Busch Lab

ZMP

gripap1

Ensembl ID:
ENSDARG00000063069
ZFIN ID:
ZDB-GENE-070112-922
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
sa34312 Nonsense Mutation detected in F1 DNA Not yet available
sa31629 Essential Splice Site Available for shipment Available now
sa16570 Nonsense Available for shipment Available now
sa34313 Essential Splice Site Mutation detected in F1 DNA Not yet available

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.
Availability:
Order Allele From ZIRC
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:
sa34312
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111853 Nonsense 388 867 16 28
ENSDART00000139414 Nonsense 140 194 7 8

The following transcripts of ENSDARG00000063069 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 10276062)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 9692644
GRCz11 8 9731229
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCACAGATCCAAACAGTGAAGACTCAGGAACTGAATTTGCTGAGAGAG[C/T]AAAATCTTGCGCTGAACGCCGAGCTTCAGCAGAGACGTACTGACCAGGAG
Long Flanking Sequence:
GCAACGCTGATATATTAATCTTAAAATAAATATGAATGATTTAATTTGCACATGAGGCTCATTTTAAAAACACTACAAAGACTAATTGGTTCAACCCTGATTGAGTTTTTTTTTAAATCTTCCACAATCATCATATTAATCTTTTTGTTTGTACTTGTGCCAGCCTGAATTAGTTCATATATGTCCACACATAGATGCATGTGCACATATGTGTGTATTGCATCATGCATGATGGTTTATTTTTAGCTTGAAAGCACTCATGGGTACGTTTAGATTGATGATGGATTTAACATTGTGCTGATCTGCACTTCTCTGCTGTTCACTAGTGCTTTTCAAGCTTCCTAATAATTCTCCTTTTGTCTTCTGTTGGCATTTTTTTTCTCATCCATACACTGACCGAAGCAGACTTAATTCAGTTGATCTGGGTCTCTGAAACTGTCTGTGTGTGTTTTTCACAGATCCAAACAGTGAAGACTCAGGAACTGAATTTGCTGAGAGAG[C/T]AAAATCTTGCGCTGAACGCCGAGCTTCAGCAGAGACGTACTGACCAGGAGAGCTTTCTAGCACAGAGAGATGATCTCAACTCACAGCTACAGGTATTTGATTCCTGCTGATTTTGATAGCAACTTAACATTTTTTATACTTAAAGCCAGGATAGTTCACCCCAGAAATGAAAATGTACTGACTATTTACTCAGTAGTGGTTATAAAGTTTCATTCTTCTGTTCAACACAAAAGAAGATATTTTGAAGAAAGCTGAAAACCTGTTTGACTTCCATAGTAGGTAAAACAAATACCATGGAAGGCAATGGTTACAAGTTTCCTGCATTAAATATCTTCCTTACACCGAGTTCAGACTTTAGCCCCGATTTCGCCGACAGGTTTTGAGAAATCGCAGACAAATGCTTGAAATAACAAGCAAATCGGTGCTCGTTCATATGAGTAACAACCACACAGTGTAAACTATCAAAGACGCGATCTGAAAGAATCTATTTATTTATTTGA
Associated Phenotype:
Not determined

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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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

Mutation Details

Allele Name:
sa34313
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111853 Essential Splice Site 841 867 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 10326771)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 9743353
GRCz11 8 9781938
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAACATGCTGGAGGAACAACTGACAAAGAACATGCACCTACAGAAGG[T/G]AAAGAAAGAGATGAACAGCTACGGTTGAAGTCAGAATTATTAGCCCTCTT
Long Flanking Sequence:
TTAAAACATGACGTCAGATTTACCAAGCAGACCGATCCTCTTGCAGCTCTTGTGAGTGTAGAACGGTGTTTATTTGGCAACTTTAAGATGTGTGTGTGGCTTTCGTCAAACCTGCGGATGATTGCACTCGAGGTGCTCGTAATGTTGTGGCGTGAAGTGAACTGCTTTCCTCCAAACGCAAGCACTCTGTATTCACTCAGCAGACACTAATGGCCCCCAGATACACATGGATTTATTCATAGATGTTGAGAGGGAAAACGGGGTTAAAAAGCATAAGCTGGATTGATTGAATGTTTGCATCTTTCTGTTTTTTTTTTTTTATATCTCAGATGTATCAGGAGGTGTTGGATTGGCTCATAGTGCTCAGCCTGACCGTGGAGGTTTGAGTTCGGTTCTGAGGGACTTGGTGAAACCCGGAGATGAGAATCTGCGCGAGATGAACAAAAAGCTGCAGAACATGCTGGAGGAACAACTGACAAAGAACATGCACCTACAGAAGG[T/G]AAAGAAAGAGATGAACAGCTACGGTTGAAGTCAGAATTATTAGCCCTCTTGAATTTTTAGTCCCCAGTATATTTATTCCCTAATTTCTGTTTAACGGAAAGATTTTTTCAACAAATTTTTAAAAACTATAGTTTAAATAACAAATTTCTAATAACTGATTTATTTGATCTTTGCCATGATGACAGTATATTTTACTAGATATTTTTCAAGGTACTAGTATTCAGCTTAATGTGACATTTAAAGATTTAACAATTAGGTAAATTAGGCAAGTTATTGTTTAGCCGTGGTTTGTTTTGTAGACAATCAAAAAATTGCTTAAGGCAGGGAATAATATTGAACTTAAAATGTTTTCAAAAAAATTTAAAACTGCTTTTATTGTAGTCGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTATAGAAATAACTGTGAAAAATTCCTTGCGCTGTTAAACATCAGTTGGCAAATATTTAAAAAAAGAATAAAAAAATC
Associated Phenotype:
Not determined