Busch Lab

ZMP

NEO1 (2 of 2)

Ensembl ID:
ENSDARG00000075100
Description:
neogenin 1 [Source:HGNC Symbol;Acc:7754]
Human Orthologue:
NEO1
Human Description:
neogenin 1 [Source:HGNC Symbol;Acc:7754]
Mouse Orthologue:
Neo1
Mouse Description:
neogenin Gene [Source:MGI Symbol;Acc:MGI:1097159]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa9577 Nonsense Available for shipment Available now
sa44213 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39468 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9577
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
ENSDART00000115280 Nonsense 359 1413 6 30
Genomic Location (Zv9):
Chromosome 25 (position 2898217)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 2805373
GRCz11 25 2931090
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGTGACGTCACCGGCTCTCCACCTCCGACTGTCAAGTGGATGAAGGAT[G/T]GAGACACGGTCATTCCTAGTGATTATTTCAGGATAGTGGTACGTCTGTGC
Long Flanking Sequence:
ATGTGCTACTGTAATTAGGTATTCAAAGACTGATTGTAGGTCATAAGTCAAATTTTTATTATGTGCAGGATTTTTACAGGTATATTCCAAATGATGAGATATAACCCATCCCTACTTGACACACTTTTGTCAGTCATCAATAATAAAACTAGCAAAACCGCAGGTATTTTTAGCATCTCTATATTCTCGTTCTTCATCTGCTCTTCCCAGATTGCACAAGTAATAAACATCAGCTCGGTCCATGATGGATGCGGTTGCCATAGGAACAGAGAGGAGAAGCACTTTACCTGCCTGTACCTGTCCCAGCACATGTTGTTGTTTTCTTCGTCTTGTAAACCCTGTGACCTCTTCTCAAGTTTCTTCTTGTTGTTGTTTGTCTTGCAGTTCCTCCACGCTTCCTGACCAGGCCTTCAAACACGTACGCGCAGGAGTCCATGGACATCATCTTCGAGTGTGACGTCACCGGCTCTCCACCTCCGACTGTCAAGTGGATGAAGGAT[G/T]GAGACACGGTCATTCCTAGTGATTATTTCAGGATAGTGGTACGTCTGTGCTCCTCACTGCTTCATATGAGATTTAAACATGCATAAGACTGAGGCTGCTTTCACACCTGTGAATCGATTCAGTTGTTCTGAAACAGAGATTACAAATGTTACATTGTTGCTCTTTGCTCTTGGAGCGGTTCGCTTTCACACTGCAAAGTTTCTAATCGGACCAAAAGCAAGTCACGTGCGAGTAAACTCTCCTCACATTGGTCAGAGTGTCAGGGTTTATTTTGCAGCGTCCCGCTCAGCTGTCAGGAGAGGTGGTGGTTTGGTGGTGATTGACAGGGTGCGCGCGCGTGACATGTCTGAGGAGAGATGCGGTGGGGTGGGGTGAGAAGGGTGCGCGACCATGCCTATTTGAGGACCGGGAGGGAGACGCAAGATTACCGGGAGATCATCACTCATTTGCGGGCATCCGGAGACTCGCGAAACTTCCCGCCATACTCATAATTCTCTCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44213
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
ENSDART00000115280 Essential Splice Site 800 1413 15 30
Genomic Location (Zv9):
Chromosome 25 (position 2946133)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 2854242
GRCz11 25 2980195
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGTCACTCTGGACTACAAGCAGCGCTTCTACAGCATTGATAACCTCGG[T/C]GAGCATCTGCACTGCCTTTAACCCTTTCACTCGTATGATCACTGAGGGAT
Long Flanking Sequence:
TTCTGATGCGCGGTTTGAACTGCAGCAGATCATCTTGACCATGTCTACATGCTTAAATGCGATGAGTTGCTGCCGTGTGATTGGCTGATTAGAAATTTCTGTTAACGAGTAGTTGGACAGGTGTACCTAATAAAGTGGCCGGTAAGTGTATATATTGTAGTGTGTGTATATGTATGTTTATATATTGGTATAAATATATCATTATCAGTTTTCTTGCTATTTTTAGTCATTAAACTTTTTTTTTCTTTTTTGTTTTTTTATGTATTGAGGTTAAAAACTATTAAACATTTCCTTCGTGTTCCAGAGTCTCAGGTTCCAGGAGTCCCGAGTTCTCTTCACGTTCGTCCGCTGGTGAACCGGATCGTGGTGAGCTGGACTCCTCCTGAAAACCAGGAGGTTTTAGTGCGCGGCTATAAGATCGGTTATGGCATCGGCAGTCCGCACGCACACACCGTCACTCTGGACTACAAGCAGCGCTTCTACAGCATTGATAACCTCGG[T/C]GAGCATCTGCACTGCCTTTAACCCTTTCACTCGTATGATCACTGAGGGATAGAACGTGGAGCACACATCATTAATCACAATTAATCTGTTTTCTCACACAAATAAAGATTATTTTAGGTTTCAAATACACATAGCTACTAGCTAAACAACATTTAAGGTTTGTAAAATACACGCAGATGTCTATGGGAGATGGCAATAATTATTATTTTTAATAATTTATTCTTTTTTATTATTATTATAAACATAATCAGTTGTATGTTTTGAATACCAGTTTAAAATATTTTAGGAATATTTTAGTTTCTTTTCAATTGTAGAATTGTAAAGTAAATTAATAAATAATATTTAAGATCATAAAATATTTATAAAATAATTAGTTTTTTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATAATAGTAATAATAACGGTTTGTATTGTTATTTTTTGTTATTGTTATTTTTATGAAAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39468
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
ENSDART00000115280 Nonsense 1006 1413 20 30
Genomic Location (Zv9):
Chromosome 25 (position 2961029)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 2869239
GRCz11 25 2995092
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGGTGGAGCCGGTGGTGGGGAACCGACTGACCCATCAGATTCAGGGCT[T/A]GACTCTGGACACCAGCTACTTCTTCAAGATCCAGGCCAGAAACTCTAAAG
Long Flanking Sequence:
TTTGTGTGAAAGAATGCACAAGTATCAGAGCGTGTGTGAAATGTTTGCTGGCATCCCGTCGGGTTGGTCAGTTTCTGCTGCAATGACTGTTAAGACGAGTTGATTTAGGATCTCATTTCCATCCATTTAGCCGCACATCTGTGTGTTTCTTATGAGTGTGTCTGTGTGTGTGCGTGCGTGTTTAATAGCTCTACTTGTGAGGTCTCACTTATATAGTGAGATATCCAAACAAGCCACTAGTGTTGACATTTCACTGCTCCTCACTGATTAAAAGTGCTTATAAATCAGACACAAGGTGTTTTATTAGTAAGGTTAAGGTCAGGGTTAGGGGCAGGCCACAGACACTAACAATAACCTGATAGAAAAACAAGTCAATGCAATGTCCTCGCATTGTGTTTCAGGCTACATCATCTACTACAGCACGGATGTGAACGCAGAGGTTCATGATTGGGTGGTGGAGCCGGTGGTGGGGAACCGACTGACCCATCAGATTCAGGGCT[T/A]GACTCTGGACACCAGCTACTTCTTCAAGATCCAGGCCAGAAACTCTAAAGGCATGGGGCCCATGTCTGACGCCGTGCAGTTCCGCACTCCGAAAGGTCCTAACACTTCTAAACATCAGCCTGTTTACTGACCTGCTCATGCTCACTCATGCTTTTGTCTGTTCATTTACAGCTGAACCCTCTGACAAGATGTCCAGCGATCAAGGTAAATCACCATGTTTAACACAGTCACCGAAAATCATGAAGTTAAATGAGTTAGTCTAGTGCAGGGGTGTCCAAACTCAGTCCTGGAGGAGCGGCGTCCTGGAGAGTTTAGCTCCAACCCTAATTAAACACACCTGAAGCAGCTAATCAAGCTCTTACTGGATATACGCTTATTTCACGCGGCCGCCATTTTAAAGAACCAAAGCGAGGCTGCGGTGGGAAGAAACCCGGAAGTATAAGACGAGCACTGTAAACATTGCAGTAACATACTGTGTACTACAAACCTCCAGCTGTTGC
Associated Phenotype:
Not determined