ZMP
gripap1
Ensembl ID:
ZFIN ID:
Description:
GRIP1-associated protein 1 isoform 1 [Source:RefSeq peptide;Acc:NP_001116792]
Human Orthologue:
GRIPAP1
Human Description:
GRIP1 associated protein 1 [Source:HGNC Symbol;Acc:18706]
Mouse Orthologue:
Gripap1
Mouse Description:
GRIP1 associated protein 1 Gene [Source:MGI Symbol;Acc:MGI:1859616]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa402 | Essential Splice Site | Available for shipment | Available now |
| sa31629 | Essential Splice Site | Available for shipment | Available now |
| sa16570 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa402
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 |
|---|---|---|---|---|---|
| ENSDART00000111853 | Essential Splice Site | 102 | 867 | 5 | 28 |
| ENSDART00000139414 | None | None | 194 | None | 8 |
The following transcripts of ENSDARG00000063069 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 10252408)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 9668990 |
| GRCz11 | 8 | 9707575 |
KASP Assay ID:
554-0369.1 (used for ordering genotyping assays)
KASP Sequence:
GGATGATTTCAGACTGCAGAACAGCACCCTCATGCAAGAGCTGTCCAAGG[T/C]GCTTTCATTATCATGAACATGTCAACACTGTAACTTTATGCACAAATGTA
Long Flanking Sequence:
CTAATAATTTTTTTTTCTTCTGCTTACACTATGGAAAATATTTTAAAGCATGCTGATAACCACAAAGTTGCTTTTCCATATATACTTCGTTAGTGTTTGAAGGGATAGTTTAACCAAAATTGAACATTCTTTCATCTTTTACTCACTTTTTACTTGTCACAAAGCTTTTTTTTTGTAGAACAAAAAAGAAGATATTTTGAAGAAAGTTGAAAACCGGTAACCATTGACTTCCATGTTATTTGTTTTTTCTACTAAGGAAGTCAATGTTTATCAATTTTCAGCAATTTCTTTTTTTATTTCTGAAAAAAATGTAATCACGTTGTAACATCTAAAGTATCATGTAAAAAAAATTATGTCTAGTAACCATGCCTGATTATTTTGTTTTTTTTAGGAGGTAGATGCCTTAATCAATGAGAATAAGATGCTTCAGGGCAAGTTACACAGTCAAGAGGATGATTTCAGACTGCAGAACAGCACCCTCATGCAAGAGCTGTCCAAGG[T/C]GCTTTCATTATCATGAACATGTCAACACTGTAACTTTATGCACAAATGTATCTGAAGCTGATTTTTCATACTCGCAGAAAAATTATCAAAAATGTATAACATAAAAATTTGTTTTACACAGTAGTGACATCACTAATTGAACAGTTTAGATAACTTTACTGCTCAAATAACATAAAGTGGGTGTAAAAACAATTTCTCATTTATTTTACTTACAGCAGCTATTACTTCAGTCTTTTTTTGTCACATGAACTCAGAATTACATTTTCTACACTGAATTATGCTAAGCAAACATTAAAAAATATACATGACATATATATTGCCCCCCCTGTTTTTTTCCCCCAATTTCTGTTTAATGGAGAGCAGATTTTATCAACACATTTCTAAACATAATAGTTTTAATAACTGCTTTCTAATAACTGATTTCCTTTATCTTTGTCATGATGACAGTACATAATATTTGACTAGATATTTTTCAAGACACTTCTATACAGCTTAAAGTG
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa31629
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 |
|---|---|---|---|---|---|
| ENSDART00000111853 | Essential Splice Site | 785 | 867 | 26 | 28 |
| ENSDART00000139414 | None | None | 194 | None | 8 |
The following transcripts of ENSDARG00000063069 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 10305985)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 9722567 |
| GRCz11 | 8 | 9761152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAAAAAAAGCGCAATTATTGAGACGTACGTCATGGACAGCCGGAGAGG[T/C]AAAGCAGCTTTTCTCCATCCCTCTTTTGTCATTGTTCGCAGCCTCTTGTT
Long Flanking Sequence:
CTGAACACAAGATCGAAATTATTAAATTAAATTATTTTTCTTAAGTTTTATGAAAAAGATGAAATCCTTTAACCATAATTAAATAGAAGTTCTTAATAAATGAAAAGATAAATGTTTAAAATATTATAAAAAAAACTGCAACATTTATTTGGTCTTATAGATAAAATTACCCAATTTTAAATGCATAATCTATTTAAGAACCATTTTGATATTTATTAATAATAAAACCTGTTGAATATCATGGGATATTGACTAAAGGTGAAAAGCATTTTCGAAAGCTATCTTTATCTGGCAGTGATTGCACTATCCTTACCTGTGTGTCTCCATATCAGGTTTATCAGGCGTTTGTGTGGCCGTGGTGTGTGGCAGTTTATTGCAGATTGTATCTCTGTGTCGTCTGTTCAGGTGAAACACTTGGAGGTCAGCTGCGCTTCAATGGCCGATGACATCTGTAAAAAAAGCGCAATTATTGAGACGTACGTCATGGACAGCCGGAGAGG[T/C]AAAGCAGCTTTTCTCCATCCCTCTTTTGTCATTGTTCGCAGCCTCTTGTTTTTCTGAAGGGTTTACAGATGAGGTCAGGTGATAGCTGATACCCATCATGCTTTTATTCTAAGGAAAAGCGACAGCTGAAGTGTATCAGACATAAGCTTGTCACTTTGTTGTGTCTGCAAATAAAAGAGCTATTTAGACTGATACAGAGAAAATTGCATAACATTTTTTTAATACTATTTTTAGATCTGCGCTTGTACTTGCGTAATCTGCCACTAAATGTTTTAGCGATACTATTTATAATGCTGCTATTTTGGTGCTACAGTACAGTCCGGCATCTTCCAAAAAGCACTTTGCGACTGGAAATAATATTTAATAATAAATGGGAGGAAGGTTTTGTTTTAGTCCTCTGATTACAATTAAAGGTGCTGTGTGTAAGTTTTTGACTCTTCTAAAGCATAAGAATACCATGATATGTTTGCAGATATTTAAGAAAAATGCTAAGTGAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16570
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111853 | Nonsense | 791 | 867 | 27 | 28 |
| ENSDART00000139414 | None | None | 194 | None | 8 |
The following transcripts of ENSDARG00000063069 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 10326617)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 9743199 |
| GRCz11 | 8 | 9781784 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATCTTTCTGTTTTTTTTTTTTTATATCTCAGATGTATCAGGAGGTGTT[G/T]GATTGGCTCATAGTGCTCAGCCKGACCGTGGAGRTTTGAGTTCGGTTCTG
Long Flanking Sequence:
ATCTTAACGACTTCTAAAAGATGAATCACTGTTTGACCATCTACAATTAGGCATGGATATAAACATTTACGATCATGATTCTCGTAGTACTACATCACACCTTCAGCATACATTAAAACCATTTGTTGTTTCCGTTTGCCATCTGATTTAGCATTTAAAACATGACGTCAGATTTACCAAGCAGACCGATCCTCTTGCAGCTCTTGTGAGTGTAGAACGGTGTTTATTTGGCAACTTTAAGATGTGTGTGTGGCTTTCGTCAAACCTGCGGATGATTGCACTCGAGGTGCTCGTAATGTTGTGGCGTGAAGTGAACTGCTTTCCTCCAAACGCAAGCACTCTGTATTCACTCAGCAGACACTAATGGCCCCCAGATACACATGGATTTATTCATAGATGTTGAGAGGGAAAACGGGGTTAAAAAGCATAAGCTGGATTGATTGAATGTTTGCATCTTTCTGTTTTTTTTTTTTTATATCTCAGATGTATCAGGAGGTGTT[G/T]GATTGGCTCATAGTGCTCAGCCTGACCGTGGAGGTTTGAGTTCGGTTCTGAGGGACTTGGTGAAACCCGGAGATGAGAATCTGCGCGAGATGAACAAAAAGCTGCAGAACATGCTGGAGGAACAACTGACAAAGAACATGCACCTACAGAAGGTAAAGAAAGAGATGAACAGCTACGGTTGAAGTCAGAATTATTAGCCCTCTTGAATTTTTAGTCCCCAGTATATTTATTCCCTAATTTCTGTTTAACGGAAAGATTTTTTCAACAAATTTTTAAAAACTATAGTTTAAATAACAAATTTCTAATAACTGATTTATTTGATCTTTGCCATGATGACAGTATATTTTACTAGATATTTTTCAAGGTACTAGTATTCAGCTTAATGTGACATTTAAAGATTTAACAATTAGGTAAATTAGGCAAGTTATTGTTTAGCCGTGGTTTGTTTTGTAGACAATCAAAAAATTGCTTAAGGCAGGGAATAATATTGAACTTAAAAT
Associated Phenotype:
Not determined