Busch Lab

ZMP

LOC100331980

Ensembl ID:
ENSDARG00000090106
Human Orthologue:
SLC17A7
Human Description:
solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 [Source:HGNC
Mouse Orthologue:
Slc17a7
Mouse Description:
solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7 Gene [Source

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa37956 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa24553 Nonsense Available for shipment Available now
sa37955 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa37956
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099869 Essential Splice Site 21 585 1 13
Genomic Location (Zv9):
Chromosome 24 (position 40110255)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 38709912
GRCz11 24 38597675
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGAGCGCTTTAAAGCGGTAGCGGCCAAAACACTTGGAAGGATAAACAG[G/T]TAAGATCCAAAAATTCATTAAACTTATTTTTAATATGCAAAAGCTGCTTT
Long Flanking Sequence:
TTCCAGATTCTCATTTAACATCTCTCATTTCAAATCCAGTGTAGTGCAACAGGATCATGATTGATTTTCTTGTAAACAAACAATGCCGTGTATAAACCATTATTTAAAGCATTCTTTAAATGACTAACAGTCATCATTTAAAGCAGTCAAAATATGGACAACCATTTGGTAGAGCAGGCAATTAAAGGGATTAGGTCGCTGTCGTTATTAGAGACCTAATATCCAGATGTCTTTCTTTTTTTATTTAATAGCATTCTGGGATATTAACGGGGCTTTAGGCATCTGAAGTTCATGTATGTGTATGTGCGCGTACTTGTCCCTGCGCGCGTGTGTGTGTGTGTGTGGCAAGGGGGCGGAAGCGCGCTGGTGCGCATGCATGAGAGCAGGAGCGCGCAGTGTCCCGGTCGGTTGGTCGGTCCCGCGGTGGAGTTGTAAAGGATGGAGGTCCGACCTGAGCGCTTTAAAGCGGTAGCGGCCAAAACACTTGGAAGGATAAACAG[G/T]TAAGATCCAAAAATTCATTAAACTTATTTTTAATATGCAAAAGCTGCTTTATATGTTAATTATATCAGTGCAATTCACTTTACTATAGAGTTAAAGCGTAAAGGGAGAGCATAATGAGGGTTAACTGTGCTTTAAAATCATTAAAGTGGCTGTTAATCAGAGCAGATGGTGTAAATTAGTAATGAAGTGTGGAGGAGGAGGATTAGAGCAGGTGAACTGCACCGTGAGCGCACTATAGATGCTCATATAGCTCACAAGATTAACACTTATTATGTTTTATATCACTATTGTGTTTGTTTGAGTGTGAATGTAAGTTGAGGAGATCCTCCTTTGTATAGCAGCTTGTTTAATGTGTGTGTGTGGGGGGGTGTTATTAACGCGTCTGTTCTGGACGACCAGATTAACTCGACTGGACGCTATTAATAGCGACTCTTGTCCGGTTTGTGTCGTCACATTTCACCTGTCAGGTGATCACTTCCGATCCGCAGTGTGACAGTATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24553
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099869 Nonsense 98 585 2 13
Genomic Location (Zv9):
Chromosome 24 (position 40090062)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 38689540
GRCz11 24 38577501
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAATCTGGGAGTGGCCGTCGTCAGCATGGTCAACAACCACACCGTCTAC[A/T]GAGATGGAAAACCCTACATTGTGGTAAGTAGAATTACGTGTGTGTGTGTG
Long Flanking Sequence:
TAGCCACACCCAATACCTCAGACTGACAAACCGAAAACAAACAGGAAGATAATTTTCAGATATTCATTTTAGAAGTGCAAACTATTTCTTTCCTAATGTCACGCACAGATGAATTGTTCACTACAAAACCAGCAATGTGAACTAACAAAATCAGATTAGTTTTGATGTGTACTTAAACGTCATTGATTTTACACTGATTGTCCTGGGTTATGTTTGATTTGGATCTAAAGTGTGTGTGATGGTCAGAAACGCTGCTGTTGTTTTTGGACAGGGTTTTGGAGAAGCGTCAGGAGAATGGAGAGACCATCGAGTTGTCAGCAGAAGGCCGTCCGGAGCTGCAGGAGGAGAAGGAGCTGCCGGTGGTGGACTGCACATGTTTCGGTCTGCCGCGGCGCTACATCATCGCCATACTGTCAGGCCTGGGCTTCTGCATCTCCTTCGGGATCCGCTGTAATCTGGGAGTGGCCGTCGTCAGCATGGTCAACAACCACACCGTCTAC[A/T]GAGATGGAAAACCCTACATTGTGGTAAGTAGAATTACGTGTGTGTGTGTGTGTGTGTGTGTGTTAAACTCCATATCCATCCACCAGGCACTGAAATATTTTATTTTGTTTCATTTGTAAGATAACATTTGGCTTGTGATGTTAGTCTAGCATTAGTTTTATTAACTCACTGATTTATAATCATGGAAGGTTGTCAAAGCTTTTGATCTAGAGAAGGCACTGATACTGATTTTAAGCAATAGGGGGCGCCGCTATAAATTTTGACTCATAGGTGGTACTGAGATAAATTAGTACTGACTGGAGGCACAAAGACAAATTTTCAAGACCTAAGACCTATAAAGTGACGTTGATTCAAACTTTGGCAAATCAGTGGTACTACGACATTTTTGTGACTAACAGGTGACACTGACCATAACCATAGTCAGCACTTATGGTCATGAGTTTTGGATCATGACCGAAAGGACAAGATCTCGGATACAAGCAGCCGAAATGAGTTTCCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37955
Status:
Mutation detected in F1 DNA
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
ENSDART00000099869 Essential Splice Site 106 585 3 13
Genomic Location (Zv9):
Chromosome 24 (position 40087989)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 38686729
GRCz11 24 38574600
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTTTGGTATGTTTTAGATAAAGTGCATGTTTTGTGTTTGTGTGTTTC[A/G]GAAAGCACAGTTCTCCTGGGATCCAGAGACTGTAGGAATGATTCATGGCT
Long Flanking Sequence:
TGGATTCACCTGATTTGTTGACAAATGGGTTGTGGATCCATTCCTTGGCAGTTCCTTCACTGGGCCTTTTCCCCTTGGCAAAAAAAACTTTCCAAAGATGTCTGTTTCTTACTAATTTTGCTGCTTTTGGGTTAAATTTGGTCGCTAAAGTGACCGAGATGTAAGCGAGAGAATACGGTCATTTTTCAAAATAAAAGACTTTTCATAATAAAAGATCATTCAGACTCCATTTAATTAATGATTTATTGTGCAGCCTGCTACCAACTGATCCACGGACCGATGGTTGAGGACCACTAAGCTAGGGAATAAAATGAACTAAGGCAACATAATCATTCTCCTTATTGTCTACTGCTAAGAGTTTTATTAAATATGAGGCGACCCCCCACAAAGCTAGTTGATGCCCCCTGTGGGCTGGGACCCCCCTGTTGGGAACCGCTGGTATATAGTATTTTTGTTTGGTATGTTTTAGATAAAGTGCATGTTTTGTGTTTGTGTGTTTC[A/G]GAAAGCACAGTTCTCCTGGGATCCAGAGACTGTAGGAATGATTCATGGCTCGTTTTTTTGGGGATATATCGTCACTCAGATTCCAGGAGGGTTTATCTGTCAGAAATTTGCTGCCAACAGGTCAGTCAGTCATCCGGTCACTGAATGAAGATGTTTAAAAGAGTTAAACGCTCTTAATGCAGTGAATGTGTCTGTGTTTTTCAGGGTTTTTGGCTTTGCGGTGGTGTCCACGTCTATCCTGAATATGATGATTCCCACTGCGGCACGAATGCACTTCGGCTGTGTGATCCTAGTGAGGATATTACAGGGGCTCGTTGAGGTAAACAAAGAGAAAGAAATGCATTTGATCAAAAGTAAACTTGATTTCTGTCAAGATCCCGATCATCAAATATATATATATAGATATTTAAAAATGTCAAAGAGATGACAGTTGTAATAGATGCTCTATGTCCCTGTCGGACCATACACACACATTTTACAACTGCCCTAAATTGATCTGG
Associated Phenotype:
Not determined