ZMP
egfra
Ensembl ID:
ZFIN ID:
Description:
epidermal growth factor receptor [Source:RefSeq peptide;Acc:NP_919405]
Human Orthologue:
EGFR
Human Description:
epidermal growth factor receptor [Source:HGNC Symbol;Acc:3236]
Mouse Orthologue:
Egfr
Mouse Description:
epidermal growth factor receptor Gene [Source:MGI Symbol;Acc:MGI:95294]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14931 | Nonsense | Available for shipment | Available now |
sa19660 | Essential Splice Site | Available for shipment | Available now |
sa11905 | Nonsense | Available for shipment | Available now |
sa19661 | Nonsense | Available for shipment | Available now |
sa16195 | Essential Splice Site | Available for shipment | Available now |
sa1683 | Nonsense | Available for shipment | Available now |
sa15365 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14931
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 |
---|---|---|---|---|---|
ENSDART00000027219 | Nonsense | 31 | 1172 | 1 | 32 |
ENSDART00000088591 | Nonsense | 17 | 1174 | 1 | 33 |
ENSDART00000108964 | Nonsense | 45 | 503 | 2 | 12 |
ENSDART00000128514 | Nonsense | 45 | 389 | 2 | 9 |
ENSDART00000131374 | Nonsense | 45 | 625 | 2 | 15 |
ENSDART00000136906 | Nonsense | 45 | 760 | 2 | 19 |
ENSDART00000147261 | None | None | 243 | None | 5 |
The following transcripts of ENSDARG00000013847 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 4264286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3938812 |
GRCz11 | 2 | 3769991 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGGAGCAAACAACAAACTGACTCTTCTGGGAACRGTGGAAGACCATTA[T/A]CAGGTTCTGCTCAGAATGTACAGAAACKGCACTGTGGTTCTGGAGAACCT
Long Flanking Sequence:
GCCGATGTGTAGTTCTCCAGGGATTTGCAAATGCTTGATCACTGATGATCATGACAGTATGATCTTATTTTACATCCCTACCCAATACCTAAACCTAACTACTACCTTGCTGACTAATAACAAGCAGCTAATTAGTAGTTTATTGAGCTAAAATTCTTGGTTAATAGTGTGAATTGTACAATAATAAAAAGCGTAACGGTTTTATTAAACCACGTGTTGCACCTTAATTGTTTTAATGTTTCAGAAAAACATTTTATCTTTGTAATAATAATACACTTTATTTATTTATTTATTTTTTTGGTTTGGATTATTTATAGATCAACACATTTCGAAATGAGTAAAATTATAATTACCAAGAAAAAGTATTGTTGTACTTTTCCCCATGAGGGCCTCTCTGGGGAAATTGAATTGAATGGTTCTTTCTGTGTGTGTTTGTGTGTTTCAGTGTGTCAGGGAGCAAACAACAAACTGACTCTTCTGGGAACAGTGGAAGACCATTA[T/A]CAGGTTCTGCTCAGAATGTACAGAAACTGCACTGTGGTTCTGGAGAACCTGGAAATTACACATATAACAGAGAAATATGACCTGTCCTTCCTCAAGGTATGATAAATCCTGCAATGATGATATTCCAATGCATCGTACATCATCTGTACACCATTGTTTAAGCATGTTACTATGATAAATTTAGATTGTACAGTTGAAGTCTGAATTATTAGCCCCCTTGTCAATTTTTCCCCAATTTCTGTTTGATGGAAATATTTTTTTCAACACTTTTCTAAACATAATAGCTTTAAAAACAAATTTTTAATGATGAATTTCTTTTATCTTTGCCATGATATTTTCCAACATACTAGTATACAGCTTAAAGTGACATTTTAAGGCTTAACTAGGTTAATTAGGGTAAAGTTAGGGTAAATAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGAAGACAAATGAAAAATAAAATCTTGCTTTAGGGGGCTTATAATATTGTGTGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19660
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 |
---|---|---|---|---|---|
ENSDART00000027219 | Essential Splice Site | 280 | 1172 | 6 | 32 |
ENSDART00000088591 | Essential Splice Site | 268 | 1174 | 7 | 33 |
ENSDART00000108964 | Essential Splice Site | 294 | 503 | 7 | 12 |
ENSDART00000128514 | Essential Splice Site | 294 | 389 | 7 | 9 |
ENSDART00000131374 | Essential Splice Site | 294 | 625 | 7 | 15 |
ENSDART00000136906 | Essential Splice Site | 294 | 760 | 7 | 19 |
ENSDART00000147261 | None | None | 243 | None | 5 |
The following transcripts of ENSDARG00000013847 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 4272705)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3947231 |
GRCz11 | 2 | 3778410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCATATGGGAAGTACAGCTTTGGGGCGACGTGCATCAAGACATGCCCAC[G/A]TAAGTCTTTTATGTGAATTTGTGCTGTTCCAGAGTTTCTACAAGGGCTTA
Long Flanking Sequence:
TAAGTGAAAAATAAAACGAAAAAATTAAACAAAAAAACTGAATGAAATGAAACAAAAAAAAATGTACAAAACAAAAAACTAAACAAAATGGAAAAATTAAACAAAACTAAATTAAATGAAGCAAAACAGGAAACAAAAAAACAAAACAAAATAAAACAAAAAAAAGAAACAAAAGCTACATAAAATATTTAACTAAACTAAATGAAAATGAAATGAAACAAAAAATGGGACAAAACAAAAAACAAGCCGAACGTGAAAGTCTCCTTTATAACAGTGAAGCTTTCATTCACAGCTGCATCAGGGCTGCGTTCAGATTACTGTGCTCATGTGAAATGCTGTGTGTGTTTGTGTCCTGCAGGCCTGTAAGGACTTCCAGGATGAAGGGACATGTAAGGACGCATGTCCGCGGCTCATGCTCTACGACCCAAACACACACCAGCTCGCGCCAAACCCATATGGGAAGTACAGCTTTGGGGCGACGTGCATCAAGACATGCCCAC[G/A]TAAGTCTTTTATGTGAATTTGTGCTGTTCCAGAGTTTCTACAAGGGCTTACTTTTTTACAAAATCTAAATTATAGGCCTAAATTTAGAAGCTGCGACTATTTTTTTCTCTTCTTATTGTCACCCAGATCTTAGAGAAACAGAATATTAAATGAGAAAACAGTGGGCGTGTCCTAGTTTTTAAACTGCGAGCTGATTGGATGTAGTAAAGTAGGCATTTCATTCAGAAAGATGGAGAAAAGAGCTTGGGGGGAGTTATTACAGCCTAACAGACTCCTCCTCCATCTCTGTTGTCAAAACTGACAGCTGGAGGGGCGTGGTTAAGTATGTTAGCCACACCCTATACCCCCAGACAGACCTAATCTGAGAATTTAACTGAAAACAAACAAAGTGCTTTTTCAGATTTTAATTAGAAGCTGCGTCCCAAATGGCACACTATACACTATGCACTCATGCACTATGTACTTATGCACTTACACACTCAACAGGATAGTACATGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11905
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 |
---|---|---|---|---|---|
ENSDART00000027219 | Nonsense | 283 | 1172 | 7 | 32 |
ENSDART00000088591 | Nonsense | 271 | 1174 | 8 | 33 |
ENSDART00000108964 | Nonsense | 297 | 503 | 8 | 12 |
ENSDART00000128514 | Nonsense | 297 | 389 | 8 | 9 |
ENSDART00000131374 | Nonsense | 297 | 625 | 8 | 15 |
ENSDART00000136906 | Nonsense | 297 | 760 | 8 | 19 |
ENSDART00000147261 | None | None | 243 | None | 5 |
The following transcripts of ENSDARG00000013847 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 4275698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3950224 |
GRCz11 | 2 | 3781403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGKTTGTGGTTAATGGTGNTTTTTTTGTCTGTTTTTTTCCTCAGACAACTA[T/A]GTGGTGACGGATCACGGGGCCTGTGTGAGAACATGCAGCCCTGGCACCTA
Long Flanking Sequence:
GCCATCCCCGCTTCGGCACTATTCGGTTCACGATTTTTGCCTTTTACATTTCTCTTTTTGAGCAAGATGCTAATGGTCTAATCTGATTCAATGATCTATGCTAAGCTAAGCTAAAAGTACAGATTGCCTGAATTGATTGAAAATAGTAAAGCTCAACTGTTTACCTCTAGAAATGCTGTAAAATAAATCTATTTCCCCCAAAGAAGTGAATATTTCTTTTTTTTTTAGTCTTAAGACTGACCTAGTAAGACCTGCAGAAACTCTGTGTTCCAGCAGCTCGTGGATTCTGGAGATTAATCTTTCAGGGAAATGGGGTTAAAATATAAATGACTCTGTCCAGCTAAAGAGAGCGAGTCTGCATCTGTTGATCTGTTGCTCAACTCTGGTTTCTGAATAACGTTTCTCCATGACCTGAAGATTAGACACAAGCACCAGTTATTTAGCTTTGACTGGTTGTGGTTAATGGTGTTTTTTTGTCTGTTTTTTTCCTCAGACAACTA[T/A]GTGGTGACGGATCACGGGGCCTGTGTGAGAACATGCAGCCCTGGCACCTATGAAGTGGATGAGGGTGGAGTTCGCAAATGTAAGAGGTGTGAAGGCCTGTGTCCAAAAGGTACAACTCAGACTGATTTTTGTTTCATTTCTAGTTTGACAAACGTAATGCGATTGCTTTTAGTTGTTTTAGTGGTATACAGGGTGTCCGCTGGGTCTAAAAAAGTATTGAAAGTCCATAAATCAGGGTGTAGAAATTTAAGGCCCTTAAGAAGTATTAAAAAGTCTTAAATGCTATTTTGCAAAGCATTCAATTTAATATTATTTTTGATTATGCAGGATATGGTAAAATTCACCTGAATTAAATCTGCGAATATCAGCATGCAGTGTTGTTTATGAAATCAGTGAAATCCTGCTAGATTTGACATCTTGCTGCTTTGTTTACCCCAGTAACCAAGACACCACCATAATTTCTGCAGTTCTATATGCACAAACCCGCTGAATTAGCTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19661
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027219 | Nonsense | 569 | 1172 | 14 | 32 |
ENSDART00000088591 | Nonsense | 557 | 1174 | 15 | 33 |
ENSDART00000108964 | None | None | 503 | None | 12 |
ENSDART00000128514 | None | None | 389 | None | 9 |
ENSDART00000131374 | Nonsense | 583 | 625 | 15 | 15 |
ENSDART00000136906 | Nonsense | 583 | 760 | 15 | 19 |
ENSDART00000147261 | None | None | 243 | None | 5 |
The following transcripts of ENSDARG00000013847 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 4286350)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3960876 |
GRCz11 | 2 | 3792055 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCAACATTTTGTCCAGGGACCCGACAAATGTACAGTGTGTGCAAACTA[T/G]AAAGACGGACCGCACTGTGTGCATCGCTGCCCGCAAGGTGTACCAGGAGA
Long Flanking Sequence:
AAATTTGAGATCTGAAAAAGCGCACACAGCAGCCTCAGCTGTATTCGCAACAACAAAAAGTGCAAAAAAGCGTACCTCCTGAGACGTATTTGGCGCTCTCCAGAAATTATTCTAGGGGTTCGTTTTTTAGAACGAGCCGGGGTTGCATTAAGCTGTCGAATTGACGATTTCAGCAATAGTGACCAGAATGTGTTTTTCTTTCTGTCTCTACAGTGAGCCGCGTGAATATGAGGTCAATAAAACATGCATGGAATGCGATCCTGAATGTCTGCTCATGAATGAAACCCAGACCTGCAACGGCCCTGTGAGTTTCAAACCAAACATGTTCTGCTTCTGTAGATATCAGATACAAAATGCTGACTCTCAAAGCAATGTATTCCGTCCCGGAGACACATCGTTAAATTCACATCAACTACAAGACCGTACAATTGCTGTTTGTTGCTATATAATTGCCAACATTTTGTCCAGGGACCCGACAAATGTACAGTGTGTGCAAACTA[T/G]AAAGACGGACCGCACTGTGTGCATCGCTGCCCGCAAGGTGTACCAGGAGAGAAAGACACACTCATCTGGAAATACGCTGACGTGACACACGTTTGCCAGCCCTGTCATGAAAACTGCACCCAGGGGTGAGACAGACATCGCATATGAGCCTTTCAATTCAATGAAAATACACAAAACACACACTTCCCAGCAGGCACACGACATTATGAGACGTTAGTATTAGGTAGATTTAGTAAGGTGACGTCAGGTGACCAAAATTTAATGTCTAGTCAGTGTCTAAAGATAACGTTATTTTGACGTCCAATAACAATGTCAAATGACGTTGATGTTTGGTTGATTTTAGGTTGTGTTGGAAAGTAACCAAAATCCAATGTCGAGCCAACATCTTAAACCAACGTCATATTTACGTCAAATACTGACAATTATTCGTCAGGTATGGCAACCAAAATCCAACATCTAATAGACGTCATAGTGGTAACGTCCACACAACGTCAAGCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16195
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 |
---|---|---|---|---|---|
ENSDART00000027219 | Essential Splice Site | 611 | 1172 | 14 | 32 |
ENSDART00000088591 | Essential Splice Site | 599 | 1174 | 15 | 33 |
ENSDART00000108964 | None | None | 503 | None | 12 |
ENSDART00000128514 | None | None | 389 | None | 9 |
ENSDART00000131374 | None | 625 | 625 | 15 | 15 |
ENSDART00000136906 | Essential Splice Site | 625 | 760 | 15 | 19 |
ENSDART00000147261 | None | None | 243 | None | 5 |
The following transcripts of ENSDARG00000013847 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 4286476)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3961002 |
GRCz11 | 2 | 3792181 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGACGTGACACACGTTTGCCAGCCCTGTCATGAAAACTGCACCCAGGG[G/T]TGAGACAGACAWMGCATATGAGCCTNNNNNTTCAATGAAAATACACMAAA
Long Flanking Sequence:
TTAGAACGAGCCGGGGTTGCATTAAGCTGTCGAATTGACGATTTCAGCAATAGTGACCAGAATGTGTTTTTCTTTCTGTCTCTACAGTGAGCCGCGTGAATATGAGGTCAATAAAACATGCATGGAATGCGATCCTGAATGTCTGCTCATGAATGAAACCCAGACCTGCAACGGCCCTGTGAGTTTCAAACCAAACATGTTCTGCTTCTGTAGATATCAGATACAAAATGCTGACTCTCAAAGCAATGTATTCCGTCCCGGAGACACATCGTTAAATTCACATCAACTACAAGACCGTACAATTGCTGTTTGTTGCTATATAATTGCCAACATTTTGTCCAGGGACCCGACAAATGTACAGTGTGTGCAAACTATAAAGACGGACCGCACTGTGTGCATCGCTGCCCGCAAGGTGTACCAGGAGAGAAAGACACACTCATCTGGAAATACGCTGACGTGACACACGTTTGCCAGCCCTGTCATGAAAACTGCACCCAGGG[G/T]TGAGACAGACATCGCATATGAGCCTTTCAATTCAATGAAAATACACAAAACACACACTTCCCAGCAGGCACACGACATTATGAGACGTTAGTATTAGGTAGATTTAGTAAGGTGACGTCAGGTGACCAAAATTTAATGTCTAGTCAGTGTCTAAAGATAACGTTATTTTGACGTCCAATAACAATGTCAAATGACGTTGATGTTTGGTTGATTTTAGGTTGTGTTGGAAAGTAACCAAAATCCAATGTCGAGCCAACATCTTAAACCAACGTCATATTTACGTCAAATACTGACAATTATTCGTCAGGTATGGCAACCAAAATCCAACATCTAATAGACGTCATAGTGGTAACGTCCACACAACGTCAAGCTGTAACATCATTAGACGTTGATATGTTGTTGATTTTAGGTTGGACATTGGACATTAACGTTGACCTGATGTTGGGTTCTGATGTCAGCCTGATTTTCATTTCCAAACAAAATGCCACGTCCCTTCGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1683
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 |
---|---|---|---|---|---|
ENSDART00000027219 | Nonsense | 1104 | 1172 | 32 | 32 |
ENSDART00000088591 | Nonsense | 1106 | 1174 | 33 | 33 |
ENSDART00000108964 | None | None | 503 | None | 12 |
ENSDART00000128514 | None | None | 389 | None | 9 |
ENSDART00000131374 | None | None | 625 | None | 15 |
ENSDART00000136906 | None | None | 760 | None | 19 |
ENSDART00000147261 | Nonsense | 175 | 243 | 5 | 5 |
The following transcripts of ENSDARG00000013847 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 4304373)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3986626 |
GRCz11 | 2 | 3817515 |
KASP Assay ID:
554-1629.1 (used for ordering genotyping assays)
KASP Sequence:
CGGACCCTCCTGCACTCCTCCCCAGCGCTGGACGAGACGGAAGAGGAGTA[T/A]CTGAACTGCTTCAAGAGCCCGGCTCCGGCTTCAGTGGTGGAGTATCTGAA
Long Flanking Sequence:
TTCCCATGCTTAAAATAGCAAAAGTGGATTCATACTGTGTGCTTAGATCCCTAAAATAGAGTTAAAATTTCTTTTGGGAGAGCAAAGTTTTTCCTTTAAAACCTAAAAACAAACTTCCTCAAGCGTTTGACCAACCCCCCCCCCCCTTTCATTTACATTGGTTTCCATCATCTTGTCCCTCAAGGGCTCCATAGATTTTGAAGGTCATAGGTTAATTAAACGACCTTAGTCGGGTCTATTGCTTTAATAGATGCTTATACTCTTGGGGGGTAAGGGGGGGGGGGGGGGGGTTGTTCAGCACGTAGATACACATTTACATCTTAATGAACTGCTGATTAAAGTCACTACTAATAACTTACCCCCCATATCATCCTTTAATCTGCAGAATATATGAACCAGAATGAGTCCAGCATGATCAACCCAGTGTACCAGCAGCCCCACGGACCCCCGCGGACCCTCCTGCACTCCTCCCCAGCGCTGGACGAGACGGAAGAGGAGTA[T/A]CTGAACTGCTTCAAGAGCCCGGCTCCGGCTTCAGTGGTGGAGTATCTGAACACGTCCCACACACAGCTGCTCTCCACAAAGCCCTTCTTCAGCATGGACAACCCCGACTACCAGCAGGACTTCTGCCCGCTGGAGCTCAAAACACACACCAACGGGCACCTGCCGGCCGCGCAGAACCAGGAGTACATGGGCCTGGAGGTGCACTAGCAGATCACTTTTCAATTAGACGCTTTAATAAAGCTGAGAGATGCAAGGACGTCTGTTTATGGGCCTTTCTGAACCCAGATCTGCCGGTTGGATTGAACAATTTGAGACTATTGATGACTACAGGACATGAGTAGACTACAGTCCCGTGATGCCAGTAGAGACGCATTGAAGTGCTGAAAGACCTTTTTAGGACTTCTGGTTTCATTCGCTTATGATTTTAATCGGCAATTTACACCAGTGTGTGTTGCTCTGTGGTGTGTGTAATCATCTTCTGTAATCATTCATTCAGAGCC
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:
sa15365
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 |
---|---|---|---|---|---|
ENSDART00000027219 | Nonsense | 1119 | 1172 | 32 | 32 |
ENSDART00000088591 | Nonsense | 1121 | 1174 | 33 | 33 |
ENSDART00000108964 | None | None | 503 | None | 12 |
ENSDART00000128514 | None | None | 389 | None | 9 |
ENSDART00000131374 | None | None | 625 | None | 15 |
ENSDART00000136906 | None | None | 760 | None | 19 |
ENSDART00000147261 | Nonsense | 190 | 243 | 5 | 5 |
The following transcripts of ENSDARG00000013847 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 4304418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3986671 |
GRCz11 | 2 | 3817560 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTAWCTGAACTGCTTCAAGAGCCCGGCTCCGGCTTCAGTGGTGGAGTA[T/A]CTGAACAMRTCCCACACACAGCTGCTCTCCACAAAGCCCTTCTTCAGCAT
Long Flanking Sequence:
GATCCCTAAAATAGAGTTAAAATTTCTTTTGGGAGAGCAAAGTTTTTCCTTTAAAACCTAAAAACAAACTTCCTCAAGCGTTTGACCAACCCCCCCCCCCCTTTCATTTACATTGGTTTCCATCATCTTGTCCCTCAAGGGCTCCATAGATTTTGAAGGTCATAGGTTAATTAAACGACCTTAGTCGGGTCTATTGCTTTAATAGATGCTTATACTCTTGGGGGGTAAGGGGGGGGGGGGGGGGGTTGTTCAGCACGTAGATACACATTTACATCTTAATGAACTGCTGATTAAAGTCACTACTAATAACTTACCCCCCATATCATCCTTTAATCTGCAGAATATATGAACCAGAATGAGTCCAGCATGATCAACCCAGTGTACCAGCAGCCCCACGGACCCCCGCGGACCCTCCTGCACTCCTCCCCAGCGCTGGACGAGACGGAAGAGGAGTATCTGAACTGCTTCAAGAGCCCGGCTCCGGCTTCAGTGGTGGAGTA[T/A]CTGAACACGTCCCACACACAGCTGCTCTCCACAAAGCCCTTCTTCAGCATGGACAACCCCGACTACCAGCAGGACTTCTGCCCGCTGGAGCTCAAAACACACACCAACGGGCACCTGCCGGCCGCGCAGAACCAGGAGTACATGGGCCTGGAGGTGCACTAGCAGATCACTTTTCAATTAGACGCTTTAATAAAGCTGAGAGATGCAAGGACGTCTGTTTATGGGCCTTTCTGAACCCAGATCTGCCGGTTGGATTGAACAATTTGAGACTATTGATGACTACAGGACATGAGTAGACTACAGTCCCGTGATGCCAGTAGAGACGCATTGAAGTGCTGAAAGACCTTTTTAGGACTTCTGGTTTCATTCGCTTATGATTTTAATCGGCAATTTACACCAGTGTGTGTTGCTCTGTGGTGTGTGTAATCATCTTCTGTAATCATTCATTCAGAGCCGCTGAAAAGTGTTCGGACACTTCAGCTGAATGGGAGAAATGTGTG
Associated Phenotype:
Not determined