ZMP
celsr1b
Ensembl ID:
ZFIN ID:
Description:
Flamingo 1b [Source:UniProtKB/TrEMBL;Acc:Q4KP32]
Human Orthologue:
CELSR1
Human Description:
cadherin, EGF LAG seven-pass G-type receptor 1 (flamingo homolog, Drosophila) [Source:HGNC Symbol;Ac
Mouse Orthologue:
Celsr1
Mouse Description:
cadherin, EGF LAG seven-pass G-type receptor 1 (flamingo homolog, Drosophila) Gene [Source:MGI Symbo
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12454 | Nonsense | Available for shipment | Available now |
sa11458 | Essential Splice Site | Available for shipment | Available now |
sa13613 | Essential Splice Site | Available for shipment | Available now |
sa44288 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa426 | Essential Splice Site | Available for shipment | Available now |
sa10133 | Nonsense | Available for shipment | Available now |
sa12090 | Nonsense | Available for shipment | Available now |
sa24665 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12454
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 |
---|---|---|---|---|---|
ENSDART00000128852 | Nonsense | 1457 | 3006 | 4 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 20279506)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19691483 |
GRCz11 | 25 | 19789434 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTGTTTTTTTRTTCATAGGTTTGCTACCAGGGAGCGAAATGCGCTTT[T/A]GCTGTATAATGGCAGGTTTAACGAAAAGCATGATTTCATTGCGATTGAAA
Long Flanking Sequence:
CTGCCCCTTTGCCATGTGCTATTTGACACCTTTCCATTTTGAAATCCCAGGTGCCCTCAGCGCAGCACCATCTGAGATACCAGAGGTTGGCAAACATTGCAGTGTCAGTTTCCCCCGTCCTTTACAGCGTCATTATTACCTCTAGCTGTGTCTCTTGGCAGCTTTTATCACTTCCTTTTCCTCCACTCCCTGTCTTTTTTTATTCCTCTGTCAAACCTGTGTCTTTTTGCTGTGAATGATTTGAGGGTTTTCCTGGTCTCTGCAGATCAGAAATCAATATTCATTAAATGTTAATTGTTAATTAATGTTAATTAAATGTTCATTAAATGTGTTTAAAAGTAACATAAAAAAACATTTTTTTGGACTGTGAATGCTAACTTACACATTAAGTTGAAATAAGAACATTTTAAAGTAATGTATTATTTGTTACACATTTTAAAATTGTGTGTTTGTTTGTTTTTTTATTCATAGGTTTGCTACCAGGGAGCGAAATGCGCTTT[T/A]GCTGTATAATGGCAGGTTTAACGAAAAGCATGATTTCATTGCGATTGAAATTGTTAAAGAGCAAATCCAGCTGACCTTCTCTGCTGGTGAGTTGTGCACTTTTACCATACATTTTATTGTAGTTTTGACAACAGTACACAATGCTTTTGTTTAATAAAAATACCCATGGAACCAAATGAAATTTGGATGAATTTTTGATATAATTTTTGAAATGAATTTTTTCTGGAGCTGCTTTTTGTGTTATTGTTTGTGTCACTGCCTTGCCTTGCTTTTATTTAATTTAATTTGTGTTTGTTTTCTAATTATTTGTGTTTTTGCTGCCATGCCTTGTTTTTTTTTATATACCTTTTTAGTTTGTTTTTGTTTTTTAATGAAATGCTCTTTTCTTTTCTTTTTTTTTCTTTTCTTTTTTTTTGTTTATTTTCTTATTGGTTGTGTGCATTGTTTTTTTTGTTTTTGTTTTTTCATGTACCCAGTGGGCTTTGAAAAAAAAAAATGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11458
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 |
---|---|---|---|---|---|
ENSDART00000128852 | Essential Splice Site | 1966 | 3006 | 14 | 35 |
ENSDART00000128852 | Essential Splice Site | 1966 | 3006 | 14 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 20314801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19726778 |
GRCz11 | 25 | 19824729 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGCTTCAAACGGGACTGYAATAAAACCACAGGAGAGTGTAGCTGCAAGG[T/C]AAGCAACAAGTGAKCACATGCTACACAAAACNAAAAAACTATRGAAAAGGA
Long Flanking Sequence:
AAAAAAAATCTAAAAAATTTAAGTCTCAATGACGGAAACCAGCTTCCAAATTAAAAGCAGCTACATTAAGAACAATAGCATCAATGTGTTAAAGATGATAGAATTTTCTGTTTCCTTCCATTACCATAAAAAGACTCTCTGTTAAATGATCATAAAGGAAGTAAGTCTACAATGATGGATTGCTTTCACAATACATCATGTCAAGTTTGCCTCGCAGTATGAAACCACTGCTTTGATTTTACAGTGCAATTTCACGTCAAATTTCAAAGCAAATCCCTCTGTTTTCCAACTTCCAATTAGCCCCAGTCTTCTGTATTAGCACTCCTGGCTTTCATTCTGTGAAGTTTAAACAGTCTTTTTCTTTTTTGACGCGCACAGAGGAGATCAGCCTTGTGCTCATGGCTGGTGGGGAAACCCGACATGTGGGCCTTGCAACTGCGACCTCAGCAAAGGCTTCAAACGGGACTGTAATAAAACCACAGGAGAGTGTAGCTGCAAGG[T/C]AAGCAACAAGTGATCACATGCTACACAAAACAAAAAACTATAGAAAAGGATAAAGAGAATGCTTGAAAATGATCAGTTTCTGTGGATTTAGAACTGTAAAAATGCTGGGTTCCACACAATTCCTTCATGTTGTCCCAACACAAATCATTTAAATTAATCATTTTTAAGTGGATTGAAAATTAAACAATTAAATTGTCCCAAAAAACCTTTGAGAATTTTTTTTTTTTTTAACTAATCTTAAATAAGTAGTTTGAAAAATGCTGAAAAAAAATGCTGGGTTCCACACAATCAATTTGGGTTGAGTTCAATTCTTAGTGTTTACAATTTTGAGTGAATCGAGCATAAAACTAATAAAGTTGTCAAAAAAAAAAAAACACGTAAGAATTGTGTTGTTTGAACTCAATTTAAATACATTGTATGAACAAGCAGCAAAAGTCATTTTATGAGTGTGCTATGTATGGTTTGAGGAAAACAGTTAAAGATTTCTTAACTTTTCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13613
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 |
---|---|---|---|---|---|
ENSDART00000128852 | Essential Splice Site | 1966 | 3006 | 14 | 35 |
ENSDART00000128852 | Essential Splice Site | 1966 | 3006 | 14 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 20314801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19726778 |
GRCz11 | 25 | 19824729 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGCTTCAAACGGGACTGYAATAAAACCACAGGAGAGTGTAGCTGCAAGG[T/C]AAGCAACAAGTGAKCAMATGCTACACAAAACNAAAAAACTATRGAAAAGGA
Long Flanking Sequence:
AAAAAAAATCTAAAAAATTTAAGTCTCAATGACGGAAACCAGCTTCCAAATTAAAAGCAGCTACATTAAGAACAATAGCATCAATGTGTTAAAGATGATAGAATTTTCTGTTTCCTTCCATTACCATAAAAAGACTCTCTGTTAAATGATCATAAAGGAAGTAAGTCTACAATGATGGATTGCTTTCACAATACATCATGTCAAGTTTGCCTCGCAGTATGAAACCACTGCTTTGATTTTACAGTGCAATTTCACGTCAAATTTCAAAGCAAATCCCTCTGTTTTCCAACTTCCAATTAGCCCCAGTCTTCTGTATTAGCACTCCTGGCTTTCATTCTGTGAAGTTTAAACAGTCTTTTTCTTTTTTGACGCGCACAGAGGAGATCAGCCTTGTGCTCATGGCTGGTGGGGAAACCCGACATGTGGGCCTTGCAACTGCGACCTCAGCAAAGGCTTCAAACGGGACTGTAATAAAACCACAGGAGAGTGTAGCTGCAAGG[T/C]AAGCAACAAGTGATCACATGCTACACAAAACAAAAAACTATAGAAAAGGATAAAGAGAATGCTTGAAAATGATCAGTTTCTGTGGATTTAGAACTGTAAAAATGCTGGGTTCCACACAATTCCTTCATGTTGTCCCAACACAAATCATTTAAATTAATCATTTTTAAGTGGATTGAAAATTAAACAATTAAATTGTCCCAAAAAACCTTTGAGAATTTTTTTTTTTTTTAACTAATCTTAAATAAGTAGTTTGAAAAATGCTGAAAAAAAATGCTGGGTTCCACACAATCAATTTGGGTTGAGTTCAATTCTTAGTGTTTACAATTTTGAGTGAATCGAGCATAAAACTAATAAAGTTGTCAAAAAAAAAAAAACACGTAAGAATTGTGTTGTTTGAACTCAATTTAAATACATTGTATGAACAAGCAGCAAAAGTCATTTTATGAGTGTGCTATGTATGGTTTGAGGAAAACAGTTAAAGATTTCTTAACTTTTCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44288
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128852 | Nonsense | 2011 | 3006 | 15 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 20318220)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19730197 |
GRCz11 | 25 | 19828148 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTGACGGGACAGTGCTCCTGTAAGACAGGTGTTGTGGGCCGCCAGTG[T/A]AACCGTTGCGACAACCCATTTGCTGAGGTCACAGTCACTGGATGTGTGGG
Long Flanking Sequence:
GGCAAAAGCAGAATAAATTCATTATTAGAAAAATCAAATTTTCTGTAATTGTGAAATCTATTATATTTAAAAACAGGTCTAATCATTATTAATGATCTTTTATTGATTATATTTGATCAGTTATGTAGTTTTTATATTCTGATATAAAATTTTGCCTTTAGAAGAATTTCATTACCAAACAGGAATTTGCGTTTAAAAGGAATTTATGCTTTATATAAAGTCTCATACCATATCTGTATTTGTTTTATTAAAATACAGTAAAACAGTAATTCATATATATGTAAACACTACACATACTGTATACATTCTGGCAAATAAAAAGTGTCTACTAAATGAGTAAATGTAAACATAATGTAACTTTTTCAGGACAACTACTTTCGTCCACTCGGAGGAGACACCTGCTACCCGTGTGACTGTTTCCACTTGGGCTCTCATTCACGGGTGTGTGACCCTGTGACGGGACAGTGCTCCTGTAAGACAGGTGTTGTGGGCCGCCAGTG[T/A]AACCGTTGCGACAACCCATTTGCTGAGGTCACAGTCACTGGATGTGTGGGTATGTATCTGTTAAAGAAACACTTCACTCAAAACGGACATCTCTGCAATCATTTACTCAACCCATCACTTGTTACAAACCTGTTTGACCTGCTAGAAGCATCCATTTCCCTGTATTTTCCCTCCTTTTGCATGAAATGTGTCTTTAAGTCAACATTCTGCAGACAAAAACACTATTTTTGCAACTCCTGAATAGGTCTTGAAACCCCCCTCTTTCGGTTCAAGTCTACCTCAGATTTTTTTTTCAAAAAATGCTCTATGATGGGTATGGAGTGTTGTGAGCAGAAGGGAGTATTGGGCATGGCTGGCAAAGCAGAGGAAAAACAGGTGGGCTCACCAGCTCAAGACAAAAAATTACTATAAATGAAGATAACTTTTCTGATCCTGAATCCCCGGGTCTGAATGCAGACAGTCACAGTGGATAGCTGTACAGCAGGTCTCTTTCCCTATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa426
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 |
---|---|---|---|---|---|
ENSDART00000128852 | Essential Splice Site | 2439 | 3006 | 23 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 20332366)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19744343 |
GRCz11 | 25 | 19842294 |
KASP Assay ID:
554-0374.1 (used for ordering genotyping assays)
KASP Sequence:
CAGTCATATGAGCAGCTTTGCCATCCTCATGGACATCTCCAAACGAGAGG[T/C]GAGACTTAATGAGCTATTGTGGTTTGTGGAGATCAAGGTTATAATAGTTT
Long Flanking Sequence:
TTCTCTCCATTAAAAAGAAATTGGGGGAAAAATAAACAATTAATAATAATTCTGACTTCAACTGTATGTGGTGTTTTCCACTTTCTCAGACTGCCAAATCGTCCTGTCATCAACACACCTATAGTTAGCGTGGTGGTCCACAAGGATGGAGAACCGCTCTTAAGCCCTCTCCAAAGACCAATACTGCTGAACTTCAGACTCCTGGAGACTCAGGAGAGGACCAAACCTGTGTGCGTCTACTGGAACCACTCCATCATGTAAGTGCTTAATGAATTAATAGTATCATTTATCTTTCATAGATTGCCCAAAGAAAGCTACAGTATCTTTGCTTTTGTAATGATTGCAGAATAAAGATGTATTTTTTTGTGATAGGGTTGCTGGTGGAGGTGCCTGGTCTTCTAAAGGCTGTGAGTTGGTCTTCAGGAACTCCACTCACATCAGCTGCCAGTGCAGTCATATGAGCAGCTTTGCCATCCTCATGGACATCTCCAAACGAGAGG[T/C]GAGACTTAATGAGCTATTGTGGTTTGTGGAGATCAAGGTTATAATAGTTTTGTATTTTTCGTTAGTTTTAGTTTTTATTTCGTTTTGACTTTTTGTTTTCAAATTCAATTAGTTTTAATTAGTTTTCAGAGGCAGATTTACTAGTTTTTATTAATTTCTATATTTTGAAATGACTTAGTTTTAGTTTAGTTTTTATTAATTTCAGTATTAGTTTTAGTTTTTTTTTCTAAATGAGGATATTTGTTTGGTGCAAGTTTCAAAATCAATAGAATAAATATTGTATAATAAAAACTTACATTTTATGAAACCTGTATTTAGAGGGTACATGAACACTATTATCTACCAATACAATACCCATCCTCAAATTCAAATACAACAGCCCACAAGATAGCAGCCTTAAGTACAATATGTGTGCAAGGCTGCTCTGAGATTAGATACACAGTAGTGATGGGAAGTTCAGATCTTTAACGCGGATGTTAGGACTCAACATTATAAAGTCA
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:
sa10133
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128852 | Nonsense | 2526 | 3006 | 25 | 35 |
ENSDART00000128852 | Nonsense | 2526 | 3006 | 25 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 20335845)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19747822 |
GRCz11 | 25 | 19845773 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGTTGTGGCCATTCTTCTACATTACTCATACATGTGCGCATTCGCCTG[G/A]ATGTTTGTGGAGGGGCTGCACATTTATCGAATGCTGACTGAGATGCGTAA
Long Flanking Sequence:
TATTATTTGTCAATACTAATTTTGGGGGGAAAAAATAACTTAAAAATGAAATTAGTCCCAGAATCAGCCATTTTGTTTGTAAAAATCATAAATCTGAATTGTCTATATTTTCTAGTATTCACACAGCTAACTTAGGTTATTCTCGGTTACAGCATGGTGACGTTCTTCCTCTGAAAGTGGTGACCTACACAACAGTGTCAGCTTCACTGGTGGCCCTCCTCATCACCTTCCTCCTGTTGGCCATTCTTCGCAAGCTGCGCTCCAATCTACACAGCATCCACAAGAACCTGGTGGCCTCCATCTTCCTCTCAGAGTTCATCTTCCTCACTGGCATCAATCAGACAGACAGTCCGGTGAGCCATACTATAATATCAGCAATGTTATTTTGTTGTAATTATAACTTAGCAGTCTCTGTGTGATACTAAACCCTTGCTTTTCTAGTTTGTTTGTACAGTTGTGGCCATTCTTCTACATTACTCATACATGTGCGCATTCGCCTG[G/A]ATGTTTGTGGAGGGGCTGCACATTTATCGAATGCTGACTGAGATGCGTAACATCAACCAAGGCCACATGCGCTTCTACTATGCTATTGGCTGGGGGATTCCCGCTATTATTACCGGTATGATGCGCTCAGCTGATCAACAGTTAACCTACTGACTGATCGCTAACATGAACTAGAGCAGCAATTCTCAATCCTGGCCCTCGTGACCTCCTGCTTGACACATTTTGCACGTCTCTCTTGTTTTACACAGCTGATCTAGATAAGCAGCTCATTAGAAGCGATTGCCTAATAAAGAAACTGTGGCTGCATCCGAAACCGCCTACTACTCAGTAGGTACTGCATTTGAATTTAAACGTACTATTCGGCTGTTAGAAAAGTATGTTCTATTGACCTTATTCTAAAATGCAGAAGTGCGCCTGTTTTCGCGATTGTCTTAGAACTTCCGATTCAGTCGCCTATGGGAGAAATGACTAGGAATAATAAACGGCGGAAAATGGTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12090
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128852 | Nonsense | 2526 | 3006 | 25 | 35 |
ENSDART00000128852 | Nonsense | 2526 | 3006 | 25 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 20335845)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19747822 |
GRCz11 | 25 | 19845773 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGTTGTGGCCATTCTTCTACATTACTCATACATGTGCGCATTCGCCTG[G/A]ATGTTTGTGGAGGGGCTGCACATTTATCGAATGCTGACTGAGATGCGTAA
Long Flanking Sequence:
TATTATTTGTCAATACTAATTTTGGGGGGAAAAAATAACTTAAAAATGAAATTAGTCCCAGAATCAGCCATTTTGTTTGTAAAAATCATAAATCTGAATTGTCTATATTTTCTAGTATTCACACAGCTAACTTAGGTTATTCTCGGTTACAGCATGGTGACGTTCTTCCTCTGAAAGTGGTGACCTACACAACAGTGTCAGCTTCACTGGTGGCCCTCCTCATCACCTTCCTCCTGTTGGCCATTCTTCGCAAGCTGCGCTCCAATCTACACAGCATCCACAAGAACCTGGTGGCCTCCATCTTCCTCTCAGAGTTCATCTTCCTCACTGGCATCAATCAGACAGACAGTCCGGTGAGCCATACTATAATATCAGCAATGTTATTTTGTTGTAATTATAACTTAGCAGTCTCTGTGTGATACTAAACCCTTGCTTTTCTAGTTTGTTTGTACAGTTGTGGCCATTCTTCTACATTACTCATACATGTGCGCATTCGCCTG[G/A]ATGTTTGTGGAGGGGCTGCACATTTATCGAATGCTGACTGAGATGCGTAACATCAACCAAGGCCACATGCGCTTCTACTATGCTATTGGCTGGGGGATTCCCGCTATTATTACCGGTATGATGCGCTCAGCTGATCAACAGTTAACCTACTGACTGATCGCTAACATGAACTAGAGCAGCAATTCTCAATCCTGGCCCTCGTGACCTCCTGCTTGACACATTTTGCACGTCTCTCTTGTTTTACACAGCTGATCTAGATAAGCAGCTCATTAGAAGCGATTGCCTAATAAAGAAACTGTGGCTGCATCCGAAACCGCCTACTACTCAGTAGGTACTGCATTTGAATTTAAACGTACTATTCGGCTGTTAGAAAAGTATGTTCTATTGACCTTATTCTAAAATGCAGAAGTGCGCCTGTTTTCGCGATTGTCTTAGAACTTCCGATTCAGTCGCCTATGGGAGAAATGACTAGGAATAATAAACGGCGGAAAATGGTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24665
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 |
---|---|---|---|---|---|
ENSDART00000128852 | Nonsense | 2632 | 3006 | 28 | 35 |
Genomic Location (Zv9):
Chromosome 25 (position 20338300)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19750277 |
GRCz11 | 25 | 19848228 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAAGCAGGGTTTTTACATTGGTTATTTGCTGTTGTTCAGCTCTGCTCTT[C/T]GAGTGGCCTTTCTCCTCCTGCTGCTCATCAGCGCCACCTGGCTGCTGGGT
Long Flanking Sequence:
TATTTAGTATTGAAATTTGGAAAGATGTTAGAAATATAAACAGATATAGTATTAGATTCTTAAAACCTGTGTAGTTTGCTCTTTGATTGCCCACTAGTGCTGATTGTGTGTCTGTATCATCAGGTCTGGCTGTGGGTTTGGATCCGCAGGGTTATGGAAACCCTGACTTCTGCTGGCTGTCTGTTTATGACACTCTCATCTGGAGCATCACGGGACCAATATCCATAGTAGTGCTGGTCAGTTTGTGTTTTATTTATCTTATTTAAAAAAAATTTTCAAACTAAAGTGCTGATTACTTATTGAAAACATATCTCTTTGTTTAACAGATAAATATAGTCCTAATTGTGCTGGCAGCCAAAGCCTCGTGTGGACGGCGCCAGCGAACAGAGAAATCTGGAGCAATGTGAGTAAAGCAAAAGTGTGTAATGATCAAAGTGAAGAATATTTTTGGTAAGCAGGGTTTTTACATTGGTTATTTGCTGTTGTTCAGCTCTGCTCTT[C/T]GAGTGGCCTTTCTCCTCCTGCTGCTCATCAGCGCCACCTGGCTGCTGGGTCTGATGGCGGTCAACAGTGATGTGCTGTCCTTCCACTACCTATTCGCCATCCTCAGCTGCTTACAGGTACAAATGCACCCATATGGTTATGGAAAAATAATGTATGTTAGAATTGAAATTAGAGACATCTTAGGTACTAAGAATGTCCATGTTGTAATTTTAAAAAGGTAAAATAAATATGAATCAGTTTCAGAATCAAGTTCAAAATGCTTTGTTTTATAGTTATTTATATTCTTCATTTAAAATGTACAGATATTATTGTTTGTTGCTGTTGCTGATAAAATAAATTATATTTATATTAATAATAATAATTCTATTATATTTGTATTTTATTTTAAATAAAAATAAACAATGTACATCAAAAATTGCTAAGTAAATAGATATAAACAAAATGTAAATAACGAAATATATAAAATAAATTTTAACAAAACAAATCCTAATAAAATTGGG
Associated Phenotype:
Not determined