ZMP
slc35d1a
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1
Human Orthologue:
SLC35D1
Human Description:
solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1
Mouse Orthologue:
Slc35d1
Mouse Description:
solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6070 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40729 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6070
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 |
|---|---|---|---|---|---|
| ENSDART00000073957 | Nonsense | 3 | 336 | 1 | 12 |
The following transcripts of ENSDARG00000011973 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 34964359)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 34877169 |
| GRCz11 | 6 | 34860552 |
KASP Assay ID:
554-3687.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGAGGCGTCAACGTGGGGAGGAAGAAAGGCGCTGCGTTCGGAATGAAG[C/T]AATGTGAGGCGAGGAATGAAGCGGCAGGGATGGCGGACCAGACGCTAACG
Long Flanking Sequence:
TAATTTAGGGGGGGGGCTAATAATTCTGACTTCAACTATATATATTTGACTATTGTACTGTTCCTTGTGTGAGGTGGTGGATATTTTAATTTATACTATTACATATCACATAACATTACATTATTATAATGAGATTATATTTTAGTGTATATTAAATAACATTTAGTTATGTAAAATATATATAAATGATGTTATATATAGTTTATTCGTATAATTTACTTCTAGATATTTATTGGGGGCCCCCAGATTTCCTGGGGCCCTACGCGGCCGCTTACCTCGCTTATTGGTTAAATCCGCCCCTGACTGTACATACCTGAAAGGGGCTTTGACTATGTTGTCGTGTTGTACTTTACAGTCAGCTGCCCCCAGGTGGCGACAGAGAGCAACGTACTGTTGGATGTAAATGAGACGGCACGTCACCGCATACGTCTCTGTAAACATGGCGGAAGTTCAGAGGCGTCAACGTGGGGAGGAAGAAAGGCGCTGCGTTCGGAATGAAG[C/T]AATGTGAGGCGAGGAATGAAGCGGCAGGGATGGCGGACCAGACGCTAACGGTACTCCTTAAACTCTCAGCTGCGGGCTTTTACGGAATCAGCTCGTTCCTCATAGTTGTAGTCAACAAAAGCGTCCTGACTAATTACAGGTAAGAAGACTTTTGGCTAGAGTTAAATACTCGGTGTATTTCAGGAGCTGGACTGGCTTTACATCCAGAGTACTTGGAATAGTTGGCAACTTTAGTGATTACAGCAGTATCAGTGATGCAGAAAGACACATCCGGGTCTGAGTTTTTCCCAAACCAAAATATAAGATGTTATTAGATTGTTTTAAGAGATATATCTTGATAATATAATGTTTATTTTGTAAACTTCAGTTATATCATTGTAATGCAACAATATTACCTGTAAGTTAGACTTTTGAGTGTCTTTTCTGTACTCTACTGTACCTGTATCTAACTGGCATGATGGTCAAAGAAGAAAAGGAGTTCAAAAACAGTTTTTTTGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40729
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 |
|---|---|---|---|---|---|
| ENSDART00000073957 | Nonsense | 239 | 336 | 9 | 12 |
The following transcripts of ENSDARG00000011973 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 34970533)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 34870995 |
| GRCz11 | 6 | 34854378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTTAGGCCTTTGATTATGATGGCTGGTCCGATGTTTTGTTTATAAGT[C/T]AATTCTTTCTCTCTTGTATAATGGGGTAAGTATAATATATTTTGTCAAAT
Long Flanking Sequence:
AAGGCTCAGTTGTTGGGGAAGGTTAGGATGACAGGGCCCTGCTCCATGAATGCCTCATTTTATTTAGCTCAGTGTGTTCACAGGGAGGCCCTGGTTTATTTGGCAGGCACTGCTTCAGGAAGGAGAGTGGACAGGAGGCAGTGTGTCTCGCGCACAAAGCTGCCATTTATACCAGTCAGCATAACTAGCAGATTGAGTTTTGTAGCTTATAGTGTTGTTCTTTAGGTGTGTTCATCTTAGACGAGGTCTTTTTTTATTGATAGGCTGAGTGGAATTAAAAAAAAATACATTTTTGTGGTTTTTACTTTAATGACTTGGAAGAATGTGAATGATGTGGAATGTATGAAATGTTACCAGAGCTAAGACTTGAGCTAGATATTTTCTTACAAACAACTCCATAGCTCTAAAATGTAATGATTAACTAAGGTAATTGCTTTGTTTTTGTTTTTTTCCTTTAGGCCTTTGATTATGATGGCTGGTCCGATGTTTTGTTTATAAGT[C/T]AATTCTTTCTCTCTTGTATAATGGGGTAAGTATAATATATTTTGTCAAATAAATACTGGTTGTGTCAAAGTTAATGTGTTGAAGTGGGGTTTAAATGTTAGTGGTTTGTAATTTTTAGTAGTTTGTGAAAATATTTTTCTTACAGATGTCAGTTAATGGCCATAAAGAGTGATCGAATTAGTCTTTTATTGTTTTATTGGGGAAGTACTTGGAGCTTTCCATTAGGCTATATACTTTACCTGAATGACTGACTAATTGTTAACAAGCTTATAAATGTTCATGATTTACATGTTTCTCTTGTGTAATGATACAAAGGAAAATGTGTCATGGCGTTTATCATCATTCAGCTTTTTCTTTTTTTTTGCTTTCACACTCTAGTTATTTAAATGGGATGTTACTCTGTGCATTTAGGAGTATTCGGTAACACTTTATAATAACTACACACTATGAATCATTACTACATTAATAAATGTTAGTAATGTAATGTGTATTTATATAGA
Associated Phenotype:
Not determined