si:ch211-173p18.1

Ensembl ID:

ENSDARG00000035823

ZFIN ID:

ZDB-GENE-030131-5459

Description:

zinc finger protein 262 [Source:RefSeq peptide;Acc:NP_001037777]

Human Orthologues:

ZMYM1, ZMYM4, ZMYM6

Human Descriptions:

zinc finger, MYM-type 1 [Source:HGNC Symbol;Acc:26253]
zinc finger, MYM-type 4 [Source:HGNC Symbol;Acc:13055]
zinc finger, MYM-type 6 [Source:HGNC Symbol;Acc:13050]

Mouse Orthologues:

Zmym1, Zmym4, Zmym6

Mouse Descriptions:

zinc finger, MYM domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1915560]
zinc finger, MYM-type 4 Gene [Source:MGI Symbol;Acc:MGI:1915035]
zinc finger, MYM-type 6 Gene [Source:MGI Symbol;Acc:MGI:106505]

Allele Name	Consequence	Status	Availability
sa9286	Nonsense	Mutation detected in F1 DNA	Not yet available
sa36894	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa43331	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa36895	Essential Splice Site	Available for shipment	Available now

Allele Name:

sa9286

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
ENSDART00000026912	Nonsense	422	525	10	12
ENSDART00000113411	Nonsense	454	1329	9	26
ENSDART00000140926	Nonsense	434	1523	10	28

Genomic Location (Zv9):

Chromosome 19 (position 41044100)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	40496638
GRCz11	19	40083758

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCTGATTCAAGCAWCCAGAACTTYTGCTCCTTTTCTTGTGTAGTGTCATA[T/G]CAGGTAAAGTGAAGCAATTTTACTAATTTCTTTCAAATCGAAATGWRCAG

Long Flanking Sequence:

CATTAACATCTGACTTTTTTTTAATGGTTATGTGCCTTTTCTATACAGTGTATGTAAACTTCTGGTTTTAACTGTAGATAGGAAAAGAGTGCGTTACCTTCATTACTTTAACAAACCAACTGCGTTACAGGTGGTTTGTGAAGCCCACTCATCTGCGTGTAGCACACTCAGAATTGCTCAATTTGTTACAAGAAGTTTAGGATGCTTGTAAGTAAGTCTCTGGTGCATATTGTCCCTTGTTTAATACTCTAAATGAATAAATTACCAGGGCATTACAGGTGGATGTCAAGCCCACTTATCTCCATGAAGCACACTTGGAATCGCAGTGTTTTTCAGAAACATCGAGGTTTAAGTTCCAATGTGTCTTTTGTTTGCATGCTTATACAAGGTGCTCCCGTGGAATGCAACAGCTGTAAGCAGAAGCTGGTGCCTCAGTACCATCTGGCCATGTCTGATTCAAGCATCCAGAACTTCTGCTCCTTTTCTTGTGTAGTGTCATA[T/G]CAGGTAAAGTGAAGCAATTTTACTAATTTCTTTCAAATCGAAATGTACAGGGTTCATACGAGTGCTGGAAATTCTTGAAAATGCTTGAATTTTAATTAGGGATGCACCGATATGGATTTGTGGGGCGATGCCAATAACTGATAACTCTTTTTTTATTTGAAGGCCGATAACCGATATATGTTCTATATGCTGTTGCTCGCATGTTAATTCATTTTTTTTAAATTAAGTATAATGTAATATTAATCTGACCAGTTAAGGGTTAATATTCGGTTAATGAGCAGCGGTTGCTGGTTAGGAAAATTAACCAAATGTTTACGTAATATTTTTATTTAATTTAAACCAAAGTACACAATGACACTCTATCAAACATATCTACAATGATAAGGAACATGGAATAAACAATGCGAGGAAAGCTTCATTATAGTGCACTGGACATGCCTGAACAAGTTCGACCTGTGCATGTATGAGGCAGGCTGTTCTGTACATTAAATTAACCTATC

Associated Phenotype:

Not determined

Allele Name:

sa36894

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000026912	Essential Splice Site	491	525	11	12
ENSDART00000113411	Essential Splice Site	523	1329	10	26
ENSDART00000140926	Essential Splice Site	503	1523	11	28

Genomic Location (Zv9):

Chromosome 19 (position 41046279)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	40498817
GRCz11	19	40085937

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACAGTGTCTCAACTCATTCTTCCACAAACCAGAACTGCTGGATTTTAAGG[T/C]AAAGATATCATGTATTCTTATTTATATTTGTAAAGTTGATTTATAAACTA

Long Flanking Sequence:

ACCGCTGTTTGTTTACCTTCAAGCTACAAATACAAATCTACTATACAATCGCTGCTGTTTTGAATTTACAAGTATTTTGGAATGGATGTGTGAATGGTCTGTTCGGAAACATTCCGTAATGTCCTTGCCTGTGTAAACATCGCTTTTTTGAACTTACCGGTAAAGTCGTTCCCATAATTTTCTGGATATTTAACCAGTATCACTGACTGAAAGGGGCTACTGTCTACATTTAAAAATGTAAGAAGGCTGAATATGTCAAGTAGAGTTATCTTAAGATTTCATTTTCTTTGTTTAGGAGTCATTTGGTAAGAAACCAAACTACCAGGTGAACACTGTAACCTCTACGACGAATGCATCAACGCCAAAACCTGCCTCTTCAGAGTCCAGCTCCTCAACCAAGACAAGCACTTCCAAGAGTCAAGTTCAGAACGTCACAAAGATCCCCTGCTCACAGTGTCTCAACTCATTCTTCCACAAACCAGAACTGCTGGATTTTAAGG[T/C]AAAGATATCATGTATTCTTATTTATATTTGTAAAGTTGATTTATAAACTAATTATGAGAGGATCATGTGCTTATGATTGTCCACGGCTGGTCCCACGTTAGTTTACGATTGATTCACCAATCAGATGATTTTTTGCTATTAGTAACCAGAGTTTATTATCTCAATATCTTTATCTTGAAAAATCCCCCCTACTCCCCCTCTCTTTTCTAGATGGGCAACACGATGGCTCAGTGATTAGCACTGTTGCCTCACAGCAAGAATGTCTCTGGTTAAAGTCCTTACTAAACCAGTAGACATTTCTGTTTAGAGTTGCTCGTTCTCTCCGTGCTCACATGGGTTTTCTCTGGGTTTCTCCAACTCTTTATAAACACCCAACCTAAGTAAATTGAACACCAAATTGGCATCATCGTCAAGCTCTTAGCAAGCCGTATATCTCTCCTTAGCCATCCCTATATCTCTCATTAACCAGAAATAAGTCTGGAAAGTTCATCGAGATCTAC

Associated Phenotype:

Not determined

Allele Name:

sa43331

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000026912	None	None	525	None	12
ENSDART00000113411	Essential Splice Site	573	1329	11	26
ENSDART00000140926	Essential Splice Site	553	1523	12	28

Genomic Location (Zv9):

Chromosome 19 (position 41047146)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	40499684
GRCz11	19	40086804

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAAGGAGGTGAAAAGGATCAACAAAATTGACCGATCTTTCTGCAGTGAGG[G/A]TAAGTGTTAAGAGCAAAATGAAAATGTTTGTGTTGTATGATGTATGCTGC

Long Flanking Sequence:

AACACCCAACCTAAGTAAATTGAACACCAAATTGGCATCATCGTCAAGCTCTTAGCAAGCCGTATATCTCTCCTTAGCCATCCCTATATCTCTCATTAACCAGAAATAAGTCTGGAAAGTTCATCGAGATCTACCTGAGCTCAAACTCCTCTCTTGCCCAGCTCGAGGATCTGATAAGCTCAGGGCTCTCTCCTGGGACGGCATGCCAAACAAGCTTATTACCAATCATCAACTAATTATTATTATTAACTATCATTAAGTTTAGCAGTTAATGGTTTGTTTTTGTTCATAATTTGTATTTGGCAAAATGGTTGACACTAATTGGTTGCTCTTTTTCCTGACCTTTCAGAGGAAAATGTACGCTTTCTGCGGTACGGCTTGTGTTGAGGAGTTCAAGCAGATCAACAACGTCATGGCTCGCTGCGAATACTGCAAGATTGACAAAATTATCAAGGAGGTGAAAAGGATCAACAAAATTGACCGATCTTTCTGCAGTGAGG[G/A]TAAGTGTTAAGAGCAAAATGAAAATGTTTGTGTTGTATGATGTATGCTGCATGTAATATATGTTTTTCTTTTTTGTTCTACTCAATATGAGCTGAAGGCTGTTGGGAAAATGCTGTATTATTTGTTGTTTATTCTTTAAAATATTTAGCTGAGTAATACATTCTGCTCTCATTAAAAACAGCGAGATTAACTGATTTTATCAAAAAACCAAATCACTTTGTTAAATGTATGTGCTATGATTATTGTTATTAATATTACACTGTCAATAATTAGTAATAATTAAGACATTTCCGTCGATGGTTTTGAATCGGTCTAAAAGAGGACACTTGTTTATTTGTTTGAAGAAAAGTTTAAGTGGCCAAACAAAATCTCCAAGAAAAATTTTGAGAACTTCATAATTTTATGTCTACATTTTGATTTAAATTCTGTCTAAATTTCAGATTTAAAATGTAAAAATTAGGGCTGCGTGATTCTGGCTAAAATGAGAATCACAATTTTCT

Associated Phenotype:

Not determined

Allele Name:

sa36895

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000026912	None	None	525	None	12
ENSDART00000113411	Essential Splice Site	799	1329	16	26
ENSDART00000140926	Essential Splice Site	779	1523	17	28

Genomic Location (Zv9):

Chromosome 19 (position 41056014)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	40508552
GRCz11	19	40095672

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAAGGGCACTTCCTGCAAACCCAATGTCTGTGACATGGATTCACAAACAG[G/A]TACTTGGAAGTACATGTTTCTAGTGAGCATTGCATATATTGACACTTGGA

Long Flanking Sequence:

CAAGTTCAGTGCTGAATACACTAGTCAAGCTTTCTTTGATTTGCTCACAGATGTCTTGTGCATCTGCCAGGTGAGACTATTTAGTTTAAAGTCTGATGGTGGGTCAAATGAAAGGTTACCATGGGCCAATTTTAGCCCGGGGGCCCTATTTTGGGAATCTCTACCTACCTTTTCTGTGGTTAATTCTGTGGATTTCTTTTTGTTTCCTCAGCTTCTGTTCCAGCTGCTGCTACAAAAAGTTCAGGAAATGTGAGTTTTTCCGCAAATCATCTGAACAGCTAAAGATCCTTTTAAAGTGTTCATGTAAATCAATGATTCATTCCAGCATTTCAATCATTCTCACATTTGTCCCCAGACGGCCAGCACACAGACAGACAGTGTGAAGCCTTCTGCTCCTCCACCTCGAATCCTGAAAAACAAAGCCTTACTGTGTAAACCCTTAAGCCAGAACAAGGGCACTTCCTGCAAACCCAATGTCTGTGACATGGATTCACAAACAG[G/A]TACTTGGAAGTACATGTTTCTAGTGAGCATTGCATATATTGACACTTGGATGACATGGAAAAATAATGAATTGTATGAAACACAACCTGGACTTTCTAACAGATTTCTAATACATTTCATATTGGACAAACAAGGCTAACTCATGTTTTTTGCTTAAAGGGTGAAGATTACACTCATTGTTTGTTCTGCAAAATTAATATCACTGTAAAACACGTTCTGTTGGATGGTTCTGCTTTTAATGACTGCAGAAGGCTTTTTCATTAAATGAACTTACTCGAGACATTCAGCAAAGTGTCAGCAGGAACAATTTTACAATTTTTATAATATTCATTTTCCTTAAGCTTAGTCCCTTATTTATCAGGGGTCGCCACAGCAGAATGAACTACCAACTATACCAGCATATGTTTTACACAGCGGTTGCGTCCTTCCAGCCGCAACCCAGTACTGGCACAGTGCTAACCACTGAGCTGCTGTGCCTCCAATTTTATTATATATTATAT

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details

Mutation Details

Mutation Details