ZMP
grik4
Ensembl ID:
ZFIN ID:
Human Orthologue:
GRIK4
Human Description:
glutamate receptor, ionotropic, kainate 4 [Source:HGNC Symbol;Acc:4582]
Mouse Orthologue:
Grik4
Mouse Description:
glutamate receptor, ionotropic, kainate 4 Gene [Source:MGI Symbol;Acc:MGI:95817]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16435 | Essential Splice Site | Available for shipment | Available now |
sa16493 | Essential Splice Site | Available for shipment | Available now |
sa13014 | Nonsense | Available for shipment | Available now |
sa15276 | Nonsense | Available for shipment | Available now |
sa16037 | Essential Splice Site | Available for shipment | Available now |
sa24983 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13341 | Nonsense | Available for shipment | Available now |
sa10219 | Nonsense | Available for shipment | Available now |
sa22637 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16435
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035812 | Essential Splice Site | 83 | 965 | 3 | 19 |
ENSDART00000035812 | Essential Splice Site | 83 | 965 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 15 (position 22298668)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23009855 |
GRCz11 | 15 | 22945120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCTGTGTCTGTAATAAATGACAGTTGGTCTTTCCCTTATCTATTGACA[G/T]TGTGCCAGATCATGTCCAARGGKGTGGTGGCGGTCCTGGGCCCCTCTGCC
Long Flanking Sequence:
TTTTGCCTGTGTCTGCAGTGTCTGCATTTATGGTCAGTGTATTTATGTGCACTTACAATGTACTACCAGAGCTAAGGTTAGGTTTAGGAGAAGGTTTGATGTCAGTACCTAGCAATTATGCAATTATTGTAATTACCATAATAGGTATGCTGCATGCTGACATCACTATAAACATTATGTTATTATATTATTATTATCTTAGTCATAAAGACTTAGTTATCCTTTTTGTGCATTTTCAAAGCAATGATTAGCTGTTACTTTACTTTAATTTAATTTTTGATTTTAAAGCCCCAGCGTCAGCAATAGCCATTGACACAAGTGTGTATGCAGACAGACTCTGCTCTTTGCTTTCTCTGTGTATTTTAGACTTACACTGCAAACAATCTACTTCACTGAAAATGGGGCAGCGGGAGCTTTTCTTTTGGCAGACTGACATCTTGCTTTCCTTCTGCTCTGTGTCTGTAATAAATGACAGTTGGTCTTTCCCTTATCTATTGACA[G/T]TGTGCCAGATCATGTCCAAGGGGGTGGTGGCGGTCCTGGGCCCCTCTGCCAGCCCGGCATCCAACTCCATCATCAGTAATATCTGCGGAGAGAAAGAGGTGAGTCCTGCCGTCCAAAGCCCACTTCATATTACCAAATCATCATTCATATCATTACTATAATGACTGGTGTGGTCAGTGACTGATCCCTAACCACAGTTGACCAATGCTGAATGATTACAATCCGCAGCTCTAATTAATAAATGCGTGATTGATTATTGACGCATCTTGCTTTGTATTCCTACTGTTCTTGAGTCAAAACATCCAGCAGAAAATAAAGTGTTTGTTCTGCCTCTGACGAACATGGAGAGGCACACAAACAGACTGAGTAAACCGCTAAGGGAAGAATTAAATAACATGGATTAGCAGAGAGTTTGTATTGATTAATTGTCGTCGTGACACAGACTGAATTGTTTGGAGCAGTTTCCCGCTCTGTCAGACAGTAAGAGGAAACTGAGGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16493
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035812 | Essential Splice Site | 83 | 965 | 3 | 19 |
ENSDART00000035812 | Essential Splice Site | 83 | 965 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 15 (position 22298668)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23009855 |
GRCz11 | 15 | 22945120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCTGTGTCTGTAATAAATGACAGTTGGTCTTTCCCTTATCTATTGACA[G/T]TGTGCCAGATCATGTCCAARGGKGTGGTGGCGGTCCTGGGCCCCTCTGCC
Long Flanking Sequence:
TTTTGCCTGTGTCTGCAGTGTCTGCATTTATGGTCAGTGTATTTATGTGCACTTACAATGTACTACCAGAGCTAAGGTTAGGTTTAGGAGAAGGTTTGATGTCAGTACCTAGCAATTATGCAATTATTGTAATTACCATAATAGGTATGCTGCATGCTGACATCACTATAAACATTATGTTATTATATTATTATTATCTTAGTCATAAAGACTTAGTTATCCTTTTTGTGCATTTTCAAAGCAATGATTAGCTGTTACTTTACTTTAATTTAATTTTTGATTTTAAAGCCCCAGCGTCAGCAATAGCCATTGACACAAGTGTGTATGCAGACAGACTCTGCTCTTTGCTTTCTCTGTGTATTTTAGACTTACACTGCAAACAATCTACTTCACTGAAAATGGGGCAGCGGGAGCTTTTCTTTTGGCAGACTGACATCTTGCTTTCCTTCTGCTCTGTGTCTGTAATAAATGACAGTTGGTCTTTCCCTTATCTATTGACA[G/T]TGTGCCAGATCATGTCCAAGGGGGTGGTGGCGGTCCTGGGCCCCTCTGCCAGCCCGGCATCCAACTCCATCATCAGTAATATCTGCGGAGAGAAAGAGGTGAGTCCTGCCGTCCAAAGCCCACTTCATATTACCAAATCATCATTCATATCATTACTATAATGACTGGTGTGGTCAGTGACTGATCCCTAACCACAGTTGACCAATGCTGAATGATTACAATCCGCAGCTCTAATTAATAAATGCGTGATTGATTATTGACGCATCTTGCTTTGTATTCCTACTGTTCTTGAGTCAAAACATCCAGCAGAAAATAAAGTGTTTGTTCTGCCTCTGACGAACATGGAGAGGCACACAAACAGACTGAGTAAACCGCTAAGGGAAGAATTAAATAACATGGATTAGCAGAGAGTTTGTATTGATTAATTGTCGTCGTGACACAGACTGAATTGTTTGGAGCAGTTTCCCGCTCTGTCAGACAGTAAGAGGAAACTGAGGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13014
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 |
---|---|---|---|---|---|
ENSDART00000035812 | Nonsense | 241 | 965 | 6 | 19 |
Genomic Location (Zv9):
Chromosome 15 (position 22360484)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23071671 |
GRCz11 | 15 | 23006936 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTCATTTGTCWTCCAGGCCTCAGAGTTGGGGATGCTGTCAGTCTACTA[C/A]ACCTACATCCTGACTTCCTTGGTGAGATGCTGTCTAATGCTGGARTTTAT
Long Flanking Sequence:
TTCTTTTTGTTCCAGGAAATGTGATTCTATTTCACTGCAGGTTATTTTTGATCAATACAATTTTTAATTCATTATTTAACATTTCACTCTGCCAGAAAGAAGACCAACACCCCCCACCGCTCAATCGCTTTCCGTCTTGTGCATTTATTGTACTCTAAACTGTCCCTCTTACTCAGTTCTCTTTCCATAGAAATAATTGTTGAAAGTGTTTTTATCCCTGACATTTGATTGACATATTGTATTTGCTGCCTGGTTTCCTTGGAGACGGAGGAGAATTGATAAATAGGATGGCAATGACAGAGCGGCAATCTTTTGTTAGCTTTCATCCATCTCTGAACAGGTTTTACAAAGCAGTGAACCTTGCTTTTGCCTTCTCAATGGTTGTGATGCAGATTCAGTATGTTTACCTGTTACAATTAGCCCAGCATTGTCAAAAAATATTCAATGTTCTTCTCATTTGTCTTCCAGGCCTCAGAGTTGGGGATGCTGTCAGTCTACTA[C/A]ACCTACATCCTGACTTCCTTGGTGAGATGCTGTCTAATGCTGGAGTTTATTAAGCATGTGCCTATACCAAAAAACAAGAAAATGTTGCTATATAGATATGATGTTGCTACATATAAATGTCACATACCTGAATCTATAGCTGAATGTAGTTGTGCTTAAGTGTTCTTCTTTGCTGCTCGAAAATGTTTAGTTGAGAGTACACTTCTATCAGTATTGGATTACGGAGATAATTTATATGCACGCTCCTCTGAATGTTTTTAAAAAAAGTTGGATATTGTTTATCAAAGTGCCTTAAGATATGTCACTCATTCAAGTGCATGCACACATCCGTGTAATTTATAAAAAGTGACAGAATGGACTTCATTACAGTTAAGGTGCTTTATTTGGTAAATTATGACAGTATATATCTTATCTGTTGGAGTACTGTTTAAATACTTACAATACCAAATCAGCAGATATACTCTTACTTAAGATTCCATTATTTCACACAGAGTTAGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15276
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035812 | Nonsense | 287 | 965 | 7 | 19 |
Genomic Location (Zv9):
Chromosome 15 (position 22408882)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23120069 |
GRCz11 | 15 | 23055334 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTCAACAGKACACATCCTTTCTTTCAGGACTTTGTGCTCAGCCTCAAT[C/T]GATCCTGGCAGGAGAACTGTGATCACGCACCRTTTGCAGGARCACCGGTA
Long Flanking Sequence:
TAGACTGTAATACTGTCAGAAGGAAGTGCTGGGACATCTCTATTAACCTTCAGCTGATGTACTGCATGTGCCGGGACGCAGACTGACAACACTGCAGACCTTTTCTCACCCGCTTTCACACAATCTCCAAAGTGTCCCTCGTGGGATCTGAAGCACAATAGCTGCTGGGATTTGCTCTCCTAAGCATTAACTTTTGCTGAATTGAATTACTTGTCCCAAGAATTGGCAGGATTACCTCAGTGCTTGTTAATGAGCCTGACGATATTGTTCTACTTCCTATGGGCATCGTTAGGTTGTTTAGACTCAACAAGGGACCTGAGCTTGGCAATTTGATAGGAAACACTCATATTGGTGAATTACCCTGAACGTTTTCTCTTTCCTTGCAGGAATTCTCTTTGCTACGATTGGACGATTTAGCTGATCAGCGAGTCAACATCGTGGGCTTTTCAGTCTTCAACAGGACACATCCTTTCTTTCAGGACTTTGTGCTCAGCCTCAAT[C/T]GATCCTGGCAGGAGAACTGTGATCACGCACCGTTTGCAGGAACACCGGTAAGGCAGAGAAACTCAAAGATTAAATCAATGTTAAAGGGATAGTTCACCCGAAAATGAAACATTTATTTTGTTTCCTTCATAAAAAAATACACTAAAGAACACACATCACTTTAAATGGGTGCTCAGTCAAACAATGCCAAAAAGTGCAATAATGTATATTCAAATAGACCGCAACACTTTAGCTCCAAAAATGCCAATTTATCAAACTAAAAGTCTGATACAAGGCGTGTTATTTTTTGAACACACCGTTTTTTCATCAGACAGTGTTTATCACAGTATGTTGCTGTTTTTTTGTTTCTTTGTTTTGTAATGTATTATCAGGATTGTTTTTGTTTTGAAAGCCTTTTTAATTTTATAAATTGCCATTTTTAAAACTTTGGTGTTGCCACCTTTTTGAATATATATTTTTATTTCCTTCATGAAACAGTAGATTTTAGGCAGATTTAACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16037
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035812 | Essential Splice Site | 353 | 965 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 15 (position 22414056)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23125243 |
GRCz11 | 15 | 23060508 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTAAGATCTGGGARCAYGGCACGAGTCTGATGAACTACCTGAGGATGG[T/G]AARAATCGCGGGGAAGAGCCCACCAGCTGCCAATCATCTCACCTGCTGCC
Long Flanking Sequence:
CCAACTCATCTGCTGGGGCTCGAACCAGCGACCGTCTTGCTGTGAGCCAATCATTCTACCCACTGTGTCACTGTGATGCCCTGATAATAATTTTATAGTTGATAATTCTTTAAAGAATTTCCCAGGTATTATGTTATAGTGAATATTGAAATGCATAAAAAAAGCATTTCTGTCATTAAAAAATGTAAAGGTTTTACTGTGTTTTTTTTTAAAATAACTTATTTAGCAGATTATTTGACCTTGATAAGTATATAGGCAACATTGCAAATCCTACTAACCTCAAACTACCATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTTGTGTGTGTGTTCCAGCTGTCATCAGCGCTGCTGTTTGATGCGGTACATACGGTGGTGGCAGCCGTGCAGGAGCTGAACCGCAGCCAGAACGTAGGAGCCACTCAGCTCTCCTGCAAGTCCTCTAAGATCTGGGAGCACGGCACGAGTCTGATGAACTACCTGAGGATGG[T/G]AAGAATCGCGGGGAAGAGCCCACCAGCTGCCAATCATCTCACCTGCTGCCGTTGCAGACTCATTCATCATTTAGTTTTTTCGCTCTCTGTACCACAGCGGCCCCAAAAACCCCTGTCAGAACTGCAGCCTTCAGCAGAATCTGAGACAGTCAGCCATTAAAGATTAACGAGCGTCAGCTTGTCATTACGGCATCATCCTATGCGTGACGTATGGCGATCTATAGCATGCTTCTGCAAATGCTGTGTTGTCCGTGTAGCTCTATAAATCGATACAGCACTGAAGTCTTATGTGTGGCTATAATCGCGTAATATCCTCAGGCGTTAACATGTGTCTTTCTCTCTCTCGCTCTCTCTGTGGATAGGTAGAGTTGGAAGGTCTAACAGGCCACATCGAGTTCAACAGCAAAGGCCAGCGTTCGAACTATGCCCTGCGGATCATGCAGAACAGCAGGGATGGCCTAAGGCAGGTAAAGTAACTCTCGGCGACATCGCCCTATCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24983
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035812 | Essential Splice Site | 424 | 965 | 10 | 19 |
Genomic Location (Zv9):
Chromosome 15 (position 22460731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23171918 |
GRCz11 | 15 | 23107183 |
KASP Assay ID:
554-7788.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGACGGACACACTATTCAACACCACTCTCACCATAACTACCATTCTGG[T/C]AAGTCCTGTCTTCTACTGCATATTCATGGTCCACATATCCTACCGATTAA
Long Flanking Sequence:
TGCACTAAGCCATATTACCATATGTCCAAAGTATTTTTATTACTAACGTTCTGTCTGACAACACAATGTAACATAAAATATCATTAACCTATAGAGTTTGAGAGCTATGGTGCATGGGAAAACGAGTTTTATTCAGGGATAAATATAATTTTGCCCGTATCTCACAGCAAAAATAAATACACAAAGGCTTTAAAGACACCAAATATAATTTAATGGCTACAGACTTTTTTTGTGATACATTCATGGTGCTCTTGGAAGATTGACAGCCACTTTTCTTGGAAAGACAGTTTCTCATTTCTTGGTGAACTATCCCTTTCAGGCTTCATGGTTGCATTTTGTCATGCTTTTTTTGAGAAGGCTTAGTATAACTCGCAGTGTGTTTCTCTCACAGATCGGTCAATGGCATTCAGAGCAGGGACTGTCCATGGAGAGGAAGCTTCCTTCACTTAACGTGACGGACACACTATTCAACACCACTCTCACCATAACTACCATTCTGG[T/C]AAGTCCTGTCTTCTACTGCATATTCATGGTCCACATATCCTACCGATTAAGGCCCTGTCCACTCAAACATGGGTATTTTTTTAAATATCCTGCTTTTTCCAAGTCTGGCTGTTCCTCCACATGCAAATGCAGCATCAGGTGACTGAAACCAAAACTTTTGAAAGAAAACTCCTGCCAGAGGGAACATTTTCAAAAACTCTGGATACAGTGTGGCCATATAGCCAATGAGTTAGCCAAGAGTTTTACACACACCCTAAGGAATAATCTTTTTTTAAAGGAGTTTCTCTTTAGCTTCCAGAAACAGTCCCGTCTGTGATCACCTCGGGGTACAATGCTGATCTAAATAAAGACTCTTCTCCACGGAGATGAGTGGAAACTAACAAGTATGCGTGTGATAGCATTTCCTGGAGCAGCAACCACCAATTGAAGATGTAATCCACTAGGCTGTTATCTAGGGGCAATTTTCTCATCTTCTCCTACACTGTATAGTGATAATGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13341
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035812 | Nonsense | 428 | 965 | 11 | 19 |
Genomic Location (Zv9):
Chromosome 15 (position 22485095)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23196282 |
GRCz11 | 15 | 23131547 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTGAGTTAATCTCTGACGCCAGTGCTGTGTTTACAGRAGAACCCGTA[T/A]GTAATGTTGAGAGCCAATCACCAGGAGCTTGAAGGGAACGATCGCTAWGA
Long Flanking Sequence:
TAGGAGCTTTCTGCACCTATTGGTAGGCTCAGAAGGCAGTTATCCATCAACATGGTTAATCATCTATAGATCACATATGGCTGTGGCCGGAAATTACCGAGAATTGTTTATATTATTTATTAAGTTGTACTTTAATAACCGCTACCACAATCCTAAACCTAACCGTCAAAGTAACATAAAAACAGACCAGGATCTGAAGTCTTCTCTATTAGTACAGCAGATTGTTGTCAAAGTAATTTATTTTAAAGGGAAACTTTTTTTAACAGTGTCTTCCCTGTTTGTAGCAACCATTTCTTATTTCTGATCCTTTGCAGCAATTTCCCAGGAAGCAACAGGTTTGCTGTGTAGAAAATATGAAATGGAAATGATATTCCATTTTTTTTTTCAACTTTTTCGACTTTCATCTGTCACACAAAAGTTTTTGCCTTTTGATATAGAAGTGTGCTGAAATGTGTGAGTTAATCTCTGACGCCAGTGCTGTGTTTACAGGAGAACCCGTA[T/A]GTAATGTTGAGAGCCAATCACCAGGAGCTTGAAGGGAACGATCGCTATGAGGGCTTCTGTGTGGACATGCTAAAGGAGCTGGCGGACATCTTGAAGTTCAAGTACCGTATTCGGCTAGTCGGGGATGGTGTGTATGGGGTGCCGGGAGCTAACGGTACCTGGACAGGGATGGTGGGAGAGCTCATCAGCAGGGTGAGTGGCATCAATCGATTAACTACACATTACAGTTATCAGCTGTCATATGATATCAACGTCTTCAAAGCCAAATTAAATACTTTACTTTACTAGACTGAAATTAGTACCGTGTCGGTCATTCAAAGTACATTTTATATTGGATTAAGTGATAATGCAAAAAAAACTAACCCCCTAGGAGAAATTAAAAGCATTTGTTTTTCTCAAAGTAGTATTTAAACCAGCATTTTTAATGTCATGTGACCACATGAAAAAGAGTACTGCTTATGTGCTATTCAGTTTTATGTATTTCTAATGTGAGTTTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10219
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035812 | Nonsense | 444 | 965 | 11 | 19 |
Genomic Location (Zv9):
Chromosome 15 (position 22485143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23196330 |
GRCz11 | 15 | 23131595 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGTAATGTTGAGAGCCAATCACCAGGAGCTTGAAGGGAACGATCGCTA[T/A]GAGGGCTTCTGTGTGGACATGCTAAAGGAGCTGGCGGACATCTTGAAGTT
Long Flanking Sequence:
AACATGGTTAATCATCTATAGATCACATATGGCTGTGGCCGGAAATTACCGAGAATTGTTTATATTATTTATTAAGTTGTACTTTAATAACCGCTACCACAATCCTAAACCTAACCGTCAAAGTAACATAAAAACAGACCAGGATCTGAAGTCTTCTCTATTAGTACAGCAGATTGTTGTCAAAGTAATTTATTTTAAAGGGAAACTTTTTTTAACAGTGTCTTCCCTGTTTGTAGCAACCATTTCTTATTTCTGATCCTTTGCAGCAATTTCCCAGGAAGCAACAGGTTTGCTGTGTAGAAAATATGAAATGGAAATGATATTCCATTTTTTTTTTCAACTTTTTCGACTTTCATCTGTCACACAAAAGTTTTTGCCTTTTGATATAGAAGTGTGCTGAAATGTGTGAGTTAATCTCTGACGCCAGTGCTGTGTTTACAGGAGAACCCGTATGTAATGTTGAGAGCCAATCACCAGGAGCTTGAAGGGAACGATCGCTA[T/A]GAGGGCTTCTGTGTGGACATGCTAAAGGAGCTGGCGGACATCTTGAAGTTCAAGTACCGTATTCGGCTAGTCGGGGATGGTGTGTATGGGGTGCCGGGAGCTAACGGTACCTGGACAGGGATGGTGGGAGAGCTCATCAGCAGGGTGAGTGGCATCAATCGATTAACTACACATTACAGTTATCAGCTGTCATATGATATCAACGTCTTCAAAGCCAAATTAAATACTTTACTTTACTAGACTGAAATTAGTACCGTGTCGGTCATTCAAAGTACATTTTATATTGGATTAAGTGATAATGCAAAAAAAACTAACCCCCTAGGAGAAATTAAAAGCATTTGTTTTTCTCAAAGTAGTATTTAAACCAGCATTTTTAATGTCATGTGACCACATGAAAAAGAGTACTGCTTATGTGCTATTCAGTTTTATGTATTTCTAATGTGAGTTTGATTACCATCCTCCGTAGTATTTATTGCCATACTAAAAGCACCAGCAGATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22637
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 |
---|---|---|---|---|---|
ENSDART00000035812 | Essential Splice Site | 567 | 965 | 13 | 19 |
Genomic Location (Zv9):
Chromosome 15 (position 22525622)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23236809 |
GRCz11 | 15 | 23172074 |
KASP Assay ID:
2260-8448.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTGCTGGCGTACCTGGCTGTCAGCTGCGTGCTCTTTTTGGTGGCGAG[G/A]TAAATTCTCAGCTCCACACTGACACCTGCAGGATCTTATTAGCACTGACA
Long Flanking Sequence:
CCGCCATCTGTAAGACACCTGTGCCGTGTTGATAGATTGGCCATGGTGCTTTCACACTTAGTTTCTCGCTGATAAGCAACTGTTTAGTTGTTGCTGACCACTGATTGTCAAAGAAGCTCCTGGAGAGATAATTGGATTTGACTATTGTGTACAGAATCGGCTCCTGAGTTCTGTTCCAGTGGTTATTGGATCTTGTGAGTGTGCCAAAATGGTTTGGAGACAGAATATCAAGCACTTTGTTTGGATCAAGCCAATCAAGCGTAAAAGCCTTTAAATGTCTTTAACCTGAAATCGCTTCAATGTTTACTTACTGGAATTGATTAATATAGGCTTATGGGATTTTTGAGATGCTGCTTTCAGAGTCTTGACGTTGTCTGTGTGTTTTTATAGGGAAGAAGACCGGGGTATTTCTCCTTTTTGGATCCGTTCTCTCCTGGGGTTTGGCTTTTCATGTTGCTGGCGTACCTGGCTGTCAGCTGCGTGCTCTTTTTGGTGGCGAG[G/A]TAAATTCTCAGCTCCACACTGACACCTGCAGGATCTTATTAGCACTGACATCTTTCTGAATGGGGCAGTGCAACTTTTAGCATTACTATTATTTTCTATTCTTGTGTCACTCTGAACCTTTATTATTAATTCATTATGAGTAATGATGGTGTACAACAACAGTTTAAACAACTACATGAATTTCCTTACAATGGCTGTGAATTGGGACTTCATTCATTCATTTTCCTTCGGCTTAGTTCCTTTATTCATCAAGGGTCGCAACAGCAGATTAAACCACCAACTTATCCAGCATATGTTTTACACAGCGGATGCCTTTCCAGCTGCAACCCAGTACTAGGAAGCATTCATGCACTCATATGCACACACATACGCCACGGCCAAGTATTAGTTACTAGTTTATTATTATTAGTTTATTCAATTCACCTATATCACATGTCTTTGGACTCGAGGAAACCCATGTGAACATGGGGAGAACATGCAAATTCCACACAGAAATGCCA
Associated Phenotype:
Not determined