ZMP
slc4a5
Ensembl ID:
ZFIN ID:
Human Orthologue:
SLC4A5
Human Description:
solute carrier family 4, sodium bicarbonate cotransporter, member 5 [Source:HGNC Symbol;Acc:18168]
Mouse Orthologue:
Slc4a5
Mouse Description:
solute carrier family 4, sodium bicarbonate cotransporter, member 5 Gene [Source:MGI Symbol;Acc:MGI:
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21891 | Nonsense | Available for shipment | Available now |
sa17754 | Essential Splice Site | Available for shipment | Available now |
sa10270 | Nonsense | Available for shipment | Available now |
sa9545 | Nonsense | Available for shipment | Available now |
sa16760 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21891
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 |
---|---|---|---|---|---|
ENSDART00000013784 | Nonsense | 58 | 1052 | 2 | 24 |
ENSDART00000142053 | Nonsense | 36 | 996 | 1 | 21 |
Genomic Location (Zv9):
Chromosome 11 (position 21444922)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 44980764 |
GRCz11 | 10 | 44827376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGCAAACACGCGTCACGACATTCCCACGATCGCGATAAACACCATAGT[C/T]GACATGAACACGCGGATCCAGAGGAAAACTGCGACCCTGAGGAGGCCGAG
Long Flanking Sequence:
TAATTGAAATTAAGCATAAATTTCGATCGATTTAAAATCGATATCGTGACACCCTTAATCAACACAATACTTTTTTCAAAATGAATGCTTCATTTGAAGATGGCTGTGATATGTGGAACTGAGTATTTATAGTGGCTTAGGATTCATCTGATTGCTGAATCATTAATTGGCTAATGCATGGCCAGCCGTGTTTAATCATAAGCACGTGCTCCTCTCCAAATTAGTTTAGAAATAATCTTCACTTGTTGTGTGTGTTGCCTCCTCCTGTTGAATCGCTGAATGTCTCCTCAATTGTAAGTCGCTTTGGACCAAAGCATCTGATAATGACTGTGTGAAATGTAAATAAACATCGCTTTTACAGCAGAGCTTCACCTGTGTGTGTTTGTCTGCTTGTAGAGTCCGTCTACATCGGCGTTCCTGTGCCCAGGAGCTACAGAAGGAAACGCAGACATCGCAAACACGCGTCACGACATTCCCACGATCGCGATAAACACCATAGT[C/T]GACATGAACACGCGGATCCAGAGGAAAACTGCGACCCTGAGGAGGCCGAGCAGGAGAACGAGCTCTCAGATGTCAACTCTACCGGTAAGAATCTGTAAACACTACTACAGTATAACTCTACGTTTCCATAACAGCGTCGAATCTGCGCACTGTACTGCTGCAAATGATACAACGACACGACTCTAGGGGCGTCTCAGATACAGGGCTAAACAGACTTGACGAAAACAGTCTGCAGAAACAATTTGATTGACACTCTATTTGTACGTGTCATCAGCGAGGGAAAGCCCCCCCCACTAGTGCCCATCTCTTCACCTCATTAGCATAAACAGCAGCCCTGAGTGAGAAGCAGCTGTCTGTCTATTAGCCGTTAGAGTGTTTGCATCAAGCACACACCTGACCAGCATTGACAACACAGCTAGTGCTGTTTTACATCTGCCGCAGCATTTGTAGCTCCGCCCTCTTCTAAAAAGAGCTCAATCTCATTTGCATTTAAAGTGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17754
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013784 | Essential Splice Site | 519 | 1052 | None | 24 |
ENSDART00000142053 | Essential Splice Site | 464 | 996 | None | 21 |
Genomic Location (Zv9):
Chromosome 11 (position 21401721)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 45023965 |
GRCz11 | 10 | 44870577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YGCCATTACTTTTGGGGGACTATTGGGGGACGCCACCGACAACTACCAGG[T/C]GCTGTTTTCATATACAGTGCACAGCATAAMCGAGTCCACCCTTCACAGAT
Long Flanking Sequence:
TTAGAACTGAAGTTTTGAGGCAAATCTTTGCTGTTAAAAATCTGTCATGTAAATAGTGAACGTGCCATTGCGCAACACAACTCACTCTTAAAGGGAATGGGAGATGAAATTCTGTTTTAATGCATGTTTAATGCCCAAAAGACACCCCATAACTCATTAAGAAAATATGACAACTGGTTTAGACCAGGCGCCTGGTGCACAGACAGCTTTTACCACCCTTAAAACAGCAAAATGGACTTAGACATGCTCTAAGTGAAACTGCGTCATGTGTTTCAGACCCTGCACTTAACTTGTTAAAATAGAGCTCTGTATGTGTTTGAGCAGGTTCTGTGGAGGACTCTGGCTAGACATCAAGCGGAAAGCACCCTGGTTTTTCAGCGATTTCTATGAAGGTTTCCACATCCAGTCGGTGTCCGCGGTGCTCTTCATCTACCTGGGCTGCATCACCAATGCCATTACTTTTGGGGGACTATTGGGGGACGCCACCGACAACTACCAGG[T/C]GCTGTTTTCATATACAGTGCACAGCATAAACGAGTCCACCCTTCACAGATCTCTCTTTATATTAAAAGTTTCTACAAGATCATTTTGAGCTTGGATGATGGTTCTCTTACTAAAATTAAAAAATCTTGGGAAAATGAATTGGGAATATGTTTTGAGGAAGAATGGTGGCTTGGTGCGCTGCAGAGAATACATTCTAGTACAATTTGTGCTTGGCTTAGTCTGATACAGTTCAAAGTAGAGGTCTGCATAAATTTCCGAATAAATCGCGGGAGCGGTCGGTAACGGGTTTAATTTGGGACGGGAGCAGGCTGTCTAGCAATATCGTGGATATTGCTATGCGAATGAGAGAGAGAGAGAGAGAGAGAGAGCTTTGCCTGTGTGTGTGCTTGGTGCTTGTGTGTGTGTGTGTTAGTGCGCGCGAATGAGAAAGAGAGAGAGAGCTTTCCCAAATAGCAAAATACACTCGGGCCAGTTCCGGCTAGATTCTCGCCTGCCGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10270
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 |
---|---|---|---|---|---|
ENSDART00000013784 | Nonsense | 584 | 1052 | 14 | 24 |
ENSDART00000142053 | Nonsense | 529 | 996 | 12 | 21 |
ENSDART00000013784 | Nonsense | 584 | 1052 | 14 | 24 |
ENSDART00000142053 | Nonsense | 529 | 996 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 11 (position 21395901)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 45029785 |
GRCz11 | 10 | 44876397 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATCGACTACATGGAGATCCGTCTGTGGATCGGTTTGCACTCCTGCCTG[C/T]AGTGYCTGATTCTRGTGGCCACAGATGCGARTTATATCATCAAATATATG
Long Flanking Sequence:
TATAAATATATATTTCTTGCAAAATTTTAAAAGATATGTAGCTCATCCCGGAACTTTACCTTGATCTTCAGTGGAAATGTTCATATCTATATACTTACATCCACATTCATAACTGTTTGGCGCCATCTTGTGTCTTAATAATGTGTAGGTTAGTGTATACTCCATCAGCTATTTTCATTTTTGTCAGCTTAGCGTTTAATTAAAGTATTAATAAACCATTATGGCTCAAAAAATAGATTTTTATCTAATAGTTGTGCCATGTAATAATCAAGATAAAGCACATCCTGGACAGTTGTTTATTGTTTGTTGTTTACCCTTCAGTCTTATACACCTGTCAGGCTTTATTCTGAGATAACAGCCTACTTGATCTACTTTATCACTAACTTCTATTGAAAATTTAGAGTACAGTTTTAAAGTTCAGTCTGTTTTCATTTGTGTTCAGAAACAACAACATCGACTACATGGAGATCCGTCTGTGGATCGGTTTGCACTCCTGCCTG[C/T]AGTGTCTGATTCTAGTGGCCACAGATGCGAGTTATATCATCAAATATATGACACGCTTTACAGAGGAGGGTTTCTCCAGCCTCATCTCCTTCATCTTCATCTCTGACGCCCTCAAGAAGATGATGAGCACCTTCAGCTATTACCCCATCAGCCCAGACTTTAAGCCCGACCTCATCATTAGCTACAGGTGTGACTGCCAGCTTCCGGACCAGGGTGAGGCAAAACACATGGCCACAATAGCAGAGTTGACCATAACAGAGTTGACGGTAACACAGTTGACAGTAAAGAAGTAGACGATATTAGAGTTGATGGTAGCAGAATTGACGGTAGCAGAGTTAATGATAATTGGATTGACGTTAGCAGAGTTGACGGTAACAAAGTTGATGGTATCGGAGTTGACGGTAGCGAAGTTGACGATTTCAGAGTTGAAGGCAGCAGAGTTGACCATGAAAGAGTTGACGGTGTCAGAATTGACCGTAGCGGCGTTGACGGTAACACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9545
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 |
---|---|---|---|---|---|
ENSDART00000013784 | Nonsense | 584 | 1052 | 14 | 24 |
ENSDART00000142053 | Nonsense | 529 | 996 | 12 | 21 |
ENSDART00000013784 | Nonsense | 584 | 1052 | 14 | 24 |
ENSDART00000142053 | Nonsense | 529 | 996 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 11 (position 21395901)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 45029785 |
GRCz11 | 10 | 44876397 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATCGACTACATGGAGATCCGTCTGTGGATCGGTTTGCACTCCTGCCTG[C/T]AGTGYCTGATTCTRGTGGCCACAGATGCGARTTATATCATCAAATATATG
Long Flanking Sequence:
TATAAATATATATTTCTTGCAAAATTTTAAAAGATATGTAGCTCATCCCGGAACTTTACCTTGATCTTCAGTGGAAATGTTCATATCTATATACTTACATCCACATTCATAACTGTTTGGCGCCATCTTGTGTCTTAATAATGTGTAGGTTAGTGTATACTCCATCAGCTATTTTCATTTTTGTCAGCTTAGCGTTTAATTAAAGTATTAATAAACCATTATGGCTCAAAAAATAGATTTTTATCTAATAGTTGTGCCATGTAATAATCAAGATAAAGCACATCCTGGACAGTTGTTTATTGTTTGTTGTTTACCCTTCAGTCTTATACACCTGTCAGGCTTTATTCTGAGATAACAGCCTACTTGATCTACTTTATCACTAACTTCTATTGAAAATTTAGAGTACAGTTTTAAAGTTCAGTCTGTTTTCATTTGTGTTCAGAAACAACAACATCGACTACATGGAGATCCGTCTGTGGATCGGTTTGCACTCCTGCCTG[C/T]AGTGTCTGATTCTAGTGGCCACAGATGCGAGTTATATCATCAAATATATGACACGCTTTACAGAGGAGGGTTTCTCCAGCCTCATCTCCTTCATCTTCATCTCTGACGCCCTCAAGAAGATGATGAGCACCTTCAGCTATTACCCCATCAGCCCAGACTTTAAGCCCGACCTCATCATTAGCTACAGGTGTGACTGCCAGCTTCCGGACCAGGGTGAGGCAAAACACATGGCCACAATAGCAGAGTTGACCATAACAGAGTTGACGGTAACACAGTTGACAGTAAAGAAGTAGACGATATTAGAGTTGATGGTAGCAGAATTGACGGTAGCAGAGTTAATGATAATTGGATTGACGTTAGCAGAGTTGACGGTAACAAAGTTGATGGTATCGGAGTTGACGGTAGCGAAGTTGACGATTTCAGAGTTGAAGGCAGCAGAGTTGACCATGAAAGAGTTGACGGTGTCAGAATTGACCGTAGCGGCGTTGACGGTAACACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16760
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013784 | Nonsense | 828 | 1052 | 18 | 24 |
ENSDART00000142053 | Nonsense | 773 | 996 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 11 (position 21386664)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 45039022 |
GRCz11 | 10 | 44885634 |
KASP Assay ID:
2260-4193.1 (used for ordering genotyping assays)
KASP Sequence:
TCTTCATGGATCAGCAGATCACCGCYGTCATCGTCAACCGCAAAGARAAC[A/T]AACTCAAGGTGTTCAGTCACACAGCTGCTGTTAGATTTTGTTACCARAAA
Long Flanking Sequence:
CTGGTTTATTAGTGTGTTTTTCTGCATCTCTGTCTTTCTGTTCTCTATACTCGTGCAGCTTCGGAAACTCATCAGTGATTTTGCAATCTTCACATCAATCATGACTTTTGTTGGTCTCGATATGTTTATGGGACTTAAAACACCCAAACTGATTGTGCCGACTGAGTTTAAGGTACGTGCTGCTGTAACCCTGATCTGATCTGATTCTGTACTAATATTAGACAATCATCACATTCATACACACTGCTGGATCATGAACTGTGTGCTCTGTACATGTGACTACCACTGGATATTGCTGTACTGACATCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCAGCCGACGCGTCCTGACCGTGGCTGGATCGTGATGCCGATGGGCAGGAACCCGTGGTGGATGTGTTTGGCCAGTTTTGTTCCTGCTCTGCTGGTCACCATTCTCATCTTCATGGATCAGCAGATCACCGCCGTCATCGTCAACCGCAAAGAAAAC[A/T]AACTCAAGGTGTTCAGTCACACAGCTGCTGTTAGATTTTGTTACCAAAAATAGATATATATGTACTATATACAGGATTGCAAAACGTAAACTCAGAATTGTGAAATGTAAAGTCAGAGTTGTGAAACCCAAAGTCAGAATTGCCAAGTGTAAACAGAATTGTAAGATGTTAAGTCATAATTGTGAAACAAACTCAAAATTGCAAGATGTAAATTTAGAATTGCGAAACGTAAAGTCTGAGTTACGAGACGTAAACTTCGAATTGCAAAACCCAAAGTCAGAATTGCGAGACATAAACTCAGAATTGTGAAACGTAGTCAGAATTGCAAAATGTAAAGGTAGAATTGTGAAACGTAAACTCAGAATAGTGAGATGTAAAAGTCAAAATTGCGAGACGTAAACTCTGAATTGTTTGACGTAAACTCAGAATTGCAAAACATGAACTCAGAAGTGCGAGACATAAATTAAAAATTACAAAACGTAAAGTCAGAATTGCAAAAT
Associated Phenotype:
Not determined