ZMP

zgc:101657

Ensembl ID:

ENSDARG00000033957

ZFIN ID:

ZDB-GENE-041010-189

Description:

tRNA (uracil-O(2)-)-methyltransferase-like [Source:RefSeq peptide;Acc:NP_001006086]

Human Orthologue:

C4orf23

Human Description:

chromosome 4 open reading frame 23 [Source:HGNC Symbol;Acc:26653]

Mouse Orthologue:

2310079F23Rik

Mouse Description:

RIKEN cDNA 2310079F23 gene Gene [Source:MGI Symbol;Acc:MGI:1926140]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa41055	Nonsense	Mutation detected in F1 DNA	Not yet available
sa44677	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa41055

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039535	Nonsense	167	340	3	7
ENSDART00000125570	Nonsense	109	574	3	12
ENSDART00000132044	Nonsense	167	625	3	11

Genomic Location (Zv9):

Chromosome 7 (position 60160656)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	59379621
GRCz11	7	59684858

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGACCTGAGCAATGGTACAGTGATGGAATAGCTTATCCTAAACTGTCTTG[G/A]CTTCGTACTGAACTTCTACCTAAACTGTCCCGGTGGTCTCTAGAGAGCAA

Long Flanking Sequence:

CCTGACTAGGAGAAACTCTTTATAGTCAAAATCTTCATTAATTTGGGCCCTGGTCTAAACACATCTTAAGAGCAGTATACATTTATATTCATAGCACCACCATTTTTTCTTTGATTTTTACCCATTGAAATGCATATTGCTCATGATACTCTTTTTTTTCCAGCTGAAAAGCACTGGATGGGGGTGGCTCCAGATCGAGAGGACATTTTATTGTTGCTTGCAGCTTTAATTTTATACAATTATTTCATCAATGTGTAATGACCAACTGATGCCAGACATGATTGAAACATGTTGTCCATTAAAAAAGATTTTGTAATCTTGTGGTCGCAAAAAAAATTATTAGCACATTCTGTATTTATTAGTGTTGTATTGATTAGATTCATCTATATATATTTTTTCTTTTTTCTTTTGTTGTTCGTTTTTTCCAGGATGTTTTCCCTTCACGTGCTGAGACCTGAGCAATGGTACAGTGATGGAATAGCTTATCCTAAACTGTCTTG[G/A]CTTCGTACTGAACTTCTACCTAAACTGTCCCGGTGGTCTCTAGAGAGCAAAACCTGTGTGTTTAAGAGTACCCTGTCTCTCATACCGGTGGACAAATACAGTATGCTCTACCAGCAGCTGAAACTGAAATATAAAGATTTAGTAAAGGTATCATATTTATTAATTCATACATCAATTCATTAATTGAATCATTTGTTAATTGAGCATATAATCTATTAAATAATAATTAAGGAAGAAAATATTAAAATATTGTCAGTGTTGAACAAAGCTTTAAATACAGTAACAAAAATACAGAACTACTGTTTTTGAGCAGTCTCTTGGTTTAATCTCATATACTACATCTAATATGTATTTTTGAGTTTGTGTAGAGGTAAAGTATTGCATATCTATATTTATAAAAATAAGTGACATTTGTTAATTTTTCAAGGTCTGGCCAGAAGTTACCGATCCACAGAAGTTTGTGTTTGAAGATGTTGCTATTGCTACGTATCTGTTGGTAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44677

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039535	None	None	340	None	7
ENSDART00000125570	Nonsense	282	574	8	12
ENSDART00000132044	Nonsense	340	625	8	11

Genomic Location (Zv9):

Chromosome 7 (position 60181241)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	59400206
GRCz11	7	59705443

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACTCGTCTATAATAGTCTTATTTTATTCTTTTTAGGTCATCTTACTCGTG[C/A]CGTTTCTTTGTGCTTCCTTGCTGCTTTTTTGACTTTTGTGGAAAGTACCA

Long Flanking Sequence:

TGTATTCTTTTTGTAATATCTTAGATATTATAAACTTATATTATAAGCTTTTTTGACAGAGATGATGCCAATATCTTTTTTGTGTATGTGTTTTTAACAAGTGTTTATTTACATGTTAGTTTTTCTGGGTCTGGTAAAAATAAGCATCAGAGTAAATTAATAAACAAAACATGTTGTCAGTCTGTTGCATTCTGTTGTAATATAACTTCATTTAATAGCTATGACATTCTGCTCTTTTGTCAATTTTATTTGTCATATCATTACAATTAAAACTTCATACGGTATATTACTCATTTATGTCTTATGGGTCACCCTGAACAGGCATGCGTTTCCACTGCCAACAATATCCTTACATTAAAGTTTGATATAATAAAAAAGTTCTAAAGTAATCAATATCATTCTCACTCAAAGAAAGTTGTTCGGGCTGTTCACATGCAGCATCTGTTGCAAACTCGTCTATAATAGTCTTATTTTATTCTTTTTAGGTCATCTTACTCGTG[C/A]CGTTTCTTTGTGCTTCCTTGCTGCTTTTTTGACTTTTGTGGAAAGTACCAACGAAGACAGTGTACAAAGTCTCAGTATAAGGAGTACATTGACTTCATCACTGATGTAAGCACAGTGTGTGGTTTCTACGCAGAGGAAGACTGTCTGAGGATACCGTCCACTAAACGGGTATGTTGGTCCAGTGTGTAGTGTTGGGATTGTAGACTGGACTGTAAATTACTAATAAATTCTCATTACCTGTTTCTCACATTATCTAATCTCATAGAAACACATCCTTGTTCTGCTGTTAACAGAACATGTTTGTTTATGATTTAGCCCAACTCAGCTAGAATACAAGATTTAAGAGACTGAACAAAGCTCCTTCATGTTCTGCATAGGTGTACACAATTTCACCTGTGATCCTCGAAAATGCAATTGTGTGCATGTGTACTTCTGCTCTAATACTTTCAGTCCTGCTGAAGTTCATTTTTGTTAAAAGAATAAGCTTTCATATGAAACTT

Associated Phenotype:

Not determined