ZMP
mll
Ensembl ID:
ZFIN ID:
Description:
histone-lysine N-methyltransferase MLL [Source:RefSeq peptide;Acc:NP_001103749]
Human Orthologue:
MLL
Human Description:
myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila) [Source:HGNC Symbol;Acc:7
Mouse Orthologue:
Mll1
Mouse Description:
myeloid/lymphoid or mixed-lineage leukemia 1 Gene [Source:MGI Symbol;Acc:MGI:96995]
Alleles
There are 11 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42541 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa137 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa24984 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa35881 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19111 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa10905 | Nonsense | Available for shipment | Available now |
| sa22638 | Nonsense | Available for shipment | Available now |
| sa2815 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa42541
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 |
|---|---|---|---|---|---|
| ENSDART00000104525 | Nonsense | 1664 | 4219 | 10 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 22753340)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 23464527 |
| GRCz11 | 15 | 23399792 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCCTTCCATCTCTTCTGCTTGGGGGAGGCAGAGCGGCCTCATGACGAA[C/T]AGTGGGAAAACTGGTGTTGCCGCCGATGCCGCTTTTGCCATGTTTGTGGG
Long Flanking Sequence:
CCCGATGGATGCACATGCTGATCAAATGTACCTTGAATACATTGCCAGTCACTTTGGATAAAAGCATCTTCGATATGCTTCTGTGTAATGTAAATATGATTGTTTACAGGAGAAACAGCTACCCAAACCTGACAGCAGTACTTTAAACTCCCAGAGCACTCCTTCGACTGGGGGCACAGCCAAGCAGAAAGCGCCCTACGATGGAGTGCATCGAATCAGAGTGGATTTCAAGGAGGACTATAACATTGAGAATGTGTGGGAGATGGGTGGGCTCAGCATTCTCACCTCTGTGCCAATCACCCCACGGGTGGTGTGCTTTCTTTGTGCCAGCAGCGGTAATGTAGAGGTGGGTCATCTTTTGTTAAAGGAGAAGAATCGAAGGCATAAAAAGGATGGGATGTGTTCTTATGCCTTGTTGTGTTTAGTTTGTTTTCTGCCAGGTGTGCTGTGAACCCTTCCATCTCTTCTGCTTGGGGGAGGCAGAGCGGCCTCATGACGAA[C/T]AGTGGGAAAACTGGTGTTGCCGCCGATGCCGCTTTTGCCATGTTTGTGGGCGGAAATATCAGAAAACCAAAGTAAGACATTTTATGAAGAATTCTGATGTAAAAGACTGCAAGAGCCATCTAAAAGTTTCCTCTAAAATGTACATCTTTCTCAGGCTCCTTTGTGTAGGTACAGTAATTTTACTTTTATGCCGAGTTTAGACTACATGATTTTAGCCCCAATTTTGACTCGCCGCTTTGAGAGATCAGCAACAAATTCTTGAAATCACAGGCAAATCGTTGCTCGTTCACGCGAGTAACAATCACACTCTGCGAACTATCAAAGTCGCGTTCTGAGAGAATCACAGTCGCCAATACCCATGAGATATTTTGCGTGCTGTTGGCGTCCTGTCGACGATTCAAAATCATGCGGTGTGAAATGTGTTCTGATTGTTAATAGCATCAGTGATCACCTATAACCAATGAGAGAGAAGCATCCACTAGTATGGGTATTGGCAAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa137
Status:
Confirmed mutation in F2 line
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 |
|---|---|---|---|---|---|
| ENSDART00000104525 | Nonsense | 1668 | 4219 | 10 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 22753326)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 23464513 |
| GRCz11 | 15 | 23399778 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGCTTGGGGGAGGCAGAGCGGCCTCATGACGAACAGTGGGAAAACTG[G/A]TGTTGCCGCCGATGCCGCTTTTGCCATGTTTGTGGGCGGAAATATCAGAA
Long Flanking Sequence:
ATGCTGATCAAATGTACCTTGAATACATTGCCAGTCACTTTGGATAAAAGCATCTTCGATATGCTTCTGTGTAATGTAAATATGATTGTTTACAGGAGAAACAGCTACCCAAACCTGACAGCAGTACTTTAAACTCCCAGAGCACTCCTTCGACTGGGGGCACAGCCAAGCAGAAAGCGCCCTACGATGGAGTGCATCGAATCAGAGTGGATTTCAAGGAGGACTATAACATTGAGAATGTGTGGGAGATGGGTGGGCTCAGCATTCTCACCTCTGTGCCAATCACCCCACGGGTGGTGTGCTTTCTTTGTGCCAGCAGCGGTAATGTAGAGGTGGGTCATCTTTTGTTAAAGGAGAAGAATCGAAGGCATAAAAAGGATGGGATGTGTTCTTATGCCTTGTTGTGTTTAGTTTGTTTTCTGCCAGGTGTGCTGTGAACCCTTCCATCTCTTCTGCTTGGGGGAGGCAGAGCGGCCTCATGACGAACAGTGGGAAAACTG[G/A]TGTTGCCGCCGATGCCGCTTTTGCCATGTTTGTGGGCGGAAATATCAGAAAACCAAAGTAAGACATTTTATGAAGAATTCTGATGTAAAAGACTGCAAGAGCCATCTAAAAGTTTCCTCTAAAATGTACATCTTTCTCAGGCTCCTTTGTGTAGGTACAGTAATTTTACTTTTATGCCGAGTTTAGACTACATGATTTTAGCCCCAATTTTGACTCGCCGCTTTGAGAGATCAGCAACAAATTCTTGAAATCACAGGCAAATCGTTGCTCGTTCACGCGAGTAACAATCACACTCTGCGAACTATCAAAGTCGCGTTCTGAGAGAATCACAGTCGCCAATACCCATGAGATATTTTGCGTGCTGTTGGCGTCCTGTCGACGATTCAAAATCATGCGGTGTGAAATGTGTTCTGATTGTTAATAGCATCAGTGATCACCTATAACCAATGAGAGAGAAGCATCCACTAGTATGGGTATTGGCAAGCCAGCGGGAAGTTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24984
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 |
|---|---|---|---|---|---|
| ENSDART00000104525 | Nonsense | 1762 | 4219 | 13 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 22751237)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 23462424 |
| GRCz11 | 15 | 23397689 |
KASP Assay ID:
554-7410.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTGTCATTAAACAATGTAATAAATGTTATTTCCCCCTTCCAGGCAACT[T/A]GTGCCCACTTTGTAATAAGGGCTATGATGACGATGACTGTGACAGCAAAA
Long Flanking Sequence:
TAAGCAACTTCCAAGTTTTAGCTTCTTTCTTTCTTTCTTAAAGCCCTTCAGAAATGACAAATGCTCAGTACTAAGATGGAAACAAACTTTTAAATGTTATTTTTTCCATCATCATTTAGCAGCTACTGGAGTGTGACAAGTGCCGAAACAGCTATCACCCCGAGTGCCTGGGACCCAACCATCCTACCAGACCCACCAAGAAGAAGAGAGTCTGGGTACTTGAATGCTCTAAATCTTAGAAGTCTGTAACATCTGTGGCAGCGTTCTCCCATAGTTATTTTTTCTTCTGCCACAGGTTTGCACCAAGTGTGTGCGCTGTAAGAGTTGTGGAGCCACCAAACCAGGAAAGGCCTGGGATGCCCAGTGGTCACATGATTTCTCTTTGTGTCATGACTGTGCCAAACGTTTAACTAAAGGTTAGTTCTAATCATCTTGAATGTTTATTGTATGCCTTGTCATTAAACAATGTAATAAATGTTATTTCCCCCTTCCAGGCAACT[T/A]GTGCCCACTTTGTAATAAGGGCTATGATGACGATGACTGTGACAGCAAAATGATGAAGTGCAAAAAGTGTGACCGCTGGGTCCATGCCAAATGTGAAAGCTTAACAGGTGAATTATCAAATTTTATTTGCATCTCTTATGTATCAAGTGGCATAACAAGGCACAATTTCATTTATTTTTTATTTGTTTATTTGGATTACAGAAATTTTATATTTTATTCTGTGAAGCAGCATAAATTTGAAAACTTACAAAGGGATTTATGATTTTGCCTAGTGTTTCTTTTTTAAATAAATCCTATTCTTTTAAAATTTAAAAAGATAAATGATTCTTCAGGCTCAAAATTTAGCAAATTAGAATCATTTCTAAAAGATCACATGCTAAGTTATTATAGTTAACGAAAACTAGAATTGAAAAACGTTTTGTTAACTGAAATAAAAATAAAAACGAGAGTTAAAAAAACAAACAAACTAGAACTAACTAAAACTGGATTGTGTATGTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35881
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000104525 | Essential Splice Site | 1954 | 4219 | 16 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 22748257)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 23459444 |
| GRCz11 | 15 | 23394709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTAGAGAGCAGGAAAGCCAACAGCATGCTCAAGTCCTTTTTTATTCGG[G/A]TGAGAAAAAGCTGGTGGACACACAGTTCTGACAGTTGGGTGTCTCGAAGT
Long Flanking Sequence:
TCTCAGTTGCCCACAGCTTTATTTCCACTATATACCTTAACATTGCCAATTGTTTCAGGCTGTTATGAAGCCACCTGAGCTCAACCCAGAGACCGAAGAAAGCCTTCCCTCACGACGTTCCCCAGAGGGTCCTGATCCCCCTGTGTTAACGGAGGTCTCTCCACCAAACGATTCGCCGCTCGATTTAGAGTCTGTGGAGAAGAAAATGGATTCTGGATGCTATAAATCTGTGGTAAGTTTTTCTCCTTTGTGAAATCCGAAAGGTAGCTTTTATGTTTTTATTCTTCTGCGAAAGATTATCTGTTGTCTTTTAAGCCTCCAGTTCAGCAGGGTTCAGGCAACGGTCACATGTGAGAGCCCAGGTGTCATTTTCTGTTCCTCTCTTTCAGCTGGAGTTCAGTGATGACATTGTGAAAATCATCCAGACAGCCTTCAACTCAGATGGAGGTCAGCTAGAGAGCAGGAAAGCCAACAGCATGCTCAAGTCCTTTTTTATTCGG[G/A]TGAGAAAAAGCTGGTGGACACACAGTTCTGACAGTTGGGTGTCTCGAAGTCCTGCGTTGTGTCTAATGACACTTGTCGCTTTTTTTTGTTACAGCAAATGGAGCGGATTTTTCCATGGTACAAGGTGAAGGAGTCCAAATTTTGGGAGACAAGCAAAGCTTCTTCCAAGTGAGTGCAAACTTTGTTTTAGTTTGCTTGCTGTTTTAATTTCAGCCTTAAAATTGATTTGATCAAAGAAGAATTTTTTCATTGCTAAGTTCCCACACAAAATATACGTTGTTTAAAGGTAAACAGTTGGACAAGTCAAGGTAGTGTTTGAGCATCGAGAGCAAACTCACCGCGGACTGTCTGTCTATTCTTTGCTCTCTGGTAGAGCAGAAATATCACCTTTCCATAGGGAATGCAGCCTGTATGGTCTAGTTCCATTGTTTGAGGTCGACAGGCAGTGTCACATTTCACATGGGGTGCTTTGACAAGTCTTGTGGTTGGCATTTGGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19111
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 |
|---|---|---|---|---|---|
| ENSDART00000104525 | Nonsense | 2976 | 4219 | 26 | 35 |
| ENSDART00000104525 | Nonsense | 2976 | 4219 | 26 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 22741496)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 23452683 |
| GRCz11 | 15 | 23387948 |
KASP Assay ID:
2260-8460.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGTCTTCCATCTATTGCTGGTATTGATCAGTGTTTGGGAAGAGGTTCA[C/T]AGATCCACAGATTCTTGAGGGACCAGGCAAAGGAGCATGAAGATGACAGT
Long Flanking Sequence:
CTGAATCAGACAGCCACATCCACCCGGATGATTCTGAAGAGCATCTCATGGACCACCAGTGTGCTGATGATGGGGAGGACAATAATTTAGAGGATGAAGGCAGTGTCGATAAACACCACGAGGAGGATAGTGATGGTTCAGCAGGTTCAGCAAAACGCAGATACCCAAGGAGGAGTGCCCGTGCTCGATCTAACATGTTTTTTGGGTTAACTCCATTCTATGGTGTTCGATCGTATGGTGAGGAAGACATACCCTTTTACAGAAGTGGTGAAATCTCTATGAAGAAGCGGACTGGGAGCAGCAAGCGCTCAGCCGAAGGGCAGGTTGATGGAGCAGATGATATGAGCACATCTTCTTCAGCAGACAGCGGAGAGGATGAAGAAGGAGGAATTGGCTCCAATAAGGATACTTACTATTACAACTTCACACGCACTATAATAAACCCTAGCTCTGGTCTTCCATCTATTGCTGGTATTGATCAGTGTTTGGGAAGAGGTTCA[C/T]AGATCCACAGATTCTTGAGGGACCAGGCAAAGGAGCATGAAGATGACAGTGATGAAGTTTCAACAGCAACCAAAAACTTGGAGCTGCAACAAATTGGTCAGCTGGATGGTGTAGATGATGGTTCAGAGAGTGACATTAGTATAAGTACCAGTAGCACAACCACTGCTACTACTTCATCCACACAAAAAGGTTCAACAAAAAGGAAAGGTAGAGAAAGTAGGACTGAAAAATCAAATGTTGACTCAGGGAAGGAGGCAGTAAATACCACTAGTAACAGCCGTGACAGTCGAAAAAATCAAAAGGATAACTGTCTTCCATTAGGAAGTGTGAAAACACAAGGACAAGACCCACTTGAAACTCAATTATCACTCACCACAGATCTGCTCAAGTCTGACTCTGATAACAACAACAGTGATGACTGTGGTAACATCTTACCCTCTGATATTATGGAGTTTGTGCTCAATACCCCTTCAATGCAGGCTTTGGGACAGCAAGCAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10905
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 |
|---|---|---|---|---|---|
| ENSDART00000104525 | Nonsense | 2976 | 4219 | 26 | 35 |
| ENSDART00000104525 | Nonsense | 2976 | 4219 | 26 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 22741496)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 23452683 |
| GRCz11 | 15 | 23387948 |
KASP Assay ID:
2260-8460.1 (used for ordering genotyping assays)
KASP Sequence:
CTGGYCTTCCATCTATTGCTGGTATTGATCAGTGTTTGGGAAGAGRTTCA[C/T]AGAWCCACAGATTCTTGAGGGACCAGGCAAAGGAGCATGAAGATGACAGT
Long Flanking Sequence:
CTGAATCAGACAGCCACATCCACCCGGATGATTCTGAAGAGCATCTCATGGACCACCAGTGTGCTGATGATGGGGAGGACAATAATTTAGAGGATGAAGGCAGTGTCGATAAACACCACGAGGAGGATAGTGATGGTTCAGCAGGTTCAGCAAAACGCAGATACCCAAGGAGGAGTGCCCGTGCTCGATCTAACATGTTTTTTGGGTTAACTCCATTCTATGGTGTTCGATCGTATGGTGAGGAAGACATACCCTTTTACAGAAGTGGTGAAATCTCTATGAAGAAGCGGACTGGGAGCAGCAAGCGCTCAGCCGAAGGGCAGGTTGATGGAGCAGATGATATGAGCACATCTTCTTCAGCAGACAGCGGAGAGGATGAAGAAGGAGGAATTGGCTCCAATAAGGATACTTACTATTACAACTTCACACGCACTATAATAAACCCTAGCTCTGGTCTTCCATCTATTGCTGGTATTGATCAGTGTTTGGGAAGAGGTTCA[C/T]AGATCCACAGATTCTTGAGGGACCAGGCAAAGGAGCATGAAGATGACAGTGATGAAGTTTCAACAGCAACCAAAAACTTGGAGCTGCAACAAATTGGTCAGCTGGATGGTGTAGATGATGGTTCAGAGAGTGACATTAGTATAAGTACCAGTAGCACAACCACTGCTACTACTTCATCCACACAAAAAGGTTCAACAAAAAGGAAAGGTAGAGAAAGTAGGACTGAAAAATCAAATGTTGACTCAGGGAAGGAGGCAGTAAATACCACTAGTAACAGCCGTGACAGTCGAAAAAATCAAAAGGATAACTGTCTTCCATTAGGAAGTGTGAAAACACAAGGACAAGACCCACTTGAAACTCAATTATCACTCACCACAGATCTGCTCAAGTCTGACTCTGATAACAACAACAGTGATGACTGTGGTAACATCTTACCCTCTGATATTATGGAGTTTGTGCTCAATACCCCTTCAATGCAGGCTTTGGGACAGCAAGCAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22638
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 |
|---|---|---|---|---|---|
| ENSDART00000104525 | Nonsense | 3090 | 4219 | 26 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 22741154)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 23452341 |
| GRCz11 | 15 | 23387606 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAATCAAAAGGATAACTGTCTTCCATTAGGAAGTGTGAAAACACAAGGA[C/T]AAGACCCACTTGAAACTCAATTATCACTCACCACAGATCTGCTCAAGTCT
Long Flanking Sequence:
TGAGCACATCTTCTTCAGCAGACAGCGGAGAGGATGAAGAAGGAGGAATTGGCTCCAATAAGGATACTTACTATTACAACTTCACACGCACTATAATAAACCCTAGCTCTGGTCTTCCATCTATTGCTGGTATTGATCAGTGTTTGGGAAGAGGTTCACAGATCCACAGATTCTTGAGGGACCAGGCAAAGGAGCATGAAGATGACAGTGATGAAGTTTCAACAGCAACCAAAAACTTGGAGCTGCAACAAATTGGTCAGCTGGATGGTGTAGATGATGGTTCAGAGAGTGACATTAGTATAAGTACCAGTAGCACAACCACTGCTACTACTTCATCCACACAAAAAGGTTCAACAAAAAGGAAAGGTAGAGAAAGTAGGACTGAAAAATCAAATGTTGACTCAGGGAAGGAGGCAGTAAATACCACTAGTAACAGCCGTGACAGTCGAAAAAATCAAAAGGATAACTGTCTTCCATTAGGAAGTGTGAAAACACAAGGA[C/T]AAGACCCACTTGAAACTCAATTATCACTCACCACAGATCTGCTCAAGTCTGACTCTGATAACAACAACAGTGATGACTGTGGTAACATCTTACCCTCTGATATTATGGAGTTTGTGCTCAATACCCCTTCAATGCAGGCTTTGGGACAGCAAGCAGAAGCTCCTTCTGCTGAACAATTCTCTTTAGATGAGAGTTATGGGGTGGATGTTAACCAAAGAAAAGACATGCTTTTTGAAGATTTTACTCAGCCTCTGGCCAATGCTGAATCTGGCGAATCTGGGGTGAGCACTACCATTGCTGTAGAAGAGTCATACGGGCTTCCTCTTGAGCTGCCCTCTGACCTCTCTGTGCTTACAACTCGAAGTCCCACTGTAAGTAATCAAAATCATGGGCCACTTATCTCGGAAACCTCTGAACGCACCATGTTAGCTCTGGCTACGGAAGAGTCAGAAGCTGGGAAAAGCAAGAAGAAAACAAGAACGGGGTCCACTGTATCCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2815
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000104525 | Nonsense | 4194 | 4219 | 35 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 22737015)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 23448202 |
| GRCz11 | 15 | 23383467 |
KASP Assay ID:
554-3171.1 (used for ordering genotyping assays)
KASP Sequence:
ATTTTTGCCACACGCAAGATCTATAAAGGCGAGGAGCTCACGTATGATTA[C/A]AAGTTTCCCATCGAAGAACCAGGCAATAAGCTGCCTTGCAACTGCGGGGC
Long Flanking Sequence:
CTTTTTAAAATGAAAAAGAAAGGTTGGATAGAGGACAGAAAACAAATATGCTGCTTCATTGCATTCAAACTTATGTTTATTCACAGATCAGCCATACATGGCAGAGGTTTGTTCTGCAGGAAGAACATTGAGCCCGGAGAAATGGTGATCGAGTATTCTGGCAATGTAATTCGTTCTGTCCTCACTGACAAGCGGGAGAAGTACTATGATGACAAGGTAGAATTCTTGATGGTTCATGAATGCAGTTTGAAATCATTATCAGTGTTACTTAACGATTTAATATTTATTTTCTTTAATACTCAGGGCATTGGCTGCTACATGTTTCGAATCGATGACTACGAGGTGGTGGATGCTACCATTCACGGCAACTCAGCCCGTTTCATTAACCACTCATGCGAGCCCAACTGCTACTCTCGTGTGGTCAATGTTGACGGTCAGAAGCACATTGTCATTTTTGCCACACGCAAGATCTATAAAGGCGAGGAGCTCACGTATGATTA[C/A]AAGTTTCCCATCGAAGAACCAGGCAATAAGCTGCCTTGCAACTGCGGGGCAAAGAAGTGTCGCAAGTTCCTCAATTGAAAGCAAATTCACAATGTAAAAGTATCTGTGAAGCGCTATCAAGAGTGTACACTTGCCAGGGAAGAGACATTTTTAAATGTTTTGTTTTTTACCGAAGCAGGCTCAGGTTATCAGAAGGTTAATGGTATTGTGCCTCTTAAGTTGTTTGGTTTTTAGAAAAAGACATTCGAGCGGAGTCACAATGGAGAAGATTGCCCTTATGTCCCTTTTAGTAATGTGCAATTTAAGAGATTAGTGCCCCTTCATTCTTAACGTTTTGTATGTGCTCTTTTATTTGACCATTTTGTTTTTATAAGAAGGATATTGTGAATAGTTTTAAATTTGTAATAAGTCGAGTCTGGCCTGCCCTTACTTACTGAGTGTGACAAATTACTGAAAAATTGCCACATCGTTCCATTCTACACCAAAGTGCAATTTCGGAA
Associated Phenotype:
Not determined