Busch Lab

ZMP

slc25a44b

Ensembl ID:
ENSDARG00000035905
ZFIN ID:
ZDB-GENE-050320-89
Description:
solute carrier family 25, member 44 b [Source:RefSeq peptide;Acc:NP_001013537]
Human Orthologue:
SLC25A44
Human Description:
solute carrier family 25, member 44 [Source:HGNC Symbol;Acc:29036]
Mouse Orthologue:
Slc25a44
Mouse Description:
solute carrier family 25, member 44 Gene [Source:MGI Symbol;Acc:MGI:2444391]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa14027 Nonsense Available for shipment Available now
sa18105 Nonsense Available for shipment Available now
sa17175 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa14027
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
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052123 Nonsense 94 316 2 4
ENSDART00000125113 Nonsense 94 316 1 3
Genomic Location (Zv9):
Chromosome 7 (position 49757480)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 48027716
GRCz11 7 48300492
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGTGACCACGTTCACACTCATATCAGGGCAGGCGTACATAACCACTTA[T/A]GAATTGGTAAGAAAATATGTCTCCAGCTACTCTAAAGACAATACGCTGAA
Long Flanking Sequence:
TTAAAATTGTAGAATGTTTTTTTTGTAAATCACCTCATTTTACACGTTACAAACATGTGACTTGCCTTTTAGTAGTAAAACATAAGATGCAGCTTAACATTTGCTTTAGCTTCCACTAAAGAAAGATAGCATAACTGATGCCACAAATATAATTTATTTGTGTATTTATAACATTTTCAGTTGGCCTGGGACTGATGCTGGGCGCTACAGGCAGGAAACATGCAGCAGAAGCGCAACATTCAGATTATAGAATGGGAGGACTTGGACAAACGCAAGTTCTACTCCTTTGGACTGTTCATGACCATGACCATCCGTGCCACGGTCTACCCAGCCACGCTAATCCGCACCAGACTGCAGGTTCAGAAGGGGAAATCTCTCTACACTGGGACCTACGACGCCTTTCGGAAGATTCTCAGAACAGAGGGTCTGAGAGGACTCTACAGGGGCTTCATGGTGACCACGTTCACACTCATATCAGGGCAGGCGTACATAACCACTTA[T/A]GAATTGGTAAGAAAATATGTCTCCAGCTACTCTAAAGACAATACGCTGAAGTCTTTAGTGGCGGGAGGCTCAGCGTCACTGGTGGCCCAGAGCATTACTGTTCCCATAGATGTCGTTTCACAGCAGCTTATGATGCAGGGCCAAGGGGAGCATCTGACCCGCTTTAAAGTTAAACCCAAAACACCATCGGGAGCAAAGCACTCTGTGTTTTTCGGCCAGACAAGAGACATTATTGGGCAGATATTTGCAGCAGATGGCATTCGTGGGTTCTACCGAGGTTATGTGGCATCTCTTCTTACATACATCCCCAACAGTGCTGTTTGGTGGCCCTTTTACCACTTCTATGCAGGTGAGAGATGCAGTAACAATCTTTTTTTTTTTTTTTTAATTATCATACAGTACTGTTTGTAAGTTTGAGGTCAGGTTTTTTCAGCAAGGATGCTTTTAAATTTTTCAGAAGTAATAAAATGTATCACACCAAAAAAATAAAAATAATAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18105
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052123 Nonsense 167 316 2 4
ENSDART00000125113 Nonsense 167 316 1 3
Genomic Location (Zv9):
Chromosome 7 (position 49757697)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 48027933
GRCz11 7 48300709
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTTAAACCCAAAACACCATCGGGAGCAAAGCACTCTGTGTTTTTCGGC[C/T]AGACAAGAGACATTATTGGGCAGATATTTGCAGCAGATGGCATWCGTGGG
Long Flanking Sequence:
ACATGCAGCAGAAGCGCAACATTCAGATTATAGAATGGGAGGACTTGGACAAACGCAAGTTCTACTCCTTTGGACTGTTCATGACCATGACCATCCGTGCCACGGTCTACCCAGCCACGCTAATCCGCACCAGACTGCAGGTTCAGAAGGGGAAATCTCTCTACACTGGGACCTACGACGCCTTTCGGAAGATTCTCAGAACAGAGGGTCTGAGAGGACTCTACAGGGGCTTCATGGTGACCACGTTCACACTCATATCAGGGCAGGCGTACATAACCACTTATGAATTGGTAAGAAAATATGTCTCCAGCTACTCTAAAGACAATACGCTGAAGTCTTTAGTGGCGGGAGGCTCAGCGTCACTGGTGGCCCAGAGCATTACTGTTCCCATAGATGTCGTTTCACAGCAGCTTATGATGCAGGGCCAAGGGGAGCATCTGACCCGCTTTAAAGTTAAACCCAAAACACCATCGGGAGCAAAGCACTCTGTGTTTTTCGGC[C/T]AGACAAGAGACATTATTGGGCAGATATTTGCAGCAGATGGCATTCGTGGGTTCTACCGAGGTTATGTGGCATCTCTTCTTACATACATCCCCAACAGTGCTGTTTGGTGGCCCTTTTACCACTTCTATGCAGGTGAGAGATGCAGTAACAATCTTTTTTTTTTTTTTTTAATTATCATACAGTACTGTTTGTAAGTTTGAGGTCAGGTTTTTTCAGCAAGGATGCTTTTAAATTTTTCAGAAGTAATAAAATGTATCACACCAAAAAAATAAAAATAATAATAAGCATAGAATGATTCCTAAATATTGGTGTAACACTGAAAACTGTAGTAATAACTAGACCCACATGGAATCTGCACACACTAAAATTCACAGATTTATTTATGTAAATATGTGTAAGTATATATTTTTTATATTAATTTCAGTAATGCCATTGAATATTATGCAAATGTTTATAAGATTTATTTACAAAAGTTTGCCTTTCATTAGATGTATGAGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17175
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:
G > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052123 Essential Splice Site 210 316 2 4
ENSDART00000125113 Essential Splice Site 210 316 1 3
Genomic Location (Zv9):
Chromosome 7 (position 49757830)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 48028066
GRCz11 7 48300842
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAYATCCCCAACAGTGCTGTTTGGTGGCCCTTTTACCACTTCTATGCAG[G/C]TGAGRGATGCAGTAAYAATCTTTTTTTTTTTTTTTTAATTATCATACAGT
Long Flanking Sequence:
ACTGCAGGTTCAGAAGGGGAAATCTCTCTACACTGGGACCTACGACGCCTTTCGGAAGATTCTCAGAACAGAGGGTCTGAGAGGACTCTACAGGGGCTTCATGGTGACCACGTTCACACTCATATCAGGGCAGGCGTACATAACCACTTATGAATTGGTAAGAAAATATGTCTCCAGCTACTCTAAAGACAATACGCTGAAGTCTTTAGTGGCGGGAGGCTCAGCGTCACTGGTGGCCCAGAGCATTACTGTTCCCATAGATGTCGTTTCACAGCAGCTTATGATGCAGGGCCAAGGGGAGCATCTGACCCGCTTTAAAGTTAAACCCAAAACACCATCGGGAGCAAAGCACTCTGTGTTTTTCGGCCAGACAAGAGACATTATTGGGCAGATATTTGCAGCAGATGGCATTCGTGGGTTCTACCGAGGTTATGTGGCATCTCTTCTTACATACATCCCCAACAGTGCTGTTTGGTGGCCCTTTTACCACTTCTATGCAG[G/C]TGAGAGATGCAGTAACAATCTTTTTTTTTTTTTTTTAATTATCATACAGTACTGTTTGTAAGTTTGAGGTCAGGTTTTTTCAGCAAGGATGCTTTTAAATTTTTCAGAAGTAATAAAATGTATCACACCAAAAAAATAAAAATAATAATAAGCATAGAATGATTCCTAAATATTGGTGTAACACTGAAAACTGTAGTAATAACTAGACCCACATGGAATCTGCACACACTAAAATTCACAGATTTATTTATGTAAATATGTGTAAGTATATATTTTTTATATTAATTTCAGTAATGCCATTGAATATTATGCAAATGTTTATAAGATTTATTTACAAAAGTTTGCCTTTCATTAGATGTATGAGAGACTTGCTTTATTTTGTTCAAACAAGTGGATATAATTGGATTTGCATTGTAAAACTTGAATACAAATTACAGTATAAAGCTGTTATTTTTAATTTTATGTGGGAAGTTTTTTTTTTTTTTTTTTTTTTTTTTTGC
Associated Phenotype:
Not determined