ZMP
mlphb
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8JI93]
Human Orthologue:
MLPH
Human Description:
melanophilin [Source:HGNC Symbol;Acc:29643]
Mouse Orthologue:
Mlph
Mouse Description:
melanophilin Gene [Source:MGI Symbol;Acc:MGI:2176380]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41417 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14687 | Essential Splice Site | Available for shipment | Available now |
sa41418 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41419 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21486 | Nonsense | Available for shipment | Available now |
sa30918 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10656 | Nonsense | Available for shipment | Available now |
sa25426 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41417
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 |
---|---|---|---|---|---|
ENSDART00000090417 | Nonsense | 65 | 579 | 2 | 13 |
ENSDART00000139725 | None | None | 135 | None | 4 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 25046075)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24201861 |
GRCz11 | 9 | 24012730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAAGACTAAAATTATGAAAGAGGACAACAAGAGAGAGCTGCTGGAATA[T/A]CAGCCTAAACTCAGTGATTCACTCTGCATTCGCTGTCTCCAACCCTTCAA
Long Flanking Sequence:
CAGCTGTGCTACAGAGATGTCATTGTCCTAGTATTCCATTGGATTTGAACGTAAAGCATGAGAAATTGGCACATTAAGAATGGAGGTTTTCATAGGAAGAATAGAGAGAAAGTCCAGGCAGAATGTGGAGTCATTTCCTCTCTTTTTATTCTGTCTAAAGCAATCTGGACATATCTGTTCAAAAGAAATTTGATCTAATTGAATTAAATCTAGAAAATTAGTTGGAATGAGGTGAAGGGATTTAGCAAGCTGTCATGCAGAATAAAGTATTTATTTGCTTTGTGATTAATAATAAACAGTCAATATCCTAGCAATATGCATGTAATAAGCATATTGAGTATGTTGCTGAATCTATGTGTTACAGATGTTTCTTTGTCAGTGTATTGTTCTAAATATGGATTTAGGTTTAATCTAGATTTAATGTTTAATGTTTATTATTAATACAGGGAACTCAAGACTAAAATTATGAAAGAGGACAACAAGAGAGAGCTGCTGGAATA[T/A]CAGCCTAAACTCAGTGATTCACTCTGCATTCGCTGTCTCCAACCCTTCAAATTCTTGGTCAACAGCAAGCGCCAATGTTTGGACTGCAAACTGTTTGTCTGCAAGTCCTGCAGTCGTTTTAACAAGAAAGACAGCGGTTGGGTGTGTGATCCATGCCACATGGCCAGGTGAGCACCTGACAGACATTGTATTCCTCCATGAAGAAAGAACAAACAGGAGAACAATAGAATTTTTTTTAAGCAAATTATTCCCCCAAAAAAGAAAAGGACAATTTTGGTAACAATAGATTATTTTTGTTTTACAATTCACCTAATATTTACTGCATAAGTTTCAATAATGAGTCTGTTTAACTTTTTAAATGTTTTGAATACCTTTTATTTATTATTCATCTTCATTTCAGCCGAATTACTACCATAAATTAACCTAAAAATGCATTTCCACCTTTTCACTCTACTGCTAATGAAACATTGTGGGACTCTGAGAATATATTAAACATTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14687
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 |
---|---|---|---|---|---|
ENSDART00000090417 | Essential Splice Site | 182 | 579 | 4 | 13 |
ENSDART00000139725 | None | None | 135 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 25049463)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24205249 |
GRCz11 | 9 | 24016118 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCACAGAGCCTCGAGACGATGACACGCACAGCATGCCTGAAGTTCACAG[T/C]GAGTAAAACAAAGTCCCATTCCTTTGTGATAWCAGACAATATTAATGTTG
Long Flanking Sequence:
TAGAATAACAACAATCAGAACAAAAATATTAATTTCTTAATTATATAATGTTCACTGTACAGATGAGTGGAAAATACTAACATAGCTTGTTGAATAGAAATGTTGGCACAGGGTTGTCATGGTTAACTAAAGCTACAATAGTTTTTTGCTTCTTAAAATAAATGTCAAGTGTGCATTTTTCACATAATTGTGTACAATGGCAATGGAATGACAATTAAAAGCAGAAGGTGACTTATGTGGAAAACACTAATTTTCTCAACAAAGTGACCCAGCAAAACCCCAGTAGCTTTTGATGTTTTCTGTTAGTAGCGCAACACAGAAAACTGAAAGAAAACACTATAAATCTGCTGCTTTCAACAGTTTCAACAGCTTCCTGTAGCCAATCACAGTTTGTTATCTGTTTCTTGTTGTTTTATGTTTAATTTTTCATCTGCCGCTGTTCTTCTCCGTCCCACAGAGCCTCGAGACGATGACACGCACAGCATGCCTGAAGTTCACAG[T/C]GAGTAAAACAAAGTCCCATTCCTTTGTGATAACAGACAATATTAATGTTGATGTCATGCAAGAATCTAAAGTAATCAGTGAATGTCTTTCATCTGTCCAAACAAGACAGCAGCAATCTGCTCTCACGTCATCTTTAATTTAATAAGGCAGAGAACAAAATGTCTGTGGAAGAAAAACACCTCGAATAGCCAGGATAAAAACTGAATATCCTTTTCTAGGCATAAACACTTAAGGTATTTTTTGTTGTCCTGGTTAAATTTAAAAATATATAATAACAATAAAAAACAGTAGTTCAGTTTTGCACCTGCCCTGTGTATATACTGTATTTCAAACGTAGTCAGTATACAAAACGTACTTAAAATAATACTGTGTAGGAAAAAACATTCATTTTCTATTCAGCTTAGTCCCTTTATTAATCAGACATCCCCACAGTGGAATGAACTTGCGACTCATCCAGTATATGTTTTACACAGTAGATGCCCTTCCAGCTGCAACTCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41418
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090417 | Nonsense | 286 | 579 | 7 | 13 |
ENSDART00000139725 | None | None | 135 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 25052484)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24208270 |
GRCz11 | 9 | 24019139 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGCAATGAGATTAAGGATATAATGCATATCAGCCAAAAGAGTCTGGAC[A/T]AAGCCTCTCATTTTGGTAAGATCTGCTCTCTGCATTTATTTCCTTTACCA
Long Flanking Sequence:
AGAATGCTCAGACTGTTAACAGTGATAAGACTTCTCTTGAAATCTTGATTGTTCCGTCACTGATAGAAATAATCAAAAAAAAAATTAGTCATGCCCAAGATAGAGTGACAGTATTTCGGTTTGATTGATTTGGGTTAGTTTGAGCCTCAGAATTTCAGCAAGGAATGAATCCAATGTATTTAAAATTAGGCAGACAAAATATTAGCTTAACAACAATGTTTGTTTTGATTTCTTCACACTAAATAATCTTTAAAAAAAACTGTCACAATGCATGGAGTGAAAGAAATAATTGTATTAATTAAGATTTAATGAATTTTAAAAGGCTGTTGTTTAATTATACCTTTAAGCATTCAGGTAGCCAGGAGAAAATAACCCAGACTAAGGACTCACTAGCAGAAGATGACTGGTCAACAACTGTTAAGCAGATACTAGAGAATGGAACTCATGGCAGAGGCAATGAGATTAAGGATATAATGCATATCAGCCAAAAGAGTCTGGAC[A/T]AAGCCTCTCATTTTGGTAAGATCTGCTCTCTGCATTTATTTCCTTTACCAACACTTAAAGAAACATATTAGAAAAAAATTCTGAAAACAAATAAATGTATGCTAGACTAGTTGAATAGACTCCGAATTTCCTTTTGTTATTTTCATAATAAAATAACACTTTACGTTGACAGAAGCCCTTTATTTTACACATTCTGTTAAATATATTTAACTGTAAGTATGTTAACTTATAGTAACTCTAACCCTATAGTTTGTCTAATAATAAGCTAATACTTTAATGCCAGTTATTGTAGGTGAACTTCAGTTGCAAAGTTACTTGTAAGTCAACAGAATGTCTGTCAAGATAAAGCGTAACCAACTTTTGTCTTTTGTTTGCTCTTTGTAGATGACTGCACACCCCACCTAAACCAGAGGTTGGCAAAGTCATGTTCCCTCTCCAAAATGAGCCTCTCTTCAGCTGGCAGCACCAACTATCACCTCCAGCGCGAGCTTTCTTACAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41419
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090417 | Essential Splice Site | 291 | 579 | 7 | 13 |
ENSDART00000139725 | None | None | 135 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 25052501)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24208287 |
GRCz11 | 9 | 24019156 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATATAATGCATATCAGCCAAAAGAGTCTGGACAAAGCCTCTCATTTTGG[T/G]AAGATCTGCTCTCTGCATTTATTTCCTTTACCAACACTTAAAGAAACATA
Long Flanking Sequence:
AACAGTGATAAGACTTCTCTTGAAATCTTGATTGTTCCGTCACTGATAGAAATAATCAAAAAAAAAATTAGTCATGCCCAAGATAGAGTGACAGTATTTCGGTTTGATTGATTTGGGTTAGTTTGAGCCTCAGAATTTCAGCAAGGAATGAATCCAATGTATTTAAAATTAGGCAGACAAAATATTAGCTTAACAACAATGTTTGTTTTGATTTCTTCACACTAAATAATCTTTAAAAAAAACTGTCACAATGCATGGAGTGAAAGAAATAATTGTATTAATTAAGATTTAATGAATTTTAAAAGGCTGTTGTTTAATTATACCTTTAAGCATTCAGGTAGCCAGGAGAAAATAACCCAGACTAAGGACTCACTAGCAGAAGATGACTGGTCAACAACTGTTAAGCAGATACTAGAGAATGGAACTCATGGCAGAGGCAATGAGATTAAGGATATAATGCATATCAGCCAAAAGAGTCTGGACAAAGCCTCTCATTTTGG[T/G]AAGATCTGCTCTCTGCATTTATTTCCTTTACCAACACTTAAAGAAACATATTAGAAAAAAATTCTGAAAACAAATAAATGTATGCTAGACTAGTTGAATAGACTCCGAATTTCCTTTTGTTATTTTCATAATAAAATAACACTTTACGTTGACAGAAGCCCTTTATTTTACACATTCTGTTAAATATATTTAACTGTAAGTATGTTAACTTATAGTAACTCTAACCCTATAGTTTGTCTAATAATAAGCTAATACTTTAATGCCAGTTATTGTAGGTGAACTTCAGTTGCAAAGTTACTTGTAAGTCAACAGAATGTCTGTCAAGATAAAGCGTAACCAACTTTTGTCTTTTGTTTGCTCTTTGTAGATGACTGCACACCCCACCTAAACCAGAGGTTGGCAAAGTCATGTTCCCTCTCCAAAATGAGCCTCTCTTCAGCTGGCAGCACCAACTATCACCTCCAGCGCGAGCTTTCTTACAGCCTGGATGACTCCGATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21486
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 |
---|---|---|---|---|---|
ENSDART00000090417 | Nonsense | 396 | 579 | 9 | 13 |
ENSDART00000139725 | None | None | 135 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 25053289)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24209075 |
GRCz11 | 9 | 24019944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTCTGAGCCGTTTGGAGCAGAAAATGACTTTGCCAATAATTGGGGGAT[C/A]AGTTGAACAGGTAAGTTAAACAGTTGTGCTGCCTAATATTTCTGTAAAAA
Long Flanking Sequence:
TGCAAAGTTACTTGTAAGTCAACAGAATGTCTGTCAAGATAAAGCGTAACCAACTTTTGTCTTTTGTTTGCTCTTTGTAGATGACTGCACACCCCACCTAAACCAGAGGTTGGCAAAGTCATGTTCCCTCTCCAAAATGAGCCTCTCTTCAGCTGGCAGCACCAACTATCACCTCCAGCGCGAGCTTTCTTACAGCCTGGATGACTCCGATGATGATGAGGATGATGATGAAGAAGAATCAGAGATGAATGTTATATACAGTCATGCCCTACATAGGGAGCCCTCACCAGATGAGGTTCCTCCACAGGTGCAGTCATACTTCTAATAATGGGGCTTCACGGCTTTCTTTCCCAAAATGTTCAGGTGTTTTTGAAAATGCAACAAAAACATTTATGCATCTCTATGACTTCAGATTATTGAGCTCAACAAGCGTATGTCAGCAATTGAATCTATTCTGAGCCGTTTGGAGCAGAAAATGACTTTGCCAATAATTGGGGGAT[C/A]AGTTGAACAGGTAAGTTAAACAGTTGTGCTGCCTAATATTTCTGTAAAAAAAAAAAACCTACCTTTTCTGGCTTAATTGGCCTTTAACTCAGGCATGGGATGAAAACCGTTTTCAAGGTACACTGCAGTTTGGAAAAGTCAAGGTTTTAAAACCACCAAAATTTTCTGTAATACCATTCCTAAGGTATGTGTAAGATTTTTTTTATTTACTTTTTTTTTGTTTGTTTGTTTTTTAGGACAACAGTATCTCCAGCAGAAAAGATTTCTAAAGATGCCATTTTAAATTGTTTAAATCTGTGTTTTTTGAAACTAACGAAGACAGCAAAAGTCAATGATTCATTTTCATTATTTTGCCTGACACATTTACTGTTCCAAAATATTTTAAATCTTTCAAAAAATAAAATAAATTGATTTCAAAGGGGGGGAAATCTTTGTTTTTACCCAAACATTTTACCCAAAATGATATATTTTAGAGCAGTAATCACAATACTGTGATACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30918
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 |
---|---|---|---|---|---|
ENSDART00000090417 | Essential Splice Site | 399 | 579 | 9 | 13 |
ENSDART00000139725 | None | None | 135 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 25053300)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24209086 |
GRCz11 | 9 | 24019955 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGGAGCAGAAAATGACTTTGCCAATAATTGGGGGATCAGTTGAACAG[G/A]TAAGTTAAACAGTTGTGCTGCCTAATATTTCTGTAAAAAAAAAAAACCTA
Long Flanking Sequence:
TTGTAAGTCAACAGAATGTCTGTCAAGATAAAGCGTAACCAACTTTTGTCTTTTGTTTGCTCTTTGTAGATGACTGCACACCCCACCTAAACCAGAGGTTGGCAAAGTCATGTTCCCTCTCCAAAATGAGCCTCTCTTCAGCTGGCAGCACCAACTATCACCTCCAGCGCGAGCTTTCTTACAGCCTGGATGACTCCGATGATGATGAGGATGATGATGAAGAAGAATCAGAGATGAATGTTATATACAGTCATGCCCTACATAGGGAGCCCTCACCAGATGAGGTTCCTCCACAGGTGCAGTCATACTTCTAATAATGGGGCTTCACGGCTTTCTTTCCCAAAATGTTCAGGTGTTTTTGAAAATGCAACAAAAACATTTATGCATCTCTATGACTTCAGATTATTGAGCTCAACAAGCGTATGTCAGCAATTGAATCTATTCTGAGCCGTTTGGAGCAGAAAATGACTTTGCCAATAATTGGGGGATCAGTTGAACAG[G/A]TAAGTTAAACAGTTGTGCTGCCTAATATTTCTGTAAAAAAAAAAAACCTACCTTTTCTGGCTTAATTGGCCTTTAACTCAGGCATGGGATGAAAACCGTTTTCAAGGTACACTGCAGTTTGGAAAAGTCAAGGTTTTAAAACCACCAAAATTTTCTGTAATACCATTCCTAAGGTATGTGTAAGATTTTTTTTATTTACTTTTTTTTTGTTTGTTTGTTTTTTAGGACAACAGTATCTCCAGCAGAAAAGATTTCTAAAGATGCCATTTTAAATTGTTTAAATCTGTGTTTTTTGAAACTAACGAAGACAGCAAAAGTCAATGATTCATTTTCATTATTTTGCCTGACACATTTACTGTTCCAAAATATTTTAAATCTTTCAAAAAATAAAATAAATTGATTTCAAAGGGGGGGAAATCTTTGTTTTTACCCAAACATTTTACCCAAAATGATATATTTTAGAGCAGTAATCACAATACTGTGATACCTTGAAATTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10656
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 |
---|---|---|---|---|---|
ENSDART00000090417 | Nonsense | 487 | 579 | 11 | 13 |
ENSDART00000139725 | Nonsense | 43 | 135 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 25054356)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24210142 |
GRCz11 | 9 | 24021011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTTCAATTGTATACTCCAGAAARCAAAGCCGAATGCACACAAATCAT[T/A]AAAAAAGCAGAAGAGGGTGAGTTCCTTTGAGTTTAGTAACACAACTAGCT
Long Flanking Sequence:
ATGCCTATAACTTAACTACAGGACACAGTTTATTCAAATATCACACAGAGACTCTCCTGACTCCCTGTAGGTTGAGCAGAAAGCTGAGGATTTGTCTCCAGCTGATTTAGAGGAGCTTGAGCTTAGGAAAAAGCTTGATGAACTCACTGAAAAAATAAGCGACAAAGGCTTTTCATCTGATGAGGAAGATGCAATTAAATCACCAATGGCCTCTCCAAAGAAAAGTGCAGTTTACCAAGTTTCACCTATAAGAGGAGCTTCAGCTGGACTTGTCCGACCTGACTGGCCTCTTGAGGCTGAATGGGTGAGAGTACTCTGTGTACACATTTAACATACATCACTATACATGCTTAGACCTATTAAACGTGACATTTTATTTATATTCCCTTACCAATACTTCATGTTAATGGTGTGTGATTTTACCACCTTACTGTCCTGAATGATCTGCTATGTTTTCAATTGTATACTCCAGAAAGCAAAGCCGAATGCACACAAATCAT[T/A]AAAAAAGCAGAAGAGGGTGAGTTCCTTTGAGTTTAGTAACACAACTAGCTGTGAGCTGTCACAGCTGGAGGGTAAAGTTGCAATGGCAGCAGCCAGCGTCCAGAGCACTCAAAGTGGGGTACGTCACTTTAGTCCATATTCTTTCTTTTAACACTAACAAAATCTGTATTCTGTATTAATATGGAATCTTGACCTTTCTACCAAAAGTAAAAAAGTAGAAAAAAGTGACTTTTATTAACATTTTTAATAGTTTAAGGTGATATATTGCTTGGGTTGGTGTTGTGCAAAAACCTTGTAATAAACTGCAATTAAATGTTTTGTTATTTTACAGATTTTTTCTCTACATATTGCTTGTAGATTATTTCAAATTGTAAATGAAAAAAATATGAAAACTGTTAATTAACAGACATTTTAACAGTATTTAACAGATGTAAAAGTTGCATGTGTGACTTGAACTACTTTAGCTGACTTTCAAAAAACCTCCCAGTCTGTGAGCTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25426
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090417 | Nonsense | 532 | 579 | 12 | 13 |
ENSDART00000139725 | Nonsense | 88 | 135 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 25055267)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 24211053 |
GRCz11 | 9 | 24021922 |
KASP Assay ID:
554-7344.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTGTTCATGGTTACTGTTTGCTTTATGTGAAGGTTACAGACATTCAG[A/T]AACGAATCGCTGCTTTGAGTGCAGCAGGGATGACAGTGGAGACATCCCGC
Long Flanking Sequence:
TTTAACAGTATTTAACAGATGTAAAAGTTGCATGTGTGACTTGAACTACTTTAGCTGACTTTCAAAAAACCTCCCAGTCTGTGAGCTCAACATACTGATAAACTTCAGCCAGATGTGATTTGATCTAGATTCCACTGATCACAGAGTAAACTACCTTATGTGCAACACATATTTTTAACATTAGATATTAAGTTTTGCACTTCATTAACTGTTTCAAACTGAACAGGATATGCACAGGTGGCAACTCTGAACCAGATTATGGTTTCACAGTCTTAAAAAAAACAACTAGAAAAAGCTCCAGATGTTTGAGTTTACATGTACACTAGCGCAGATGTGTCAAGTGTATGTGTTCGTTGTACATGGTATTAAATTAAGTAAACTTCGTTTGCAAGGATGTGCAACTTCATCTGTGACCATATACAAAAAGAACTGAACTATACTTTAACTACCTGTCTGTTCATGGTTACTGTTTGCTTTATGTGAAGGTTACAGACATTCAG[A/T]AACGAATCGCTGCTTTGAGTGCAGCAGGGATGACAGTGGAGACATCCCGCAGACGGGTATGTAGAGATGCACATACTCGCACATTCCTATTTTTCCAGAACAGGATCAAGCACAAAGCCATTTACATATAAAATATATTTTTGACCAAACATGAGCCAGCCAATCATAAATTCTGTTATGTTTATAACAGCTGTTTGCAGCAAATTCAGACAAAGGCTAAATATATTTTTCTGTTCTTCCCTTTTTCATTTAGACTCCTCAGCCATCGAGGATGTTGCATGCATTTCCAATTAGTAAGAGCAAAGTTTTACACTGCATTTTCAAGAACATGTAATCTGTTATCAGTGCTGGGTAGATTACTTACAAACTGTAGTCTGTTACTGATTACAAATTACATGTTGAAAATTGTAGTTAGTTACATAATCGTTTAGGTTATTACTTTTAGATTTTTTCTTCTATTTTATTTTATTATTTTATTAAAATACTTTGACCTAACTTGT
Associated Phenotype:
Not determined