Busch Lab

ZMP

slc36a1

Ensembl ID:
ENSDARG00000075618
ZFIN ID:
ZDB-GENE-061117-1
Human Orthologues:
SLC36A1, SLC36A2, SLC36A3
Human Descriptions:
solute carrier family 36 (proton/amino acid symporter), member 1 [Source:HGNC Symbol;Acc:18761]
solute carrier family 36 (proton/amino acid symporter), member 2 [Source:HGNC Symbol;Acc:18762]
solute carrier family 36 (proton/amino acid symporter), member 3 [Source:HGNC Symbol;Acc:19659]
Mouse Orthologues:
Slc36a1, Slc36a2, Slc36a3
Mouse Descriptions:
solute carrier family 36 (proton/amino acid symporter), member 1 Gene [Source:MGI Symbol;Acc:MGI:244
solute carrier family 36 (proton/amino acid symporter), member 2 Gene [Source:MGI Symbol;Acc:MGI:189
solute carrier family 36 (proton/amino acid symporter), member 3 Gene [Source:MGI Symbol;Acc:MGI:266

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa45517 Nonsense Mutation detected in F1 DNA Not yet available
sa24957 Nonsense Mutation detected in F1 DNA Not yet available
sa35693 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa45517
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115133 Nonsense 32 468 2 11
Genomic Location (Zv9):
Chromosome 14 (position 27004154)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 25697356
GRCz11 14 25994601
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAGACGAGAGCCCGACTGAAGACGAGCCCATCCATTCGCCTGGTTCA[C/T]GACAAACAGAATATGAACGAATCGGGGGAAGAACTGGATCCTCGTAAGCA
Long Flanking Sequence:
AACAATCAACAAAGCAGATCAAAGTAAGGTTTAAGGGAAAAAAAAAACAGAAAAATAAAGAAAATAAAGGATTGATGGCTGGCAGTGAGGTTTCCCCTAATTAGTAATTAGGCTAGTTATTGTATAATGATGGTTTGTTCTGTAGACTATAAAAATAGATTAAAGGGGCTAATAATTTTGACCTTTAAATGGTGTTTAAAAAAATAAAAGCTGCCTTTATTCTAGCTGAAATAAAGCAAATAATTCTTTCCCCAGAAAACAAATATTATCAGACATACTGTGAACATTTCCTTGCTGTTAAACATCATTAAGGAAATCATTTAAAAAGAAAAAATTCAAAGGGGGGGCTAATAATTATGACTTTAACTGTTTGTATATTTATTTACTTTTTTATAAAAGTGATGTGAAAGCCATATTTGTGTGTTGGTTGTATAGGCCCAGACTTTTCTAGAAGAGACGAGAGCCCGACTGAAGACGAGCCCATCCATTCGCCTGGTTCA[C/T]GACAAACAGAATATGAACGAATCGGGGGAAGAACTGGATCCTCGTAAGCACTGTGATCTTCACCTATTAAAACTTTTCTCTTCCTAAATACCTGTTTTGATTTTTGGGGGATTTTCTCAGTGTTTTACAGACCATCATTCATTTACTAAAAGGTAATATTGGCACAGGGCTGCTCGGTTTGCCTCTGGCTGTCAGGAACGCAGGACTCCTGGTAAGATGGAAAATTGAATTTGGAAATAAATGCCTGGTGTTGTCTTTTTTATTTTCAACTCCTCCGCTCTTGAACTCTGGTTATCTTCTATAATTGCTAGCTGGATAATTGCTGAGCTTTAGATGATCATGATTTTCTTATGTCAAACACCATGTCAGCTTTACGTTTTCTATTCTCTCTTGTTTCCTCTAAGTATTATGGTAATGTAATGTGTGTTAGCCTGCTTTTTAGAGAACAGTTCAAATGTTTCTTTTTAACTTTAATACATTAAACAAAAGTGAAATTAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24957
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115133 Nonsense 54 468 3 11
Genomic Location (Zv9):
Chromosome 14 (position 27004298)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 25697500
GRCz11 14 25994745
KASP Assay ID:
554-7678.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTGATTTTTGGGGGATTTTCTCAGTGTTTTACAGACCATCATTCATT[T/A]ACTAAAAGGTAATATTGGCACAGGGCTGCTCGGTTTGCCTCTGGCTGTCA
Long Flanking Sequence:
GACTATAAAAATAGATTAAAGGGGCTAATAATTTTGACCTTTAAATGGTGTTTAAAAAAATAAAAGCTGCCTTTATTCTAGCTGAAATAAAGCAAATAATTCTTTCCCCAGAAAACAAATATTATCAGACATACTGTGAACATTTCCTTGCTGTTAAACATCATTAAGGAAATCATTTAAAAAGAAAAAATTCAAAGGGGGGGCTAATAATTATGACTTTAACTGTTTGTATATTTATTTACTTTTTTATAAAAGTGATGTGAAAGCCATATTTGTGTGTTGGTTGTATAGGCCCAGACTTTTCTAGAAGAGACGAGAGCCCGACTGAAGACGAGCCCATCCATTCGCCTGGTTCACGACAAACAGAATATGAACGAATCGGGGGAAGAACTGGATCCTCGTAAGCACTGTGATCTTCACCTATTAAAACTTTTCTCTTCCTAAATACCTGTTTTGATTTTTGGGGGATTTTCTCAGTGTTTTACAGACCATCATTCATT[T/A]ACTAAAAGGTAATATTGGCACAGGGCTGCTCGGTTTGCCTCTGGCTGTCAGGAACGCAGGACTCCTGGTAAGATGGAAAATTGAATTTGGAAATAAATGCCTGGTGTTGTCTTTTTTATTTTCAACTCCTCCGCTCTTGAACTCTGGTTATCTTCTATAATTGCTAGCTGGATAATTGCTGAGCTTTAGATGATCATGATTTTCTTATGTCAAACACCATGTCAGCTTTACGTTTTCTATTCTCTCTTGTTTCCTCTAAGTATTATGGTAATGTAATGTGTGTTAGCCTGCTTTTTAGAGAACAGTTCAAATGTTTCTTTTTAACTTTAATACATTAAACAAAAGTGAAATTAAAATATAAGTAGCTAAAAAATTTTACCTTAGAACTAAAACAAACAAAAGTAAAATAAAACCAATTTAAAATGATCTAAAACCATAGCATATTGATATTCAAAGCGGACTTGCACTATTAATACAAGTTAAAATAGTTACCCAGTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35693
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115133 Nonsense 343 468 10 11
Genomic Location (Zv9):
Chromosome 14 (position 27021537)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 25714739
GRCz11 14 26011984
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATATCAGATTGTGAAGCTGCTTTACTCTTTTGGTATCTACATCACCTA[C/A]GCGCTGCAGTTTTACGTGTCAGCAGAAATCCTGATCCCGCCAGCGGTGGC
Long Flanking Sequence:
GATATTTTAGAAAGTTTTAAGATTTAGGGTTTGTTTGTATCAGTCATATACTGTAGAGATGAAGCAGTTTGAATGAGTCAGTGCCCTGACAACAACAAAAAAGCTGACCCACAAACTACTTTGAAAGTGGGAACAGGCCCAAATCCAGCCATTAGAGTTTGTCAGCAGGGACCAGTGATGTGGAATGAGAAGCTGTGGGCTCCATGCACAATCACAGAGGTGTCAGTCTTCTGCTGCTGTTAACGGCAGTGCAGTGATTGATGTGTCACTACAGAGACCAAAACGCTCTTTCAAGAGCATTCGTGATTATTACAGATATCAGTGATACCTCTGTGATACTTTTATTTGTAATCTATTCCTTTTATGCTTCTCATTTTCTTTACCTTTATGATTTTGACATCAATAGCTTGAGAAATAAGAAAGGTATGCGATGTCTGTCTGTTCTGCAGGTTATATCAGATTGTGAAGCTGCTTTACTCTTTTGGTATCTACATCACCTA[C/A]GCGCTGCAGTTTTACGTGTCAGCAGAAATCCTGATCCCGCCAGCGGTGGCGCGATGTGGTCCCAGATGGGCATTGATGGTAGACCTCAGCATCCGCGTGGCTCTTGTAGGCCTCACATGTGAGTCGAACTACAGCAAATACAAAACTAAAGCTTTTTTCACACACACAATCAAATTTAGTGTTCTACATTTGCATACCTGTGTCCACAGGGGGGTGTTATCCCTTATTTTTACATCTCAATGTTGACAGGTATGGAATAGATTAGTTTAGCCTATTAAAACTAATACCAGATATTGAACCCAATTATCAAGTTTCATTCACTTTTTCATTACTTTATAATATAAATATAAACCTACACTGATTCTGATTAAAATTACCATAGTTATTTAATGAAGAGCTGGGAATAAATCCCTTATTTTTATATTTTCTTTAAAAAAAAATTATTAACATTGAGTAACACAGGTGTCACTTTAAGACCTTCAGATCTATAATGACAAGCA
Associated Phenotype:
Not determined