ZMP
LOC798983
Ensembl ID:
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 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41787 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41786 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13492 | Nonsense | Available for shipment | Available now |
sa35031 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6192 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21853 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41787
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 |
---|---|---|---|---|---|
ENSDART00000091923 | Nonsense | 288 | 1074 | 7 | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 10777794)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 10730108 |
GRCz11 | 11 | 10713800 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCACTTCATGAAAAAAATCCCACCGGGGGCTGAGGCGTCTAACATCT[T/A]GGTGGGTGAGCTGGAGTTTCTGGAGAAACCTGTGGTGGCCTTCATCCGTC
Long Flanking Sequence:
GTTTAGACTCTTGTTTGGTAAATCTTACTTTTTAAAGGTTTGGGTGAGTAGAATCTACATGGTATTAATGATAATAAATGACAAGACCACAAATAGATACCCGCAATACGATGATAGTGTCAGTATTAAGGATTTAAATAAATTTGTATCTGAGGAGGCGTGTGTTTGAATTAAGTGTCATACTGTTGGTTTTATAGTATACAGTAATTATAGGTATAATATAATTTCTTGGTGGATTGTTAATTTTTTTGAAATGTTGTAAATGTCATGTATTTTGAAACTTATTTCTAAAGTTATTCGTATTTATTTTGTATTGATTCATTGCTTTATATTTTAGCTATACTGTTTTACTATTAGTCCAAAGACTGTTGGTATATAATCCCTGTCAAATAAACCAGAAAAAATGTATAACAATAAAATAAAAAAAGTTTTCTTTTGTCTGCAGATAGACCTCCACTTCATGAAAAAAATCCCACCGGGGGCTGAGGCGTCTAACATCT[T/A]GGTGGGTGAGCTGGAGTTTCTGGAGAAACCTGTGGTGGCCTTCATCCGTCTGTCTCCTGCTGTGCTGCTCAATGGGCTGGCAGAGGTCCCGATCACCACCCGGTATATATCTGCGCAAAAAACTCATAACTGTCTCAATCTTTCAAGCACATTTTGCAAAATGGTGTACCCAAGGGTTCGCTTCTTAGTTCGCTGTCATTTTGCAGGTTTCTCTTCATTCTGCTGGGGCCAATGGGAAAAGGACCACAGTATCATGAGATTGGTCGTTCCATTGCCACACTCATGACAGATGAGGTCAATATTATTGCCATTATTATCTATTTATTTTTATGCATGATGCTATACTAACTGGCTGTTACTGTATATATGCTAAATTCACATCAGTGTGTCTTTTCTAGGTGTTTCATGATGTGGCGTATAAAGCAAAGGAGCGTTCTGATCTTGTGGCTGGAATTGATGAATTTTTGGACCAGGTGACTGTGCTGCCTCCTGGCGAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41786
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091923 | Nonsense | 399 | 1074 | 9 | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 10777253)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 10729567 |
GRCz11 | 11 | 10713259 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCGAATGGGATCCCACCATCAGAATAGAGCCACCTAAAAACGTGCCCT[C/A]ACAGGTAATCAGTGATCAAACTTTACTGTACATGCACTGATCCATAGCAG
Long Flanking Sequence:
TTCATCCGTCTGTCTCCTGCTGTGCTGCTCAATGGGCTGGCAGAGGTCCCGATCACCACCCGGTATATATCTGCGCAAAAAACTCATAACTGTCTCAATCTTTCAAGCACATTTTGCAAAATGGTGTACCCAAGGGTTCGCTTCTTAGTTCGCTGTCATTTTGCAGGTTTCTCTTCATTCTGCTGGGGCCAATGGGAAAAGGACCACAGTATCATGAGATTGGTCGTTCCATTGCCACACTCATGACAGATGAGGTCAATATTATTGCCATTATTATCTATTTATTTTTATGCATGATGCTATACTAACTGGCTGTTACTGTATATATGCTAAATTCACATCAGTGTGTCTTTTCTAGGTGTTTCATGATGTGGCGTATAAAGCAAAGGAGCGTTCTGATCTTGTGGCTGGAATTGATGAATTTTTGGACCAGGTGACTGTGCTGCCTCCTGGCGAATGGGATCCCACCATCAGAATAGAGCCACCTAAAAACGTGCCCT[C/A]ACAGGTAATCAGTGATCAAACTTTACTGTACATGCACTGATCCATAGCAGATCCGATGATGCAATTGGTGATGCATTAGTGATGAATTATCAAAACCAAAATAATTCCAATAAAAAAATGTCACTTTTGTGTGAAACATTTTTTTGAGGGCCACATTAGAAAGAAACAAAACAACTTTCTGGAATTAATTATGTCTCATGCAATTGCTCAACCACAGAAATACATCAATAAATCCAACATACAGTAGACTCATTCTGAAAGCGTAGCCCTATATATATTTTTAAAGATTGCCAGTTCTTTCAAGACGTCCTCGCTGTAGCCTTGATGACGTAGGTGATCGTCAACTAAAAAGCGGACCTGCTACTGTGACAGTTGGGCTTAGGGTAGGCGATCGTCAACTACCTAGCAGACCTTGTACCGTCCACTAAGGTAACACCCATGCTACTGTGATGGTTGTGTTTAGGGTAGGGGGAGGTGTAGGCAATTGTCAACTACTGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13492
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 |
---|---|---|---|---|---|
ENSDART00000091923 | Nonsense | 514 | 1074 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 10773021)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 10725335 |
GRCz11 | 11 | 10709027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTTTTTGGAGCCTCTATGACGGGTATTGCATACTCATTGTTTGCCGGG[C/T]AGCCCCTCACTATTCTGGGCAGTACAGGGCCTGTATTGGTCTTTGAGAAA
Long Flanking Sequence:
GGAGGAAGAGGAACATGGAGGCCATGGTGGACCAGAGCTACAACGCACTGGGAGGTCAGAAATCTGTCCATATCTACTGTTTATTTTATGTTTGATAAATCCCCATATTTGAGACCGACCTGGATCTCAGATGTTCTGTTAATTGTACAGGATTTTTGGTGGCCTTTTCCTGGACATCAAGCGCAAGGCTCCTCACTATCTGTCAGACTACACAGACGCCCTCAGCCTGCAGTGTCTGGCCTCCTTCCTCTTCCTCTACTGCGCCTGCATGTCTCCGGTCATCACCTTCGGAGGTCTGCTGGGAGAAGCTACTGAAGGACGCATAGTAAGAATGCATATAGGCAATTTATTTAGCAAGTTTATAGACGCAAAACTGTATTTCAAGAGACCTGGGTTGATTATGCTGCCATTGTGATATCTTTTCATTTGTCTTTTAGAGTGCAATAGAGTCTCTTTTTGGAGCCTCTATGACGGGTATTGCATACTCATTGTTTGCCGGG[C/T]AGCCCCTCACTATTCTGGGCAGTACAGGGCCTGTATTGGTCTTTGAGAAAATCCTCTTCAAATTCTGCAAGTAAGGCTCCTTTGGTTTCAAATAGTTCTGTTCTTTTATTTTGTAATGTTTCATTAGGTTTATAGTGGAAGAATAAGGAAATGCACTTTCACAGTAGTCTGCTTGATTATAAGAATGCATGTACAGTGGTCTGCATTGTTGTAGTATGATATATAATTAAAAGAGAAAATGCAGAATACACTACTTGACAAAAGTCTTGTCGTTGATCCCAGTTGTAAGAGCCGCTTGATCTAGTTGATCATTTGGAAAAGTGGCAGAAGGTAGATTTTTCAGATGAATCATCCGGTGAGCTGCATCCCAATCATTACAAATACTGCAGAAGACCTACTGGAACCTGCATGGACCCAAGATTCTCACATAAATCAGTCAAGTTTGGTGAAGGAAAAATCATGGCTTGGCGTTACATTCAGTATGGGGGTGTGCGAGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35031
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091923 | Essential Splice Site | 709 | 1074 | 16 | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 10758086)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 10710400 |
GRCz11 | 11 | 10694092 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGAAATCTATATAATCTGTAATGTTGTTCTCTGTGTTATTTTGCAAC[A/G]GGTGAGGCAGATTATCAGTGATTTTGCTGTTTTCATCACCATCATGACCA
Long Flanking Sequence:
CCTCAGCTGGGTCAGTTGGCATCTCTGTGTGTAGTTTGCATGTTCTTTCTGCGTTCAGGTGAATTGGGTAAGCTTAATAGTCCATAGTGTATAAGTGTGTGGGGATGTTTCCCAGTGATGGGTTGCTGCTGGAAGGGTATCCGCCGCGTAAAAACGTGCTGGATAAGTTAGCGGTTCATTCCGCAGTGGCAACCCCGGATTTATAAAGGGACTAAGCCAAAAAGAAAATGAATGACTGAATGATAATATAATATAATAATAGTATGAGTATATTTTGATCAAAAATACTGTAAAAAATACTGTAAATTTTTGAACTGCTATTACAGTTTGAAATAACTGTTTTCTGTATGAATAAATTTCTTTTTTTTTTATTAATATTAATATAATAATAATTATTATTATTAATAATAATATTATTAATATGACACTCTTTAGTGCTGTAAAAATTCCCCCAGAAATCTATATAATCTGTAATGTTGTTCTCTGTGTTATTTTGCAAC[A/G]GGTGAGGCAGATTATCAGTGATTTTGCTGTTTTCATCACCATCATGACCATGGTTCTGATCGACTATGGTCTGGGGGTTCCTTCACCCAAACTACAGGTTCCTAATGTGTTCAAAGTGAGTGGTTAGAAGAAGTTTTACTATTTTAATTATTCATCAATTTTCCCATCAATATGTATTCAACATATTTATTTGACCTCTCACAGCCAACCAGAGATGACCGTGGCTGGATTATCAGTCCACTGGGACCAAACCCGTGGTGGACTGTAATTGTGACCTGCATCCCAGCCCTGCTGTGTACTATCCTCATCTTCATGGACCAACAGATTACTGCCGTTATTATTAACAGGAAGGAACACAAGCTGAAGGTTTTAATAAGAATCTTCTTTTGATTATCAGATATTCTTGTAGACTTAATGTTACGGTATGTTTTTGGTTGTGGATGTCGGAATGACAACAATTTCCTAATTTTTTATGTCACTGCTTAGCAAAGTTGGGTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6192
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091923 | Essential Splice Site | 965 | 1074 | 20 | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 10753343)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 10705657 |
GRCz11 | 11 | 10689349 |
KASP Assay ID:
554-4727.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCTGGGTCATTAAAACCTCCAGAGCCGCCATAGTCTTTCCAATGATGG[T/C]AGGACACCTATATTTATATGTATTTGAGTGTGTGCATGATCACCAAGAGC
Long Flanking Sequence:
TAACTAGAATTTTTTATTAGTAATGTTGGTAATTTTGTCAATCTATGTAAATAAAAAAAGCTTTATCTCATTTGTTGTTTTAACGTAAATTGTATTGTAATGTGTACTTATGTTTTTTTTAAGCTTTACATTTCTTAAGAAATCACTTAAGAAATCGCTTTCTTTTCAATTAATATTTATCATGTAATATTTATATCTTATTTTAACTCTATCCCAAATAATAGTTTTTGTCAAAAAGGACTAAATTGTGTCTAGATGCACTTCAGGTTCAAACTATTTACAGTAGTTCTGACCATATTTAGATGTGTTTGTGTTTGCCATTCAGTTCTTTGATCGCCTGAAGCTGTTTGGGATGCCGGCGAAACACCAGCCTGATTTTATCTATCTGAGACACGTTCCGCTGAGAAAAGTCCACATGTTCACCATTATCCAGCTCAGCTGCCTGGTGCTTCTCTGGGTCATTAAAACCTCCAGAGCCGCCATAGTCTTTCCAATGATGG[T/C]AGGACACCTATATTTATATGTATTTGAGTGTGTGCATGATCACCAAGAGCTGAGGAAATTAGGACTGGTTATCAATTCAGATTTAGTCAATTCAATTTCAAGAGCAGTGAATGTTTTCTCTTTTGTTCCTTAATTAAAGTTCCTGTGAAATTAAAATATAGTTTTTTAGATGTTAGTGTCAGTATGTTAAAACAGTGAAAGAATTTGCATTTAGAAGATATTAATATTTACAGTTGAAGTCAGAATTATTAGCCCCCTTTGAATTTTTTTCTTCTTTTAAAATATTTCCCAAATGATGTTAAACAGAGTAAGGAAATTTTACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCGACTAGAATAAAAGCATTTTTTTTTTAGCATTTTAGGGACAAAATTATTAGCCCCTTTAAGCTATATTTTTTCTCAATAGTCTACAGAACAAACCATCGTTATACAATAACTTGCTTAATTACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21853
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 |
---|---|---|---|---|---|
ENSDART00000091923 | Nonsense | 1020 | 1074 | 22 | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 10750995)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 10703309 |
GRCz11 | 11 | 10687001 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACTTTTAGGAGAATCAGTGTGTCTTGATTGAGGATGAAGGGATTGTA[C/T]AAGTACCCCTAGAAGGACATTATAAGTAAGTTGGACAATTTTTAGTGCCT
Long Flanking Sequence:
AAGAAAACAGATTCCCATAACATTCATCCCATTCCATCCTCCACATGTTATCAGTAAAAGAGTTTATCAGTGGTTTTACATCAGAAAGGGAATATGACCTTATGAAGAGTTAAATTTTGCCTGTTTTCAATGTTTTTTTAAAGCCAGAACATACACAAATTGTATTCACAACAATATCATGTCAGCCACTTTTTACCAAATTTTACTGCTGGATTAGATGACATGTCTGTGTGTTTCTGTGCAGGTATTGGCTCTCGTCTTCATCCGTAAGCTGCTGGATTTTGTCTTTTCTAAGCGAGATCTCAGCTGGCTCGATGACCTCATGCCCGAGAGCAAGAAGAAAAAGATGGAAGATGCACAGCAGGAGGTATTAACAACACCACCCTAACACACACTGGTCAATCAGTAAAAATAGTGTTCTAAAACAACAGATGACTAGTGTGTTCTTCTCTCACTTTTAGGAGAATCAGTGTGTCTTGATTGAGGATGAAGGGATTGTA[C/T]AAGTACCCCTAGAAGGACATTATAAGTAAGTTGGACAATTTTTAGTGCCTTTTTTTTAATGTATTTATTTATTTAGAAAGCTGTAGTCAGTAAGATTTCATTAGTTTAATTAATTGAATTATTTATTTTTAAAGATATTAATATTATTCTGCAAGCAAGCAGTAAATTGTTATAATTATATTACAGCTAACATTAACTTTCTTTCTTTGATGTAATAAAATGTAAAAATGTAAAAATGTACTGATCAGAAAAGAAAACATTCACTTTCATGTGGACTACAATTTTGCAACCATAAAGAACTATAAATCCCATCAAGCACCACACACACACACACCTGTTCCGATTTTCTGTTAATTACACACAGAAATGGCTGGGAGCTGCTCATGAACAAGTTAGATGGACTTTTTTATTTATTATTTTTATTTTTCTTATTTATACAGCAAACAAACACACAGATTTTGCTGAGTCTTGTTTAACTGTTTTGTGACATTAAGTTGCGT
Associated Phenotype:
Not determined