ZMP
slc4a1ap
Ensembl ID:
ZFIN ID:
Human Orthologue:
SLC4A1AP
Human Description:
solute carrier family 4 (anion exchanger), member 1, adaptor protein [Source:HGNC Symbol;Acc:13813]
Mouse Orthologue:
Slc4a1ap
Mouse Description:
solute carrier family 4 (anion exchanger), member 1, adaptor protein Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45618 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23155 | Nonsense | Available for shipment | Available now |
sa16732 | Nonsense | Available for shipment | Available now |
sa36489 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45618
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 |
---|---|---|---|---|---|
ENSDART00000046003 | Nonsense | 125 | 768 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 41038833)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 40924461 |
GRCz11 | 17 | 40879776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCCGAGAGATTAAAGGAACCGAGAGTACAGCCGAAATCAAAAGACATC[A/T]GACCCAAGATCCCTCCGGCTGGTAAATTCCCTCCGCTCCCGTACACCGAG
Long Flanking Sequence:
AACCCTATGTCATGTATATATATCTATGAGCCTATAGTCTCAGATTGTCCCTGCAGGAAGGGAATTATTAAGGTGTAACACCAAACACACCAGAACGCGTTGAGCGAACAGTGTTCGCCGAACGCACGATGGAGTTTGATGGCAGCGAACTGACAGAAAACATTCCCACTGAAACGATGAAAACGGAGAAAAGCCAGGACCCAGAAAATGGAAAAATCTGCGATTCTAAACAAGACATCACCAGCACAAACGAAACCGCTGACGATCCGTTTAAGAAACCCGTACTGACCCCTTCTCTCGCGGTGAAGAAATCATTAGGACCCAGTAAGAAGCCTACAGAAGAAGTGAGCAGCAGCGTATCAGAAAATACAGACGCAGATCATGATACTAAACACCTGCTGTCAACTGCAAAGGCTAAAGACACAAAAATAGACCCATCGGATCATCCGCCATCCGAGAGATTAAAGGAACCGAGAGTACAGCCGAAATCAAAAGACATC[A/T]GACCCAAGATCCCTCCGGCTGGTAAATTCCCTCCGCTCCCGTACACCGAGCCCCCATGGGGAGCTGTCCCTGACATCAACTACTCGTTTGAACTGCTGAAAAATGGAGCTATCCTAGACACCGTCCCGCTGACCCACAGGAGTTATTTTGTGGTGGGTCGGTTGCCTGTGTGTGATGTGTCTCTGGAGCACCCGTCCATCTCTCGCTATCACGCCGTGGTCCAGTACCGGGGCAGAGCCGGGCAGGAAGGCGTCGTGGGAGAGGAGAGGGGCTTCTACGCTTATGATTTAGGCAGCACCCATGGAACCTTTATCAACAAGAACAAAATACCACCTAAAACATACATAAGACTCCGAGTGGGGCATGTTCTAAAGTTTGGGGGGAGCACACGACTCTTTATCTTGCAGGTATGTGGGTATAATAGTGTTATAGTTCGTCAAAAACTAAAAGTTCACTCACTGTTTACTCACCCTCAAGTCACAACTTTGAAGTTTCTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23155
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046003 | Nonsense | 152 | 768 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 41038916)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 40924544 |
GRCz11 | 17 | 40879859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCTCCCGTACACCGAGCCCCCATGGGGAGCTGTCCCTGACATCAACTA[C/A]TCGTTTGAACTGCTGAAAAATGGAGCTATCCTAGACACCGTCCCGCTGAC
Long Flanking Sequence:
AACACACCAGAACGCGTTGAGCGAACAGTGTTCGCCGAACGCACGATGGAGTTTGATGGCAGCGAACTGACAGAAAACATTCCCACTGAAACGATGAAAACGGAGAAAAGCCAGGACCCAGAAAATGGAAAAATCTGCGATTCTAAACAAGACATCACCAGCACAAACGAAACCGCTGACGATCCGTTTAAGAAACCCGTACTGACCCCTTCTCTCGCGGTGAAGAAATCATTAGGACCCAGTAAGAAGCCTACAGAAGAAGTGAGCAGCAGCGTATCAGAAAATACAGACGCAGATCATGATACTAAACACCTGCTGTCAACTGCAAAGGCTAAAGACACAAAAATAGACCCATCGGATCATCCGCCATCCGAGAGATTAAAGGAACCGAGAGTACAGCCGAAATCAAAAGACATCAGACCCAAGATCCCTCCGGCTGGTAAATTCCCTCCGCTCCCGTACACCGAGCCCCCATGGGGAGCTGTCCCTGACATCAACTA[C/A]TCGTTTGAACTGCTGAAAAATGGAGCTATCCTAGACACCGTCCCGCTGACCCACAGGAGTTATTTTGTGGTGGGTCGGTTGCCTGTGTGTGATGTGTCTCTGGAGCACCCGTCCATCTCTCGCTATCACGCCGTGGTCCAGTACCGGGGCAGAGCCGGGCAGGAAGGCGTCGTGGGAGAGGAGAGGGGCTTCTACGCTTATGATTTAGGCAGCACCCATGGAACCTTTATCAACAAGAACAAAATACCACCTAAAACATACATAAGACTCCGAGTGGGGCATGTTCTAAAGTTTGGGGGGAGCACACGACTCTTTATCTTGCAGGTATGTGGGTATAATAGTGTTATAGTTCGTCAAAAACTAAAAGTTCACTCACTGTTTACTCACCCTCAAGTCACAACTTTGAAGTTTCTTTCTTCTGTTGAACATAAGATATTTTGAAGAAAGCTGAAAACCTGTAACTATTGACTTTGATAGTAGGAAAACAAATACTGTGGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16732
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 |
---|---|---|---|---|---|
ENSDART00000046003 | Nonsense | 424 | 768 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 41046416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 40932044 |
GRCz11 | 17 | 40887359 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAAAGAAAGAAGCGGCAGTYCAGTGCTGCCTGGAGGCCTGTCGTATCT[T/A]GGAGGCCCGTGGCCTWTTRAGACAGGAGGCAGGTAGGTKGACRTTAACAA
Long Flanking Sequence:
CTTAGATCAATATCGAGTAAAAATGTCCACAGCTAATCATTGATTATCATGATTTCCGCTATTGGCACAGCCCTAGTTGGAACGTTTCCTGGTTTTATGTGCTGGGGTGCCAGACAGAAACTTTTTTAAAAGAAAGAATTTAAAAGTCAAGAAACTATAGTAATGCCCGTTTTTAATCTATGATCAATGTTTACTGACCCATAAGTTATGGTAAAAACATTTAAAATAACCACTCAACATGCACATTTACATCACCAGAAATTAAGTTGCAGAAATCACAAATCAAATCGGAAACCAAATGTATATTCCCACACAATGACATATAATCTTTTTGGTTATTGTCATCACTGTATATTAAAGGGAAAATACTGTGTTTTATTTCTCTCTTTTTAGGTTACCTGTGGATGATGCTGTGGGCAGGCAACTGGTAGCTGAGGTCACTCACACAGGGAAAAAGAAAGAAGCGGCAGTTCAGTGCTGCCTGGAGGCCTGTCGTATCT[T/A]GGAGGCCCGTGGCCTTTTGAGACAGGAGGCAGGTAGGTGGACATTAACAATAAAAATCACATTCAGGGTTCAGATTCTTAGCATTGTTGCATTCAGTTATCTTAAGTATCTATTTTTTTCCAATTCGTCTCCTTAGAATTATGACTTTTTTGTCAAAACTGAGTTTTATATAAGTTATATATTGTAATTATATATACATAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATCATATATAAAATAATGTAACTTATTGACATTTTGGGATGTATATGTTTTATTTACAGTATGGGAAGATTTTTTAAGTTGTTTACATTTTAAGACAAATATTACACACATATTGTTTGCTACATGGAATGCAATCACTTTGAAGCTCAATATCTCAAAATCATTCAGAACATAGATAGAACCTTATCATTCCAAGGTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36489
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 |
---|---|---|---|---|---|
ENSDART00000046003 | Essential Splice Site | 576 | 768 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 41048847)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 40934475 |
GRCz11 | 17 | 40889790 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAGTGGAGCTGGCTAAACCCACACAGCTGCCTTCATTGCTGTCTAGCGG[G/A]TGAGATCATGAGATCTGTGTTTTCTTTCAAACTTTTCATTCTTTTTTTAT
Long Flanking Sequence:
TGTTCAATAGAAGAAAGATACTCAGAAATGTTTGGAACTACTTGTGGGTGAGTAAATATTCCTTATTGCGTGAACTTTCCTTTTAATTACCCTTGCTGCTGTATGTTCTATAACTGGTATTAATGTAGAATATGTTCTTTCTTAGCTAGCCAAGCTGGCTGATGTTGAAAAAGAGCTGGCTGACACCGAGAAAAAGCTAAATTTATCTGGGAAAGGTGAGGCAGTGGAAGACTTTTCCAATTCATCTCAGTATTTTATCATCTGTAAGGTAAGGTCACGCTTGTTTTTTTTTGTTATTGTTATTCAGGAGGCTCCGGTTCATCCACCGAGGATCCTCTGGATGCTTTTATGACCGCTGTACGGAGCGAGGTTGCTCTGGATGGGGTGGAAAGAAAGAAGTTGCACTTACATATAGCCGACTTAAAGAAGGAAGGTCAGAGATTGAGCAGGCTAGTGGAGCTGGCTAAACCCACACAGCTGCCTTCATTGCTGTCTAGCGG[G/A]TGAGATCATGAGATCTGTGTTTTCTTTCAAACTTTTCATTCTTTTTTTATAAGTTTTATAAGGATTCCCACGCTTCTTGAAAGTACTTTCATTTCAGACATATGGATTCAAGGCCTGGAAAGTATTTAAAAACCAACATGGAGCCTTGAAAGTGCTTGATTTAAATTTGAAGTAATTTGTTTATTAAATGTATTTGTCAAAAAGGTCAAAAGGTTTTTTTATTTTATTTTTGTACATTCAGATCTCATACTCAGTCTTCAGACTCCGACAAACCTAAGAAATTATCTTTACCGATGTTTGGAGCCATGAAAGGAGGGAGTAAATTCAAACTGAAGACTGGAACTATTGGAGTAAGTCTTTCTAACATTTTTATTTTTACCAGCAGTGTAGGTCATTGCTTTCAAAACTCTGTAATTTCTGTAATTTTCTGTCTTACATAAATAAGTAGAATTTACCACCAAAGCGGACAAGTTTGCCTCCAGAGCTCTTCACTATGAAGG
Associated Phenotype:
Not determined