ZMP
zgc:123207
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC641419 [Source:RefSeq peptide;Acc:NP_001032485]
Human Orthologues:
SLC16A1, SLC16A7
Human Descriptions:
solute carrier family 16, member 1 (monocarboxylic acid transporter 1) [Source:HGNC Symbol;Acc:10922
solute carrier family 16, member 7 (monocarboxylic acid transporter 2) [Source:HGNC Symbol;Acc:10928
solute carrier family 16, member 7 (monocarboxylic acid transporter 2) [Source:HGNC Symbol;Acc:10928
Mouse Orthologues:
Slc16a1, Slc16a7
Mouse Descriptions:
solute carrier family 16 (monocarboxylic acid transporters), member 1 Gene [Source:MGI Symbol;Acc:MG
solute carrier family 16 (monocarboxylic acid transporters), member 7 Gene [Source:MGI Symbol;Acc:MG
solute carrier family 16 (monocarboxylic acid transporters), member 7 Gene [Source:MGI Symbol;Acc:MG
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16042 | Nonsense | Available for shipment | Available now |
sa24262 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16042
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 |
---|---|---|---|---|---|
ENSDART00000023099 | Nonsense | 175 | 465 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 9994864)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9953005 |
GRCz11 | 23 | 9887975 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCYACCCTGGCTCCAGTCAACCAATTTCTTTTTGACCAGTTTGGATGG[C/T]GAGGAAGCKTCTTCATYCTCGGAGGAGTGCTKTTCAACTGYTGYGTAGCT
Long Flanking Sequence:
TTTCTGTATCTACATTTGTAATTACACTGTTGTCCACCCTTTACACCTTAACCTAAACCTACCCATCCTACCAAACCTGTTCCTAACCTTACCCGAGTCCCACCTCAAGAGCACCTGAAGTGTTCTTCAATACATTATGTACATATTTATTTGCGTGTTTAGTTTATGATGCAAGTAGGCCACCTAATATAAAGTGGGATTGAATATTTTGTGTATTTTTAAGAGACTTTTTTTTAACTTTACTCGAGTAATGAACTTTTTACCGGAGTAATATGTCATCAAGGTATCTATTCTTGTCAAATGCTAACTACTGCACATAAAACTGCTTTTGCTTTACAGGCTTTGGCTTGGCTTTTAACCTGCAACCAGCTCTTACAATAATCGGCAAGTACTTTCTTGTCAAAAGGCCAATGGCAAATGGTATAGCAATGGCGGGCAGCCCAGTCTTCCTGTCTACCCTGGCTCCAGTCAACCAATTTCTTTTTGACCAGTTTGGATGG[C/T]GAGGAAGCTTCTTCATTCTCGGAGGAGTGCTGTTCAACTGTTGTGTAGCTGGATCTCTAATGAGACCCATCAAAATCCCAGTGAGTAAAACCACTGAAGACAACATCAGCCCTCAGACAGCAGGACAAGACGAGTCCAAACCCTCAGGCTGTTCTTCAAAGCTCAACCAATTCATAGACATCTCCCTCTTCAAGCACAGAGGCTTCCTCATCTATCTGGTAGGGAATGTACTCATGTTTTTTGGATTTTTTGCCCCTGTGGTCTTCTTGGCACCATATGCCAAGCATCAGGGAGTAGACGAGTACTCTGCAGCATTCCTGCTCTCTATATTTGCTCTTGTAGACATGTTTGCACGTCCAGGAACCGGTTTGGTCGCCAACACTAAATGGATCAGACCCAAGATCCAGTATTTCTTCAGTTTTGCTGTGACATATAATGGTTTGTGCCATTTAATGTGCCCACTTTTACCAGGTTACATAGACCTGGTGGTTTACGCGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24262
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 |
---|---|---|---|---|---|
ENSDART00000023099 | Nonsense | 363 | 465 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 9995428)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 9953569 |
GRCz11 | 23 | 9888539 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTTGGCATGGTTTGCGCTCTTTTGTTTGAGGTACTCATGGATTTGGTT[G/T]GAGCTCAACGGTTCTCTAGTGCGGTTGGACTTGCTACGATTATAGAGTGT
Long Flanking Sequence:
GACCCATCAAAATCCCAGTGAGTAAAACCACTGAAGACAACATCAGCCCTCAGACAGCAGGACAAGACGAGTCCAAACCCTCAGGCTGTTCTTCAAAGCTCAACCAATTCATAGACATCTCCCTCTTCAAGCACAGAGGCTTCCTCATCTATCTGGTAGGGAATGTACTCATGTTTTTTGGATTTTTTGCCCCTGTGGTCTTCTTGGCACCATATGCCAAGCATCAGGGAGTAGACGAGTACTCTGCAGCATTCCTGCTCTCTATATTTGCTCTTGTAGACATGTTTGCACGTCCAGGAACCGGTTTGGTCGCCAACACTAAATGGATCAGACCCAAGATCCAGTATTTCTTCAGTTTTGCTGTGACATATAATGGTTTGTGCCATTTAATGTGCCCACTTTTACCAGGTTACATAGACCTGGTGGTTTACGCGGTGTTATTTGGCCTGGCTTTTGGCATGGTTTGCGCTCTTTTGTTTGAGGTACTCATGGATTTGGTT[G/T]GAGCTCAACGGTTCTCTAGTGCGGTTGGACTTGCTACGATTATAGAGTGTGGACCCGTCCTGCTGGGGCCACCAATATCTGGTGAGTTCAACGATTGGTGTACTTCTCTCTGATATAATGTTCAGGACGTTTATTAACAATAAGTATGGCATAAAGCTCTTTATACAAGTAAACCTGAAGATTATTCACAGATCTCTTTTTTTTAGGTTTACTGGTCGACATCTTCATGGATTATAAATACATGTACTTTGCTTGTGGCATGATGATGCTGGCTGGAGGTGTCTTCCTCTTCATTATGAACTATTACAACTACAGATGGTTAAAAAAGGAGGAAAAACAGAGAAATGCAGAAGAGCTACAGATCTTCTCAACCAAAGAACTTGCCGCCATTGATGAAGAGATCAAACTTAGTATTGAGGAGAAGCTTAAAGACTAGAGCTGCAAATACCATTGAATCTGTCCTCTTTTCTTTAAGAAACTTCCATCTATCCATCCATCTA
Associated Phenotype:
Not determined