Busch Lab

ZMP

ENSDARG00000086721

Ensembl ID:
ENSDARG00000086721
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 7 alleles of this gene:

Allele Name Consequence Status Availability
sa34537 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa13976 Nonsense Available for shipment Available now
sa41326 Nonsense Mutation detected in F1 DNA Not yet available
sa27307 Nonsense Mutation detected in F1 DNA Not yet available
sa34538 Nonsense Mutation detected in F1 DNA Not yet available
sa41327 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa34537
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127352 Essential Splice Site 144 1399 2 11
Genomic Location (Zv9):
Chromosome 9 (position 522594)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 538053
GRCz11 9 537686
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGATCCCAGATTGTTTGGAGTATATGAAGCAGAAACAACACTTAACGG[T/A]AAGATATTTATTTAAGTTTGACTTTATTCAATGGCATCTCCCATCTAGAG
Long Flanking Sequence:
AATTGCATCTTAAAATCTGGTCACTAAATTAAATTTGTTACCAAACTGAACAGAGCAAATCATGACAACGGCATCATTTCAAGTATATTTAAAGATATTTATTGTCTGTCTAACGCCACTCTCCACACAGATCAGTGTGACGGTCAGCGTGTGGTCCAGATCCAGGATGGCCCCCTGTACAGAGTGGAAGGATTTCCCTTCTCCATCTTCTGTAGTGTTAGTGGGTTTAAAGGCTCGAGTGAGCAGGACTTCGAATTTGGTGTCAAAAAAAAAAAAGGTGAATTCAACATCATCAGTACTAAAGAGCCAGACTTTGCCTTTGCGAGGTTCTCCGACAGGGTGAAGCAAAAAGAAATTGAGATCGAGAGGATGACGGGGTCTTCGGCTCTCTTGAGGATCAAAAAAGCGATGATGGATGATGCGGGACAAATCTTCTGTCACACCCCAAGTACAGATCCCAGATTGTTTGGAGTATATGAAGCAGAAACAACACTTAACGG[T/A]AAGATATTTATTTAAGTTTGACTTTATTCAATGGCATCTCCCATCTAGAGATCTCCAGGTTTCTTTTATTCCAGCGATAACTTTATTATGCATGTCAGTTTGACTGCTTATCAATGCACATATTTAATCAGCCATGTCTCATGTCTTAAACTCAGTGCATTTAGGTGTTAAGTTCAAACTGAGCAACAGAATGGAGAAGAAAGAAGACTTACATGACTTTAAACTCGCAGTTGTTGACAAATGTGTTGGTCTGAATACTTCCAAAACTGCTAGTCAGGAGGGATTATATCTTATATCATGTTGATGGCTGAATAGACTTGATTAAATTAAACGTGATTGGATTAAAGGATTCGCTTTGAGTTGACAAAACCAAGCTAGCTGTTGTAGTTGAAAAAGCCAGCAGTAATTTCCTGCTGTAACAAGATTAAACCTCAGAGAAGGTAAGGAGGCAGGAACCATTACACATTTTAAACAACTTTAATAAGCAAATAAACACATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13976
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127352 Nonsense 252 1399 3 11
Genomic Location (Zv9):
Chromosome 9 (position 523528)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 538987
GRCz11 9 538620
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACTGAAGATKCCTCAAGTGCAGCAGTCAGACCAGGGGAAGTTCTACTGC[A/T]AAAYCGTCMAGTGGATCCAAGACCCAGATCGWAACTGGACAGAGATTGCG
Long Flanking Sequence:
AGAGAAGGTAAGGAGGCAGGAACCATTACACATTTTAAACAACTTTAATAAGCAAATAAACACATAATAAATGTGTCTTGTTCCTAGAAGTTAGTCACTAGTACTATCTTTGCTCAATAACAAATGTGCTGCTTTTGATAATTGGCAAGTTGTCAAGAAGGTTTGTTTTATTCACAGTGGTACCGGACACCCTGAAGGCCATATATTCTGGTTCTCCCACTCAGAGTCTGTTTGAGAGTGATCCACTTCAGCTTGAGTGCCAGGTCTACAGTGAGACTTTTCAACACACCCATCTGTCGGTCACCTGGTACGTCCATAGTGCAGAAGATGAGGACCCCCGACCAGTCATCACTCTGGACAGAGATCTCACTGTAAAGCCAGGAGGAGGATTTGAGGATCGCTACCATGCAGGTCTGATCAGCATGGATAAAGTAGAGGACACAACATACAGACTGAAGATGCCTCAAGTGCAGCAGTCAGACCAGGGGAAGTTCTACTGC[A/T]AAACCGTCCAGTGGATCCAAGACCCAGATCGTAACTGGACAGAGATTGCGCACAAAACCTCTACAGCATGTGATGTGGAGATCAAACCAATCGGTGAGGTTTACGTTTTCTAATTTAAAATATTTTTTCTTGTTTGAAGTTTCATGCGTTCTCCATTTAATACTTTGAAGCTCAAACAGTAGATTTCTAATCAATGCACTCTGTGACCTTGAGTGGTTTTCTGTTACCTGCGGTGGTTTGCATTTAGTTTTTGAAAATGAGGGCGTTACACAGCCTTCCCCATGTTTTACTTCTACAAAATGACAGATGCATGAGCCTGATAAATCTTAGACCTTTTAAAATGAATAGCTAAAGATATCGGACGTTTTCTTTCATTGTTTTATTGTTAGTTATCCCTGCTGTCTTTGTATCCATCCAAAAAGAGTAGTAACTTACTATAACATGAGAACTTCTTGTGTAATCTATACAGATCAGAGCCTGGTGTAATGACAGTGTCACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41326
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
ENSDART00000127352 Nonsense 404 1399 4 11
Genomic Location (Zv9):
Chromosome 9 (position 524456)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 539915
GRCz11 9 539548
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGGCAGGAGAGCATGAATGAAGACGGCACCTTCAAAAGAGTGCAAAAA[C/T]AACTGTCCAACCCTGAGACTGTGAACATCACGACTAAAGGTAATTGCTCC
Long Flanking Sequence:
TAACTTACTATAACATGAGAACTTCTTGTGTAATCTATACAGATCAGAGCCTGGTGTAATGACAGTGTCACTAAGACTGCAATCAGGAAGCTGCACAAGAGAATCTGTTTGACCTCATTATATTTCCTGTCTCAACAGAGGCCCAAGATGTAGGATCATTCAGTGTTTCCACAAAGGCCTCAAAAGGGCCCCTACAGGAGAGAGATGCACTGGACATCCGCTGCAGTGTGAAAGCACAGAATCTTCCTGGCTATTTCTATTCTGTGACGTGGATGAAGAACGGAAAGAACGTGGCCCAGATCGGGCCTTCTGGGATGCTCACCGTATTTGATAGTTATAAAGACAGAGAGAATTCAGCAGAGATGAGAGCAGTGAAAACAAGTCTAACAGACTACCTGCTGAGCATCCATTCAGCTCGAACTGAAGATCAGGGCCAATACCAGTGTGAAGTATGGCAGGAGAGCATGAATGAAGACGGCACCTTCAAAAGAGTGCAAAAA[C/T]AACTGTCCAACCCTGAGACTGTGAACATCACGACTAAAGGTAATTGCTCCTCCTCTACAATCTTAAAATACTCCACACATTGGTTTGCATCTTGTAGATAAACATTATTTGTACAATGAAAGCTTTAGCATGACCATGCGCACCCTGACACTGTCTGTTCTTGCTTGTCTGGTCAGAGAGTGATCTGGCTGTGGTCATGATGATGAAGGATGCAGTGACTGAAGGAGATGCTCTACAGGTCACCTGCTCTGTGTCGGGGTTCAAGGGTTCTTTATCAGTATCATGGCAACACAAGAAAGACTCTGTGGACTCCTTCAGTGACGTCACTAGTCTGACCCATGAGGGCGTGATGAAAGATACTGGGAAGAGGTACCAGAGTCGGCATGTTCAAACTCTCCATTCTCCAGCTGGAAACTTCACCCTGGAGATTGGTGAAGCTGGATTATCTGACAGTGGTGAATACAGGTGCATTGTGTCTGAGTGGATCATACAGAGCAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27307
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
ENSDART00000127352 Nonsense 536 1399 5 11
Genomic Location (Zv9):
Chromosome 9 (position 524989)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 452756
GRCz11 9 452389
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATCATACAGAGCAATGGCGAGATGAAGAAAACACACACCCAGTCTCAG[C/T]AAAATAAAGTTGCAGTGCGTTCAGTTGGTAAGACTACACACACACACTAA
Long Flanking Sequence:
ACTAAAGGTAATTGCTCCTCCTCTACAATCTTAAAATACTCCACACATTGGTTTGCATCTTGTAGATAAACATTATTTGTACAATGAAAGCTTTAGCATGACCATGCGCACCCTGACACTGTCTGTTCTTGCTTGTCTGGTCAGAGAGTGATCTGGCTGTGGTCATGATGATGAAGGATGCAGTGACTGAAGGAGATGCTCTACAGGTCACCTGCTCTGTGTCGGGGTTCAAGGGTTCTTTATCAGTATCATGGCAACACAAGAAAGACTCTGTGGACTCCTTCAGTGACGTCACTAGTCTGACCCATGAGGGCGTGATGAAAGATACTGGGAAGAGGTACCAGAGTCGGCATGTTCAAACTCTCCATTCTCCAGCTGGAAACTTCACCCTGGAGATTGGTGAAGCTGGATTATCTGACAGTGGTGAATACAGGTGCATTGTGTCTGAGTGGATCATACAGAGCAATGGCGAGATGAAGAAAACACACACCCAGTCTCAG[C/T]AAAATAAAGTTGCAGTGCGTTCAGTTGGTAAGACTACACACACACACTAATCTCAGGAACACAGAAACCTTCTGCATCAGTAGACGTGCAACCTGTGTCATTACTTTTCTCCTATTTTCACTGCATGTTACTGAGAGCCGAGTATGAATAATCACAGCATGTTTTCCTTTCAGAATCTCTAATGAAGGTCACCTTGATAAGTCGCGAAATAACTGCACCTATAGATTCTCCAGTCAAGTTACTGTGTATAGTTGAAAGACCTGAGGTTTCTTTGGCTGTACGCTGGATGTTTCGGTCTTTCAATTCAACTGCACAGAAGGATATCTTAACAATACACAACGCTGGAGAAATCACCTGGTTAACAGATCAGAGAAATTATCAGCTGTCAGTTCAAGAACAGCCTTCCAGCACAATATTCACTCTCATCATGCCGAGAGCCAGCAAGCGGCAAGAAGGACAGTACCAGTGCCAAGTTGATGCCTATCAAAGGGGTAGACAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34538
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
ENSDART00000127352 Nonsense 667 1399 6 11
Genomic Location (Zv9):
Chromosome 9 (position 525528)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 540987
GRCz11 9 540620
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGGTAGACAGAAAGCCATAAAGAACTCCAACTTACTAGCAGTGACTATA[C/T]AAAAACCTGGTAAATACAGCTGTATATGTTGATGTATTTATAAAGTGCAT
Long Flanking Sequence:
CACACACACTAATCTCAGGAACACAGAAACCTTCTGCATCAGTAGACGTGCAACCTGTGTCATTACTTTTCTCCTATTTTCACTGCATGTTACTGAGAGCCGAGTATGAATAATCACAGCATGTTTTCCTTTCAGAATCTCTAATGAAGGTCACCTTGATAAGTCGCGAAATAACTGCACCTATAGATTCTCCAGTCAAGTTACTGTGTATAGTTGAAAGACCTGAGGTTTCTTTGGCTGTACGCTGGATGTTTCGGTCTTTCAATTCAACTGCACAGAAGGATATCTTAACAATACACAACGCTGGAGAAATCACCTGGTTAACAGATCAGAGAAATTATCAGCTGTCAGTTCAAGAACAGCCTTCCAGCACAATATTCACTCTCATCATGCCGAGAGCCAGCAAGCGGCAAGAAGGACAGTACCAGTGCCAAGTTGATGCCTATCAAAGGGGTAGACAGAAAGCCATAAAGAACTCCAACTTACTAGCAGTGACTATA[C/T]AAAAACCTGGTAAATACAGCTGTATATGTTGATGTATTTATAAAGTGCATTCCTATTTTAAACCTATTTGTTTTCCTAACCCTACACTTATCCCAACCTGGTGTAAGTGTAAGGTGGAAATAGAAATAGAAGCCATATACAGGAGTTCTTATAGGCAAAGTAAAAAAAAAAACAAATAAAAAAAATAATCTAAACGTGTAATCAGACACTGGGTAAAAACACAGAAGAAGCAGTCCATACAGTAGACAAAGCCAATGGGTAATAAAGAGCAATAGTAGAAAAATCAGAAATAGAGGTCAAACTCAAAATAAGCAATCCAAACGGTTGATCTTCAGTTCTTAAACGAAGTTATTTTTAGCCAGTTCCCAGAAGTAAAAATGTTGATTGCCAAATTGAATGAATTACCTCTTGTATTTATTAGCATGTTTGTGTTTCTTAGTCTCTGCACAGCATAACCTGCTGAAAAATCCAGCTTAAACCAGCCTAGGCTGGTTGGCTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41327
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127352 Nonsense 889 1399 8 11
Genomic Location (Zv9):
Chromosome 9 (position 528936)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 544282
GRCz11 9 543915
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTCCATTTCTTCAGTCCAGCGGTGGGTATCTTCCAATTGACCATCCAT[A/T]GAGCCATTCAGACAGACAGGGGGCGCTACCACTGTCAAGCTCAACAGTAC
Long Flanking Sequence:
AGGTGTGTTTGATCAGGGTTGGAGCTGAAGTCTGCAGGAAGGTAAATCTCCAGGAACAGGGATAAACACCCCTAGGCTACTATTATGAAGATCTTACTCTAATAGGTAAGACTCGCAAATGGCGAATGGATCCGGAGTCTTCAGGATAGTTCCCTGCTAGAGCAAGGTTGGTGATCCCTGATTTAAAAACTCATACTAACCCTCTGTTGTAATTGTCTTCTGTTTCAGCCAGTGATTTCAGAATGAATAAAGCTGACACTGAGCTGAATGTTAAAGAGGGAGAGCCGCTGATGTTGAATTGCTCAGTGGATGGTTCTGGCTCTGACTCCACACTTCGCTACTCTCTTACCTGGTTCTTTACCCAAGATCAGTCCGCCAGTGTGACACTTCTGACGTACTTTTATGATGGCCGCCTGATATACAGCAGCTATGACCCAGAGCTTGCAGGACGACTCCATTTCTTCAGTCCAGCGGTGGGTATCTTCCAATTGACCATCCAT[A/T]GAGCCATTCAGACAGACAGGGGGCGCTACCACTGTCAAGCTCAACAGTACCAGGTGGACTGTAAAGGCCACTGGTCAGCTAAGGCAAGCGATAAGTCCGGTTACACCAATGTTGCTGTTCAGCTTATAGGTGAGTACTTCATATTTAAAAAATCTGAAAAATAAAGAAAATCTCTGATAATAACTGAAAGTCCTCTATGATATTTAGAGAACAAACTGAGCGTGCGCAAAGAGGACCAAAGCCGCAGTGTTACCAATCTGCAAGAGGGATTTACCATTGACTGCATCATTGACTCGCGGTCCAGTGATGCATCTGTGTTTGAGGTGACTTGGTCTAAAGGTCTGGAAAATGAGCGACCCATCATCATCTTCAATGCCAGTCGTGATGGAACTCTACACAGCGCAATCAATGATAAAGATCTGGTCTTCAAACGCCCAGGTGCCAAGCAATACATGCTGACCGTGCCAAACACCAACCTCGCTGATTCTGGCCTTTACCAT
Associated Phenotype:
Not determined