ZMP
LOC555258
Ensembl ID:
Human Orthologues:
SLC47A1, SLC47A2
Human Descriptions:
solute carrier family 47, member 1 [Source:HGNC Symbol;Acc:25588]
solute carrier family 47, member 2 [Source:HGNC Symbol;Acc:26439]
solute carrier family 47, member 2 [Source:HGNC Symbol;Acc:26439]
Mouse Orthologues:
Slc47a1, Slc47a2
Mouse Descriptions:
solute carrier family 47, member 1 Gene [Source:MGI Symbol;Acc:MGI:1914723]
solute carrier family 47, member 2 Gene [Source:MGI Symbol;Acc:MGI:3588190]
solute carrier family 47, member 2 Gene [Source:MGI Symbol;Acc:MGI:3588190]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5881 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9619 | Essential Splice Site | Available for shipment | Available now |
sa6380 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35896 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa5881
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 |
---|---|---|---|---|---|
ENSDART00000087632 | Nonsense | 12 | 607 | 1 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 25972919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26703702 |
GRCz11 | 15 | 26636578 |
KASP Assay ID:
554-3908.1 (used for ordering genotyping assays)
KASP Sequence:
CGCTGAGAAGAAGATCATGGACGTCTCCAGTCCTGGAACYGACAATTTGT[C/A]AATGGAGCCCAGYGCCAAGCTGTTTTGCTGTGGTTTCATGAGGCGTTGCA
Long Flanking Sequence:
AAATTTTACGGATTCATTTTTTACAGTGTATAATTGTATTACAATTTTACAATTTGACCATGATTTCCAGCAGACACCCTCTAAAATGTCATTCAGTTTAACATTTTTACACACCCCTAACATTTTCTCACTATATCCACAACTTATCATTACTCTAATGTACTTTTACATCCCATACATCCTGTCATTAATCAACTCAAACTGTATCTTGAAAACAACTGATTGATCTCAAGAAACAATCAATCGTCCTACAATGCAACTTTCTGCCAGGACTGCAAACATCCTCCTCCCATCCTGTGGATTAAATCAAAGCGTCATTGTCTTCACCTCGGTTAATCGGTAAGCCTTCAAAGGTGCTGAATTTGGACCTGGGGAACGAACAGCTGTAGAAGGGCCCCTCGCAGTCTATGAAGCAACACACGGGCCCCTGACAGTGACTTGGAGGATCAGCGCTGAGAAGAAGATCATGGACGTCTCCAGTCCTGGAACTGACAATTTGT[C/A]AATGGAGCCCAGCGCCAAGCTGTTTTGCTGTGGTTTCATGAGGCGTTGCATCCCTCTGGTGTATCGAGAGGAGCTGTACCACATCCTGCGCATGACGGGACCCCTGGTGAGGCTTCAGTCGCATTCACTTCATGATAATATGCTACACTTGTCCTGTGTGAAAACTGAGCGCCACGAGAGAAATGTAGTGGCTTTGTGTGTTTGTGTGTATTTTTTCTACATGCATGTCTGTTTAAATGCAAATTAATCCCGGGTGATTGGATATTTGATTGTTAAATGCTTGCGTAATCTTGCATGATATGCCTTCAGTCTTGCGTGCAACAAAAACCATAGTAAAATATGTCTTTTATGAGATTTTCTAAGTAAATCAGTCAAGGTGCATAATACAAATTTGACTTGTGTGGCTAGTTTTAATGTTATTTTAACTTAATTTAGTAAGATAATTAAGTTATAGAGATTTTAACCTGACATTAAAATTGACAAAGTCAGTACATCACTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9619
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087632 | Essential Splice Site | 168 | 607 | 5 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 25966571)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26697354 |
GRCz11 | 15 | 26630230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTAGGATTGCACAGCTTTATGTGGTGGTTTATTTGCCAGCAATTCCAG[T/C]AAGGTTCACTAGTGGATGATTATRGGTTGCATTTTCAGCTTACCTTAATT
Long Flanking Sequence:
ATTAATATTAAATGTTGCTAAATTTGTTGCTAGGTTAATTTTAAAAAGGAAAATTTTATAGCGTCGTACCAAAGTTTTCTATAAAAAAAAAGGCTAAGTTTACCACACTGGTTGTTAATAAAGCCCTTCTGTGATAACAACCGAATGTAGGCCTATTTTATCCCCTACCCCTAAACCCAAACCTCACAGGAAATGGCAAATTTTGAATGTTAAAAGACTGTTAAGATTGTTATATATGATTTCTAAGCGTTTTGAATTACGAGGACACAAGGCATGTCTTTGTAAACCATCTTAATATAGAGCTACTAGGTCATTCCCTTGTCATTATACAATTTTTACACACACACACTGAATACATGTAGACCGATATTGACTGTTGAATGCTTGAACTGAGTATCGATGCATTAGAGCTCACATCTGTCTGTGATTTTTAACTGAAATCTCTCTCTTTCTTAGGATTGCACAGCTTTATGTGGTGGTTTATTTGCCAGCAATTCCAG[T/C]AAGGTTCACTAGTGGATGATTATGGGTTGCATTTTCAGCTTACCTTAATTATTTGTATGCATTGCTGTCCATCCTCATGTTGATTGTGTCATGTTTCTATACTACAGGCCATGTTTCTGTATCAGCTGCAGCTGTCATATCTTCAGAACCAGGTACATAAAATATACATTTAAGAAACTGAACAAAGCAAATAAGTGCTTTCAGGTGTTGTATGTGGTTGTTGTAATATTTATGAACCCTCTGTAGGGAGTGATCAAACCTCAGATGTACGCATCTGCTGTGGCCAATGTTGCCAATGTCATCGCGAACTATTTTCTGCTGTACTGGTGGGATTTTGGAGTTTAGTAAGTCGAATATGTTTTCATATTTCTTTCATTCACCTATTTATCTATTTGTTCATTTATACATACTTTTCTTGGTTTTAAATTTCAGCATGATACTTTTTTCTCTTGTGCATTTTTAGTGGATCTGCTGCCGCAAACACCTTTGCTCAGGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6380
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 |
---|---|---|---|---|---|
ENSDART00000087632 | Nonsense | 179 | 607 | 6 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 25966431)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26697214 |
GRCz11 | 15 | 26630090 |
KASP Assay ID:
554-5192.1 (used for ordering genotyping assays)
KASP Sequence:
CATGTTTCTATACTACAGGCYATGTTTCTGTATCAGCTGCAGCTGTCATA[T/A]CTTCAGAACCAGGTACATAAAATATACATTTAAGAAACTGAACAAAGCAA
Long Flanking Sequence:
CCGAATGTAGGCCTATTTTATCCCCTACCCCTAAACCCAAACCTCACAGGAAATGGCAAATTTTGAATGTTAAAAGACTGTTAAGATTGTTATATATGATTTCTAAGCGTTTTGAATTACGAGGACACAAGGCATGTCTTTGTAAACCATCTTAATATAGAGCTACTAGGTCATTCCCTTGTCATTATACAATTTTTACACACACACACTGAATACATGTAGACCGATATTGACTGTTGAATGCTTGAACTGAGTATCGATGCATTAGAGCTCACATCTGTCTGTGATTTTTAACTGAAATCTCTCTCTTTCTTAGGATTGCACAGCTTTATGTGGTGGTTTATTTGCCAGCAATTCCAGTAAGGTTCACTAGTGGATGATTATGGGTTGCATTTTCAGCTTACCTTAATTATTTGTATGCATTGCTGTCCATCCTCATGTTGATTGTGTCATGTTTCTATACTACAGGCCATGTTTCTGTATCAGCTGCAGCTGTCATA[T/A]CTTCAGAACCAGGTACATAAAATATACATTTAAGAAACTGAACAAAGCAAATAAGTGCTTTCAGGTGTTGTATGTGGTTGTTGTAATATTTATGAACCCTCTGTAGGGAGTGATCAAACCTCAGATGTACGCATCTGCTGTGGCCAATGTTGCCAATGTCATCGCGAACTATTTTCTGCTGTACTGGTGGGATTTTGGAGTTTAGTAAGTCGAATATGTTTTCATATTTCTTTCATTCACCTATTTATCTATTTGTTCATTTATACATACTTTTCTTGGTTTTAAATTTCAGCATGATACTTTTTTCTCTTGTGCATTTTTAGTGGATCTGCTGCCGCAAACACCTTTGCTCAGGTTTTTAATTGTTTTGCCCTGTTTTGTTTCATTCGCTGGCAGAAGCTCCATGAGAAAACTTGGGGAGGTGAGTGTTTATGTTGAAAGAATTGCTTTAAAACTGCAAGTTTGCAAAGCTAGTGTCTGTTTAAAATGACTAGTTTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35896
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 |
---|---|---|---|---|---|
ENSDART00000087632 | Nonsense | 589 | 607 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 25952873)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26683656 |
GRCz11 | 15 | 26616532 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTCACTGTGCCCTTACCACAAGTATCTTACGGTGCTGGTGCAAACTA[T/A]ACTGTGGACTCCAACTTTACCACAGCCAATCCCATCTATTCAACGAGTTT
Long Flanking Sequence:
AAAACATGAGACACAGGTGAATTGGGTAAGCTAAAGTGTTCGTTGTGTATGTGTAAAAAAATGTGCTGGATAAGTTGGCGGTTCATTACGCTGTGGCAACCCCAGATAAATAAAGCGACTAAGCTGAAAAGAAAACGAATAAAAAAGTATGCCATGTGTATTCGCCATGTTATGTGTGTAAAAGCACAATCAATAAATTCTACAGTACGTCTAATCCCTGGGAAACACTTATAATGGTGAAATTGTGTCTTTCAGAACGGAAATGGATACATGGTTGTGAGCTCTCAGGATCAGGACGAGAGGCTCAACAGTACTGCGGTACCCGAGGAGCCAAACGTGACTGGCGTGGAGGAAAAGCCTCCAGTTCTGCTGTCCACCACTCAGCTGGTTCTCAGGAGGGGTTTGACCACCGTCGCCGCTCTCCTCATCCTCGCCGTAGGAATAATCATCCATCTCACTGTGCCCTTACCACAAGTATCTTACGGTGCTGGTGCAAACTA[T/A]ACTGTGGACTCCAACTTTACCACAGCCAATCCCATCTATTCAACGAGTTTCATTTGAAATCAAGACTTCAGACAGATTCACTGTGAACTTTTTATATCTGTATATGCTGCGTGAGACCAAAAAACAAGTCTTTTAACGGCAATCCCAGGCTGTAGATTGTGACCTAAACAGATGATAATATTTTTATTTTGAGCACATTTGCTTTGTCCACAGCATTAGGCTGGAGGAGTATGAAAATCAACCAGCTTAGCAGAAAAAAAGGTCATATAATCTCTTTGGTTGACATTTCTAGTCAGATGACTGCTGGAGAAATACTGCCAAAAAGAAGATATTCTACAAAGCCACTGTCAAGATTGAGAAAGATATGTTATTAAGCACGATGGAGATGTAGAAATTGAAGAAGTTGCATGTGAAAAAAGATTTCTCTGAATTATATTTTTCTCTTTTTAGAATGCTGCTGACGCTGCAAAAATCGCAAGAAAACTTTCACACACACACAC
Associated Phenotype:
Not determined