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 |
sa6205 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41816 | Nonsense | Mutation detected in F1 DNA | Not yet available |
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:
sa6205
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013784 | Nonsense | 630 | 1052 | 14 | 24 |
ENSDART00000142053 | Nonsense | 575 | 996 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 11 (position 21395761)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 45029925 |
GRCz11 | 10 | 44876537 |
KASP Assay ID:
554-5122.1 (used for ordering genotyping assays)
KASP Sequence:
TTCATCTTCATCTCTGACGCCCTYAAGAAGATGATGAGCACCTTCARCTA[T/G]TACCCCATCAGCCCAGACTTTAAGCCCGACCTCATCATYAGCTACAGGTG
Long Flanking Sequence:
ATGTGTAGGTTAGTGTATACTCCATCAGCTATTTTCATTTTTGTCAGCTTAGCGTTTAATTAAAGTATTAATAAACCATTATGGCTCAAAAAATAGATTTTTATCTAATAGTTGTGCCATGTAATAATCAAGATAAAGCACATCCTGGACAGTTGTTTATTGTTTGTTGTTTACCCTTCAGTCTTATACACCTGTCAGGCTTTATTCTGAGATAACAGCCTACTTGATCTACTTTATCACTAACTTCTATTGAAAATTTAGAGTACAGTTTTAAAGTTCAGTCTGTTTTCATTTGTGTTCAGAAACAACAACATCGACTACATGGAGATCCGTCTGTGGATCGGTTTGCACTCCTGCCTGCAGTGTCTGATTCTAGTGGCCACAGATGCGAGTTATATCATCAAATATATGACACGCTTTACAGAGGAGGGTTTCTCCAGCCTCATCTCCTTCATCTTCATCTCTGACGCCCTCAAGAAGATGATGAGCACCTTCAGCTA[T/G]TACCCCATCAGCCCAGACTTTAAGCCCGACCTCATCATTAGCTACAGGTGTGACTGCCAGCTTCCGGACCAGGGTGAGGCAAAACACATGGCCACAATAGCAGAGTTGACCATAACAGAGTTGACGGTAACACAGTTGACAGTAAAGAAGTAGACGATATTAGAGTTGATGGTAGCAGAATTGACGGTAGCAGAGTTAATGATAATTGGATTGACGTTAGCAGAGTTGACGGTAACAAAGTTGATGGTATCGGAGTTGACGGTAGCGAAGTTGACGATTTCAGAGTTGAAGGCAGCAGAGTTGACCATGAAAGAGTTGACGGTGTCAGAATTGACCGTAGCGGCGTTGACGGTAACACAGTTGACCATAGCAGAGTTGACGGCAGCAGATTTGATGGTATCGGAGTTGACGGTAGCGGAGTTGATGATACAGGAGTGGACGGTAGCAGAGTTAATGATAACTGGATTGACGATAACAAAGTTGACGGTAACAAAGTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41816
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013784 | Nonsense | 795 | 1052 | 18 | 24 |
ENSDART00000142053 | Nonsense | 740 | 996 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 11 (position 21386761)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 45038925 |
GRCz11 | 10 | 44885537 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCCTGACCGTGGCTGGATCGTGATGCCGATGGGCAGGAACCCGTGGTG[G/A]ATGTGTTTGGCCAGTTTTGTTCCTGCTCTGCTGGTCACCATTCTCATCTT
Long Flanking Sequence:
CAAGTCCATATTTTGACCCACAGAACTCATGTAAACGTTCCCGGAAGCACTTGAAGGCATCGATGGTGTCCGTTTCCTCTTCTTGTCTGGTTTTGATCTGGTTTATTAGTGTGTTTTTCTGCATCTCTGTCTTTCTGTTCTCTATACTCGTGCAGCTTCGGAAACTCATCAGTGATTTTGCAATCTTCACATCAATCATGACTTTTGTTGGTCTCGATATGTTTATGGGACTTAAAACACCCAAACTGATTGTGCCGACTGAGTTTAAGGTACGTGCTGCTGTAACCCTGATCTGATCTGATTCTGTACTAATATTAGACAATCATCACATTCATACACACTGCTGGATCATGAACTGTGTGCTCTGTACATGTGACTACCACTGGATATTGCTGTACTGACATCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCAGCCGACGCGTCCTGACCGTGGCTGGATCGTGATGCCGATGGGCAGGAACCCGTGGTG[G/A]ATGTGTTTGGCCAGTTTTGTTCCTGCTCTGCTGGTCACCATTCTCATCTTCATGGATCAGCAGATCACCGCCGTCATCGTCAACCGCAAAGAAAACAAACTCAAGGTGTTCAGTCACACAGCTGCTGTTAGATTTTGTTACCAAAAATAGATATATATGTACTATATACAGGATTGCAAAACGTAAACTCAGAATTGTGAAATGTAAAGTCAGAGTTGTGAAACCCAAAGTCAGAATTGCCAAGTGTAAACAGAATTGTAAGATGTTAAGTCATAATTGTGAAACAAACTCAAAATTGCAAGATGTAAATTTAGAATTGCGAAACGTAAAGTCTGAGTTACGAGACGTAAACTTCGAATTGCAAAACCCAAAGTCAGAATTGCGAGACATAAACTCAGAATTGTGAAACGTAGTCAGAATTGCAAAATGTAAAGGTAGAATTGTGAAACGTAAACTCAGAATAGTGAGATGTAAAAGTCAAAATTGCGAGACGTAAACTC
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