Busch Lab

ZMP

ftsjd2

Ensembl ID:
ENSDARG00000030830
ZFIN ID:
ZDB-GENE-040426-696
Description:
Cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 1 [Source:UniProtKB/Swiss-Prot;Acc:Q803R5]
Human Orthologue:
FTSJD2
Human Description:
FtsJ methyltransferase domain containing 2 [Source:HGNC Symbol;Acc:21077]
Mouse Orthologue:
Ftsjd2
Mouse Description:
FtsJ methyltransferase domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1921407]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa24383 Essential Splice Site Available for shipment Available now
sa44029 Nonsense Mutation detected in F1 DNA Not yet available
sa32458 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa24383
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049373 Essential Splice Site 390 829 11 24
ENSDART00000142038 None None 192 None 6

The following transcripts of ENSDARG00000030830 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 35434447)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 35284039
GRCz11 23 35382953
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACTGCTCCTGTGTCAATTTCTTACCGCCCTGTCTGTCGTCAGACCAGG[T/C]GATGTGTGTGTGCTTTTGTTTTTGTGTGTACGTATATTTATATATATATA
Long Flanking Sequence:
GAACAGACAATTACAGTTATATCAACAAATTTCTTTTATTTCATTGAAATTTAAAATATGTATTATATAAATGCAGCCTTGGTGAGCTTTTGAGACTTCTTTTGGTCTTAAATTCATAAAATATTCCTTATTATAATGTATTCAGTACATAATATGTTCCTTTTTTTGACTGTCTTATTGCGGGGTGTTTTAGGTGAGGGTGGGATCGATGGCGATGGTGACATCACACGGCCCGAGAACATCAGTGCGTTTCGTAATTTTGTCTTGGACAGCACTGAGGGCCGGGGCCTGCACTTCTTAATGGCGGATGGGGTGAGACATGCTGTTCTGTGATTGGTGCAAATGTAAATATTGCTTTGTGTGATTGGTGGTTGAATATTCTGATGGTGTGTTGCTCCTCAGGGCTTTTCTGTGGAGGGACAAGAAAACCTTCAGGAGATTCTGAGCAAGCAACTGCTCCTGTGTCAATTTCTTACCGCCCTGTCTGTCGTCAGACCAGG[T/C]GATGTGTGTGTGCTTTTGTTTTTGTGTGTACGTATATTTATATATATATATATTATTAATTATTATATATATTATTATTAATAAATTAAGTAGTTTTCAAATTCAATCACTCCCTTATAAGGTAATAAAATATCCTAATTGTTGTTTTAATGAAATGAATATTATTATATTTCAAAAAGCAGAGAATAATGTGTCCTAAGATTCCAGAAGCATTGACTGCATGATGAGGCCTATTAAAATGCAACCTGAATCAACTTTTTGAATCAAACTATTCCAGTCTTGTAAGACTTTTAGCCACATTTTAGCAACAGGAAAAGGCATACACACACAACTGTTTGACACTTTTGCCTGCACCTATCGAGTCAGTAAAGTACCACAGACACATGTCCTCTGAATGCGCACACAAACGGTGAACTACTAGAGACACACTCGTCGTCATCATCATCACCAAACACACATTAAAAAATTAAAAATTTAAAAAAAAATTTATATTCAATTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44029
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049373 Nonsense 450 829 13 24
ENSDART00000142038 None None 192 None 6

The following transcripts of ENSDARG00000030830 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 35425940)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 35275532
GRCz11 23 35374446
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGTACGTGGTGTGCAAGGGTTTAAAACCAGGCACGGATGCCGTCAGA[G/T]AATACATGTTCACCATCAACCTGAAGCTGAATCAGTTCAGACACTCAGAC
Long Flanking Sequence:
TTGTGATTCTTAACTTATTATTTGATTGCAACAATGTGTTGCTTGGATTTTTAATATATAATTTAAGAATAAAATCATCTTATTATAATAATTTAGACATTTTTGTAACACTGTAAATGCTGGTTTCACACAAATCAACTAAGTTCACTTCATTGTTTTTTTTTTTTTTACAAATTTAAGTGTATTAAATATAACATAATTAAGTTGTGCCAAAAAAAAAGAAACTTAGGAATTGTTGTTTCAACTAATTTTAAATAGTAAAAAAAGTTTCTAAAAACATTTTAAATAGTTTGAACAAACAGCAAAAGCCGTGTTTGACTGAATTTTAAAGTTACTTCAATTTAGTTAACTTTCCTGTAATAAAATGGGAAAAGGAAGAAGGATTTTAATCTTAGAAAAAGTACTCCCCTCCATGATAGCAACTGATTTTTTTTATATGTATGTCCACGTGCAGGTACGTGGTGTGCAAGGGTTTAAAACCAGGCACGGATGCCGTCAGA[G/T]AATACATGTTCACCATCAACCTGAAGCTGAATCAGTTCAGACACTCAGACAGAGACGTTATTGAAGTCGTCCCTCTGGACATCATTAAAGGAGACACTGACTTCTTCCAATACATGATCGGCTCCAATGAAAGGTATCATCGTCACTTTCTGATCCTCTTTCTGTCTCTCCCTCCATGCATTCATTCATGCTTAGGTTTGTTTACTGAACTCTGATCTCCTGTCTTGCAGCTATTGTGCGGTTCAGATCAAAGCTCTGGCGAAGATCCACGCGTACGTCAGAGATACGTGAGTCACACATTTTTCCTCTGGTGTGTTTCAGAGCGTTCATTTCATACTCTTTCATTTGAATGCGCGCACGTGTGTGTGGGTCTATAAAGGCATTACTGATGAGGCTGTGTCATTCTAGGACGCTGTTTGAGGCCAGGCAAGCAGACATACGCAAAGAATGCTTGAAATTGTGGGGGGTGAGTCTTAAAATATTTATTTACATGCATGGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32458
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049373 Nonsense 827 829 24 24
ENSDART00000142038 None None 192 None 6

The following transcripts of ENSDARG00000030830 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 35414787)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 35264379
GRCz11 23 35363293
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGACAAGCTCTCCAAAGATGATGTGGTTTCCTTCATCCATAAGCACTA[T/A]CAACAATAACCACACACATGCACACACAAAGTAACAGACTGTTCATTCTC
Long Flanking Sequence:
CGAGCGAGCATGACGTCGACTGAAACTTTCTGTCATATACCACGCCCACCAAAAGGCTACCCTTGGTAGTGGAAACGCAAGCCTGATAAAGGTAACCCGTACCGACCTGAACCATACCGTACTGTACCAGTCAGTGGAAACGAGCCATAACATCATGTTTTGTTTATGGCTGTGTTTTTGTTCAATACTAATTTCCCTTACTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTACATTCATATAAACCCTGCATTCTTTCTTTATTTTGACAATATTTTAGTGTTTTTCGGGCAATGCTTTGACAGTTTGTTCTCTCTGTTCTTCTGCTCCTCAGCGTGTGTCATCAAGACAGGCTGTTTTGGGCTTGGGAGGAAGGCGTCCGAGTTCACGACTCCCAGACGAGGATCAACCCTGACAAGCTCTCCAAAGATGATGTGGTTTCCTTCATCCATAAGCACTA[T/A]CAACAATAACCACACACATGCACACACAAAGTAACAGACTGTTCATTCTCCTGTCCACCAGGAGGCACTGTAGCTTTCAAAACAGTCCAGCATTCTGCTCAGTTTCTACACACTTCAGGGCTTCAGAAATAGACAGCAGTGTGTATCTGCATGTGTCTGGCATTTCTAGAGGAGAAACTTAGATCACACTGCTTTTCGCTTGTTGGTGTGTTTTTCTCCTGAACTTCAACCCCCCTCCACCCCACGCCCCTGATTCCTCGTATGAATTTTTCCTCTGCTAAACCGTTCGATTTTTAGATCCATCCCGTCAGTGCGATAACCGCGTTTAACAAAAGCGCATGGCGGTTAGCATTGGCTCTACTGTGTTGCATGTGTCGCCTTGCGCTCTTCATTTTGGTTTGTATTTCTTTTTTCAGTGTTTACAAATATTAGACTGACTGTTCTGAGGGGAAAACATGTCGATTTTAAGACTATTCGTGATCATGGTTGTATTAAAATCA
Associated Phenotype:
Not determined