ZMP

yth2

Ensembl ID:

ENSDARG00000014498

ZFIN ID:

ZDB-GENE-040426-948

Description:

YTH domain family protein 2 [Source:RefSeq peptide;Acc:NP_956544]

Human Orthologue:

YTHDF2

Human Description:

YTH domain family, member 2 [Source:HGNC Symbol;Acc:31675]

Mouse Orthologue:

Ythdf2

Mouse Description:

YTH domain family 2 Gene [Source:MGI Symbol;Acc:MGI:2444233]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36430	Nonsense	Mutation detected in F1 DNA	Not yet available
sa1176	Nonsense	Confirmed mutation in F2 line	Not yet available

Mutation Details

Allele Name:

sa36430

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000127043	Nonsense	25	613	3	6

Genomic Location (Zv9):

Chromosome 17 (position 27275965)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	27400081
GRCz11	17	27417044

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTACCTTAACTTTCTCTGTTTTCTTTTCAGTACAAAACGGAGCTGTTACC[C/T]AAAAGGATACTTTGAACGATGATGAGTTCGAGCCTTACCTGAATGCTCAG

Long Flanking Sequence:

TGGGTGCTTGGCTCACTGGAGTGGAAAAACAAGGCATTTTAACATTTTTTTTTTTTTTTATGAAACTACGTTGATCCAGTGTACTTTATATGCTTTTAACATGCAAATATGACATTCCTGACATGAACTTAAACACCCCGTCAGAGCAATGCACCTGCTGCTGAATTGGACAGGTCATTGATTCTTATCATATTTAAAAGATATCACTAGATAACAACAGAAAATATGTTTCATCAAAAATATAATCTGACTGAATATAGTCATAAATACAATGCATAGACAGATTCAGGAGAGGACTCGTTTAACAAAATCTTAGGGTTTACATATAATTAAAAGGGATTTTAATCTTTTAGATGACACAGAACCCCAATTGAACATTCCTCATCCTGTAATTATGCATGCATGCATGCATGCATGCATGTGTATGGATGGATGGATGAGACGAGACCTGTACCTTAACTTTCTCTGTTTTCTTTTCAGTACAAAACGGAGCTGTTACC[C/T]AAAAGGATACTTTGAACGATGATGAGTTCGAGCCTTACCTGAATGCTCAGCCCAGACAGGTAGGTCTTGTTTCAAAGTTTTAACAAAAGAAGGATCTCATAGAGACAGCGTGCCGTAGCAATTGTTTTTCTGTCTATTGTTTTAAGGATTTATTATGGTCCGTAATTGCATCCTGGCCACGGGGCTTTGTTTTCTTATTAGGGTGTCTCTGTGGCCTTTTACATTGTGGCTTATCACTGTATGCGTAGTTTAAAGCAGTTTGTGGACTTAAGTCAATTCATCCATTACGTGTATTGAGAAATATTTAGTTGCTGTCTAGGTTGAAGTACATGCGGATGAGTCATAGGAAATTATGCAAAAAGCAGCACAGTCGTTTACCAGGAAGTGGAGAAAGGTGATTGCGTTTATGTTCCTGTCCAGATATTCTGTAATAGAATTCCATTCAAATTAAAAATGAATCAGTCCTGGCACTGATAAAGAGGGTTCTGGCAATGGATGTC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa1176

Status:

Confirmed mutation in F2 line
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
ENSDART00000127043	Nonsense	149	613	4	6

Genomic Location (Zv9):

Chromosome 17 (position 27273787)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	27397903
GRCz11	17	27414866

KASP Assay ID:

554-1086.1 (used for ordering genotyping assays)

KASP Sequence:

GCTTGGGGCAACAGCAGCTCTCAGGGACAGTCCACACAGAGTTCAGGTTA[C/A]AGCAGCAGTTACGCCTATGCCCCTAGCACGCTAGGAGGTGCAATGATTGA

Long Flanking Sequence:

ATCTACAGTTAATGTACTTAAGTTTTTACTCAAAGGGTTAATGCTACAAGGGGAGAAATGTTTCCAGGTGACAACAGGGAGCAATTGTCACCTGGCAATATTTTCCAGGTTGTTGCATTACCTTTCTAATCCTACTTGTCTGGAGTTGATAATGACTAATCACAATTTATGTTGTTGTTTTTACAGAGCAATGCCTATACGGCCATGTCCGACTCCTACATGCCCAGTTACTACAGCCCCTCAATAGGCTTCACCTATTCCCTGAATGAAGCGGCATGGTCAACAGGTGGAGATCCCCCGATGCCTTACCTGGCCTCTTATGGACAGCTTAGCAATGGGGAGCACCACTTTCTCCCGGATGCCATGTTTGGACAGTCTGGAGCACTGGGGAACAACCCTTTCCTAGGACAGCATGGCTTCAACTTCTTTCCCAGTGGGATTGACTTTCCCGCTTGGGGCAACAGCAGCTCTCAGGGACAGTCCACACAGAGTTCAGGTTA[C/A]AGCAGCAGTTACGCCTATGCCCCTAGCACGCTAGGAGGTGCAATGATTGACGGACAGTCTCCCTTTGCAGCCAATGAGCCACTCAACAAGGCAGTGGGGATGAATAGCTTGGATCAGGGCATGGCAGGGCTTAAAATTGGGGCAGGGGACATGGCACCAAAGGTTGTTGGTTCTGGACTTCCCGGAGGGCCATTGAGTCAGGTGTCTACAGCTCCAACCATGCCTCCTGCCTCCATGGCTCCTGCGAAAACTGCTTCTTGGGCGGACATTGCCAGCAAGCCAGCCAAACCACAGCCTAAATTGAAAACTAAGGGGGGACTTGGTGGGACAAATCTGCCACCACCTCCAATAAAACATAACATGGATATTGGGACATGGGACAACAAGGGGAATATGCCTAAACCAGCAGCCCCACAGCAGACTTCCCTGCCCACTAATGGACAGCCACCCAATCAGTCGTCTCCTCAACCAGGTGCTACTGCTGGTGGGGTGCCTCAGTT

Associated Phenotype:

Not determined