ZMP
eif2c3
Ensembl ID:
ZFIN ID:
Description:
Protein argonaute-3 [Source:UniProtKB/Swiss-Prot;Acc:A3KPK0]
Human Orthologue:
EIF2C3
Human Description:
eukaryotic translation initiation factor 2C, 3 [Source:HGNC Symbol;Acc:18421]
Mouse Orthologue:
Eif2c3
Mouse Description:
eukaryotic translation initiation factor 2C, 3 Gene [Source:MGI Symbol;Acc:MGI:2446634]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17616 | Nonsense | Available for shipment | Available now |
hu2484 | Nonsense | Available for shipment | Available now |
sa23461 | Essential Splice Site | Available for shipment | Available now |
sa23462 | Nonsense | Available for shipment | Available now |
sa43240 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44906 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39235 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23463 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17616
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 |
---|---|---|---|---|---|
ENSDART00000091813 | Nonsense | 49 | 860 | 2 | 19 |
ENSDART00000091813 | Nonsense | 49 | 860 | 2 | 19 |
Genomic Location (Zv9):
Chromosome 19 (position 11289237)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10748466 |
GRCz11 | 19 | 10667391 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGCCAACTGCTTTCAGGTGGACATCCCCAAGATGGATGTCTACCTGTA[C/A]GATGTSGACATCAAGCCAGAAAAGTGCCCAMGRCGTGTTAACAGGTGCAA
Long Flanking Sequence:
TTGTCTGTCGTGTTTGTGTTGTTTCCAGTGAGTGGGCATTTAGAGGAAATTTCCTGATAACACAGATAACACCCACTGTTTATATGTCAGTGTCAAGAAACAAGCGGGTGATTGCTGCGCTGTTATTAATTCAGGCATTAATCAGTTTTCACTAAATGTCAATGTTGACAATGAGAAATACCACTCGTATGTCTGTATGAAGGTAGTTTTTGATCATGACACATTGGCTGCACACTTTTACACATTTCTTCTCTTGTGGGGGCTTGTTTAGATTTTTACTTTCAGTTCTCTGGTAATAACTGATGTGTAAAGTCGAATATATTAAGTGTCGAGAAGTCGTACTAATGGAAATCCCCTCTAATTTTCCTGACAGGAGCCGTTGGGGCTGCGCCCCAGTTCTCCGTACCTCGGAGGCCTGGCTATGGCACCATGGGGAAGCCCATCAAGCTGCTGGCCAACTGCTTTCAGGTGGACATCCCCAAGATGGATGTCTACCTGTA[C/A]GATGTGGACATCAAGCCAGAAAAGTGCCCACGACGTGTTAACAGGTGCAAAACATTCAGCCTTTACAATAATTGATATAGTTTGCAACACTTGATTTGTTTTAAATCTTTCATTCTCAAGAGACTTCTCCATTATTGAGTCTTTATAGTCAAGCTGAGCAGCTTTGAGCCCATGATAATGGTCATAACATTTTCTTTGATGGCTTTCAGGGAAGTGGTGGATTCTATGGTGCAGCACTTTAAAGTGACAATCTTTGGGGACAGAAGACCAGTTTATGATGGCAAGAAGAGCCTTTACACTGCTCAGCCTTTACCAGTGGCCTCAGCGGGGGTAAGATACAGTAACGGGCACCAGGGCGGCTGGGAAGCACCTAACAGTAAAAGTAGAACTTGATACATGCCATGATTAAATGTGTTCATTATGATAGTCCTTTTATGATGCATACTGTAGTTTTTACAAATATTTATTGAAAACATTAAAGGCGTACAAAACTGTCAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu2484
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 |
---|---|---|---|---|---|
ENSDART00000091813 | Nonsense | 49 | 860 | 2 | 19 |
ENSDART00000091813 | Nonsense | 49 | 860 | 2 | 19 |
Genomic Location (Zv9):
Chromosome 19 (position 11289237)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10748466 |
GRCz11 | 19 | 10667391 |
KASP Assay ID:
554-0088.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCCAACTGCTTTCAGGTGGACATCCCCAAGATGGATGTCTACCTGTA[C/A]GATGTGGACATCAAGCCAGAAAAGTGCCCACGACGTGTTAACAGGTGCAA
Long Flanking Sequence:
TTGTCTGTCGTGTTTGTGTTGTTTCCAGTGAGTGGGCATTTAGAGGAAATTTCCTGATAACACAGATAACACCCACTGTTTATATGTCAGTGTCAAGAAACAAGCGGGTGATTGCTGCGCTGTTATTAATTCAGGCATTAATCAGTTTTCACTAAATGTCAATGTTGACAATGAGAAATACCACTCGTATGTCTGTATGAAGGTAGTTTTTGATCATGACACATTGGCTGCACACTTTTACACATTTCTTCTCTTGTGGGGGCTTGTTTAGATTTTTACTTTCAGTTCTCTGGTAATAACTGATGTGTAAAGTCGAATATATTAAGTGTCGAGAAGTCGTACTAATGGAAATCCCCTCTAATTTTCCTGACAGGAGCCGTTGGGGCTGCGCCCCAGTTCTCCGTACCTCGGAGGCCTGGCTATGGCACCATGGGGAAGCCCATCAAGCTGCTGGCCAACTGCTTTCAGGTGGACATCCCCAAGATGGATGTCTACCTGTA[C/A]GATGTGGACATCAAGCCAGAAAAGTGCCCACGACGTGTTAACAGGTGCAAAACATTCAGCCTTTACAATAATTGATATAGTTTGCAACACTTGATTTGTTTTAAATCTTTCATTCTCAAGAGACTTCTCCATTATTGAGTCTTTATAGTCAAGCTGAGCAGCTTTGAGCCCATGATAATGGTCATAACATTTTCTTTGATGGCTTTCAGGGAAGTGGTGGATTCTATGGTGCAGCACTTTAAAGTGACAATCTTTGGGGACAGAAGACCAGTTTATGATGGCAAGAAGAGCCTTTACACTGCTCAGCCTTTACCAGTGGCCTCAGCGGGGGTAAGATACAGTAACGGGCACCAGGGCGGCTGGGAAGCACCTAACAGTAAAAGTAGAACTTGATACATGCCATGATTAAATGTGTTCATTATGATAGTCCTTTTATGATGCATACTGTAGTTTTTACAAATATTTATTGAAAACATTAAAGGCGTACAAAACTGTCAAGA
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:
sa23461
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 |
---|---|---|---|---|---|
ENSDART00000091813 | Essential Splice Site | 264 | 860 | 6 | 19 |
Genomic Location (Zv9):
Chromosome 19 (position 11293602)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10752831 |
GRCz11 | 19 | 10671756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTCCTCTCACCGATTCCCACAGAGTCAAATTCACCAAAGAGATCAAAG[G/A]TTAGTGTCAATGGGCAAAAGTGGCTATAAAGATTGTTCAAACTCTGCATT
Long Flanking Sequence:
GTCGCCGTGAGCACAGAGGTGCTATATGTTGGCGCATTCAACCAGTAGGCTATTGGAACTGTCATGTTTCATTCTTCATAACTTATATTAATAGAGCATGTATGCTCCCTGATTATCATGGTGCGTTGTGGGACTTTTCGGAAGGCATACGTTTCAGCACACTGGAAGAATTTTGGAATTGAGAGCCCTTAAAATACCTGACTCCTTTATCAGTGCCCTAACTAGTGAACAAGGCACTGCTTGAGACAAACCAATTGTTTTTATGCAAACTGTAAACTTTGTTTCCAGTTCTTGTATAGTAATTTGAATTTAAGCTCATTTATTTTGCATTAACGTTGACCGGATATTATAATTATTTTCCTTAGTGTCTGCCACTGCTTTCTACAAAGCTCAGCCTGTGATTCAGTTCATGTGTGAGGTTCTTGATATCCACAACATCGATGAGCAGCCCCGTCCTCTCACCGATTCCCACAGAGTCAAATTCACCAAAGAGATCAAAG[G/A]TTAGTGTCAATGGGCAAAAGTGGCTATAAAGATTGTTCAAACTCTGCATTTGAGCTGCATTTCATTAAACCATCCTGAAAAAAGGTATAATTAGGTGGCCTTAACTACTGTGTACTTGCATCAGAAAATAGATACAGTGTACTTACTAAGGTCATAATGTATGGCAGAACACTTCTGGTGCACTTGAGGTGGAATACGGGTAGGGTTAGGGACAGGTTTGGTGGTATGGGTAGGTTTAAGAGTGGGTTGAGTTGTAAGGAATGGTCAACAGTGTAATTACACTGGTATTTAATCAGTCATAACTACAATGTAAAAACACGCATTTACACAATAACAATACATTGTAACAAATGAATAATTTCTGTACAAGGTAAGGCCACCTAATATAAAGTGGGATTGAAATTTCTTGGGCTTTAGTTTAACAGAATGATCCGTGAAAGATACTGCAACTGATGCTTTTTTTTTTCTTATGTATTATTGCATTATTTACACAATTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23462
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 |
---|---|---|---|---|---|
ENSDART00000091813 | Nonsense | 342 | 860 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 19 (position 11295138)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10754367 |
GRCz11 | 19 | 10673292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGCCCTGCCTGCAAGTGGGACAGGAGCAGAAACACACATACCTACCTT[T/A]AGAGGTGAGGCGTCTGATAACTTATGTTAACAGGAAACGTGATGCTGTTT
Long Flanking Sequence:
AAACTGGAAGAACCTTCTTAGAATTTTCAAAGGGATAGTTCACCCAGAAATTAACATTTTTCTCACCGTGTTTCTAAACTTTCATGAATTGTGTTGAACACGTAGGAACTTACCCTGAAGAATGTTGGAAACCAGCAGCTATTGACATCCATAGTAGAAACAAAAATTGTATGGAAGTCAATGGTTGCTGCTTTCCATCATTCATCAGTATATCTTTCTTTGTGTTAAACAGAAGCAATAAACAGTAGGGTGAGTAAATACTGACAGAATATTCATTTTTTGGGTGGACTATCACATTAAAATCCCAGCTCCCTGTTCATTTTTAATAATTATATAGTTTTTGTATTCATTTGCCAGGTTTCCTCTACAGCTAGAAAATGGACAGACTGTGGAGAGAACAGTGGCACAATATTTCAGGGAAAAGTACAACTTACAGCTCAAGTACCCCCATTTGCCCTGCCTGCAAGTGGGACAGGAGCAGAAACACACATACCTACCTT[T/A]AGAGGTGAGGCGTCTGATAACTTATGTTAACAGGAAACGTGATGCTGTTTCTTTGCACTGAAGCACAATCTAGCCATCGTTTGTTTTTCCCTGATTAGTGGAATTCATCATTTCTAGATACCTAACAACAGCTTTTTTGAAGCTTATTTTTTTCCACCACAAAAATACAGCTTAGAATTCACACAGTTTTGATTTTATATCTCACAATTTTGAGTTATAAACGTGCAATTGTGGGTTTGTGTCTTGCAATACTGAAACAAAACTCAGAATTGCAAGAAATAATGTTAATTTTAAAGTCTGAAAAAAGTATATTTAAATACATAAATTATTTTTAAATTGTTTATTTATTGCTATTTGGACTATTTTTCTCAGATTTCCAACATGATTTAACCTAATTCTGACTTTCTTTGTCAGAAATGGTCAGTTTTGTGTAATATAAACAATGCAAATGCTTACATCTGATTTTTTCATTAGGATTTCATCATTCTCAGATTTGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43240
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091813 | Nonsense | 377 | 860 | 9 | 19 |
Genomic Location (Zv9):
Chromosome 19 (position 11296218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10755447 |
GRCz11 | 19 | 10674372 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAAACCTCCACCATGATCAAAGCCACGGCCCGCTCCGCACCGGACAGA[C/T]AAGAGGAGATCAGCAGACTGGTGAGTCCTAAAAGATACTCAGAAACATCC
Long Flanking Sequence:
AGCTGCGTTTCTTTTGTATGCTAGCGACAACAATGTTTTTCTCCTTCTATAGTTCAGTATTTGGTTTATTTCTGGCATAAAAGCAGCTGCATTAATGAGAAAGTTTGTAATAAAAAGTTGAACCCGCAAAAAGTCTCACCCATTCATGTTTACAAATACAAATGCAGCTGTTTAGAGGTCATTTCTGATTTATGATGTAAGAATTTACTGCTTTTTTATGATTAAATTTACCGGTGAAGTCTTTTCAGTAATTTTACAGATGTTTACTATTATAACTGTGTGAAAAGGGCTATTAGCACTAGCTCTGATCTAGTGTCTTGTAGTACTTGCTTTAGTTAAAGCTTATTGGATTTTTTTGTTCCTTTTTAATGCTGTCATTATCAACTGTCCTTTTCCCTCAGGTGTGCAACATAGTGGCAGGTCAACGCTGCATAAAAAAACTGACCGACAACCAAACCTCCACCATGATCAAAGCCACGGCCCGCTCCGCACCGGACAGA[C/T]AAGAGGAGATCAGCAGACTGGTGAGTCCTAAAAGATACTCAGAAACATCCCTGCTAGTGTTTATGACTGAAGATGCCTTTCTTAAGTGTCCTAACTCTGAAGCCTCAATCTTTTGCTTATTTCTCAGGTGCGCAGTGCCAACTATAATTCAGACCCATTTGTGCAAGAGTTCCAGTTCCGTGTGCGGGACGAGATGGCGGAGGTGACGGGTCGAGTTCTGCCCGCCCCCATGCTGCAGTACGGCGGCAGGGTGAGCTCTGAACACTTTATGGTACCCGCCCCCTTTCACTCATGCACCGTGTGTGTTTGTGTTTGAGTAGAAGACTAGAGATTTTGCTGGCTTTATGTCTAGATTTAACATCTAAATGGGTAGCTAAACCCAAAATAAACCCAAAATAAATAATAAAATAATAATAATTGTCATTTACTTACTTAATTGTTTTGCACACTTGAAACACCACATTTCTGCCCCATCACAGAAAATCCAGTGCTTTAAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44906
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091813 | Nonsense | 462 | 860 | 11 | 19 |
Genomic Location (Zv9):
Chromosome 19 (position 11299112)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10758341 |
GRCz11 | 19 | 10677266 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGTGGAGATCAAGATGTGGGCCATCGCTTGCTTTGCCACTCAGAGA[C/T]AATGTAGAGAGGAAGTTCTCAAGTAAAGCTTCCTCCATCTTTTTTTTTTG
Long Flanking Sequence:
TTTTGCATTTGGAAAATGAAATTACATTTTCTCCTTATGTATTTAGTATTTTTATTTTTGAATGTGTCCGAATATATACATTTATCTTTTCAGATATCCATAAAATATATCTTTATTTTGATTAGAAAACTAGTAAAGTAGTACCAATATTTACTAGTACTTTCCAAATTTAGTAAGAGTTTGACAAATGACTGCTGTGTAAAAAAAATAAAAATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACAATGATTAAAATGCAGTCAAACATATAGTATTTGACAAACTTATTCTTGAAATTACAATTATATTTCTCCTTGTGTTACAGAATCGTACTGTAGCCACCCCTAGTCATGGAGTGTGGGACATGAGAGGCAAGCAGTTTCACACTGGAGTGGAGATCAAGATGTGGGCCATCGCTTGCTTTGCCACTCAGAGA[C/T]AATGTAGAGAGGAAGTTCTCAAGTAAAGCTTCCTCCATCTTTTTTTTTTGGTCATTAACAAAGCTTCAATTATCAGTAGAAGTGAAATACTCGGCTATCTCTTTTGTAGGGGCTTTACAGACCAGCTGCGGAAGATCTCCAAGGATGCAGGGATGCCTATTCAGGGGCAGCCGTGCTTCTGCAAGTATGCTCAGGGAGCAGATAATGTGGAGCCCATGTTCCGGCACCTGAAGAACACTTATGCTGGTCTTCAACTCATCATCGTCATTCTGCCTGGAAAAACTCCAGTCTACGGTAACTATACATGGACAGAGGTGCCATTTATGTTGGTCAAGTTTACTAAAGAGCTCCGTATTGAAGCTTCCCAGTACATTTATTTGCATTGTTTTAGCCTGTTGTTGTTATTTTTTTAATTTTTTATTTTTTTTGATGAATCAATATTCCTGAGAGTGGCTTAAAAGTTGAAGTGCATTGGTATTTGTAAAAATCTTGATGTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39235
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091813 | Nonsense | 637 | 860 | 15 | 19 |
Genomic Location (Zv9):
Chromosome 19 (position 11303218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10762447 |
GRCz11 | 19 | 10681372 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCTCACCCCAGCAGATACTGCGCTACCGTCCGTGTCCAGAGGCCCAGA[C/T]AGGAGGTGATTCAGGACCTGGCATCCATGGTGCGAGAGCTGCTCATCCAG
Long Flanking Sequence:
TCACTGATTATTTTGCTTAACCCATTCACTGATTATTTTGCTTGTTTTAAGGAAAAACGTACGTAATATTGGCGTATTATTTATGAAAACAAGACAATATGTTGTGCTTTCCTAGAAAATGCTTCTTGATATAAGAATTTTTAGATATTTGGACTAGAAATAAGACAAAAAAAATCTAAGTAAGAAAAGCATTTTTTGCAGTGCATTAATCTATGATAAATCCTAAAGGCACAGTATGTCATTTTGTTTTTCAGTAGTTGGACAAAATGAAAGACTAAATAAAAATAATGTACATCATTTATAACAAATACTGCAGTGTATCATTTTTAAAATGCTTGATTTTATTTTATTAAATTTTTTTTTTGTATGATTTTAAGGGAATTTTTTTTTACAATGTGTTTTTCTTTTTTTTTCCACTTACCTCTCTTCTTCAGGTGGTGGGTAGCATGGATGCTCACCCCAGCAGATACTGCGCTACCGTCCGTGTCCAGAGGCCCAGA[C/T]AGGAGGTGATTCAGGACCTGGCATCCATGGTGCGAGAGCTGCTCATCCAGTTCTACAAGTCTACTCACTACAAACCCACCAGAATCATCTTCTATAGGGATGGAGTGTCTGAGGGGCAGTTCAGACAGGTGAGGAACTACAGAATATATCGCTTTAAAGCACTACACATAGTCAAAACTCTCTCACTTCTCAGTTCCCTTTGAAATAGTCTCTCCAGTGATGCGCATCATGAAACATTTGCGTGTGTATTGCGAGAATTAGTGCCACAGTTTCGTCATGTGTGAAGATTTTCAGGTGTTTTCAGGGTCTGCAGTCTCACTATATGACAACATGAACAAGCTGTTCTCTTTTTCATTTGAGAAAACTCTTGTTAGATACAAATAGAAACTTGCAGGTCTTCATTTTAACCTGGGAATAAAGTGATTTAACTTGAAATGAGGACAAATGCGTTACTCTTATATAATAAAATTTACTTCAAAAATAATAATAAAAATAATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23463
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 |
---|---|---|---|---|---|
ENSDART00000091813 | Essential Splice Site | 825 | 860 | 19 | 19 |
Genomic Location (Zv9):
Chromosome 19 (position 11307216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10766445 |
GRCz11 | 19 | 10685370 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTCATTGTTTAAGTAATTTGCTAATTTCTCTCTCCTCTTTTCACACA[G/A]TGCGGAAGGCAGCCATGTGTCGGGTCAGAGTAACGGTCGAGACCCTCAAG
Long Flanking Sequence:
TTTGATTTGATCTGATTTTGTTACAGTATTTTCGATATTTATTATTCTGGAGAAAGTCTTATTTGTTTTATTTCGGCAAGAAGAAAAGCAGCTTCTTTAATCATTTTAAGGTCACTATTATTAACCCCCTTAAGCTATATATTTTCGAATTGTCTACAGAACCAACCATCATTATACAACGACTTGCCTAATTACCCTAACCTGCTAGTTATGCCGTTAAATGTCACTTTAAGCTGAATAAAAGCACCACGAATACTATCTAGTAAAATATTGGGAACTGTTATTATGACAAAGATAAAATAAATCAGTGATTAGAAATGAGTTATTAACTATTATGTTTAGAAATGGGTTGAGAATTTTCATTCCATTAAAAACAAACTGGGGAAAAAATTAGGGGGGTTAAAAATTCAGGAAGGCTAATAAATCTGACTTTAATTATGTTTATTAAAATTATTCATTGTTTAAGTAATTTGCTAATTTCTCTCTCCTCTTTTCACACA[G/A]TGCGGAAGGCAGCCATGTGTCGGGTCAGAGTAACGGTCGAGACCCTCAAGCCCTGGCCAAAGCTGTGCAGATCCATCACGACACTCTGAGGACCATGTACTTTGCCTAGCACCGCCTCCACAGACCTGTCAATCACCAGTCATTGTGCACTTAGAGGAGGAGGGAGAGGAGCTTCTCCCAATCACAGGCTGCTAAAGAGAACCAAATGTAATAGAACTTACAGGCGGAACTAGCACAGTTATGCAATAGAAAAACAGCCAATCTTTCCAAGCTTACTAATTGTTTTTAATATCTAGATTGCAGCTATAATGTTATTTATTAGATTTCTAGATCTGTTTAACTATTCATTTTGCAGCCTTGGGTCACAAAACCAAGTTTAAAGATGAGGCAGATCAGCGAATGAGGCAGTGTTATTTCCCTGTTTGTGTAGGTTTCTCTCATCCTGTAGAGTTTCACGACTCATCGGACACGCAAAAAGCTGAACAGTTTTAAAAAACGTC
Associated Phenotype:
Not determined