ZMP
slc2a12
Ensembl ID:
ZFIN ID:
Description:
Solute carrier family 2, facilitated glucose transporter member 12 [Source:UniProtKB/Swiss-Prot;Acc:
Human Orthologue:
SLC2A12
Human Description:
solute carrier family 2 (facilitated glucose transporter), member 12 [Source:HGNC Symbol;Acc:18067]
Mouse Orthologue:
Slc2a12
Mouse Description:
solute carrier family 2 (facilitated glucose transporter), member 12 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24373 | Nonsense | Available for shipment | Available now |
sa37756 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12204 | Essential Splice Site | Available for shipment | Available now |
sa12272 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24373
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 |
---|---|---|---|---|---|
ENSDART00000053531 | Nonsense | 456 | 610 | 3 | 6 |
ENSDART00000143335 | None | None | 241 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 31858218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 31693108 |
GRCz11 | 23 | 31619639 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCTATAATCATAGGACTGCTTTAATGGAAACCGCTGAGCTTTCGAAG[A/T]AAGACAGTGCAAAGATTGCGCTTCAGTCTCTTCACGAAGTGTCGCCTTCG
Long Flanking Sequence:
TTGGCGCTGCGCTGGTGTTCTTGCAGCAGGCCACAGGACAGCCTAATATTTTAGCATATGCCTCGACTGTTCTCAGTAGCGTAGGCTTTCATGGGAATGAGGCGGCGACTCTTGCGTCTACAGGGTTTGGTGTGGTTAAAGTGGGTGGAACCATTCCTGCAATTTTTCTAGTGGACAAAGTTGGGCCTAAAGCCCTTCTGTGTGTTGGAGTGGTTGTCATGATGTTGTCAACAGCAACGCTGGGGGCCATTACTATGCAGAGCCGCACACACGTTTCCAGCCTATGCAGAGGCCCCGGTAATACAGCAAACTTCACGTTATTTGAGACCGGAGATGAGACTGATATCCAGACCAACACTCCACTGGGCTTATACCAGCCTCAAAACAAGCTCAAAACAAACACTTTTCTCACAAGCATTAATGACACTAGAGAGCATTGGATTTTAAATCACACCTATAATCATAGGACTGCTTTAATGGAAACCGCTGAGCTTTCGAAG[A/T]AAGACAGTGCAAAGATTGCGCTTCAGTCTCTTCACGAAGTGTCGCCTTCGCTGAAATGGATCTCTCTGGTCAGCCTGCTGGTGTATGTAGCTGGATTCTCCATCAGCTTGGGACCAAGTAAGATTCAGACTCAAACAAATGATATCTGTTTATATTACAAATTAAATTCTGACTGACTTGCTGCGTTTCAATTCGCATACTTATACTACGCCCTAAAAGGATGTATTTTTTTGTAAAGGCAAAGTATATAGTTTTGAGTATGTAACAGAAGAATATTGCAAGCTTTGGGACACACTACTTCTTTGTTAACAGATCTTTATATTGCTTGGTTATGTCCCTTGTCAACCATCTGGACACATCATCCATATTTCTTTCTTATTTAATTTCCTACTTTATTGGAAAAGCAGCAGCAGGATAATCTTCCAATCGCGAGTCTTTCATGCAGAGAAATCTGCCCAGGTGTTTGTATAATTATGCATTCAGGCATTAATGTCCAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37756
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 |
---|---|---|---|---|---|
ENSDART00000053531 | Essential Splice Site | 494 | 610 | 3 | 6 |
ENSDART00000143335 | None | None | 241 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 31858100)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 31692990 |
GRCz11 | 23 | 31619521 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCAGCCTGCTGGTGTATGTAGCTGGATTCTCCATCAGCTTGGGACCAA[G/A]TAAGATTCAGACTCAAACAAATGATATCTGTTTATATTACAAATTAAATT
Long Flanking Sequence:
TACAGGGTTTGGTGTGGTTAAAGTGGGTGGAACCATTCCTGCAATTTTTCTAGTGGACAAAGTTGGGCCTAAAGCCCTTCTGTGTGTTGGAGTGGTTGTCATGATGTTGTCAACAGCAACGCTGGGGGCCATTACTATGCAGAGCCGCACACACGTTTCCAGCCTATGCAGAGGCCCCGGTAATACAGCAAACTTCACGTTATTTGAGACCGGAGATGAGACTGATATCCAGACCAACACTCCACTGGGCTTATACCAGCCTCAAAACAAGCTCAAAACAAACACTTTTCTCACAAGCATTAATGACACTAGAGAGCATTGGATTTTAAATCACACCTATAATCATAGGACTGCTTTAATGGAAACCGCTGAGCTTTCGAAGAAAGACAGTGCAAAGATTGCGCTTCAGTCTCTTCACGAAGTGTCGCCTTCGCTGAAATGGATCTCTCTGGTCAGCCTGCTGGTGTATGTAGCTGGATTCTCCATCAGCTTGGGACCAA[G/A]TAAGATTCAGACTCAAACAAATGATATCTGTTTATATTACAAATTAAATTCTGACTGACTTGCTGCGTTTCAATTCGCATACTTATACTACGCCCTAAAAGGATGTATTTTTTTGTAAAGGCAAAGTATATAGTTTTGAGTATGTAACAGAAGAATATTGCAAGCTTTGGGACACACTACTTCTTTGTTAACAGATCTTTATATTGCTTGGTTATGTCCCTTGTCAACCATCTGGACACATCATCCATATTTCTTTCTTATTTAATTTCCTACTTTATTGGAAAAGCAGCAGCAGGATAATCTTCCAATCGCGAGTCTTTCATGCAGAGAAATCTGCCCAGGTGTTTGTATAATTATGCATTCAGGCATTAATGTCCAAACATATCTTTATATAAGTTCACATTGTTGTTGCAGATGAAATATAACACTGAGTACGCGGTTTAAATATTTTCCAGTTGGCAAATAATCATTCAAGCAGCTTTACTGAAGCCTATCTACGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12204
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 |
---|---|---|---|---|---|
ENSDART00000053531 | Essential Splice Site | 580 | 610 | 5 | 6 |
ENSDART00000143335 | None | None | 241 | None | 3 |
ENSDART00000053531 | Essential Splice Site | 580 | 610 | 5 | 6 |
ENSDART00000143335 | None | None | 241 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 31852204)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 31687094 |
GRCz11 | 23 | 31613625 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGACCAAAGGCCGATCATTGGAACAGATCTCAAAGGAACTTGCAATGAA[G/A]TGAGTGGACATAAACACACACATTGGTTTTGGTGGTKTATAAGGACTCTA
Long Flanking Sequence:
AAAATATATAACCACTTTTATATAACCACTTTTATGGCAATGGAACAATAGCTTTTGGTCATTCTTAACTTCATCAATAAATAAAAAAAACGAAATAGACATAGAAGCAATACAATACGTTAGAAACAAAGTTATATTCCCAGAAACGGATCACCAAGTAAAGATTAAGTTTGCAGTGTGTGTTTAAAGGCTGTCCGCCAAACATTAATTTGCCACCTGTGGGGATGATCCTGCAGAGAAGGAATGAAAACACAAGGAAACACATACTTACAAGTTTTTGCACAGAACAATAAACAAAAAATAGTTTTGGCTGCAGAAAGGAGTGCTATATTGTAAGGTGATTTACTGTAATGTGATGTGCTTGTAGAGCGGATCGGCCTCCCTACTGTCATCTTCTCCTACTCTGCTATGAGCTTCCTGTTGGTGGTGTTTGTGATTGTGTTTGTGCCAGAGACCAAAGGCCGATCATTGGAACAGATCTCAAAGGAACTTGCAATGAA[G/A]TGAGTGGACATAAACACACACATTGGTTTTGGTGGTGTATAAGGACTCTACAGAGGCGTAAGTATTTTATACTGCAAAAACACTTATTAGATGGCCTTACCCTACCTAACCCTCAAATTATTAATGCGAAAACACCCCATTAAGTAGGATTTTTAACAGTTTTGCATTAGGAGGATACAAGGGATGTCCTCATAAACATTGTAAATTGTAATACAGAGGACATACCAATGTCATTGCACAAATGTGTGTCTTCACAAACCACTAAAACCAACACACACACTCTCTATTACATACACACAAATATGTTGATTGTTAGAACAGATCTCAAAGGAACTTGCCATGAAGTGAGTGAACACACAGACTGTTTTTTTTGCGGTTTATGAGGACTCTCCAAAGGCGTAATGAATTTTTAACTGTAAAAACGCTTATTATATGGCCTCAACCTACCCCTAAACCCAACCCTTAAATTATGTAATGTCGAATGTAAAAATACCCCATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12272
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 |
---|---|---|---|---|---|
ENSDART00000053531 | Essential Splice Site | 580 | 610 | 5 | 6 |
ENSDART00000143335 | None | None | 241 | None | 3 |
ENSDART00000053531 | Essential Splice Site | 580 | 610 | 5 | 6 |
ENSDART00000143335 | None | None | 241 | None | 3 |
Genomic Location (Zv9):
Chromosome 23 (position 31852204)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 31687094 |
GRCz11 | 23 | 31613625 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGACCAAAGGCCGATCATTGGAACAGATCTCAAAGGAACTTGCAATGAA[G/A]TGAGTGGACATAAACACACACATTGGTTTTGGTGGTKTATAAGGACTCTA
Long Flanking Sequence:
AAAATATATAACCACTTTTATATAACCACTTTTATGGCAATGGAACAATAGCTTTTGGTCATTCTTAACTTCATCAATAAATAAAAAAAACGAAATAGACATAGAAGCAATACAATACGTTAGAAACAAAGTTATATTCCCAGAAACGGATCACCAAGTAAAGATTAAGTTTGCAGTGTGTGTTTAAAGGCTGTCCGCCAAACATTAATTTGCCACCTGTGGGGATGATCCTGCAGAGAAGGAATGAAAACACAAGGAAACACATACTTACAAGTTTTTGCACAGAACAATAAACAAAAAATAGTTTTGGCTGCAGAAAGGAGTGCTATATTGTAAGGTGATTTACTGTAATGTGATGTGCTTGTAGAGCGGATCGGCCTCCCTACTGTCATCTTCTCCTACTCTGCTATGAGCTTCCTGTTGGTGGTGTTTGTGATTGTGTTTGTGCCAGAGACCAAAGGCCGATCATTGGAACAGATCTCAAAGGAACTTGCAATGAA[G/A]TGAGTGGACATAAACACACACATTGGTTTTGGTGGTGTATAAGGACTCTACAGAGGCGTAAGTATTTTATACTGCAAAAACACTTATTAGATGGCCTTACCCTACCTAACCCTCAAATTATTAATGCGAAAACACCCCATTAAGTAGGATTTTTAACAGTTTTGCATTAGGAGGATACAAGGGATGTCCTCATAAACATTGTAAATTGTAATACAGAGGACATACCAATGTCATTGCACAAATGTGTGTCTTCACAAACCACTAAAACCAACACACACACTCTCTATTACATACACACAAATATGTTGATTGTTAGAACAGATCTCAAAGGAACTTGCCATGAAGTGAGTGAACACACAGACTGTTTTTTTTGCGGTTTATGAGGACTCTCCAAAGGCGTAATGAATTTTTAACTGTAAAAACGCTTATTATATGGCCTCAACCTACCCCTAAACCCAACCCTTAAATTATGTAATGTCGAATGTAAAAATACCCCATTA
Associated Phenotype:
Not determined