAAGTTTTCATTTGTTTTGACCAGTTCTATCTCTCTCTTTCTGTCATTCTGTTCTGTTGTTCTACTATTATGTGATACTGTTCTTCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCAATCTTATCGTTATGTGTATTGTTTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCGTTGAAAGCAGAAGTTAACATACACTGAACAAAAAGGCACATAACCATTTAAAATAAGTCAGATGTTAATGTGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41117
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092426 | Nonsense | 404 | 736 | 10 | 16 |
The following transcripts of ENSDARG00000063337 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 7786175)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 7172978 |
| GRCz11 | 8 | 7216526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGAAGGGCAAACCTCTGAGCGAAGCCATTCACCTGCTGCAGACCGCT[G/T]GAGACACGGTCACACTCAAGATCAAGAAACGATCCGACCGTAAGAGTGTG
Long Flanking Sequence:
TTTTATAATTTCATTTATTTCTACAATTTTGTGAATCCGATGTTTGATTGTTTTGTGTATACATCGTGGAAAACCCTATCTGTATGTGAATTTGGAAACTGCAATAAAAAACAAAATGGAAAAAAAAGAATATAATGTGTTAATAATAGATCAAGTGTTGCTAGAAGTGTTGAATCTTTAAAATGATCATGAGAATGACTGAAGACTCCACTGACAATACAGACATTATAATCAATTGTCATGAATGTTTGAGTAGGTACACTTATTTGAGATCAGTTTTAGTTTTTTTAACAGAAATGTCAATATATATCAAAACACATTTCATCTTTAGCTTCAGTTAACCATAATAGACATTGAATAAGTGTTAACTGTGTTAAACATGGAATTATGTGTGCTTTAGGACTGGCGCTCTTCATATCGGTGACCGAGTTTTGGCCATTAACAACATGAGTCTGAAGGGCAAACCTCTGAGCGAAGCCATTCACCTGCTGCAGACCGCT[G/T]GAGACACGGTCACACTCAAGATCAAGAAACGATCCGACCGTAAGAGTGTGTGTGTCTGTGTCTGTGTGTCTGTGTGTCTGTGTGTCTGTGTCTGTGTGTCTGTGTCTGTGTGTCTGTGTCTGTGTCTGTGTCTGTGTGTCTGTGTCTGTGTGTGTGTTTGGAGAAGTGTATGTTAACATTTCCGTCATGTAATCCACCGAAAAGAGCTTCTCATAAATATTACATCAGGTCTTGTCCTCATGACCCACATCTGTGCTTTCCAGCACTTTTGGATTCAGAGCGGGGCAGTCCGTCCAGAACAGCCTCATGCGTGAGCGACATGGAAGACGATCGCTCCGATTCATTCCGGAGAGGGAAATACTCTGATCTCCTCCGTCAGACCACGCCGCCCAGTCTGGATTCAGCCATGGACTCGTGGGACAGTTCGGCCCTCGATGCTGGCTATGGAAGTCAGGGTATGGAATGAAATCATGAATATCCTAATTGAATGTTAACAAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa883
Status:
F2 line generated
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092426 | Nonsense | 497 | 736 | 12 | 16 |
The following transcripts of ENSDARG00000063337 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 7783006)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 7169809 |
| GRCz11 | 8 | 7213357 |
KASP Assay ID:
554-0790.1 (used for ordering genotyping assays)
KASP Sequence:
GGCGTATATATTCATAGGCCATCAGACTTCACTCTTCATCCCAGCGACTG[G/A]AGACAGACCAATCACAGGAGCCCGCTGATGTCAAGAAGACCCGCCCACCG
Long Flanking Sequence:
TTTGGATGAATTGCCCCTTTAAACTAAAATATCAAAAATGATTAGTTATAGTATAAAATCAAATTTCTTTTGGCAAATCATATTCATGTTTGTGCTTAATCAAATCTCAAACTCTGTTTTCCGGTGTGTATATTCATATTTAATTTTTAGGCTTCAGAACAAACCACTTCATTAACTTTATTCATTCATTTTCCTTCGGCCTAGTCCTTTATGTATAAGGGGTTACCACTGTGGAATGAACCACCAACTAACAACTCCAATAACTTTCCAAAAATAATTAAACTTGCCTTGGTTAACATAATAATCTACTTAAGTCTTTAAATTGCACTTTAGGATGACTCCTAGCATCTTAAAAAATAAGAAATTAGTTATTAGAAATTAGTCATAAAAATCATTAGGCTTAAAATGTGTTGAAAAATCTTGTAATCAAACCTCAACCTTTATATTTCAGGCGTATATATTCATAGGCCATCAGACTTCACTCTTCATCCCAGCGACTG[G/A]AGACAGACCAATCACAGGAGCCCGCTGATGTCAAGAAGACCCGCCCACCGTCCTACAGTGTATGATGGGAGACTGAGTGAAGAAGACTGGACGTACTCTGGGTGAGAGTTTCTTTAGAGACACAACTCGTTGAATTAGTCAGTACAGGTCTTCATCTTATGAAGATAATAGTCAGCGATTCGAGGGTTAAAGAAGCATAATGGAAGATGAGAAAGACAATTATGCCAAAGAGCATTTCAGTTTTGGTTACTAACGCAATCTTGTGGCTGTTCTGTCAATTATTATTTCTCATGTGTATGTGTGCTTAGGAATGAATGTCATTAAGAAAATGTTCAGGTCATATTTCAGAAATGTATTTCGTTTGAATTATAATACATTGATATTATGACGGTAGTATTTGTGATACTAGCTGATTTGTCATAAATTTTAATATTGTGAAAAAAGAAAAAGTGGACTGTGACCTGAACATGTGATCATGCACTGTAAAATCAGTCCCTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15003
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 |
|---|---|---|---|---|---|
| ENSDART00000092426 | Essential Splice Site | 626 | 736 | 14 | 16 |
The following transcripts of ENSDARG00000063337 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 7776559)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 7163362 |
| GRCz11 | 8 | 7206910 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CWGAGGACCTRAAGGRGAACAGCCCGTCAGTGCCTCTAGAGCTTCATAAG[G/A]TAATGTTCACCTTCCAGCAGCTGGATTCACGTCTTGAACTCTTGCTTTTG
Long Flanking Sequence:
TCCACAAAGAATACCGTTATAATAGCTTATCGTCTTACATTTGCTATAATTGTCAACATACACAAATTAGCGAATTAAATTTAGAAAATATTAAAATCTCTTTAGACTACTGCTTTTTTACTTCTATCTTTGAGAATTTTTCCAAATCTGACACTGCCTGAATCCCTTTATTTTCACAGCGTGTGACTAAACATCAAACATTTGACTTGTGACAACTAATCTTTTAATTCGATTCATTTTGGAGAATAAATTAGTCTTGCTTTGAACAAAAAACATCCAACATCTCTGTCTCTTCTTTGAAATCTCATGTTTTTTTTTTTAATATTTATTATTTGGAGGCTACAATAATGTCAGGCAGCACGTTGAGTTTGGGAGAAGACTTCGAGAAGCAGAATGAAAGCAAGACCAAATTTCTGGAACTGAGCCCGGAGAATACCTCCGTGAACACACCAGAGGACCTGAAGGAGAACAGCCCGTCAGTGCCTCTAGAGCTTCATAAG[G/A]TAATGTTCACCTTCCAGCAGCTGGATTCACGTCTTGAACTCTTGCTTTTGATGGCCTGATCCATGTTTTCTCCATCAGATCTGCATTCAGAAGGATGCCGACAGCAGGGATTTTGGCTTCAGTGTGTCCGACGGTCTGCTGGAAAAGGGTGTTTATGTGAACATGATCCGTCCGGATGGCCCTGCAGATCAGGCTGGGTTACGTCCATATGACCGGATTCTGCAGGTGATGCTTTCTTCCCTCTAACCTTTTCTTAATGGGAAAGTTTACAGAAAATGGGAAAAGTCACTATTCACCTACGCTTTTTATAAACCGTCAGACTATCCCAAGACCCAGTTCAAACTTTCTCACTTCTCTGATCGTTTTCCACAGGTCAATCACGCGCGGACTCGTGATTTCGACTGTTGTCTAGCTGTGCCATTGATCACGGAGGCCGGAGAGAATCTGCAGCTGGTCATTAGCAGGAATCCTCTCGCTCAGGCGCACGACTGGCCACCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21192
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 |
|---|---|---|---|---|---|
| ENSDART00000092426 | Nonsense | 718 | 736 | 16 | 16 |
The following transcripts of ENSDARG00000063337 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 7776060)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 7162863 |
| GRCz11 | 8 | 7206411 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGGTCATTAGCAGGAATCCTCTCGCTCAGGCGCACGACTGGCCACCT[A/T]AAGACTGTCAGGACACTTCCCAACAGTCTGCACAAAATCCAAGAAAAGTT
Long Flanking Sequence:
GGTAATGTTCACCTTCCAGCAGCTGGATTCACGTCTTGAACTCTTGCTTTTGATGGCCTGATCCATGTTTTCTCCATCAGATCTGCATTCAGAAGGATGCCGACAGCAGGGATTTTGGCTTCAGTGTGTCCGACGGTCTGCTGGAAAAGGGTGTTTATGTGAACATGATCCGTCCGGATGGCCCTGCAGATCAGGCTGGGTTACGTCCATATGACCGGATTCTGCAGGTGATGCTTTCTTCCCTCTAACCTTTTCTTAATGGGAAAGTTTACAGAAAATGGGAAAAGTCACTATTCACCTACGCTTTTTATAAACCGTCAGACTATCCCAAGACCCAGTTCAAACTTTCTCACTTCTCTGATCGTTTTCCACAGGTCAATCACGCGCGGACTCGTGATTTCGACTGTTGTCTAGCTGTGCCATTGATCACGGAGGCCGGAGAGAATCTGCAGCTGGTCATTAGCAGGAATCCTCTCGCTCAGGCGCACGACTGGCCACCT[A/T]AAGACTGTCAGGACACTTCCCAACAGTCTGCACAAAATCCAAGAAAAGTTGACCTCTGATTCCCACAAATGAGAAACACAGAGCACAAGTTTGTTTTTCTTCCACACACAAATGTTGTCTCTCTCTCACTCTCACATTAGCACCAGTGTTTTGTATTTCACATATGTTTATTTATTGATATTTATTTATTATTCTCAAGCCAAGTTCAATGTTTTTCTCACAATGTGTGTTTTTTTTTTTGTGATGATCCTCACTTCAAACAAGCCACAAACAAGTTCTCACAGACGCACATGAGATTTCTGCTCGCTCTCAGTTACACAAAACATCATGTTCACCTCCATCCAAGCCTCTTTTGTTTGTATTTGAAATAATGGCGCACTCATTTAGTTCGTCCTGTCAACAGAAACTCTTTGATGAAGCAGATCTGTGGGTTTTACCGAACACGACGAGAAATTCAAAGCCATGTGTTTGACTGTCTAGATGCAATTTCTGAGATCAAA
Associated Phenotype:
Not determined