ZMP
slc25a44b
Ensembl ID:
ZFIN ID:
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 |
|---|---|---|---|
| sa40995 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34167 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| 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:
sa40995
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000052123 | Nonsense | 12 | 316 | 2 | 4 |
| ENSDART00000125113 | Nonsense | 12 | 316 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 7 (position 49757234)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 48027470 |
| GRCz11 | 7 | 48300246 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACAGGCAGGAAACATGCAGCAGAAGCGCAACATTCAGATTATAGAATG[G/A]GAGGACTTGGACAAACGCAAGTTCTACTCCTTTGGACTGTTCATGACCAT
Long Flanking Sequence:
TTTCTTCTATTGATGTTGACTACCGGTTTCAACATTCTTCGAAATATCATCTTTTATGTTCAGCAGTCGAAAGAAACTTAAACTGATTTGTAACCAAGTCTGATTTAATAAATGGTTTTCATTTTCATTATTGGGTGAACTGTCCCTTTAATAAGAAATTGATAACATTCAGAAAATAAGAAACTTCTTCTGATTTTTATAAGATTGCTAATTAGTTCATGTGTTTTCTTTTAATGTAATGGCTTGTTAAAATTGTAGAATGTTTTTTTTGTAAATCACCTCATTTTACACGTTACAAACATGTGACTTGCCTTTTAGTAGTAAAACATAAGATGCAGCTTAACATTTGCTTTAGCTTCCACTAAAGAAAGATAGCATAACTGATGCCACAAATATAATTTATTTGTGTATTTATAACATTTTCAGTTGGCCTGGGACTGATGCTGGGCGCTACAGGCAGGAAACATGCAGCAGAAGCGCAACATTCAGATTATAGAATG[G/A]GAGGACTTGGACAAACGCAAGTTCTACTCCTTTGGACTGTTCATGACCATGACCATCCGTGCCACGGTCTACCCAGCCACGCTAATCCGCACCAGACTGCAGGTTCAGAAGGGGAAATCTCTCTACACTGGGACCTACGACGCCTTTCGGAAGATTCTCAGAACAGAGGGTCTGAGAGGACTCTACAGGGGCTTCATGGTGACCACGTTCACACTCATATCAGGGCAGGCGTACATAACCACTTATGAATTGGTAAGAAAATATGTCTCCAGCTACTCTAAAGACAATACGCTGAAGTCTTTAGTGGCGGGAGGCTCAGCGTCACTGGTGGCCCAGAGCATTACTGTTCCCATAGATGTCGTTTCACAGCAGCTTATGATGCAGGGCCAAGGGGAGCATCTGACCCGCTTTAAAGTTAAACCCAAAACACCATCGGGAGCAAAGCACTCTGTGTTTTTCGGCCAGACAAGAGACATTATTGGGCAGATATTTGCAGCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34167
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 |
|---|---|---|---|---|---|
| ENSDART00000052123 | Nonsense | 44 | 316 | 2 | 4 |
| ENSDART00000125113 | Nonsense | 44 | 316 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 7 (position 49757328)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 48027564 |
| GRCz11 | 7 | 48300340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACCATGACCATCCGTGCCACGGTCTACCCAGCCACGCTAATCCGCACC[A/T]GACTGCAGGTTCAGAAGGGGAAATCTCTCTACACTGGGACCTACGACGCC
Long Flanking Sequence:
CAAGTCTGATTTAATAAATGGTTTTCATTTTCATTATTGGGTGAACTGTCCCTTTAATAAGAAATTGATAACATTCAGAAAATAAGAAACTTCTTCTGATTTTTATAAGATTGCTAATTAGTTCATGTGTTTTCTTTTAATGTAATGGCTTGTTAAAATTGTAGAATGTTTTTTTTGTAAATCACCTCATTTTACACGTTACAAACATGTGACTTGCCTTTTAGTAGTAAAACATAAGATGCAGCTTAACATTTGCTTTAGCTTCCACTAAAGAAAGATAGCATAACTGATGCCACAAATATAATTTATTTGTGTATTTATAACATTTTCAGTTGGCCTGGGACTGATGCTGGGCGCTACAGGCAGGAAACATGCAGCAGAAGCGCAACATTCAGATTATAGAATGGGAGGACTTGGACAAACGCAAGTTCTACTCCTTTGGACTGTTCATGACCATGACCATCCGTGCCACGGTCTACCCAGCCACGCTAATCCGCACC[A/T]GACTGCAGGTTCAGAAGGGGAAATCTCTCTACACTGGGACCTACGACGCCTTTCGGAAGATTCTCAGAACAGAGGGTCTGAGAGGACTCTACAGGGGCTTCATGGTGACCACGTTCACACTCATATCAGGGCAGGCGTACATAACCACTTATGAATTGGTAAGAAAATATGTCTCCAGCTACTCTAAAGACAATACGCTGAAGTCTTTAGTGGCGGGAGGCTCAGCGTCACTGGTGGCCCAGAGCATTACTGTTCCCATAGATGTCGTTTCACAGCAGCTTATGATGCAGGGCCAAGGGGAGCATCTGACCCGCTTTAAAGTTAAACCCAAAACACCATCGGGAGCAAAGCACTCTGTGTTTTTCGGCCAGACAAGAGACATTATTGGGCAGATATTTGCAGCAGATGGCATTCGTGGGTTCTACCGAGGTTATGTGGCATCTCTTCTTACATACATCCCCAACAGTGCTGTTTGGTGGCCCTTTTACCACTTCTATGCA
Associated Phenotype:
Not determined
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.
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 |
|---|---|---|---|---|---|
| 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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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