ZMP
si:ch73-255e3.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate solute carrier family 4, sodium bicarbonate cotransporter protei
Human Orthologue:
SLC4A10
Human Description:
solute carrier family 4, sodium bicarbonate transporter, member 10 [Source:HGNC Symbol;Acc:13811]
Mouse Orthologue:
Slc4a10
Mouse Description:
solute carrier family 4, sodium bicarbonate cotransporter-like, member 10 Gene [Source:MGI Symbol;Ac
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6119 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa15332 | Nonsense | Available for shipment | Available now |
| sa13363 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6119
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084806 | Essential Splice Site | 76 | 900 | 2 | 21 |
| ENSDART00000139316 | None | None | 573 | None | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 52701570)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 51823792 |
| GRCz11 | 9 | 51355205 |
KASP Assay ID:
554-3707.1 (used for ordering genotyping assays)
KASP Sequence:
CGCTGACATCGGCAAGAAGCAGTCAGAGTCCAACTGCTTGGACAAAAACG[G/A]TACTCGATTACCATCATTCAGAATTCACAGAAGGTATTSGTGTTATTACT
Long Flanking Sequence:
TGCAGAAATAAAGAGATGGTCTTGATACGAGGGTGGCCAAGTAGGCACACTGTCCCCCAGAAGCTAGCACATCACTCTTATTTATATGATCTAAACCAACCAGCAACCAGGCACCCAATCAGGATCTGCCACATCCAAACTGGAATCCTGGGGTCATCACTGGGACTAAGCTGAAAAGAAAATGAATTAATTAATTAACGAATGTTAATGTGTACCGTATTAATATCTAAATGTTAAGTTACATATAATGTATGTTCTACATATAATAATTATATGTTCCTTTTGTACTGTTGTGTATTGGATGTTTTTAGATATGATACTGGACCAACAGGAAGTGGCTGGTCATCTTGAAGACGATGTCAGGAAGAAGGTGAAGGAGGCTCTTCTAAAGCAGCACCATCATCAGAACCAGAAGAAACTGGCCAATCGGATCCCCATCGTCCGCTCTTTCGCTGACATCGGCAAGAAGCAGTCAGAGTCCAACTGCTTGGACAAAAACG[G/A]TACTCGATTACCATCATTCAGAATTCACAGAAGGTATTGGTGTTATTACTTGGTGACTCGCTCTGACCAGATCATTTGAATCAGTGAGTCTTTAACTGGTGACTCACTCTGACCTGATCATTTGAATCAGTGAATCTTTAACTGATGACTTGCTCTGACCAAATCATTTGAATCAGTGAGTGTTTAACTAGTGACTGGCTCTGACCAGATCATTTGAATTAGTGAGTCTTTAACTGGGAACTCGCTCTGATCAGATTAATTGAATCAGTGAATCTTCAACTAATGACTCACTAACGACCAAATTGTTTAAATTGTGAGTCTTTAACTTGTCACCCGCTCTGACCATATCATTTGAATCAGTAAGTCTTTAACTGGGGACTCGCTCTGATTAGATAATTTGAATCAGTGAGCCTTTAACTGTGGACTCGCTCTGATTAGATCATTTGAATCAGTGATTCTTTAACTGGGAACTTGCTCTGACCAGATCATTTGAATCGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15332
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 |
|---|---|---|---|---|---|
| ENSDART00000084806 | Nonsense | 174 | 900 | 5 | 21 |
| ENSDART00000139316 | None | None | 573 | None | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 52687019)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 51809241 |
| GRCz11 | 9 | 51340654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAGGTTTCTGTTCATCCTTCTCGGACCTCTGGGAAAAGGAGCTCAGTA[T/A]CACGAGATYGGCAGATCCATCGCAACCTTGATGACAGATGAGGTATCTCA
Long Flanking Sequence:
TTCATCTTCCAGCAGGACAATGACCCAAAGCACACCGCCAAAATATCAATGGAGTGGCTTCACAACAACTCGGTGAACGTCCTTGAGTGGCCCAGCCAGAGGCCAGACCTAAATTCTATTGAAGATCTCTGAGAGATCTGAAAATGGCTGTACACTCTCATTTCCCATCTAACCTGATAGAGCTTGAGAGGTACTGCAAAGAGTGCATCAACACAGTATTGAGTAAAGGCTGTGAATACTGATGTACATGTGATTTTTCAGGGGGGTTTTTTTCTATAAATTTGCAACAATTTCAAAAACTCTTTTTCACATTGAATGTTGAGGAAATGAATGAATTTAATCCATTTTGGAATAAGGCTGTAACATAAAAATGTGTGGAAAAAGTGAAGTGCTATTAATACTTTTCGGATGCAATGTAAATGCAGCAGTACATTAGTGTTGCGTGTGTGTTTCAGGTTTCTGTTCATCCTTCTCGGACCTCTGGGAAAAGGAGCTCAGTA[T/A]CACGAGATTGGCAGATCCATCGCAACCTTGATGACAGATGAGGTATCTCAAGATATTATTTTATTTTGTCTTTATATATTAAATTATGAGGGATTTTATAATAATTATAAATTTACTTTTATTTAATTATATTATAAGATTAAATATATTATTAAATGTATTAGATTGTGGAGGTTTATTCCGCTGTGGTGAAAATTAAATGAAATGTATTAGATTGCTCAATTAGATGAGCAAAAATAATTTAGAAAAATAATGTATCGATTTATTTAGGGTGACACAGTGGCTCAGTGGGTTGCTCTGTTGCCTCACAGCAATACGGTAGCTCCCGGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTGCGTGTTCTCCCCATGTTGCCTCCGGGTTCTCTGGTCTCCCCTACAGTCCAAACACATGTGCTATAGGTAGTTTTGGGAGTAATGCTTTACAAAAGTGATGTATTATGTATTAAGCAATGTATTAATGCTGCATATTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13363
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 |
|---|---|---|---|---|---|
| ENSDART00000084806 | Nonsense | 747 | 900 | 17 | 21 |
| ENSDART00000139316 | Nonsense | 479 | 573 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 52648829)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 51771141 |
| GRCz11 | 9 | 51302564 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGACATGTTTRCTTCTGCTTTTTCTYGTGATCTTAGTTTTTCGAYCGTT[T/A]GAGATTGTTCGGGATGCCGGCTAAACAYCAGCCAGACTTCATTTACCTGA
Long Flanking Sequence:
ATGAGACTCTAATTGGTTTATTCTCAAAACACACCTATGACTCATTAAGAAAATAAACTCAACCCTTTTAAACCATGCGCCACGGCGCAAAGCAGATTTTCCCCCTCCTTAAATTAGCAAAAATGTGTTCTGACACGCCCTGAAAGCGTTTGCGCCCTGTGTTTTGCGCTCTGCGCATGGATCGTCAAAATAGAGCCCGAAGACAGACAATGACAGGAATTGAGTGCTTGATTCGAGAAAACTTGATCCGAGCACAACATACAAGACATGACTGGACTAGTGTCTGGACTCTGCCACTAAAACAAGAATGAACAAGACTGAAGTGGCTGAATCCTGACAATTAAAGACTTTCGATATGGATTATGTAGTTGTAGAAACATGGAAGCGTTTCTGACCATTATGACTGGTGCATGAGAAAGGAAGGAGTGTATCCTATGTTTACCTATTGCTCTGACATGTTTACTTCTGCTTTTTCTTGTGATCTTAGTTTTTCGATCGTT[T/A]GAGATTGTTCGGGATGCCGGCTAAACACCAGCCAGACTTCATTTACCTGAGGCACGTTCCCCTGCGAAAGGTTCACCTGTTCACCATCATCCAGCTCAGCTGTCTGGTCCTCCTGTGGGTCATCAAAACCTCCAGAGCCGCTATCGTCTTTCCCATGATGGTATACATCTGACATACTACTATAATGTTATATTATAATGTTGTTTTTCATGTAACACAGGGAGAGTAAACCCATTATATGTACAGTTGAAGTCAGAATTATAGCCCTTCTGAATCCTGTATATTTTTCCCCAATTTCTGTTTAACTTAAAGATTGTTTTCAACACATTTCTAAACATAATAGTTTTATTAACTCATCTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTGCATAATATTTCACTAGATGTTTTTAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGCTAATTAGGATATTTAGGCAAGCCATTATA
Associated Phenotype:
Not determined