ZMP
zgc:153443
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC751686 [Source:RefSeq peptide;Acc:NP_001038865]
Human Orthologue:
SLC24A2
Human Description:
solute carrier family 24 (sodium/potassium/calcium exchanger), member 2 [Source:HGNC Symbol;Acc:1097
Mouse Orthologue:
Slc24a2
Mouse Description:
solute carrier family 24 (sodium/potassium/calcium exchanger), member 2 Gene [Source:MGI Symbol;Acc:
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16853 | Essential Splice Site, Missense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16853
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 > A
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080100 | Missense | 210 | 619 | 2 | 10 |
ENSDART00000111805 | Essential Splice Site | 209 | 231 | None | 3 |
The following transcripts of ENSDARG00000042988 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 11274952)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 11328352 |
GRCz11 | 1 | 12015152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTCATCTCACACAGCAAYGTSGGCATCGGGACCATCGTGGGCTCYGCCG[T/A]CTTCAACATCTTGTTCGTGATCGGGATGTGCGCTCTCTTTTCACGTGAGA
Long Flanking Sequence:
CCTGAGCGTCTCTGCCGTCACGTCGTTCCTGTCCTGGAGTGCCTTTACCTCCACTTTGGGCCCGATCCCGAGATGGACGCCACTCAGCTCTCTCACCAACCATGAGGGACTTGCAGAGCCAGTGCCACACAGAACTGTTCTCTCTTCCGACGAGGAGCGCAACGTTTCGGCAGACGTGCCTATCGCCATGGCCTCGTCCGCCGAACACAGCAAGGGAGAATATCCTGAAGATCTGTTCACGCTGGAGCAGAGGAGGCAAGGTGCCGTCGTGCTGCATATGTTCGGGATGATGTACATGTTCATCGCCCTGGCCATCGTCTGCGATGAGTTCTTCGTCCCGGCCCTCACTGTGATCACGGAGAAACTGGAGATCTCGGATGACGTAGCAGGAGCTACATTTATGGCCGCCGGTGGTTCTGCTCCTGAGCTCTTCACCTCAGTGATCGGTGTGTTCATCTCACACAGCAACGTGGGCATCGGGACCATCGTGGGCTCCGCCG[T/A]CTTCAACATCTTGTTCGTGATCGGGATGTGCGCTCTCTTTTCACGTGAGATCCTCAACCTCACCTGGTGGCCTCTGTTTAGAGATGTCAGTTTTTATATCATTGGACTAATAATGCTCATCGTCTTCTTCCTGGATAACTACATTACCTACGTCGAGAGCTTTGCGCTGCTGAGCTGTTACGGTAGCTATGTCACTTTTATGAAGTTCAACAGCAGTGTAGAGACTTGGATCAAGACTCGACTACTGGGGAATCAAGTGGATGACATTGAAGCTCCTCCTAAGGTGAGTCACATGTTTCCAGGTGAACAAAATGCAGGTCAAAGTTGGCTTTTGGTGGATGTGATTAACCTGCCACTGGTGTTAGAAAACTGTGTATCACAGTCAGGGATGGGCAACTTTGGTCCTGGAGGATCATAAAGCTGCGGTCACACTGCACTTTTCGCCCCATAGACTTCCATTCATACGCAGGTGAGTGCAGCAGACCAGAAACGCAAGCTCA
Associated Phenotype:
Not determined