ZMP
si:ch211-195h3.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate netrin G2 (NTNG2) [Source:UniProtKB/TrEMBL;Acc:B0UX66]
Human Orthologue:
NTNG2
Human Description:
netrin G2 [Source:HGNC Symbol;Acc:14288]
Mouse Orthologue:
Ntng2
Mouse Description:
netrin G2 Gene [Source:MGI Symbol;Acc:MGI:2159341]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21214 | Nonsense | Available for shipment | Available now |
| sa18661 | Nonsense | Available for shipment | Available now |
| sa18579 | Nonsense | Available for shipment | Available now |
| sa10911 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21214
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 |
|---|---|---|---|---|---|
| ENSDART00000114432 | Nonsense | 108 | 1256 | 2 | 13 |
| ENSDART00000132492 | Nonsense | 100 | 343 | 2 | 3 |
| ENSDART00000138101 | None | None | 156 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 12533702)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11978465 |
| GRCz11 | 8 | 12016170 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCACCAAAGAACTGGCTCATCCTCCAGAGCTGATGCAAGACAGCGAG[C/T]GAACCGGACTCATCACCTACTGGCAGACGGTAACATGGAGTCGATATCCT
Long Flanking Sequence:
TCTTACTTCTTTCAAAATATGTGATCATAGGTTGCCATGTTTTATAAAAATTTTGGACAGATCCCTTAATTAAATACTTAATTTTTTTTTATTTCAAATATAAAATCAGATCACACATCCACATTGAAGCTTTAGGTGAAGCTGCTAATTTCCACTCAAGTAGTATTCTTCTCCTTGCTAACAAAGTAGTGAAGACGAATAAATTTTTTTTCTTGTTTGTCAACAATATATTGCCCCAAAGATAGCTAACTTAACACTAGGTTTTATCTCTAAATTAAAGGCGTCATTTAATGTTTACAACAGATTAGTTTTAACAATACAGAACACATTAAGTATAGTGCAATGTTGTTGTCATGCTTCATTTTATATCACTCTTTGTTTGCCTTTTTATTAACTCTATTTATCTGTGTTTTTAGGAAAACCCATACCTGTGTAGTGACGAATGCGATGCCTCCACCAAAGAACTGGCTCATCCTCCAGAGCTGATGCAAGACAGCGAG[C/T]GAACCGGACTCATCACCTACTGGCAGACGGTAACATGGAGTCGATATCCTGAGCCTCTTCTGGCCAACATATCCTTATCCTGGAACAAAAGCCTTGAGTTAACAGATGACATCCAGATATCCTTTGAGTATGGTCGGCCCACAATAATGGTGCTAGACAAGTCTCTGAATTATGGACGAACCTGGCAGCCTTACCAGTACTACGCTGACGACTGCATGGAGGCTTTTGGGATGTTGGCAAAAAGAGTGCAGGATCTTTCGGCCACCAACGTGACCAGAGTTATATGTACCGAGCAATACTCTCGCTGGGTTGGTTCCAAGAATGAGAAGAACGTGCGCTTTGAAGTCCGGGAGCGCTTCGCCATATTTGCTGGGGCAAAACTGCAGAACATGGACAACTTGTACACACGCATGGAAAGTATGAAAGGTCTCCGAGACTTTTTCACCTTCACAAACCTACGACTTCGGCTGCTGAGACCGGCGCTCGGAGGAACATACGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18661
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114432 | Nonsense | 135 | 1256 | 2 | 13 |
| ENSDART00000132492 | Nonsense | 127 | 343 | 2 | 3 |
| ENSDART00000138101 | None | None | 156 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 12533785)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11978548 |
| GRCz11 | 8 | 12016253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATGGAGTCGATATCCTGMGCCTCTTCTGGCCAACATATCCTTATCCTG[G/A]AACAAAAGCCTTGAGTTAACAGATGACATCCAGATATCCTTTGAGTATGG
Long Flanking Sequence:
TTTTTTTATTTCAAATATAAAATCAGATCACACATCCACATTGAAGCTTTAGGTGAAGCTGCTAATTTCCACTCAAGTAGTATTCTTCTCCTTGCTAACAAAGTAGTGAAGACGAATAAATTTTTTTTCTTGTTTGTCAACAATATATTGCCCCAAAGATAGCTAACTTAACACTAGGTTTTATCTCTAAATTAAAGGCGTCATTTAATGTTTACAACAGATTAGTTTTAACAATACAGAACACATTAAGTATAGTGCAATGTTGTTGTCATGCTTCATTTTATATCACTCTTTGTTTGCCTTTTTATTAACTCTATTTATCTGTGTTTTTAGGAAAACCCATACCTGTGTAGTGACGAATGCGATGCCTCCACCAAAGAACTGGCTCATCCTCCAGAGCTGATGCAAGACAGCGAGCGAACCGGACTCATCACCTACTGGCAGACGGTAACATGGAGTCGATATCCTGAGCCTCTTCTGGCCAACATATCCTTATCCTG[G/A]AACAAAAGCCTTGAGTTAACAGATGACATCCAGATATCCTTTGAGTATGGTCGGCCCACAATAATGGTGCTAGACAAGTCTCTGAATTATGGACGAACCTGGCAGCCTTACCAGTACTACGCTGACGACTGCATGGAGGCTTTTGGGATGTTGGCAAAAAGAGTGCAGGATCTTTCGGCCACCAACGTGACCAGAGTTATATGTACCGAGCAATACTCTCGCTGGGTTGGTTCCAAGAATGAGAAGAACGTGCGCTTTGAAGTCCGGGAGCGCTTCGCCATATTTGCTGGGGCAAAACTGCAGAACATGGACAACTTGTACACACGCATGGAAAGTATGAAAGGTCTCCGAGACTTTTTCACCTTCACAAACCTACGACTTCGGCTGCTGAGACCGGCGCTCGGAGGAACATACGTACAGAAAGACAACCTTCTCAAGTATTTCTACGCCATCTCCAACATCGACATACCAGCAAGGTAAAGTTGCACAACACTATAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18579
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 |
|---|---|---|---|---|---|
| ENSDART00000114432 | Nonsense | 505 | 1256 | 8 | 13 |
| ENSDART00000132492 | None | None | 343 | None | 3 |
| ENSDART00000138101 | None | None | 156 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 12608186)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 12052949 |
| GRCz11 | 8 | 12090654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
MAGCAACTGACACCGTCTTTGCAACAACTGCCTTYGGTGCAAGCAATCCA[C/T]GATCTGCTCTTCCTGAGGTTACTGATGCACTTGCTTCATCATCTGATGCC
Long Flanking Sequence:
GAAGGCCGAAGCTCAATTCTTTCAGATCTATTTTTGAATAGCGATTGAATGAACAGCTGCTAAATATTTCATAAGAGAAAAGAGACCGGGTCATGGTAAGGAAGACCAAAAAGGGTCCAATTTATTGAACTTACGGAGAGAGAGATAGATACATGAAACCATAACAGGAAAGCGCAGCGAGTCCTGTCCTTGAACGCTTGTACGGGGGCACGGGCAGGAAGTGATTCTATCAGGGCTCGTGTATCCCGTTTCTGCTGAACTGGAAATGGCGAAAGGTTGAATCGCTGCAATAACATCTATTATGTACGGAATGTAAGCCCTAAGGGCAGCAATGGCATCCATAGGCATATTTACTGCTTTTGACTGAACGGTTTAGATATCTGACTCTTTATATTCTGTCCACAATTACAGTTTCCGCAGCACCAGATGTGATACCCGATGCAGCCACCACAGCAACTGACACCGTCTTTGCAACAACTGCCTTTGGTGCAAGCAATCCA[C/T]GATCTGCTCTTCCTGAGGTTACTGATGCACTTGCTTCATCATCTGATGCCACTGCAACAACACTTAATATGGTCATCCGAGCAACCATGGCAACAACACCTTCTGTAACCATGGCAACTTCTGAAACAACATCAGATAACACTATTCAGCTGCCAACATCTCCTTCTAATGATGCAGTTTCACCTCCAGTGGAAACCAGTACAGCGGGTTCAGAAAATATGGCAGCTGTTCCTTCAACTGATGCAACAATGAAAACAGTTGATGAACTCCCTCCAGACATTGATGTGGTCGTCTCAGCAACTAGTGTTCCTTTACCTTCTCCATCAGATAGAGATGCACCTGTAATTGATGCTGACCCCACTATAACAGATGCTCCTGCACCAGAGGCTGGTTCTATTGCACCTGCAAGAGATGCAGATGCTCCTGCCACTGCTGCTGTGGCTCTTGAAACTGATGAGGATGCAGAAGTTACAAATGTGTCAGATGAAACCAAAGCAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10911
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114432 | Nonsense | 994 | 1256 | 8 | 13 |
| ENSDART00000132492 | None | None | 343 | None | 3 |
| ENSDART00000138101 | None | None | 156 | None | 3 |
| ENSDART00000114432 | Nonsense | 994 | 1256 | 8 | 13 |
| ENSDART00000132492 | None | None | 343 | None | 3 |
| ENSDART00000138101 | None | None | 156 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 12609653)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 12054416 |
| GRCz11 | 8 | 12092121 |
KASP Assay ID:
2260-0236.1 (used for ordering genotyping assays)
KASP Sequence:
CCCCTGATCGTAAACCTTYATCCAAAGTAGGRGAAAACAGCGAAGAGTCC[A/T]ARGAATCGAAAACAGCTTTAAATTCGGAGAARAAAGATAAAGATGCAGAA
Long Flanking Sequence:
TCCAGGAGGAAAAACAGAAAACAAATGTTGAGAATGAGGATAAAGATACTCCTGACATTAAACCTTCATCTGAAGTAGAAGAGAAGAGTGAAGTTCCTCTCGGTGAGACCACGGAGGATAAACCGTCAACCAAGCTGGATGATAAAGATACTCTTGACGTTAAAACTTCTCCTGAAATAGAAGAGAAGAATGAAGATCCTCTTGTTGAGACCAAGGAGGAAAAAACAACAAAGAAAGATGAAGATGCTTCCGACAGTAAACCTCCATTCAAAGTAAGAGAAAACAGTGAAGAACCCAAAATGGAAAAACCCGAAACAAATTTGGAGAAGAAAGATAACAACACCCCTGATATTAAACTTTCATCTGAAGTAGGGGAGAAGAGTGAACTTCCTATTGCTGAAACCAAGGAGAAAAAAGAGATAAAGAATTTAGAAAAGAAAGATAAAGATGCCCCTGATCGTAAACCTTTATCCAAAGTAGGAGAAAACAGCGAAGAGTCC[A/T]AGGAATCGAAAACAGCTTTAAATTCGGAGAAGAAAGATAAAGATGCAGAAGCCTCAGGTATCCACAGAAATTCTGACATCTGAATTCTCTAACAATTATATACACAATAATACACATTAAAAGCAGCTCAAATGTTACATATCGAGCACAATTCATGGAAGTTTGTCACACAACCAAAATTGCCTCCAACACAGTAAGCAAACGCCTTCGCTCTGAGCGGAATTGTAAATGAATATGTCATCATTTACTCAGCATCATGTCTTTTCAAACCTGTTAGACTTACTTTCTTCTGTGGAACTCAGAGGTTGACGTTACTCCACATGACAGCGTTTTTGGAATATTCTACACAGATAAATAAGATCTTTTGAATTCTTTTCCACAGAAGAACACAGTCATCCTATGTCTTCAGAATCACTGAAGTATGAAGAAATAATGACAGAGTTGTCATTTCTTGTGAACAACCCACTTATACTTTTTAAACAAACCACAAAAGTTTTAGA
Associated Phenotype:
Not determined