ZMP
si:ch211-87l8.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate solute carrier family 24 (Sodium/potassium/calcium exchanger), m
Human Orthologue:
SLC24A4
Human Description:
solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 [Source:HGNC Symbol;Acc:1097
Mouse Orthologue:
Slc24a4
Mouse Description:
solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 Gene [Source:MGI Symbol;Acc:
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37169 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa10429 | Essential Splice Site | Available for shipment | Available now |
| sa37170 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37169
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 |
|---|---|---|---|---|---|
| ENSDART00000031139 | Essential Splice Site | 213 | 636 | 5 | 17 |
| ENSDART00000145132 | Essential Splice Site | 80 | 165 | 3 | 7 |
| ENSDART00000148149 | None | None | 203 | None | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 50475792)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 50360533 |
| GRCz11 | 20 | 50163537 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATGGCTGCGGGAAGCTCAGCGCCCGAACTCTTCGCTTCGGTTATAGG[T/A]AAATGCGTCCCTCAGTCACAATCATTTTGCACAAAGAAACAATCCCATTA
Long Flanking Sequence:
GCAATGCAAAAGCAAAAAAATAGACAATCACAAGACACAGGAATCTGTTTACAGTCAATTTCTTCCACAGTGTAATGAGATATTAAAGAGTTTTTGTTTGTTTGTCGTCTCCATCCAGGCTCTCTACATGTTCCTGGCGCTGGCGATCGTGTGCGACGACTACTTCGTGACGTCTCTGGAGAAAATCTGTGAGGTAGGATTGTTCCGATCGCACGAACACAAACCAAACAATCCTGAGGAATTCCCATTAGAGCTGAGTAATACCGCAGTACAATGAGAGCAGCAGAATTCTTCCTCTGACCCACTTTGAGGCTTTCAGAAGCTCATAAAACACACCGCTCCAGATCTGGCGGCTGTTTCTGCCAACAGGCTTTGTCGGATGTGAAAGTGTCTGCTGTTTATTGTGTTGTGCAGAAGCTGAATCTGAGCGAGGATGTGGCTGGTGCAACGTTTATGGCTGCGGGAAGCTCAGCGCCCGAACTCTTCGCTTCGGTTATAGG[T/A]AAATGCGTCCCTCAGTCACAATCATTTTGCACAAAGAAACAATCCCATTATTCATCACAAACTCTGGGAATGTTTAGTTTTCCTTCATCAATGTTTATTCTGTGGACAACACTCATTTTTGACTAAAGTAAAGGGTGTATTTCCTAATGCGAACAGTACCTTAGTCTGTCAACAATAATTAATGAGGGGTAGGTCTAGTTTGAGGGTTACGTGTACAAATGGAAATACAAGTACAAATACAAGTGTATTTAAACCTGAGACATTACTGTCCAGCATTAACCATTTTCCCTGACTTTCATTTTCGTCTGAGACTTTTATGCACTATTGCAAATATAATTGCAATATACCATGTCATAAAGCGTGAATCATCTCAGACTGGTTTCTTGAACATGTCAATGAGTTCACTGTACTCAAATGGCCTTAACAGTCACCAGCTCTCAATCCAATAGAGCACCTTATATATATATATATATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10429
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000031139 | Essential Splice Site | 272 | 636 | 7 | 17 |
| ENSDART00000145132 | Essential Splice Site | 139 | 165 | 5 | 7 |
| ENSDART00000148149 | None | None | 203 | None | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 50477906)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 50362647 |
| GRCz11 | 20 | 50165651 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTCCGTGACTYTTTCTTCTACATATTGTCTGTAGTCGCCCTGATTGTG[G/A]TGAGTCTTAAATMAAACACGCTAACAYCTYTCTGTAATGAGTTTCCCGAG
Long Flanking Sequence:
GGGCTGTTTTTGTGTTATGACAAGGCTTTTCTTATTAATTTGCATAATTTTGGATTTGATCTACTGTTGATGGTAAAAATTTTATTATATTTATTATTAAGTGATTTTTAAAAGTGCAAGTACATTATTTCCTTATATATTTTAATAGAAAAGGTGTTATTTATTTAGTTTTGCTGTAGTAATAATAATAATACAAAATAATAATAACAATAACAATAACAACAACAATAATAATAATAATAATAGTAATAATAATAATAATAATAAATTTTTATAAACTTAATTTAATTTAAACGATTAATTTCCCTGCTCTGCTAAACATCACTTGGAAAATATGTGAAAAGGCATCGCAATATTCACTGGAGGGCTAATAATGTTGCCTTCAACCGCGTGTATTTAACAGTTGTCTGCGTTTATGTCTTTAGGTGGTCTTACTAACCTGGTGGGCTGTTTTCCGTGACTCTTTCTTCTACATATTGTCTGTAGTCGCCCTGATTGTG[G/A]TGAGTCTTAAATCAAACACGCTAACATCTTTCTGTAATGAGTTTCCCGAGCTGTCATATAATTTTAAAATAACAACAATCAAAACATCATGCTAATTTGACTCATTTTGTAAATCTTATCCTACATTTTGTTTACCTGTGACCATTTACTAGCATTAGACAGCCACACACACTCTATTCCAACACAATCTCACGGCAATTCGTAACTTTTTCATTTAGTGGCTAATTCGTATGAATTCGTACGATCTAATTCGTACAATTTAGTATGATTTGCTCATCCCCCAATGACGGTTGGGGTTAGGGGTGGGGTCAGGTGCCACGCCTCCTTTTTAAAATTATACCATTTCGTACGACTGAACTCGTACAAATTCGTTTGAATTAGCCACTAAACTGGCAAAACGTAAAATACTTACATTTTCTCGTGAGATCAGGCTGTCTATTCTGTTGGTAAAGGCACAGTATGTACGATTTTATTCATTGAAATATCTCAAAATCACTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37170
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000031139 | Essential Splice Site | 490 | 636 | 14 | 17 |
| ENSDART00000145132 | None | None | 165 | None | 7 |
| ENSDART00000148149 | Essential Splice Site | 57 | 203 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 50501077)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 50385818 |
| GRCz11 | 20 | 50188822 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTATATCAACATACAGATGACACTTGACCAGTTTCCATTACTTCTTCC[A/G]GGTGACAATTATTGGATATACGCTGGGCATTCCTGATGTCATCATGGGTA
Long Flanking Sequence:
CCAAGAGCACCATCTGCTGCTGAAAACTAGCCTACAGCTCCATCTGCTGTTAAAAATAGGCTAGAACACGTCTTCCTTTAAAAACTAGAATAGATTGCAGACTACAGTTAAAAACTAGCCTAGAGCGCCGTCTGCTGTTAAAAACTAGCCTTGCATGTTTAAAACAAGCTTCTTCAAATAACAGTGTGTGTGTGTTTGTGTGTGTGTGTTTCAGATGGCTGTATGAACAGAACTAAATGGCTGATCTCTTGGCCGTTGTTGTTGATCCTGTTTTTTACCATCCCGAACTGTGCCAAGTCTCGCTGGGAGAAATACTTCATGCTCTCTTTTATCCTCTCCACTGTTTGGATCGCCGTCTTCTCATACTTCATGGTGTGGATGGTATGTATGAAACTGTATCTGTCTGTCTGGATCAGATGTGTCTCTCTTGTTTTTAAGTGCCACTGTTAGGCTTATATCAACATACAGATGACACTTGACCAGTTTCCATTACTTCTTCC[A/G]GGTGACAATTATTGGATATACGCTGGGCATTCCTGATGTCATCATGGGTATCACGTTTTTGGCTGCAGGAACGAGTGTCCCGGACTGCATCGCCAGTTTGATCGTGGCTCGTCAAGGTAGATTGATCATGTTTTAATGTCTAATGCTAGATCAATAAAACGGAGGCTTTTAACATTAAATACTGAATATTTTAGCATCAAGGAGCAGAGTAGAGCATATGATAAGAGAGGCACAAAACATCATCAGGAACATTCCTGTGTCACTCTCCGTCACTGAACTAATACTAATCCATACTAGCACTAGTCCTAACAACATGTTAATTCATGCTAGAAACACACTAATTTATGTTACAAACATGCACATTCTTGCTAGCAACATGTTAGAAAGATGCTAACAATGTGTTAATTCACGGTAAGACCTAATGTTTACGTAATAGCTATAAGATATATAAGAGAAGGTTATGCTAGAAACATGTTAGTTGATGCTAAATCTTAGTAACA
Associated Phenotype:
Not determined