ZMP
inpp5f
Ensembl ID:
ZFIN ID:
Description:
Phosphatidylinositide phosphatase SAC2 [Source:UniProtKB/Swiss-Prot;Acc:A8E7C5]
Human Orthologue:
INPP5F
Human Description:
inositol polyphosphate-5-phosphatase F [Source:HGNC Symbol;Acc:17054]
Mouse Orthologue:
Inpp5f
Mouse Description:
inositol polyphosphate-5-phosphatase F Gene [Source:MGI Symbol;Acc:MGI:2141867]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22302 | Essential Splice Site | Available for shipment | Available now |
sa35491 | Nonsense | Available for shipment | Available now |
sa38941 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22303 | Essential Splice Site | Available for shipment | Available now |
sa18211 | Nonsense | Available for shipment | Available now |
sa9903 | Nonsense | Available for shipment | Available now |
sa8676 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22304 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22302
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087604 | Essential Splice Site | 33 | 1126 | 2 | 20 |
ENSDART00000140634 | Essential Splice Site | 33 | 1120 | 2 | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 25735269)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25380929 |
GRCz11 | 13 | 25511379 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTAGCTTAAATGTTTTGATCCTAAGTGACTCATATCCATCTTTCTTTC[A/G]GCAACCGACTTGTTGCTAGCATGGAACCCTGTCTGTCTGGGCCTTGTAGA
Long Flanking Sequence:
AAAAAAATAACAAAACATTTTAGCGGTTTTAAAACTATGATTTTTATAAAACCATATTATACCTTCAAACCAGTTATTGTCCATGCTTAGTTTAGACTACTTAATTGTTGCAATTATAAATAAGGAAAAAAAAAATGTTAAATGGCTATAATATAATATTATTATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATACACACTCAAAGTGAATGTGTATTTTCCAAAACATTATTAACACCAAATATTTAAAAACATAAAGAGTATTGGAGGGGAAAAGTAAGTCTAGACTCTTGAAAATGCACTATTATCTACACCTCATCCCCCAACCCCATGTTTTATCTTAATTACCAATAGATTCAGTGCACTATGATTCTGTTACTAGCTTAAATGTTTTGATCCTAAGTGACTCATATCCATCTTTCTTTC[A/G]GCAACCGACTTGTTGCTAGCATGGAACCCTGTCTGTCTGGGCCTTGTAGAGGGCATCATTGGAAAAATGCAGCTTCATGTTGGTAAGTCTGCTTTGTACTAAGGTAGGAAGGATGAGAGTAACATGTTAATGTTTGCAATGCATTCGGTGGTTCTGAATCTTGGAATAAAACAGATTTAGAGTCTAATGTAATTATTGTTAAAGTACCATTCTGAGCCTGATTTAATGTCAAATGTGATCATTTCCATTTGGTTCTACTGTAATTCAGTTTGTCGCAGGAAGAAACTGGGTACCAGAGACTCATAATGATTAACATAATGAAAAGCTGTTCCAGCACCAGAACAAAATGTCAGCATTATTTGGTTTATTATTGTTTTGTAATTGCTAAATATCTTTCAGAGCTTTGTTGTGAATGTGTCTTGTTGTAGGTTTACAGAAACCATTCAACTAAACAACTGCCCTTTAATGGATTAAAAAAGGAAACTCTTTAGGGATACAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35491
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087604 | Nonsense | 160 | 1126 | 5 | 20 |
ENSDART00000140634 | Nonsense | 154 | 1120 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 25740542)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25386202 |
GRCz11 | 13 | 25516652 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTCACTCCTATCCAGTATTCCCCTGCCTTTCAGGTCAAAGAGAATAAA[G/T]AGAAGGAGCGTCTGGAGAGGAGGCTGCTTGATGAGCTCTATAAGATATTC
Long Flanking Sequence:
CACCGGATGAAACCAAGTTCCTGATGAAGACCCTGAGTCAGATCAAATCCAATGTTGGCGCTCCCATCAAGAAAAAGGTTGATGTTTTTTTTTTTAATGCCTATAATTTTGAGACTAAATATTGCTGTTTCATCTTATCTGGTAGTTCCTTCACTTTAGGGCTAGTGTGCATAGAATACATTTTTGCATTTAAAAAATTAAGGAGCTAGGCCGTGACACATGGCCTATAGTCAATGTAAGAGACATTGCAAAGGATTGAGTGCTTCACAACAGTTTGTTTTTCCAATTTCAATAAAAAAAAATGTGCATCTTTATAGTATGTAGAAAAACTATGGACAATGTGTTCTGTGTAAGGCCCCTTAACATGGTTAATATAAAAGCTAACCATTCTGTTTCCTCCATGAAAGTAATTCTTATTTTTGGCATTGTCTCTTTTAACCTCGATTTGTTTGTTCACTCCTATCCAGTATTCCCCTGCCTTTCAGGTCAAAGAGAATAAA[G/T]AGAAGGAGCGTCTGGAGAGGAGGCTGCTTGATGAGCTCTATAAGATATTCATGGACTCGGATTCTTTTTACTATAGTCTGACCTATGACCTCACCAATACGGTCCAGCGACAGGGAGAGTTGGGCAAGTCAGATCAGCCCCTGTGGAAAAGGGTAAGAAGCCGACTCACAGCCGTACATGAAAAATTTCCATCTTTTAATTGTGTGGCATTTATTATTGTTTTAAAATGTATTTTAACTCAAAGTACATTTGAAACTAATTAAGATTTTGTTAGTCTGTTGCTCATTGAAAAGGTGATGGATTGCAATTTAATTGCAATATTATATAGATCAATAGGTCAAAGATAAGATAAGCCCCATTTCGGTGTTTGAATGAAGAAAAATGTACAAAATAAATGTTACACATTAAATGCAGGTAAAGTGCCTGCTTTAAATGGTCATGACACTCCACTCTTTTTGATTTAAGTCGACCTCAGAATTAAAAAAAAAAAGTTTCATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38941
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 |
---|---|---|---|---|---|
ENSDART00000087604 | Nonsense | 254 | 1126 | 7 | 20 |
ENSDART00000140634 | Nonsense | 248 | 1120 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 25742920)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25388580 |
GRCz11 | 13 | 25519030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCCTATCATCCAAGGCTTCGTGCAGGTGGAGGAGCTGGTGGTGAACTA[T/A]AATGAGAGCTCAGATGAAGAGCGAAGCAGCCCGGAGACGCCTCTGCAGGA
Long Flanking Sequence:
ACCCAGATGCTTGCGGCAACCCGAATTCAATTCCTGGCTTGAGGTTCTTTGCCCATCCTTCCCCTATCTCTACTTCCAACACTTTCATGTCTGTAAATCTCCACTGTCCTAATGAAGGTGAAAACCCCTAAATATATATTATTATAACAAAGTTTTAATAGTCTCCATTAATAAATACTATACAAAACTAAAGTAACACCTGTTCACCAGTATTGAAAGTTTATATCAGTGCTTTCATTTCATTGTGTTGTGGTGCTGATCCCCACTTGTTTTTCATGTTAGGTGGATGATAGATTCTTCTGGAACAAGCACATGATCAAAGACCTTGTAGACTTGCAGGTGAAAAACTTATTTGAATTTTAACAATTAACATTTTAACATGTGAAACGGACCTGAGTGGTTCTAATACAAGCTGTCTTTTTACAGGCGCCTCAGGTGGACTTTTGGGTGATTCCTATCATCCAAGGCTTCGTGCAGGTGGAGGAGCTGGTGGTGAACTA[T/A]AATGAGAGCTCAGATGAAGAGCGAAGCAGCCCGGAGACGCCTCTGCAGGAGCCCACCTGTGTGGACGACATTCACCCTCGCTTCACCGTGGCCCTCATCTCCAGGCGGAGCCGCCACCGTGCAGGTAGAGTGTATAATAATTTCTATTTGATAGGGATACACAGTACTGTCTGAATATTCTTTAGTTCAGTGATAATCTTGAAATGTGAATATTGGCATTGACCTGATAAATAAGATAATATAGGTGGGCGATTACGAACAAAATAAATTGTATCCAGATGATGTCAATGTTTTTAAGATATTCAATATATACTGCAATATGTTTGCTTTTGTTTTTAAATAATAAAAAGGATGATATTCTTGCGCCCTCATTAAAAAACAAACAAAAAATGTTTTCGAACAACTACTGTTAAAGACACTTAAAAACAAAATCTTTAGTAGTTATAAAAAATCTAGACCAGGGGTCACCAATCTCGGTCCTGGAGGGCCGGTGTCCTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22303
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087604 | Essential Splice Site | 296 | 1126 | 8 | 20 |
ENSDART00000140634 | Essential Splice Site | 290 | 1120 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 25745261)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25390921 |
GRCz11 | 13 | 25521371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACTCATCATGTTATCAGAGAAGTAACATCATCATGCATTTCCCACTGC[A/G]GGAATGCGCTACAAGAGGAGGGGGGTTGATACAGACGGACATGTGGCCAA
Long Flanking Sequence:
GTAAATGATGACAGAATTTAAATTTTTTGGTCAACTATCCCTTTGAATTTGCATTTGGTGGGCCAAATGAAAAATGAAATGGTGGGCCAAATTTGCCCTTCAGACCTTAAGTTTGCTCATTATCTAATGATTAGAATCTATGACTAAGACTAACCGATTCTTTGAGAATTAAATATCTGCTCACAATATTGCTTCCAAGCAACTGAAATATTAGGTTTACTTAAATACATAGCATTGCTATGAACTAGATTGATATTTAACCATTAATTGATGTCATAAAATCACAATTCTGATTTGCTTTAATGGTCAGAAGCTACAGGTTTTGGGGAATAAATATCAGTAGTCTGACTTTCCATTTAAACACTTAAAATAAAACTGAACAAAAACGATAACAGTATTTATATAAGGCACAAGCAGTTTTAAAAATCCAGTATTGTGCATCACTTACATCTACTCATCATGTTATCAGAGAAGTAACATCATCATGCATTTCCCACTGC[A/G]GGAATGCGCTACAAGAGGAGGGGGGTTGATACAGACGGACATGTGGCCAACTATGTAGAGACAGAGCAGTTAATCCACGTACACAGTCACACTCTGTCCTTTGTGCAAACGCGAGGCTCCGTGCCTGTGTTCTGGAGCCAGGCTGGGTACCGATACAACCCCAGACCTCGCATAGAGAAAGGTGGGTCGTATCTGTGTAATCCATTCTCTCCTGGAATAATAAATGAGATCAAACTCACTGATCAAGCAGTATATCACTTTGATGCATCAGCGTAGTTGTTGTGTGGAATGTTTTAGGCCTGTGAAAGGTGTCAGATGTGGAGCAGGTGTGTTTTCAGGCTTTTTTGGTTAAAAATAATGCTCCGAGAGGATTTTTGTGCTGGACTGTGGCTTCAATGCTGTGATCCACCTGGTGATATGATTTATCTCATCGATGTGCTTTCTTGCAGGAGAGAGGGAGACTATGCCTTACTTTGCCTCTCATTTTGAAAAGGAGGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18211
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087604 | Nonsense | 308 | 1126 | 8 | 20 |
ENSDART00000140634 | Nonsense | 302 | 1120 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 25745298)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25390958 |
GRCz11 | 13 | 25521408 |
KASP Assay ID:
2260-6440.1 (used for ordering genotyping assays)
KASP Sequence:
CMTTTCCCACTGCAGGAATGCGCTACAAGAGGAGGGGGGTTGATACAGAC[G/T]GAYATRTGGCCAACTATGTAGAGACAGAGCAGTTAATCCACGTACACAGT
Long Flanking Sequence:
TCCCTTTGAATTTGCATTTGGTGGGCCAAATGAAAAATGAAATGGTGGGCCAAATTTGCCCTTCAGACCTTAAGTTTGCTCATTATCTAATGATTAGAATCTATGACTAAGACTAACCGATTCTTTGAGAATTAAATATCTGCTCACAATATTGCTTCCAAGCAACTGAAATATTAGGTTTACTTAAATACATAGCATTGCTATGAACTAGATTGATATTTAACCATTAATTGATGTCATAAAATCACAATTCTGATTTGCTTTAATGGTCAGAAGCTACAGGTTTTGGGGAATAAATATCAGTAGTCTGACTTTCCATTTAAACACTTAAAATAAAACTGAACAAAAACGATAACAGTATTTATATAAGGCACAAGCAGTTTTAAAAATCCAGTATTGTGCATCACTTACATCTACTCATCATGTTATCAGAGAAGTAACATCATCATGCATTTCCCACTGCAGGAATGCGCTACAAGAGGAGGGGGGTTGATACAGAC[G/T]GACATGTGGCCAACTATGTAGAGACAGAGCAGTTAATCCACGTACACAGTCACACTCTGTCCTTTGTGCAAACGCGAGGCTCCGTGCCTGTGTTCTGGAGCCAGGCTGGGTACCGATACAACCCCAGACCTCGCATAGAGAAAGGTGGGTCGTATCTGTGTAATCCATTCTCTCCTGGAATAATAAATGAGATCAAACTCACTGATCAAGCAGTATATCACTTTGATGCATCAGCGTAGTTGTTGTGTGGAATGTTTTAGGCCTGTGAAAGGTGTCAGATGTGGAGCAGGTGTGTTTTCAGGCTTTTTTGGTTAAAAATAATGCTCCGAGAGGATTTTTGTGCTGGACTGTGGCTTCAATGCTGTGATCCACCTGGTGATATGATTTATCTCATCGATGTGCTTTCTTGCAGGAGAGAGGGAGACTATGCCTTACTTTGCCTCTCATTTTGAAAAGGAGGTTGAAACTTACAAAAAACTGGTAAGATGCGTTTAAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9903
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 |
---|---|---|---|---|---|
ENSDART00000087604 | Nonsense | 555 | 1126 | 14 | 20 |
ENSDART00000140634 | Nonsense | 549 | 1120 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 25749650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25395310 |
GRCz11 | 13 | 25525760 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTTAGCRGGGGTGAWGAAGGATGGTGTGAATTCAGCTAACCGTTACTA[T/A]CTGAACCGCTTCAGGGACGCCTAYCGACAGGCCGTCATYGGTGAGCATAA
Long Flanking Sequence:
TATTAAAATCATGTAAATATTATAGAAATAATTTCTTTACTTTATTTTAATTTCTGTGTTTATTATGATTACTGAGTTTATAATGAATTAAAATTGTTTAAAAAAATAAATGGAATTTTTATTTGATTTAATTAGTTTTTGAGTATGAATGTATTTATGTATGTAGGGTTGGGTCGATAGGCGACGCGATCCTCCTCCCTGCCCCCATCGCAGCAGCAACCCGCTCACGAAAAATACACACTTAAACCCCTTTTACACAAATATGTCATCGTTTTACATGGTAGACTTTTAATTAAGTATTGTCTCAATCGCATTAAAATGGGTTTGGTGTCCATGTCAACGTACTCACTGTCACTGTAATGTCATTTTCATTTGAGATTTAGCCCTGTCAGCTTACTCTGCTGTGTGCGATCTGTTGTTTAGGGAGATTTCACACGAACAGGCGAGCGAAAGTTAGCGGGGGTGATGAAGGATGGTGTGAATTCAGCTAACCGTTACTA[T/A]CTGAACCGCTTCAGGGACGCCTACCGACAGGCCGTCATCGGTGAGCATAATTAGACTCCATGTTATGAACTCTTTGACTCCATGTTAGCCTCACTTTGCTAAGAGCCAAGCTTGCCGCCTCATCGGTCATATGCTGTTATCTCTGGTTCTCCCAGACCTCATGATGGGCCATCCCGTAACAGAAGACCTGTACTCCATCTTCAGCAAAGAGAAGGAGCATGAGGAGAAGGAGAAGGAGAGCCAAAGAGGAGCTCAGGAGCAGGTCAGTCTTCTGCTGCAGACCTACATGCAACTGCTACTTCCTGATGATGAGAAGTTTCACGGCGGATGGGCTCTAATCGACTGTGACCCCAGGTGAGAGCACTACACGTTAAGCAGTGCTTCAGACAGTCGATTTTATGTGCTGTGTATAAAGGGGCTGTTCACACAATTTTGAGTTTAAAATTACATGGAAGATGATGGGCGGTGGTATAAAACTGTGTTCCAGTTTTGATTTCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8676
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 |
---|---|---|---|---|---|
ENSDART00000087604 | Essential Splice Site | 635 | 1126 | 16 | 20 |
ENSDART00000140634 | Essential Splice Site | 629 | 1120 | 16 | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 25753258)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25398918 |
GRCz11 | 13 | 25529368 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTAAGGATTTTGACCTTTGAATATGCTGTTTTTCTCTCCATCTTTTTA[G/A]TCTTATAGATGCTACTCACAAAGATGTCGACGTTCTTCTGCTGCTCTCCA
Long Flanking Sequence:
AATAATAAAGCTTGATTTTAATAAATGATATTTTTAGTGTACTCTTTCTTCTACAGATTTTTGTCAATGGCACAGAGGTACTGGTACACATTGTATTTTCCCTCTATTTAATTGTAATTGTTTGGGTGAGGGAGTCAAATTTTCTTAAACCTTTTGAGCATTTTTGGTGGTAGGTCATGGTGATAGATGCCTAAAGCCTGGTACTGGTGGGGCTGGAGTCTAGAATCTTGCAAATGCACACTTTGCTAAGTAATCTCTGATGATAATATGTGTTGCATATTTGGGTTAACAAATCTTCAAATAGGATGTAATGACACCGTCAATTAAGCATCAATTGTTATGGACAGATGATGAATTGCATCATTGTGAAATTCCTTGCATTGAGTTTTTTTCCTGTGTTTCTCTTTCTCTGATATGGCCAGGGTTTAATGGTGCCTTTTATGAGCCTCCCTTTAAGGATTTTGACCTTTGAATATGCTGTTTTTCTCTCCATCTTTTTA[G/A]TCTTATAGATGCTACTCACAAAGATGTCGACGTTCTTCTGCTGCTCTCCAACTCTGCATATTATGTAGCCTAGTAAGTCCATTTTCTCTTCATGTTTGTGTCCTTTTTTCTTGGCATTGCTTCAGTAATGTCAATTTACTTTTACTGTTTAGTTACGATGAGGAGGCGGACAAAGTCAACCAGTACCAGAGACTCAGTTTAGAAGGACTCGAAAAGATTGAAATTGGTAAGATCTGTTGATGAAGGCGTAATTAAAATGTTCTGTGAGATCATGACAGTTTGCCAATATTGGTGTTTTTAGGTCCAGAACCAACTCTATTTGGAAAGCCTAAATACTGCTGCATGCGGCTGCACTATAAGAATGGGGAGACGAGTGGTTACTTTCATACACTGAGATCTGTCACACGAAATCCAGAGGACGATGGGAAAGGTTTGTACCGAGGAGCCATGATTTGGTGTGGCACTAGTTCAAGTTTTGTATTGTGTAATTCAGTGATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22304
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087604 | Essential Splice Site | 727 | 1126 | 19 | 20 |
ENSDART00000140634 | Essential Splice Site | 721 | 1120 | 19 | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 25753885)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25399545 |
GRCz11 | 13 | 25529995 |
KASP Assay ID:
2260-6443.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATAAATAATTGATTCTTTCCTCTCCACTTGTTGGATTGTTTCCATTTCA[G/A]ACACACTCCAGTGCATTGCTGAAATGCTTCGAATTACAAAGCAAGCTATG
Long Flanking Sequence:
AATGTCAATTTACTTTTACTGTTTAGTTACGATGAGGAGGCGGACAAAGTCAACCAGTACCAGAGACTCAGTTTAGAAGGACTCGAAAAGATTGAAATTGGTAAGATCTGTTGATGAAGGCGTAATTAAAATGTTCTGTGAGATCATGACAGTTTGCCAATATTGGTGTTTTTAGGTCCAGAACCAACTCTATTTGGAAAGCCTAAATACTGCTGCATGCGGCTGCACTATAAGAATGGGGAGACGAGTGGTTACTTTCATACACTGAGATCTGTCACACGAAATCCAGAGGACGATGGGAAAGGTTTGTACCGAGGAGCCATGATTTGGTGTGGCACTAGTTCAAGTTTTGTATTGTGTAATTCAGTGATTGACTTCATGGGTTAAGTTGGTAAAAGATATAACTTGGCTCTGTGGATGCTGGTGTTGCTTGAATAAGTTTTGTGTTGTGATAAATAATTGATTCTTTCCTCTCCACTTGTTGGATTGTTTCCATTTCA[G/A]ACACACTCCAGTGCATTGCTGAAATGCTTCGAATTACAAAGCAAGCTATGGGGCTTGATGTTCAGGTCGTTGAGAAGAAACTAGAGAGGTAAAAAAAAACTATTCTTCGTACATTTATTTAAACTTTCTGAATAAAAAATGTTTTACCTGATTTGTAAAGATCTGTTTGTATTTTTGGGGAAAATCATGTGCACAAAACTCATGCTTGTTCATATTTTCACTGCCTGAACGATTGATGATTGATAAAAGAAAAAAACTCACTTTTACCAATATCTCAGATTAGATGCATCAATATATGAATAATATATGAATAAAATGAAGAGTGATGAAGCCAATTATGAGAATGGACAGGGGCCAGTGGGCAAATTTGGCCAGGATGCCAGGTTAAACCCCTACTCTTTTCGAAGGACATCCAGTTTAACGTCTCATCCTAAAGATGGTGCTCACTGACAGTATAGTGTCCCCTTCACTATACTGGGGCGTTAGGACCCACACAGACC
Associated Phenotype:
Not determined