ZMP
slco1d1
Ensembl ID:
ZFIN ID:
Description:
solute carrier organic anion transporter family, member 1D1 [Source:RefSeq peptide;Acc:NP_001082802
Human Orthologues:
AC087309.1, SLCO1B1, SLCO1B3
Human Descriptions:
liver-specific organic anion transporter 3TM12 [Source:RefSeq peptide;Acc:NP_001009562]
solute carrier organic anion transporter family, member 1B1 [Source:HGNC Symbol;Acc:10959]
solute carrier organic anion transporter family, member 1B3 [Source:HGNC Symbol;Acc:10961]
solute carrier organic anion transporter family, member 1B1 [Source:HGNC Symbol;Acc:10959]
solute carrier organic anion transporter family, member 1B3 [Source:HGNC Symbol;Acc:10961]
Mouse Orthologue:
Slco1b2
Mouse Description:
solute carrier organic anion transporter family, member 1b2 Gene [Source:MGI Symbol;Acc:MGI:1351899]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30489 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38230 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30489
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084568 | None | None | 599 | None | 12 |
| ENSDART00000127944 | Nonsense | 418 | 682 | 8 | 13 |
Genomic Location (Zv9):
Chromosome Zv9_NA995 (position 22832)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 76022734 |
| GRCz11 | 4 | 77407436 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTGGCGTCGGTTCTGGCTTTCTGTTCAATGCTCATCCAGTATTTCCTA[C/T]AGTGTGACAACTCACAAGTGGCGGGACTTACAGTCACGTACCAAGGGTAA
Long Flanking Sequence:
TGATCACGTTCAAGCCGAAGTTCATGGAGCAAGTTTACGGCCAATCGGCATCAAGAGCAATATTCTTGATAGGTGGGTTTCTGTTTGCTGGCTTTGTTATAGTATGTGTAATATTAATTTCTGGGGAAGATATATAAGAACAGATTGTATTTGTACACGTATAGTGTACAGTAGTAGTATATTCCAATTCATAGTGTTCAAAAGCTATATAGTGCAAAAAGTGTCCTACTACTACAGATTAAATTTAAATCCAAATGATCGGATATATTTCTATACAACTACGAATTGTTAATGAAGTCAAATATTCGCCAATATAAATATTGATGAATTGAGTTCATTTGGTCTTTGCAGGCATCATGAATCTCCCAGCCGTGGCTCTGGGAATCGTCACTGGAGGGTTTATAATGAAGAGATTTAAGGTGAATGTTCTCGGAGCGGCCAAGATCTGCATCGTGGCGTCGGTTCTGGCTTTCTGTTCAATGCTCATCCAGTATTTCCTA[C/T]AGTGTGACAACTCACAAGTGGCGGGACTTACAGTCACGTACCAAGGGTAAACACAGCAGAAATACGACTATGACATTGATTTTGCTTGCTTAGTTGTGACCTGTGACCTTTCCCGATCAAAACTTCTACTCATTTGAATGCAATTGTTGTAAAGCAGTTTAATAATCGAGGTCGGATAGGCAAGGGTCATGAACAGGAGCAAAACAGTACCATAAGGGTAATCCAAAAATCGATGTACAGGGGAGAGGTCAGATTAGGCGGCAATAGATCAAGGCAAGGATCAGAAACACACAGGGAAAGCGACAAAGGCTCTGGCAGCAGTGCACGCTTTGGCAGCTCTGGTAGCGACGAAGGCTCTGGTAGTGATGAAGTTGATGAAGCGTTGCGGTTGGTGGAGAGTAGCAAACCCAAGAGGGAGGGTCGCAAACTGAAGACTGGGGTCCCGTTGGGATTCCAGGAGTTTTCCGGAAGACAGAACAAAACAGGAGATGGGTCTGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38230
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084568 | Nonsense | 536 | 599 | 12 | 12 |
| ENSDART00000127944 | Nonsense | 619 | 682 | 13 | 13 |
Genomic Location (Zv9):
Chromosome Zv9_NA995 (position 39009)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 76006265 |
| GRCz11 | 4 | 77390967 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAAGCACCGTTTTTGTCTTTCAGGAATGCTTTCTTGGGGTTAATTTA[C/A]GCCCTGTACAGCTCATCCTACCTGCTGTTTGGACTTCTCTACAACAGACT
Long Flanking Sequence:
TAGCTTAGCATAAGTCATTGAATCAGATTAGACCATTAGCATCTTGCTCAAAAGTTTCAATTAACTATATCGAAAGTTTTGAGTGAGATGCTAGTGGTCTAATCCGATTCAACTATTTATGCTAAGCTAAGCTAAAAGTGCTCCCGCCAGACCCAGTGATCAGCTGAATGGATTAAAAAAAGTTAAAACTTAGCTGTTTAACTCTAGGTGACTTGTAAACTGGAGGGTTTCATTAAATATCAATAAAAGTCACTGAATATCAATAAAAGTCAACCAAAGTTGTCAGAGCGGAGATCAAGGTCCGGTAATGCAATCAGAAAGCCTAAAGAACAACAACAAAAGACACCCATCGCCAACATTTCTCCTTTCATTCTGTCACAGTAGCTCCATGGTGTCATGTCATACAAGCGCACTGTAGCCAAAACCACACAACCGTTGTCTTTCCATGTCATGGAAGCACCGTTTTTGTCTTTCAGGAATGCTTTCTTGGGGTTAATTTA[C/A]GCCCTGTACAGCTCATCCTACCTGCTGTTTGGACTTCTCTACAACAGACTGTCTCATCGAGAAAAGAAGCAAGCGCTAAAGGACCAGTTAAAAGCTCCAGAGCAGGACAGCTGTGGTGTATCGACCACCAATGGAAATGCGTCTTCGGCGATCGTAAAATGCGAAAACCCAGACCAGGAGACCACCATCTGAAGTCCTGCAGGCAGAAACAAACCAAACACTAGAAAACATTGTAGTATTCTAATGTTTATATAGAAATTGCATGGGTTTTAATGTCCAACGATACTCTGGAAACCATCGAAAAGTACACTGTGAAGTTGACTCAACTTAAAATTGGATGGAAACTCCAACTTTTCGAGTTGACTCAACTTAATTCATGTGTTGAAGTTGCCTCACAATTTTAAGTTGAGTCAGTTGAGTTTTTACTGTTTTAATGGTCAAAAATGAAGGGTGGAAACCGTTCTGTTCTGGTTAATATTGAGTTGAAGTCAGAATTATTA
Associated Phenotype:
Not determined