ZMP

zgc:111982

Ensembl ID:

ENSDARG00000051920

ZFIN ID:

ZDB-GENE-050417-342

Description:

hypothetical protein LOC550506 [Source:RefSeq peptide;Acc:NP_001017808]

Human Orthologues:

NSMAF, WDFY3

Human Descriptions:

WD repeat and FYVE domain containing 3 [Source:HGNC Symbol;Acc:20751]
neutral sphingomyelinase (N-SMase) activation associated factor [Source:HGNC Symbol;Acc:8017]

Mouse Orthologue:

Nsmaf

Mouse Description:

neutral sphingomyelinase (N-SMase) activation associated factor Gene [Source:MGI Symbol;Acc:MGI:1341

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa41052	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa34207	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa34206	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa9529	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa41052

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
ENSDART00000073635	Essential Splice Site	144	911	7	31

Genomic Location (Zv9):

Chromosome 7 (position 59417040)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	57869649
GRCz11	7	58172089

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTTGGGGTCACCCATTAAAACTGAAGATGTGGTTCAGATTTTATTACAG[G/A]TTTGCCATTATTCTTTCTTTAGGTTTTTAATTTTTATTGGGAATTTTGAT

Long Flanking Sequence:

CGGCCCATAACCCATTTATTGAGTAATACAGAATCATTTATTATCAGAAATATTTATTTATTTGTTTGATCATTTTTTAGGGTTATATAATACTTTTCTTTTACTTTTCTGTGTTTGCAGAAGTAAACCCGCTTGTATTGTTATAAAAACGAAGCAGGTGAGTGTGCCTCATGTTACCCCAGTGTACTCCATCCTTCTTATTTTGTAAAGATAGTTCAGTATTTGATCAAGTTTTATTGTATTTCTTCATTAGATTTATCAAATTAAAGAAGAAAATGTGGTTGCTCCATATAAATATGACAGGGTGAGCTCATTTTTGTCTCTGCAAGTAAACATTTTCAGCAGTGATATATATTTTTCTGTTGTTTATTCTCTCTTTATAATGTTGGTACATTGTATATAATATTATTTACTGCTTGATTTGTTAGGGAGAGAAGAAGATCACATTCCAGTTGGGGTCACCCATTAAAACTGAAGATGTGGTTCAGATTTTATTACAG[G/A]TTTGCCATTATTCTTTCTTTAGGTTTTTAATTTTTATTGGGAATTTTGATATAAGCTAATTTGCTATTTGCTGTTTATTTTCCAGTTACACAGAGCATCCCGTCTGGATAAGCAGAGTGATCAGACAGCAATGGTTAGTGAAGTAACTTTTCCATACATTAATACATCCATACATAAATTATTAGCTTGCATTATGGATGATCTGGATGTCTGTGTATCTGCTAAAGATTGCAGCTATATTGCAGTCCAGGTTGGCAAGAACACGCTTTGATAAGAACAGGTAAGAATCAAAACTCCACATTTTTTAAATTCGTCATATTCCTTCAGTTGTTGATGTCAGATTTTGGGGTAAAAATGATTAGGTTTTAGACCTTCTGTGCAGTTTAATTTTCTCTTTGAGCCTTGTTCCGACTCAAATCACTTTTGAATAAATTCTAAATTTCGATAAAAAAGTTATTATGATATCCAAAAACTAAAATGATACTAAAACATATCGGAGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34207

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
ENSDART00000073635	Essential Splice Site	625	911	22	31

Genomic Location (Zv9):

Chromosome 7 (position 59401175)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	57853784
GRCz11	7	58156224

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCAACATGAACAAACTTGTCTTGCAGTCTTGCCATAAAATACACAAAGAG[T/C]GAGTATTTGTTTGTCCACTTGAGAACTGATGTAAAGAATAATTACAGAAT

Long Flanking Sequence:

GCTTCTTTAATGTCTAATCCTACCCCTTTTCGCAGCGCCGGATGGCAAAATTTTGCACACACAAACTCTAATATGACCCCTGTATGAGTGTGTTGAAGCATGGTTAGAACTAAACTGTGCAGAGCTGCCGCCCTCCAGGAGCTGGATTTGACACTTCTCCGTCAAGCCTTCCTTACCATTAAGCTTATTTTGTTGGAATGTGAAATTTATTATATATATATATATATATATTAAGTTATTATATAATCATAGATTGATATATGTTTTTATTTAAATTGATCTTGCCATTGAATATTCATAAGTTGCTAATGTGGCATTAAATAAACAAACAAACAAATCTCCAGAAGGGTGTCATTACAGAATCTAATTGACCTCAGTGTTTTTGTGCAGTTTCTCCTTGCATGGAGTCATTTGAGGACCTGACTGAGGAAAGTAGGAAGATGGCCTGGAGCAACATGAACAAACTTGTCTTGCAGTCTTGCCATAAAATACACAAAGAG[T/C]GAGTATTTGTTTGTCCACTTGAGAACTGATGTAAAGAATAATTACAGAATAGAATTATAGAATAGAATAGTTTTTGACTCTTGTTTATTTTTTATTTAAATGTTAATTTTGCGGGATTTTGCAGAGCAGTAACAGGCGTTGCTGTGACCCTCAGTGGAGATTCCATCTTCACAACATCCCAAGGTTAGGAATTCCTCAGTTATTTGGTCTCTTAAGTAAAATGATCACTGACTGGAAGGTCTAAGATGTAAACTTTTTTTTTCTTTGTGTAGACTCTACATTAAAGATGTTCTCAAAAGAAAATGGCCTACAAAGAAGTGTTTCCTTCTCCAACATGGTAACCTTTCAAAATATTTTTGGTATCACAGTTTTGTACCCTAAAGGTATTTGTATATTAAAGGTACACTCACTAAATTAATTGCTTTTAACTATAGCTTTGGTTCTTTGGACCTGCCACTTTAAATATTTGACATCTCCCTAATTTAACACACTTAAGATCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34206

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
ENSDART00000073635	Essential Splice Site	645	911	23	31

Genomic Location (Zv9):

Chromosome 7 (position 59400990)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	57853599
GRCz11	7	58156039

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGCGTTGCTGTGACCCTCAGTGGAGATTCCATCTTCACAACATCCCAAGG[T/C]TAGGAATTCCTCAGTTATTTGGTCTCTTAAGTAAAATGATCACTGACTGG

Long Flanking Sequence:

TATTTTGTTGGAATGTGAAATTTATTATATATATATATATATATATTAAGTTATTATATAATCATAGATTGATATATGTTTTTATTTAAATTGATCTTGCCATTGAATATTCATAAGTTGCTAATGTGGCATTAAATAAACAAACAAACAAATCTCCAGAAGGGTGTCATTACAGAATCTAATTGACCTCAGTGTTTTTGTGCAGTTTCTCCTTGCATGGAGTCATTTGAGGACCTGACTGAGGAAAGTAGGAAGATGGCCTGGAGCAACATGAACAAACTTGTCTTGCAGTCTTGCCATAAAATACACAAAGAGTGAGTATTTGTTTGTCCACTTGAGAACTGATGTAAAGAATAATTACAGAATAGAATTATAGAATAGAATAGTTTTTGACTCTTGTTTATTTTTTATTTAAATGTTAATTTTGCGGGATTTTGCAGAGCAGTAACAGGCGTTGCTGTGACCCTCAGTGGAGATTCCATCTTCACAACATCCCAAGG[T/C]TAGGAATTCCTCAGTTATTTGGTCTCTTAAGTAAAATGATCACTGACTGGAAGGTCTAAGATGTAAACTTTTTTTTTCTTTGTGTAGACTCTACATTAAAGATGTTCTCAAAAGAAAATGGCCTACAAAGAAGTGTTTCCTTCTCCAACATGGTAACCTTTCAAAATATTTTTGGTATCACAGTTTTGTACCCTAAAGGTATTTGTATATTAAAGGTACACTCACTAAATTAATTGCTTTTAACTATAGCTTTGGTTCTTTGGACCTGCCACTTTAAATATTTGACATCTCCCTAATTTAACACACTTAAGATCATGGAGTGCTTCATGAATAGAGTTCCATGTTATTTCCACTATAATCCAGATTGTTCTGACTTGTAAATATTTTGGCTTCTTTCCACACTTATACACTATTTTTGTCCAGCACAAACTGAGCTCTTCTTAGTCAATACATTTGACAGTGTATTGAAGCATGGACTATAAAAACTGTGATTGCGTGTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9529

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
Order Allele From EZRC

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000073635	Nonsense	756	911	27	31

Genomic Location (Zv9):

Chromosome 7 (position 59398007)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	57850616
GRCz11	7	58153056

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCTCCAGTAATAAAAGGACTCARTTTGACCCACTTGCTGAATTTGAGCAT[G/T]AGGCCGGGGTTAGTAAWAAGGAATCCTTAAAAAAAAAAAAMCNNTCAAATTT

Long Flanking Sequence:

ACTCAATTGCTTATGGAAGAAGACAGGACACTTTGATGGGTCATGATGATGCGGTTAGTGATATTTGCTGGAGGGATGACAAACTTTACACGGCTTCTTGGGACTCCACTGTGAAGGTATTGAAGTGTTTTAACTCCGAATGCAAAAGCAGTTACATAGGACTTTCTATTTATTTTAGTCTTAAATGTTTCAAATAAAACTTCTAGTCAACGCAAACAAAAAGTCTTGCAGTTTTTACTGAAATCTTGTCTGTCTTAAAATGAAGTTGCAGTAATGTTTTAACTAATTTAAAACTTTTAATTAAAACCCTTAATTTGAAAACCTTTTTGATTTTACTGATTAATTAGAACTGATTTACACACTTTAAAACATTTTTTGATACATCTGTTGTCTCTGCATTCATCATTTTTCTGTCTTTTTTTAAGGTTTGGGAATGTGTAGCTGCTGACATCTCCAGTAATAAAAGGACTCAGTTTGACCCACTTGCTGAATTTGAGCAT[G/T]AGGCCGGGGTTAGTAATAAGGAATCCTTAAAAAAAAAAAAACTCAAATTTATTCAACTATATTTAACCCATGATTCATTTGTGGCACTTTTCAGACTAGGGTACAAAAGTTGGACCTAAATCTCTAAAGTGCTTAAAATATAGAAATATTAGTCCTCATATTAATATTAATCCTCTCGTGCTGTATACTTTATCAGTTTTTAACAATTTGTTAATGGGTTGGTTCATCTCAAAATAGGAATGTGTTACTGTTTGGTTACTTTTTATGCTTTTCTGAAATGGTAAATCTAATGCTGTGTTCACACCAGACGTGGCACATGTTATACATGTACATAGATGCTTGAACATTTTGAGTTTGCTTGCTTCATTCACGCATCAAATTCACTTTACAATAGACGTGGATTTGTGTCATGAGGAGGGCTTCTGTCTTCCCAGTGACTCCCTCTTCTTTGTTAAATGGCTGAAAAACAGTGAAGATTCGTTTAGCGCCTAGTCTAATAG

Associated Phenotype:

Not determined