ZMP
slc17a9a
Ensembl ID:
ZFIN ID:
Human Orthologue:
SLC17A9
Human Description:
solute carrier family 17, member 9 [Source:HGNC Symbol;Acc:16192]
Mouse Orthologue:
Slc17a9
Mouse Description:
solute carrier family 17, member 9 Gene [Source:MGI Symbol;Acc:MGI:1919107]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34387 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21280 | Essential Splice Site | Available for shipment | Available now |
sa31653 | Essential Splice Site | Available for shipment | Available now |
sa34388 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34389 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34387
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036801 | Nonsense | 62 | 458 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 24007547)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23133365 |
GRCz11 | 8 | 23154604 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCGGACATGGACCCTGATGCTACTGCTGGTCACATGTGTTCTCCATTG[G/A]TCACGGATGGCCATGCCGATCTGTGCCGTCACCATGGCTAGAGAATTTGA
Long Flanking Sequence:
ATATTTATTAAAATAATATTTTATTAAATTCAAAACATTTAGAATTTTAAAGAGAATACAATTAAATTCAAGCTAAATATTGCACAAAAAAATTACAACCTACAAAATTTCAACAAATTTTTTTTCATTTTTTTGCTTTTCTTGATTTTTCCTATTTTTTTTATTTGTATTTAATGTTTTTCTATAACATACATTTGGTTGTACTAGTTTTTGAACCGTTATCGTAAGTTATTTTGTTAGATATGCTCCAGATTTGCTTCAGTACTGTCTAATCTAATGTATATGCACAAATATAATATTGTACAGCTTTCTATAAAAATATGAATTTTAAAGATAGATTTGTGTAGGATGTACTTGTATATGGTGAGCACTGCACCTATGAACATTTGAGATACAGCAAGCCTATTAGGCACTGTTATAATTGTAATGTCCATCTGCTGCAGGCCACTGGCCCGGACATGGACCCTGATGCTACTGCTGGTCACATGTGTTCTCCATTG[G/A]TCACGGATGGCCATGCCGATCTGTGCCGTCACCATGGCTAGAGAATTTGAATGGAGCAAGACAGAGACTGGCATGGTGCTGGGGGCTTTTTTCTGGGGCTACTGTTTCACTCAGGTGGTTGGGGGTCACGCCAGTGACAGGTAAGTGTTTAGGTCAAAGTCTGAGGCTCTAGATGATGTAGATTCTGATTATGAAGTTTTTTTTTTTTCAGGATTGGAGGAGAACGAGTGCTGCTTCTTTCCACCTCCTCATGGGGCATAATGACAGCTCTGACCCCAATACTGGCAAAGACTGGACTCTCACCTCTTCTTACAATGACAGCGTCCAGGTTTCTATTGGGTGTAATGCAAGGTGAAGACTTTAGGAGGCACAGGAGAGGAAAAAGTGTATAAAGAAAGAAAGATATTTGACAGTATACAGAATGAATCTAAGAAATGTGTCAGCATGTTTGAACTAGTCATTTCCCTTCTAATAAGCCTGTGGGATCAGATGCTGGGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21280
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036801 | Essential Splice Site | 109 | 458 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 24007757)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23133575 |
GRCz11 | 8 | 23154814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGAGGCTCTAGATGATGTAGATTCTGATTATGAAGTTTTTTTTTTTTC[A/T]GGATTGGAGGAGAACGAGTGCTGCTTCTTTCCACCTCCTCATGGGGCATA
Long Flanking Sequence:
TTGAACCGTTATCGTAAGTTATTTTGTTAGATATGCTCCAGATTTGCTTCAGTACTGTCTAATCTAATGTATATGCACAAATATAATATTGTACAGCTTTCTATAAAAATATGAATTTTAAAGATAGATTTGTGTAGGATGTACTTGTATATGGTGAGCACTGCACCTATGAACATTTGAGATACAGCAAGCCTATTAGGCACTGTTATAATTGTAATGTCCATCTGCTGCAGGCCACTGGCCCGGACATGGACCCTGATGCTACTGCTGGTCACATGTGTTCTCCATTGGTCACGGATGGCCATGCCGATCTGTGCCGTCACCATGGCTAGAGAATTTGAATGGAGCAAGACAGAGACTGGCATGGTGCTGGGGGCTTTTTTCTGGGGCTACTGTTTCACTCAGGTGGTTGGGGGTCACGCCAGTGACAGGTAAGTGTTTAGGTCAAAGTCTGAGGCTCTAGATGATGTAGATTCTGATTATGAAGTTTTTTTTTTTTC[A/T]GGATTGGAGGAGAACGAGTGCTGCTTCTTTCCACCTCCTCATGGGGCATAATGACAGCTCTGACCCCAATACTGGCAAAGACTGGACTCTCACCTCTTCTTACAATGACAGCGTCCAGGTTTCTATTGGGTGTAATGCAAGGTGAAGACTTTAGGAGGCACAGGAGAGGAAAAAGTGTATAAAGAAAGAAAGATATTTGACAGTATACAGAATGAATCTAAGAAATGTGTCAGCATGTTTGAACTAGTCATTTCCCTTCTAATAAGCCTGTGGGATCAGATGCTGGGGCAATGGGTGTAATTACTAGGGTGGGTCTAAGTCAGTTTAATCTGAATCTGCTCATCCGCAGTCATTTTAGTGGTTAATTTTGGATAGAACATGTTTTTTTAGCCTTCACTTACAGTTGAAGTAAGAATTATTAGATCCCATGAATTATTAACCCACCTGTTTATTTTGTCCACAATTTCTGTTTAACAGAGAGCAGATCGAAAAAATATAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31653
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036801 | Essential Splice Site | 156 | 458 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 24008878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23134696 |
GRCz11 | 8 | 23155935 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAGACAATTCAGGGGCAAAGAATTTCAGTGACCATCGTTGTTATTTAC[A/T]GGTGTTCACTACCCTTCTCTGGTCAGCATCTGTTCTCAGCGGGTGACAGA
Long Flanking Sequence:
ATCCTTGCTCTGTTAAACATAATTTGGGAAATATTTAAAAAAGAAAAAAATATATAATAAATACGACTTCAACTGTATATCTCATCTGGCTCTTTATTAAAGGATGATTCCATCACATAAGAGAAAAAATGTAAATGCTTTGCTAATTGAGAATTACAGCATATTAAAATAAAAATATGATTCATAATTAGGAATAATATATTACATAAATATGACAATTATAAATATGTTGTGAAAAGTAAAATACATGTAGGACAAAGTCAGTTATTAATGTTTTTTTTTCTAATGCATGCTGCATTTATAATAAACATTTTCTTTATTTTTTATTCCAAAATAATTGACATTTTAAATTGTATAAATATTAGATTGTGAACATCAATGAAACCCATCTTAGCATAACTGACTTTTTGCTATATTTATCTCTGACTAAAGAATGTTTTTTGGTTTTTATAAAGACAATTCAGGGGCAAAGAATTTCAGTGACCATCGTTGTTATTTAC[A/T]GGTGTTCACTACCCTTCTCTGGTCAGCATCTGTTCTCAGCGGGTGACAGAGGGGGAGAGAGGTTTACTGATGAGCACTTTGGCCTGTGGCTGCTACCTTGGGTAAGAAAACTAGACCTGGCTTACAATAATGTCCAAAATCATACATTTTTGATCTATAGAAACTTGTTTCAAGTCTTTTTGATGGGTATCTGTGGACTTATACCTTAATTCATTGTCTAATATACTCTTAATAAATGCTGAGTTATTTTTATGCAAATTGAGATAAAATATATCAACAAATCCAACACTTTACTATTAAATATTTTACTCAGTTGTTGGGTTTTTCAGTATTTTACTTAAATATTGGTTAAAACAACCCATCCATTTGTACTCTTGTTGGTTTTCTGTCAGGATGATGCTGGTTGGAGGAGTGGGCTCCCTGATGCTGGACTGGTTTGGGTGGCAGAGTGTGTTTTATGGAGCTGGTCTCCTTGCTGTTTTCTGGGCCTGTTGTGTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34388
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036801 | Nonsense | 206 | 458 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 24009321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23135139 |
GRCz11 | 8 | 23156378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGATGCTGGTTGGAGGAGTGGGCTCCCTGATGCTGGACTGGTTTGGGT[G/A]GCAGAGTGTGTTTTATGGAGCTGGTCTCCTTGCTGTTTTCTGGGCCTGTT
Long Flanking Sequence:
GTTTTTATAAAGACAATTCAGGGGCAAAGAATTTCAGTGACCATCGTTGTTATTTACAGGTGTTCACTACCCTTCTCTGGTCAGCATCTGTTCTCAGCGGGTGACAGAGGGGGAGAGAGGTTTACTGATGAGCACTTTGGCCTGTGGCTGCTACCTTGGGTAAGAAAACTAGACCTGGCTTACAATAATGTCCAAAATCATACATTTTTGATCTATAGAAACTTGTTTCAAGTCTTTTTGATGGGTATCTGTGGACTTATACCTTAATTCATTGTCTAATATACTCTTAATAAATGCTGAGTTATTTTTATGCAAATTGAGATAAAATATATCAACAAATCCAACACTTTACTATTAAATATTTTACTCAGTTGTTGGGTTTTTCAGTATTTTACTTAAATATTGGTTAAAACAACCCATCCATTTGTACTCTTGTTGGTTTTCTGTCAGGATGATGCTGGTTGGAGGAGTGGGCTCCCTGATGCTGGACTGGTTTGGGT[G/A]GCAGAGTGTGTTTTATGGAGCTGGTCTCCTTGCTGTTTTCTGGGCCTGTTGTGTATGGAAATGTCTTCTTCAAGGTAATTAAAATCTTGCTCTTAAATAATCTGTTAAAATGTAAATAACATTGTTCCTGAGATTTTGTACATACAGTTGAAGTCAGAATTATTAGCCCCCCCTGAATTATTAGCACCCCTGTTTATTTTTTCCCCAATTTCTGTTTAACGAAGAGAAGATTATTTCAACACATTTCTAAACATAATAGTTTTAACAACTCATTTCTAATAATTGATTTCTATTATTTGTCATGATGACAGTAACTAATTTTTAAATAGATATTTTTCAAGACACTTCTATACAGCTTGAAGTGACATTTAAAGGCTTAACTAGGTTGATTAGGGTAACTATGCAGGTTAGGATAATTAGGCAAGTTAATAATGGTTTGTTCTGTAGACTATCAGGAAAAAATATAGCTTAAAGGGGCTAATAATTTTGTCCTTAAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34389
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 |
---|---|---|---|---|---|
ENSDART00000036801 | Essential Splice Site | 337 | 458 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 24014420)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23140238 |
GRCz11 | 8 | 23161477 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTCATTCTGGCAGGTTGTGGGACAGCGGCTGTGAGGAAACTGATGCAG[G/A]TAACACATCAGCTATGAGTTTTCTTTGCCCTCATACTGTATACCGTATTA
Long Flanking Sequence:
GGGAAACATTCATACACACTCCTTCACACACATTCACTAAGGCCAATTTAGTTTATTCAACTCACCTGTACCGCATGTCTTTGGACTTGTGATGACACGCAAACAAGGAGAACATACAAACTCCACACAGAAATGCCAACTGACCCAGCCGAGGCTCGAACCAGCGACCTTCTTGCTGTGAAGCGACAGCACTTCCTACTGTGCCTCTGCGTCACCTTTGAAATTAATATTATTTAATGTTGCTTTATTTTACCTTTATTTAGTTTATTATTTTTATTTTTTAAATTTTGAATTCAATTTTACTTTTTTTTTTTTTACAAAAAAAATATTTAAATTCCTACAACATTGCTTCCCCATAAAAAAGTTGCATTTTCTCATGAAGTAGGGTTAATAAGAAATCCTGCCAGTACTTTTAATAAAATATGTTGCTATAATTTTTTTTTGCCATTTTTGTCATTCTGGCAGGTTGTGGGACAGCGGCTGTGAGGAAACTGATGCAG[G/A]TAACACATCAGCTATGAGTTTTCTTTGCCCTCATACTGTATACCGTATTATTATTAGTAGTATTAGTAATTGTTGTAATAATAATAATAATAACAACAACAAAATTCAAAATGTGTGTTTGTTTGAAATGCGGTCTAGTTCTGTTCAATGGGAGTTGCCAGTGTGTTCATCCTCTTTCTCTGCAAGACGAGCAGTTTCATTCAGGCTGTTGCTTGTGTGTCTGTGACTATCGGACTCTCCACCTTTCATAATAGGTAAGACAATTAAAACCTGATTATCTGGTATTGATTTTGTACACAGAGAGGGTGTATTGTTGATGCCCAGATATGAATGTTTACAAGATTAGAGATAAGAGAAAGTGCAACAAAGTCACTGTGCCTGTTTTGTTGTGTAGTGGAGTGTCTGTAAATGTGAACGACCAGGCGCCATCATGTGCAGGAGCTCTGTATGGTGAGACAACACCATTTTTATTTTATTTTTTATTTATTGTATTTTATTTA
Associated Phenotype:
Not determined