ZMP

si:ch211-105d11.3

Ensembl ID:

ENSDARG00000070553

ZFIN ID:

ZDB-GENE-041008-25

Description:

mRNA cap guanine-N7 methyltransferase [Source:UniProtKB/Swiss-Prot;Acc:Q1MTD3]

Human Orthologue:

RNMT

Human Description:

RNA (guanine-7-) methyltransferase [Source:HGNC Symbol;Acc:10075]

Mouse Orthologue:

Rnmt

Mouse Description:

RNA (guanine-7-) methyltransferase Gene [Source:MGI Symbol;Acc:MGI:1915147]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44910	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa23481	Nonsense	Available for shipment	Available now
sa5919	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44910

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000088917	Essential Splice Site	109	400	3	11
ENSDART00000103675	Essential Splice Site	109	400	3	12

Genomic Location (Zv9):

Chromosome 19 (position 13277540)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	12735886
GRCz11	19	12655414

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATAGTCTACATGCGCAATTTCAACAACTGGTTGAAGAGTGTGCTTATTGG[T/A]GAGAAGAAGCGCTTGCTTATGTTTAACTCCCAAAACAAGCATGTTTAATT

Long Flanking Sequence:

CGATGGACCATTTTCACAAGAATTTTATGACGCAAATAACGGTCATCAGCATCCTGACAGCATCATCTTGGTCAGAAAGAACCGTCTCATTTGCATTTAAAGGCACACGCACAAAACGGCTCAAATTTGCTCTGACCCAAAAATGGACATTTTCAGTCGTGTATAATGCATAAGCTGGTGGATATTTTGAGCGGAAACCTTTCAGATACTTTCTGGAGACACCAAAAACGTATTTTACATCTTGTTGAAAGAAGCAAAAGAGTACCCCTTTACCTCTGTTTTCTGTTATTTCATGGCAATACAATACAACACAAACTACAAGATTATAAATGTACATCATTATTACACTTTGTTTTGCAGGTCACAGAAGATTCATTACACAGTCAAAAGGTGGCCACACATTACAACAAAATTAAGGAGTGTGGTCTGGCAGAACGAAATAAAAGCAGGATAGTCTACATGCGCAATTTCAACAACTGGTTGAAGAGTGTGCTTATTGG[T/A]GAGAAGAAGCGCTTGCTTATGTTTAACTCCCAAAACAAGCATGTTTAATTTGTGCTCTTATTTGGTGCTCAAGAGCCATGCTGAGGTCTCTCTGTGTTGGTTTTCTCAGCTGAGATCTTGGACAAGGTCAGGCAAAAACGAAGAGAGGTGACTGTACTGGATCTGGGCTGTGGAAAAGGAGGAGACCTTCTGAAATGGAAGAAAGGGCGTATTGATAAACTGGTCTGTGCAGGTAAATACAAAAAATCCTGTTGAAATTTTTATTTGTGCCTAGATTTATAACTTTGTCTTGTTTAAAGCATTTTAAACATTTTTATTCTTCCATCGGTCGATGAGGTAGTTTCCTGGTCCTGTCCCCAACTTTTCTTTCCTGTTAATTCTTGTCATCTCTAATGTTTTGGGCCAGTAAAGCCATCAAGTTTGAAATATTTTATCCTATAATAAAGTATACTTCTGACACACAAATAAGTAAATTTATCAATTGTTGAAATTCATTAATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23481

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000088917	Nonsense	119	400	4	11
ENSDART00000103675	Nonsense	119	400	4	12

Genomic Location (Zv9):

Chromosome 19 (position 13277679)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	12736025
GRCz11	19	12655553

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTCTGTGTTGGTTTTCTCAGCTGAGATCTTGGACAAGGTCAGGCAAAAA[C/T]GAAGAGAGGTGACTGTACTGGATCTGGGCTGTGGAAAAGGAGGAGACCTT

Long Flanking Sequence:

AAAATGGACATTTTCAGTCGTGTATAATGCATAAGCTGGTGGATATTTTGAGCGGAAACCTTTCAGATACTTTCTGGAGACACCAAAAACGTATTTTACATCTTGTTGAAAGAAGCAAAAGAGTACCCCTTTACCTCTGTTTTCTGTTATTTCATGGCAATACAATACAACACAAACTACAAGATTATAAATGTACATCATTATTACACTTTGTTTTGCAGGTCACAGAAGATTCATTACACAGTCAAAAGGTGGCCACACATTACAACAAAATTAAGGAGTGTGGTCTGGCAGAACGAAATAAAAGCAGGATAGTCTACATGCGCAATTTCAACAACTGGTTGAAGAGTGTGCTTATTGGTGAGAAGAAGCGCTTGCTTATGTTTAACTCCCAAAACAAGCATGTTTAATTTGTGCTCTTATTTGGTGCTCAAGAGCCATGCTGAGGTCTCTCTGTGTTGGTTTTCTCAGCTGAGATCTTGGACAAGGTCAGGCAAAAA[C/T]GAAGAGAGGTGACTGTACTGGATCTGGGCTGTGGAAAAGGAGGAGACCTTCTGAAATGGAAGAAAGGGCGTATTGATAAACTGGTCTGTGCAGGTAAATACAAAAAATCCTGTTGAAATTTTTATTTGTGCCTAGATTTATAACTTTGTCTTGTTTAAAGCATTTTAAACATTTTTATTCTTCCATCGGTCGATGAGGTAGTTTCCTGGTCCTGTCCCCAACTTTTCTTTCCTGTTAATTCTTGTCATCTCTAATGTTTTGGGCCAGTAAAGCCATCAAGTTTGAAATATTTTATCCTATAATAAAGTATACTTCTGACACACAAATAAGTAAATTTATCAATTGTTGAAATTCATTAATTTTCTTTCGATTTAGGCCTGATCCCAATTCTATTTTTGTACCCCTTACCCTTCCCCTTGGCCCTTACAACTGAGGGTTAAGGGGAAGGGCTTCAAAATTTACCCCTAAGAATTGGGACAGCACTACGATCTCTTGCTTCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa5919

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000088917	Nonsense	246	400	6	11
ENSDART00000103675	Nonsense	246	400	6	12

Genomic Location (Zv9):

Chromosome 19 (position 13281265)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	12739611
GRCz11	19	12659139

KASP Assay ID:

554-3938.1 (used for ordering genotyping assays)

KASP Sequence:

GAGAGACTCCGGCCTGGAGGATTCTTCATCGGGACAACTCCTGATGCATA[T/G]GAGCTGGTGTAAGATNNNNNNCACACACACACACACACACACACACACTT

Long Flanking Sequence:

ATATAGTAAGTTAATTTCAGACTGTTCGCTCTGCGGGAAAGTGTGTTAGATTTCCATCGGAGGAAGAATTTGATTACAATGTCTATTAATTGACGGTGGCTAAACATGTCAAACCAGTGATTTAAAAACTCCAGATTTAATCCTAAGATTATAGAAATCTTTTAGGATTTTAAAAATGTGTCTCCGATTATATATCATACCCAGATTCACACAGTGCGAACTCAGCTTTAGAGGGTTTCAGTTCATTGTCAAAATAAATAAACGTTTGTCTGTGATCATCATTCAGTACATGACAGTACAGGGTCACATACTCTCCGTCTGTCTCAGGAACTGCTGTCTGAGAAGTTGCAAGACCCTGAGCTGCAGTTTGACGTGTGCAGCTGTCAGTTTGTGTATCATTATTCCTTTGAGAGCGAGTCGCAGGCTGACACCATGCTGAGAAATGCCTGTGAGAGACTCCGGCCTGGAGGATTCTTCATCGGGACAACTCCTGATGCATA[T/G]GAGCTGGTGTAAGATCACACACACACACACACACACACACACACACACTTAGGACCTACTCACACTATGCTATACGAACCGTGCCCAGGCCCATTTCCCGGATCGTTTGAGAAGTGTGAGTGCGCTGAATCAGGCTCAGGCACGGTTCACTTGGCCGGCCCTGGCCTGGTTGGAAGAGGTGTGCCTGAGCGCGGTTCACTTGGGCTTTGGCGCGGTACGCTTGGGTGTGAGTGCAAAACGCGCCAAAGCCCGAAACTGAAAGCGAGATGTGACTTTTAAGGGACCGTTTCATATGGATTTATTAATCATTCTTACTGTTCAGTGAACGCAAACTTCCGCAACCTATTAAAAACGCAAACCCCTCACTGCATGACATCTGCGCACATTCAGCAAACCTCCTAATTCCTGCAGCACGAGGGCTTTATGATTGTTTATGAGCGCCAAAAGTGGCGGATCTGTTCGGCGAAATATCTGACTGCGTGTCACTGCATCCCAAACGA

Associated Phenotype:

Not determined