ZMP
slc9a2
Ensembl ID:
ZFIN ID:
Description:
sodium/hydrogen exchanger 2 [Source:RefSeq peptide;Acc:NP_001107567]
Human Orthologues:
SLC9A2, SLC9A4
Human Descriptions:
solute carrier family 9 (sodium/hydrogen exchanger), member 2 [Source:HGNC Symbol;Acc:11072]
solute carrier family 9 (sodium/hydrogen exchanger), member 4 [Source:HGNC Symbol;Acc:11077]
solute carrier family 9 (sodium/hydrogen exchanger), member 4 [Source:HGNC Symbol;Acc:11077]
Mouse Orthologues:
Slc9a2, Slc9a4
Mouse Descriptions:
solute carrier family 9 (sodium/hydrogen exchanger), member 2 Gene [Source:MGI Symbol;Acc:MGI:105075
solute carrier family 9 (sodium/hydrogen exchanger), member 4 Gene [Source:MGI Symbol;Acc:MGI:105074
solute carrier family 9 (sodium/hydrogen exchanger), member 4 Gene [Source:MGI Symbol;Acc:MGI:105074
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34552 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21430 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34552
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081718 | Nonsense | 259 | 795 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 9 (position 7025905)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 7005998 |
| GRCz11 | 9 | 6984389 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCTCCATTTCAGGTACTGTATAATCTCTTCAATCATGTAGCAGCGATG[G/T]AAGTGGATGAACCTGCAGTCATTTTCATGGACATTGGCGGATTTTTTGTG
Long Flanking Sequence:
TCTGAAAACAATCACCTACTGCACCCTGAAAGGCTAAAAAATATTGGAGGGAATGTGGAGACAACATATAAAATAATATGTTTTGCTACTCATTTACGAATAGAAATTTATTTTTATTGAGACTTTTTCTGACTCAAAAAATAACGGAAAAACTCAAATTTTTAATCTCGAGTGGCACGGACCTGCTTGGACAACACTTAAATACATCACATCCGGTCGGCCGGTCGCATACGGTCTAGTCGCAGGAGTTCAACTCAGATCCGATTTTACCGCATATAGAGATGATCGGAACTCCACACAGCTCCTGGACTACTCTCCATTGGAAATGAATGACTTCCGGTCTGTCGCTTGTCATGTACAGTTGAAAGGAGGCTTTAAAATTCATCGTATCTGTACTCTAATTGTATTAGTCATTTTTTTGTGCATCAGTTTTTGTATGTCATAGATGTCACCCTCCATTTCAGGTACTGTATAATCTCTTCAATCATGTAGCAGCGATG[G/T]AAGTGGATGAACCTGCAGTCATTTTCATGGACATTGGCGGATTTTTTGTGGTGGGTTTGGGTGGGATATTCTTCGGCTTGCTGTTTGGGTTTTTGACAGCCTTCACCACACGTTTTACTGGAAAAGTGAGAGAGATCGAGCCCCTGGTCATCTTCATGTTCAGTTACATGTCCTACCTCATCGCTGAGCTATTTGCACTCTCCAGCATCATGGCGTAAGTAAAGCCCTCTTAGTAAATTTGCTTCTGATCGTCTGAAGAAATGATAGATTTTCCTGAAAGTTGTGCTATTCATATTTTACAGTATCTTAATCTGCACCTTGAGTATGAAGTACTACGTTGAGGAGAATGTGTCCCAGCGCTCCTGCACCACTATTCGCCATGTCATTAAGATGGTTGGAAGTGTGTCGGAAACACTGATCTTCTTTTTTCTGGGTGTTGTTTCAATCACAACGGAGCACGAGTGGAACTGGGGCTACATCCTCTTTACTTTGTTCTTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21430
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081718 | Nonsense | 732 | 795 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 9 (position 7004908)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 6985001 |
| GRCz11 | 9 | 6963392 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCTGAACGATCTGAGGGAAGATAATGAACCAAATGAAGAAATTCCTTA[C/A]AAGATGTCACATCCAAGGTCAAAATTCAGACATTCAGGACATCAAACCTC
Long Flanking Sequence:
ATCACTCTAGCTTGACGTGCGTTCCACGTCGGGTGTGAACGCAGCATGAGGCTGTGTCCTTCAGGTTGTTATCACAGAATGACGCATTATCAGTCATTAAGCACTGATAATAGGATATTTTTAAAGAAAAATACAGGTTACACTTTTACATGCAAATGGTTTGATATGCAAATATCTACATGTTTAAAAACAAACACATTAAAATTGTAACATATCCTGCGTTAAAATTGTCAGGCAAGTAAGTTCCCTGCTGGTGAACCATTTTTACCTTGTGAAAATACTAGTGTTTCTGGTTATTTTTGTTCATAACCCTGATTATAGTGGATAGTAACATGCATTGTTGTGTTTTCAGACCACATTGATGCTGAATCTGAGACTGCGTATCCATCAAACAGATCAACGTTCAGGCATCAGCGGAGATCGTCATCTAAAGCAGGGATTCCTCTCAGGCCGCTGAACGATCTGAGGGAAGATAATGAACCAAATGAAGAAATTCCTTA[C/A]AAGATGTCACATCCAAGGTCAAAATTCAGACATTCAGGACATCAAACCTCACGTCAGTATTATGGCACATCTAGAAACTGTAGGGACACAGACTTTGAAGAGCAGCAGTCGAGCTTGTCTCCTCATGGATGGACAGAGGAACCACAAAACAACAGTGATGTCCAACATCCCCTGATGAGAAAACCACAGTAGATGCGACAGAAACCACATGAACAATGTGATCATACTTTTAAAGCAGCTGACCTGACATTACTTGATCCGACTACTTTGAAACGAAGTAAACAATGCAAAAGAAGTCTACGTGTGAGAAAGGGAAGAACGTTCTCCATGTTAAACAAAATTCTGCTCAAATATAAACAATAGAGCTTTCCATGACACTAAATCCACATTACTCACTCTAAATATAAGGTCACACTTTATTTTGATGGTTCGTTTTTTACATTGCATTTACATGTCAACTAATTCTTGTTAGATTATAAGTAGACTGATAGGTTGGGATT
Associated Phenotype:
Not determined