ZMP
mocs3
Ensembl ID:
ZFIN ID:
Description:
Adenylyltransferase and sulfurtransferase MOCS3Adenylyltransferase MOCS3Sulfurtransferase MOCS3 [Sou
Human Orthologue:
MOCS3
Human Description:
molybdenum cofactor synthesis 3 [Source:HGNC Symbol;Acc:15765]
Mouse Orthologue:
Mocs3
Mouse Description:
molybdenum cofactor synthesis 3 Gene [Source:MGI Symbol;Acc:MGI:1916622]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14956 | Nonsense | Available for shipment | Available now |
sa23157 | Essential Splice Site, Missense | Available for shipment | Available now |
sa16784 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14956
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009528 | Nonsense | 114 | 459 | 4 | 13 |
ENSDART00000134111 | Nonsense | 114 | 459 | 4 | 13 |
The following transcripts of ENSDARG00000008239 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 42657641)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 42556381 |
GRCz11 | 17 | 42831787 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATTTGTCGTTGTTAATGTGTATTTAGGACGCTTGGGTTTGTTGGACTA[T/G]GATGTGGTGGAACTGAGWAACCTGCACAGACAGGTGCTTCACACAGAACT
Long Flanking Sequence:
AGTTCTTTTAACCTTTTAATTATCTTTTACATTTTAAATACTTTCATTTTTCATATTTTAAGATATTTGTCTGCTACTGTGCATCACGGTGTATGTAAAAAGCTCTGTATACACATTTTGGACCCGCATAGGTTCATATGCCAATCATAACATCATAAATAAAAAAATAAAAAATAAAAAAAAAACTGCGCTATTGACTTAAGACCAACTTTTCATTGATCAATGGCACAGCAACACAAACAATGTGCCTTAATCTACCTCCTTTTCAGACCTTTTTGTTCAATGGTAGTGTCTAACAATCAAATGATGCATTTAATAAAGATGTGATAGTAGTTCTGTTTAATTTAAAAGAAAAACATATAAAACTAGTTACAAAAAGGTTAACTGTCTAAATGCTTAAAATAGAAGCAATGCAGACTGAATCTGTGGTTTGTGATGCATACAGTGAAACAATTTGTCGTTGTTAATGTGTATTTAGGACGCTTGGGTTTGTTGGACTA[T/G]GATGTGGTGGAACTGAGTAACCTGCACAGACAGGTGCTTCACACAGAACTTACTCAAGGTCAGCCAAAAGCATTGTCTGCCGCTCAGGCCATTAGCAGGTATTGTCTCACTCCCTCGTAAAATATTTTAAAAGGGATAGTTCACTCAATAAAAGAAAATACAGATAATTTACCCTCAGATCATCCAATATGTCTTCTGTAGAACCCTAAAAAAGATTTTTAGCTGAATCAATAGTCCTTTGTGATTCACTATAATAAAGTCAAAATGGGGGCCGCCATTTTAAACAGCGATGCGGTGCTGTGGTGGGAAGAAACCTGGAAGTACGGCATGAGTCACACAGGAATGTTCTGTAAGAGAAAGTGACACAAATTTATAATTTCACCACCTTCAGAGTGACCTGAAGGTCCGTTCTGAACAGAGGTCGCGTTAGACTTTGTCATTGTCCGTTATTTTGACGGAGAGTGTTGTAAAAATTCTGTCATAACCTACCTATTATTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23157
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 > C
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009528 | Essential Splice Site | 172 | 459 | None | 13 |
ENSDART00000134111 | Missense | 173 | 459 | 5 | 13 |
The following transcripts of ENSDARG00000008239 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 42655197)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 42553937 |
GRCz11 | 17 | 42829343 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTATCACCTCCAGCTGTCCAGAGAGAATGCCATACAACTCATCCAACAG[T/C]ATCCACTCTGGTTAATTGCTGATGAGTGTTAATTTACTTTCTACAGTTTT
Long Flanking Sequence:
ATGTTATTTAATGCATAATAAGCTTTTAACTGTTTAAATTAAGCTTAACTTAATCATGTTAAAGTGATGTTTACACCATTTCTGCATTTTGAAATCACAGCAACAGCTGGAGGTTTGTAGTCAACAGCATGTTGTTGCAATGTTTACAGTGCTGATCCTATACTTCCGGTTTTCTTTCCACCGCAGCCTCGCTTTCGTGTTTTAAAATCGCTGTCGTGTGAAATAAGCGTATTGACTTGAGTTAGACAAATCACCAAATGTTATATGAATCACCAAGGCCTACGGATTCAGCTACTGAAAAAAAATCAACATTTTTCATGGCCTGAGTATGACTAAATTAACTAAACTGCTATATATTTTTGGGTGAACTATCTCTTTAAGACACAGGTGAATAGATGAGAGTTGACTAGCTGTTCTCTTCCAGAATGAACTCCACTGTACAGTGTGTTCCCTATCACCTCCAGCTGTCCAGAGAGAATGCCATACAACTCATCCAACAG[T/C]ATCCACTCTGGTTAATTGCTGATGAGTGTTAATTTACTTTCTACAGTTTTGTGTTTAGTGCAAGTTTGACTTCTTTGTCTCCTTGACTGTTCGTCTTATGTATGACATTGTGGCAGACTGTTCAGACAATGTTCCCACACGGTACCTCGTGAATGATGCCTGTGTTCTGACCAGCAGGCCTTTAGTGTCAGCAAGTGCCTTACGAATGGAAGGACAGGTGAGAGATCTCTTCATTATCTTTATCATAGCTGCAGCCAGCGAAATCTCTACTGGCTCTTGCAGGGTTCATTTAAAGTTGTAGATTTAATTTAAGGTCCTAGTAATTTTAAAGTGTCAGATGCTTTAAACACAGTGCAGCACTACTTTTTCATCCAGCGTGCAACCGACATTAGAATAACTAAAGGAGGCAGAAAGGGTGTCATTATTATGATGTATAGATACTGATTACAACAGAATTGTTTGTAACCATTACTGCACTTTACAGGTGAGTAAAGGCACGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16784
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 |
---|---|---|---|---|---|
ENSDART00000009528 | Nonsense | 179 | 459 | 6 | 13 |
ENSDART00000134111 | Nonsense | 179 | 459 | 6 | 13 |
The following transcripts of ENSDARG00000008239 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 42655076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 42553816 |
GRCz11 | 17 | 42829222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTTGTCTCCTTGACTGTTSGTCTTATGTATGACATTGTGGCAGACTG[T/A]TCAGACAATGTTCCCACACGGTACCTCGTGAATGATGCCTGTGTTCTGAC
Long Flanking Sequence:
CAACAGCATGTTGTTGCAATGTTTACAGTGCTGATCCTATACTTCCGGTTTTCTTTCCACCGCAGCCTCGCTTTCGTGTTTTAAAATCGCTGTCGTGTGAAATAAGCGTATTGACTTGAGTTAGACAAATCACCAAATGTTATATGAATCACCAAGGCCTACGGATTCAGCTACTGAAAAAAAATCAACATTTTTCATGGCCTGAGTATGACTAAATTAACTAAACTGCTATATATTTTTGGGTGAACTATCTCTTTAAGACACAGGTGAATAGATGAGAGTTGACTAGCTGTTCTCTTCCAGAATGAACTCCACTGTACAGTGTGTTCCCTATCACCTCCAGCTGTCCAGAGAGAATGCCATACAACTCATCCAACAGTATCCACTCTGGTTAATTGCTGATGAGTGTTAATTTACTTTCTACAGTTTTGTGTTTAGTGCAAGTTTGACTTCTTTGTCTCCTTGACTGTTCGTCTTATGTATGACATTGTGGCAGACTG[T/A]TCAGACAATGTTCCCACACGGTACCTCGTGAATGATGCCTGTGTTCTGACCAGCAGGCCTTTAGTGTCAGCAAGTGCCTTACGAATGGAAGGACAGGTGAGAGATCTCTTCATTATCTTTATCATAGCTGCAGCCAGCGAAATCTCTACTGGCTCTTGCAGGGTTCATTTAAAGTTGTAGATTTAATTTAAGGTCCTAGTAATTTTAAAGTGTCAGATGCTTTAAACACAGTGCAGCACTACTTTTTCATCCAGCGTGCAACCGACATTAGAATAACTAAAGGAGGCAGAAAGGGTGTCATTATTATGATGTATAGATACTGATTACAACAGAATTGTTTGTAACCATTACTGCACTTTACAGGTGAGTAAAGGCACGTGCCTTGAGCAACTGCACGTGTTGAAGTCGAATGAAGCATTGTGAACATGAACTGCTTGTTTTAAAGTTAGTTTTGTGGCTCTGAACTAAAAGCAATTCCAGAGTCCAAACATTGGTAATTT
Associated Phenotype:
Not determined