ZMP
si:dkey-22o22.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
FAT4
Human Description:
FAT tumor suppressor homolog 4 (Drosophila) [Source:HGNC Symbol;Acc:23109]
Mouse Orthologue:
Fat4
Mouse Description:
FAT tumor suppressor homolog 4 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:3045256]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36223 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16390 | Nonsense | Available for shipment | Available now |
sa36222 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15888 | Nonsense | Available for shipment | Available now |
sa16692 | Nonsense | Available for shipment | Available now |
sa13663 | Nonsense | Available for shipment | Available now |
sa22920 | Nonsense | Available for shipment | Available now |
sa42791 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36223
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 |
---|---|---|---|---|---|
ENSDART00000111951 | Nonsense | 347 | 2780 | 3 | 33 |
ENSDART00000146565 | Nonsense | 117 | 2395 | 2 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 43377743)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 40762136 |
GRCz11 | 16 | 40712168 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAGGGCAGGAGGGGTACACACGCCTCTCTCTTCATTCTGGCCGGCTTT[C/T]GACCCCCTCAGTTCACCAACACCACCTACACCATCCACATCCCAGAGAGC
Long Flanking Sequence:
ATTTAATTAAGAAAGCATATATATAAGTATACTTCATAATACAGTTACATAAATCTGTGCTGTAATATTTAAATATTTTTTATTTCATTTATGTTAATTAATTCAATGTATTTAATTTTTAAAATATTTATTTTATATTTAATTAGTTCTTTCATTCATTCGTTTTCTTTTGGCTTAATCCCTTTATTAATCTGGGGTTGCCACAGCGGAATGAACCGCCAACTTATCCAGCATGTTTTACTCAGCAGATGCCCTTCCAGCTGCAACTCTGCAACCTTAATATTTAATTTCATCTTAATTGTATTTCAAGCAATATTAAATGACTGTATTTTTTTGTCACAGGTGGAGAAGATTCATTTGAAGTGGACCAAACAACAGGAGAAGTGAAAACCACAGGTCGCCCTCTGACCCCGAGTAAGGAATACACACTGACCGTCCAGGCCGTGGACTCTCAGGGCAGGAGGGGTACACACGCCTCTCTCTTCATTCTGGCCGGCTTT[C/T]GACCCCCTCAGTTCACCAACACCACCTACACCATCCACATCCCAGAGAGCAGCGCGGTGGGCCAAGCGTGAGTACAGCAAACTGTGTGTCAGTGGGTGTATTGCTGTGCATCTGTGTGTAAGAAGATTCACAATTTGCTGCTCATTAGAGGGTAAGAGAAGGATTGTGTGAACGTGGCCAACTCCAAAGCTTTATGTGTCATCTGTTGCATGAAACAATTGGCCCGCAGGGAGAGCGGAGGTTGAGAGAGGGGGGGACGGACTCAATAGAAGAGAGGGTTGTGGCAGAGACGGGGAACACAGATGCATCATTTTGTCCCCAGGCTCTGAATTTGAAAGCGTGCTCAAATTCAAATATTTATTAAAAGAAACTTCTGGATAAACATGAAGAGCAGTGTCTGAACTCCCCCCTTCGGGCACTGGCACAGAACCGAGCATAATAATCTGTGTGAAGGAGGAGAGGACAGCTAATCATGGGAAGAGCGACGTATTAAAAGAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16390
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 |
---|---|---|---|---|---|
ENSDART00000111951 | Nonsense | 1037 | 2780 | 15 | 33 |
ENSDART00000146565 | Nonsense | 807 | 2395 | 14 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 43308955)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 40693348 |
GRCz11 | 16 | 40643380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AWTCTGAAGGACCAAAGCGGTGACTCGCAGTTCTTCAGCATTAATTCCTA[C/A]ACAGGCATCATCCACACGCGGGCCACCTTCGACCGTGAGCAGAAAGGCTC
Long Flanking Sequence:
AAAGTAATGAGAAAGAGGATAAATGCTGATCTGAAGAAAGAAGTCTAAAAAATATTGAATATCGTTAAAAAAAGAAGAAAAAAAAGAGGCTCATTTGCTTGCAGGTCTCATCTCTTGCAATTAAAGTATCCTTCTATTTGTATACATTTTTGAAACTTGTATTTACATGTACTGTAAACGCATGCTTGTTACTAATCTAATCTCCTCTTCATCTTTTTTTTTCTCCAGATGTGAATGACAATGTTCCCTTCTTCATGTCGTCCACGTATGAAGCAACAGTTCCAGAAGGGGCAGAAATTGGCACATCAGTCGCTCAGGTCTCAGCCACCGATCTAGACTCTGGTCTTCATGGCATGGTGAGCCTCGTTTCAGCTCTTTAACCCATGTCTGTTTGGCCTTTGCAACAAGGTCTTTTCGAAATCCTCTTTCTCTTCTCAGATTAACTACATCATTCTGAAGGACCAAAGCGGTGACTCGCAGTTCTTCAGCATTAATTCCTA[C/A]ACAGGCATCATCCACACGCGGGCCACCTTCGACCGTGAGCAGAAAGGCTCGTACTTGATCGAAGTCCAGTCTCAGGACAGCTCCGAATCTGCCCGACCCGGTCAGCAGGGCCAACCCAACACAGGTGTGATCAATCAAGCGTGTCTTCTTCATCCCTTGGTTTCCCCCTCCACCAATTAAAGACGGGCCACAGCAGCCTCCAGCATGAACTCCATTCATTAAGACTTCAATGAGTCATGCCTAATGAAGAACTAATGCCGTCCTAGGGATTTGTGTGTAATATAGGCCACGTTTAATACAATAAGTCCACAGTTGCAATATTAAACAGCCATTAAGATGTTTAATACATTTTATGGAATAAATCATTACAAGTTTTCACAAATAATAGTTTCTCATTAATGCTTTCTAAGAAGACTACAGTCTTGTAAATATGTTTTCATAACAGCGAAATAAGTTTGTTAAAAACTCTGCAGTCTGTAAGAGTTTTTTTAGAAGTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36222
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111951 | Nonsense | 1179 | 2780 | 17 | 33 |
ENSDART00000146565 | Nonsense | 949 | 2395 | 16 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 43300337)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 40684730 |
GRCz11 | 16 | 40634762 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAGGTGCAGCGCTACGAGTTACGGCTGGTTGCGTCGGATGGAAAGTG[G/A]GAAAACCAAACAATGGTCGTCATTAATGTCATCAACCAGAATGATGAGGC
Long Flanking Sequence:
AATGATTGATTAAAATAAGATACATTTTCAATTTCAAATCAAAACTATCACATTTAAAAAGTCAAATAGGATTCGTTTAATTATGATTTGATCAAGTATCATCTGTGTGTTATGTTGAAAATGATGCACAGTTTGTTTGTGACATACTGTATTGTGTTCATATGTATGTTGATTTCCGTATTTAAGCACAATCATATCATGCCTGTGTGCATTAGAGCCGCCTTGTCCTTTATGTAATCCTCATCAAATGAGCACAGATTAATGCTGACATTCTCTTTTTCATCCAGCTCAGCCAAGCTTAACACTTCCTAGTATGCTAACACTTCCCAAACCCCCCAAACAGGTGCCAATGCCAAACTGCGGTACCAGATTACCTCTGGGAACACAATGGGCACGTTCGATGTGGAGCCAGAGGTTGGCACGATATTCATTGCCCAGCGGCTAGACTATGAGCAGGTGCAGCGCTACGAGTTACGGCTGGTTGCGTCGGATGGAAAGTG[G/A]GAAAACCAAACAATGGTCGTCATTAATGTCATCAACCAGAATGATGAGGCACCCCTTTTCACTCAGACTGAGTACCATGCCAGCGTCATGGAGGAACTTACAGAGCTTCCAGTTCTTGTGCTAGAGGTGAGAGGTCAAAGCAGACATCAAACAATTGCAGTAATGTTGTCGATGCAACTTGTTGCAGTTTCATATTGGGATTTCCTGAAGTGATGTACAATATTTATTAATGTGCTCATGTAGTTTAAAGCTTAGAAAGAAAAGAGGAAGCCTATTTGAATCAATATTTTGGCACACCCTTCCACGGTTTTAATTCTACTCTAGTGTGTCTCAATATTGCTGTCTATTGTTTTGTCAGTGTAAAAATAGACTTCAAAGGTTTCAAATAAACATACCGGAAAAGAGGCGGAGAGAACCATCAGCATTTCTTTGCTGCGTCTATTAACTTTTAATTGCCTCATGTGTTCCGTGACTAGTGTGTTGAATTCTAATATGCATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15888
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 |
---|---|---|---|---|---|
ENSDART00000111951 | Nonsense | 1784 | 2780 | 19 | 33 |
ENSDART00000146565 | Nonsense | 1554 | 2395 | 18 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 43295399)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 40679792 |
GRCz11 | 16 | 40629824 |
KASP Assay ID:
2261-0165.1 (used for ordering genotyping assays)
KASP Sequence:
CTTGGACAGGTTCAATCCCCTGACCTTGATGACTGGAGCGAGAAGGTTTA[C/A]AAGTTCGAAGGCAAACCCCCCAGGTGCTTTGATCTTCTATTGAAGTTTGA
Long Flanking Sequence:
AGCTTTAACCACTCTCAATATATATTTTTAGCATTTTCCTCTTGCATTAGCCCTCTCATGCATTAGCCTTCTAATAAGAATTTGTCATGTAGCTCAAACATGGCATGATGCTAACAATTTGCTTAAATCCCAGGTTTAAGAAGCACATAAACACGAGGCATTTTAAAGGATGTTGATTTCATGACTAACAGGATTACAGCATTTCGTTTTGCCTTTTGGAGAAATGGCAATGTTGCATGCTAATAGCATTGCATCCCCCCCACTGTGCTGTTTAAGTGGGTCCATATGTGCCAATGAGATGCTCTGCTTTTTGCTTATCTCCTTAAAGATACCTCTCCTCCACCCTCCCACACAGGCACGCATCGCCCCAGGTATCGCACAGCCTGGATGGAGGTAGCTTTTCTCTAACCTCATTATGTATTTTCCCCAGGTACACTCCCCACGACGGTACTTGGACAGGTTCAATCCCCTGACCTTGATGACTGGAGCGAGAAGGTTTA[C/A]AAGTTCGAAGGCAAACCCCCCAGGTGCTTTGATCTTCTATTGAAGTTTGATTCAAACTCTGCTGTGTGTCAAGTGACACCTACAAGGGAAGAAAAAAAAGAACAAAAGCGAGGGGAAGATAAAGGATGAGACCGTGCATATTAGCTCACTGACATCTCGCCTGTCACTCTTCTTTTTAATTTCAAAATTTGCTCTGAAGTGATACATGAATTCTCACCTAGTAACCCATAAGAAAGATTACATTGGCTAGAGGTGCTCTCTAAAGAGCTGCATCTAAGTGATGGTCTTTGTCCAAACCAGATTCTGTGGCTCATGCCAGCGCTAGCACCTTCAAGCAAAGCGATTATGCTAGCACTCCAGCAACCAGTGCCAACTCAATCAGTTTAGTCTTGAGTTCAATCACACTCTATTTCAAGTTCCATCTAAAGCTGTGCCCGACGGTGTGTTATGCAGGATCCGCTCTCATTAATTTGGATAATTAACACATTAATACATTAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16692
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 |
---|---|---|---|---|---|
ENSDART00000111951 | Nonsense | 2051 | 2780 | 23 | 33 |
ENSDART00000146565 | Nonsense | 1821 | 2395 | 22 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 43282571)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 40666964 |
GRCz11 | 16 | 40616996 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGAATGCCAGCAAACCAAACACAGCTTTCTTGGCAACGGCTATGCTTG[G/A]TTCCATCCCATAMARCCGTGCTTCCAGAGCCACATCTCTCTGGAGTTCAT
Long Flanking Sequence:
GGTGATCATAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATCATATGCTCTGATTTTTAATCAAACCAGATTTCTACTAGCCATTACAGCTACACATCTTCTATAAAAGTTCACTGATGCAGGGTTTAGATAACCTTTCACTAAGTGGTTACAGGTTTTCAACATTTTTTTAAAGTAACATTTTTTTTTGCATTCAACAGCACAAAAAATAAACTCAAATTTATATGAAACATGTAAGGGGTGAGTAAATGATGGCAGAATTTTGGATGAACTATCCCTTTAAGTTATGACTGATCTTCTGCTCTGTCACAGGTGTAAATGTCCCCCAATGTTTGATGGGCCAGAATGCCAGCAAACCAAACACAGCTTTCTTGGCAACGGCTATGCTTG[G/A]TTCCATCCCATAAAGCCGTGCTTCCAGAGCCACATCTCTCTGGAGTTCATCACGGAGGCAGCCAATGGCCTGTTGTTCTACAACGGCCCAATGGGAGCACCTCAGCCCAGAGAAAAAGAGGACTTTATTGCCCTGGGTATGAATCATCATATTTACATGTTTTTGTGCATTCAAAATGAGCAGCTGCATATATATTACACATATCACATATAAACAAGCACAATGTAAAGTCACTTTAGAATACACTGTGTTATTGTAGTATTATTTATATAGTGTTATCTTTTTTTGTTTGTATCTTGAATGAGCATTTATTTTTCTGTTTTCAGTTTACATTATTTTACATTTATTTTTATGAAACATTTGGTTTTATTTGTTTTTAAGGGGGTGTAAGTAAATTATATGTTTAAATATATAATTTTTAAAGATATAAATATATATATATATATATATATATATATATTTATAAAGACTAGTACATGACAATTTTTTTGTATATACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13663
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 |
---|---|---|---|---|---|
ENSDART00000111951 | Nonsense | 2076 | 2780 | 23 | 33 |
ENSDART00000146565 | Nonsense | 1846 | 2395 | 22 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 43282497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 40666890 |
GRCz11 | 16 | 40616922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGAGCCACATCTCTCTGGAGTTCATCACGGAGGCAGCCAATGGCCTGY[T/A]GTTCTACAACGGCCCAATGGGAGCACCTCAGCCCAGAGAAAAAGAGGACT
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATCATATGCTCTGATTTTTAATCAAACCAGATTTCTACTAGCCATTACAGCTACACATCTTCTATAAAAGTTCACTGATGCAGGGTTTAGATAACCTTTCACTAAGTGGTTACAGGTTTTCAACATTTTTTTAAAGTAACATTTTTTTTTGCATTCAACAGCACAAAAAATAAACTCAAATTTATATGAAACATGTAAGGGGTGAGTAAATGATGGCAGAATTTTGGATGAACTATCCCTTTAAGTTATGACTGATCTTCTGCTCTGTCACAGGTGTAAATGTCCCCCAATGTTTGATGGGCCAGAATGCCAGCAAACCAAACACAGCTTTCTTGGCAACGGCTATGCTTGGTTCCATCCCATAAAGCCGTGCTTCCAGAGCCACATCTCTCTGGAGTTCATCACGGAGGCAGCCAATGGCCTGT[T/A]GTTCTACAACGGCCCAATGGGAGCACCTCAGCCCAGAGAAAAAGAGGACTTTATTGCCCTGGGTATGAATCATCATATTTACATGTTTTTGTGCATTCAAAATGAGCAGCTGCATATATATTACACATATCACATATAAACAAGCACAATGTAAAGTCACTTTAGAATACACTGTGTTATTGTAGTATTATTTATATAGTGTTATCTTTTTTTGTTTGTATCTTGAATGAGCATTTATTTTTCTGTTTTCAGTTTACATTATTTTACATTTATTTTTATGAAACATTTGGTTTTATTTGTTTTTAAGGGGGTGTAAGTAAATTATATGTTTAAATATATAATTTTTAAAGATATAAATATATATATATATATATATATATATATATTTATAAAGACTAGTACATGACAATTTTTTTGTATATACATTCACCGGCCACTTTGTTAGGTACACCAGTCCAACTGCACAATACCGTAAATTTCTAATCAGCCAATCACATGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22920
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 |
---|---|---|---|---|---|
ENSDART00000111951 | Nonsense | 2393 | 2780 | 29 | 33 |
ENSDART00000146565 | Nonsense | 2163 | 2395 | 28 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 43272316)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 40656709 |
GRCz11 | 16 | 40606741 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGGCATGACAACATCTTCATCCTGCGACTGGAGCAGGGCGGAGGCTCA[C/T]GAGAGGTGACAGGGGTCCTGGGACAGAAGAAGGAAATTGTAGTTCACCCC
Long Flanking Sequence:
AGAAATTTTCAAATGCATAATTGCATACATGCATAATTTGAAGCTCCTAGTGCACTTTGAAGGAAATGTCACTCCCAGGGGCGGGGTTTATGTAAATTTAAGGGTTAACTTGGTAAACCAAGGGTAAACTTGGTGATGTCACAAACCCAAGGAAAAGGCCAAGGAAAAGCTTGTTGTAGGCCTTAAAATGCAAATTCTGTTAAATAAAAGATCTCACTTTGCATTACACCTTAAATCCCGTAACTTTTCATTAAAGTTTATGTTCAGAAATCATTCAAAACTAATTTTAATAAAATGTTGAATCCCATTTAAAGCTAACACTGTGCACTGTACTTTTTCAGATAGTGGATGGGTACCTCAATGTTCGTGCTAACCTTGGTGACGGCACTCACTCGCTAAAACTAACAGGCCAGCGTGTAAACCATGGCCAGTGGGTGCTGATCAGCATTCTCCGGCATGACAACATCTTCATCCTGCGACTGGAGCAGGGCGGAGGCTCA[C/T]GAGAGGTGACAGGGGTCCTGGGACAGAAGAAGGAAATTGTAGTTCACCCCTCCAGTGTGTTTCTGGGAAACAGCGCCAGCCCAAACACACAGGGAGACTTTCAGGGTGAGTTTACTCATCACTTTCTTCCTCACTCCTGGGATTTTTATCTTAAACTAATTTGTTTGTTTTCGGTAATGATGATAGCGCGAGAAATAATTGATTAGCCATCAAATTATCATCACATAATGAAATAGATTGAGGTGATTTGTTCTCTAGATTGTTTTCTAATAATTCAGCAGACTTATACTATGGTTTCCACACCCACAGACATTATTTAGGTCTTCTATTTCAGGACATTTGTTGTGACTATTTTGGTGTAGATTTTTCTCCATCTCATTCAAACATTTAGATTTTAAGTTGTAGATTGTAACTGTGTTTTTCTCTGAAAATAATTGAACCATTCATTTCAGGTTTTCCAGTCTCTTCTAATGTTCAAATGAGTAGATTCAGGAGTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42791
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111951 | Essential Splice Site | 2626 | 2780 | 33 | 33 |
ENSDART00000146565 | None | None | 2395 | None | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 43260149)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 40644564 |
GRCz11 | 16 | 40594596 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTCAAACAGGAGCTCTTCTGATGCACTTTTCTGAATGTTAAACCCACA[G/T]AACGCGTATGACATCACTGAGCTGAAGAGGCCGCTGTGTTCCAGCTTGTC
Long Flanking Sequence:
TGCTAAACATCTGGAGCTGTCGGCGATTCAAATCATGCCGTGTGAATTGAGTTTTGACCAGGGTTTTGACTGAAAATAACATCAGCGATCGCCTACAGCCAATGAGAGAGCAGCTTTCACTTGCGTGTGAGTGTGTAAAGTCATGCAATGTGAAAGTCCCTGTCGCTGATACCTCTTGCAGTGTAAACAAAGCAGCGACGAAACGCTAGCCCAGATAGTCAAGCAGTGTGAAAACATCTGTGACACGACTACTTTGAAAATCATGCAGTCTGAACTCTGCATTAATCTAAGAATTAAAGGTGTATTTTCAGATTTCCAGTAAAGATTACAAGCGCTAACAATTATTGTTCTTCTTAATAACATGCACAGATGAATTGTTTACTACAAAGCTAGCAATGTGAGCTAACAAAATCAGTATGTTAGTTTTGATTTCATTTGTACTTTAAGATAAAGTCAAACAGGAGCTCTTCTGATGCACTTTTCTGAATGTTAAACCCACA[G/T]AACGCGTATGACATCACTGAGCTGAAGAGGCCGCTGTGTTCCAGCTTGTCCCAGTCCTCGTCCTGCACCACTGCGCCCCTCATCAAATCCTCCCAGGGTTCTCAGGAGGAGGTTCACCCCTGCGGAGCCATCCAGAACGCAGCCATGCTTCCGTACCAGCACCACAGTGGAGGCCACTGCTCTATGGACTTCAAGAGCTACGTGTCCCGCATCATCTGGGAGGCGGACAACGACAGCCTGTCATTCCCCATGGACACCTATCACGTGTACTGCATCGAAGGCTCAGGTTCCAACGCCGGCAGCCTCAGCTCTCTGGGCTCCTTCATCTCTGACGATGGCTTCAGCTACGACACGCTTCGCCGCTGGGGGTCCAAGTTCGAAGGCCTGAGCGAGCTTTACCGCCGACCCGAGCTGGACATCCCATACATGGACACAGTGCAGAGCCAGAGTCTGGAACAGCAACAATGAACACTTGAAGGTTTTGAATGTGTGTGTTTGTG
Associated Phenotype:
Not determined