ZMP

si:ch211-14a17.7

Ensembl ID:

ENSDARG00000038720

ZFIN ID:

ZDB-GENE-030616-590

Description:

hypothetical protein LOC368669 [Source:RefSeq peptide;Acc:NP_001007181]

Human Orthologues:

POMZP3, ZP3

Human Descriptions:

POM121 and ZP3 fusion [Source:HGNC Symbol;Acc:9203]
zona pellucida glycoprotein 3 (sperm receptor) [Source:HGNC Symbol;Acc:13189]

Mouse Orthologue:

Zp3

Mouse Description:

zona pellucida glycoprotein 3 Gene [Source:MGI Symbol;Acc:MGI:99215]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa1906	Nonsense	Available for shipment	Available now
sa44542	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa1906

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000044552	Nonsense	26	228	3	10
ENSDART00000112834	Nonsense	109	311	3	9
ENSDART00000132621	Nonsense	109	311	3	10
ENSDART00000148281	Nonsense	26	228	2	9

Genomic Location (Zv9):

Chromosome 2 (position 37986794)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	38301708
GRCz11	2	38284036

KASP Assay ID:

554-1896.1 (used for ordering genotyping assays)

KASP Sequence:

AGATCACTTCTGTGGCTGAAACYGTGTCTTATCCAGTGGCATGYGTTTTT[G/T]AAAGGTGATTGCTTTGTCCATTTTAGAATGTGTAACTTTAAACCAAKATG

Long Flanking Sequence:

TTTCTGTGCAATGGAGTGAAGTAGTCTCTCAAATAGATCCATTTCTTCTCCGGTTGGGGAGCTGCCCTCCATCTCGAGCATCTGTGAACGCTCAAGGGTCCGAAGCAGTGTTTCATGCTGAATTTGGGGCCTGTGACATTAGGAGGCTGGTGAGTTTAAATAAGTTCACTTAATTCATTGAACCCATAACTATTAGTTAATGGCTTGAGTAAAGTGGTACTTGGTTTAAACCCCATAATTACCATTAAAAAAAAAAAAACTAAATTCAGGTCTCCTTTTACCTTGGTCTTATTTGAGATTCATTTAGAAAAAAGTGTAGCAATACTGATTTTTTTTTTTTCATTTTTTTCAAATAAATAAATGGAAACCCATAGAGTTCAATCTTTTTCTCAAAGTTCACATTCTCTTCCTCTTCTTAGGTGACAATGGGTGGGATTGTATTTGAGACTGAGATCACTTCTGTGGCTGAAACTGTGTCTTATCCAGTGGCATGTGTTTTT[G/T]AAAGGTGATTGCTTTGTCCATTTTAGAATGTGTAACTTTAAACCAATATGCTCCACTGTCTTGATCTTCTGATAACTATAAATCTAAACCATTGACTTCCCCTCAGGCCAAAAGAGTGGTCTCCTCCTTTGTATGATCCTCTGGCGTTTCAAACATATGGCCAGGGGGGTTTGGCCTTTCACTTGACTCTTATGAATGGTGGGTATAAACTCAGTGAAATGTTCTTGAATTAACCTCTTGACCATTTTAATGATCTTTCTGATGCTTTCTATTTTTGTAGATGACTTCAGTGGTTTGGCCACTTCCACAACATTTTCTCTAGGCTCAACAATTCCAATTTCCGCCTCTGTTGAACAATTGGGCCATCAGCCTTTAATACTGTTCTTGGATGAATGTTGGGCCACTACAACACCAATATTGAGTCCAGAGTCTCTCATTCACCCACTAATTACAAATAGCGGGTATGTGTTTGAATATTGTGTGCTTTATTCTAAAACAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44542

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
ENSDART00000044552	Nonsense	184	228	8	10
ENSDART00000112834	Nonsense	267	311	8	9
ENSDART00000132621	Nonsense	267	311	8	10
ENSDART00000148281	Nonsense	184	228	7	9

Genomic Location (Zv9):

Chromosome 2 (position 37985834)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	38300748
GRCz11	2	38283076

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATTGGTTTACCTTGTATTACAAATAGGCTCTCTCTCTCTCTTTGCAGATG[G/A]GTGTTGTTGGATGATCCTTCCCAGAGTTCTCTCTGCAGCTGTTGTGACAC

Long Flanking Sequence:

GGGTATGTGTTTGAATATTGTGTGCTTTATTCTAAAACAATTTTCAAGATTGGTGGATTAATATCTTTATTTTGGAATTGATAAACCACCTGTTTGTTTTTAAGATGTCTGGTAGACAGCAAAAAGACAAACTCTAGATTTCTGCCAAGAAACCAGCTTTCAGAGATCCGATTAGGTCTTCAAGCTTTCAGATTTGCCACAGGGCAAGATGTAAGTTGGCTTTAAATTATTATTATTATTATTATTTTTTTTTTTTTTTGGAAACCGCTTTCCTTATTACAAATGTATGTCATCTTCAGATCTACCTGCACTGCAGACTTGTGGCATGGGACCCTCAAGCTCTGGACAGTAGCAAGAAGGCATGTCAATATGACAGTGCCAGCTCACAGTATGAATATTTAATTGCTTGACATTCCTAAATTCATACAATTGAGTCTAACTTGAATGCAAATTGGTTTACCTTGTATTACAAATAGGCTCTCTCTCTCTCTTTGCAGATG[G/A]GTGTTGTTGGATGATCCTTCCCAGAGTTCTCTCTGCAGCTGTTGTGACACTAGTTGTCAAGGAACAAAGAAAAGGGAAATAACAGCAGGTGCGTTTAGTGTTTTCAATGGTATAAAGATGAACAGTTGGTCATTTTAAGTGTTAGTACTGAACATAATCTGGTTGCGTGATCTACAGGTTCCTCTGCAATATCTATGCTTGGGCCTCTGGTTATTACAAAGTGATTACAGTGTCAAATACCTTTTTAGGCATGTCCAGGTTTGTACCCTTTATTTAAATTGCTTTTGAGTTTTTATTTATTTTTTATTAATTTGTTGAATTATTTCAGATTGTTCTCCATGCAACTGGAGCTGCTTTGGACACCCTAAGGGTTGAGTTCTTTCTGTTCCTGTTAAACTGTTTATTAAAATTAATAAACTGTTCAAATGATTCTGGTGTTATTCATTTTATTGAAATAAACTTGATCCTATTTCTGCAGAGCAAAATAAGCTTAATGGTGT

Associated Phenotype:

Not determined