ZMP
zgc:153639
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 22, member 13 [Source:RefSeq peptide;Acc:NP_001070840]
Human Orthologues:
SLC22A13, SLC22A14
Human Descriptions:
solute carrier family 22 (organic anion transporter), member 13 [Source:HGNC Symbol;Acc:8494]
solute carrier family 22, member 14 [Source:HGNC Symbol;Acc:8495]
solute carrier family 22, member 14 [Source:HGNC Symbol;Acc:8495]
Mouse Orthologues:
Slc22a13, Slc22a14
Mouse Descriptions:
solute carrier family 22 (organic cation transporter), member 13 Gene [Source:MGI Symbol;Acc:MGI:214
solute carrier family 22 (organic cation transporter), member 14 Gene [Source:MGI Symbol;Acc:MGI:268
solute carrier family 22 (organic cation transporter), member 14 Gene [Source:MGI Symbol;Acc:MGI:268
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37868 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37868
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082201 | Nonsense | 227 | 508 | 4 | 9 |
ENSDART00000121740 | Nonsense | 227 | 415 | 4 | 7 |
ENSDART00000146340 | Nonsense | 227 | 542 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 24 (position 20621214)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 19868343 |
GRCz11 | 24 | 20012762 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAGGTACTGAGTGGTGTGGTTCAGCCAAGCGGGCCCTTTTCACCATAT[T/G]ATCGCACTGCTTTTTTGCCATTGGTCTGATGTTGCTGTCTGGTGTGGCCT
Long Flanking Sequence:
TATCAACACATTTGTTCTGGGTATTGCCTTTGACTCCTTTCAATGCCCGCACATGTCTGAAATTTCATAGCATGTAGGAAGAGCTTATGAAGTAGTTAAAGTTGTAAATGTAAAAATGTAAAACTATTATTATTTAACGCAGTGTTCAAGTCCACATGAATCAGAAGCTGTGACCTTTCTTTTTTGTATTGTGACAGATTGGATGTAGAGAAATGGGATATTAAATGAGACAGCAGTGGGCGTGGCTTGTTTTTTCTATCGTGAGCTGATTGGATGTAGTAAAGTAGGCATTTCATTGAGAAAAATCAGGAAAAGGGTTTGGGGGAGTTATTACAACCATACAGACAACTCCTGCTTACGATTTCAGTTTGTTGATGACTTTAAACAGATTTCTTGTTTGTGATTATTATTAGCAGTATTTTTATACATAGTATCTCAACTGTCTTTCACTGTAGGTACTGAGTGGTGTGGTTCAGCCAAGCGGGCCCTTTTCACCATAT[T/G]ATCGCACTGCTTTTTTGCCATTGGTCTGATGTTGCTGTCTGGTGTGGCCTATGGGATTCGAAACTGGAGGGTTTTACAGCTGGTTTTGTCAGCACCAGTTGGGCTTTTCTTTATCTATTACTGGTGAGAGTATTCAGAGATGATCAAAATTTTATTTATTTATTTTTTTGTCAGATGAATATTTACTTATCTAACTAATTTTAATTAATCTTTTAATTGTTTAACAAAACATTTGCGTGATAATGATTTTCTGATATCAGCTAAGGCTCTTGTGACATGCACATATACAAATAACATATTTTATATTTTTACTGTGTTAATTAAGCTATTATTATAAGTTTTTGTTGTAAAGTAATTTTAAAATATTCATCCATTTATTCATTCATTTAGCTTAGTTCCTTTATTCATCAGGGGTCATCACGGCGGAATGAACCGCCTACTTATCCAGTTTATGTTTTACTCAGTGGATGCCCTTCCAACCACAACGCAGCACTGGGAAA
Associated Phenotype:
Not determined