ZMP
si:dkey-246g23.4
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC559426 [Source:RefSeq peptide;Acc:NP_001106809]
Human Orthologues:
AC037487.1, SLC16A1, SLC16A3, SLC16A5, SLC16A6, SLC16A7, SLC16A8
Human Descriptions:
solute carrier family 16, member 1 (monocarboxylic acid transporter 1) [Source:HGNC Symbol;Acc:10922
solute carrier family 16, member 3 (monocarboxylic acid transporter 4) [Source:HGNC Symbol;Acc:10924
solute carrier family 16, member 5 (monocarboxylic acid transporter 6) [Source:HGNC Symbol;Acc:10926
solute carrier family 16, member 6 (monocarboxylic acid transporter 7) [Source:HGNC Symbol;Acc:10927
solute carrier family 16, member 7 (monocarboxylic acid transporter 2) [Source:HGNC Symbol;Acc:10928
solute carrier family 16, member 8 (monocarboxylic acid transporter 3) [Source:HGNC Symbol;Acc:16270
solute carrier family 16, member 3 (monocarboxylic acid transporter 4) [Source:HGNC Symbol;Acc:10924
solute carrier family 16, member 5 (monocarboxylic acid transporter 6) [Source:HGNC Symbol;Acc:10926
solute carrier family 16, member 6 (monocarboxylic acid transporter 7) [Source:HGNC Symbol;Acc:10927
solute carrier family 16, member 7 (monocarboxylic acid transporter 2) [Source:HGNC Symbol;Acc:10928
solute carrier family 16, member 8 (monocarboxylic acid transporter 3) [Source:HGNC Symbol;Acc:16270
Mouse Orthologues:
Slc16a1, Slc16a3, Slc16a5, Slc16a6, Slc16a7, Slc16a8
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 3 Gene [Source:MGI Symbol;Acc:MG
solute carrier family 16 (monocarboxylic acid transporters), member 5 Gene [Source:MGI Symbol;Acc:MG
solute carrier family 16 (monocarboxylic acid transporters), member 6 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 8 Gene [Source:MGI Symbol;Acc:MG
solute carrier family 16 (monocarboxylic acid transporters), member 3 Gene [Source:MGI Symbol;Acc:MG
solute carrier family 16 (monocarboxylic acid transporters), member 5 Gene [Source:MGI Symbol;Acc:MG
solute carrier family 16 (monocarboxylic acid transporters), member 6 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 8 Gene [Source:MGI Symbol;Acc:MG
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa28999 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10653 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa28999
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009363 | Nonsense | 5 | 425 | 1 | 5 |
ENSDART00000125033 | Nonsense | 5 | 457 | 1 | 4 |
ENSDART00000136120 | Nonsense | 5 | 121 | 3 | 4 |
ENSDART00000141813 | Nonsense | 5 | 118 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 14152987)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14598405 |
GRCz11 | 18 | 14566917 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTTTTGTAGTTGTAGGATGATCTATTAAGCTTTCAATGGAAAGGAAG[A/T]GAGGAACAGCCGGGCCTGCAGGTCCTCCTCTGGATGGTGGTTATGGCTGG
Long Flanking Sequence:
TAAAAAATATTTAGCTTTTAAGGCATAAAATCAGCTTGCATATATTGAAAAACAAGGTAAAAATCACCCAAGAAAGTTTTTTTGATTTGGGTTTCTGGTTTGCCCAACATGACATCCTATAGCTAATCACGCTATTCATACACGTGCTATATATAAACACAACCGGTAAACTTGTTGGCTATACTCTTGAAACCACCCTTATGTGAATGACAGAAGAGACCTGTATAAACATCAACTGTACCTGCAACTGACTAAAAAATATTAAGAAAAATGCATGTACTACAGTACAAGTGTTGTTTTGTTACTATGGCATGTAATATAGTTAATCATTCTTCAGTTGTTTTAGCACTTGGAGATAATAATTGATGAACTAAATCACTTGTCATGTCATGTTCCTAAGCTTGAAAAACTTCACTGCTGACATAGCATTCTGCTTGTATGTTTTTCCTCTTGTTTTTGTAGTTGTAGGATGATCTATTAAGCTTTCAATGGAAAGGAAG[A/T]GAGGAACAGCCGGGCCTGCAGGTCCTCCTCTGGATGGTGGTTATGGCTGGTTCATTGTGCTCTCCACTTTCCTTGTGTTTGGGCTGACGTTCGGCGTAATCAAGTCCTTCGGTGTGTTCTTTGTAGAAATTCACCACTACTTTTCAACTACAGCAACTGCAAGCTCATGGATCACATCCATCTCTGTGGCCACGGTGCATATTGGGGGTATGTGCGAGTTTAACTGTTCCACCAGCAGGGGGCTCTATCCACTGACACTCTCACTTACATTTGCCTTTGAGTTTAAAGGGAAAGTTCACCCCAGAAAATAACTGATAACTTACTCACCCTTAAGTGGTTCTAAACCTTTATAGCTTACTATTTTCTGCTGAACCTAAAAGAGGATTTTTTTAAGAAAGCTGGAAACTGGTAACCATTCACTTCTATAATAGGAAAAAATTAATATATGGAAGACAGTAACAGAGTTCAACTTTCTTCAAAATATCTTATTTTGGTTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10653
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009363 | Nonsense | 21 | 425 | 1 | 5 |
ENSDART00000125033 | Nonsense | 21 | 457 | 1 | 4 |
ENSDART00000136120 | Nonsense | 21 | 121 | 3 | 4 |
ENSDART00000141813 | Nonsense | 21 | 118 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 14153037)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14598455 |
GRCz11 | 18 | 14566967 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGGAACAGCCGGGCCTGCAGGTCCTCCTCTGGATGGTGGTTATGGCTG[G/A]KTCATTGTGCTCTCCACTTTYCTTGTGTTTGGGCTGACGTTCGGCGTAAT
Long Flanking Sequence:
AACAAGGTAAAAATCACCCAAGAAAGTTTTTTTGATTTGGGTTTCTGGTTTGCCCAACATGACATCCTATAGCTAATCACGCTATTCATACACGTGCTATATATAAACACAACCGGTAAACTTGTTGGCTATACTCTTGAAACCACCCTTATGTGAATGACAGAAGAGACCTGTATAAACATCAACTGTACCTGCAACTGACTAAAAAATATTAAGAAAAATGCATGTACTACAGTACAAGTGTTGTTTTGTTACTATGGCATGTAATATAGTTAATCATTCTTCAGTTGTTTTAGCACTTGGAGATAATAATTGATGAACTAAATCACTTGTCATGTCATGTTCCTAAGCTTGAAAAACTTCACTGCTGACATAGCATTCTGCTTGTATGTTTTTCCTCTTGTTTTTGTAGTTGTAGGATGATCTATTAAGCTTTCAATGGAAAGGAAGAGAGGAACAGCCGGGCCTGCAGGTCCTCCTCTGGATGGTGGTTATGGCTG[G/A]TTCATTGTGCTCTCCACTTTCCTTGTGTTTGGGCTGACGTTCGGCGTAATCAAGTCCTTCGGTGTGTTCTTTGTAGAAATTCACCACTACTTTTCAACTACAGCAACTGCAAGCTCATGGATCACATCCATCTCTGTGGCCACGGTGCATATTGGGGGTATGTGCGAGTTTAACTGTTCCACCAGCAGGGGGCTCTATCCACTGACACTCTCACTTACATTTGCCTTTGAGTTTAAAGGGAAAGTTCACCCCAGAAAATAACTGATAACTTACTCACCCTTAAGTGGTTCTAAACCTTTATAGCTTACTATTTTCTGCTGAACCTAAAAGAGGATTTTTTTAAGAAAGCTGGAAACTGGTAACCATTCACTTCTATAATAGGAAAAAATTAATATATGGAAGACAGTAACAGAGTTCAACTTTCTTCAAAATATCTTATTTTGGTTTTAATTGAAGAAAGAAATTTGTGACAAGTAAAGAGTGAATAAATGATAACAGAG
Associated Phenotype:
Not determined