ZMP
slc9a5
Ensembl ID:
ZFIN ID:
Description:
sodium/hydrogen exchanger 5 [Source:RefSeq peptide;Acc:NP_001106943]
Human Orthologue:
SLC9A5
Human Description:
solute carrier family 9 (sodium/hydrogen exchanger), member 5 [Source:HGNC Symbol;Acc:11078]
Mouse Orthologue:
Slc9a5
Mouse Description:
solute carrier family 9 (sodium/hydrogen exchanger), member 5 Gene [Source:MGI Symbol;Acc:MGI:268554
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2382 | Essential Splice Site | F2 line generated | Not yet available |
sa34118 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12316 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2382
Status:
F2 line generated
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081338 | Essential Splice Site | 268 | 970 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 7 (position 36085686)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 34359529 |
GRCz11 | 7 | 34631006 |
KASP Assay ID:
554-3330.1 (used for ordering genotyping assays)
KASP Sequence:
CTTCATCATYGTCTTTGGCGAGTCATTGCTCAATGATGCTGTCACTGTGG[T/G]AAGTCAGTTTTTAAAAAATAGAATMTTCTCTTGTATTACTCACRTTTGCT
Long Flanking Sequence:
TTATTTTTTTCAATAAATACCCTCAGTGCAATAAAAGTGATCAGTATTCATCATTAATGTTACAATTATTTAGCGCAAAATACAAAAAATTATTTATTGCATTTAAACATTTGCTCAATTTTGGTCACATACTAAGATTCTATCTAATTTTCTAATCTAATAATCAAATCATTTGTTTTGATTTGGCACATTCAAGTTTCATACTGTTATTTATACTATTTTATTAAACACAGGTTGCTCCTGGACAGTCGCAGTGGAGCAAGTGCATGTTAAGCTATGGTTAAATTGGTTGTAATTATTGACTGGATTTGTTTATGTGTTGTGTGTGAGTGCAGATGAAAAAGTGGACGCAGGTTTGATGGAATTCTTGTTGTTTGGAGCTCTGATCTCAGCTGTGGATCCTGTAGCAGTGCTCGCTGTGTTTGAAGAAGTCCATGTGAACGAGACACTCTTCATCATCGTCTTTGGCGAGTCATTGCTCAATGATGCTGTCACTGTGG[T/G]AAGTCAGTTTTTAAAAAATAGAATATTCTCTTGTATTACTCACGTTTGCTTTCATCTCTAACTTATAAATTGTATTTACATGATTAACATGCTACTAGTAGAGTGGAATGATACGTCCAACACAGGCTCATTGTGAAAATATACCCCAGTATACATTTCTGAAGAGCGCGAATTATGTAGCCTGTTCACGCTACCGTCTGATCGCTTACCTCTGTGTGGATGGTTTTTACACTGTTACTGCATTGCCCAGTGCATATTGCCTATTTGATTTGTTTTAAAAGCCCATTAATGAATATTTCTAAACTGATTTTTTTTAGCCACATCGCTAAAGTCTTCAGTGTCACGTTCAAAACAGTTTTTTTTTGTTTTTTATCATTTGTTTTGCTGAATTTCGAAAGAGTAAGATTTGTTTTAAATGGCATTTTAGTCTTCATAATTTAAGTGTATAAAAGTATTTACTGTCACTTTTCATCAATGTAATGTTTTCCTCGCTGAATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34118
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081338 | Nonsense | 362 | 970 | 6 | 16 |
Genomic Location (Zv9):
Chromosome 7 (position 36092036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 34365879 |
GRCz11 | 7 | 34637356 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAATGACAATGTTGATTCACCACAGGTTGACTTTCTGTGGAATTGGCTG[T/A]AACAAATATGTGGAGGCTAATATATCCCAGAAGTCCCGGACTACTGTAAA
Long Flanking Sequence:
ATATGTAGAGTAGGCCTATAGTGAATGCACTGTATATTTGGGATAATGGCATATCTTTGTCTCATATAAGAACATGTTAAATTGGAAAATGTAAATCACTAAACATGGTTAAGGTGTTTACTAATTTATTTTTAAGTATGGGCATTAGTATAGTATGCAAAAACTAGAAAGACAATCAAAAATCTCACAGGAAATAAAAGAATACATCGACTGCAACATTCATTCATAAATTTTCCTACGACTCAGTCCCTTTATTCATCAGGGGTCGCCACAGCGGAATGAACCGCCAACTTTGACTGCAATATACAGTATTGCATTTAAATTATTTTCTTTGTGTAATCAAATATTAAAAGCACTGCTATATTATATATGGAATTAAAAGGCAAGGATGTCACTCCTAATCTGGCCACCACAATAATTCTGTTGGACTATATCATATTGCACAACATCTTAATGACAATGTTGATTCACCACAGGTTGACTTTCTGTGGAATTGGCTG[T/A]AACAAATATGTGGAGGCTAATATATCCCAGAAGTCCCGGACTACTGTAAAGTACACCATGAAGACCCTGGCCAGCATTGCAGAGACGATCATCTTCATCTTTTTGGGAATCTCAGCTGTGGACAAGTCAAAATGGGCCTGGGACACTGGTCTCGTTGTCAGCACACTCATATTTATCTTAGTCTTCAGGGCTATGGGTGAGAAAGAGAATTCTCTATTCAATTCCATAACATGATATGCTGAAGTTTTCAAGTTGAAAAGTGAATGCTAACTGAATATTCTGCATTAAAACTAAGTGAAGTTTATTCATGAACTGATTTCGAGAGTAGCACATGCTTATGATTGTTAGCAGCTGGTCCTGCATTAGCTTATGCATTATTTACCAATCAGATGACTCTTAACCCACTATATTCAATTCAATTCAATTCAATTCACCTTTATTTGTATAGCGCTTTTACAATGTAGATTGTGTCAAAGCAGCTTCACATAAATGATCATAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12316
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081338 | Nonsense | 948 | 970 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 7 (position 36106369)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 34380212 |
GRCz11 | 7 | 34651689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCCACYTGCTGCACAATCTGCAGGAAAGAGAAGGAATCCTTGTGTTTA[T/A]CTTAGGAGTCTGGTGACAGTGCCACCTACTGGTGCRGAGCCACATAGCAG
Long Flanking Sequence:
GCAGTACCAGCAGCTCTGGATGTCTGTCAGAGCCCGATCACAGCTCCTCCCTCACTGACATGCGGAGAGAAAAACCTGCCGTGGAAAAGTGGCATGGGTTCCCTCCCTCCCTGTGTGTCTGTGGAGGCAACCAAAATCATCCCAGTAGACCTTCAGCAGGCCTGGAATCAGAGCATCTCCTCTCTGGAGAGTCTGGCTTCTCCTCCTGCTCCCGCAGAGCCTCTTCACCCGCGCATTAGCGCTCTCTCGCGGCTAGGAGGACCCCTGCGCACCCCTGCCAAGGACAAAAGTGCTGGTGTTGATGCAGGATTAGAAAGCACTACAAGTTCCCCAAGTTCAGGGCAGTTCAAATACCCTATGGGGAAGGAGGAAGAGGAGGAAGGTGCTCTTTCTCAGCAGCATCGGGAAATGCAGCCGCTAATGTCATCTTTGAGGCCGCCACCGCCTCCTCCTCCACTTGCTGCACAATCTGCAGGAAAGAGAAGGAATCCTTGTGTTTA[T/A]CTTAGGAGTCTGGTGACAGTGCCACCTACTGGTGCAGAGCCACATAGCAGGAAGCCAACCCAACTATAGACTCTCTCGCTTTTTTACTGTGTGGTCATTTAAGGACCTTCAATCATCTCACAGTAGGCATTTACCTCCTCAGGCCATACTTTATTTTTGAAGTCAGTAAATTAATAACTGAGAGGTTACTCGTTTGGTTTCTTTTTTTAGCACTTCATGGGTTTATAAATGCAATTATTTGTTGGTTTGAAGTGATCTTCAAGCTGTGATCTGCCCTGTATCATGTACCTCTGCATGTGTGATTGTCAAGGTTAAAAGCGACTGAACATCTTAAGGCTAAACCACATTCCAAGTACCATGTACTGGGAGTGTCTGTTGAACAGTGTTTTTACTGAAATGTCCTCCCTCAGTCACTCAATCACACATCTAAGAACGGCAAATCACTTTATGGTTATTCTTAATCTCACAGATTTATTCTTCAAATCAGCCAATCCATTTTA
Associated Phenotype:
Not determined