ZMP
SLC4A7
Ensembl ID:
Description:
solute carrier family 4, sodium bicarbonate cotransporter, member 7 [Source:HGNC Symbol;Acc:11033]
Human Orthologue:
SLC4A7
Human Description:
solute carrier family 4, sodium bicarbonate cotransporter, member 7 [Source:HGNC Symbol;Acc:11033]
Mouse Orthologue:
Slc4a7
Mouse Description:
solute carrier family 4, sodium bicarbonate cotransporter, member 7 Gene [Source:MGI Symbol;Acc:MGI:
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1291 | Essential Splice Site | F2 line generated | Not yet available |
sa22928 | Nonsense | Available for shipment | Available now |
sa22927 | Essential Splice Site | Available for shipment | Available now |
sa36235 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1291
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000112879 | Essential Splice Site | 90 | 1092 | 3 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 45572891)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 42831081 |
GRCz11 | 16 | 42734839 |
KASP Assay ID:
554-1206.1 (used for ordering genotyping assays)
KASP Sequence:
GAAAGACAGATGCTCTGAGCGAGAGGACGGCAGAGATTCACCAACGTACG[G/A]TAAGAAAAGCAGGTCATAATGGGGCTAATCTATCTGTTTTATTTGCTTGG
Long Flanking Sequence:
TTATGAATTTTTGGGTGAACTATCCCTTTAAATATGTAGAGTCATTAAAAAAGTATTATGCTTATCACTTTTGGCCATTATGCTTAAGTTATTTAAACAAATGTGATGCAATTTGCTAGTAGACCATTTTCCTCATTGCTCATTTGTTTATTGATCTCTATTTTTGGTGTGCATTAAAATGTGCCTCAGGGAATATGTATTGCTGGGATTAGCAGTTTGTAGAATGAATTATTCAGCTTGTGTGTCTGGAATGCTGTTTGTTGTATCGCACTCCTTTTCTTGTGTATTATGGATCTCAAAAGAGTTTCCTATCTCTCACATTACAGGACAAAGTTCTAATGTCTTTCTCTTTACAGGTCACAGAGCAGTTTATGTTGGCGTACATGTACCTTTAGGAAGACAAAGCAGAAGGAGACACCGCCACCGTGGTCATAAGCACCATCGGAAAAGGAAAGACAGATGCTCTGAGCGAGAGGACGGCAGAGATTCACCAACGTACG[G/A]TAAGAAAAGCAGGTCATAATGGGGCTAATCTATCTGTTTTATTTGCTTGGTGTAAATATTTTGGCTCTGTGCTTTTCCACTGGTGGCTTCAGACACTCCTTCACAGAGGGTCCAGTTTATCCTCGGCACTGAGGATGATGACGAGGAGCACATTCCTCATGACCTCTTCACTGAGCTTGACGAGCTGTGCTTCCGCGATGGACTCACTTGTGAGTGGAAAGAGACAGCCAGGTGAGAAGCTAAATGAAGCCGAGAGAGTGCATACAATAAATTAATGATAAGATAATAAGTATTAAATAATTTAAATAAAAGATCAGAAAGCTATTAAATGCAACGGAATGTTTAAATAAATAAATGTACATTACATTTAAGCATAATAATAAATAGTGTGTGAAATACACTTTACATTTTTTTTTTTACTGATGCTTATAATCACGTTATACATATGTATAATTTCATATTTTACGTTGTGTGCTTTTTTTGAAAGTGTGGTTTAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22928
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 |
---|---|---|---|---|---|
ENSDART00000112879 | Nonsense | 275 | 1092 | 7 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 45563697)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 42821887 |
GRCz11 | 16 | 42725645 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCCCAGTCGGCCCCGGGCATCCTGGAGAACAGTAAGTCCAGTGAAAGC[C/T]GAATAAATGGCACCGGTGGCAGCAGGGAAAATAGCACAGTGGACTTCAGC
Long Flanking Sequence:
GGAGAGTTTGTTTCCATGAAATGTCCCCTCATGTTAACACAGTTTTGCAGTCTCTTTATGGATATCGAGAGATGATTTTCGATCGCTACTCTTTGTGTAGCTAAAATCCTCAGTCAGAAGCCAGGAACAATTTATCAGACCTCAAGTTAATGATTTAGCCTTAATGCTCACCCCAGATGAACTCATCATTTTAAATAAAAGGTTTGATTTCCATCCAATACATTCTCTGGGATGGAAAATCTACAAATCTTTCAGCATCGTATCCATGAGCACTGTTGTGTGATGTTATGCAGAAAGCATGTGACCTACTCTGCATGTCCACACACTGAGTGTGCAGTAAACCTTCTCTGGATATTAGAGATTTGAGTCGCCATCAAATGTCTAACTGCAATCTTTTTCTTGTGTTTTTTTTTCTTTCTTTTTTTCTCACCCCAACAGGTCTTCTTGCGTCGCCCCAGTCGGCCCCGGGCATCCTGGAGAACAGTAAGTCCAGTGAAAGC[C/T]GAATAAATGGCACCGGTGGCAGCAGGGAAAATAGCACAGTGGACTTCAGCAGAGTGAGTTTCTTTCAGCTAGTTGTAGATGTTGCAGATGAGTTAAGACTGTTCAGACAACAGAATCACACAAACACAAATCAGCCCATTTTGACATAAAAAACTCAAATAATAATAATAATAATGATAATAATATTTGTATCATTTTATTTTTATTTGATTTATTCTGGAATGCAAATTTTCTTAAAAACAAAGCAATACGGTAAAAATTTTAATGCACTAAAAATACAACATCAATTAAAAACAGCTAAAATAAATTGGCTAATTAAAAGTGATCCATGTGCCTTTATGATATTTAAAAGTGAGAGCATTCCTTAATTTGCAGGCTTTGAATGAAAAAACTATTTTTACCACAGTCTTTTATAAGTTTACATGGTGGCTGATGATCATGAGACCCCCACATCATTTCACATTGTTTGTAAGTTTATTATTGTATTCCATTTAATCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22927
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 |
---|---|---|---|---|---|
ENSDART00000112879 | Essential Splice Site | 345 | 1092 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 45558586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 42816776 |
GRCz11 | 16 | 42720534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGCCTGCTGTTCTTCTCACCGGACTGACCGAAGTGCCCGTTCCGACAAG[G/A]TAGGACTACTGAAAACATGACTTGTTTACATGAATGGAGCCCCTTATAGA
Long Flanking Sequence:
TTCTGTAGCCTGTGGATTGTGAAAGATCACCTAATTCTCATGTGTCGCTGGTTTGGTGTAATAGTTTGTTGTGCAATTGTTTCTTTTGTTCATTGTCAGTGGTTTACTGTAGAATATATATATTTTTTTGTTTAATAGGACTTATGTTTGTCTGTGTTTCCATTGTCACTGATCACCACGTTAAACTGGCCTGACTAGAGTTTGTTTTATTTCCTTTTAATTTTTGCATGTTTACTTAAAGGAAAGAAGTGTTTTTTTCTGAATTTGGTTTTCTACTACAAACCTTGGTGTTACCCATTAGTGTCCATTATGAATGATCTTCCGCTAATCTGTGCTCTATAGGTGGACATGAATTTTATGAAGAAAATCCCGCCTGGGGCTGAAGCTTCAAATGTTTTGGTGGGGGAGGTTGATTTCCTTGAGCGTCCAATCATTGCCTTTATCCGACTCTCGCCTGCTGTTCTTCTCACCGGACTGACCGAAGTGCCCGTTCCGACAAG[G/A]TAGGACTACTGAAAACATGACTTGTTTACATGAATGGAGCCCCTTATAGAACAGGGGGATTTCATGACCGAAATGTGAAACTTTCTTTTCCTAAAGATTTATCTATTTCCTTGTCTTGTTTTTACAGGTTTCTCTTCCTGCTGTTAGGGCCTTTCGGTAAAGGAGCCCAGTACCATGAGATTGGCAGATCTATAGCTACGTTGATGACAGATGAGGTGAGGTATCTGCCCTGCAAGGTCCATACGGATTGGTTAAAACTCCTATTTAGATGCTTTAACCTTAAGTAAAGTATTCGTTTTTTTATTTAACTTATAAATAAAGTTAAATAAATTAGATTTTCTTAATCTGTGGGCTTGTTAAATAGACCCATTTCACATTCTCAGCAGCAGAAGTCGTCATAGTTGAGTCAACTTAGAGCGCAGTGAATGGGAGAGAACAACAAATACTTTTTTACAATCCTATTTGCTGCGGTTGTGTTATCAATACTTTCAGAAAAAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36235
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 |
---|---|---|---|---|---|
ENSDART00000112879 | Nonsense | 497 | 1092 | 12 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 45553718)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 42811908 |
GRCz11 | 16 | 42715666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTTAGCCTGCAGTGTTTGGCCTCCATCCTTTTCCTCTATTGTGCCTG[T/A]ATGTCCCCCGTCATCACCTTCGGAGGCCTTCTGGGGGAAGCCACCAAAAA
Long Flanking Sequence:
ACTCTGTACCCTGTATGAAATGTATGATGTCTTAAAGTCTTAAATTTAATTTGCTGTAACCTGCAGAAACCCTGCATGGTTATTATAATTTTAAATATAGTATAAAATAAAAAAATATAGTATCTAGTATAAAACTAAAACCATAACTTTTTCATTATCAGAAAATAAAATGTTTAATTACATTCAAAATTAATATAGAATTTAATGAAAATAACATTTTTGTCATTTTTATTTCGTGAAATCTGTTGTACTAAAAAATACAAACCAAAGGAAAATGAATTGAAAAACTATGTAGGCAACTGCAAAAACTAGTAGTGTTATTTATGTAAATTTGATTGCTTTCATAAATATGAACTACTTTGGTTTTTTTTCTCTTCTTTCAGGATATTTGGGGGCCTGGTGCTAGACTTGAAGCGGAAAGCTCCGTTTTACTGGAGTGATGTTCGGGATGCTTTTAGCCTGCAGTGTTTGGCCTCCATCCTTTTCCTCTATTGTGCCTG[T/A]ATGTCCCCCGTCATCACCTTCGGAGGCCTTCTGGGGGAAGCCACCAAAAACAACATAGTGAGTCTCGTAGACCTCTGATGGGAATGATCTGTAGAGGATTAAAGGAATACCAAAAATTATAACTCTGTCATCATTTACCAATTTTTCTTCAGCTGATCGCAAAAGAAGATATTTTGAAACCATTGACTTCCATAGATATTTTTGACTTCCATAGTATTTGTTTTTTCCTACTGTGGAAGTCAATGTATACAGGTTGCAGCTTCAAAATGTCTTCTTATTGTGTTTAACAGAAAAAAGATTTGAAACCTCTTGTAAGTTGTGTGTACATTTTTAGTTTTTGGGGGAATTTTCCCTTTAAAGCACTGGACAAAATAGATTTTACTGGAATCATTGTGTAGCCCAATCGCTATGTTTTTATTCTTTACTTGACCTCATTTGTGATTACTTCTCTTTTGTCTGCATTTGATCCAGAGTGCCATTGAGTCTCTATTTGGAGCTTC
Associated Phenotype:
Not determined