ZMP
LOC100333073
Ensembl ID:
Human Orthologue:
SLC4A3
Human Description:
solute carrier family 4, anion exchanger, member 3 [Source:HGNC Symbol;Acc:11029]
Mouse Orthologue:
Slc4a3
Mouse Description:
solute carrier family 4 (anion exchanger), member 3 Gene [Source:MGI Symbol;Acc:MGI:109350]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34759 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34758 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41548 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34759
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 |
---|---|---|---|---|---|
ENSDART00000075745 | Nonsense | 41 | 1172 | 2 | 23 |
Genomic Location (Zv9):
Chromosome 9 (position 47251726)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 46803373 |
GRCz11 | 9 | 46603852 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAGTACATTAACATCATGCTGATTTTAACCTGTCTTTGTTTTCTCAGA[T/G]CACCGGCACACCTTCCACCATACCCACCACCCCCTGTCCACACATCTTCC
Long Flanking Sequence:
CTGCGATACCTGTTTCTGATTGATGCTCTGAACATCGGTGGTGGCATTCTCTGAGCAAATATGTTTGTATAATGATACTCAACTATATAATTGGCCATTTGTCAAAGCTAGTCGATTGCCTACATTGCTGTACTAGTCTCTAGTAGCATTCTCAATGTTATCTGTTATTTGAAGTTTGTGTGAAATTAAAATTTACAGTGTTCCTTTTGATAGCGCACATTGTTATTCTTTAGGTGAACAATAAATTTGTTTGTTTTGGTAATATTCAATCAAAGTCTGACCGTTTTCTTCTGTGTTTGGATGGGCGATCCATCTATGATGATGTCAGTTTGAAGGCTTCAGCCACACTATTATTAACCACGCCTCTCTTGTCATTAGCTTGCAATTAGGTAATGTTGTACAAAAAGAAAGCTCCGCCCCCTACTCAATATTCAATACTCCATTTCAGTTGGAAGTACATTAACATCATGCTGATTTTAACCTGTCTTTGTTTTCTCAGA[T/G]CACCGGCACACCTTCCACCATACCCACCACCCCCTGTCCACACATCTTCCACCGCAGCGTTTCCGAAAAAGGGTGCTCAGTATGGACCGCCGGCGGAAGAGAAAGAGGAAGAAAAAGAAGACGTCTATGCCTCCGTCAGATGTCACACCCACTATTCATGAAGTGGATGAGGAGGAGGCGGAGTCTGAAATCGAGGGGCAGTGTCAAGCAGCCACACCTACTGAGCCATCTGAAGAGCTGCCACAGGTAACCTGAAAGAAAATATCATACTACTGTTTAGGGCAGAAAGTGCACACTGCCATTAAAGAAGTGCAAGTTACCTTTGCCAAGTGCACTGACACAACCCATTCCACGACAGACCCCGGCTTTTTGACTTGTTGGAGTCTGGATGATCCTTTTCTTCTTTGGTCTGGAGCATACAGCATCCATTTCTCCTCAAAAATACCTGAAATACTGATTCATCTGACTACAGTACAAGTTTCCACTGTGTGATGGTCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34758
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075745 | Nonsense | 123 | 1172 | 2 | 23 |
Genomic Location (Zv9):
Chromosome 9 (position 47251482)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 46803617 |
GRCz11 | 9 | 46604096 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGGCAGTGTCAAGCAGCCACACCTACTGAGCCATCTGAAGAGCTGCCA[C/T]AGGTAACCTGAAAGAAAATATCATACTACTGTTTAGGGCAGAAAGTGCAC
Long Flanking Sequence:
ATTTGTTTGTTTTGGTAATATTCAATCAAAGTCTGACCGTTTTCTTCTGTGTTTGGATGGGCGATCCATCTATGATGATGTCAGTTTGAAGGCTTCAGCCACACTATTATTAACCACGCCTCTCTTGTCATTAGCTTGCAATTAGGTAATGTTGTACAAAAAGAAAGCTCCGCCCCCTACTCAATATTCAATACTCCATTTCAGTTGGAAGTACATTAACATCATGCTGATTTTAACCTGTCTTTGTTTTCTCAGATCACCGGCACACCTTCCACCATACCCACCACCCCCTGTCCACACATCTTCCACCGCAGCGTTTCCGAAAAAGGGTGCTCAGTATGGACCGCCGGCGGAAGAGAAAGAGGAAGAAAAAGAAGACGTCTATGCCTCCGTCAGATGTCACACCCACTATTCATGAAGTGGATGAGGAGGAGGCGGAGTCTGAAATCGAGGGGCAGTGTCAAGCAGCCACACCTACTGAGCCATCTGAAGAGCTGCCA[C/T]AGGTAACCTGAAAGAAAATATCATACTACTGTTTAGGGCAGAAAGTGCACACTGCCATTAAAGAAGTGCAAGTTACCTTTGCCAAGTGCACTGACACAACCCATTCCACGACAGACCCCGGCTTTTTGACTTGTTGGAGTCTGGATGATCCTTTTCTTCTTTGGTCTGGAGCATACAGCATCCATTTCTCCTCAAAAATACCTGAAATACTGATTCATCTGACTACAGTACAAGTTTCCACTGTGTGATGGTCCATTCCAGATGCCTCCTAGCAAAGTTAGGTTGACAGCGATTTTGGACACTGTTAACATATGGCTTCCTTTTGGCATAGTACAGTTTTATCTGGCATTTGTGGATGTAACAACATATTGTGGTACTTGACAAAGGTCTGCCAAAGTGGTCCTGAGCTCATGTGGTGATATTGCTTATAGATGATTCTATAGAGACAATTCTTAATGCAGCTTTTGAAAAAAACAGTGCCTATATGGTATAAATGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41548
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 |
---|---|---|---|---|---|
ENSDART00000075745 | Nonsense | 472 | 1172 | 11 | 23 |
Genomic Location (Zv9):
Chromosome 9 (position 47198612)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 46856487 |
GRCz11 | 9 | 46656966 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTTGTGTGGTTTGTGATTTTTACCGCAGTAAATGTGTTTATAGGGTG[T/A]GTGGAGTTCCTAGAGAAGCCTGCGATGGCCTTTGTCCGGCTGAACGAGTC
Long Flanking Sequence:
GGTTTAGATTTGCTCTCGGTGATGCAAAACAGGCACAATGGTTCATTAAAATTCACCAAACGCACATGCATGCTGAATCCATGAACGAAACAGCCGTATGGAACAATAAACAATCGCAGCGAGGGTAGCTGTGCATGTGCTATCTGCCAACGCTTGCCTGTCACAGCTCCAGGCTGATGTGTGTGATGTTTGAATGGCACTAACTATTTTCTTCTCTCCACAAAAGAAAAGCCTCCACCCCATCCCAGCTGAGGGACACGCCGCCTCCAGATCTTTGAAACTCTTGGCAAAGATTCCCAAGGATGCCGAAGCAACTGTGGTCTTAGTGGGTAAGCTTCGTTCCAGCGTTTGTTGTTTTCAGGTCCTGCGAAGATGTTGAGTCACCGCACCAGAGCTCAGCTAACCCAAGACGAATGCTTTCTGTTGTGTTTGATTTCTGTCACTAGTTCTTGGTTTGTGTGGTTTGTGATTTTTACCGCAGTAAATGTGTTTATAGGGTG[T/A]GTGGAGTTCCTAGAGAAGCCTGCGATGGCCTTTGTCCGGCTGAACGAGTCTATCCTGCTGGAGTCCATTCTGGAAGTCCCTGTTCCCATTCGCTTCATCTTTGTGCTGTTGGGTCCCACGCAGACCAACGTGGACTATCATGAGATCGGGCGCTCCTTTTCTACCCTCATGTCTGATAAGGTTGATATGCATCCATTATGAATCATGATTTGCTTATTATTAGGTCACAAATTTCAAGATGGTACAAACCCAGTGATATATTTAAGTGAACCTATTATGCAAGAATCACTTTTATAAAGGGTTTAAACACAGTCAGAGACAGCCCTCAGTGAGAAGCAGCCGTCCGCCATTAGAATTTTCATGCAGTACAAACTAAATATAATGTGGAATAAAGATAAAAAGCATAGTGTAGTTTTTCAGAGAGATAATATTAGCCCTGTTTTAAATCTGCCGCTATGCTGATTCATAGGTGTTTGTAGCTCCTCCCTCTTTTGAAAAGA
Associated Phenotype:
Not determined