ZMP
si:ch211-101b18.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
ULK4
Human Description:
unc-51-like kinase 4 (C. elegans) [Source:HGNC Symbol;Acc:15784]
Mouse Orthologue:
Ulk4
Mouse Description:
unc-51-like kinase 4 (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:1921622]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36032 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36033 | Essential Splice Site, Missense | Available for shipment | Available now |
sa17493 | Nonsense | Available for shipment | Available now |
sa22745 | Nonsense | Available for shipment | Available now |
sa6405 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
sa36034 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa792 | Essential Splice Site, Splice Site, Nonsense | Available for shipment | Available now |
sa16618 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36032
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 |
---|---|---|---|---|---|
ENSDART00000060519 | Essential Splice Site | 128 | 1048 | 4 | 32 |
ENSDART00000143540 | Essential Splice Site | 127 | 753 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 16 (position 7162671)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6007202 |
GRCz11 | 16 | 5906828 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTTTTTTTATTGTCAGAACTTAGCAATGTGTCACTTTGTGTTTCTGCA[G/T]ATTTTATTGGATGGACCGGGAACTCTTAAGTACTCCAATTTCTGCCTGGC
Long Flanking Sequence:
TTGGAGCAAAATGAATGATTCCTCTGTCCAAACATCTTTTTTTTATTTTATTTTTTTTAAGATAAACGGTGTTTATTATAATGATTTATCCATAAACATAGCTTTTTCAAACGAAGGTGCTTTTGTTCTTTTTATTCAAGATATACTTTAAAATGTCTTGCAACCGGTCACTTACATGAAATCATATGGTTAGCAAGCATCAATGATCTTTTGATATCCATGCAGCTTCTGTCTCAAACTGATCTATTATTTTCAGGATGATTCACAAAATTTTCAAGATACGACTTTTTATGACGTTTTCTTTACTTCATCAATACCATTTAGAATTCAACAGTTTCTGAATTAATCATATCAAAAGGAATATTATTTATCAAATCGCTTTAATCTTTTATCTAAAAATGTTGTATGCTTGTCATGTATATAAGGAATGTCATGCTATTTGCTACCAGTCTTTTTTTTTATTGTCAGAACTTAGCAATGTGTCACTTTGTGTTTCTGCA[G/T]ATTTTATTGGATGGACCGGGAACTCTTAAGTACTCCAATTTCTGCCTGGCCAAAGCTCAAGGAGAAAGTTTGGAAGAGTTTTTTTCTCTTGTCATGGCTGAGGAGACAGGACTTGGAGAAAGCAAAGAAAACAACAGCTCTCCTCGAAACATCAAGAACAGAATTAAAGGTCTGATGACTCATCAGAGTGCCGTCATTTTTATTTATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCTTTCTGTCTTTTCTCGTTACTAAAATGTATGGTCAAACTGATTGAACTCCATCCATCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36033
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060519 | Missense | 150 | 1048 | 4 | 32 |
ENSDART00000143540 | Essential Splice Site | 148 | 753 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 16 (position 7162739)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6007270 |
GRCz11 | 16 | 5906896 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAACTCTTAAGTACTCCAATTTCTGCCTGGCCAAAGCTCAAGGAGAAA[G/A]TTTGGAAGAGTTTTTTTCTCTTGTCATGGCTGAGGAGACAGGACTTGGAG
Long Flanking Sequence:
GTGTTTATTATAATGATTTATCCATAAACATAGCTTTTTCAAACGAAGGTGCTTTTGTTCTTTTTATTCAAGATATACTTTAAAATGTCTTGCAACCGGTCACTTACATGAAATCATATGGTTAGCAAGCATCAATGATCTTTTGATATCCATGCAGCTTCTGTCTCAAACTGATCTATTATTTTCAGGATGATTCACAAAATTTTCAAGATACGACTTTTTATGACGTTTTCTTTACTTCATCAATACCATTTAGAATTCAACAGTTTCTGAATTAATCATATCAAAAGGAATATTATTTATCAAATCGCTTTAATCTTTTATCTAAAAATGTTGTATGCTTGTCATGTATATAAGGAATGTCATGCTATTTGCTACCAGTCTTTTTTTTTATTGTCAGAACTTAGCAATGTGTCACTTTGTGTTTCTGCAGATTTTATTGGATGGACCGGGAACTCTTAAGTACTCCAATTTCTGCCTGGCCAAAGCTCAAGGAGAAA[G/A]TTTGGAAGAGTTTTTTTCTCTTGTCATGGCTGAGGAGACAGGACTTGGAGAAAGCAAAGAAAACAACAGCTCTCCTCGAAACATCAAGAACAGAATTAAAGGTCTGATGACTCATCAGAGTGCCGTCATTTTTATTTATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCTTTCTGTCTTTTCTCGTTACTAAAATGTATGGTCAAACTGATTGAACTCCATCCATCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATTCTAATTACTAAAATGTATGGTCAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17493
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 |
---|---|---|---|---|---|
ENSDART00000060519 | Nonsense | 242 | 1048 | 6 | 32 |
ENSDART00000143540 | Nonsense | 207 | 753 | 6 | 22 |
Genomic Location (Zv9):
Chromosome 16 (position 7163769)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6008300 |
GRCz11 | 16 | 5907926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTATGACTGGTCTAGTTGATCTCATTTTAAAWGAAGATCCTCCACCYT[T/A]AAGACCTAAAGGTTTGASGCTTTTAATAAACTCAACCTTTTCAAAGCWGT
Long Flanking Sequence:
CCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCTATCTGTCGGTTTTATACCTGCTCACTATTACACACCTGTCTATTAATGTATCTTCCAGCCATACAAACAATCACTTAGTAAAGTCTAAAATGTTATTTTAGCACCTTAATTTTCACTTGCTTTATTATATGATGTTGCTCTGGCAGGTTCTCCTGTGTATTGTTCTCCTGAGGTGTTGAGAGGATCAGAAACCAATGTCGACAGTGACCTGTGGGCTTTAGGCTGTGTTCTGTATGAGATGTTCACAGGTTACACATTTCACATTAATCCACAATTTCCAGCTTAGCAAACTAGTCAAATCATTCTGTAATTAAATATTTAATTACATTGTCTTGTTTTCTCTTTGTTTTCTAGGAAAACCTCCCTTTGTATCTGAGAGTATGACTGGTCTAGTTGATCTCATTTTAAATGAAGATCCTCCACCTT[T/A]AAGACCTAAAGGTTTGACGCTTTTAATAAACTCAACCTTTTCAAAGCAGTTGCTTTCATGTAATATTTAATGACGTCTTTTGTTTTCTTTCTAAGAACCGGCTTCCTCACAGCCCAGCCCAGATTTTGAGAACCTGGTAATGGGTTTACTTCAGAAAGATCCTGTTTTAAGGTACAGTCATTATTTTATTTAGTTTCTCTTAAATTTGTAATAGTGCTTCTTCGCAAACGTAATCAGTTAATGAATCAGTTGTAGTGAGGAAACTTTAATTTCTCAGTTTGAATGATAATCAAATGACTCATCACAACATTAATCATTAATATGAGATGGACAATGCGATAGAGGCCAAAACATTCTTTCTAATTTTTAATTTCAAATTAATGTCACTATTCATAGTCTTAGATGTTTAATCAAAACGACGTGATATGACCAGGCATTAAAGCATTCATTTTTTATGCATCATTGAGCCTGTCACATTACGTTAGTATTGTAGCTTCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22745
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 |
---|---|---|---|---|---|
ENSDART00000060519 | Nonsense | 665 | 1048 | 22 | 32 |
ENSDART00000143540 | Nonsense | 564 | 753 | 18 | 22 |
Genomic Location (Zv9):
Chromosome 16 (position 7236088)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6080619 |
GRCz11 | 16 | 5980245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATCCGCTCAGGGATTCATCACTGCAGAGGTGGGACCTGCTCTCTGGTA[T/G]CTGTTCACACACTCCACGGTGGATGCTCTGAGGGTCAGCGCTATATCTGT
Long Flanking Sequence:
TAGTTAAACCTTTAAATGTCCCTTTAGGCTGAATACTAGGATCTTTAGAAATATCTAGTCAAATATTATTTACTGTCATCACGGCAAAGATAAACTAAATCAGTTTTTAGAAATAAGTTATTAAAACTATTATGTTTATTTTTCCGTTAAATAGTAATTTGGGAGTAACTTGTATTGATGTTGTAATACACAGCACTTGTTTGCAATAAAATAAAGAAAAAAAGCACATGAGTTGCATGTATGTATATGATTTGAATATGTGAAATGTAATTATTCAGTCATTTGTGGCTCAGCGTGGGGCTGGTGTGATATTGAACCTTTTGCACATGTTGTTTTAAGCCATAGCTGTATTTGAATGATTTATATGGGGGATTGGTGTTTGTTCAGGAGGACTTGGTGGTGAACCACATGGCTGCCAAAACAATTGAGAACGTGTGCAGCCGAGAGTCTCAATCCGCTCAGGGATTCATCACTGCAGAGGTGGGACCTGCTCTCTGGTA[T/G]CTGTTCACACACTCCACGGTGGATGCTCTGAGGGTCAGCGCTATATCTGTGAGTATTAAACACACCACATTCACATCATTCCAACACAAACGCAACACTCAAATGCATCAGTCCAGTTTCCGTTACGTTTTTCACCTTTGACAACTTGCGTTATGCATTATATTACATCACATCACATTATATAAACATTGTACATTATACTGTATCTGCCATACACAAAATCAAACAAAAAATGCTTTGTGTATTAAACTTAGGCATCTATAAGTTTTTTGTTGTTGTCCTTTTTGAGCTTTTTAAAGTGTAAATGATGGATTGTAAAGGCCAAAGGAAATTCTTTCCAGAGATCCAAAATCTGTGAATGAGCAAGTCCAGCGTTATGCATGTGACATTTGCATAAAAACACAGAGAATGCACACTGTAAAACCCAACAGTCAAATGAAATGAGAGTAGTTAACTCAAAATTGACTAAACGTTAATTCTACCCATTTGAAAAGAGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6405
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060519 | Essential Splice Site | 681 | 1048 | None | 32 |
ENSDART00000143540 | Missense | 581 | 753 | 18 | 22 |
Genomic Location (Zv9):
Chromosome 16 (position 7236138)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6080669 |
GRCz11 | 16 | 5980295 |
KASP Assay ID:
554-5242.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGTTCACACACTCCACGGTGGATGCTCTGAGGGTCAGCGCTATATCTG[T/A]GAGTAWTAAACACACCACATTCACATCAYTCCAACACAAACGCAACACTC
Long Flanking Sequence:
ATATCTAGTCAAATATTATTTACTGTCATCACGGCAAAGATAAACTAAATCAGTTTTTAGAAATAAGTTATTAAAACTATTATGTTTATTTTTCCGTTAAATAGTAATTTGGGAGTAACTTGTATTGATGTTGTAATACACAGCACTTGTTTGCAATAAAATAAAGAAAAAAAGCACATGAGTTGCATGTATGTATATGATTTGAATATGTGAAATGTAATTATTCAGTCATTTGTGGCTCAGCGTGGGGCTGGTGTGATATTGAACCTTTTGCACATGTTGTTTTAAGCCATAGCTGTATTTGAATGATTTATATGGGGGATTGGTGTTTGTTCAGGAGGACTTGGTGGTGAACCACATGGCTGCCAAAACAATTGAGAACGTGTGCAGCCGAGAGTCTCAATCCGCTCAGGGATTCATCACTGCAGAGGTGGGACCTGCTCTCTGGTATCTGTTCACACACTCCACGGTGGATGCTCTGAGGGTCAGCGCTATATCTG[T/A]GAGTATTAAACACACCACATTCACATCATTCCAACACAAACGCAACACTCAAATGCATCAGTCCAGTTTCCGTTACGTTTTTCACCTTTGACAACTTGCGTTATGCATTATATTACATCACATCACATTATATAAACATTGTACATTATACTGTATCTGCCATACACAAAATCAAACAAAAAATGCTTTGTGTATTAAACTTAGGCATCTATAAGTTTTTTGTTGTTGTCCTTTTTGAGCTTTTTAAAGTGTAAATGATGGATTGTAAAGGCCAAAGGAAATTCTTTCCAGAGATCCAAAATCTGTGAATGAGCAAGTCCAGCGTTATGCATGTGACATTTGCATAAAAACACAGAGAATGCACACTGTAAAACCCAACAGTCAAATGAAATGAGAGTAGTTAACTCAAAATTGACTAAACGTTAATTCTACCCATTTGAAAAGAGTTTTAAACTCAGTGTTGAAGGTAATGAGTTAATGACATACTTCATCACTTTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36034
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 |
---|---|---|---|---|---|
ENSDART00000060519 | Nonsense | 849 | 1048 | 26 | 32 |
ENSDART00000143540 | Nonsense | 713 | 753 | 21 | 22 |
Genomic Location (Zv9):
Chromosome 16 (position 7277774)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6122305 |
GRCz11 | 16 | 6021931 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGTCCGTGTTAGGCAGTATTGTGGGACGGAAGCACCCCTCGCCCACA[C/T]AGTCCCGTCAGCTGAAGCAGAGCCTCCCCATGATGGCTGTGGTGCTGCAT
Long Flanking Sequence:
AATTACTTTAATTAGGCAAGTTAGCATAATTCGGCAATTCATTATATAATGATGGTTTGTTCTGTAGACTTATCTAAAGAATATTGCTTATAATATTGACCTTAAAAGGGTTTAAACAAATTTAAAAACTGCTTTTATTCTATCCGAAATAAAACAAATAAGATCTTCTCCAGAAGAAAAAATATTATCAGAAATACTGTGAAAATTTTCTTGCTCTGTTTAACATCATTTAGGAAATATTTCAAAAAGTTAGGCTAACAATTTAGATTTGAACTGTATATTAGCATACTGTTATTAACATGTAAATTGTTTAATTTCTATTGTATTTCATGTATTTCATTTGTATCAACCAGCAAAGCACAAACAAAACATCAGCTCATGATCGTGAGAGTTTGTTTGTGATTGGCTGATTTCTCACAGACTGTGTTTTTGTGGTCTCCCTAGATGACATCCTGTCCGTGTTAGGCAGTATTGTGGGACGGAAGCACCCCTCGCCCACA[C/T]AGTCCCGTCAGCTGAAGCAGAGCCTCCCCATGATGGCTGTGGTGCTGCATCTGCTCACCTCACAGGTGTGTGTGTGTCTGTGTCAGGACTTACTATATTTACCTTTTTCACTAAGTTATTTTCGGTTTTTCGGTCTCAAGGGGATGGTGCAGCTTGGGGAAGAGAAATAAAATAACTTGTGCGGACCTACCTTGTGGTGCAATAGATAATATATCATATTTCAAATAACACGTTTAAAGTCAGGGTCATGGTTTTGCTGATTCTCTAACATTCAATTGTTCATTCATTCGTTTGTGTATTCTTCACTCCATTTGTTTAATTAAAGCAAAGTACACAAGCCAAATTAAATGGCATGTGTAAAGTTATTTGCATAAACCCTGATGATAAATCTTTACAGAAACTAATTAATGTAGTGAATACAGTGCTCTGCATGAAACCATATATAATTATTTTGTTTTGCTTTTTATTTAGTCTTATTATTGTTTGACAGTCATTTGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa792
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:
Essential Splice Site, Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060519 | Essential Splice Site | 869 | 1048 | 26 | 32 |
ENSDART00000143540 | Splice Site, Nonsense | 734 | 753 | 21 | 22 |
Genomic Location (Zv9):
Chromosome 16 (position 7277837)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6122368 |
GRCz11 | 16 | 6021994 |
KASP Assay ID:
554-0697.1 (used for ordering genotyping assays)
KASP Sequence:
TGAAGCARAGCCTCCCCATGATGGCTGTGGTGCTGCATCTGCTCACCTCA[C/T]AGGTGTGTGTGTGTYTGTGTCAGGACTTACTATATTTACCTTTTTCACTA
Long Flanking Sequence:
GTAGACTTATCTAAAGAATATTGCTTATAATATTGACCTTAAAAGGGTTTAAACAAATTTAAAAACTGCTTTTATTCTATCCGAAATAAAACAAATAAGATCTTCTCCAGAAGAAAAAATATTATCAGAAATACTGTGAAAATTTTCTTGCTCTGTTTAACATCATTTAGGAAATATTTCAAAAAGTTAGGCTAACAATTTAGATTTGAACTGTATATTAGCATACTGTTATTAACATGTAAATTGTTTAATTTCTATTGTATTTCATGTATTTCATTTGTATCAACCAGCAAAGCACAAACAAAACATCAGCTCATGATCGTGAGAGTTTGTTTGTGATTGGCTGATTTCTCACAGACTGTGTTTTTGTGGTCTCCCTAGATGACATCCTGTCCGTGTTAGGCAGTATTGTGGGACGGAAGCACCCCTCGCCCACACAGTCCCGTCAGCTGAAGCAGAGCCTCCCCATGATGGCTGTGGTGCTGCATCTGCTCACCTCA[C/T]AGGTGTGTGTGTGTCTGTGTCAGGACTTACTATATTTACCTTTTTCACTAAGTTATTTTCGGTTTTTCGGTCTCAAGGGGATGGTGCAGCTTGGGGAAGAGAAATAAAATAACTTGTGCGGACCTACCTTGTGGTGCAATAGATAATATATCATATTTCAAATAACACGTTTAAAGTCAGGGTCATGGTTTTGCTGATTCTCTAACATTCAATTGTTCATTCATTCGTTTGTGTATTCTTCACTCCATTTGTTTAATTAAAGCAAAGTACACAAGCCAAATTAAATGGCATGTGTAAAGTTATTTGCATAAACCCTGATGATAAATCTTTACAGAAACTAATTAATGTAGTGAATACAGTGCTCTGCATGAAACCATATATAATTATTTTGTTTTGCTTTTTATTTAGTCTTATTATTGTTTGACAGTCATTTGAATATTTATAATACACTACCTGACATGTCAAATGCTTTTAGAACAACAAATAATAACTCACAAATA
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:
sa16618
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060519 | Essential Splice Site | 940 | 1048 | 29 | 32 |
ENSDART00000143540 | None | None | 753 | None | 22 |
Genomic Location (Zv9):
Chromosome 16 (position 7294295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 6138826 |
GRCz11 | 16 | 6038452 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGGCCATTTCCCAGCATCCYGCTCTGCTCAGCCTCTACCCYTTCATTG[T/A]AAGCACAAGCACTGATGCACTTTTCATTTTGTGTCTTTYTCACAGTTGCT
Long Flanking Sequence:
TAGCAGGAGGTAAATATATGTGTGTGTAATGTCTCTTTTCTTTTTTCTCTTGTGGAAAGAATCACATAACTTCCATTGACTCGAATGAGACGAGTTTGGGAAGTGCAATAGGTAGGTTTTACTTTTATTTACTTTTTTATTTCATTAATTAATTCATTCATTTATTTATTCATTAATTTATTATATATTATTAACTTTTCAACTATTTTTCTTTCTCATCCTCTTATTTAATCTATTCTTGCGTAAATTGTAAGGTAATATAATGTAGCTCTAGTTTTTTAGTTTTGTTTGTTAGATCAAATGCTGTTTTTCATCTATTACATATAAAATGAATTGCTGAAAGGTGAGATTACCATTTTATTCCTTCCTTAATACTTTTTATTTTTTTGTTTTCTCCAAAACAGGCCAAGCGTCATCTGAGGAGCTGATCAGAAACACACTGTCAGCAGTGGAGGCCATTTCCCAGCATCCCGCTCTGCTCAGCCTCTACCCCTTCATTG[T/A]AAGCACAAGCACTGATGCACTTTTCATTTTGTGTCTTTCTCACAGTTGCTTCAAAATGATTTAAGCATTTACATATAATGCGATTTGATTCAGCATATTTTCTTTTTTTTTCTTATTAAATATCGAGTTTACGTTGAATTTGAATTATTAATTCGTTATTTAATCATTACTTTCTTTGAATTTTAAAGATTAACTTTGAATTGGAAGTTTATTTTTGTGTTTTTTTTATTATTTTTTAATTAATTACTCTTTAATAGTAAAACAAAGCAATTGTGTTAATAATAATTGTGTGCATTGTGTTAAAATTGTACAAAAAAAAAAAAAACTAAGTGCTTTAAAAGAATAACAGGCACACACACACATCTGTGTAATTTGAAGTGGACGCTGGACAACGTGCCGATCCAAACGCAGGTTTATTAAACAGAGCTGGTCAGGCAAGCAACGAAAATCGAGCAAAAGCAAAAGGAAATCAAGAGTTATGGTAGATAAAACAGGCAGAT
Associated Phenotype:
Not determined