ZMP
zgc:162756
Ensembl ID:
ZFIN ID:
Description:
translin-associated factor X-interacting protein 1 [Source:RefSeq peptide;Acc:NP_001093570]
Human Orthologue:
TSNAXIP1
Human Description:
translin-associated factor X interacting protein 1 [Source:HGNC Symbol;Acc:18586]
Mouse Orthologue:
Tsnaxip1
Mouse Description:
translin-associated factor X (Tsnax) interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1919486]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11452 | Nonsense | Available for shipment | Available now |
sa15477 | Nonsense | Available for shipment | Available now |
sa17810 | Essential Splice Site | Available for shipment | Available now |
sa17203 | Nonsense | Available for shipment | Available now |
sa36649 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36648 | Essential Splice Site | Available for shipment | Available now |
sa5909 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23300 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11452
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 |
---|---|---|---|---|---|
ENSDART00000043452 | Nonsense | 30 | 673 | 2 | 17 |
The following transcripts of ENSDARG00000030512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 21729982)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21960205 |
GRCz11 | 18 | 21949271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTAGGTCATCGTCTCAATTTGAGTCTAATGATGACAACAATAGAGRAT[T/A]ACAGCGACACATTGCAAACAAGATGTCTAGAGCAAAATTGATAAAAGTAA
Long Flanking Sequence:
ATTTATGTGATGACATTGAATGTAATTTGTGCTGCCTGTTTTTTTCTGTGATGTGTGTAATATGAACGCTGATGTGGTTGTGTGGTGAAGCCAAAGATAAATTTCCACTTGTGGACAATAAAGAAAGTAAACTTACTCATCTGTCAACCAAAAGCATTAAAGTAACGCCAATTATTTATAATGTAACATAAATAAGCAGGACGACTTATCATTTTTATACATTTAAATAAGTACAGGTGAGAAACAGAATAAGTTTATTTTTTTGCACAAATACGTTATCATGAATGAAAGTAGAACACCGTTTTAACTATATTTTATTTTATTTTCTTACGAAAGTTATTTGGAATAATAAAGTAGACATGAGACAAATTTTACCATCTATAAAAGCCATAGAAATTGTGTGTTATCGAAAGTCACAGCATCTCAAATACCCAAGTTGTCTGTCTTCTGTTCTAGGTCATCGTCTCAATTTGAGTCTAATGATGACAACAATAGAGGAT[T/A]ACAGCGACACATTGCAAACAAGATGTCTAGAGCAAAATTGATAAAAGTAAGTTATGAATTTGCAAGTTAAATTATCCCGGTTGTAATATATATACAGGGATGGGCAGTATTTAAGGTTCATGTATTTCAAATTAGTATTTTAAATACCAAATAGTATTTTATAACTTGTATTTTATTGGGTATATGAAAATGGGTTAATTTTCTTTATTAAAATACTTTAGTGTCTTGTATTTTTAAAATACTGTAAAATACTTTGTAAGAAGTATATGATCACATCATAAAAATGTGGCCTGGTCTTGAAATCAGAACAGAAAATTGATTAAGAAGGTGGTCAATGCTTGGAGTAGGGATGAAAATTATGCAACACACACAAAAAAAAAAACAAGAGACAAATGGCATTGTGTATATTTCAAAACAAGTCAACAATCATTAAAAATAGTATACTGCACAATGCCTAGACCAGTAATATATAATGGCAGTATAGTGTACATTTTGTCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15477
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 |
---|---|---|---|---|---|
ENSDART00000043452 | Nonsense | 84 | 673 | 4 | 17 |
The following transcripts of ENSDARG00000030512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 21727962)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21958185 |
GRCz11 | 18 | 21947251 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGTATCTWCATGTCCTGCAGGTCTCTTGCCAAGCCTCGTTTCTYAGAG[C/T]AACTGGAGTGTCTTCTCAAGAGAGAACTAGAAGYTTTAGACAACACACAS
Long Flanking Sequence:
ATTTCAATGTATTTTTGCCCATCCCTGATAACACGTTTACATATATGCCAAAAAACATATATGTATTCTACATTTATAACACATATACGTCCCATATATGTCAGAAACATATATGTTCACTTATATGCCATAAACATTTATGTCCCATATAGCTATTTACATTTACAAGCAAGATTAACAGGTGTACCTAATATATTGGCTGGTGAATGTATATTGTATTAATGCAAATCACTCCATTTCCAGCAGACCAAAGAGAAGGAAAAGAGTTATTTTTCATCTGAGCCTGCTGAAGTTACATTTCAAAAGCCCAGACAAATAAGAAATTATGGGTATGGCAAGAATTCCACATAGAGCATATGTGTTCATGTTAACAATAGTTTCATAATTTTACAATGTTTAGTCATATTCTTTTGTTTTCAGTCAGTTCTGAATATCAGTGCCTTGGTCCTGATGGTATCTTCATGTCCTGCAGGTCTCTTGCCAAGCCTCGTTTCTTAGAG[C/T]AACTGGAGTGTCTTCTCAAGAGAGAACTAGAAGTTTTAGACAACACACAGGACTCTAAAGTCCAAGAGCTCAGACTGCAGGTAAACTTCTTACATCAAACTGGTTTTCTTAACAAAACAACACAGTTCAAGGCTTTGGGGTGAAAGCAAATGTTCAGTGTCACATGATTCTTTAGAAATCATTCTTATACTGTATGCGGAATGATTGTTGTAGTTGAAAAATAAATATGGAAACAAAAATACATTGATTATTTTTCTCCCCAAGATTATGTGGTTCATAGTTAAAAGAACATTGTCTATTGAAATAACTAATTGTTAATTGAAGTTGAACATTTTAGAAGTTTGACTTTCATGTAAACTGCAAAAAATGCTTTTTTACTGAATTTTTTTACTTGTTTCCAGTACAAAATCTGTTTTTTTTTTAAACAAGCAATTACACTGTTTTGTTTTGTTTTAAGAATAAACATGTCAAAATGAAGTGAGATTTTTTTAAACAAGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17810
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 |
---|---|---|---|---|---|
ENSDART00000043452 | Essential Splice Site | 207 | 673 | None | 17 |
The following transcripts of ENSDARG00000030512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 21726175)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21956398 |
GRCz11 | 18 | 21945464 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCGTCATTGAAAGCATGAGGTCACAACAGAGTGCTCTGCAGATTCAGG[T/C]GGAGCTCAGTTTACTTTRAWTTATTTTACTCTGTNNNNNNNNTYTTCTGTAGAGATCT
Long Flanking Sequence:
GTCTTTGGCCATTTAATTGAAGAATTTAAAACCTATAAGCCTATTTTGTCTGCCATCAAAAAGGAGTATGACATCACATTAGGTATGTACATTCGGAATGTTCAATCAAATATTTGAGTAAGCAGGCTATCTCCATTTCCATTGGTATTATTATTTTAAAATCAATTTAACAAAAAGAAATAGTTTCACAAAATGTTGCAGCAAAATAAAGAAATCTAATTCCACAAATAAATAAAATACCAATGAAACTCAGTTAACTATTTCATTTTAGACACTAATCGAAGTGCTAATGTCTCTCTCAGCACATCTGCGAGATCAGATCAGGGATCTGCTACCGCTACGGCCGAAGCTGGTGCTCGTGTCAGAACAATGTGACAAGAAGATTCTGGAAATGAGAGTACAGGAAAGAGAGGAGGTTCGAGCTCTGAAGCAAGAGTGCAGGCATCTGCAGAGCGTCATTGAAAGCATGAGGTCACAACAGAGTGCTCTGCAGATTCAGG[T/C]GGAGCTCAGTTTACTTTAAATTATTTTACTCTGTTCTTCTGTAGAGATCTGGTTACTTTGGATTATTCAGATTTAGATGCCTGCTTTGAATTTGTGTGGTTAATCAGATGTTTGGCTTTAATTAGGTAATTTTGTGATGGATAGTTGATGTTTTTCTTTTAAATACTTTTTGTTTTCAGATTTAGTAACTTTATAAATTCAATTTACAGGGTTAGGTCACCCCAAATAATTATATAATTTATAATAATAATTATTATATTATATTGTCATATTGTTCCAAACAGATGTCTGTCCCGCCATTGAAAGTCTTTTCACCGACACTGCAAAAAAAAAATATTTACTTAGAGTTGTTTTCTTATTTATAGTCCAAATATTTAAAAGTTTCTAAGTCAAGAAGCTCTACACCAGTAAACATATTTTATTGTTTTCAGAAATAATGTCAAGCTAAATAATTTTTGCAACATTTTTCTTAGCCCATTGGCTCATTATTTTTCTTGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17203
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 |
---|---|---|---|---|---|
ENSDART00000043452 | Nonsense | 229 | 673 | 7 | 17 |
The following transcripts of ENSDARG00000030512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 21725123)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21955346 |
GRCz11 | 18 | 21944412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGASGAWCTAGCCACCCAGTATCAGCTCTACAGGGACGAACGTGATGCA[C/T]GAAAGCTGCTCATCACYAGAATMAGCAYAATGCAATCTACCCAAGATGCM
Long Flanking Sequence:
AAGACAATATTTTTTTAACTTGTCAAGAAAATGCTTCTTGATTTAAGATTTTATTTGTACTAGAATTTGGATTACGAGACAAAAAAACTAAGTATGAAATGTTTTTTATTTACATTGTAAAACTCAAAACTGATGCTTCAAATATTCATAAAGATAATTTAAGCCAAAATGAAATCTGCTCATCATACAAAGCAAAGACTTGAATTAAACTGCTTAATGTCTTTACAAATGCTCTGAACAAATTCCATATGGGTTTGGAGCAACATTATGGTAAGTAAATGAAGAATTTTTAAATTTGGGAAGAAATAACTCTTTAACCTTAATTTTTTTTTTAATCCAATACTTATTTTATAATATTCACAGTGCTGCTGCTTTATTAAAGCAAACAGAAGACATGATAAAACACTACATCATGATTATCTCATCTCTCCCCAAAGGTTGATCATCTAAAAGAGGATCTAGCCACCCAGTATCAGCTCTACAGGGACGAACGTGATGCA[C/T]GAAAGCTGCTCATCACCAGAATCAGCACAATGCAATCTACCCAAGATGCCGAACATGATGATAATAATGAAGGTTACGTTAATAGTGGAGTCTGAAAAAAAACAATAAACATGAAAACAAAATACTATTTGAATTTATGTATCAATATAAGGACTTGAGCAGAGGTGTGACGGTAGGCAAAGTTTTACATGTTATGCCATATTTTCTACATTTATAGATAAGTTTATTATTTTTATATATTTATAGCTTAATTTTTTTGATACATTTACAGTTAACAATTACATTTATTCATTTAGCAGACTCTTTTATCCAAAGGGACTTGCATGCAAGTAGAAAAGAAGCTATATATAAATGCTTTCACATGTCTAAGTTATTAGCTAGACTAGTTAGTAGCTCTAGCTTGACTCCCGTCTTGCACCCCTAAACTTCTATAAATGATCCAGAACACTGCAGCTCATCTGGACTTCAATGAGCCCAAGAGAGCATCGCATAGGTGAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36649
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 |
---|---|---|---|---|---|
ENSDART00000043452 | Nonsense | 269 | 673 | 8 | 17 |
The following transcripts of ENSDARG00000030512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 21723938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21954161 |
GRCz11 | 18 | 21943227 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGATGAGTCTGAGGATCCTGTGGTGGTGAAAATGGCTTTACAGGTGTG[T/A]CGAGAAGATCTTACCAAAGCCCAGATTGAACTCAACCGCCTTCAAGCTGA
Long Flanking Sequence:
AACTTACTCTAACACCTAATTCTCTGATCACTAACAGTTCTTTTTTATAATTAGCACTTCTTGTGTGTATTGCCTCTTCTTGTTAAATTGCTGAATGCCTTCTCAATTGGAAGTCACTTTGGACAAAAGTGTCTGCTAAATGTAAATGTACTTACAATATTAACAGTGACTGGCATACTGTACAAAAAGTGGAATAAAAGCCAGCTTTTCCTGATCTGATTCTGCCAATGGGCGTGAAGTCAGATTACTAGATTATATTGAATATTAGCTATGCTGGAGTTTCTGTAGAGGTAGCAGGTAGTCAAGATGAAAGCACATTACAACCTGTACTTGAAGCTAGAGTAGCTTGTCTGGTAAGACTTGAGAGTGTTTTATTGGAATGTTTGTGTTAATGAGGTTGAAGATTTAGTAGTGAGGAGCAGGAGTTTTGACAGAAACTTGTTCTTCTCAGAGGATGAGTCTGAGGATCCTGTGGTGGTGAAAATGGCTTTACAGGTGTG[T/A]CGAGAAGATCTTACCAAAGCCCAGATTGAACTCAACCGCCTTCAAGCTGAATACAGTGATGTGGTCCCTCGACGAGATTGGGACAACTTGAATCACTTGCATGAGGAGACGCTAATGAAGGTATGGGAACAATTGATATGAAACATATTATAGAAATGTACACTTATTGGCAACGTTCTTGGTACATCTTCCTTATGCCAAATTGGACCCCTTTTGCTTTCAGAACTGAATGGCATAGGTCCTGAAAGGGCTTTAATCATTCCTTATAGGTCATGTGAAATTCAAATATTTTTTATATGTCAGAATCACATGTTATCCCCACGTTCGTGTGGGTGCTCCGGTTTCCCCACAAGTCTAAAGACATGTGATACAGGTGAATTGGATGAACTGAATTGTCCGTAGTGTGTGTGTGTGTGTGTGAATGGATGTTTCCCAGTGATGGGTTGTGGCTGGAAGGGTATCTGCTGCGTGAAAATGTGCTGTATAAGTTGGCGGTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36648
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 |
---|---|---|---|---|---|
ENSDART00000043452 | Essential Splice Site | 442 | 673 | 12 | 17 |
The following transcripts of ENSDARG00000030512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 21721757)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21951980 |
GRCz11 | 18 | 21941046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAGGTAATAAAAGAAATATGGAGAAACAAAATGGCGGATAATGAAAAG[G/A]TATGGTATACGAATGTTCTTTCTTAATTTGATTTATCGTTCGATAGATAT
Long Flanking Sequence:
TCAGATAGCCAACACATTGCCACAACTCCCAGGCCAAACTGGGAACAGTGTTCAGGTATCAATTTCTGAACTTACCATACAGATTTTCTGTAGTCATAAGCCAGATGTTGCCTTCTTTATATAGCACATCTGAGCATATGTTCAAGATGGTAATTATGCAATATGGGCTATAGATATACTCGGAGGGACTGAGCGATGTAAAGAGCTTTTTGAAGGTCAGTCCAGCCAAAAGAGGCTGGAGATCTTGATGAAGGAGATTAATAGCCAAAATCAGTTCTTCACTGGACTTGTAAGTGTTTTTAACCTCACATATTTAGCATTGGAGACAATTGTACCATCTTTGCTTGGTTTAATTAAAGTTGTTTTGACAGGGAACATCCAGTGACGTGCCCATTTATCTGCGATATGAGGGGAAACTTAAAAATCTTAAGCTCAAGAAAGCAGATGTTATTAAGGTAATAAAAGAAATATGGAGAAACAAAATGGCGGATAATGAAAAG[G/A]TATGGTATACGAATGTTCTTTCTTAATTTGATTTATCGTTCGATAGATATGAGTGTTTGATTCTCCACACATTTCTCTTCATCAAAGAATGATGACCCCAGAGATCTGCAGACGTTTCTTCACAGCTATCTTGTGGAACAGTATAAAGATAAAGCAGGAGAATGGGCTTACAGCCTCATGGAAAGCGTACAAAACAATCTCAAAGATGATCTCATTTGCCTTTTCAATGATGTCTTGACTGGAAAGGTTTGTACTTAAGCTAAATAATTTCTTCCAAGTGTTCTTAATATCAAAAACATGTAGCATGCCTCCAAATGTTTATTTGGATAGTTATACATTAAAATTAGTGCTGGGCAAAGATTAACAGTGATTAATCGCATCCAATTTTTTTTTGACATAATTATAGTGTATATGGGATTCACACATACATAGAAACAAAACTATACAAAACAAATTTGTTAAATAGATATTTAAATTTATATATAATTTGTATCATATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5909
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043452 | Nonsense | 470 | 673 | 13 | 17 |
The following transcripts of ENSDARG00000030512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 21721586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21951809 |
GRCz11 | 18 | 21940875 |
KASP Assay ID:
554-3646.1 (used for ordering genotyping assays)
KASP Sequence:
CACAGCTATCTTGTGGAACAGTATAAAGATAAAGCAGGAGAATGGGCTTA[C/A]AGCCTCATGGAAAGCGTACAAAACAATCTCAAAGATGATCTCATTTGCCT
Long Flanking Sequence:
AGATATACTCGGAGGGACTGAGCGATGTAAAGAGCTTTTTGAAGGTCAGTCCAGCCAAAAGAGGCTGGAGATCTTGATGAAGGAGATTAATAGCCAAAATCAGTTCTTCACTGGACTTGTAAGTGTTTTTAACCTCACATATTTAGCATTGGAGACAATTGTACCATCTTTGCTTGGTTTAATTAAAGTTGTTTTGACAGGGAACATCCAGTGACGTGCCCATTTATCTGCGATATGAGGGGAAACTTAAAAATCTTAAGCTCAAGAAAGCAGATGTTATTAAGGTAATAAAAGAAATATGGAGAAACAAAATGGCGGATAATGAAAAGGTATGGTATACGAATGTTCTTTCTTAATTTGATTTATCGTTCGATAGATATGAGTGTTTGATTCTCCACACATTTCTCTTCATCAAAGAATGATGACCCCAGAGATCTGCAGACGTTTCTTCACAGCTATCTTGTGGAACAGTATAAAGATAAAGCAGGAGAATGGGCTTA[C/A]AGCCTCATGGAAAGCGTACAAAACAATCTCAAAGATGATCTCATTTGCCTTTTCAATGATGTCTTGACTGGAAAGGTTTGTACTTAAGCTAAATAATTTCTTCCAAGTGTTCTTAATATCAAAAACATGTAGCATGCCTCCAAATGTTTATTTGGATAGTTATACATTAAAATTAGTGCTGGGCAAAGATTAACAGTGATTAATCGCATCCAATTTTTTTTTGACATAATTATAGTGTATATGGGATTCACACATACATAGAAACAAAACTATACAAAACAAATTTGTTAAATAGATATTTAAATTTATATATAATTTGTATCATATACATTTAAATGTTATCACTAAATTTAAAAATTTTCACAAATATTTCCATGCGGGCGAAGCAGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTGGTTCGAGCCTAGGCTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCTTGCGTTTGCGTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23300
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 |
---|---|---|---|---|---|
ENSDART00000043452 | Essential Splice Site | 573 | 673 | 15 | 17 |
The following transcripts of ENSDARG00000030512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 21716632)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21946855 |
GRCz11 | 18 | 21935921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGGAGAGCAGTGGAGTGCGCATTTCTTATCAGACACTTTATACAGAG[G/A]TCAGTTCCAAAGTTTTCGCTAAGAATATGTAATTCTTTGATTGTAAAAAG
Long Flanking Sequence:
TTATTTACATGGCGTCTACACTCAAAAGATGATTCACGAGCACACGAAATGGCACTTAATAAAAACCAATCCGGCGCTTTCAGTAGTGAGTGAATTCTGTGAATCTAGAGAAATGACAGATCAATATCCGTGAACCTGATTTAGAATCTGTAATTGTGTTGACTGTAATGTTGTGGCAGGTTGATGAGAGTATCTACCATGGACAGACACAGCTGCTGTCTCACTTGCTTAAGGTTTTAATTCAAAGTGACATAACGCAATGCGGATCACTGACTGTCTCAGAATTTAGGTGAGGATAAAAAAAGTCACATTTTCTTATCAGTAAATGTATGATTGTCATTTTATTTTTTCACTATATATGTGTGGTGGTTTTCAGCGAGGCATTGAGGAAGGCTTTCCCTCTGAAGTCGGATCAGGACATTGAGGAGCTGTTGGCGGCGGCTCAGACAGAGCTGGAGAGCAGTGGAGTGCGCATTTCTTATCAGACACTTTATACAGAG[G/A]TCAGTTCCAAAGTTTTCGCTAAGAATATGTAATTCTTTGATTGTAAAAAGGAGTAGATTTTGTGGCTTTAAGCTCATCATGATAGGGATTGGTGTGACCAAAATATCATGCAAATATTAGGTACTGCATGGATTGTCATGTGTTTGAATTTTTAAAAATATTTATAATCTACAAATGTCGGAAATAATAAGATACAACTTCAAAGTAATTATTAGTTCTCTTGATTTGCCATTTAACAGTCACATATTTTGGTTATTTGTTTTGTTTATTTTATAAACTGCTGATAATGTATAATATTTTTTGTCAAATAAGTTTTATTTTAGACACAGATTCAGAAAGAAAATAATTCTCTGTTTTACATATTTTGTCCATATATAACAATGGCAGAGCAAAGAAAAAGAAAGAAAAGGAAAGAAAAGGAAAAACAATAGGAAAATCAAAATAATAAATAAAAAACCCACCCACATAAAAAGCCAACTTGTTTACAAAGACCTGTTTGA
Associated Phenotype:
Not determined