ZMP
vmhcl
Ensembl ID:
ZFIN ID:
Description:
ventricular myosin heavy chain-like [Source:RefSeq peptide;Acc:NP_001070932]
Human Orthologues:
MYH6, MYH7
Human Descriptions:
myosin, heavy chain 6, cardiac muscle, alpha [Source:HGNC Symbol;Acc:7576]
myosin, heavy chain 7, cardiac muscle, beta [Source:HGNC Symbol;Acc:7577]
myosin, heavy chain 7, cardiac muscle, beta [Source:HGNC Symbol;Acc:7577]
Mouse Orthologues:
Myh6, Myh7
Mouse Descriptions:
myosin, heavy polypeptide 6, cardiac muscle, alpha Gene [Source:MGI Symbol;Acc:MGI:97255]
myosin, heavy polypeptide 7, cardiac muscle, beta Gene [Source:MGI Symbol;Acc:MGI:2155600]
myosin, heavy polypeptide 7, cardiac muscle, beta Gene [Source:MGI Symbol;Acc:MGI:2155600]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18394 | Nonsense | Available for shipment | Available now |
sa6839 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa19748 | Nonsense | Available for shipment | Available now |
sa19749 | Essential Splice Site | Available for shipment | Available now |
sa39820 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16260 | Nonsense | Available for shipment | Available now |
sa39821 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18394
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 |
---|---|---|---|---|---|
ENSDART00000078958 | Nonsense | 555 | 1943 | 14 | 37 |
ENSDART00000123064 | Nonsense | 546 | 638 | 16 | 17 |
ENSDART00000123565 | None | None | 242 | None | 8 |
ENSDART00000128784 | Nonsense | 551 | 1936 | 16 | 39 |
ENSDART00000137560 | None | None | 99 | None | 2 |
ENSDART00000141922 | None | None | 167 | None | 4 |
The following transcripts of ENSDARG00000079782 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 23579941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24628554 |
GRCz11 | 2 | 24284205 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTGCATGTTTCCCAAAGCCAGTGATGCAAYCTTTAAAGCAAAGCTTTA[C/A]GACAACCATCTTGGGAAATCAAACAATTTCCAGAAACCCAGGCTTGTKAA
Long Flanking Sequence:
CCTCGCCAGTATTTCATCGGAGTATTGGATATTGCTGGCTTTGAGATCTTTGATGTAAGTACTGAATGCCTAGTTCGACCCAAATTAATTTCCACACAGCAGCATTTCGTCTCATACTGAAACCTGTAGGAACAATTGTGGTTTTCCAATATTTTTTGTTTGCAGTTTAACACCTTTGAGCAACTCTGCATCAACTTTACCAATGAGAAACTGCAACAGTTTTTCAACCACCACATGTTTGTGCTGGAACAAGAGGAGTACAAGAAAGAAGGGATTGAATGGGAGTTTATTGACTTTGGCATGGACTTGCAGGCCTGCATCGATCTCATTGAGAAAGTGAGTCATTAATGATACAAAATGCAAATATTAAAACTGAATTATATGCTATACTTCACCATTACTTATTCCTGACTCCTTCAGCCTATGGGCATCATGTCCATCCTTGAAGAGGAGTGCATGTTTCCCAAAGCCAGTGATGCAACCTTTAAAGCAAAGCTTTA[C/A]GACAACCATCTTGGGAAATCAAACAATTTCCAGAAACCCAGGCTTGTGAAGGGCAAGCCAGAGGCTCACTTTGCTCTTGTTCACTACGCTGGCACAGTAGACTACAACATTAACAACTGGCTGGTGAAGAATAAGGACCCTCTTAACGAAACTGTGGTTGGATTGTACCAGAAGTCCTCTCTGAAGCTGTTGTCTAATCTGTTTGCCAACTACGCTGGTGCAGACTCAGGTGTGCTTTATCAAATAGAATTGCCATCTTTACTAGTAAAGTCATTATATACGACTTATGTCATTAATGTAAAAAAGGGAAAGTTCACCCAAAAAAGAAAATTCTGCCACCATTTACTCATCTTTTACTTTTTGCAAACTTATTTATTTTTGTTTCTGCTGTTGAGCACAAAAGAAAATAATTACAAAAATGCTGATAGTATTAACCCATTAATAGTGCTGGGCTATCAATCAAAAAGTAATCGAAATCAACATTAGGCTACAACCATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6839
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078958 | Essential Splice Site | 901 | 1943 | 20 | 37 |
ENSDART00000123064 | None | None | 638 | None | 17 |
ENSDART00000123565 | None | None | 242 | None | 8 |
ENSDART00000128784 | Essential Splice Site | 894 | 1936 | 22 | 39 |
ENSDART00000137560 | None | None | 99 | None | 2 |
ENSDART00000141922 | None | None | 167 | None | 4 |
The following transcripts of ENSDARG00000079782 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 23583582)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24624913 |
GRCz11 | 2 | 24280564 |
KASP Assay ID:
554-5235.1 (used for ordering genotyping assays)
KASP Sequence:
AATACAAGATCTGTATGCAGGTAATGCATTATCTATTAAATATATTTAAC[A/C]GGAGCAAGACAACCTCTGTGATGCTGAAGAAAGGTGTGAAGGTCTGATCA
Long Flanking Sequence:
AATCACAGGCATTCAAGCCAAGTCTCGTGGTCTTCTCTCAAGGGCTGAATACATAAAGATGGTAGAACGCAGGTACTGATTATCCTATACTTAAACAAGTAATGTGTGCTGTTGTCTTTTTTAATGGTGTTTGATTATGTTTTTTTGTGTTTTCTACTAATAAAAAAAGGGATGCCTTACTTGTGATTCAGTGGAATGTGCGTGCATTCATGGCGGTCAAGAACTGGCCCTGGATGAAGCTCTTCTTTAAAATCAAACCATTGCTGAGATCTGCTGAAGCAGAAAAGGAAATGGCCAATATGAAAGAAGAGTTCTTGAAGCTAAAGGAAGCTTATGCGAAGTCTGAGGCACGTAGAAAAGAACTTGAAGAAAAAATGGTGACTCTTCTCCAAGAAAAGAATGACCTACAACTTCAAGTGCAAGCGGTATGTTTGTAAAAAAAAAATCATAAATACAAGATCTGTATGCAGGTAATGCATTATCTATTAAATATATTTAAC[A/C]GGAGCAAGACAACCTCTGTGATGCTGAAGAAAGGTGTGAAGGTCTGATCAAAAACAAGATTCAGATGGAGGCTAAAGCCAAAGAGCTCACAGAGAGACTTGAGGATGAGGAGGAGATGAATGCAGAGCTGACAGCTAAGAAGAGAAAGCTGGAGGACGAATGCTCTGAGCTGAAGAAGGATATTGATGATCTGGAGCTCACTCTGGCTAAAGTGGAGAAAGAGAAGCATGCTACTGAGAACAAGGTTTCAGACAAACAATAATTTACTGTGAAGAGAAGTCCATTTGTCTGATGTTTACTTATTACTAGCTTTTCACACACAGGTGAAGAACCTGACAGAAGAAATGGCAGCTTTAGACGATATCATTGCTAAACTGACAAAGGAGAAGAAAGCCTTGCAGGAAGCTCATCAGCAGACACTGGATGACCTGCAGAGTGAGGAGGACAAAGTCAACACCCTCACCAAGGCAAAAGTAAAACTAGAGCAACAAGTGGATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19748
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 |
---|---|---|---|---|---|
ENSDART00000078958 | Nonsense | 1110 | 1943 | 23 | 37 |
ENSDART00000123064 | None | None | 638 | None | 17 |
ENSDART00000123565 | None | None | 242 | None | 8 |
ENSDART00000128784 | Nonsense | 1103 | 1936 | 25 | 39 |
ENSDART00000137560 | None | None | 99 | None | 2 |
ENSDART00000141922 | None | None | 167 | None | 4 |
The following transcripts of ENSDARG00000079782 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 23584459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24624036 |
GRCz11 | 2 | 24279687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATCAGTCAGCTCAACAGTAAAATCGACGATGAGCAAAGCATAATTATC[C/T]AACTCCAAAAGAAACTCAAGGAGTTGCAGGTACATTGACCATACGTGATG
Long Flanking Sequence:
GACAAAGGAGAAGAAAGCCTTGCAGGAAGCTCATCAGCAGACACTGGATGACCTGCAGAGTGAGGAGGACAAAGTCAACACCCTCACCAAGGCAAAAGTAAAACTAGAGCAACAAGTGGATGATGTGAGTAAGCATTGTTTTTGACGTAGCATTCAGTTGTGATGAAGTAAACTACAGTACTACATTAAGAACTTCTGTTGCTAATTCTGTTAGCTTGAGGGATCTCTAGAGCAAGAAAAGAAAATCCGAATGGATCTAGAAAGAGCCAAGAGGAAACTTGAAGGAGATCTGAAGTTAACCCAGGAGAGCATAATGGACCTGGAGAATGACAAGCAGCAACTGGAAGAAAAACTGAAGAAGTAAGACACACTGCTTAATTATTATTGTTGTTTTACATGTTTTGAATGCCTTAAACGAATTCCATGATTTCAATTTCAGGAAAGACTTTGAAATCAGTCAGCTCAACAGTAAAATCGACGATGAGCAAAGCATAATTATC[C/T]AACTCCAAAAGAAACTCAAGGAGTTGCAGGTACATTGACCATACGTGATGTTCTGTTCATCTTTGTAGTGTGCATTTTTAAGAAAAAATGTATCTTCTCCTTTATGCTAGGCGAGAGTTGAGGAGCTGGAGGAAGAGCTTGAGGCAGAAAGAGCTGCCAGAGCCAAAGTGGAGAAACAGAGAGCAGATTTAGCCAGAGAGCTGGAGGAGATCAGCGAGAGACTGGAGGAGGCTGGAGGAGCTACAGCTGCTCAGATTGAGATGAATAAGAAACGAGAGGCAGAGTTTCAGAAGCTCCGCAGAGACCTTGAAGAGGCCACTCTGCAGCATGAGGCCACTGCCGCCACACTCAGGAAAAAACAAGCCGACAGTGTGGCTGAACTTGGAGAGCAGATAGACAATCTGCAGAGGGTCAAGCAAAAACTGGAAAAGGAGAAAAGTGAACTTAGGCTGGAGTTGGATGATGTAGCCTCCAGCATGGAGCATATTGTGAAGTCCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19749
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 |
---|---|---|---|---|---|
ENSDART00000078958 | Essential Splice Site | 1119 | 1943 | 23 | 37 |
ENSDART00000123064 | None | None | 638 | None | 17 |
ENSDART00000123565 | None | None | 242 | None | 8 |
ENSDART00000128784 | Essential Splice Site | 1112 | 1936 | 25 | 39 |
ENSDART00000137560 | None | None | 99 | None | 2 |
ENSDART00000141922 | None | None | 167 | None | 4 |
The following transcripts of ENSDARG00000079782 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 23584490)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24624005 |
GRCz11 | 2 | 24279656 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGCAAAGCATAATTATCCAACTCCAAAAGAAACTCAAGGAGTTGCAGG[T/C]ACATTGACCATACGTGATGTTCTGTTCATCTTTGTAGTGTGCATTTTTAA
Long Flanking Sequence:
CATCAGCAGACACTGGATGACCTGCAGAGTGAGGAGGACAAAGTCAACACCCTCACCAAGGCAAAAGTAAAACTAGAGCAACAAGTGGATGATGTGAGTAAGCATTGTTTTTGACGTAGCATTCAGTTGTGATGAAGTAAACTACAGTACTACATTAAGAACTTCTGTTGCTAATTCTGTTAGCTTGAGGGATCTCTAGAGCAAGAAAAGAAAATCCGAATGGATCTAGAAAGAGCCAAGAGGAAACTTGAAGGAGATCTGAAGTTAACCCAGGAGAGCATAATGGACCTGGAGAATGACAAGCAGCAACTGGAAGAAAAACTGAAGAAGTAAGACACACTGCTTAATTATTATTGTTGTTTTACATGTTTTGAATGCCTTAAACGAATTCCATGATTTCAATTTCAGGAAAGACTTTGAAATCAGTCAGCTCAACAGTAAAATCGACGATGAGCAAAGCATAATTATCCAACTCCAAAAGAAACTCAAGGAGTTGCAGG[T/C]ACATTGACCATACGTGATGTTCTGTTCATCTTTGTAGTGTGCATTTTTAAGAAAAAATGTATCTTCTCCTTTATGCTAGGCGAGAGTTGAGGAGCTGGAGGAAGAGCTTGAGGCAGAAAGAGCTGCCAGAGCCAAAGTGGAGAAACAGAGAGCAGATTTAGCCAGAGAGCTGGAGGAGATCAGCGAGAGACTGGAGGAGGCTGGAGGAGCTACAGCTGCTCAGATTGAGATGAATAAGAAACGAGAGGCAGAGTTTCAGAAGCTCCGCAGAGACCTTGAAGAGGCCACTCTGCAGCATGAGGCCACTGCCGCCACACTCAGGAAAAAACAAGCCGACAGTGTGGCTGAACTTGGAGAGCAGATAGACAATCTGCAGAGGGTCAAGCAAAAACTGGAAAAGGAGAAAAGTGAACTTAGGCTGGAGTTGGATGATGTAGCCTCCAGCATGGAGCATATTGTGAAGTCCAAGGTGAATTGAATTGCTTGACTTTTTTAAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39820
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 |
---|---|---|---|---|---|
ENSDART00000078958 | Essential Splice Site | 1249 | 1943 | 24 | 37 |
ENSDART00000123064 | None | None | 638 | None | 17 |
ENSDART00000123565 | None | None | 242 | None | 8 |
ENSDART00000128784 | Essential Splice Site | 1242 | 1936 | 26 | 39 |
ENSDART00000137560 | None | None | 99 | None | 2 |
ENSDART00000141922 | None | None | 167 | None | 4 |
The following transcripts of ENSDARG00000079782 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 23584960)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24623535 |
GRCz11 | 2 | 24279186 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGTTGGATGATGTAGCCTCCAGCATGGAGCATATTGTGAAGTCCAAG[G/A]TGAATTGAATTGCTTGACTTTTTTAAAAGAACAACGAAATTACAATTCAA
Long Flanking Sequence:
AACTCCAAAAGAAACTCAAGGAGTTGCAGGTACATTGACCATACGTGATGTTCTGTTCATCTTTGTAGTGTGCATTTTTAAGAAAAAATGTATCTTCTCCTTTATGCTAGGCGAGAGTTGAGGAGCTGGAGGAAGAGCTTGAGGCAGAAAGAGCTGCCAGAGCCAAAGTGGAGAAACAGAGAGCAGATTTAGCCAGAGAGCTGGAGGAGATCAGCGAGAGACTGGAGGAGGCTGGAGGAGCTACAGCTGCTCAGATTGAGATGAATAAGAAACGAGAGGCAGAGTTTCAGAAGCTCCGCAGAGACCTTGAAGAGGCCACTCTGCAGCATGAGGCCACTGCCGCCACACTCAGGAAAAAACAAGCCGACAGTGTGGCTGAACTTGGAGAGCAGATAGACAATCTGCAGAGGGTCAAGCAAAAACTGGAAAAGGAGAAAAGTGAACTTAGGCTGGAGTTGGATGATGTAGCCTCCAGCATGGAGCATATTGTGAAGTCCAAG[G/A]TGAATTGAATTGCTTGACTTTTTTAAAAGAACAACGAAATTACAATTCAAAATGGTCTAAATTAATGCAACACTTACTTAAACAGACTAATATGGAGAAAGTTAACAGAACCCTTGAAGATCAAATGAATGAATACCGTAACAAATGTGAGGAATATCAAAGGTCCCTCAATGATTTTACAACTCAGAAGGCAAAGCTTCAGGCAGAAAATGGTAAATCAAGCATGTTGTTTTTGTTCAACTTTAAATCATTGAGAGAAATACAAGAAAAGAGTATTTGATTGTTTCTTTCACTACATTAGATGAATTTTCAAGACAATTAGAAGAAAAGGAATCATTAGTCTCCCAGCTAACAAGGGGTAAGAATTCCTTCAGTCAACAATTGGAGGACCTAAAAAGGCAGTTAGATGAGGAAATTAAGGTAACATACACTTTTCCTATATTTCTACCACTGTTTGACAGTCTACAACAAGGTAATCCAATATTTTCTTTTTTCCAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16260
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078958 | Nonsense | 1507 | 1943 | 29 | 37 |
ENSDART00000123064 | None | None | 638 | None | 17 |
ENSDART00000123565 | None | None | 242 | None | 8 |
ENSDART00000128784 | Nonsense | 1500 | 1936 | 31 | 39 |
ENSDART00000137560 | None | None | 99 | None | 2 |
ENSDART00000141922 | None | None | 167 | None | 4 |
The following transcripts of ENSDARG00000079782 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 23586853)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24621642 |
GRCz11 | 2 | 24277293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AKTTGAAGAACTCATATGAGGAATCTATRGATCACCTGGAAACCATGAAG[A/T]GAGAGAACAAGATTCTGCAAGGTTTCTATTTTATACACSTTTCCAWAAAC
Long Flanking Sequence:
GTGGATGTGGAGAGATCTAACACTGCTGCTGCTTCTTTAGACAAGAAACAAAGACACTTTGATAAAGTAAGTGAAAGTATAGTACTTAACATGACCAAAACTGTTTTAACGGTTCAAATTTTCTACTGCAATCTTCTACTCTTAGATGTTAAAGATTGTTTATCAGCATTGGTTTTGGGGAGAATGGTTAATATTTTTCATCGCACAGTTTAGTGGAAAAGTGTTCAATATGTTATTCATATATTCTTCAAACATCATTTTAAAATCTTTAGTTTTAAGAGTCTATAATCACCCTTTTTCACACTATTAATTTGAATAATTTAACCTCATTTCAACATTTACAATCTTTCTTTCAGATCATATCTGAATGGAAGCAGAAGTATGAGGAGTCTCAGTGTGAACTGGAGAGCTCTCAGAAGGAAGCCAGATCTTTGAGCACAGAGTTGTTCAAGTTGAAGAACTCATATGAGGAATCTATGGATCACCTGGAAACCATGAAG[A/T]GAGAGAACAAGATTCTGCAAGGTTTCTATTTTATACACGTTTCCATAAACTCAGAAGCATGTTTTTATTTTTGTATTAATAGTCTCAATAGGCTATCCTAACCTAATTCTATTTATCATTTAGAGGAGATCTCCGATCTGACTGAACAGCTTGGCGAAGGTGGAAAGACAATACATGAGCTGGAGAAAGTCCGTAAGCAGCTGGAGCAAGAAAAAGCTGAGATACAGGCGGCTCTGGAAGAGGCTGAGGTAGGAGGGTGCCCACAAAATAAATGAAAAAAGAGCAGGTATGACATGAGGAAACTAATTATGTGTATTACAGGGATCTTTGGAGCATGAGGAGGGTAAAATCCTGAGAACGCAGCTCGAATTTAACCAAATAAAGGCAGACATTGAGCGCAAGCTGAGTGAGAAAGATGAGGAAATGGAACAGGTGAAGAGAAACCAACAGAGGACCATAGACACCCTGCAAAGTGCTTTGGAGTCTGAAACCCGCAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39821
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 |
---|---|---|---|---|---|
ENSDART00000078958 | Nonsense | 1809 | 1943 | 33 | 37 |
ENSDART00000123064 | None | None | 638 | None | 17 |
ENSDART00000123565 | None | None | 242 | None | 8 |
ENSDART00000128784 | Nonsense | 1802 | 1936 | 35 | 39 |
ENSDART00000137560 | None | None | 99 | None | 2 |
ENSDART00000141922 | None | None | 167 | None | 4 |
The following transcripts of ENSDARG00000079782 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 23588105)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24620390 |
GRCz11 | 2 | 24276041 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATGGAGCAGACCATTAAGGACCTGCAGCATCGCCTGGATGAAGCAGAA[C/T]AAATCGCTATGAAGGGAGGAAAGAAACAAGTCCAGAAACTGGAGGCCAGG
Long Flanking Sequence:
CAAATGATGATCTGAAGGAGAACACTGCCATTGTGGAGAGACGTAATGCTCTGCTTCAGGCTGAGCTTGAAGAGCTCAGGGCTGTTTTGGAGCAAACAGAGCGTGGACGCAAACTTGCTGAGCAGGAGCTCCTGGACGTCACTGAGAGAGTACAGCTTCTGCATTCTCAGGTAAAACACAGAGTCATCATGGATGTTGTTAAAATGATTATTTGCAACCCCTTTAACAAAAATTGACAACATTATCTGATACAGAACACCAGTCTCATAAATCAAAAGAAGAAGCTGGAGACGGATTTATCCCAGTTTCAGACAGAAGTGGAAGAGGCAGTGCAAGAATGCAGGAATGCTGAGGAAAAAGCCAAGAAGGCCATCACTGATGCTGCCATGATGGCGGAGGAGCTGAAGAAGGAGCAGGATACAAGTGCTCACCTGGAGAGGATGAAGAAGAACATGGAGCAGACCATTAAGGACCTGCAGCATCGCCTGGATGAAGCAGAA[C/T]AAATCGCTATGAAGGGAGGAAAGAAACAAGTCCAGAAACTGGAGGCCAGGGTGAGATCAATATAAAGTTTTTGGGACTCTAATAATTTTAGAAGACATAAACAAAGCATTGGCTAATGTACTTCTAATGGATCAATCCTAGGTCAGAGAGCTGGAATGCGAAGTTGAGGCCGAACAGAAGAGAAGCAGCGAATCTGTGAAGGGAATCCGTAAATATGAACGCCGCATCAAGGAACTTACTTATCAGGTGGGATTAGAAGATTTAGATGTCATGGAGCATTGAAGAAACCTGGTAAAAATCTAAATAAATCATGTACACAGAATTAATCTTTAGTTATGAATCTTAGACTGAAGAGGACCGTAAAAACATAGCCCGTCTTCAGGATTTGGTTGACAAGCTGCAACTAAAAGTCAAAGCTTACAAAAGAGCTGCAGAGGAATCTGTAAGTGCTGTTACAATTCAGGTACAATACTAGAAAGTGGTGTTGTCTAAATTACAAT
Associated Phenotype:
Not determined