ZMP
si:ch211-14a17.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
SLC7A8
Human Description:
solute carrier family 7 (amino acid transporter, L-type), member 8 [Source:HGNC Symbol;Acc:11066]
Mouse Orthologue:
Slc7a8
Mouse Description:
solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 Gene [Source:MGI Symb
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10767 | Essential Splice Site | Available for shipment | Available now |
sa1219 | Nonsense | Available for shipment | Available now |
sa20925 | Essential Splice Site | Available for shipment | Available now |
sa14212 | Essential Splice Site | Available for shipment | Available now |
sa20924 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10767
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 |
---|---|---|---|---|---|
ENSDART00000010124 | Essential Splice Site | 50 | 531 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 25394393)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23956145 |
GRCz11 | 7 | 24227302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTATTTTAATTTACATTTCCAATACTCAACCTCTATGTTTTGTCATTTKC[A/T]GGTAACATCATTGGCTCTGGAATCTTTGTCAGCCCAAAGGGAGTGTTGGA
Long Flanking Sequence:
TAAGAAAGCACTATATTCTGTCATTAATTTTCAGAATAATATCGAGAGGAAGTGGAAGTGATTTAGATCATCATCCAGCATTAATGTAAAGAGATTAGGATTTATCCTAGATTAAAAGGAAGATTCAACTCTTCATATTCTATCTCTTGAAGAATGTTTAATAGTGGATGTTTAATTAATATTCCATGAACATGTAATTGTAAATTCATAATACTGATCATACCATGAAAATAATTATTCATTTAAAATAAAGTTGGACATATTTTCAAAATGTATGTCCTTAATGCACTCCTGACAAATCCCAAATCTCTTTAAATCCTTTACTCGTGATAACGTCTCTCTGGCTTTTCATTTAGAGCACTTTAGTAAATTCATCCAGACATCCATTAGGCATATAGGTTTTTGAATTCATAATCAGTGCAATTCCCTTCTATCTTTCTGACCTGCTTTCTATTTTAATTTACATTTCCAATACTCAACCTCTATGTTTTGTCATTTTC[A/T]GGTAACATCATTGGCTCTGGAATCTTTGTCAGCCCAAAGGGAGTGTTGGAAAATGCCAGTTCGGTAGGCCTGGCCCTCATTGTATGGATTCTTACAGGCATTATAACAGCGATTGGCGCACTCTGCTATGCTGAGCTGGGCGTTACTATACCAAAATCTGGAGGCGACTACTCTTATGTCAAGGACATCTTTGGAGGACTTGCAGGGTGAGAGTTTTCGGCCACACGTTCATTTTAATAATATTTTTAGTGTCTTTTACTAATTGACTAAAGTCAGAAATCTATAAGTTATGTCTAAAAGCTGCAGCCGTTTTTCCTTTTTAAGTAGTTAAATTAATTATAGAAATGTAGACTTTAGAGTAATTGTATCATGAAAATCCTTTAAGTCAGAGATTTAACAAACCTGATGAAAAACAATGCATTGATTTCAAAGACATGAGTGTTCAGAGATTCGGCAGAATTTAGTTTTCATTAATGTGCAATAAATACAGTTCTGTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1219
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 |
---|---|---|---|---|---|
ENSDART00000010124 | Nonsense | 412 | 531 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 25381423)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23943175 |
GRCz11 | 7 | 24214332 |
KASP Assay ID:
554-1128.1 (used for ordering genotyping assays)
KASP Sequence:
ACCTCTTCTACGGTGTCACTGTTGCTGGGCAGATTGTGCTGCGGATTAAA[C/T]AACCAGATATGCACCGACCAATTAAAGTAAGAATTGCTAATGATAAAAWA
Long Flanking Sequence:
ATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTTCACATACTCTCTCTCCTCCATGTCATGTTCTCCTGAATAACAGTATTGCTGGACTGTCCTCGTGTTGTTCAGGTTGTTTTTCGCGGGTGCTCGTGAAGGCCATCTGCCTAGTCTGCTGGCTATGATTCATGTGAAGCGCTGCACTCCTATTCCAGCCCTGCTCTTCACTGTGAGTATAATACAGTATACATGCACTGTCATGCATCATGTAATCCAACTGTACATCTGTCAAATTTAAGATTTCACTTGGTCCCTTGTCTATTTCATGACATCATCATCATATTTAATGTTACCTCGTTTGTTAAATAAACCTCTCTGTTGCTATTTTGCAGTGCATTTCAACACTTCTGATGCTGTGCACCAGTGACATGTACACACTCATCAACTATGTGGGTTTCATCAACTACCTCTTCTACGGTGTCACTGTTGCTGGGCAGATTGTGCTGCGGATTAAA[C/T]AACCAGATATGCACCGACCAATTAAAGTAAGAATTGCTAATGATAAAAAAATAATTATTGTCTTTCTGTTGAATTTTTAAGAAACACTCCACTTTTTTTTTGGAAAAGGCTCCCCTATTAACTCCCCTAGAGTTAAATAGTTGACTTTCACCTTTTTTTTTATCTGTTTAACCAATCTCCGGGTCTGGCTGGAGCACTTTTAGCTTAGCTTAGCATAAATCACTGAATTGGATTAGACCATTAGCATCTCGCTCAAAAAATGAAAAAATAACTGCTTAGATAATTTTCCTATTTAAAACTTTACTCTTCTCTAATTACATCATGTTCAAAGGCTGACAGAAACCATTACCTAGCTGGGGACTATTTTCAGGCGATGCAAAATATTATTGCTCCTGATGATACGGCAGCAAAGGTCCTTGTTTATTACACCAGAATGAGAGTAAAGTTCCTAAACATACTGACCTAGAAAATATCCACTTTTCATTTTCTGTTGGACTTAG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa20925
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 |
---|---|---|---|---|---|
ENSDART00000010124 | Essential Splice Site | 421 | 531 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 25380554)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23942306 |
GRCz11 | 7 | 24213463 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAAGATTATTTTTTCCTTCAGATTGCTAACCTCTCTTTTACTCCTCAC[A/T]GATCAGTCTGGTGTGGCCTGTGATCTACCTGCTCTTCTGGGCCTTCCTGC
Long Flanking Sequence:
AGGCGATGCAAAATATTATTGCTCCTGATGATACGGCAGCAAAGGTCCTTGTTTATTACACCAGAATGAGAGTAAAGTTCCTAAACATACTGACCTAGAAAATATCCACTTTTCATTTTCTGTTGGACTTAGTACACAATTTATTACAGAAGGGTTACTATTTAAATAGCTTGTTTTAAGAGAGAGTGAGTGATGCTAATGGTCTAATCTGATTCAATGATTTATGCTAAGCTAAAAATGGTCTTGCCAGGCCCCACAATCGACTGAATGGATTAAAAGGGTAAAAATTAACAGTTTTTCTCTAGATGACTTGTAAAATGAGCCTTTTTTAAAATGTGTTCCTTTCACTGACAACTTGCCACCTGTATTCCATTATTCTGGTATCAATTTTGCTATTTTGATGTGCTTGTCCAGTTCGTGGTATTTTTCGTACATTCCTGCCATATCAGATGAAAGATTATTTTTTCCTTCAGATTGCTAACCTCTCTTTTACTCCTCAC[A/T]GATCAGTCTGGTGTGGCCTGTGATCTACCTGCTCTTCTGGGCCTTCCTGCTGATCTTCTCTCTGTACTCGGAGCCTGTGGTTTGTGGCATTGGCTTGGCCATCATGCTTACTGGAGTCCCTGTCTATTTCTTGGGCGTTTACTGGGACAACAAGCCCCAATGTTTCAATACATTTGTTGGTGAGTGGAATACAGTTCACACACGTGTGGGACTTCATGATTGCTATATTATGTTTGAACAGAGACAGCATAACAAAGATGATTAAGACTAATTAGCAAGGGTACATTAAAATGGTTAAAAGGGGCAGTATTTATAATGATACAGAGTATTTAACTTTAAATAACTGCTTTTTTTTTTTTTACTTTTGTGGAAAAAAAGTATCTTTAAAAAGTGTATCACGATTTCCACAAAAATATTAGGCAGCATAATAAAACATATTTGTAATCAAATAATAGCAAACTTGATGTTATTGTAGTATGAGTGTTATACTTTTGTATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14212
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 |
---|---|---|---|---|---|
ENSDART00000010124 | Essential Splice Site | 479 | 531 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 25380374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23942126 |
GRCz11 | 7 | 24213283 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTGGGCGTTTACTGGGACAACAAGCCCCAATGTTTCAATACATTTRTTG[G/A]TGAGTGGAATACAGTTCACACAYGTGTGGGACTTCATGATTGCWATATTA
Long Flanking Sequence:
AGAGAGTGAGTGATGCTAATGGTCTAATCTGATTCAATGATTTATGCTAAGCTAAAAATGGTCTTGCCAGGCCCCACAATCGACTGAATGGATTAAAAGGGTAAAAATTAACAGTTTTTCTCTAGATGACTTGTAAAATGAGCCTTTTTTAAAATGTGTTCCTTTCACTGACAACTTGCCACCTGTATTCCATTATTCTGGTATCAATTTTGCTATTTTGATGTGCTTGTCCAGTTCGTGGTATTTTTCGTACATTCCTGCCATATCAGATGAAAGATTATTTTTTCCTTCAGATTGCTAACCTCTCTTTTACTCCTCACAGATCAGTCTGGTGTGGCCTGTGATCTACCTGCTCTTCTGGGCCTTCCTGCTGATCTTCTCTCTGTACTCGGAGCCTGTGGTTTGTGGCATTGGCTTGGCCATCATGCTTACTGGAGTCCCTGTCTATTTCTTGGGCGTTTACTGGGACAACAAGCCCCAATGTTTCAATACATTTGTTG[G/A]TGAGTGGAATACAGTTCACACACGTGTGGGACTTCATGATTGCTATATTATGTTTGAACAGAGACAGCATAACAAAGATGATTAAGACTAATTAGCAAGGGTACATTAAAATGGTTAAAAGGGGCAGTATTTATAATGATACAGAGTATTTAACTTTAAATAACTGCTTTTTTTTTTTTTACTTTTGTGGAAAAAAAGTATCTTTAAAAAGTGTATCACGATTTCCACAAAAATATTAGGCAGCATAATAAAACATATTTGTAATCAAATAATAGCAAACTTGATGTTATTGTAGTATGAGTGTTATACTTTTGTATTTTTATTAATTGTTTTAATTTGTTCTTATTTTTATACTTATTTTTTTATATATATTTAAATTATTGAGTTTTTGACATTATTTGTGTTATGTGTCATTTATTTATTAATTATAAATTATTCATGTTTTTTTAGCACATCTAGTAAGCTAAATAAAAATGATAATGTTTGTTTGATTTCAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20924
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 |
---|---|---|---|---|---|
ENSDART00000010124 | Essential Splice Site | 480 | 531 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 25379603)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23941355 |
GRCz11 | 7 | 24212512 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATTATTGACGTATGACACGTGAACCAAATTCCTCTCTTTGTGTTTAC[A/T]GACAAGATGACATACCTGGGCCAGAAATTCTGTGTGGTGGTGTATCCAAT
Long Flanking Sequence:
AATAGCAAACTTGATGTTATTGTAGTATGAGTGTTATACTTTTGTATTTTTATTAATTGTTTTAATTTGTTCTTATTTTTATACTTATTTTTTTATATATATTTAAATTATTGAGTTTTTGACATTATTTGTGTTATGTGTCATTTATTTATTAATTATAAATTATTCATGTTTTTTTAGCACATCTAGTAAGCTAAATAAAAATGATAATGTTTGTTTGATTTCAAATAAGAAATGGTTAGTTTTAGTCGACTAAACTAAAGGATTCTGTCTACAATATATCAAATATTAATTAAAAAATGTAATAAGTGTCAGTTTACACTTTTAGGAATAAAATATATTCTAAGTTATTTCAGAATGTATGGCTGATTGCAGAGATTAGCAAATTGATAGATAGATATAAAGCCTTTATATTGATTTAAAGAAGATTGTTGCTGACGTTTGAAGAAGATTATTATTGACGTATGACACGTGAACCAAATTCCTCTCTTTGTGTTTAC[A/T]GACAAGATGACATACCTGGGCCAGAAATTCTGTGTGGTGGTGTATCCAATGGAGGAAGTAAAGAAAACCGATGAGTCTGCAGAGGGGATTGAGCTGAAGGAGCAGACTGCTCCACTGTCAGCAGAGGGCGAGGAGACGCCCAAATCAGCCGACTGCTGAAGAGACACACTCCTTCACACATATTCAAACAGACACTGGAAATCAAACTCAGATTGTTCACATACCTCTATAGTTTGCCTTTTGTATAAAGAGGGGGTTGCACTGGGGGCTGAAGCTCAGGAGAGAGTCATGAACAGAGACCAGCTGCTCCTCGATCTCTGTTCGCTGGTTTCTTAGCAGCTGCTTTCTACTCCATCGGCTGTGCAACAGAATTACAACATTAAAATGTGAGATAAGGAAAAGCTCTAGAATGTATAAAGTACAAGCACAGGTTTTGGGATTAAAAAGAACACCTTTCTGGACATTCTGTGAGACACAGGAGAGTTACAGATCGTGCCAAA
Associated Phenotype:
Not determined