ZMP
rerea
Ensembl ID:
ZFIN ID:
Human Orthologue:
RERE
Human Description:
arginine-glutamic acid dipeptide (RE) repeats [Source:HGNC Symbol;Acc:9965]
Mouse Orthologue:
Rere
Mouse Description:
arginine glutamic acid dipeptide (RE) repeats Gene [Source:MGI Symbol;Acc:MGI:2683486]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32440 | Nonsense | Available for shipment | Available now |
sa8509 | Essential Splice Site, Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10433 | Essential Splice Site | Available for shipment | Available now |
sa9631 | Nonsense | Available for shipment | Available now |
sa13495 | Nonsense | Available for shipment | Available now |
sa24320 | Nonsense | Available for shipment | Available now |
sa1112 | Nonsense | F2 line generated | Not yet available |
sa24321 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32440
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 |
---|---|---|---|---|---|
ENSDART00000111345 | Nonsense | 72 | 1531 | 1 | 21 |
ENSDART00000135130 | None | None | 1390 | None | 19 |
ENSDART00000142085 | Nonsense | 72 | 131 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 23114326)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22893633 |
GRCz11 | 23 | 22820184 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATGATGACAACGAGACACCCGGGGCCGCCACCGCCGAGGAGGCCACT[A/T]AAAAGAGCAAGAAGAAGCTGCCCAAGAAGAAGTCACGCTATGAGCGGACG
Long Flanking Sequence:
TAGATAGATGGATTCATAGATAGATACATAGAAAGATACATATATGTCTTACTGTGTCAGGGAAGGTGAAACTAATCTCTGTTAATGAATAGGTCACGTCATTGACCCATCTAAAATGCCATTATTTTCTGTTCTCCCTTTAGCTCTTCTGAAACACTGGGGTTGTTGGTGTGGCCAAATTTTCCCTGGATTTGATTGGTAAATTCAGAAGACTGAAGCCCAGGCTCACAGTCTACCTTTCACGGAGGCCCAGCCGTGAGAGGACAGAAGAAGGCACGTGGCGAATCATGACTGCCGACAAAGAGAAAGACAAAGAGAGGGAGCGCGACCGGGACCGGGACAGAGACCGTGAGAAGCGGGACAAAACACGGGAAAGTGAGAGCTCACGGCCCAGGCGCAGTTGCACGCTGGAAGGCGGCGCTAAGAACTATGCAGAAAGCGAACACAGTGAGGATGATGACAACGAGACACCCGGGGCCGCCACCGCCGAGGAGGCCACT[A/T]AAAAGAGCAAGAAGAAGCTGCCCAAGAAGAAGTCACGCTATGAGCGGACGGAGAACGGCGAGATCACTTCCTTCATTACGGAGGACGACATTGTTTACAGACCTGGTGGTGAGTTATGCTTGTATAATCTTTATTTAGTATGTCTGGATATCAAAGTTTACTTTAATACACTATAAAAAATGATTAAAAAATCCCTTGCTTCAAAAGTGGCAAGTTGATTTTACTTAATGTTGGTAATTATGTTGTATTTAACTTAATGGTTTGAGAATTACGTACATATCACCTTAGCATTAAGTAAATGAACGTAATGCTAAGTATGCTGAGCTTACTCACTTTTTTCACAGTAAACTAAACACTTTTCACAGTGTATGGACCCTATAGAATATGTTGGGTATGCTACTGTTAAATTGATGATTGATTAATTGATCATTATCCTTTAAATCAGTATACTATTGATGGTCGATTAAGTGTTGACGTCTCTGTTGTGCTTGTTTTTGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8509
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, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111345 | Essential Splice Site | 108 | 1531 | 1 | 21 |
ENSDART00000135130 | None | None | 1390 | None | 19 |
ENSDART00000142085 | Splice Site | None | 131 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 23114436)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22893743 |
GRCz11 | 23 | 22820294 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGATCACTTCCTTCATTACGGAGGACGACATTGTTTACAGACCTGGTGG[T/C]GAGTTATGCTTGTAWAATCKTTATTTAGTATGTCTGGATATCAAAGTTTA
Long Flanking Sequence:
CTAAAATGCCATTATTTTCTGTTCTCCCTTTAGCTCTTCTGAAACACTGGGGTTGTTGGTGTGGCCAAATTTTCCCTGGATTTGATTGGTAAATTCAGAAGACTGAAGCCCAGGCTCACAGTCTACCTTTCACGGAGGCCCAGCCGTGAGAGGACAGAAGAAGGCACGTGGCGAATCATGACTGCCGACAAAGAGAAAGACAAAGAGAGGGAGCGCGACCGGGACCGGGACAGAGACCGTGAGAAGCGGGACAAAACACGGGAAAGTGAGAGCTCACGGCCCAGGCGCAGTTGCACGCTGGAAGGCGGCGCTAAGAACTATGCAGAAAGCGAACACAGTGAGGATGATGACAACGAGACACCCGGGGCCGCCACCGCCGAGGAGGCCACTAAAAAGAGCAAGAAGAAGCTGCCCAAGAAGAAGTCACGCTATGAGCGGACGGAGAACGGCGAGATCACTTCCTTCATTACGGAGGACGACATTGTTTACAGACCTGGTGG[T/C]GAGTTATGCTTGTATAATCTTTATTTAGTATGTCTGGATATCAAAGTTTACTTTAATACACTATAAAAAATGATTAAAAAATCCCTTGCTTCAAAAGTGGCAAGTTGATTTTACTTAATGTTGGTAATTATGTTGTATTTAACTTAATGGTTTGAGAATTACGTACATATCACCTTAGCATTAAGTAAATGAACGTAATGCTAAGTATGCTGAGCTTACTCACTTTTTTCACAGTAAACTAAACACTTTTCACAGTGTATGGACCCTATAGAATATGTTGGGTATGCTACTGTTAAATTGATGATTGATTAATTGATCATTATCCTTTAAATCAGTATACTATTGATGGTCGATTAAGTGTTGACGTCTCTGTTGTGCTTGTTTTTGAGGTGCATATGACAATGTGTGGCAGATTTGACGAGAACATGAAACAAGTAGACATTAGTTTAGTAACTCCAGTACTGTGCTTGTAGAAACAAAATGAACAAAACCTTTATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10433
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111345 | Essential Splice Site | 199 | 1531 | 5 | 21 |
ENSDART00000135130 | Essential Splice Site | 68 | 1390 | 3 | 19 |
ENSDART00000142085 | None | None | 131 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 23170870)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22950177 |
GRCz11 | 23 | 22876728 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAAGTGTATTCACACTGTGACACTGATTTGTTTGCTCTATTTCTTTGC[A/C]GGGGGAAATGTAACATTTCACACTTTTCTGACATATTCGCTGCMAGRGAG
Long Flanking Sequence:
ATCTTATGAGCAAGGTATTGAACCAGTGCAAAAACACAGACGCCTATTATTTTGATAGCCCCTGACGTCGGAAATGGAAAGCGCAGAAAGGTGGATAGAGAAAATGTCATGATTTGTGTGGAGCTTGTTGGCTCGGCATTGTTTGAAAAGCCTATGGTGTCTGTCACCTTTTGTTTGTCTAACAGGATGAAGGGAAAGGGCATTAATAAAACAACTGTGCTGAAATATTGTGATCCTGTAACCCGCAAGATTCCTTTGAAACCTATATCAGTATCCTAGATGTGTCAGTAGTCACACATTTTCTGTAAACCAGTGTTATTTTAGGCTTATGGTACAATTGAAGTTTTTTTATTAGTTTAATATATTTTTTATTATTGTTTACAAAAAGTTGTAACATATTTTTAGCATTTAGCTGGAAATATTTTTTTTGCCAAACATTTTTTTGTGATCTGGAAGTGTATTCACACTGTGACACTGATTTGTTTGCTCTATTTCTTTGC[A/C]GGGGGAAATGTAACATTTCACACTTTTCTGACATATTCGCTGCAAGGGAGTTCAAAGCAAGAATCGACTCTTTCTTCTACATCTTAGGATATAACCCAGAAACCAGGTAAGCCTTTACTGACTTCAATAATCAGCCTTCCTCAGGCGTGTTCTGTCTTCTGATCCTCTGTTGCGGGATTTCACAAATAAAGGTTTTGGTTCACATCAGGAATGCAGCTGCTGGTTTTGCTCTATTCCCTTTAAATTGCCCAGTGGTAATGAGGGCAGTTTGGGGATAAATTCGATTTAGGATATATTTATCTGTTTTATAGCTTGTCTTTGAGGTCTAAAGTTTCGTTTTGAAAGAATTGATCGCTTTCTTATTATATATAGCACATATGAGTAAAGTTTTCTTCCAATGTTTGAGGTTGATGTAATTATAGAGGAAGATTCTTACATTTACTTAATCAATAGTAACATACGCACACACACACACACACACACACACACACACACACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9631
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 |
---|---|---|---|---|---|
ENSDART00000111345 | Nonsense | 225 | 1531 | 5 | 21 |
ENSDART00000135130 | Nonsense | 94 | 1390 | 3 | 19 |
ENSDART00000142085 | None | None | 131 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 23170950)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22950257 |
GRCz11 | 23 | 22876808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACATATTCGCTGCMAGRGAGTTCAAAGCAAGAATCGACTCTTTCTTCTA[C/A]ATCTTAGGATATAACCCAGAAACCAGGTAAGCCTTTACTGACTTCAATAA
Long Flanking Sequence:
GCGCAGAAAGGTGGATAGAGAAAATGTCATGATTTGTGTGGAGCTTGTTGGCTCGGCATTGTTTGAAAAGCCTATGGTGTCTGTCACCTTTTGTTTGTCTAACAGGATGAAGGGAAAGGGCATTAATAAAACAACTGTGCTGAAATATTGTGATCCTGTAACCCGCAAGATTCCTTTGAAACCTATATCAGTATCCTAGATGTGTCAGTAGTCACACATTTTCTGTAAACCAGTGTTATTTTAGGCTTATGGTACAATTGAAGTTTTTTTATTAGTTTAATATATTTTTTATTATTGTTTACAAAAAGTTGTAACATATTTTTAGCATTTAGCTGGAAATATTTTTTTTGCCAAACATTTTTTTGTGATCTGGAAGTGTATTCACACTGTGACACTGATTTGTTTGCTCTATTTCTTTGCAGGGGGAAATGTAACATTTCACACTTTTCTGACATATTCGCTGCAAGGGAGTTCAAAGCAAGAATCGACTCTTTCTTCTA[C/A]ATCTTAGGATATAACCCAGAAACCAGGTAAGCCTTTACTGACTTCAATAATCAGCCTTCCTCAGGCGTGTTCTGTCTTCTGATCCTCTGTTGCGGGATTTCACAAATAAAGGTTTTGGTTCACATCAGGAATGCAGCTGCTGGTTTTGCTCTATTCCCTTTAAATTGCCCAGTGGTAATGAGGGCAGTTTGGGGATAAATTCGATTTAGGATATATTTATCTGTTTTATAGCTTGTCTTTGAGGTCTAAAGTTTCGTTTTGAAAGAATTGATCGCTTTCTTATTATATATAGCACATATGAGTAAAGTTTTCTTCCAATGTTTGAGGTTGATGTAATTATAGAGGAAGATTCTTACATTTACTTAATCAATAGTAACATACGCACACACACACACACACACACACACACACACACACACACACACATATATTTATCCTTTTGTGAGAGGAACTACCTCCATTTATTCAAATCTGCAGCTGACGGTCAGAACGAACAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13495
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 |
---|---|---|---|---|---|
ENSDART00000111345 | Nonsense | 496 | 1531 | 13 | 21 |
ENSDART00000135130 | Nonsense | 365 | 1390 | 11 | 19 |
ENSDART00000142085 | None | None | 131 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 23212426)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22991733 |
GRCz11 | 23 | 22918284 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCGAGAACATCTTGCTGTGCAMCGACTGCCGGATCCATTTTAAGAAGTA[C/A]GGCGAACTACCACCCATTGAGAAGCCTGTAGACCCGCCACCGWTTATGTT
Long Flanking Sequence:
GAAATGTTGGTGGTATTAACTTAATATAAGTGATACAATGAGACAGGTGAAGACTCTATAACTGTTTTCCCATCAGAGGACTCAATAAATCCCTCTGCAGGCCTGTAATTACTCTCAGTTTGAGAGAGCACTGATGCTCGCCTCCATCCCTCATCTGGCAGATGGACATCAGTGTGTGTCATTTCTAATTTGATTCAATCTGACACTTACTCATTCGTTTTTGCCTCATTAAATCCTCTGACCTGTTGGATGCAATTGGCATTCATATCGCTCTCGCATCTGATACCAAAACAACCTCAGCATGGATAAGTAAGAGCCTTTGACCTTAGCATGTCCACGAGGTGTTTGGGTAGCCCTTGAGCACTTTCTGTAAGTGTAATGTTTAATAAGCAGAGCTCAGCTAAACTTAAATTTGTGTTTACAGCCTCCAAGGACTGGCACCACGGGGGTCGCGAGAACATCTTGCTGTGCACCGACTGCCGGATCCATTTTAAGAAGTA[C/A]GGCGAACTACCACCCATTGAGAAGCCTGTAGACCCGCCACCGTTTATGTTCAAACCTGTCAAAGAGGAAGACGATGGACTCAGTGGGAAGCATAGCATGAGGACTCGACGGAATCGCGGCTCAGTAAGATGCCTAAATTTGCTTCATTTTAGCTTCATTTAAACCGTTTTATTATTGTTTGCTGTTTGTTACATCACATATTTTATTGATTCAGATGTCAACGCTACGAAGTGGCCGCAAGAAGCAGACCGCTAGCCCAGATGGCAGAGCCTCACCAACCAATGAGGATCTGCGATCCAGCGGGCGAACCTCACCTAGTGCAGCAAGCACCTCCAGCACTGACAGCAAGACTGACTCGATGAAGAAACCCAGCAAGGTATGACCCACAGACACAAACTGTAACATTGAAATCACACTAAGTTTCCCAGGAACACATGAACGTAAGAAACATGAGAAAACATGTTTTTGTTTTGTCAAAACAGAAGACAAAGGAAGAAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24320
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 |
---|---|---|---|---|---|
ENSDART00000111345 | Nonsense | 522 | 1531 | 13 | 21 |
ENSDART00000135130 | Nonsense | 391 | 1390 | 11 | 19 |
ENSDART00000142085 | None | None | 131 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 23212502)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22991809 |
GRCz11 | 23 | 22918360 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTAGACCCGCCACCGTTTATGTTCAAACCTGTCAAAGAGGAAGACGAT[G/T]GACTCAGTGGGAAGCATAGCATGAGGACTCGACGGAATCGCGGCTCAGTA
Long Flanking Sequence:
AGGACTCAATAAATCCCTCTGCAGGCCTGTAATTACTCTCAGTTTGAGAGAGCACTGATGCTCGCCTCCATCCCTCATCTGGCAGATGGACATCAGTGTGTGTCATTTCTAATTTGATTCAATCTGACACTTACTCATTCGTTTTTGCCTCATTAAATCCTCTGACCTGTTGGATGCAATTGGCATTCATATCGCTCTCGCATCTGATACCAAAACAACCTCAGCATGGATAAGTAAGAGCCTTTGACCTTAGCATGTCCACGAGGTGTTTGGGTAGCCCTTGAGCACTTTCTGTAAGTGTAATGTTTAATAAGCAGAGCTCAGCTAAACTTAAATTTGTGTTTACAGCCTCCAAGGACTGGCACCACGGGGGTCGCGAGAACATCTTGCTGTGCACCGACTGCCGGATCCATTTTAAGAAGTACGGCGAACTACCACCCATTGAGAAGCCTGTAGACCCGCCACCGTTTATGTTCAAACCTGTCAAAGAGGAAGACGAT[G/T]GACTCAGTGGGAAGCATAGCATGAGGACTCGACGGAATCGCGGCTCAGTAAGATGCCTAAATTTGCTTCATTTTAGCTTCATTTAAACCGTTTTATTATTGTTTGCTGTTTGTTACATCACATATTTTATTGATTCAGATGTCAACGCTACGAAGTGGCCGCAAGAAGCAGACCGCTAGCCCAGATGGCAGAGCCTCACCAACCAATGAGGATCTGCGATCCAGCGGGCGAACCTCACCTAGTGCAGCAAGCACCTCCAGCACTGACAGCAAGACTGACTCGATGAAGAAACCCAGCAAGGTATGACCCACAGACACAAACTGTAACATTGAAATCACACTAAGTTTCCCAGGAACACATGAACGTAAGAAACATGAGAAAACATGTTTTTGTTTTGTCAAAACAGAAGACAAAGGAAGAAGCGCCATCGCCTATGAAGAGTGCCAAACGCCAGAGGGAGAAAGGAGCCTCAGACACAGAGGAGTCCGAAAGGGCAAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1112
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111345 | Nonsense | 705 | 1531 | 16 | 21 |
ENSDART00000135130 | Nonsense | 574 | 1390 | 14 | 19 |
ENSDART00000142085 | None | None | 131 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 23213977)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22993284 |
GRCz11 | 23 | 22919835 |
KASP Assay ID:
554-1014.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGCCCAGCAGCAGATCCTTCAGGGCCAGCACCCTCCAGTCATCCAGTG[C/A]CAGACAGGGACTTTACCCCCAGCCCCTCCACCGGCAGCTGCAGCTTCYAC
Long Flanking Sequence:
AAAGTTCACTGAAAGGTTTGTGGCAGCTCTGTTTGGCCCAGAGTCCAGTGAAGACACTAGATTTTAAGGTTGTATTTACTTTGGCTGTTACCTTTGGTAGCAGCTTGATTGCACAGAGTGATTTCATATCCTTTAAATGTCATGAGTTCATTGCAACTCAATGACTGTGAAATGCAAAGGTTATTTGTTCTTGATCATGACTGCACCTATTATCATCAGTAACCCCTGCTTCGGTCAAGTTTGTTGACCCTTTCTCCTGTTTATCTCACACAGGAAATAAGTGTGCCGAACTCGCCTTCAGAGTGTGAGGGAGAGGGCGAGGGTGAAAGCTCAGATGGGCGAAGTGTGAACGATGAGGGCAGCAGTGATCCTAAGGATATTGACCAGGACAACCGCAGCTCTTCTCCAAGCATCCCTAGCCCACGAGACAACGAGAGTGACTCTGACTCCTCAGCCCAGCAGCAGATCCTTCAGGGCCAGCACCCTCCAGTCATCCAGTG[C/A]CAGACAGGGACTTTACCCCCAGCCCCTCCACCGGCAGCTGCAGCTTCTACAACACCCACCTCAGGCGCACCTTCACTGTCCTCTCAACCATCTCCATCCATCCCCCCTACCTCCATGCCTCCTCAGCAGATACCACCCGCGGGTCCGCTGTCTCTCATTCAGTCAGGGGTGCAGAGGCTGCCGTCACCTCATTCCCCATTGCAAGGCATGCCTCAACCGCCTCCACCCTCTCAAACCTGCCCACAAGCCCTGCAGCCTCCACTACATGGTCCCATGCCACCCATGGGCCACCCTCTGCAGGCAGGGCCCTCACACATGCCTCACCCTCATGCTTTACCCACTCAGCCCTTCCCAATGGCTCAGTCTCAGGTTCCCCCTTCACCCCTTTCTGGTCAAGCCCAAGCTGCCTCCCTGTCCCAACAACAGCGACCTCACACACCTCCATCACAGTCGCAGTCCTCTTCACAGAGCGGCAGTCAGCCTCCCAGAGAGCAGCCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24321
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 |
---|---|---|---|---|---|
ENSDART00000111345 | Essential Splice Site | 1404 | 1531 | 18 | 21 |
ENSDART00000135130 | Essential Splice Site | 1273 | 1390 | 16 | 19 |
ENSDART00000142085 | None | None | 131 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 23217787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22997094 |
GRCz11 | 23 | 22923645 |
KASP Assay ID:
2261-7690.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATCCATTCGCACCTACACCTGCACCAACAGGATCCATTGCACCAAGG[T/C]GAGGGACCATTCTCTCTGTTCTTGTGTGACAAATTGTTTTATTAGGCCCA
Long Flanking Sequence:
CTCAACCCTACAGACCCTTTACTGGCATACCACCTGCCAGGCCTCTACAACGCCGACCCCAGCATGCGTGAGCGGGAGCTGAGAGAGCGGGAGATCCGGGAAAGAGAGATTCGTGAGAGGGAGCTCAGGATGGAGAGGATGAAGCCTGGCTTTGAGGTCAAACCTCCAGAGTTGGACAGTCTGCATCCTTCCGCCAACCCTATGGAGCACTTTGCCAGACACGGGCCCATTGGTCTACCTCCCATGGCTGGCCCTCATCCGTTTGCTTCTTTTCACCCGGGACTGAATCCATTGGAGCGGGAACGGCTGGCGCTGGCCGGCCCACAGCTACGGCCTGAAATGACCTACCCTGAGCGGTTAGCCGAGAGGCTACATGTGGAGAGGTTGGCAAACGACCCCATGGCACGATTGCAGATGTTCAACGTGACGCCGCACCACCATCAGCACTCGCACATCCATTCGCACCTACACCTGCACCAACAGGATCCATTGCACCAAGG[T/C]GAGGGACCATTCTCTCTGTTCTTGTGTGACAAATTGTTTTATTAGGCCCACATGGAATGTGCGTGCACAGATCTTATTAACTAACTACTTCACAATTTTTGTGTATTTATGTAATGTAGTAACAAATCAGATTGTTTTTTTGTTGACAAATTAGAGCTTTTTGGCTACCAATTAGAGAACAGAACTGTAAACTGTAACAGAACTGTAAAGAGAAATTCGTTGTTTAAATGTGTTATTCTGTGTTCTTAAAGAATTCTTACAGAAAATGTGAAAACTGTCCACAGATTTCATTTGGGCCATTAGAATTCATTAAATTGTATAAGTATAAATGTATTTAATCTGTCTATAAAGGAATTTTATAAATGTCTTAATCAGGGGTGCCCAAACTTTGTCCTGGAGGGCCGGTGTACTTCAGATTTTAGCTCCAACTTGCCTCTAAACACCTGCAAGGGATGTTTCTAGAAAGTCTAGTTAGAGCTTGATTAGCTAGTCCAGGTGTG
Associated Phenotype:
Not determined