ZMP
si:dkey-83k24.4
Ensembl ID:
ZFIN IDs:
Description:
UDP-galactose translocator [Source:RefSeq peptide;Acc:NP_001123545]
Human Orthologue:
SLC35A2
Human Description:
solute carrier family 35 (UDP-galactose transporter), member A2 [Source:HGNC Symbol;Acc:11022]
Mouse Orthologue:
Slc35a2
Mouse Description:
solute carrier family 35 (UDP-galactose transporter), member A2 Gene [Source:MGI Symbol;Acc:MGI:1345
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15127 | Nonsense | Available for shipment | Available now |
sa34305 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18618 | Nonsense | Available for shipment | Available now |
sa16989 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15127
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 |
---|---|---|---|---|---|
ENSDART00000081983 | Nonsense | 79 | 395 | 2 | 6 |
ENSDART00000131215 | Nonsense | 79 | 374 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 8 (position 9498923)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 8915505 |
GRCz11 | 8 | 8954090 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACACCACATCGGCTGTGGTGATGGCAGAAGTTCTTAAAGTCATCACCTG[T/A]CTGTTCATCATCCTKATACARAAGAGAGGTGCGTTCACTAGACACTMCAC
Long Flanking Sequence:
GTGCAAAAAAACCTTGTGCAAGTGTCAGTTAAAGTGTCAGAGAGATGAAAGAGTGTGTTTTCTACAGGTGGTTTGTCAAGCCCACTCACCTGTGTGGCACACTCAGAATTGATAATGTTTTCGTGTATTGTAGTTGTGGTGAGAGAAGACAGGGTCCTGGTTTTGTTTACAGGTGTTCAGGTGATGGCATAAGGGATTGGTATACATAAACTGTCGCTGTAATTCTGACGTCAGTTTTTTAGATCAGTAAATTCACCATCCTTCTATTACATTTTCACACTTTTAACAAAAGAAAAGAAGCCACTCTTTGTTGACTGAAATGTTTTCATATGTGTGTTTCTTGCAGTCAACAAGAAGCTGAAGTACACCAGTCTGGCAATTCTGGTGATCCAGAATGCGTCGCTCATCCTCAGTATCCGCTATGTGCGGACGCTTCCGGGTGATCATTTCTACACCACATCGGCTGTGGTGATGGCAGAAGTTCTTAAAGTCATCACCTG[T/A]CTGTTCATCATCCTTATACAGAAGAGAGGTGCGTTCACTAGACACTACACAGCCTGTCACGTTTACACTGAGCATTAAAAGGAATAGATGTATACTGGATTGTTTTAGGACTTCTGACATGGTGAGATGAGCAATGATGATGTTGAGTTTTGCAATTAAAAAATGTTATAATTTCTCTAGAGAAATTCTATTTTTATTAGCCCTTTTTAAATAAAATAATTAATACAATGAATAAAATACTCAAATAAATGTGTAATATACATTTATCTAATTTAATTATATCTTATATAAGTCAAGGATCAGTAATATCATACAAGTGATGTTTTTAATTTGTGTGTGTGTGTAAATGCAGGTAATGTGAAGAGCTTCGTGTCGTTGTTGTATGACTCTATAGTCATACAGTATTGGGACACGCTGAAGTTAGCAGTTCCTTCACTCATCTACACTTTACAGAACAACCTGCAGTATGTGGCCATTTCCAATTTACCAGCAGCCACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34305
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081983 | Nonsense | 183 | 395 | 4 | 6 |
ENSDART00000131215 | Nonsense | 183 | 374 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 8 (position 9501934)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 8918516 |
GRCz11 | 8 | 8957101 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATCTCTCTGGTGCTGCTGTTCGCCGGTGTGGCCATCGTCCAGGTGGAG[C/T]AAGAGAGCGGCAAGCAGAAGGAGGCCGTGACTGCGGCCAACCAGAACTAC
Long Flanking Sequence:
GTTATTAGAAATTAGTTATTAAAACTATTATGTTTAGAAATGTGCTTAATAAATCTTTTCTTTGTAAAACAGAAATTGGTGATAAAAAAACTTAGGGAGGGGGGGGTTCTAATAATGACTGCAACTGTATACATTTCACTTTATGCTTTAACATATTTTTATTTATATTATCATTTATTTTAGCACTTAAAATTATTTCAATTTGTTTTTCCAAAGCTAAAAAGAGATTCATAATTTTTTTTTAACATGACATTTGGATCTTTTAAAATCTAAATTTAGATTAAGACAATATTTATCATGAAAGAAGCAGGTTAAGTTTGGTAAAAATGAAAAGATTGCAGTGACGTGTATTTTGATGACTTCCCCTGCAGGTCACATATCAGCTGAAGATCTTGACCACGGCTCTGTTTTCAGTGCTGATGCTGCGGAAGAGTCTGTCCAGGATCCAGTGGATCTCTCTGGTGCTGCTGTTCGCCGGTGTGGCCATCGTCCAGGTGGAG[C/T]AAGAGAGCGGCAAGCAGAAGGAGGCCGTGACTGCGGCCAACCAGAACTACTTCAAGGGTCTGCTGTCCGTCATCATCTCCTGCCTCTCCTCGGGCTTCGCCGGCGTCTACTTCGAGAAGATCCTGAAGGGCAGCTCGGCGTCAGTGTGGATGAGGAACATCCAGCTCGGGATCTTCGGGACTGTTTTGGGTCTGCTCGGCATGTGGTGGAACGACGGCGCCGCCATCGCTGAAAAAGGCTTTTTGTTTGGATACACACCAATGGTGTGGGGTGTCATTTTCAATCAAGCGTTCGGCGGCCTCCTGGTGGCCGTTGTGGTGAAGTACGCGGACAACATCCTCAAAGGCTTCGCCACTTCTTTTTCCATCATCGTGTCCACCATCACATCCGTCTACCTCTTCGGCTTCCACGTGGACCTGGTCTTCACGCTGGGCGCAGGATTGGTCATAGGAGCCGTCTATATGTACAGTCTCCCCAAAGCGAACACCAGCACTTCCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18618
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081983 | Nonsense | 199 | 395 | 4 | 6 |
ENSDART00000131215 | Nonsense | 199 | 374 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 8 (position 9501984)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 8918566 |
GRCz11 | 8 | 8957151 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGAGAGCGGCAAGCAGAAGGAGGCCGTGACTGCGGCCAACCAGAACTA[C/A]TTCAAGGGTCTGCTGTCCGTCATCATCTCCTGCCTCTCCTCGGGCTTCGC
Long Flanking Sequence:
AAATCTTTTCTTTGTAAAACAGAAATTGGTGATAAAAAAACTTAGGGAGGGGGGGGTTCTAATAATGACTGCAACTGTATACATTTCACTTTATGCTTTAACATATTTTTATTTATATTATCATTTATTTTAGCACTTAAAATTATTTCAATTTGTTTTTCCAAAGCTAAAAAGAGATTCATAATTTTTTTTTAACATGACATTTGGATCTTTTAAAATCTAAATTTAGATTAAGACAATATTTATCATGAAAGAAGCAGGTTAAGTTTGGTAAAAATGAAAAGATTGCAGTGACGTGTATTTTGATGACTTCCCCTGCAGGTCACATATCAGCTGAAGATCTTGACCACGGCTCTGTTTTCAGTGCTGATGCTGCGGAAGAGTCTGTCCAGGATCCAGTGGATCTCTCTGGTGCTGCTGTTCGCCGGTGTGGCCATCGTCCAGGTGGAGCAAGAGAGCGGCAAGCAGAAGGAGGCCGTGACTGCGGCCAACCAGAACTA[C/A]TTCAAGGGTCTGCTGTCCGTCATCATCTCCTGCCTCTCCTCGGGCTTCGCCGGCGTCTACTTCGAGAAGATCCTGAAGGGCAGCTCGGCGTCAGTGTGGATGAGGAACATCCAGCTCGGGATCTTCGGGACTGTTTTGGGTCTGCTCGGCATGTGGTGGAACGACGGCGCCGCCATCGCTGAAAAAGGCTTTTTGTTTGGATACACACCAATGGTGTGGGGTGTCATTTTCAATCAAGCGTTCGGCGGCCTCCTGGTGGCCGTTGTGGTGAAGTACGCGGACAACATCCTCAAAGGCTTCGCCACTTCTTTTTCCATCATCGTGTCCACCATCACATCCGTCTACCTCTTCGGCTTCCACGTGGACCTGGTCTTCACGCTGGGCGCAGGATTGGTCATAGGAGCCGTCTATATGTACAGTCTCCCCAAAGCGAACACCAGCACTTCCAGCACAAGCACGGCTTCATCCAGCAAAGCAGGAGAATCGGAGCTGGATGCGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16989
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081983 | Nonsense | 221 | 395 | 4 | 6 |
ENSDART00000131215 | Nonsense | 221 | 374 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 8 (position 9502048)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 8918630 |
GRCz11 | 8 | 8957215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCCGTCATCATCTCCTGCCTCTCCTCGGGCTTCGCCGGCGTCTACTTC[G/T]ARAAGATCCTKAAGGGCAGCTCGGCGTCAGTGTGGATGAGGAACATCCAG
Long Flanking Sequence:
ATGACTGCAACTGTATACATTTCACTTTATGCTTTAACATATTTTTATTTATATTATCATTTATTTTAGCACTTAAAATTATTTCAATTTGTTTTTCCAAAGCTAAAAAGAGATTCATAATTTTTTTTTAACATGACATTTGGATCTTTTAAAATCTAAATTTAGATTAAGACAATATTTATCATGAAAGAAGCAGGTTAAGTTTGGTAAAAATGAAAAGATTGCAGTGACGTGTATTTTGATGACTTCCCCTGCAGGTCACATATCAGCTGAAGATCTTGACCACGGCTCTGTTTTCAGTGCTGATGCTGCGGAAGAGTCTGTCCAGGATCCAGTGGATCTCTCTGGTGCTGCTGTTCGCCGGTGTGGCCATCGTCCAGGTGGAGCAAGAGAGCGGCAAGCAGAAGGAGGCCGTGACTGCGGCCAACCAGAACTACTTCAAGGGTCTGCTGTCCGTCATCATCTCCTGCCTCTCCTCGGGCTTCGCCGGCGTCTACTTC[G/T]AGAAGATCCTGAAGGGCAGCTCGGCGTCAGTGTGGATGAGGAACATCCAGCTCGGGATCTTCGGGACTGTTTTGGGTCTGCTCGGCATGTGGTGGAACGACGGCGCCGCCATCGCTGAAAAAGGCTTTTTGTTTGGATACACACCAATGGTGTGGGGTGTCATTTTCAATCAAGCGTTCGGCGGCCTCCTGGTGGCCGTTGTGGTGAAGTACGCGGACAACATCCTCAAAGGCTTCGCCACTTCTTTTTCCATCATCGTGTCCACCATCACATCCGTCTACCTCTTCGGCTTCCACGTGGACCTGGTCTTCACGCTGGGCGCAGGATTGGTCATAGGAGCCGTCTATATGTACAGTCTCCCCAAAGCGAACACCAGCACTTCCAGCACAAGCACGGCTTCATCCAGCAAAGCAGGAGAATCGGAGCTGGATGCGTTCCTCCCAAAGTCAGTCCTGGTGAAATGAGCCAACTAAAAGTGTCTTCTCTGTGTCCCCTTTCAT
Associated Phenotype:
Not determined