ZMP
slc9a6a
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 9 (sodium/hydrogen exchanger), member 6a [Source:RefSeq peptide;Acc:NP_001091
Human Orthologue:
SLC9A6
Human Description:
solute carrier family 9 (sodium/hydrogen exchanger), member 6 [Source:HGNC Symbol;Acc:11079]
Mouse Orthologue:
Slc9a6
Mouse Description:
solute carrier family 9 (sodium/hydrogen exchanger), member 6 Gene [Source:MGI Symbol;Acc:MGI:244351
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35711 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa8605 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35711
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000026195 | Nonsense | 550 | 697 | 14 | 16 |
The following transcripts of ENSDARG00000009209 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 32506400)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 31296207 |
| GRCz11 | 14 | 31636521 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCCGCCTGCAGATCGGCCCTGATGGAGTTGAAAGGAGGAGCACTAAA[C/T]AGGAAAGCGCCTGGCTGTTCAGGATCTGGTACAACTTTGATCACAAGTAT
Long Flanking Sequence:
TAATAGCTTAGGGGATATGCCTTTCTAAGAGCATGTAAAAAGGCTAAAAACTAAAAAGTTGCAAAGGCTACAGTACATCAGCCTGTACTGAATTTAAGAAGAATTTTAATCAACACTGTTAAGGGGTTTGGGTCTATTGATAATGAAAAAAACACCTGAAGTCTTTCTCCCAAAAGGAACAGAATATTTAGAATTAAAGCAACTAAAGCAAGACAATCAGAATCCTGTTTTAAAGCGCTCAATATTTTAAAGGGCAACATTTTATTATAATTAATAAACAGAACATTAAAGTTGTCTTTATAGTCATAATTATTGTTGTCAACATGTGTTTTGTTTTTGACAGTGTTGGAGTGGACACAGATCATGAGAACTCTGTAAGTGCTTTTGCTCTGGTGTGGACAGGTGAACATTGTCTTATCAGAGCAGATCAGTGTAATGATGGTTTCCTCTGTGTCCGCCTGCAGATCGGCCCTGATGGAGTTGAAAGGAGGAGCACTAAA[C/T]AGGAAAGCGCCTGGCTGTTCAGGATCTGGTACAACTTTGATCACAAGTATCCTTTGCAGTGTAGCTCTAATTAGCAAACTGCATAAAGACAGAATCAGATGGGAATGAAAAAAACAACGTTATAAGTGTTATAAGCTAAGTGTTATAAGCTAAGAGTGTTATAAGCTAAGAATACATGCATTTAAAAAAGGTAATGTTTCTGCCACTTCCGATAGCGTGAACTCAAAGTTAGGGCATTTTTTCTACCTGCATGCATGTATCAGACTAAAACTTGATTCATTCATGTGGAGATTATTAAATTGGCTGCTGCTCCAGTGTCATGGTTATTTTGGATGTAAGTGATTGCAAGTGTCAACTTTGGCTGGAAAATCCTTAACCCTCTTGACCTACAGTTATCTAAAGCCCATTCTGACCCACAGCGGACCACCGCTCACTGCCACACTTCCAGCCTGCTGTAGTCCTCTGGCTCGCTGCCTGACCAGCCCACAGGCCTATGAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8605
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 |
|---|---|---|---|---|---|
| ENSDART00000026195 | Nonsense | 612 | 697 | 16 | 16 |
The following transcripts of ENSDARG00000009209 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 32511566)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 31301373 |
| GRCz11 | 14 | 31641687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGWGTTTCATTCCAGAATGAAGGCGAGCTGAAAAACGCAGACTCCGATT[T/A]GATCCTGAACGATGGTGACATCACTCTTACGTACGGTGACATCGCTGTGA
Long Flanking Sequence:
TTAAAATGTTCAAATAATCGAGATTTCAATTAATCGACAGGCCTAACGCGTTGTTTTCATGTCACTTCTCGTGTATGTTTGGTTGTGAGATGTAGTTTGTGGACCAAAACAACGTTGTCGGCAATTCTTCCTATTATAAATTCATGCAGTGTGAAACCCCGTCACCAATTGCAGTGTAAACACAGCACCGACAGAAGGCTACCCCAGATAGTCATGCAGTGTGAAAATTTCTGACACGACTATTTTGAAAATCGTCTGAACTCAACATTAGTGTGATCTTACTGAAAAAATATAATAATCTTGATTAGTGATGTTAAACAGTTGTATGTTTTTAATCACTCTAACTGTTATTACATTAGGCTCTAGGACAATTTCATGCTTGTTGTAAGTCTCTTTGCAGTATGACTATTCGCAGTCTGACACATTCCCCCCAAAAATTAGGTCACTGTTGTGTGTTTCATTCCAGAATGAAGGCGAGCTGAAAAACGCAGACTCCGATT[T/A]GATCCTGAACGATGGTGACATCACTCTTACGTACGGTGACATCGCTGTGAGCACGGATGGCACAGGTGCCCACTCAAGCGGCGTCCTCATGGGAGGAGCAGCGGTGAACTCGGACGAGGCCTTGGATCGAGAGCTGGCGTTCGGCGACCACGAGCTGGTAATCCGAGGAACCCGACTGGTCCTTCCAATGGACGACTCGGAGCCCCCGCTAACTCTGGACTCCCACCGCCAACGGCACAGGAACGAATTCATGAGCTGAATGGGTGACAAAAAAACGAGTCTCTTCTCTCTATCATCTCTCATGCAGAGCAATCTCTCCTGTCTCTGAAGTGGCTGGTTTGATGTCTCTACCTCATTCCTCACTCTTTTCTTTTACACTGAATTCTCAATTATTTATTCACCTCTCTTCTGCAGATTTGTTTTGTTTCTCATTCTTTTCGGCTAACCAGACCACTTGGCATCTGACAGATGGGAAGCATGCTCTGGTTTCTCATGATGAC
Associated Phenotype:
Not determined