ZMP
slc8a1b
Ensembl ID:
ZFIN ID:
Description:
sodium/calcium exchanger 1 [Source:RefSeq peptide;Acc:NP_001034233]
Human Orthologue:
SLC8A1
Human Description:
solute carrier family 8 (sodium/calcium exchanger), member 1 [Source:HGNC Symbol;Acc:11068]
Mouse Orthologue:
Slc8a1
Mouse Description:
solute carrier family 8 (sodium/calcium exchanger), member 1 Gene [Source:MGI Symbol;Acc:MGI:107956]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa28843 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36395 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23060 | Nonsense | Available for shipment | Available now |
sa19172 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23061 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa28843
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 |
---|---|---|---|---|---|
ENSDART00000000804 | Nonsense | 20 | 944 | 2 | 7 |
ENSDART00000089919 | Nonsense | 20 | 942 | 2 | 7 |
ENSDART00000128875 | Nonsense | 20 | 608 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 17 (position 22211321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22361470 |
GRCz11 | 17 | 22381306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTGAGACCTCCCCACGCCTCTTCCTGACCTTTCAGTGTCTAGTCCTTT[T/A]GGTTATAGTGGTCCACAATGTCCACCATGTGACAGCCGAACATGCCCCAG
Long Flanking Sequence:
GACTTTTTAAGGAAAATCAATTTGTAAATTGTATATTGAAAATAACATTGTTGCTATAAGTCTTAAGGAAGCATGTACTGTACCATTCTGCTGAAAAAAATGCTGATTTAATTGATTAACAATAAATGATTTAACATGGGTATATAGATCTTCACATAGAAATGATTTCACATGGATATACAAGTCTAGTTGCTTCAGAAGGAGTTTTCTCTTGACATTTCAGGAACTTGCCTTTCAGCAAACACTGTTGAAATGCTCCCAAAAAAATCTGTTTTAAATCAGTGTCAGAAATCTAGCTATATAGTAACCTTTATGAGAACGTGTGTCAGTACCTGTTGGTGATTAGTGTCCTGGTTTCGTTTCAATTAATGGATGATCTATTTTTTTCTTCACCTTTTTTTTCTTTCTTTTTTAGCAGAAGTTTGCCGCCGAGTAAGGAAAGATGAGGCATCGTGAGACCTCCCCACGCCTCTTCCTGACCTTTCAGTGTCTAGTCCTTT[T/A]GGTTATAGTGGTCCACAATGTCCACCATGTGACAGCCGAACATGCCCCAGATCACAGCCAGGATCATAGTTCTCCTGCCAACAAATCTTTGAGCTGTGGGGGCGGCTCAGCCATATGTGCCCCTGGAGTCATCCTTCCAGTGTGGGAACCCCCAAATCCTTCCTTTGGGGACAAGGTAGCCCGGGCCACCGTTTACTTTGTGGCACTGGTATACATGTTTCTGGGGGTTTCGATTATTGCTGATCGCTTCATGGCATCTATCGAGGTCATCACCTCACAGGAAAAGGAGATCACCATTAAGAAACCAAATGGTGAAACGACCACCACAACTGTACGCATCTGGAATGAAACCGTGTCCAACCTTACCCTCATGGCTCTGGGTTCTTCGGCTCCTGAAATTCTGCTGTCGGTCATTGAAGTGTGCGGCCATAACTTTGAAGCTGGTGACCTCGGTCCCTCTACCATCGTCGGCAGTGCAGCTTTCAACATGTTTGTCATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36395
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 |
---|---|---|---|---|---|
ENSDART00000000804 | Nonsense | 192 | 944 | 2 | 7 |
ENSDART00000089919 | Nonsense | 192 | 942 | 2 | 7 |
ENSDART00000128875 | Nonsense | 192 | 608 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 17 (position 22211838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22361987 |
GRCz11 | 17 | 22381823 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCGGCAGTGCAGCTTTCAACATGTTTGTCATTATTGGAATCTGTGTCTA[T/A]GTGGTGCCCGACGGAGAACATCGCAAAGTGAAACACCTGCGTGTGTTTTT
Long Flanking Sequence:
AATGTCCACCATGTGACAGCCGAACATGCCCCAGATCACAGCCAGGATCATAGTTCTCCTGCCAACAAATCTTTGAGCTGTGGGGGCGGCTCAGCCATATGTGCCCCTGGAGTCATCCTTCCAGTGTGGGAACCCCCAAATCCTTCCTTTGGGGACAAGGTAGCCCGGGCCACCGTTTACTTTGTGGCACTGGTATACATGTTTCTGGGGGTTTCGATTATTGCTGATCGCTTCATGGCATCTATCGAGGTCATCACCTCACAGGAAAAGGAGATCACCATTAAGAAACCAAATGGTGAAACGACCACCACAACTGTACGCATCTGGAATGAAACCGTGTCCAACCTTACCCTCATGGCTCTGGGTTCTTCGGCTCCTGAAATTCTGCTGTCGGTCATTGAAGTGTGCGGCCATAACTTTGAAGCTGGTGACCTCGGTCCCTCTACCATCGTCGGCAGTGCAGCTTTCAACATGTTTGTCATTATTGGAATCTGTGTCTA[T/A]GTGGTGCCCGACGGAGAACATCGCAAAGTGAAACACCTGCGTGTGTTTTTTGTTACTGCTGCTTGGAGCATTTTTGCCTATTTGTGGATGTACCTGATCTTGGCTGTTTTGTCACCTGGTATTGTCCAAGTGTGGGAGGGTCTTCTCACTCTTTTCTTCTTTCCCATTTGCGTGGTCTTCGCTTGGATCGCTGACCGCCGCCTCCTGTTTTACAAGTATGTTTACAAGCGCTACCGAGCTGGCAAGCACCGTGGCATGATTATCGAGACAGAGGGGGACCGGCCTTTACCATCCAAGGTGGATATCGAGATGGATGGGAAAATGCTGAACTCCCATGCCGTGGACTTCTTGGATGGAACTCTGGCTTTGGAACTGGAGGATAAAGACCTGGATGAGGATGAAGCTAGACGTGAAATGGCGAAGATCTTGAAGGAACTGAAGCAGAAACATCCAGATAAAGAGGTGGAGCAGTTGATTGAGCTAGCTAATTACCAGGTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23060
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 |
---|---|---|---|---|---|
ENSDART00000000804 | Nonsense | 462 | 944 | 2 | 7 |
ENSDART00000089919 | Nonsense | 462 | 942 | 2 | 7 |
ENSDART00000128875 | Nonsense | 462 | 608 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 17 (position 22212648)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22362797 |
GRCz11 | 17 | 22382633 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGTGGAATTTCGCACTGAAGATGGAACCGCAAATGCTGGCTCAGACTA[T/A]GAGTTCACTGAAGGTACCGTTGTTTTCAAGCCTGGTGAGACACAGAAGGA
Long Flanking Sequence:
ATGGATGGGAAAATGCTGAACTCCCATGCCGTGGACTTCTTGGATGGAACTCTGGCTTTGGAACTGGAGGATAAAGACCTGGATGAGGATGAAGCTAGACGTGAAATGGCGAAGATCTTGAAGGAACTGAAGCAGAAACATCCAGATAAAGAGGTGGAGCAGTTGATTGAGCTAGCTAATTACCAGGTGCTCAGCCAGCAGCAGAAGAGCCGTGCATTCTACCGATGCCAGGCAACCCGCTTGATGACCGGAGCAGGTAACATTCTGAAGAAACATGCGGCAGACCAGGCTCGTAAAGCAGTGAGCATGCATGAGGTACGCAGTGACACTGGTGAGAATGACCCAATTTCTAAGATCTTTTTTGACCCTTGCTCATACCAGTGCCTGGAAAACTGTGGCACCGTGGCAGTGAATGTGATCCGTCGTGGAGGCGATCTCAATCAAACCGTGTCCGTGGAATTTCGCACTGAAGATGGAACCGCAAATGCTGGCTCAGACTA[T/A]GAGTTCACTGAAGGTACCGTTGTTTTCAAGCCTGGTGAGACACAGAAGGAAATCCGAGTTGGAATTATTGACGATGACATCTTTGAAGAAGACGAGAACTTCCTCATCCACCTAAGCAATGTCCGTGTGGTTCATGAGGGTGATGAGCCAGAGACCACTGAAGCCAATCATGTGGAGACCATTGCAACACTCGGTCTGCCCTCCACAGCAACAGTCACCATCTTTGACGATGACCATGCTGGAATCTTCACATTTGAAGAGCCGGTCACCCATGTGAGTGAGAGTGTGGGTGTCATGGAAGTGAAGGTCCTGCGTACGTCTGGTGCCCGTGGGGTGGTGTCAGTGCCATATAAAACCATTGAGGGAACAGCCCGTGGAGGGGGAGAGGACTTTGAAGACAGCCATGGTTTTCTGGAGTTCCAAAACGACGAAATTTTGTAAGTCACAATCTCATATTATATCATACAGCAAAATGTGTTTGGGTTCCTGTCCTGATAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19172
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 |
---|---|---|---|---|---|
ENSDART00000000804 | Nonsense | 562 | 944 | 2 | 7 |
ENSDART00000089919 | Nonsense | 562 | 942 | 2 | 7 |
ENSDART00000128875 | Nonsense | 562 | 608 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 17 (position 22212946)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22363095 |
GRCz11 | 17 | 22382931 |
KASP Assay ID:
2261-0965.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACATTTGAAGAGCCGGTCACCCATGTGAGTGAGAGTGTGGGTGTCATG[G/T]AAGTGAAGGTCCTGCGTACGTCTGGTGCCCGTGGGGTGGTGTCAGTGCCA
Long Flanking Sequence:
CAGTGAGCATGCATGAGGTACGCAGTGACACTGGTGAGAATGACCCAATTTCTAAGATCTTTTTTGACCCTTGCTCATACCAGTGCCTGGAAAACTGTGGCACCGTGGCAGTGAATGTGATCCGTCGTGGAGGCGATCTCAATCAAACCGTGTCCGTGGAATTTCGCACTGAAGATGGAACCGCAAATGCTGGCTCAGACTATGAGTTCACTGAAGGTACCGTTGTTTTCAAGCCTGGTGAGACACAGAAGGAAATCCGAGTTGGAATTATTGACGATGACATCTTTGAAGAAGACGAGAACTTCCTCATCCACCTAAGCAATGTCCGTGTGGTTCATGAGGGTGATGAGCCAGAGACCACTGAAGCCAATCATGTGGAGACCATTGCAACACTCGGTCTGCCCTCCACAGCAACAGTCACCATCTTTGACGATGACCATGCTGGAATCTTCACATTTGAAGAGCCGGTCACCCATGTGAGTGAGAGTGTGGGTGTCATG[G/T]AAGTGAAGGTCCTGCGTACGTCTGGTGCCCGTGGGGTGGTGTCAGTGCCATATAAAACCATTGAGGGAACAGCCCGTGGAGGGGGAGAGGACTTTGAAGACAGCCATGGTTTTCTGGAGTTCCAAAACGACGAAATTTTGTAAGTCACAATCTCATATTATATCATACAGCAAAATGTGTTTGGGTTCCTGTCCTGATAAGTCACTCCTAAAAAGAAGAGCAGTACTTTTTTAAGATCTGAATTTAATTTGGGTTCTTGTAGTGCTCTGTCAGAACAGGAATGTAATGCATGCAAGATGTTTTTGAATTATATGTGCTTGGAGTAGCATGCTTGATGCTAAGTATTTTGCTGTGTGGCATCATTGTGATGTCACTGTGATATGAGAAGCATTGTGTGCTAAAAGCAGCCAATGGAGGATGTCATCAAATAGAAACTCCCCAGATATATTTCCCATCTTCTTCTCTTCTCCATCTTTTCATGTATCTTTCATTCACAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23061
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000804 | Nonsense | 632 | 944 | 3 | 7 |
ENSDART00000089919 | None | None | 942 | None | 7 |
ENSDART00000128875 | None | None | 608 | None | 1 |
Genomic Location (Zv9):
Chromosome 17 (position 22302075)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22452224 |
GRCz11 | 17 | 22472060 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCAATCGAGAGGAGTACCATAAGCAATGCAGCTTTTTCATAGAGCTA[C/T]AGACGCCACTTTGGAGAAGGAGAGGATGGACAGTATACAGAGGTTTCTCT
Long Flanking Sequence:
TCTCTCTCTTCTTCTCCTTGGTCTGTCTTTTCCTCACTTTCTTCTTTCTCTCCCTCTTTCTTTTTCTCTCCCCGTCTGTCCAGCAAAACGATAAAAGTCAGGATAATTGATGATGAAGAATACGAGAAGAACAAGAGCTTCTTTCTGGAGATCGGAGACCCTCAGCTCGTAGAGACCGATGAGAAGAGAGGTGGGGGGGGGGCATGACCTGCACCAGCAGAGGAATACACACTACACACACACATACACTGAACACCAGTCCACCCTCTGCTCTGGATCATCATCAGGATCAACTACAGGCCAAACGACACTGTCAACAGCCCTCCGGCCCCCGCGTGTGTGCTTGTATCTCTGTGTGTGTGCACGTGTGAGAGTGTGTGTTTCATGCATGCATTATTCCAACCCCCCTCCTGTTGTCTTGTTTCTGCAGGAAGACGATAACAGTCAGGGTTCTCAATCGAGAGGAGTACCATAAGCAATGCAGCTTTTTCATAGAGCTA[C/T]AGACGCCACTTTGGAGAAGGAGAGGATGGACAGTATACAGAGGTTTCTCTTCCTCTCACAGTGTCTCAGCTTTGCTTTATTTGACTCCTCTTTCCCTCTGGGCAGAGTCTTACCCTCTGTTTCTCTCTGTAACTCCTGGTGTTTCTGTGCTATGTTATTAATCTAATGGTATTCCTTAACTTTCGCTGATCATACAACTACTCACAAGATAACACTCATGCATTAAAGTATTGTTTTATTGTTAGTCATAGAAAAATAACATAATTAAGACTAAATTTGAAAAGGATAAAGTAAAATAATTTAAATGGAGGTGTTAATGCGAGGTTGGCAGTGAAGTGTGGAAATTAAGGGGGGAAATTAAGCAATGGTCTTGGCAGAACAGAATAATGTTTTGGAATACTTTGGTGGACTCTTGTCTTCAGATATATGTCAATTAATGCAATATAATCTTATCTCATATAATGTAATAATATCTTCTAATTTCAAGAGTAATGGCATCT
Associated Phenotype:
Not determined