ZMP
si:dkey-119m7.4
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC560629 [Source:RefSeq peptide;Acc:NP_001038399]
Human Orthologues:
SLC22A10, SLC22A11, SLC22A12, SLC22A24, SLC22A25, SLC22A6, SLC22A7, SLC22A8, SLC22A9
Human Descriptions:
solute carrier family 22 (organic anion transporter), member 6 [Source:HGNC Symbol;Acc:10970]
solute carrier family 22 (organic anion transporter), member 7 [Source:HGNC Symbol;Acc:10971]
solute carrier family 22 (organic anion transporter), member 8 [Source:HGNC Symbol;Acc:10972]
solute carrier family 22 (organic anion transporter), member 9 [Source:HGNC Symbol;Acc:16261]
solute carrier family 22 (organic anion/urate transporter), member 11 [Source:HGNC Symbol;Acc:18120]
solute carrier family 22 (organic anion/urate transporter), member 12 [Source:HGNC Symbol;Acc:17989]
solute carrier family 22, member 10 [Source:HGNC Symbol;Acc:18057]
solute carrier family 22, member 24 [Source:HGNC Symbol;Acc:28542]
solute carrier family 22, member 25 [Source:HGNC Symbol;Acc:32935]
solute carrier family 22 (organic anion transporter), member 7 [Source:HGNC Symbol;Acc:10971]
solute carrier family 22 (organic anion transporter), member 8 [Source:HGNC Symbol;Acc:10972]
solute carrier family 22 (organic anion transporter), member 9 [Source:HGNC Symbol;Acc:16261]
solute carrier family 22 (organic anion/urate transporter), member 11 [Source:HGNC Symbol;Acc:18120]
solute carrier family 22 (organic anion/urate transporter), member 12 [Source:HGNC Symbol;Acc:17989]
solute carrier family 22, member 10 [Source:HGNC Symbol;Acc:18057]
solute carrier family 22, member 24 [Source:HGNC Symbol;Acc:28542]
solute carrier family 22, member 25 [Source:HGNC Symbol;Acc:32935]
Mouse Orthologues:
AB056442, BC014805, BC026439, C730048C13Rik, D630002G06Rik, Gm5631, Slc22a12, Slc22a19, Slc22a20, Slc22a6, Slc22a7, Slc22a8
Mouse Descriptions:
RIKEN cDNA C730048C13 gene Gene [Source:MGI Symbol;Acc:MGI:2442750]
RIKEN cDNA D630002G06 gene Gene [Source:MGI Symbol;Acc:MGI:3605624]
cDNA sequence AB056442 Gene [Source:MGI Symbol;Acc:MGI:3042283]
cDNA sequence BC014805 Gene [Source:MGI Symbol;Acc:MGI:2385316]
cDNA sequence BC026439 Gene [Source:MGI Symbol;Acc:MGI:2446114]
predicted gene 5631 Gene [Source:MGI Symbol;Acc:MGI:3645714]
solute carrier family 22 (organic anion transporter), member 19 Gene [Source:MGI Symbol;Acc:MGI:2442
solute carrier family 22 (organic anion transporter), member 20 Gene [Source:MGI Symbol;Acc:MGI:2685
solute carrier family 22 (organic anion transporter), member 6 Gene [Source:MGI Symbol;Acc:MGI:89200
solute carrier family 22 (organic anion transporter), member 7 Gene [Source:MGI Symbol;Acc:MGI:18595
solute carrier family 22 (organic anion transporter), member 8 Gene [Source:MGI Symbol;Acc:MGI:13361
solute carrier family 22 (organic anion/cation transporter), member 12 Gene [Source:MGI Symbol;Acc:M
RIKEN cDNA D630002G06 gene Gene [Source:MGI Symbol;Acc:MGI:3605624]
cDNA sequence AB056442 Gene [Source:MGI Symbol;Acc:MGI:3042283]
cDNA sequence BC014805 Gene [Source:MGI Symbol;Acc:MGI:2385316]
cDNA sequence BC026439 Gene [Source:MGI Symbol;Acc:MGI:2446114]
predicted gene 5631 Gene [Source:MGI Symbol;Acc:MGI:3645714]
solute carrier family 22 (organic anion transporter), member 19 Gene [Source:MGI Symbol;Acc:MGI:2442
solute carrier family 22 (organic anion transporter), member 20 Gene [Source:MGI Symbol;Acc:MGI:2685
solute carrier family 22 (organic anion transporter), member 6 Gene [Source:MGI Symbol;Acc:MGI:89200
solute carrier family 22 (organic anion transporter), member 7 Gene [Source:MGI Symbol;Acc:MGI:18595
solute carrier family 22 (organic anion transporter), member 8 Gene [Source:MGI Symbol;Acc:MGI:13361
solute carrier family 22 (organic anion/cation transporter), member 12 Gene [Source:MGI Symbol;Acc:M
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10047 | Nonsense | Available for shipment | Available now |
sa3051 | Essential Splice Site | F2 line generated | Not yet available |
sa9186 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1625 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10047
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 |
---|---|---|---|---|---|
ENSDART00000104807 | Nonsense | 18 | 413 | 1 | 7 |
ENSDART00000129429 | Nonsense | 18 | 542 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 325947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 316542 |
GRCz11 | 20 | 305177 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAACTTTGACAAGGTCCTGGACCGGATTGGTGGGTTTGGACGTTTTCAG[A/T]AGACTCTTTATGTTTGGATCTGTCTGCCACAGAWCTTTTTGGCCTTCCAC
Long Flanking Sequence:
GATAGAGAGAGTGTGAAAATATTCCTCCCCTTATGGCCCCACCCCTTCTCTCGGTGACCCCTCCCTCTTATGCTCACTGGCTCATTTCAGGTATCTGGGTCACTCCCAGCCCTCCCCTCCTTATATTTCCCTCATACAACACAGCCAAACAGCCAGAACTCTGCGGCAGCGCTCTCTGCCTCTTTTCCTGCATCCCTCCCTTTCTCTCTGCTACAGGTGTGAGGAGACCAATACCAGCCACACACAGGCACCTGTACCGCCCGGCCGTAACCAGACCTCCATCTCATAGCATTTTAATAATCATAACAGTGACCTGACGTTCTCCATAGCGTTGCTCACATATACACTCACACACCAACTTCTGTCCCGAGACGCTTGTGCCTGGCCATCTTCACCCGAGCAGATTCACAGTTCACATGTTCATGAAGTGATATTCACGGACAGGCAGGATGAACTTTGACAAGGTCCTGGACCGGATTGGTGGGTTTGGACGTTTTCAG[A/T]AGACTCTTTATGTTTGGATCTGTCTGCCACAGATCTTTTTGGCCTTCCACATGTTGGTGTCTGTCTTCACTGGGGCCGTGCCCCCTCACCTGTGCAGATCTTCTTGGCCAGTGGGGGACAGTGCCGGTCCCAGGCTGAACCTGAGCTTCAGCAGTGCTCCAGGGGAGTCCTGCACACCTTCTCAGGACGGCTCTCTGCCCCAGCGTAACCACAGTCTGCCGATTACCGAGCACTCGTCCACCGCGAAGGGCTGCACCGGAGGATGGGAGTTCAGCAAGGAGGTCTTCCTCAGCACTATCGCCACAGAGGTGAGTGCCCTCAAAATATAGCAGTTGTGTAGCAGGATGTGTCGGTGATAACATGCACAGCACTTCAACACAGATCTTTTTTTAGTTTCTCTTCTGCTTCTGGAGTTATTCGTGTGTTGTGGTTTCGATGGTTTAGCTGCATTGAGAGTTTCTGGCCACCTGTGGTGAAGGCATCTGACTTATAGAGATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3051
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000104807 | Essential Splice Site | 120 | 413 | 1 | 7 |
ENSDART00000129429 | Essential Splice Site | 120 | 542 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 326256)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 316851 |
GRCz11 | 20 | 305486 |
KASP Assay ID:
554-2543.1 (used for ordering genotyping assays)
KASP Sequence:
GAGGATGGGAGTTCAGCAAGGAGGTCTTCCTCAGCACTATCGCCACAGAG[G/A]TGAGTGCCCTCAAAAYATAGCAGTTGTGTAGCAGGATGTGTCGGTGATAA
Long Flanking Sequence:
TGACCTGACGTTCTCCATAGCGTTGCTCACATATACACTCACACACCAACTTCTGTCCCGAGACGCTTGTGCCTGGCCATCTTCACCCGAGCAGATTCACAGTTCACATGTTCATGAAGTGATATTCACGGACAGGCAGGATGAACTTTGACAAGGTCCTGGACCGGATTGGTGGGTTTGGACGTTTTCAGAAGACTCTTTATGTTTGGATCTGTCTGCCACAGATCTTTTTGGCCTTCCACATGTTGGTGTCTGTCTTCACTGGGGCCGTGCCCCCTCACCTGTGCAGATCTTCTTGGCCAGTGGGGGACAGTGCCGGTCCCAGGCTGAACCTGAGCTTCAGCAGTGCTCCAGGGGAGTCCTGCACACCTTCTCAGGACGGCTCTCTGCCCCAGCGTAACCACAGTCTGCCGATTACCGAGCACTCGTCCACCGCGAAGGGCTGCACCGGAGGATGGGAGTTCAGCAAGGAGGTCTTCCTCAGCACTATCGCCACAGAG[G/A]TGAGTGCCCTCAAAATATAGCAGTTGTGTAGCAGGATGTGTCGGTGATAACATGCACAGCACTTCAACACAGATCTTTTTTTAGTTTCTCTTCTGCTTCTGGAGTTATTCGTGTGTTGTGGTTTCGATGGTTTAGCTGCATTGAGAGTTTCTGGCCACCTGTGGTGAAGGCATCTGACTTATAGAGATGCAGCTCCCTGGACTTGGAATGGACCAATGGAATGGCATTCCTTTAGCAACATGTGACCGACGATATGGGTTTCTCACAGCAGGACATCCTGGCAGAACCTGCTTTGATTTACAAACACTGGACCTTGGCCAAGCCTCACAACGGGAGGTGACTATATGATACCGCTCTCTGCTGTCCAGCTGCAAGGCCGAGGTGGAGGAAAGGGTGGGGCTGGAGAAAGAGTGCAGCAGACCAATCTGTCTCCAGTCCAGGTGTATAGAGGGGGAGGATAGAGTTAATAACCCAAACTAACTGTAAGACCACTGCAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9186
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104807 | Nonsense | 138 | 413 | 2 | 7 |
ENSDART00000129429 | Nonsense | 138 | 542 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 329169)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 319764 |
GRCz11 | 20 | 308399 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATCTCGTGTGTGAAAACGCCACTATGAACAACATTGGCTCTTCTATCTA[T/A]ATGTTTGGGCTGCTGGTTGGAGCGGTGCTGTTCGGAGCCCTTGCTGATAA
Long Flanking Sequence:
AAAAATCCTTTAGGGCAACTGTTTTTCTGTCGCCTCACAGCAGAAAGGTCGCTGGTCTCCTCTGTGTGCTCCGGTTTCCCGCACAGTCCGAACACATGCGCTATAGGAGAACTGATGGACTAAATTGGCCATAGTGTGTGAATGAGTGTATGGATGTTTCCCAATACTGGGTTGCAGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGTGACCCCTGATGAATAAGCTGAGGGTGAATAAATGAATGCATGAATGAAAATGACTCATTCATTGATATCGTGTGCAGGTGAAAGTGAATGCTATTGTATTTGGTTGACAGTATGATTGACAAAATCTTCTACACTGTAAAATTGTTGTGATTTCAGTGGAGATGTTAAAATGCAACAGTAAATATCTGGGATGAGCTGGTTATGAGTTTTAGCATTGACCCATGTTCTTGTCTTGCAGTGGGATCTCGTGTGTGAAAACGCCACTATGAACAACATTGGCTCTTCTATCTA[T/A]ATGTTTGGGCTGCTGGTTGGAGCGGTGCTGTTCGGAGCCCTTGCTGATAAGTAAGAACCTCGAGATCATTCGCACACAAACACATCATTATCCTCTAGTGGAAAACCCTGAATCTGAAACTCAAGCGCTGATATCAGTTTAGAAGCAGTCCTGATTGACATGAGATGATTAACAGACTGCATGTCTGGACACGAGCTCGAATACCAGGAAGTTTGGGATATTTTACATAAACAAGTCCTGAGGAAAAGTCCTGATTCACGTGTGGAGCACACCCATTCATTTAAGCAGGCAGCGAGCTGACAAAGTTTGCTGCTGCTGCTGCTAGGAGGGCTTCTATTTAAGTGGTCCTGGGTTTATTTACTGATATATATATATATATATATATATATATATATATATATATATATATATATATACACAGAGGAAGTCAGAATTATTAGCTCTCCTTTGTTTTTGTTTTTTTCTTTTTTAAATATTTCCAAAGTGATGTTGAACAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1625
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104807 | Nonsense | 319 | 413 | 6 | 7 |
ENSDART00000129429 | Nonsense | 319 | 542 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 20 (position 336511)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 327106 |
GRCz11 | 20 | 315741 |
KASP Assay ID:
554-1566.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCTGCAGAGTCCTAAAAGCTCAGAAAAACTTCAGGAGCAGAGGAAGTA[C/A]ACAGTCTTGGATCTGGTCCGAACGCCTAGAATGAGGAAACAGTCCCTCAT
Long Flanking Sequence:
AAACACAGGAATAACTTAAACAGTAAGCACAGGAAGCCATGCCACACCAGCTGCCCTTCTGAATCTGTGTATTTTGTCTCTTTGTACATGAATAGTTGTAGCCACCTCAGTAAACGGGGACCACCATGTCATAAAGGTCAAACAGGAACAAAATGAGGGTCAAGTCATAGCTAGAATATTCATTCTGGGATGAACAGACCTGTTAAGATTGTTGAAAATCTTTATTGCCAGAGGAATAGTCTTACATTCCGTCTAGCATGGGCTTATTTACAGTCAGCTGGACAATAGCACGCTGTAAGACACAGTCAGACCGACATGCTAACTGTCAGGTAGGGCTATTTGCATTTTATCTGGAATGCAGTGGAGTTCGAGCTCTCTTTAGAAATGAATATTCAAATGAGCCTCCGTCACTGAGAAATCAACTTGGAAATATGTCAATGTGTTTCTCTTCTGCTGCAGAGTCCTAAAAGCTCAGAAAAACTTCAGGAGCAGAGGAAGTA[C/A]ACAGTCTTGGATCTGGTCCGAACGCCTAGAATGAGGAAACAGTCCCTCATCCTCTTCTACCTGTGGTAAAATGCACCTGATTGCAAACATTTATTCATTTTCCTTCAGCTTAGTCCCTTATTAACAGCAGAATGAACCAACAACCATTCTAGCATATGTTTTGCGCAGCGGATGCCCTAACACAGTACTGGGAAACACCCATACACACTCATTCACACTCATACACTACGGCCAGTGTAGTTGATCAGTTCCCCTATAGCACATGTGTTTGGCCTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACACCAACACGGGGAGAACATGCAAACTCCACACAGAAACACCAACTGACCCAGCCGAGGCTCAAACCAGAGACCTTCTTGCTGTGTTTGGCAATTCTGTCCATAACATCTTAACATGCATTCCCAATGAATTACTTGACCAGAGGTGGGTAATAATGAATTACGTTTACTTCGTACATTTACTTGAGTAAAA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |