Busch Lab

ZMP

rimbp2

Ensembl ID:
ENSDARG00000001154
ZFIN ID:
ZDB-GENE-040724-96
Description:
Novel protein similar to chicken and human RIM binding protein 2 (KIAA0318) [Source:UniProtKB/TrEMBL
Human Orthologue:
RIMBP2
Human Description:
RIMS binding protein 2 [Source:HGNC Symbol;Acc:30339]
Mouse Orthologue:
Rimbp2
Mouse Description:
RIMS binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:2443235]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa13674 Splice Site, Nonsense Available for shipment Available now
sa34470 Nonsense Mutation detected in F1 DNA Not yet available
sa41282 Nonsense Mutation detected in F1 DNA Not yet available
sa34471 Nonsense Mutation detected in F1 DNA Not yet available
sa12091 Essential Splice Site Available for shipment Available now
sa2429 Nonsense Available for shipment Available now

Mutation Details

This allele has been removed from public view.

Allele Name:
sa3694
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001313 Essential Splice Site 34 1085 1 22
ENSDART00000136269 None None 1165 None 16

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 46121800)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 44021689
GRCz11 8 44015108
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTGGCCGTCCTCAGTGCCAAGCAGCAGGAGATTGACCTTCTGCAGAAG[G/A]TGAGAGGCCACACYAGACCCCAGGATCCACTGCAGAAGACCCCGTGTCGT
Long Flanking Sequence:
GACCTGCTTCACCCAAAAGTGAATATTTGATCATTTACTCACCCTAATGGCTGTCTAAATGCAAAAATACAATCATTTCAGTTTTCTTGTTCCCTGTATAGAACAAAAAGTAGTTCTCAACAAGCATGTCTAAGCTGCTGTTTTACTATAAAACTCAATAGCTAATGATTGCTGGTCCTCATCTGCTTTCATCTGCATGAAAACAAAAGCAGCTTGGACATTCTTCTTAATATCTTCTTTTTGCGTTCCATTCAAGAAAGTAAGTCATCATGAGGGTGAGTAAAAGATAAGATGGTTTTCTTTTTTTGGGTGAGCTGTCCCTTTATGAATGATTGATGGATGCTCTCATTCTGTCCTCCTGCTTTCTCTCTCTCTCTCTCTTCTGTGTTTTCCAGCATATGCGAGAGGCTGCGGAGAGGAGGCAGCAGCTAGAATTAGAGCATGAACAAGCATTGGCCGTCCTCAGTGCCAAGCAGCAGGAGATTGACCTTCTGCAGAAG[G/A]TGAGAGGCCACACCAGACCCCAGGATCCACTGCAGAAGACCCCGTGTCGTGTCTCAAATGACAAGGTTTCTGGTGGATGATTAAACAGAAGTCATTAATTTAGAGCACATTCTGCTGATACAGTAGATGATTTTTACTTGGTTTCAGACTGGTTCAAGCTGGTGTGGATGGTTAAAGGAACAGAAAGAAAGTATTGTCAAAAATATTGAGTCTGGAACCAATCGGTACAGAATATTTACAAACGTCATTTCCCGCAAACATTTAAGCACAGTTGAGTGCATATTTAAACAAAGCTGATTGGTCATTGGGTTCATGTACTTAATAGAAATGACTGTGATTGGCCGTGAAGGTCAACTCGTCATTGCTGTTCACCAAGTGCAAACACAGATAGACAGACAGTGGATCATTTCAAAGCAGCGTAAAGGTACCAGTGTCTAATGACATAGATACTTACAACAACCATACTCTCATTCTGGAGTAATAATCAAAGATCTTTGCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13674
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:
T > A
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001313 Splice Site, Nonsense 123 1085 5 22
ENSDART00000136269 Splice Site None 1165 None 16
Genomic Location (Zv9):
Chromosome 8 (position 46135178)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 44008311
GRCz11 8 44001730
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCAGTCACCTTTGTGTATATGTGTGTGTGTGTGTGTGTGTGTGTGTTA[T/A]GAAGGTAATGAGGATTCGATGAGTAAGATCTCGGAGCTCATCCGGCCTCT
Long Flanking Sequence:
ATTATGAAAAAAAAGATGCCTGACCCCAAATTTTTGAAATTGAATATAGTATGTTGTTTGTGTTTTAATCAAGATATCAGTTGATTATTGTGCACTTCACAATTGTTCATCTTCAGGTTATTATTTTCATCCTCTCCCTTTCTCACATTATACAGCAGGCATGTGCTTGATCCTGGAGGGCCGGTGTCTCTGCAGAGTTTTGCTTCAACACTAATCAAACACACCTGAACACCCTAATCAGTGTCTTCAAGATCACTAGAAAGCTACAGGCAGGTGTGTTTGATTAGCAAAACCATGCGGGACATCGGCCCTCCAGGATGGAGTTTGCCCATCCCTGTTATCAAGTATCTTGCTATCAAGGTGCAAGGAAACTCTTTTGAAGTTTGCTCTGATAAACCAGCGGTGATGATGACGGAAGGAGGAGGATGTGGTTATACGCAGTAATGAAGTAATCAGTCACCTTTGTGTATATGTGTGTGTGTGTGTGTGTGTGTGTGTTA[T/A]GAAGGTAATGAGGATTCGATGAGTAAGATCTCGGAGCTCATCCGGCCTCTGCAGATGACTGAGGGGGAAAAGGTAGAGCTCCTGTCTGTCAAACCTAGTTTCCTGTCACGCAGCACACCCTCCAGCCCACGGCGGGCCTTCCTCTCTGAGGTGCGGCCCGTCATCGCCACTGCTGTGAGTATCACACAACCACTGCTACTTCTGTTTACCCAGAATTTGATCCATGCTTTATTTTTTAGTGTGAGAAAAAAGAGTGAAATACATCATAGGAACTAAAGCACTGTAGAATGAAATAGATGAGATTAGCTTTTTTTTTTTGGAGAAGACAATTTGATTCTGTGTGTAAACAAAATGATGAATAAAGAAATATTCATTCATTCATTTTCTTTTCGGCTTAGTCCCTTTATTAATACGGGGTCGCCACAGCGGAATGAATCGCCAACTTATCCAGCACATGTTTTGCGCAGCGGATGCTCTTCCAGCTGCAACCCATCGAGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34470
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001313 Nonsense 201 1085 7 22
ENSDART00000136269 Nonsense 147 1165 4 16
Genomic Location (Zv9):
Chromosome 8 (position 46142025)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 44001464
GRCz11 8 43994883
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGGATTTAATTCACATGGATCGATTTAACTGGTTCTGTTTGCAGTTA[T/A]AACCCTTACGATGGCCCCAATGAGCATCCTGAAGCAGAGCTCCCCCTGGT
Long Flanking Sequence:
AAAATGCATGTAGTTGTGTTTACAAAGCATTTATTAACATACAAAGTTACCATTACTATACGCCTGAATAATAAGATACATAAATGTTGATTTCAATAGTTTGTTAATCATTTACTTATGCATTCTGAATTCTCTAAAAAACCATCGACTACTCTTAAATACAAATGCAATGCTTAATTTAGTAATGAAAAATTTATTACTCATATGTTATGAAAATACAGTTTTTTTATAAATTAAGAATAGAGCATTTCTAACTGCAGTTATAAACTGCTTAATAACGTTTATTAATGTAGAGTTCATGTTTAACAGATAATGAATTCACTATACTAATGCCTAATAAATGAATCGTAGTTTATAGTTATTATAAAGTGTTACCCAAATTTATTTGTCACATCATAGTTAAAAGACAATAGGCAAATAGAAAGTTTAATTGGATAGATTTAAAATTTTAGGAGGATTTAATTCACATGGATCGATTTAACTGGTTCTGTTTGCAGTTA[T/A]AACCCTTACGATGGCCCCAATGAGCATCCTGAAGCAGAGCTCCCCCTGGTGGCTGGGAAGTACCTGTATGTCTATGGAACCATGGATGAGGACGGCTTCTATGAGGGTACGTTATACTTTGGCAAGTGGAAATTGAGGATGAAGCTTATCGAAATTGTGTCATGAAGCTTATTGCTGCATGAATCGCCACAATTTCAAGAGTGAATTGCTGAGTGGATGTATTGAAATTAAGAATGGATTATAGCCTAAAAAGGGTCCAGAGAGCACTACTGTTATTTCATTGAAAATATGTCATTTATCTTGATTCATTGCCATCTTAAAGATCCATTGTAGAGACGTTTTTTTAGGGCGCACAGTAAAATGTATTACATTTTGTCCACACTTCATTCGTTATAATGAGAAGATTTATGAGCATACTTTATACTGAGCAAAACTTTAACATTTAAAATTAACATTTTTAAAAATATTTTGAAACATACTGTAAATGAATGCTATTGATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41282
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001313 Nonsense 455 1085 10 22
ENSDART00000136269 Nonsense 429 1165 5 16
Genomic Location (Zv9):
Chromosome 8 (position 46146112)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43997377
GRCz11 8 43990796
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGAGCAACAGCAACTACAGTCACATGATCTACTTGAATGATGTGGAGTA[T/A]GATGTAGTAAAGCCTGGAGGCTACAAATACCACTTCTACAACCTGAAGCC
Long Flanking Sequence:
AGCTTGGGCATGAGCACGGGGCTGGGCATCGATTATCTGGGACCCTGCAGCAACGGGACAGGCACGCTGGACGTGAACATCGACGAGATCGGAGAAGACATCGTGCCTTACCCTCGCCGCATTACCTTGATCAAACAGCTGGCCAAGAGTGTCATTATAAGTTGGGACCCTCCAGTGGTGCTGCCCGGATGGACGCCTATCAGCGGCTACAATGTGCTGGTTGACCAGGAGGTGCGCATGAGCATTCCCTTCGGTGGACGCACCAAATCTCTGATCGAGAAGTTGAACTTGACTGTCTGTACGCACCGCATCTCCATCCAGAGCATGACGGAACGGGGCCTTTCCGATCCGCTGCGCTGCACACTTCTGGTGGGGAAAGACGTGGTGGTGGCGCCCTATTACCTTCGTGTGGAGAACATCACTCAAGCGTCTGCCGAGCTCACCTGGATGCCGAGCAACAGCAACTACAGTCACATGATCTACTTGAATGATGTGGAGTA[T/A]GATGTAGTAAAGCCTGGAGGCTACAAATACCACTTCTACAACCTGAAGCCCATGACGGTGTATAAGATACGGGTGGTGGCGCGACCCCATCAGATGCCCTGGCAGCTTCCTCTTGAGCAGAGGGAAAAGAAGGAGGTCTCGGTGGAGTTCTGCACACAGCCAGCCGGTGGGTCACTTAGCGCATGCTTCATTTTTGCATGTTCACTTCTTATTACTAAGTGATTTGAGATCTGGTTATCACTAGGGCTGTTAATCGATTCTAATATTCATGTGGATTAATTGCATAATATTTCATTGCGTCACAGCTCGCCATGCGTTCTTGCAAAAACCTGAAGTTGGTACTTCAAGACTGAATTGCTCCAGTGGTAGGAAAATTTCTTATTACAGAATTTACATGCAAGTCGGGGGTTAATATATGTTGCATTTTTACTTTTTCTAATGAAAATATTATATGGGGAGAGGCCTAAAATTTAAAGGTAATAACACCCTAGTGGATGCCT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa2435
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001313 Nonsense 489 1085 10 22
ENSDART00000136269 Nonsense 463 1165 5 16
Genomic Location (Zv9):
Chromosome 8 (position 46146213)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43997276
GRCz11 8 43990695
KASP Assay ID:
554-2967.1 (used for ordering genotyping assays)
KASP Sequence:
CATGACRGTGTATAAGATACGGGTGGTGGCGCGACCCCATCAGATGCCCT[G/A]GCAGCTTCCTCTTGAGCAGAGGGAAAAGAAGGAGGTCTCGGTGGAGTTCT
Long Flanking Sequence:
CGTGCCTTACCCTCGCCGCATTACCTTGATCAAACAGCTGGCCAAGAGTGTCATTATAAGTTGGGACCCTCCAGTGGTGCTGCCCGGATGGACGCCTATCAGCGGCTACAATGTGCTGGTTGACCAGGAGGTGCGCATGAGCATTCCCTTCGGTGGACGCACCAAATCTCTGATCGAGAAGTTGAACTTGACTGTCTGTACGCACCGCATCTCCATCCAGAGCATGACGGAACGGGGCCTTTCCGATCCGCTGCGCTGCACACTTCTGGTGGGGAAAGACGTGGTGGTGGCGCCCTATTACCTTCGTGTGGAGAACATCACTCAAGCGTCTGCCGAGCTCACCTGGATGCCGAGCAACAGCAACTACAGTCACATGATCTACTTGAATGATGTGGAGTATGATGTAGTAAAGCCTGGAGGCTACAAATACCACTTCTACAACCTGAAGCCCATGACGGTGTATAAGATACGGGTGGTGGCGCGACCCCATCAGATGCCCT[G/A]GCAGCTTCCTCTTGAGCAGAGGGAAAAGAAGGAGGTCTCGGTGGAGTTCTGCACACAGCCAGCCGGTGGGTCACTTAGCGCATGCTTCATTTTTGCATGTTCACTTCTTATTACTAAGTGATTTGAGATCTGGTTATCACTAGGGCTGTTAATCGATTCTAATATTCATGTGGATTAATTGCATAATATTTCATTGCGTCACAGCTCGCCATGCGTTCTTGCAAAAACCTGAAGTTGGTACTTCAAGACTGAATTGCTCCAGTGGTAGGAAAATTTCTTATTACAGAATTTACATGCAAGTCGGGGGTTAATATATGTTGCATTTTTACTTTTTCTAATGAAAATATTATATGGGGAGAGGCCTAAAATTTAAAGGTAATAACACCCTAGTGGATGCCTACACATGCTTTTTTGATCAGGTGGTACACTAACGTTTGACTTACACTAATTAGCCTTCTGTACATACTGCACATCACATCACAAAGTCATAAGTAAGGTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34471
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001313 Nonsense 489 1085 10 22
ENSDART00000136269 Nonsense 463 1165 5 16
Genomic Location (Zv9):
Chromosome 8 (position 46146214)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43997275
GRCz11 8 43990694
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACGGTGTATAAGATACGGGTGGTGGCGCGACCCCATCAGATGCCCTG[G/A]CAGCTTCCTCTTGAGCAGAGGGAAAAGAAGGAGGTCTCGGTGGAGTTCTG
Long Flanking Sequence:
GTGCCTTACCCTCGCCGCATTACCTTGATCAAACAGCTGGCCAAGAGTGTCATTATAAGTTGGGACCCTCCAGTGGTGCTGCCCGGATGGACGCCTATCAGCGGCTACAATGTGCTGGTTGACCAGGAGGTGCGCATGAGCATTCCCTTCGGTGGACGCACCAAATCTCTGATCGAGAAGTTGAACTTGACTGTCTGTACGCACCGCATCTCCATCCAGAGCATGACGGAACGGGGCCTTTCCGATCCGCTGCGCTGCACACTTCTGGTGGGGAAAGACGTGGTGGTGGCGCCCTATTACCTTCGTGTGGAGAACATCACTCAAGCGTCTGCCGAGCTCACCTGGATGCCGAGCAACAGCAACTACAGTCACATGATCTACTTGAATGATGTGGAGTATGATGTAGTAAAGCCTGGAGGCTACAAATACCACTTCTACAACCTGAAGCCCATGACGGTGTATAAGATACGGGTGGTGGCGCGACCCCATCAGATGCCCTG[G/A]CAGCTTCCTCTTGAGCAGAGGGAAAAGAAGGAGGTCTCGGTGGAGTTCTGCACACAGCCAGCCGGTGGGTCACTTAGCGCATGCTTCATTTTTGCATGTTCACTTCTTATTACTAAGTGATTTGAGATCTGGTTATCACTAGGGCTGTTAATCGATTCTAATATTCATGTGGATTAATTGCATAATATTTCATTGCGTCACAGCTCGCCATGCGTTCTTGCAAAAACCTGAAGTTGGTACTTCAAGACTGAATTGCTCCAGTGGTAGGAAAATTTCTTATTACAGAATTTACATGCAAGTCGGGGGTTAATATATGTTGCATTTTTACTTTTTCTAATGAAAATATTATATGGGGAGAGGCCTAAAATTTAAAGGTAATAACACCCTAGTGGATGCCTACACATGCTTTTTTGATCAGGTGGTACACTAACGTTTGACTTACACTAATTAGCCTTCTGTACATACTGCACATCACATCACAAAGTCATAAGTAAGGTTAA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27257
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001313 Nonsense 523 1085 11 22
ENSDART00000136269 Nonsense 497 1165 6 16
Genomic Location (Zv9):
Chromosome 8 (position 46160254)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43983235
GRCz11 8 43976654
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTTTATTGCAGGTCCTCCTTTACCTCCTCAGGATGTGCAAGTGCAGT[T/A]GGGACAAACACCTGGAGTCTTGCAGATTCGGTGGAAACCCCCTACCCTCA
Long Flanking Sequence:
TCTCTCTCTCTCTCTCTCTCTCTCTGTCTGTCTCTAAGTCTATTCTCCCCAGCACTGTTGTGCAACAGCTCAAATAATAACTGCACATTGTTTGTTTTAGGTTCTAAAATGGTGCGGTCCATCGCTGGCAGCCACATATAACACTCAGTATGATTAAGACAAATCAGCCCACATAAATTCAGAGTGCTGACATAAGCAAATACACTGAGAGTCTATGCCCAGCTGGCATCCCTTACGGCTATAAAACACACACACACACACACACACACACACACACACAAGCCCACACGCACATTTACATGGCTATTACACATGCATCATATTTCATGCACAAGCATTCACGTGTTTCTGAAAGCAGACTGCATGTCATGGTCCACCTACAAACTCGACAAGCAGACATAATCAAATTTGCAAGTGTAGCAATTTGCAAATTTTGTTTCCTGAGCATCATCTCTTTATTGCAGGTCCTCCTTTACCTCCTCAGGATGTGCAAGTGCAGT[T/A]GGGACAAACACCTGGAGTCTTGCAGATTCGGTGGAAACCCCCTACCCTCACTCCAAACGGCACTTCCAACGGAGCCAGTGTAATGGGCTATATAGTCTTCACTAAAGGTCAAAAGGTGAGGTGACGTTGCTGATTCTTATTATACTCATGCCATTTGTGCATATCTGCTAATTATTTACAATATGCAGTGAGCCCTGCTAATGAAGCCAAAGAAAGGTCTAGGATCAGCTACTAAGGTTACACGTGTTATTCCAGTTTATGTTTGAAGTGTAGGTTTCATTTTACTCACTGGCTCCATCTGGTGATAACTTGTGTCAGTGAATGGCTTATGTTTCCTCTGTGTTATATAATTCAGGGAGTCTATGTAAGTCATTTTGGAGAATATGTTAAAAAGGTGTATAAATATAGGTGTAAATATATATATATATATATATATATATATATATATATATATATATATATAAACAGTTGAGGTCATAATTATTAGCCCCACTTTATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12091
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001313 Essential Splice Site 974 1085 19 22
ENSDART00000136269 Essential Splice Site 1056 1165 14 16
Genomic Location (Zv9):
Chromosome 8 (position 46187911)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43955578
GRCz11 8 43948997
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGCTCYAGCACTTGTATATATTTGNTTTTTTGTCCTTYTTTTGTCTCTC[A/T]GAAAGGAAMAAAAGGAGTGGAAGACAGCATGCAGTGTCGACGCGGAGGAT
Long Flanking Sequence:
GCAAATCCACAGAATGATGATGATGATCTTTTTCCATGTACATGGAGATACAAGGTTTCTGTCTGACAGTAACATGTTACATTTTTTCCAGATTTATTTCCATTTTTTATTGGTTAAATATTCAATATAGATTAGTTTGGACTCCACAGTGCATGATTTGGGAACTTATTTAAAGTCATTCAAGACAAGGTGCTGCACGTGTCAGGGAAAAACACAGTATTTTGTTGTATAATTATTGTCCTAAAAAGCATTTAATTAATTAAAAATCATGCCATTGGCTGAATCCAGTAGTTTGGACAATAGATTTTTTTGATCAATAACATCAAATTCTTGTCATCCTGCAAAACTGTCTTTCTTGTTGTTCATTAATTATGCATTTGTTGTGTATTTATTTTGATATTCATTTATTTGTAGTTAACAAAAGCTATTAAAGATAATTTCGCTTTACTATCGCTCCAGCACTTGTATATATTTGTTTTTTTGTCCTTTTTTTGTCTCTC[A/T]GAAAGGAACAAAAGGAGTGGAAGACAGCATGCAGTGTCGACGCGGAGGATGGTGGCACTGTATGATTATGACCCCAGAGAAAGCTCGCCTAATGTAGATGTGGAGGTACTAATGGAGTCCATTTTTTCTGGGCTTTCTTGTACTTATGGTCTCATCCCATAAGTTTTTGATTTTTATGCTGGCTTGCCTGGATGTCTGCCTCTGTGATAGCCACGAAATTCATTTTCAGCTTATTGTCTGCTTCTGCGGCTAAAGTGTGATTTGTATTTTTATGTTACTGTTCATTCAGGTGGCACATGTTTAGAGACAAAAGTTTTATATCAAATACTTATAATGTCATTCCAAACCTAAATTAACTTCTTGGAAGTTTTTTTAATGCTGAATGTGTATTTTTTCATTATCTTTAAATAGATTTACCATATACATCTCTTTTCTGCCTAATTATTTTTAGCACCATTTATACATATATATATAGGCCCCCTTTGAATTTTTTTTTTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2429
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001313 Nonsense 996 1085 19 22
ENSDART00000136269 Nonsense 1078 1165 14 16
Genomic Location (Zv9):
Chromosome 8 (position 46187980)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43955509
GRCz11 8 43948928
KASP Assay ID:
554-2878.1 (used for ordering genotyping assays)
KASP Sequence:
GGAAGACAGCATGCAGTGTCGACGCGGAGGATGGTGGCACTGTATGATTA[T/A]GACCCCAGAGAAAGCTCGCCTAATGTAGATGTGGAGGTACTAATGGAGTC
Long Flanking Sequence:
TAACATGTTACATTTTTTCCAGATTTATTTCCATTTTTTATTGGTTAAATATTCAATATAGATTAGTTTGGACTCCACAGTGCATGATTTGGGAACTTATTTAAAGTCATTCAAGACAAGGTGCTGCACGTGTCAGGGAAAAACACAGTATTTTGTTGTATAATTATTGTCCTAAAAAGCATTTAATTAATTAAAAATCATGCCATTGGCTGAATCCAGTAGTTTGGACAATAGATTTTTTTGATCAATAACATCAAATTCTTGTCATCCTGCAAAACTGTCTTTCTTGTTGTTCATTAATTATGCATTTGTTGTGTATTTATTTTGATATTCATTTATTTGTAGTTAACAAAAGCTATTAAAGATAATTTCGCTTTACTATCGCTCCAGCACTTGTATATATTTGTTTTTTTGTCCTTTTTTTGTCTCTCAGAAAGGAACAAAAGGAGTGGAAGACAGCATGCAGTGTCGACGCGGAGGATGGTGGCACTGTATGATTA[T/A]GACCCCAGAGAAAGCTCGCCTAATGTAGATGTGGAGGTACTAATGGAGTCCATTTTTTCTGGGCTTTCTTGTACTTATGGTCTCATCCCATAAGTTTTTGATTTTTATGCTGGCTTGCCTGGATGTCTGCCTCTGTGATAGCCACGAAATTCATTTTCAGCTTATTGTCTGCTTCTGCGGCTAAAGTGTGATTTGTATTTTTATGTTACTGTTCATTCAGGTGGCACATGTTTAGAGACAAAAGTTTTATATCAAATACTTATAATGTCATTCCAAACCTAAATTAACTTCTTGGAAGTTTTTTTAATGCTGAATGTGTATTTTTTCATTATCTTTAAATAGATTTACCATATACATCTCTTTTCTGCCTAATTATTTTTAGCACCATTTATACATATATATATAGGCCCCCTTTGAATTTTTTTTTTAAATTTCATTAATAATTAATGTTCTACAGAAAAATTTTCACAGCATGATATTTTTTCTTCTGGATAAAGTCT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27258
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000001313 Nonsense 1000 1085 19 22
ENSDART00000136269 Nonsense 1082 1165 14 16
Genomic Location (Zv9):
Chromosome 8 (position 46187990)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43955499
GRCz11 8 43948918
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAGTGTCGACGCGGAGGATGGTGGCACTGTATGATTATGACCCCAGA[G/T]AAAGCTCGCCTAATGTAGATGTGGAGGTACTAATGGAGTCCATTTTTTCT
Long Flanking Sequence:
CATTTTTTCCAGATTTATTTCCATTTTTTATTGGTTAAATATTCAATATAGATTAGTTTGGACTCCACAGTGCATGATTTGGGAACTTATTTAAAGTCATTCAAGACAAGGTGCTGCACGTGTCAGGGAAAAACACAGTATTTTGTTGTATAATTATTGTCCTAAAAAGCATTTAATTAATTAAAAATCATGCCATTGGCTGAATCCAGTAGTTTGGACAATAGATTTTTTTGATCAATAACATCAAATTCTTGTCATCCTGCAAAACTGTCTTTCTTGTTGTTCATTAATTATGCATTTGTTGTGTATTTATTTTGATATTCATTTATTTGTAGTTAACAAAAGCTATTAAAGATAATTTCGCTTTACTATCGCTCCAGCACTTGTATATATTTGTTTTTTTGTCCTTTTTTTGTCTCTCAGAAAGGAACAAAAGGAGTGGAAGACAGCATGCAGTGTCGACGCGGAGGATGGTGGCACTGTATGATTATGACCCCAGA[G/T]AAAGCTCGCCTAATGTAGATGTGGAGGTACTAATGGAGTCCATTTTTTCTGGGCTTTCTTGTACTTATGGTCTCATCCCATAAGTTTTTGATTTTTATGCTGGCTTGCCTGGATGTCTGCCTCTGTGATAGCCACGAAATTCATTTTCAGCTTATTGTCTGCTTCTGCGGCTAAAGTGTGATTTGTATTTTTATGTTACTGTTCATTCAGGTGGCACATGTTTAGAGACAAAAGTTTTATATCAAATACTTATAATGTCATTCCAAACCTAAATTAACTTCTTGGAAGTTTTTTTAATGCTGAATGTGTATTTTTTCATTATCTTTAAATAGATTTACCATATACATCTCTTTTCTGCCTAATTATTTTTAGCACCATTTATACATATATATATAGGCCCCCTTTGAATTTTTTTTTTAAATTTCATTAATAATTAATGTTCTACAGAAAAATTTTCACAGCATGATATTTTTTCTTCTGGATAAAGTCTTATTTGTTTT
Associated Phenotype:
Not determined