ZMP

zgc:91849

Ensembl ID:

ENSDARG00000014323

ZFIN ID:

ZDB-GENE-040718-438

Description:

hypothetical protein LOC572021 [Source:RefSeq peptide;Acc:NP_001002687]

Human Orthologues:

CD101, IGSF3, IGSF8, PTGFRN

Human Descriptions:

CD101 molecule [Source:HGNC Symbol;Acc:5949]
immunoglobulin superfamily, member 3 [Source:HGNC Symbol;Acc:5950]
immunoglobulin superfamily, member 8 [Source:HGNC Symbol;Acc:17813]
prostaglandin F2 receptor negative regulator [Source:HGNC Symbol;Acc:9601]

Mouse Orthologues:

Cd101, Igsf3, Igsf8, Ptgfrn

Mouse Descriptions:

CD101 antigen Gene [Source:MGI Symbol;Acc:MGI:2685862]
immunoglobulin superfamily, member 3 Gene [Source:MGI Symbol;Acc:MGI:1926158]
immunoglobulin superfamily, member 8 Gene [Source:MGI Symbol;Acc:MGI:2154090]
prostaglandin F2 receptor negative regulator Gene [Source:MGI Symbol;Acc:MGI:1277114]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa34532	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa7166	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa34532

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
ENSDART00000002954	Essential Splice Site	23	986	None	11
ENSDART00000142964	Essential Splice Site	23	986	None	9

Genomic Location (Zv9):

Chromosome 9 (position 27710)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	456800
GRCz11	9	456433

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGGCTGTGGCGCTTGTTTCTGCTGTGTCTCACAGGACTCCTGCGCTGGGG[T/C]GAGTCTCAATGTTTTTATTATATCGCGAAAATATATCTGATTTTTATTGA

Long Flanking Sequence:

AATTGGCTTGAGGTTTAATGTTGACTTTTTAATGAATAAATGTTGAATTTGGTGTATACAAACGTACAAACAGGTATGAGAAATACAGGTGTCTGTAAAGAATATACCTGTGAGGAACATGAAAATATGAGTCCTTCAGCCTGTCATTAAAAACAAAAGGTAAATGTAACGTTACAATTAATGTAATATGTGGTAATAAAGCAAAAATGGTGGCATAGCCTATAGCTCTTCTGTTAAAATATAACTTTAAGATTAGATTCAGAGATTAAATCAACTGTGAGTTTTCCTGCCTCTCCGGCTGGGTTTAGTGTGATGTCACCGGCTCTTGCTTCAGAGAAAATGAATCAGGTTCAGCCTGGCTCCTGTCGAAACCCGCATTATCATGTAGAGAGGAAATAAGAGAGTAAGAGAAAAGGATCTGCTCATTTAAGGATGGTGGACTGTGGCTTTCGGCTGTGGCGCTTGTTTCTGCTGTGTCTCACAGGACTCCTGCGCTGGGG[T/C]GAGTCTCAATGTTTTTATTATATCGCGAAAATATATCTGATTTTTATTGACGCTATTTTAAACACACACCGTTTCTGTGTGAACTGCTGTCTTTGATTATCACGAACACAATGTAGAAACATGTTGGATGGTTAAAGTGTTAGCTCATTCAAAAAATCTACCTGTTGAATGATCTCCGTCAGTTAGCAAACATAACCAACTAGCCGAATGACCGTCAAATATTATTTAACAATATCGTAAAAGTTACAGGTGATCTTTACTACTTGTGAATTATATTATATCACATCTAAAGCTAAACAATAGATTCGTTCTGTATTTGTGTTAAAAATAAAATATCCACGTCGGCTATATTCAGTTTGTTGTTTCACGAAACAAACCCTCAACCGGGTGAACAGGATCCTGAAACAAAGCGAGACAATTCCCAGCGCAAACAGGTTGAAACAAGACATACACAGGTCATCATGATGTAGGAGAGAAAGAGTTCTTGGGTAATCTAATAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7166

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
ENSDART00000002954	Essential Splice Site	285	986	3	11
ENSDART00000142964	Essential Splice Site	285	986	3	9

Genomic Location (Zv9):

Chromosome 9 (position 30779)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	453731
GRCz11	9	453364

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ATTGCRCACAAAACCTCTACAGCATGTGATGTGGAGATCAAACCAATCGG[T/C]GAGGTTTASATTTTMTAATTTAACCCAGGGGTTNNNNNCTAACCTAACCT

Long Flanking Sequence:

TGCACTGCCCAACCTAAGATCATGGTCATGTTGAGACTATCAGTATGTAGGTACCCTCACACTGCTTGTGTTTTATCGACAGTGATACCGGACACGCTGACGGCTTCGTTTTCTGGTTCTCCCTCTCAGAGTCTGTTTGAGAGTGATCCACTTCAGCTTGAGTGCCAGGTCTACAGTGAGACTTTTCAACACACCCATCTGTCGGTCACCTGGTACGTCCATAGTGGAGGAGATGAGGACCCCCGACCAGTCATTACTCTGGACAGAGATCTCACTATAAAGCCAGGAGGAGGATTTGAGGATCGCTACCATGCAGGTCTGATCAGCATGGATAAAGTGGAGGACACAACATACAGACTGAAGATGCCTCAAGTGCAGCAGTCAGACCAGGGGAAGTTCTACTGCCATGTAGTTCAGTGGATTCAAGACCCAGACCGAACCTGGACAGAAATTGCGCACAAAACCTCTACAGCATGTGATGTGGAGATCAAACCAATCGG[T/C]GAGGTTTAGATTTTATAATTTAACCCAGGGGTTCTAACCTAACCTAACCTGTTTGACCTCATATTTCCTGTCTCAATAGTGGCCACTGATGTAGGATCGTTCAGTGTTTATATGAAGGCCTCAAAAGAGTCTCTTCAAGAGGGAGATGCACTAGACATCCGCTGCAGTGTGAAAGCACAGAATCTTCCTGGCTATTTCTATTCTGTGACGTGGATGAAGAACGGGAAGAACGTGGCCCAGATCGGACTTTCTGGGATGCTCACCGTATTTGATAGTTATAAAGACAGAGAGAATTCAGCAGAGATGAGAGCAGTGAAAACAAGTCTAACAGACTACCTGCTGACCATCCATTCAGCTCGAACTGAAGATCAGGGCCAATACCAGTGTGAAGTATGGCAGGAGAGCATGAATGAAGACGGCACCTTCAAAAGAGTGCAAAAACAACTGTCCAACCCCGAGACTGTGAACATCACGACTAAAGGTAATTGCTCCTCCTCTAC

Associated Phenotype:

Not determined