ZMP
si:ch211-48m9.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate solute carrier family 4, sodium bicarbonate cotransporter, membe
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11294 | Essential Splice Site | Available for shipment | Available now |
sa1335 | Essential Splice Site | Available for shipment | Available now |
sa26483 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45206 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11294
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042002 | Essential Splice Site | 193 | 1134 | 4 | 25 |
ENSDART00000138140 | Essential Splice Site | 169 | 1017 | 3 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 29733938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 27489236 |
GRCz11 | 5 | 28089389 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCACCGTGCTGCTGGACCTGGAGGGATACTCGCTCCCACAGATYGTMGG[T/A]AAGCTTCTGRACATAAAACAGMAATTGTCTAGCATACTGAAGTGTGCATY
Long Flanking Sequence:
TATTTAAAGAGCAGGGGAAAAATGCAGCTAAAGCTTGAGTTTTATTTTAAATGTTTTAAAATCTCACACTGTTTACATTGAATCAGATAATATAAGTGTATTTAAAATATTTAAAAATGTAGTTATATCGTTGGATATAATGCAACATTTTTTTCCGCCTAAGGCTGAATATCTGATGCAAATAAAATGTATTTTATGACCAAATTTTGGCCCATTTTTTTCACACATGTCATCTTAGAATAAACAGTGTCTGCATCTGAACAACATCAGAAACTTTGAGATCCTTTTTTCTCAGCTTGACTTCAACTGAGTGTGTGTGTGACTGTGTATGTCTGCAGGTGGGTGAAGTTTGAGGAAAAAGTTGAGGAGGGTGGAGAAAGATGGAGCAAACCACACGTTTCCACACTGTCCCTGCACAGCCTGTTTGAACTGCGGACATGCCTGCAGACCGGCACCGTGCTGCTGGACCTGGAGGGATACTCGCTCCCACAGATCGTCGG[T/A]AAGCTTCTGGACATAAAACAGAAATTGTCTAGCATACTGAAGTGTGCATTCGAATGTGTTTATTTTTATGATAATGCCTATTGTGTCATCCAGCTGAACATATAAAGGTAAACTAACTTTGCTTTTATTCCATGTAGATGACATCATCGATCGTCAGGTAGAGGAAGGGTTGATCGGTCCTGAATTGAGAGACAAAATCAGCTTTGTACTGCTGAGAAAGCACAGACACCAGACCAAAAAGCCCATCCATCGCTCCCTTGCGGATTTGGGCAAGTCTGGTTCAGGAGGCAGTGAGTGTTCAAATGTTTTTCTGTCTCTCCATCTGTATGCACACACATACACACACACACACGCCCACATCCACACCCACACACATATATATATATATATATATATATATATATATATATATATATATATAAAGAACTAATCTATACCTCTGCAATGGAATTGTAGCAATCAGTTGTTCAGTATATTGGAACCCAGTTGACCCAATTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1335
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042002 | Essential Splice Site | 779 | 1134 | 17 | 25 |
ENSDART00000138140 | Essential Splice Site | 740 | 1017 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 29710747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 27466045 |
GRCz11 | 5 | 28066198 |
KASP Assay ID:
554-1249.1 (used for ordering genotyping assays)
KASP Sequence:
TGCTAATAGGTTTGAAAACACCCAAACTCATTGTGCCTACCGAGTTCAAG[G/A]TGAGAGTATAAATTAGGTTGATGTTGTGTGACTTTTTCAATGAAGTTCCT
Long Flanking Sequence:
TTCATTGTAATTTGTTTCTAAAGATTATTTTCTCTTTGTATTCCCAACTGTAATATTACATTTAAGTGTGTAAAATTGCTGTGGAAATTCTTGTTTTGAGATTTTGGGTTTATTCATAGTCTGCTGAAAGTCATTTGTTAAATAATAGCTTTCCTTTTGAAAATGGATGGATATACTGGACAGCTCATTGATCACACTCCTTTAAAACCCTTTGCTGATTGTTTAGAGTTTATTGGAAGATACTCCTATAATCCACGCAAAGCATTATGGGGTTCAGGAAAAAATGTAGCTCTTTAGCAACACTGTGCTGCTATATTTCTGAAGCTGCAACTACATGTCTAATTCATATTTAATAAAATACCTATTTTTTTTTTTTGTCTATCCAGTTGAGGAAGTTAATTAGTGACTTCTCCATCTTCATGTCCATCATGACGTTTGTGGGTCTGGACATGCTAATAGGTTTGAAAACACCCAAACTCATTGTGCCTACCGAGTTCAAG[G/A]TGAGAGTATAAATTAGGTTGATGTTGTGTGACTTTTTCAATGAAGTTCCTTATAATTTTATTCCAACACATTGTTTTGTTTTATTTTTTTTTCAATCATGTAGCCCACACGTCCTGACCGAGGATGGTTTGTGATGCCATTTGGAAAGAATCCATGGTGGGTTTACCTGGCAAGCTTCGTCCCTGCTCTCCTCGTCACCATCCTTATCTTCATGGATCAGCAGATCAGCGCTGTTATCGTCAACCGGAAGGAAAACAAGTTAAAGGTCTCCATGCAGTTTGCTGCTATTTTAAAGGGGACCTAATATTCAAAAATATTTTATAAGGGGGTTAAGCTGTTTTTTTATAATCTCACACTGTAAAAAAGAGTCTACAGAGACACTTTATTTTGAGTTTCTTCCTTGTACATGTCATCGGAGGTTGGGTTGGGCTGATAGACAATGTCATCGACCATCGCCGATGGCCAAAACTTCACGATGCTGAGCTGACATAGCCCCGCCC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa26483
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 |
---|---|---|---|---|---|
ENSDART00000042002 | Nonsense | 838 | 1134 | 19 | 25 |
ENSDART00000138140 | Nonsense | 799 | 1017 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 29709006)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 27464304 |
GRCz11 | 5 | 28064457 |
KASP Assay ID:
2259-5883.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCTTTTTCAGTTTTTTTTTTTTTTGTTTTTACAGAAAGGCTGTGGGTA[T/A]CATCTGGATCTATTGTGGGTTGGCGTTCTGATGGCAGCCTGCTCTTTTAT
Long Flanking Sequence:
ACAAACTGATTGGATGTCTTGTCAAATGATAATCAGTTTAACTGAAGTGGTAAAGACGTTAAAGTTAAGGAACGAAACATTTCAAAATACAACAATACACACATTGAACTTAGAAAAAGATAAGGTTAAAGTGACTTTATCTGTTTTCTCTGGATGGGATAACGTTACTCCATGGTCTTGTACGGCAGCCCTTTTAATGTTCCTTAAAGCCTGTAAAGCTTTCAAAATAAGAGTCCCACATACATAGGAAATATTAGTGATTTTTTCCGATTGGCCTGAGATTTTACATTGATTTACATGAGATTGAGAAAACAATGGTATTCGTGTCTCACTGTATAGCATTATCATGTACTAAATTCTTATCATTCAGCTATGTCTAGGTATATCCAGATTTTTATTCTATGGCCACTTTAATCACCCCAGTTTTTTTATTTCCACTGATTTCCTCACATTCTTTTTCAGTTTTTTTTTTTTTTGTTTTTACAGAAAGGCTGTGGGTA[T/A]CATCTGGATCTATTGTGGGTTGGCGTTCTGATGGCAGCCTGCTCTTTTATGGGTCTGCCGTGGTATGTTGCGGCCACTGTCATTTCCATCGCTCACATTGATTCACTGAAGATGGAGAGCGAGTCTAGTGCTCCAGGGGAACAGCCACAGTTCTTGGGTGTGAGGTGAGGCACGCACTACTTGTTTGTCAACTGCAGCAGGTGTGGATTGTGCTCCTACATTTAGAGTGTCTGATGCAGAAAGTGCTTTATGCAGGAAAAAAAAGAAAAGAATGTTTTTAGCTGTAACTATGCTGTGATAAACCTGACCAGAATGATACTGTAGAGAACTCAAAGGCAGATTATTTCACTTTAGTGCAAATCTGAAAATCTGAACATAAGCCATAAAGCTATTGCATGAAACTAAACATTAATGATTTCCATATCAAAGTAGCAAAGTCACATGATTTCAGTAAACAGGAATGTTTTCATGTTAGTGAAGATTGATATCAGTTATCTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45206
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042002 | Nonsense | 1121 | 1134 | 25 | 25 |
ENSDART00000138140 | None | None | 1017 | None | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 29693165)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 27448463 |
GRCz11 | 5 | 28048616 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATTGAGATGGAGTCGGACTATGAAGACACAGATATAAACCCTAGAGGC[A/T]GACACAGGGATCACAGGGACATGAGCAGCGAAACAACGCTGTAAAAACTT
Long Flanking Sequence:
GATTGCTGGTCTCCAACATTCTTTAAAATATATTCCTTTGTGTTCAGCATAGGAAAGCAACTCATTAGTGTAGAACTACTTGAGGGTGGGTAAATGTAAAAAGAGCTTTTTAAGGTTTATCAAAGCTACTCTAGTATTCTCGCATTTTAAAACTTTAGATACCTGGAAACATTCTTCCTAAATTTGGATCTTCTAATCCCAAATCTTTCCCATGGAACATTTGTGCAGTCTCACCCGCCGTCTGTTACCTCCATCCAACATGTCAATACAGCCTGCTGTGCGTCCTGATCCTCATCTGTTCCTCCTCCCCATCGTAACCTCCTCCTACTCCTCACTGTTGTAACTGGAAGTTGCCATTTCACAGCATCACTCTGCACCTGAAGATCTCCTGCCCGTCGTCTCCAGCGATGCCACTGGCCAGAGGCATGCCGTGTCCTGTTCCCCAGGTCAAGATTGAGATGGAGTCGGACTATGAAGACACAGATATAAACCCTAGAGGC[A/T]GACACAGGGATCACAGGGACATGAGCAGCGAAACAACGCTGTAAAAACTTCTTGTTGAAGCTCCTGTGATTTGTGGTCAGATGGCACTTTATGGGTTGGCAAAACGGTGGCATGGCAACTCAATTTTAAAGAATGTCAAGATAAAATGTCGAGTTTAAGCTAATTTCTCAAACACAATATATTTTTCTGATTTTAAAAACCAAAGCAACTGAAAAATGATGCCGATGCAGTATATTTGCTCTAATTAGAATTGATATAACACCATAGATAATGTATATGACAGAGAGAATATTTTGACCTTCCAACTTCAAAATTTAAGTTTCTCTCATTTTAAAAGCCAAAGGTTTCTGAAAATAAAAGATTATTTTTATGCTAGAAATGAAAGTATATTTTAGACAAAATCAGATATATTTATGCAGTGCAACCTTTTTAGATCACCTTTATATCTTTGATAGAATAAACAACTGTGATTTTTCCCTTTATCCTTCTAGTAGTGTTGT
Associated Phenotype:
Not determined