Busch Lab

ZMP

PITPNM2

Ensembl ID:
ENSDARG00000041100
Description:
phosphatidylinositol transfer protein, membrane-associated 2 [Source:HGNC Symbol;Acc:21044]
Human Orthologue:
PITPNM2
Human Description:
phosphatidylinositol transfer protein, membrane-associated 2 [Source:HGNC Symbol;Acc:21044]
Mouse Orthologue:
Pitpnm2
Mouse Description:
phosphatidylinositol transfer protein, membrane-associated 2 Gene [Source:MGI Symbol;Acc:MGI:1336192

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa38815 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa6138 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa7288 Nonsense Mutation detected in F1 DNA Not yet available
sa9834 Nonsense Available for shipment Available now
sa41742 Nonsense Mutation detected in F1 DNA Not yet available
sa7289 Nonsense Mutation detected in F1 DNA Not yet available
sa17312 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa38815
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
ENSDART00000060194 Essential Splice Site 27 1285 2 32
Genomic Location (Zv9):
Chromosome 10 (position 46421877)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150191.1 11751
GRCz11 KN150191.1 11751
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATGCATTATAAAGAAGCTGTGTGTGTGTGTGTGTGTGTGTGTCCATC[T/A]GCAGAAGAAGAGTCGTGAGGAGAGCGAGGGCGAGGGCAGCGGTGTGGAGA
Long Flanking Sequence:
TACTGATAATGAAAATCTACTGATGCATGACAGGCTTATGATAGATAAGAAGAGCTACTGATGATGAAGGGGAGGAGCAACTTATGCGTGAGATGGGAGGAGCTACTGATGATGAAGGGAAACTGATGATAAATGGGGAGGAGCTATTGATGTATGGGAGGGGCTACTGGTAAAGGGGAGGAGCTGTTAGTCGCTGAGCTTGGATTAGTTTATTTACTGAACTGGACTGAGCTGTGTTAGTGGTTCTGCTGGTGAGTGTGGTTATGTTCATCATAGTTTGCTGGTTTATTTCACTGATTCTGCTGATGATGAATGGTCTGAATGATCCTACAGTGAAACACTGCTCATTTGGGACGACACTAAATACCACACGACACGGTTGAGTGTATGAGTCCGCAGTATATAAGTGTTCAGTGTGTCATGTGTGACGCAGCCCTGGTGTGTGTTGTGTAAATGCATTATAAAGAAGCTGTGTGTGTGTGTGTGTGTGTGTGTCCATC[T/A]GCAGAAGAAGAGTCGTGAGGAGAGCGAGGGCGAGGGCAGCGGTGTGGAGATCCTGGAGAACCGGCCCTACACCGACGGCCCTGGCGGATCCGGACAATACACACGCAAGGTGTACCACATCGGCCAGCACATCCCCAGCTGGTTCCGCTCCATCCTGCCCAAAGCAGCGCTGCGCGTGGAGGAGGAGTCCTGGAACGCATACCCATACACACGCACACGGTCAGTATGAGCACACACACACACACACACACACGGTCAGCTCATTCTGCAGGACCCACAACACATTTAGAAAGGGTCAGTTCACACACAAATGATGTTCAGCCATGCAGACCGGTCACCATTGACTTCTACAGTAACAAAAACAATACAGAAGTCAATGGTGACCGGTCTCCAGCATTCTTCACAGGATCTTCTTTAGTGTTCAACAGATGAAGGAAACTCATGAAGGTTTGAAACAAGCATGTCTGTATGATCATTTGTGTGTGAACTGACCTAAATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6138
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
ENSDART00000060194 Essential Splice Site 552 1285 13 32
Genomic Location (Zv9):
Chromosome 10 (position 46437860)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150191.1 27734
GRCz11 KN150191.1 27734
KASP Assay ID:
554-3657.1 (used for ordering genotyping assays)
KASP Sequence:
AATCCAYCACCTTCCTGCACGATGGTGMCATSAGAAATGAAGTCAAACAG[G/A]TGRGCAATGAGTGAAGCTGCTGCTGCTGCNNNTCTGCATATTAACCGCAR
Long Flanking Sequence:
ACCCTCAAAACACACAGACATAAAGAGTCAGCGTACGCTTCTCAACTATAGTGAGCTTTGTTTTCCTGCAGTGCATGCTGGGAGCTATGGGTGAATGTGGTATGAGTCTTTTACCATCCACTGCAGCCAAAACAAGTAAGACATCTCTCAGCACTGTTAAGATAGACACGCTGATCATTGATCTCTGTCTCTAGAGTGATTCAGATGCTCAATGTGTTTTAAAAATAAGCACAGCTGAGGTCCATTCTCCTAAAAACACTGAATTATGTTTCTTAATGATCAACCATCATTTAAATATAGTTTGCAGAGTCAGGCATAATCTCTTATATTTCTCACCAAGAGTAAGAATCAATACAGAATCAGTCAACCTGATCATATTTACTCTCTTTATTCTTATCATAACAAGCAAAGACTAATCAACACTAGAATTTGAGTCAAAGAGCCCAAGTAAATCCACCACCTTCCTGCACGATGGTGACATCAGAAATGAAGTCAAACAG[G/A]TGGGCAATGAGTGAAGCTGCTGCTGCTGCTCTTCTGCATATTAACCGCAGGTGTTCATCATCAGCACTTAATTAACCCCCTCATTGTCTCGTTAACTTGAACTCTGCTGTTGAGTAAATTTAACTCCATTTAGAGAGAGCAAATACTCTCTGAACTGAGCAACTTTTACTGTGAGGAGTTTGCTGTGGGCTGGAGATTAGCTCTTGTCATTGGGGGGACGTACATCCCTAGAGCGCATGCATAGAGCAGCACACATTCACACTTTTAAAAACATGAATAAAATACCCAATAATGTCAAATAAACACTTAATAATACAAATAACAATCCCGCTCCATGCTGCAAGAGTCAGTTACCATGATTGTACTGCAGTCGGGCTTTGAGCAGGTAGAGAGGTGTGGAGAGGTGTGTGACGCAGTTCACTGGTTTGCAAAACTGATTGGCCAAATGCAAAACTATTTTGAGTGATTGGCACTGCCGTGGGTAATAGTATAACGGTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7288
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
ENSDART00000060194 Nonsense 558 1285 14 32
Genomic Location (Zv9):
Chromosome 10 (position 46440385)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150191.1 30259
GRCz11 KN150191.1 30259
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTCGCTGTTTCCATCRCAGKTYATGCRCATCTCWGCGTTTCCATCAAT[C/T]GATTTTCATRTTGTGTGTGTTGGAGACAAAAAATACCCACACACTTRCAG
Long Flanking Sequence:
TTCAGCTCATGCTGATCTGCTCTCTCATTGGCTGCAGCTCGTCACTACATCTGACCACACGTGGGGTTGAGTCGGCCGACTGCTCTGGAATATTCAGCATGCTGAATGTTGGATTTCCGTCTGCGAGGTGTCGGCGACGCGTCAGCGAGCCTCGTTGATGCGTTGTTCAGTAGTTCACACATAAAGAGCGGCGAGCGCCGAGCACCCGCAGATTTCTTCCCGATCACAGCCCGATCTGTCGGCGAGCTCGTTAACTTCCACATCGGGCTCAAATCAGGCTTAAAATCCGTTAGTGTGAACTAGGCATAAGGAGATTTAGATTGACCAAATCAACATGTCAGATGTTCTACAGTGTGCTCAGCCTGCTGGATTATCCATTTACACACGTGTTCATCATCATACCATCTCTCATAACACAATCACATCACCTTTAACTCGCATACTGGAATTTATTCGCTGTTTCCATCGCAGGTCATGCGCATCTCAGCGTTTCCATCAAT[C/T]GATTTTCATATTGTGTGTGTTGGAGACAAAAAATACCCACACACTTACAGATTTGCTCTGAGTACAGATTCACTGATACACACTTTACAACCACACATGACACTTCTACAGCTGCTTGGGAGTTTTGCACCAAAAAGACCTTCATAAGTGTGTAACACCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTCCTGCAGGACAGTGAGCTGTTGTCTCCAGGCATCATCATCAACTGTAGCGGCTCTGGCGGCAGCAGTAACAGCGCTCTGTCTCTAGAGGGCAGCCGTCACCTGAGCCGCAGCAACATCGACATCCCGCGCTGCAGCGCTGCAGACGAACACAAGAAGCAGCTGCCGCGCAAACGCAGCGACTCGTCAACGTACGAGATCGACACCATCAAACAACACCAGGCCTTCCTCAGCAGGTGCGCGCACACACACACACACACACACGCACACACACACACACACGCACACACATACACACACACAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9834
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060194 Nonsense 579 1285 14 32
Genomic Location (Zv9):
Chromosome 10 (position 46440450)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150191.1 30324
GRCz11 KN150191.1 30324
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGTTGGAGACAAAAAATACCCACACACTTRCAGATTTGCTCTGAGTA[C/A]AGATTCACTGATACACACTTYACAACCACACAKGACACTTCTACAGCTGC
Long Flanking Sequence:
GTTGAGTCGGCCGACTGCTCTGGAATATTCAGCATGCTGAATGTTGGATTTCCGTCTGCGAGGTGTCGGCGACGCGTCAGCGAGCCTCGTTGATGCGTTGTTCAGTAGTTCACACATAAAGAGCGGCGAGCGCCGAGCACCCGCAGATTTCTTCCCGATCACAGCCCGATCTGTCGGCGAGCTCGTTAACTTCCACATCGGGCTCAAATCAGGCTTAAAATCCGTTAGTGTGAACTAGGCATAAGGAGATTTAGATTGACCAAATCAACATGTCAGATGTTCTACAGTGTGCTCAGCCTGCTGGATTATCCATTTACACACGTGTTCATCATCATACCATCTCTCATAACACAATCACATCACCTTTAACTCGCATACTGGAATTTATTCGCTGTTTCCATCGCAGGTCATGCGCATCTCAGCGTTTCCATCAATCGATTTTCATATTGTGTGTGTTGGAGACAAAAAATACCCACACACTTACAGATTTGCTCTGAGTA[C/A]AGATTCACTGATACACACTTTACAACCACACATGACACTTCTACAGCTGCTTGGGAGTTTTGCACCAAAAAGACCTTCATAAGTGTGTAACACCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTCCTGCAGGACAGTGAGCTGTTGTCTCCAGGCATCATCATCAACTGTAGCGGCTCTGGCGGCAGCAGTAACAGCGCTCTGTCTCTAGAGGGCAGCCGTCACCTGAGCCGCAGCAACATCGACATCCCGCGCTGCAGCGCTGCAGACGAACACAAGAAGCAGCTGCCGCGCAAACGCAGCGACTCGTCAACGTACGAGATCGACACCATCAAACAACACCAGGCCTTCCTCAGCAGGTGCGCGCACACACACACACACACACACGCACACACACACACACACGCACACACATACACACACACACACACAACAGAAGCAGGAGGAGTAGTGTAAAATAACCTTGTGTGTGTGTGTGTGTGTGTGTGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41742
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
ENSDART00000060194 Nonsense 597 1285 14 32
Genomic Location (Zv9):
Chromosome 10 (position 46440504)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150191.1 30378
GRCz11 KN150191.1 30378
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCACTGATACACACTTTACAACCACACATGACACTTCTACAGCTGCTTG[G/A]GAGTTTTGCACCAAAAAGACCTTCATAAGTGTGTAACACCTGTGTGTGTG
Long Flanking Sequence:
TCTGCGAGGTGTCGGCGACGCGTCAGCGAGCCTCGTTGATGCGTTGTTCAGTAGTTCACACATAAAGAGCGGCGAGCGCCGAGCACCCGCAGATTTCTTCCCGATCACAGCCCGATCTGTCGGCGAGCTCGTTAACTTCCACATCGGGCTCAAATCAGGCTTAAAATCCGTTAGTGTGAACTAGGCATAAGGAGATTTAGATTGACCAAATCAACATGTCAGATGTTCTACAGTGTGCTCAGCCTGCTGGATTATCCATTTACACACGTGTTCATCATCATACCATCTCTCATAACACAATCACATCACCTTTAACTCGCATACTGGAATTTATTCGCTGTTTCCATCGCAGGTCATGCGCATCTCAGCGTTTCCATCAATCGATTTTCATATTGTGTGTGTTGGAGACAAAAAATACCCACACACTTACAGATTTGCTCTGAGTACAGATTCACTGATACACACTTTACAACCACACATGACACTTCTACAGCTGCTTG[G/A]GAGTTTTGCACCAAAAAGACCTTCATAAGTGTGTAACACCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTCCTGCAGGACAGTGAGCTGTTGTCTCCAGGCATCATCATCAACTGTAGCGGCTCTGGCGGCAGCAGTAACAGCGCTCTGTCTCTAGAGGGCAGCCGTCACCTGAGCCGCAGCAACATCGACATCCCGCGCTGCAGCGCTGCAGACGAACACAAGAAGCAGCTGCCGCGCAAACGCAGCGACTCGTCAACGTACGAGATCGACACCATCAAACAACACCAGGCCTTCCTCAGCAGGTGCGCGCACACACACACACACACACACGCACACACACACACACACGCACACACATACACACACACACACACAACAGAAGCAGGAGGAGTAGTGTAAAATAACCTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7289
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060194 Nonsense 877 1285 22 32
Genomic Location (Zv9):
Chromosome 10 (position 46445195)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150191.1 35069
GRCz11 KN150191.1 35069
KASP Assay ID:
554-5138.1 (used for ordering genotyping assays)
KASP Sequence:
AAACGCAGCTTCACGTCTCGTTGTCAGATCAGTGTGTGAGCCGCWGGAGY[T/A]GACGGCGTCCCSCTMCTGTAGAGCTAACGTTACCCTAATTACCCYAGTGA
Long Flanking Sequence:
ATCTGCTTTTCCCTTCACTCATGTTGAATCAGATCAGCCTTTTACAAATGAAGCATTGTGAGTGTGTGTAGCGCTGGGTTGGGGAGCATGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGACCTGTGCTCTGCTCTCCACAGCGGACGTCATGCAGTCTCACGGCCTCATGTTTTCCGAGCACTCGAACCCGTCGTCTCCGGCGGCCATTCCAGCGTTTCGAGGAGCGCGGCGGGCGAGCGAGACCAGCATCGCCAGCCAGGTGTCAGGACTCGCAGACAGCTACACCGCTAGCAACATCGCTAACAGTGAGTCTCACACACACACACACTCAATCACACACTTTCACACACACACTTCAGCAGTTGCACACACATACAGTAATGCAGTGTGTGCGTGTGTGTGTGATGGTGTAGAGGAAACGCAGCTTCACGTCTCGTTGTCAGATCAGTGTGTGAGCCGCTGGAGT[T/A]GACGGCGTCCCCCTCCTGTAGAGCTAACGTTACCCTAATTACCCCAGTGAAGCCTTACATGTCTGAACACTGGTGTCTTGAAGAAGATCTAGTCTCATATTATGTGCTGTGGTGACGGCACGGTGGCGCAGTGGTCAGCCCTGTGGCCTCACAGCAAGAGGGTCTCTGGTTTGAGTCTCGGCTGGGTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTGGTGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCGCTATAGGGGAACTGATCAACTACACTGGCCATAGTGTATGAGTGTGTGTGTGAGAATGAGTGTGTATGGGTGTTTCCCAGTACTGGGTTGCAGCTAGAAGGGCATCCGGTGTGTGTGAGTGAGTGTGTGAGTGTGTGAGTGAGTGAGTGTGTGATTGAGTGAGTGAGTGTGTGAGTGAGTGAGTGTGTGAGTGAGTGTGTGAGTGAATGAGTGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17312
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:
C > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060194 Essential Splice Site 886 1285 22 32
Genomic Location (Zv9):
Chromosome 10 (position 46445223)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150191.1 35097
GRCz11 KN150191.1 35097
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGTGTGTGAGCCGCTGGAGYTGACGGCGTCCCSCTMCTGTAGAGCTAA[C/A]GTYACCCTAATTACCCYAGTGAAGCCTTACATGTCTGAACACTGGTGTCT
Long Flanking Sequence:
TCAGATCAGCCTTTTACAAATGAAGCATTGTGAGTGTGTGTAGCGCTGGGTTGGGGAGCATGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGACCTGTGCTCTGCTCTCCACAGCGGACGTCATGCAGTCTCACGGCCTCATGTTTTCCGAGCACTCGAACCCGTCGTCTCCGGCGGCCATTCCAGCGTTTCGAGGAGCGCGGCGGGCGAGCGAGACCAGCATCGCCAGCCAGGTGTCAGGACTCGCAGACAGCTACACCGCTAGCAACATCGCTAACAGTGAGTCTCACACACACACACACTCAATCACACACTTTCACACACACACTTCAGCAGTTGCACACACATACAGTAATGCAGTGTGTGCGTGTGTGTGTGATGGTGTAGAGGAAACGCAGCTTCACGTCTCGTTGTCAGATCAGTGTGTGAGCCGCTGGAGTTGACGGCGTCCCCCTCCTGTAGAGCTAA[C/A]GTTACCCTAATTACCCCAGTGAAGCCTTACATGTCTGAACACTGGTGTCTTGAAGAAGATCTAGTCTCATATTATGTGCTGTGGTGACGGCACGGTGGCGCAGTGGTCAGCCCTGTGGCCTCACAGCAAGAGGGTCTCTGGTTTGAGTCTCGGCTGGGTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTGGTGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCGCTATAGGGGAACTGATCAACTACACTGGCCATAGTGTATGAGTGTGTGTGTGAGAATGAGTGTGTATGGGTGTTTCCCAGTACTGGGTTGCAGCTAGAAGGGCATCCGGTGTGTGTGAGTGAGTGTGTGAGTGTGTGAGTGAGTGAGTGTGTGATTGAGTGAGTGAGTGTGTGAGTGAGTGAGTGTGTGAGTGAGTGTGTGAGTGAATGAGTGTGTGAGTGAGCGAGTGAGTGAGTGAGTGAGTG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27691
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060194 Essential Splice Site 951 1285 24 32
Genomic Location (Zv9):
Chromosome 10 (position 46446778)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150191.1 36652
GRCz11 KN150191.1 36652
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGTGCAGATTCATTTCACATAGTCCCCCATTGCTTCAATCATACAGG[C/A]ACATTATTCACAGTATCTACAACTAGAAAGTGTGTGTGTGTGTGTGTGTG
Long Flanking Sequence:
AATAAGCAGGACGGTGACTCTAAGAGTTGCAGAACTCTAGCTCCTCTGGTATTATAGCCTACTCTTGTGTTAACCCAGAATGAAGCGAGTGCATTGATACCTATTCTGGCCAATCACAGACGTTCCTGTTGAGCTCTTGAGCACACAGCCAATCAGCTCATGCTGATATGCTCTCTCATTGGCTGCAGCTCATCACTACATGTGACCGCACGTAGGCTCGAGTCGGCCGTCTGCTCTGGAATTTTCAGCATGCTAGATATTGGATTTCCATCTGTGAGGTGTCGGCGACACTTCAGCGAGCCTCTTTGATGCCTTGCTCAGTAGTTCACACATAAAGACTGCCGAGCACCAACAGCCTGATCTGTCTGTGAGCTCGTTAACTTCCAGATCGGGTTCAAATCAGGCTTAAATTCCTGTAGTGTGAACAAGGCTTTATTCAGCACCGCTCACTCCTGTGCAGATTCATTTCACATAGTCCCCCATTGCTTCAATCATACAGG[C/A]ACATTATTCACAGTATCTACAACTAGAAAGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGCAGGTGATGAGACATGAGAACTCCAGCATCCTGGAGCTGGATGGGAAGGAGGTGTCAGAGTTCACTCCGTCCAAACCGCGAGAGAAGTGGATAAGGAAGAGGACGCATGTGAAGATCAGGGTGAGCCACACTGCTGCTCCGCTAACAGATGCATTGTGGGATTGAAGCTCACATTGTGTGTGTGTGTGTGTTGCAGAATGTGACGGCGAACCATCGTGTCAATGATGCTGTGTTCACAGAGGACGGAAATCAGGTGGTCACGGGACGCTTCATGTACGGCCCGCTGGACATGGTCACGCTGACCGGAGAGAAGGTCAGAAAAAACACACAGAATGGCATGCAGGAAACACACAAACATGCAGACGACACACAATCATGCAGACGACACACAATCTTGCAGACGAGACACAAACATGCAGACGAG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27692
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060194 Nonsense 1189 1285 32 32
Genomic Location (Zv9):
Chromosome 10 (position 46451826)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150191.1 41700
GRCz11 KN150191.1 41700
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCAGTTCATCACGGACGGGTACGCGTCTCACCTGTCCCAGCTGGAGTA[T/A]AATCAGAGATCCAGACCTGCCAAGACCGGCAGCACCCGCATGGTTCTGCG
Long Flanking Sequence:
GTGTGTTTCTGGTCTGCTGTAGATGTTGTGTAATGTCGATCTGCTGTTCTCAGGCTCATATGAAGATCTTCGCTGCTTACGGCTCCACCAAGGACATCTCTGTGTACACGTCACTCGGCCTGCCGCCGGCACAGATCTACATCGTGGGCCGACCCACCAAGAAGATGCAGCACCAATGCCAGGTACACCAACAACATCATCATTGTCATTTTAGACATCATGCAGAACACATGCAGACATGCAGACAGCGCGCAAAAAACATCCAGACAGCATGCAGAAAACATGCAGATAACAAATAAACATGCAGAGAACACACAGAAAACCTGCAGAGAACACACAGAAAACATGCAAACATGCAGATAACACAGAAAACATACAGAGAACAGAAAACGTAGACGACACAGAAAACATGCAGATGTTGAGAGTGTTGTGTGTGTGTGTGTGTGTATTCTGCAGTTCATCACGGACGGGTACGCGTCTCACCTGTCCCAGCTGGAGTA[T/A]AATCAGAGATCCAGACCTGCCAAGACCGGCAGCACCCGCATGGTTCTGCGCAAGGGCAGCTTCGGGCTGGGCAGCGGAGACTTCCTGCGGAAGAGGAACCACCTGCTGCGCACCATCTCCAGCCAGCCCTCGCCCACCACACCACTGCCGGCGGCCCGACCCGAGCGCGCCCAGAGCCAGTCGGAGTGTGACCGCGAGCGGGCCGAGCGAGCCCAGAGGAGCATGAGCATCGCCGCCGGCTGCTGGGGGCGGAGCACCAAACTGGAGGGTGGAGCCTTGAGCCCCAAATAGGATCCACCCACCGCCCTTCCCTGAGTTCCGCAGGATCCGGACAGTGTGACCGCAGACTCTCACCACTGCTGCATGGAGATCTTCATTTCAGTCCGGCACACACACCTGCTGCAGGAGCCCCGAGCGGGCCAGGGGCTGCTGACCAATCACTGAGTGTGTGTGTGCGGACTCTCCTCACCTGTGTGTGTATTTACATGTGTGTGTGACTC
Associated Phenotype:
Not determined