ZMP
slc38a4
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 38, member 4 [Source:RefSeq peptide;Acc:NP_001005944]
Human Orthologue:
SLC38A4
Human Description:
solute carrier family 38, member 4 [Source:HGNC Symbol;Acc:14679]
Mouse Orthologue:
Slc38a4
Mouse Description:
solute carrier family 38, member 4 Gene [Source:MGI Symbol;Acc:MGI:1916604]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31368 | Nonsense | Available for shipment | Available now |
sa20170 | Nonsense | Available for shipment | Available now |
sa14136 | Essential Splice Site | Available for shipment | Available now |
sa31369 | Nonsense | Available for shipment | Available now |
sa2147 | Nonsense | F2 line generated | Not yet available |
sa25270 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20171 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31368
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 |
---|---|---|---|---|---|
ENSDART00000031135 | Nonsense | 51 | 310 | 3 | 11 |
ENSDART00000067446 | Nonsense | 63 | 538 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1397964)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 1689596 |
GRCz11 | 4 | 1538909 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAGTTTCTCACCAATGGCTTGATGAAGAAGAAGAAATATGAGGAATA[T/A]AATGAAGAATATGTAAGACTTTACTTCTGAAACACATTCATTATGTTCAT
Long Flanking Sequence:
TAGACGCATTTACATTTACAAAAAAGTCTTAATGTATACATGAAGAATCTCCTTTTATTATTGATTCCAAACTAATAATCTGTGGTTTCGTTTCCAGTAGTTTTCCCCGAGGCATAACCCGAATAAACAGCTGTAAAGATGGAGCGAATGGAGCTGAAGAAAGTGAGCGCAGAGATGGAGGATGAGAGCAGTGTGGACGACAGCTACAGAGAGAACATGGACTCTGAAAAGGCCACAATCAACAGGTCAGAGTCTTTGCACTGTGTGTTTAACCCTGAAGCTGTCTGATACACACACACACACACACAGAACACTGTGACACAGGAATCAGGAGTGTATCTTTAACAGCAAACTAATGTGAGTGTAAAATAACGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTTGTGCTTTACAGCCAGTTCCTGGATGAAGATGATGCAGAGAGTCAGAAGTTTCTCACCAATGGCTTGATGAAGAAGAAGAAATATGAGGAATA[T/A]AATGAAGAATATGTAAGACTTTACTTCTGAAACACATTCATTATGTTCATGACACCCCTCACTCCACCATACCTGATTCTGATTGCTCAATAATGACATTATAATGTATGCTATTCATTGTTTATATATTTCTCAGGTGCTGATCTTTTTATAAACACATTTTTAAGCATACATTTAATAACTAATTTCTAATGTGATGACAGTGCATGATATTTTACTAGCTATTCTGCAAGATACTAGTATTCAGCTGAAAGTGACTTTTAAAGGCTTAACTAGGTCCATCTTTTTGCATGGTTTACACTTAATTAAAGAGCTAGTAAATGATTACAGCTCAGATTAATGTTTTGTGTCTAATAGTTTTTTGTAATAATCAGTATAATGCACATCCAGTCGGTTGTTATCACAGAATAAACCCTTCAGTCCTACATAACAGCCCATGATAAACCTGTCAGGCTTTATTCCTCTAGATCAGCTGTCTGCATGTGCATTATTCCTTGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20170
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 |
---|---|---|---|---|---|
ENSDART00000031135 | None | None | 310 | None | 11 |
ENSDART00000067446 | Nonsense | 197 | 538 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1405664)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 1697296 |
GRCz11 | 4 | 1546609 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATCATTTGTCTGTGTGTGTGCAGTGAATGGTATCTGAATGGGAATTA[T/A]GTGGTGGTGCTGGTGTCCATCGGCATCATTTTACCTCTATCTCTGCTGAA
Long Flanking Sequence:
AGTTGAGGAGTTACCATAGCAACTGTAGAATCACCACGACAGACCAAATACTATAGTCAATGTGTTACAGTAGCAACTGTAGAATTACCACAAAAGATCAATTACTATAGTTGATGTGTTACCGTAGCAACTGTAGAAAGTCCACAATAGATCAAGTACAATAGTCAATGTGTTACCATAGCAAGTGTAGAATCAGCAAAAGATCAGTTACTATGGTCGATGTGTTACAGTATCAACTGTTGAATCACCACAACAGATCAATCACTATAGTTGATGTGTTACAGTAGCAACTGTAGAATCACCACAATAGTACTTTACTATAGTATAGATAAAATATTACTACAGTATTTTTCAGCAATTGTGAGATTGCTTGAACTGTGCGAGAGTTCTGGGTAATGAGTGTTTATGATTAGTGGGATTAATCAAGTCCTAATTATACAGTGTGATGTTCTGATCATTTGTCTGTGTGTGTGCAGTGAATGGTATCTGAATGGGAATTA[T/A]GTGGTGGTGCTGGTGTCCATCGGCATCATTTTACCTCTATCTCTGCTGAAAAACCTGGGTGAGTCCTGCGTTAGAGCAACAGAGAAAGTTTGTGAGGGTGTTTGTGATGTGTCTCTGAATGTTTGCCGTGTCCTACAGGGTATCTGGGCTACACCAGCGGCTTCTCTCTCTCCTGTATGGTCTTCTTCCTGGGAGTGGTACGTTTACTGATGCTGATTCACTTTATTTGCTTCGCTTTTAGTTCTTAAATGCCCTACTACGTGTTTTAAATTTTCTTTTATGTTATTCAGAATTTTTTTAATTATTTTAATCATGAACTGATTTTTTATTTGATGTGTGAGATAATAAAATAAACTAAAATATAGTTTTTATTCATAATTTTTTTAAATTTTAAAAATAATTTTCCAACTAGTATAGTAATGAAACAGCTTGTCTTTTTATTCTATCTGCAATAAACTTACCTGTGAGCAATTGCTGTTATGCATTTGATATATTTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14136
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031135 | Essential Splice Site | 266 | 310 | 9 | 11 |
ENSDART00000067446 | Essential Splice Site | 382 | 538 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1409751)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 1701383 |
GRCz11 | 4 | 1550696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGTTATGTACCTGCTGTCTGCTCTCTTCGGTTATCTGACGTTTTATGG[T/A]ATGTCACACAMATTCNTTCATCGCTTCTTGTGTGTRTTGCCTCTTKKTGAA
Long Flanking Sequence:
TGGCTTGGCTAAATTGTCCATAGCGTATGAGTGCGTATGTGTATGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTCCGTAAAAACTTGTTGGATAAGTTGGTGGTTCATTCCGCTGTGGCGACCCCAGATTAATAAAGGGACTAAGCAGACAAGAAAATGAATGAATGAATAATCTATAATTTTTGGTTTAAAACAGCTCCAGATCCAGCATACAAAAGCAAAGATGCCATTTAGTATATATCAGGAATTTTGTAGCATTAGGCATTAAAACCAACAGCTGCATGACAATATAACCACATCCTTTCACCCCCGACATCTCAGATGTGTGTTAGAGCTGTTAGTGTTGTGTTTGTGACGTGTGTGTGTGTTGTTGTGTTTCAGTCGCTCTCGTCGGAGGATGCAGTCTGTCTCAAACCTCTCCATCTTGGCTATGCTGGTTATGTACCTGCTGTCTGCTCTCTTCGGTTATCTGACGTTTTATGG[T/A]ATGTCACACACATTCTTCATCGCTTCTTGTGTGTGTTGCCTCTTTGTGAATCACTCCTCAATTGTTAGTCGCTTGGGCAAAAGCATCTGCTTAATGTAATGTAGATGTACATGCCATTACACACTGTTGTGGAGCAGAAACACTTACTGTGTGTTTGTGTCTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCAGATCATGTGGAGGCCGAGCTGCTGCACACCTTCACCAAGGTCTACAAGTTCGACACGATGCTGCTGATGGTGCGACTGGCGGTGCTGACGGCCGTGACGCTCACCGTACCTATCGTACTCTTCCCCGTGAGTGACTAAACACACACACACACACATCTGCAGGAAACATGATGCACATCACCCTCCCTCATGCTCATACACCTGAAGTGTGTTCGATGGCATTTTGCTGCTCTTCTACTCATTAATACACTCCTGTAGTGTCTGCAAATGTCCAGCAGATGGTGCAGAACAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31369
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031135 | None | None | 310 | None | 11 |
ENSDART00000067446 | Nonsense | 440 | 538 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1421004)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 1712636 |
GRCz11 | 4 | 1561949 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCGCTCGTCGGTCATCACGCTGTGTTTCGCAGGGAAAGAGTTCAGCTG[G/A]ATTCGACACTTCCTCATCGCCGCTGCTATTCTGGCCTTCAATAATCTGCT
Long Flanking Sequence:
TTCTCTTTTAAAAATTATTTTAAAATAATGACCATCGTGGAAAAAAGTGGTTATAGCATTGAAAATAATGCTGAAAAAATACATGGAAGTCTAAAATTAAAAGTAGCACAGGAATCCAGTGTGTTTGTGTTGAAAATGCTGGAGAAATGACTACGATTGCTCAATTGACTAGATCAGATTGCTTACACGAGCTGGATTCACTGGTCAGATCTGCTAGCAGCACACTGAGACTGACACCTGCTGGTCAAAAGGGATAATGCATAATTAAAATCATCATCTAAAAATAACCAGATCATAATTGTTCGTCTGTGTGGGCACAAATATATTCCTCCTTATCTTTATGGTTATCGTGCTTAGTGTAAATTGGCCTTAAAATGTTCATCAGCCAATCAGAATCAAGCATTCTCAGACGCATAATGTTAATTGTGATATCTCTGTGTGTGTTTTCAGATCCGCTCGTCGGTCATCACGCTGTGTTTCGCAGGGAAAGAGTTCAGCTG[G/A]ATTCGACACTTCCTCATCGCCGCTGCTATTCTGGCCTTCAATAATCTGCTGGTGATCTTCGTGCCCACCATCAGAGACATCTTCGGCTTCATCGGTCAGCAGCTTGTGCTTGTTTGTGCACTTGTGTTTTCATTCTAGAGAGGAGAAGACTTCTAATAATAGTTGTTTCTCCTTCTTTAGGTTCGTCTGCAGCCACAATGCTCATCTTTATCCTGCCAGCGGCTTTTTACCTGCGGCTGGTTAAGAGTTTACCAATGAAGTCTCCTCAAAAAATATCTGTAAGTACTTTTATTTCAGGTTTTGTTATTTTGATTTGTTTTATTTTTTGGTCAAACTGTTAATTACACCCAAAATAAGTTGTGTGCATATTTATGTATAAATATATATGAACATATAAAGTAACACAAAATAAATATACAATAGAAAAACATGTATGTGTGTGTATAAATATAGGTATTCTTTATCTATATGCATACAAATATGAAGATAAATGAACATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2147
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000031135 | None | None | 310 | None | 11 |
ENSDART00000067446 | Nonsense | 465 | 538 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1421077)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 1712709 |
GRCz11 | 4 | 1562022 |
KASP Assay ID:
554-2526.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCTATTCTGGCCTTCAATAATCTGCTGGTGATCTTCGTGCCCACCATC[A/T]GAGACATCTTCGGCTTCATCGGTCAGCAGYTTGTGCTTGTTTGTGCACTT
Long Flanking Sequence:
AAAAAATACATGGAAGTCTAAAATTAAAAGTAGCACAGGAATCCAGTGTGTTTGTGTTGAAAATGCTGGAGAAATGACTACGATTGCTCAATTGACTAGATCAGATTGCTTACACGAGCTGGATTCACTGGTCAGATCTGCTAGCAGCACACTGAGACTGACACCTGCTGGTCAAAAGGGATAATGCATAATTAAAATCATCATCTAAAAATAACCAGATCATAATTGTTCGTCTGTGTGGGCACAAATATATTCCTCCTTATCTTTATGGTTATCGTGCTTAGTGTAAATTGGCCTTAAAATGTTCATCAGCCAATCAGAATCAAGCATTCTCAGACGCATAATGTTAATTGTGATATCTCTGTGTGTGTTTTCAGATCCGCTCGTCGGTCATCACGCTGTGTTTCGCAGGGAAAGAGTTCAGCTGGATTCGACACTTCCTCATCGCCGCTGCTATTCTGGCCTTCAATAATCTGCTGGTGATCTTCGTGCCCACCATC[A/T]GAGACATCTTCGGCTTCATCGGTCAGCAGCTTGTGCTTGTTTGTGCACTTGTGTTTTCATTCTAGAGAGGAGAAGACTTCTAATAATAGTTGTTTCTCCTTCTTTAGGTTCGTCTGCAGCCACAATGCTCATCTTTATCCTGCCAGCGGCTTTTTACCTGCGGCTGGTTAAGAGTTTACCAATGAAGTCTCCTCAAAAAATATCTGTAAGTACTTTTATTTCAGGTTTTGTTATTTTGATTTGTTTTATTTTTTGGTCAAACTGTTAATTACACCCAAAATAAGTTGTGTGCATATTTATGTATAAATATATATGAACATATAAAGTAACACAAAATAAATATACAATAGAAAAACATGTATGTGTGTGTATAAATATAGGTATTCTTTATCTATATGCATACAAATATGAAGATAAATGAACATTTTCTCATATATACAGTACATACAAGTGTGTATTTACCGTATACATACATGATAAATATACACAATGCACACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25270
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031135 | None | None | 310 | None | 11 |
ENSDART00000067446 | Essential Splice Site | 504 | 538 | 15 | 16 |
ENSDART00000031135 | None | None | 310 | None | 11 |
ENSDART00000067446 | Essential Splice Site | 504 | 538 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1421284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 1712916 |
GRCz11 | 4 | 1562229 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGCGGCTGGTTAAGAGTTTACCAATGAAGTCTCCTCAAAAAATATCTG[T/A]AAGTACTTTTATTTCAGGTTTTGTTATTTTGATTTGTTTTATTTTTTGGT
Long Flanking Sequence:
AAAATAACCAGATCATAATTGTTCGTCTGTGTGGGCACAAATATATTCCTCCTTATCTTTATGGTTATCGTGCTTAGTGTAAATTGGCCTTAAAATGTTCATCAGCCAATCAGAATCAAGCATTCTCAGACGCATAATGTTAATTGTGATATCTCTGTGTGTGTTTTCAGATCCGCTCGTCGGTCATCACGCTGTGTTTCGCAGGGAAAGAGTTCAGCTGGATTCGACACTTCCTCATCGCCGCTGCTATTCTGGCCTTCAATAATCTGCTGGTGATCTTCGTGCCCACCATCAGAGACATCTTCGGCTTCATCGGTCAGCAGCTTGTGCTTGTTTGTGCACTTGTGTTTTCATTCTAGAGAGGAGAAGACTTCTAATAATAGTTGTTTCTCCTTCTTTAGGTTCGTCTGCAGCCACAATGCTCATCTTTATCCTGCCAGCGGCTTTTTACCTGCGGCTGGTTAAGAGTTTACCAATGAAGTCTCCTCAAAAAATATCTG[T/A]AAGTACTTTTATTTCAGGTTTTGTTATTTTGATTTGTTTTATTTTTTGGTCAAACTGTTAATTACACCCAAAATAAGTTGTGTGCATATTTATGTATAAATATATATGAACATATAAAGTAACACAAAATAAATATACAATAGAAAAACATGTATGTGTGTGTATAAATATAGGTATTCTTTATCTATATGCATACAAATATGAAGATAAATGAACATTTTCTCATATATACAGTACATACAAGTGTGTATTTACCGTATACATACATGATAAATATACACAATGCACACATTTATTATGTAAATACAAACTTCTTTTTTGGATGTGACTTAATTATTTGTCTGCACATGCATTGTTTAGTGCTGGGTAATTGCATCCAGATATATAAATATATTTATTATGTATGCGTGATTCACACACATACAAAACAGTTTTTGTTAGACACGTATTTAAATTAATATCTAATTTGTATCATATATATATATATATATATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20171
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031135 | None | None | 310 | None | 11 |
ENSDART00000067446 | Essential Splice Site | 504 | 538 | 15 | 16 |
ENSDART00000031135 | None | None | 310 | None | 11 |
ENSDART00000067446 | Essential Splice Site | 504 | 538 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1421284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 1712916 |
GRCz11 | 4 | 1562229 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGCGGCTGGTTAAGAGTTTACCAATGAAGTCTCCTCAAAAAATATCTG[T/A]AAGTACTTTTATTTCAGGTTTTGTTATTTTGATTTGTTTTATTTTTTGGT
Long Flanking Sequence:
AAAATAACCAGATCATAATTGTTCGTCTGTGTGGGCACAAATATATTCCTCCTTATCTTTATGGTTATCGTGCTTAGTGTAAATTGGCCTTAAAATGTTCATCAGCCAATCAGAATCAAGCATTCTCAGACGCATAATGTTAATTGTGATATCTCTGTGTGTGTTTTCAGATCCGCTCGTCGGTCATCACGCTGTGTTTCGCAGGGAAAGAGTTCAGCTGGATTCGACACTTCCTCATCGCCGCTGCTATTCTGGCCTTCAATAATCTGCTGGTGATCTTCGTGCCCACCATCAGAGACATCTTCGGCTTCATCGGTCAGCAGCTTGTGCTTGTTTGTGCACTTGTGTTTTCATTCTAGAGAGGAGAAGACTTCTAATAATAGTTGTTTCTCCTTCTTTAGGTTCGTCTGCAGCCACAATGCTCATCTTTATCCTGCCAGCGGCTTTTTACCTGCGGCTGGTTAAGAGTTTACCAATGAAGTCTCCTCAAAAAATATCTG[T/A]AAGTACTTTTATTTCAGGTTTTGTTATTTTGATTTGTTTTATTTTTTGGTCAAACTGTTAATTACACCCAAAATAAGTTGTGTGCATATTTATGTATAAATATATATGAACATATAAAGTAACACAAAATAAATATACAATAGAAAAACATGTATGTGTGTGTATAAATATAGGTATTCTTTATCTATATGCATACAAATATGAAGATAAATGAACATTTTCTCATATATACAGTACATACAAGTGTGTATTTACCGTATACATACATGATAAATATACACAATGCACACATTTATTATGTAAATACAAACTTCTTTTTTGGATGTGACTTAATTATTTGTCTGCACATGCATTGTTTAGTGCTGGGTAATTGCATCCAGATATATAAATATATTTATTATGTATGCGTGATTCACACACATACAAAACAGTTTTTGTTAGACACGTATTTAAATTAATATCTAATTTGTATCATATATATATATATATATATATATATA
Associated Phenotype:
Not determined