ZMP
BPTF
Ensembl ID:
Description:
bromodomain PHD finger transcription factor [Source:HGNC Symbol;Acc:3581]
Human Orthologues:
AC005829.1, AC103810.3, BPTF
Human Description:
bromodomain PHD finger transcription factor [Source:HGNC Symbol;Acc:3581]
Mouse Orthologue:
Bptf
Mouse Description:
bromodomain PHD finger transcription factor Gene [Source:MGI Symbol;Acc:MGI:2444008]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33174 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38389 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13237 | Essential Splice Site | Available for shipment | Available now |
sa7544 | Missense | Mutation detected in F1 DNA | Not yet available |
sa12837 | Nonsense | Available for shipment | Available now |
sa20012 | Nonsense | Available for shipment | Available now |
sa20011 | Nonsense | Available for shipment | Available now |
sa20010 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33174
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109601 | Essential Splice Site | 161 | 2725 | 1 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 25521716)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 25289901 |
GRCz11 | 3 | 25420449 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGACGATGCGAGTTACTGCACGGAGAGCAGCCACGGCAGCAACACAGG[T/A]ACGGACGCTTCGTCGGACCCACGAATTGCTGATAAGTGCGCTGCGATGAG
Long Flanking Sequence:
AATAGATTTTTATCCATAATGAGGGGGAGACGAGGCAGGCCGCCCAAAGCCCAGCTGGTGCAGGAGCCCTCAACGGGGCCGGTGCGCGGGCTGAGACCCCGCCGAAGCTTGAAACCGAAGGTGAAAGGGGGCTCGGATGAGGATTATGTCACTCCGAAACGAGGGACCCATCACCATTCAACACGAGGCCGGAGAAAAGCGCGATCCACGGCATCGAGAGGCAGAGGAAGAGGCAGGGGGACGGCCAGAGGCAGGGGGCGGCGGAGCACCGCGAGCGGGGTGGTTTACGACGACCACGAGAGCGATGAGGACGACGAAGATGCGGTCAGTTTGAGATCGGAGGAGGACGAATACATCGAGGAGCCTCTGACGGACGAAGAGGAGGAAGAAGAAGAGGAGGAGGCCATCAACGACGAGTCCGACTACCTGGAGGAACTGGACGAATTGGATGAAGACGATGCGAGTTACTGCACGGAGAGCAGCCACGGCAGCAACACAGG[T/A]ACGGACGCTTCGTCGGACCCACGAATTGCTGATAAGTGCGCTGCGATGAGTGCGAAATTAAACTTGAACGCTCGCTCTTTTGTTGACCAAAACACTCAAAATGGATCCTGGTGCTTTTCTATGCTGGCAGAGGCCGCTGGTTTAGCACTTAGCTTTAGCGCGGCAGTGCTTTATTGTGGTTAAATTAAGATTGCATGACGTTATCGCGATGAAAAAGGTTTAGAATTAAACATTGGACCTAATTTGACATTGCACAATAGTGAAACAGATTTTAAAGTCATTAACAAAAAGTTAGCTTCACTCGTCAATTATGTATTTGCTAACATTAGCCTGTTAGCGTATTAAATTAAGGCATCCTTTTTGCATTTTTATTGAATGATTTTAAATAATTCTTTCTAATCATATGACTGTTTTTGTGTTGTGACAGTAATTGGATCTGTTTTTAAGTCCACTCACGAGAACTGCAAAAGTTTGTTAGCCCGTCATCTGGCTAATTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38389
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 |
---|---|---|---|---|---|
ENSDART00000109601 | Nonsense | 577 | 2725 | 5 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 25513311)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 25281496 |
GRCz11 | 3 | 25412044 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGCTCGAACGATTCATGTCCACAACAAGACTCTAGTAATGGGAATGCA[C/T]GAAATGAGCAAACGTCTTCAGACGGTGAGAGATGTGTTTGCTCGTTTTGT
Long Flanking Sequence:
CAATGTACTTACTGTGTTCATAATTTTATTGCAGAACACTTCTGATGCTCTTGAGGTGGGTTAGGGCTAAGGTCAGGGACAGGTTTTACGGAGGCATAAGTTGTAATAAATGGTCAACAGATAATAATAGTAATACATACAGGTATTTAATTAATCATAAGTACACTGTAAATATTTATTTACACAAAAAGTACATTGTAATAAATTATTAATTTTGGTGTAGTAACATATTAGTTAAGGCCACATATTATAAATTGAGAGCCAGTATTGTTTCAAAGTGGACAACAACTAATCCTTTTTGTGTGTTTCCTCCAGATGTGATCCTGGACCGTCTGAAGACCAAGCAGGAAGCTGAGCTTGAGGAGGTGAAGCGGCGGGCAGCGGAGGAGGCTGAGAGGGCCAAGCTAGAGCCGAAAACTCTATCTGATGAACCAGCTTCAGGCGATCAGATGAGCTCGAACGATTCATGTCCACAACAAGACTCTAGTAATGGGAATGCA[C/T]GAAATGAGCAAACGTCTTCAGACGGTGAGAGATGTGTTTGCTCGTTTTGTAGCTGCTTATGTGATTGTGTGTTTAAATTTCAGAGGAAGATCATCATTCTAACACAAAGTACATTATTTAGTCATTTGTGGTCTGTTTAAAGCGCCACGAACCCTCCACCCCCCTTCAGCAGGGTGTTTTCACACCTCTAGTTTGAAAAACGTCAGGAAAGTGGGTGAGTCCAGCTCTGTTTGGGTGGGAGTGTTGAAAGAGGGAAGGGTTTGCAAGAAAAAGAGGAGTTTCATTACGTGCACAACAGCTGGTTTTTACACCAGCAACACAAAAGCAGACACACGGGGAGATAGACAGTGATTCGATGAGCAGATCTGAGAGCTGTGTGGAAGTGGAAGATTTGCACTCCATAATATTGTAGGGATTTCACTGTAAACTTAGCAACTAAATCATTTTAACTAAGGTATGTCTTTAAAAACTGAGAGTGTACTGCTGATGGTAGTAACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13237
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 |
---|---|---|---|---|---|
ENSDART00000109601 | Essential Splice Site | 942 | 2725 | 14 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 25506754)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 25274939 |
GRCz11 | 3 | 25405487 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGCAGCAGGCCACATGGGTGAAGTACACTTTCCCCATCAAACACCAGG[T/C]ACGTTAGAGCACTTGCAAGCTATGTGTTTCTGTTAAAAAAATAMCATCYG
Long Flanking Sequence:
ACTTATCATATTTAGAAGCTTTCGTTAATAGTCTGTGGAATTTAGGGTTTGTTTGAAATTGTGCAGAGAAAAAAAATGAGATAAAATCTTACATCATTCAGTCAGGAAGGGGGTTTGTTAAAAAGAAAAGGGTCAATAAAAGAGGTATGCTGGCTTTTTTTAATTAAACATAATTAATTGTCATGTTCAATTTATTGTCAAGGTAATTAAACAATGGATAATTCCTTGTACAATGCTACTCCTAAACACAAAATCATCCATGTGTGTACTTCAGCAAATTCTGTGCTGGAGGCATTCCAAAAATGTACAGTGAGTCACCTGTATGTCCCAGTTTTGATGATTTTTTTTTTTTGTATTTTTCTCCCGCAGGCTTCATCGTATGACCTCTGTGGAGCGGGAAGAGAAAGAGAAGGTGAAAAAGAGAGAGAAAAAGCTAGAGGATGAAGAAACTATGCAGCAGGCCACATGGGTGAAGTACACTTTCCCCATCAAACACCAGG[T/C]ACGTTAGAGCACTTGCAAGCTATGTGTTTCTGTTAAAAAAATACCATCTGCATCAGTATTTGAGCTGCAGGCAATCAGTAACTGAACAGATGTGTTCTGTAGGTGTGGAAGCAGAAAGGTGAGGAGTACAGAGTAACTGGGTATGGAGGCTGGAGCTGGGTTAGTAAGACGCACGTCCATCGATTTTTCACAAAACTTCCAGGAAACACAAACGTCAATTACCGCAAGGCACTTGAGGGTATGTGGTTTACTTGCATAGAATACCATAAAAGAATTATCAAACTGTCTTGGAAACAGAAAAACCTTATTTTGGAAGTACTTTTTACATTAAACTTTTTTATTTTTATAGCAGCTAAAACTGGAATGGACAATCAGGCAGCTCTCCCAGGGGCACCAAAAACTGTGGTTAAAAAAGACGAAATGTCATCTCAAAATGTGCCTGATAAGGATAATGCCCAGGTCCTATCACTGGATTCTTCTGAGGAAAAGCTATCAGTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7544
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 > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109601 | Missense | 1093 | 2725 | 17 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 25505836)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 25274021 |
GRCz11 | 3 | 25404569 |
KASP Assay ID:
554-4058.1 (used for ordering genotyping assays)
KASP Sequence:
ARCAATGCTTTTGGCATGATGTTGTAAAYGTTAGTGAAGGCTTTTTACAA[C/G]GCACAGCATACAAGAAATTAAAGCCATCAAAACTTGATGGCCTTTTGGAG
Long Flanking Sequence:
GAAATGTCATCTCAAAATGTGCCTGATAAGGATAATGCCCAGGTCCTATCACTGGATTCTTCTGAGGAAAAGCTATCAGTGGAAAAAGATCATGTGTTAAAAGTTGAAGAACAAGATGAAGAAAAAATGAATGAAACAACTGAAGAGAAATGTAATGAGAAAAACGAATCTGTGGAAGAAATGGACACCAGCAGTCCTAACTCTGCAAATGAGGGAAAAGGTAATTCTACAGTTTTTCCTGTAAAAATACAGCATATTAAGAATTATATAGCATGTATTCTCTGATATTGGAATGCATTAAAATAGTTGCCATGTGGAACAGCTGCTAAATGTGCCTCTCTCTTTCAATGTCTACAGTTGAAATCACCAACGCCTCAACCGATGACTCTACTATGAAAGAAGAGCCTTTGGATAGTGAGGTGGTGAAAGATAACACTCTGAATCAACCCCAACAATGCTTTTGGCATGATGTTGTAAACGTTAGTGAAGGCTTTTTACAA[C/G]GCACAGCATACAAGAAATTAAAGCCATCAAAACTTGATGGCCTTTTGGAGAGGCGAGTCAAACAGTTCACAATAGAAGAGAAGCAGAGGATTGATAAACTCAAACAGGCACCTACTTCTAAACCCTTGACTGAAACGGCAGTGGAAAACAAAGAGACAACCTTAGCTGCTCAGGACCATAAGGTCAAGATTGAAGGAACTATCTCTGAAACTCCTAAGGCTAGACAGACTGAGGGGGTAGCGTGTCTTGCGATACAAGAAAAAGACAATGTAGTCAAGCGGCTTGTTTTTAACCAAGAGGATGAACAGGCAAAGACAAACACTTCAGGACAGAAGAACACTCTGGATGTCAGATTAAATGATTCTGTTGAATTGGCCCCAAAAGAAAATCAGCAGAAGTTGGCAGAAACCGATCCCAAGACCGCCAGTAGGGTCGCAATGTCTGAGCTTAATGGAAACTCTCAAAGTCTGGATCAAAGTCTCAGCTTAAACGCTAAACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12837
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 |
---|---|---|---|---|---|
ENSDART00000109601 | Nonsense | 1348 | 2725 | 17 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 25505069)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 25273254 |
GRCz11 | 3 | 25403802 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAAAGGAACCAGTAAAGTCACTAATGAATGGTGACGCCASTCAAGAGTG[T/A]CTTAAAGAATGGACTAATAGCACGATTCCTCAGGTGAATTTGGATGAGGA
Long Flanking Sequence:
AATGTAGTCAAGCGGCTTGTTTTTAACCAAGAGGATGAACAGGCAAAGACAAACACTTCAGGACAGAAGAACACTCTGGATGTCAGATTAAATGATTCTGTTGAATTGGCCCCAAAAGAAAATCAGCAGAAGTTGGCAGAAACCGATCCCAAGACCGCCAGTAGGGTCGCAATGTCTGAGCTTAATGGAAACTCTCAAAGTCTGGATCAAAGTCTCAGCTTAAACGCTAAACCTGATAAAAATATTACAGAAGCTACTTGTCCACCTGAAGACTCTGCGGGAAAGGACAACATTGAAAACAGTGAGAATGATCTAGATGTGAAGAAAACTGTGCCTGTGCAAGTAAACGGGAAGGATGTTACTGTTGACCCAGAATGTAAGAATTTGACTGATAACGGTGACACAAAGGAGTTAACCAATACCATTGTAGAGGATATCAAAGCAATATCACCAAAGGAACCAGTAAAGTCACTAATGAATGGTGACGCCACTCAAGAGTG[T/A]CTTAAAGAATGGACTAATAGCACGATTCCTCAGGTGAATTTGGATGAGGAGAAAGCAGTTACTAAGCTTGACCCTGATTATCCACCACCTCAGAAAGTGGCCAAGTTGGAAAACAACATCGAAAAACCTATAGATTCCTCTGTTAGCCTCTCTGTACCTGAACCTTCTCCTGTAGCTTCTGAGCCAAATGAAAGATCCGAGGTGCCTAGTCATAGCTCTAAGGTGGAGCCGATGCAAGTGGTGGAGGCAAAGCCTTCTGTTCCTTCACCTGTCCCTTCAGCAGAGGAGTCCAGCTTAAGCAGTGACCTCACTGAAAACAGCAGCAGCATTGGCGAGACTACTGTCGTTACTCAAGTCACCACAACTACAACCACAGTATCCACAGAGTCCCGCATGGTGTTGACCTCTCGTGATAGTCTTGCTTCCAAGAACGGCCTCAATACCGCTGTGCTAACAGATTCTAAGGTGGAGTCTAGCAGCTCTGTTTCAACACTCTCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20012
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 |
---|---|---|---|---|---|
ENSDART00000109601 | Nonsense | 1573 | 2725 | 17 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 25504396)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 25272581 |
GRCz11 | 3 | 25403129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTAAAATCTATGACTGTAAGTCATGAATATTCCACCAGGGACAGAGTA[C/T]GACTATTAAAGTTTTCTCGCACCAAGAAAACGAGGTCGGGAACAGCCTTG
Long Flanking Sequence:
TAGCTTCTGAGCCAAATGAAAGATCCGAGGTGCCTAGTCATAGCTCTAAGGTGGAGCCGATGCAAGTGGTGGAGGCAAAGCCTTCTGTTCCTTCACCTGTCCCTTCAGCAGAGGAGTCCAGCTTAAGCAGTGACCTCACTGAAAACAGCAGCAGCATTGGCGAGACTACTGTCGTTACTCAAGTCACCACAACTACAACCACAGTATCCACAGAGTCCCGCATGGTGTTGACCTCTCGTGATAGTCTTGCTTCCAAGAACGGCCTCAATACCGCTGTGCTAACAGATTCTAAGGTGGAGTCTAGCAGCTCTGTTTCAACACTCTCCTCTACAACTACCACTACTGTTACCAAGGTTTTGAGCTCATCCCAGGAAGCCACTCTAACAACAGAGTGCAAGACTATGGTCATGAAAACACTGACAGATACCACATCAAGTCCTAGTGGGTCCACTGTAAAATCTATGACTGTAAGTCATGAATATTCCACCAGGGACAGAGTA[C/T]GACTATTAAAGTTTTCTCGCACCAAGAAAACGAGGTCGGGAACAGCCTTGCCCTCCTACCGCAAATTTGTGACCAAGAGTAGCAAAAAGAGTATCTTTGTGCTTCCCAATGATGAGCTAAAGAAGCTTGCAAGGCGTGGTGGCATCCGTGAAGTTCCCATCTTTAACTATAATGCCAAGCCAGCCCTAGATATCTGGCCTTACCCATCCCCTCGACCAACATTTGGGATCACATGGAGGTCTGTATCTTGTTCATCTGTATTGGATGTTTTTATTTAGAAATGTTAGTTGCTAAAGCAAATGTATAAGGGTAGGGCAGGGTTGTCTGTTGCGGCTTTTTGAAGGTCACTTTCCAGGAGAATTTTGCTCTAGATCTAAAGCCTTTTTTCTACTCGACCCGTCTGCTAGTTTGCTTGAGTGTGCGAGGTGAATGTGACATCATCGCTGAGTTGGCGGAGGTTCACTTTGGGCGAATTTTTGAGATTCAAAACAAATGCATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20011
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 |
---|---|---|---|---|---|
ENSDART00000109601 | Nonsense | 2003 | 2725 | 25 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 25499225)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 25267410 |
GRCz11 | 3 | 25397958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTCCCCACACCAAACCAACCCCAGACCCCACAGACGCCCGCTTCTCCA[C/T]GACCACAGCAGGGTCAGGTCAAACTCACTCTGGCCCAGCTCACACAGCTC
Long Flanking Sequence:
TGCTTTGTGTGTTCCAGTTGTAATAATTAATGTAATGGTTTATGCTCAGGTCCTGACAACTGGAACCACCCTACGGCCAGGGATGACTGTAATACGTTCCCCCTTGCAGCAGGCCACCACTCTGGGGAAGACTATCATTCGCACACCCCTGATGGTTCAGCAAGGTATTTAATTAATCCTAAATAGGATTAATTATTAGTTTTTTACTTATTATTTATTAGGATAGGAGAAAACATGACATGATAGGACCTCGTTCGAAATAGTGGTCATTATACAGAAATATTTTGTATACAAATATCCACACGGAATATCCACAATGTGTTTTAGGCAACGCTTTTGAATGCATCACAGTTTTCTGACTCTGTAATTGTCAATGATTATACCACACAGGCCAAACACAGCAGCAGGTGCAGACAAGTTCAGGCACTCAGGTGGTGGGCACTCCTCCTCGCCTCCCCACACCAAACCAACCCCAGACCCCACAGACGCCCGCTTCTCCA[C/T]GACCACAGCAGGGTCAGGTCAAACTCACTCTGGCCCAGCTCACACAGCTCACCCAGGGGGCTCAGGTATGTACAGTTGTTAAGCTTATTGTGGCAAATTCATCTGTGCACTTCATAGAGCTCTGCAGTGGTGGCATATTTTAAAAGGTCTACCTGGATATTAACATCACCCTGGTTTCCTTGACAAAACTCATATCTCAATGGCTTTTAGATTATTGAATAAATAAGCTTTCTTGGCATATAAAAATGCAAAAGTGTATTGGACGTTTTGTCCATCATGATAGTCTTTATAGATGAACACAACTTAGCTGTTAATAGCTGACAGCGAATAGTTCTGATATCACATTTTGTGCTTATTAAAAAAAAAAAAAGTTTAGTTTGTTTTAGTTGGCTTGGAAAAACTTACCAGAAAGTTTGAAGATGTTTTTAAAAACTTACATATAACATGTATATAAATTTTTATATTTAACATGTATAATATTTTTATTGTCCGGTCAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20010
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 |
---|---|---|---|---|---|
ENSDART00000109601 | Essential Splice Site | 2478 | 2725 | 30 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 25491976)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 25260161 |
GRCz11 | 3 | 25390709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGAAGAAAAGAGCTCTGCTGGATAAGGAACTGCAGCTGCAAGTGCAG[G/A]TAAGCAACAGCAAAAGACCAAACTTTCTCTGATTTACACTGATCTGAGAT
Long Flanking Sequence:
GAAGCAGAATGTGGCTATAGAGCAGTTAAAGCAGAAGAAAACCATGACTCCTGCTGAAAGAGAGGAGAACCAGAGGTAAAGACTTTCTTTCATCTATCTTTTTCTCATTTGTTCCTATTCAAGTAACTTTTTGTTCCAGAAATTATATTGATTTTTAAATCCCAACTAACAAAGCATTATTCGATCCACAGATAAACTGTATTTACTGAGCTCTTACTTAAGAATAGACTGAATTTAATGAGCCAGATCCATTGTCTTTTGTCTGTTCGGGCAGGATGATTGTCTGTAACCAGGTGATGAAGTTCATCCTGGATAAAATCGATAAGGATGAGAGGCAGGCGGCCAAAAAGAGGAAGCGGGAGGAGTCTGTGGAGCAGAAGCGCAGCAAACAGAACGCCAGCAAACTGTCGGCTCTACTCTTCAAACACAAAGAGCAGCTCAAAGCTGATATCCTGAAGAAAAGAGCTCTGCTGGATAAGGAACTGCAGCTGCAAGTGCAG[G/A]TAAGCAACAGCAAAAGACCAAACTTTCTCTGATTTACACTGATCTGAGATGCTTTTTCGTTCAGGATGTGTGTTTGAACTGTTAAGCTTTTTTTTTCTTTCTTTTTACAAATTCTAAGACCAACTCACTCCTGTCTGTTTCCTGTTCTGTTTTCTTTTGATACTTATATAAAAATTACTTTCATCTTCTAACATTATTAAATAGGGCTGGGCGTTTTGGCCTAAAAAAAAATCTAATTGAATCTAATCTTTAATTGAACATTTTAACTCTATTATGATTCATGAACGATTATTTTATTTATTTATTTTATGTTTTTAGTTCACTGAAAAGTTTTGTACAGTTTTGTATATGCTCACATATTACAAGTGAGAAGGGGGGATACTTGATTTTAATTGAAGGAATCGAGGGAAACACACACTATCTACTATCTATGATTATTTACTGAACATCAGCGTTGAACAACTGAAATTAAAACACACACTGCCTGAAACCAACAGTCA
Associated Phenotype:
Not determined