ZMP
slc24a1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to solute carrier family 24 (Sodium/potassium/calcium exchanger), member 1 (SL
Human Orthologue:
SLC24A1
Human Description:
solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 [Source:HGNC Symbol;Acc:1097
Mouse Orthologue:
Slc24a1
Mouse Description:
solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 Gene [Source:MGI Symbol;Acc:
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18070 | Nonsense | Available for shipment | Available now |
| sa29018 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa43082 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36625 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18070
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 |
|---|---|---|---|---|---|
| ENSDART00000060735 | Nonsense | 270 | 724 | 1 | 9 |
| ENSDART00000135729 | None | None | 205 | None | 4 |
| ENSDART00000139601 | Nonsense | 121 | 197 | 1 | 1 |
| ENSDART00000140447 | None | None | 36 | None | 1 |
Genomic Location (Zv9):
Chromosome 18 (position 18790230)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 19020453 |
| GRCz11 | 18 | 19009519 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAATTGGAAWGTGTGCAYTGTTTTCACGCRARATGCTTCACCTCACCTG[G/A]TGGCCTCTCTTTCGGGAYGTGTCCTTCTATATCCTGGATCTCATCATGCT
Long Flanking Sequence:
ACAACAACAAACAGGACAATCGTCCACTGTATCTATGTGGATCCAGACCTCCCAAAACCCACTCCAGTTCCAACTCCAGCAACTGAAACGACCACTCTGGTGCCCAACACTACCGCGTCCCAACCTGGAGATGCACCACACATGAAGGGCGAGTATCCGGAGGACATCTTTTCCATTGAGGATCGACGCAAAGGCTGGGTCTCTCTCCATATTTTTGGAATGGTATACATGTTTGTTTCTTTGGCCATCGTCTGCGACGAGTTTTTTGTCCCAACTTTAGGGGTTATAACAGACAAACTGGCCATCTCTGATGATGTAGCCGGGGCGACGTTCATGGCCGCTGGAGGCTCAGCTCCTGAACTTTTCACCTCTTTGATTGGAGTCTTCATTTCTCATAGCAATGTGGGCATTGGGACCATCGTTGGCTCGGCTGTTTTTAACATCCTCTTCGTAATTGGAATGTGTGCACTGTTTTCACGCGAGATGCTTCACCTCACCTG[G/A]TGGCCTCTCTTTCGGGACGTGTCCTTCTATATCCTGGATCTCATCATGCTTATCATCTTCTTCCTGGACAACACCATTATGTGGTGGGAGAGCATGATGCTGGTGGGAGGTTATGCTCTATATGTAACCTTCATGAAGTTCAATGTTCAGTTAGAGCGCGCCTTTAAGTCTCAGCTCAGCAAACACAAGAGCATCGTCAAAGTCATTGCGGTGGAAGAACCAGAGAAGGTACGTCTAATTGTTTTTGCTTTGGGTCAGATGGATTTGGCTACATGCCTCATGTGCAGGGCAGAACAATTTTGGCTATTTCTCCACAGAATTTTGTAAAAAAAATCTGATCAGATTTATGTGGAATGATTTTGAGAGTACAAGATCTGAAAAGAGTGGCAGAGTGGCTCAGTGGTTATCACTGTCACTTTGTAGCAGTAAAACGTCACTGGTTTGAGTCCCGGCTGGGCCAGTTGACATTTCTGTGTGGAGTTTGCATGTTCTCCTCATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29018
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060735 | Essential Splice Site | 347 | 724 | 2 | 9 |
| ENSDART00000135729 | None | None | 205 | None | 4 |
| ENSDART00000139601 | None | None | 197 | None | 1 |
| ENSDART00000140447 | None | None | 36 | None | 1 |
Genomic Location (Zv9):
Chromosome 18 (position 18796191)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 19026414 |
| GRCz11 | 18 | 19015480 |
KASP Assay ID:
2261-2076.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTCTCTGAATATTTTGCATACTCTGTAATTCTAAATGGTGTTGCACAC[A/T]GGATAATGGAACCTCAGGTGAAGAGAACAGGCCACCTGAACCAGAAGACA
Long Flanking Sequence:
ACCAAGGCTCGAACCAGTGACCTGCTTGCTGTGAGGCGACAGCACTACCTACTGCGGCACTGCGTCGCCCCTTTAAGTATACTAGTGTAGAATATTACAAATATCCATCTTTCCAATGAGGCGATAAACCGAGCTCCTGACTCTTTGTGGTCATTAAAATTCCCATGGCACTTCTCGTAAAGAGAAGGGGTGTGACTCCGGTGCGCTGTTCCACCAAATTGGCTCTCCACAACACCTATAGCTAGTGTGTGGTGAGCGCACTGGCACCCTTGTCATGTGGTTGCCGTTGCATCATCCAAGTGGATACTGCACACTGGTGGTAATCTGGAGAGACCCCCCCTCATGATTGTGAAGCGCTTTGAGTATGTGGCCATGCACAATAGAAATACACATTACATTAGATATTTACAACATTAAAAATAAACTTTATAATAATAATATAGTCACCTTTATTCTCTGAATATTTTGCATACTCTGTAATTCTAAATGGTGTTGCACAC[A/T]GGATAATGGAACCTCAGGTGAAGAGAACAGGCCACCTGAACCAGAAGACAAGAATCGATTAAAGGTAAACAGAAATGTGCAAAAATATGTACAAACATCAATAGATAAATATATGTAAATAAATCACTGGATTAGGAGTCAGAATATATGTGATCCTCTGATAACTTTTTCAAATTAGAGTGTAAGTGGCTAGAGAAGCAGCTGTCAATCTCAACTAGTGGACCAATGATAATGTTGAAGCCCTCCGTGATTTAAATTAAAGTCTAAGGACATGGTTTGTTCACACAAGTGCAAAATGTGGAAACAAAGCAAAGGGGATAAGACTATATGTTTATATATAATTGGAAAAAAAACTGATTTTGTTTGTAATTTAGAAAACTTTTAATGCAGAGTTCAATCTTGTGCAAAAGAGATTTAAATGTGTGGGGGGTTTTTTGATTCACAGTTATTATTTTTTATCCCTGACCTCATTGTTTCTTATTCTAAAATAATGTAGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43082
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 |
|---|---|---|---|---|---|
| ENSDART00000060735 | Nonsense | 442 | 724 | 5 | 9 |
| ENSDART00000135729 | None | None | 205 | None | 4 |
| ENSDART00000139601 | None | None | 197 | None | 1 |
| ENSDART00000140447 | None | None | 36 | None | 1 |
Genomic Location (Zv9):
Chromosome 18 (position 18804037)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 19034260 |
| GRCz11 | 18 | 19023326 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTATCATGGTTTAAATAAGGTGATGATCAATCGGAGCAGACCAAGGATT[C/A]AAAAGACGCGCCTCCAGGAGCCAAAGATGAAGACACCAATCAGAAGTCTG
Long Flanking Sequence:
GCTTTGTAGACAGGTCTCTGCATTGTCCTACCTCACAGATGAGCTCTGTTGCATATTCAAAACGGATTTTAATGTTGCATTTCCACAAGCGCTAACGCAGCAGCTGTGTGCTGGATGAAAGCTACAAAGAGAGGGCACGCTGCCAGGAGTTTGGCCCGTTTTGCCCTCTGCGCCGCATCCCGCATTCCATATTTCCACCTTTTGTTTCTACTTGAGAGCTGCTTTACACATTAGCTGACATAATGACCAAGCTCCATCTCATGAATTAAGCATGAGTGGCTTGGAATCAATTGCGGATTATCTTGCGCCGCGACTGTGGGCTTTGAAATTGCCGCCAAAAAGATACCGCAACATTACTCACTCCTATTGAGGAAATCTTCACTCCACATCTGAGAGGAGCTTGTAGTATTGTTACATGCAAGACTTAACTGCAGGATTCATTCATGTTTTACTATCATGGTTTAAATAAGGTGATGATCAATCGGAGCAGACCAAGGATT[C/A]AAAAGACGCGCCTCCAGGAGCCAAAGATGAAGACACCAATCAGAAGTCTGAGGCACAAAAGGTGGGCCTACTGCATCAAAACAAATGTTTGGAAGAACAAGCAAGAGCTCTGAGACACTTGCGTGCTTTTAATGAGCTTATCAATTCTTTACCCTGTTGTAAAGCAGACAGAGGTGATCTGATTTATATAGTACGTCATTCATATTCACATTTTTGTTCAGATGAAAAGTCTGTCATCTTGGGCTGGGCGATTTGGACTAAAATCTAAATTTTGATTAAAACTCTATTACGATTAATGAACGATTATTCATTTATTAATTTATTTTTTGTCCTCCATGTTTACTGACAAGTTGTGTACAGTAAATATGCTCAAATATTACAAGTGAGAGATTTTTAAATGGTGCATTACTTGATTTTAAAATAATTGAAGGAAGCAAACACTATCTACTATCTATGGTCATTTATTGGACATGAACGTTGAACAAGTGAAATTAAAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36625
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060735 | Essential Splice Site | 556 | 724 | None | 9 |
| ENSDART00000135729 | Essential Splice Site | 37 | 205 | None | 4 |
| ENSDART00000139601 | None | None | 197 | None | 1 |
| ENSDART00000140447 | None | None | 36 | None | 1 |
Genomic Location (Zv9):
Chromosome 18 (position 18815239)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 19045462 |
| GRCz11 | 18 | 19034528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCATTGTCTTTCCACTGTGGCTGACCGTTCCAGATGTCAGAAACCCTG[T/A]GAGAACCAAAACCAAATCACTTCAGCTTTAATTTTATTTGTTCTTCTTTT
Long Flanking Sequence:
CTATATTTTACCCAAGTTAGCTTTGAAATACTGAGATTGAGACTTTTGACATTTCAATTGTAAATTCAATATTGGTTACAAAATTGGGCAATTTATAATCATTGGAGGGGAATTTGTCCATCTCAGTGTCTAGGAGTTACAGCCATCTTTATATTTGTTGTTGTTTGTCTAATTTTTTAGATTATTATATGATGTTTTCACCTGCCTCTGTTTTAAGGATGGAGACATTGCAGCAGGAGGAGGTTCTGAAAATCCAGGAGGTTCAGACAATTCAGGGGATGATGATGAAGATGACAGTGATGAAGAGAGTGATGATGACGATGACGACGATGATGATGATGACGACGATGATGATGAAAATGAAGATGAAGCTGGGGAAGATGGAGATGAACCGTTGTCTTTAGAGTGGCCGGACACCAGACGTAAACAGGCCACGTATTTGTTTTTGCTGCCCATTGTCTTTCCACTGTGGCTGACCGTTCCAGATGTCAGAAACCCTG[T/A]GAGAACCAAAACCAAATCACTTCAGCTTTAATTTTATTTGTTCTTCTTTTTATATTATGCTATTGTACGTTACAGGCATCCAAGAAGTTCTTCGTCATTACCTTTCTTGGCTCAATAGTGTGGATTGCTATATTTTCCTATCTGATGGTGTGGTGGGCACATCAGGTCAGTTGCGCCTGCTTTTTTAAAAAAAAAAGGTTTTTGAAAAGGCACAATATGTCAGATTTTTTCATTAATATATCCAAAAACGACCATAACAGTGTTGTATATTTAGCTGATTTATGGGCTAACATTATCACAGATGTTTTAAAGAATGTTCAAACAAGCAATTCCTCAATTTTTCTGTTTGGTTTTAGAGAAAACCGGGAAGCATAGCATTAATATATTGTATGTTTTCTCTGCTTCTTCTTCAAATATTGATTTCAAATATTTTCCCCAGTGTCTTCTCATAATTCCAAAAAGGTTTAGAGGCAGGTGATTATCTAATGCTGGTTGAGTTA
Associated Phenotype:
Not determined