ZMP
NHSL2 (1 of 2)
Ensembl ID:
Description:
NHS-like 2 [Source:HGNC Symbol;Acc:33737]
Human Orthologue:
NHSL2
Human Description:
NHS-like 2 [Source:HGNC Symbol;Acc:33737]
Mouse Orthologue:
Nhsl2
Mouse Description:
NHS-like 2 Gene [Source:MGI Symbol;Acc:MGI:3645090]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14872 | Nonsense | Available for shipment | Available now |
sa34184 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31596 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14872
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082464 | Nonsense | 1016 | 1221 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 7 (position 52929117)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 51198867 |
GRCz11 | 7 | 51473937 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATTGAGGGAGATTTGCTTAAAGATGAAGAGGAAGACTATTCTGCCAAG[C/T]AAATTTCACATGAAAACCACCAAATTCCTGAACTTTATGAGACCTTTGGG
Long Flanking Sequence:
CCCCATTGACACCTGAATCTCCTCCATCCTCCCCTGTGGACCGACCTATGCCTGTTGGTAATATTTATATGGTTGTAAGGAAACCCAAACCTAAAAGACCAGCTCAGGCATCACTCAGCACATCTGCAATAGCCACACAAGAGCCCATCCGCAGCCATGTATCTACTTTTCCAGAGTTTGACCTAGAGCATGGGATTCCCATCGAAGAAGATCTTCCATCCCCAAGTAGCCCAGAAAGGGAGGATAAATGTAAAACTCTTCCAAGTAGAATGACAATATCTTGTTTGGCAGAATTAGACAAAAGGAAGCCCAAGGTACCACCACCAGTACCAAAAAAACCCAGTGTCCTTCTACTTCCCTCTCCAAGCATCCAGACCAATGGTGGGGCAGAGAGGCAAACTCTACTTTCAGAAAGCATCTCTCAGTCACCTACCGGTACATCAGCATCTGAGATTGAGGGAGATTTGCTTAAAGATGAAGAGGAAGACTATTCTGCCAAG[C/T]AAATTTCACATGAAAACCACCAAATTCCTGAACTTTATGAGACCTTTGGGAACGAGGAGAATGATGTAGTAGTTGAAGAATACAGTTCAGAAGACAGAGGTTCTCATCATTTTATGGAAAGGGAGACACCTCCAGCAGAGATAGTAAAAGGTTAAACATTTGCTTATATTTCCATTTATGCTTGAAATAAATGAAATGCAATCTATGTTTGTTAGTTTAAAACTAAAGCCATTTTTTTTGCTCCACAGAAATTTACACAGAAACAGAAATATTGGAAGAGAACATCTCTGCAGTTGACAAAACTGAACTACACATTACAGAGGAAACAGAGGATGAAGTATTTGTCAACACACCCACAACTCACACCACTGAAGATCTCTTCACCATAATACACAGGTATATAATTTGCAGTTAACTTTCATTGAGTTATTCCTATACTTGATGTCAGGGGCCATGTCTTCTAATGCAGAGGTCACCAAGTAGGTACTTGATTATTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34184
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000082464 | Nonsense | 1118 | 1221 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 7 (position 52928200)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 51197950 |
GRCz11 | 7 | 51473020 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTGCTGTTATTCTAACATTTCTATTGTTCTGCCTTTCCTAGGTCAAAG[A/T]GAAAAGTTCTTGGTCGAAAGGAACCATCAGATTCTTTTGGAAGAAGTCAG
Long Flanking Sequence:
TTTCATTGAGTTATTCCTATACTTGATGTCAGGGGCCATGTCTTCTAATGCAGAGGTCACCAAGTAGGTACTTGATTATTTTGTAAACAAATAATAACTGTCAAAAGTGTTTGAGTGCGAAATTGAGTACTCAGTTTTGTATTTCTTTAGCTGATTTGGACATTAGATTTAAGATTTTAGAAAGGGATAGCTATAAGTAAAGGGATGCCCTTGCTGAATAGGTGTGTCACAAAGAAGTCAGCACAATAATTTACCATAGTGATTAAGTGTCCCCAGTCCTGTTCCTGGAGAGCTACTGTTCTGCAAATTTTATCTCCAATCAAACACACCTAAACCAACCTATCAATGTGTTCAGAAATACTTCTTCACACCTGAAGTCAGGTGTGTTTTAACAGAGTACGAAGTAAAGTTTGCAAGATGGTACAGTAGCTGAGGAGTAAAGATGGTCACGGTTGCTGTTATTCTAACATTTCTATTGTTCTGCCTTTCCTAGGTCAAAG[A/T]GAAAAGTTCTTGGTCGAAAGGAACCATCAGATTCTTTTGGAAGAAGTCAGTGTCTGGTCTCGCCTGTGAAAAGCAGTAGTACAGACTTCAGAACTCTGGGCCTTGGGACTACACCTCGGTCAAGCTCACGAAATGAAAACTTTATGGCTCTCCTCCAAAAGAGGAGCAGCAAAGCTAGCAGTGGGACCAGAGTTTCTGCCATGGAGTTGCTGAAGAGCACAAACCCTTTGGCACGACGAGTCACGGAATTCTCTCAGTCACAACCAGATGGGAGCGCAATGAACACACCAAAACCATCTTCGCAGGACCAGTGATTCTACTTGTACGGAACCACATGCTGGAAATCAATATGGCTGGATTTCCGTTATGCTCCACTGTCCATCTAAATGGTTTCATTATCAAAGACCTTATGCTGAAGGACTTTAAGTGGTTTTGTGTTGTTGCGTTCAGGCAAGGGGATCACATTTGATGGTTTAAAATTGTAGAGGAGTATAGACGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31596
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082464 | Nonsense | 1161 | 1221 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 7 (position 52928071)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 51197821 |
GRCz11 | 7 | 51472891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACAGACTTCAGAACTCTGGGCCTTGGGACTACACCTCGGTCAAGCTCA[C/T]GAAATGAAAACTTTATGGCTCTCCTCCAAAAGAGGAGCAGCAAAGCTAGC
Long Flanking Sequence:
CTCAGTTTTGTATTTCTTTAGCTGATTTGGACATTAGATTTAAGATTTTAGAAAGGGATAGCTATAAGTAAAGGGATGCCCTTGCTGAATAGGTGTGTCACAAAGAAGTCAGCACAATAATTTACCATAGTGATTAAGTGTCCCCAGTCCTGTTCCTGGAGAGCTACTGTTCTGCAAATTTTATCTCCAATCAAACACACCTAAACCAACCTATCAATGTGTTCAGAAATACTTCTTCACACCTGAAGTCAGGTGTGTTTTAACAGAGTACGAAGTAAAGTTTGCAAGATGGTACAGTAGCTGAGGAGTAAAGATGGTCACGGTTGCTGTTATTCTAACATTTCTATTGTTCTGCCTTTCCTAGGTCAAAGAGAAAAGTTCTTGGTCGAAAGGAACCATCAGATTCTTTTGGAAGAAGTCAGTGTCTGGTCTCGCCTGTGAAAAGCAGTAGTACAGACTTCAGAACTCTGGGCCTTGGGACTACACCTCGGTCAAGCTCA[C/T]GAAATGAAAACTTTATGGCTCTCCTCCAAAAGAGGAGCAGCAAAGCTAGCAGTGGGACCAGAGTTTCTGCCATGGAGTTGCTGAAGAGCACAAACCCTTTGGCACGACGAGTCACGGAATTCTCTCAGTCACAACCAGATGGGAGCGCAATGAACACACCAAAACCATCTTCGCAGGACCAGTGATTCTACTTGTACGGAACCACATGCTGGAAATCAATATGGCTGGATTTCCGTTATGCTCCACTGTCCATCTAAATGGTTTCATTATCAAAGACCTTATGCTGAAGGACTTTAAGTGGTTTTGTGTTGTTGCGTTCAGGCAAGGGGATCACATTTGATGGTTTAAAATTGTAGAGGAGTATAGACGGTAGTAAAGGAATCTGAGCCCGCCACTGCTGAAAAAAATTCTGGTGTAAAAATCTGCAATTCTGGGAATATGAAAGTGAAACAACGTATTTTCAGACTTTTTAGGACCCAGCCTATATTTGTGGCCAAAGC
Associated Phenotype:
Not determined