ZMP
GPRIN2
Ensembl ID:
Description:
G protein regulated inducer of neurite outgrowth 2 [Source:HGNC Symbol;Acc:23730]
Human Orthologues:
GPRIN1, GPRIN2
Human Descriptions:
G protein regulated inducer of neurite outgrowth 1 [Source:HGNC Symbol;Acc:24835]
G protein regulated inducer of neurite outgrowth 2 [Source:HGNC Symbol;Acc:23730]
G protein regulated inducer of neurite outgrowth 2 [Source:HGNC Symbol;Acc:23730]
Mouse Orthologues:
Gprin1, Gprin2
Mouse Descriptions:
G protein regulated inducer of neurite outgrowth 2 Gene [Source:MGI Symbol;Acc:MGI:2444560]
G protein-regulated inducer of neurite outgrowth 1 Gene [Source:MGI Symbol;Acc:MGI:1349455]
G protein-regulated inducer of neurite outgrowth 1 Gene [Source:MGI Symbol;Acc:MGI:1349455]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18582 | Nonsense | Available for shipment | Available now |
sa42312 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18582
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 |
---|---|---|---|---|---|
ENSDART00000121508 | Nonsense | 92 | 550 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 13 (position 53360372)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 45679180 |
GRCz11 | 14 | 50830412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGRTTGATGATCCAGCATGCAAAGAGAGATGTAAGGAGATGTGCATTGAT[C/T]AGGAGATCACCAWTCTRGTGACCAATCMTGAYTGCAATTTAGAGGAGGAA
Long Flanking Sequence:
GTGTTTTATAATAGTGTTTGTTTTTACAATGAATAAAATTGAACCCAGAATAAATCTCTGATGTAATACGCCTCCTAAAATGTCAGTCACTTTGGACAAAAATATCAGCTAAATCTGTTATATGTTTTCAATAAGTACTAATGCATTTATGTGCATGCTTTCCAGCTAACCCTCAGTGGTGTGAAACACATTTCACTTTGCTTCGCCACAAACTCATCTCTGAACTCATGGAGGGTCCGGTTTTGACAGAGAGTGAAGTTTGGAAAGTTGGCTCGGAGACCAGCACAAGTATAAACCCAGAAGACCGAAGCATTGACTATCCTCTCATTAATGACACTGATGAAAAAGTGAAAGCACCAGAGAGTGCAGTCCAAGAGGAGATCATCCAACAGTCTGTGAATCCACCTGAACTGCGAATCGAGGATTTATCTTCCCCTCAAACTGAAATGGAGGTTGATGATCCAGCATGCAAAGAGAGATGTAAGGAGATGTGCATTGAT[C/T]AGGAGATCACCATTCTGGTGACCAATCATGATTGCAATTTAGAGGAGGAAGAGGATGAGGACACAAATGAAGAGCAGACGGCTTGTACTGAAGCTGTAATATCTAGTGTTGATGTTCGAGAACTGATTGATGAGGATAATCTTGATGGATCAATTGTTGTGGCCAACATGATTGAAGTAAGTCAAATCCAGAAAACCAACGTCGTAAACAACACCTCAACTAATACAACAACTGAAGAACAACCTAAATCTCAAGAGGATCCAGACCCAATTTGCACAAAGTCAAACCCACCACAGGAATCGGATGTTTGTAGCACACAAAGTCTGAAAGATCAGCCCACACAGTCTGAGGATGTAGGAAAAGTCGATGCAAATAAAAGCGAACCGGCTAAAGAGAAGCTGGATTTGAGTCGATCTCCTATTCGCACTCAACATGTGCAAACACAAGTCAGTCTTGAGGTGATGTACCATTCGGTGGCCACCAGTCCCATGACTCCACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42312
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121508 | Nonsense | 240 | 550 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 13 (position 53360816)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 45679624 |
GRCz11 | 14 | 50830856 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGCTGGATTTGAGTCGATCTCCTATTCGCACTCAACATGTGCAAACA[C/T]AAGTCAGTCTTGAGGTGATGTACCATTCGGTGGCCACCAGTCCCATGACT
Long Flanking Sequence:
AAATGGAGGTTGATGATCCAGCATGCAAAGAGAGATGTAAGGAGATGTGCATTGATCAGGAGATCACCATTCTGGTGACCAATCATGATTGCAATTTAGAGGAGGAAGAGGATGAGGACACAAATGAAGAGCAGACGGCTTGTACTGAAGCTGTAATATCTAGTGTTGATGTTCGAGAACTGATTGATGAGGATAATCTTGATGGATCAATTGTTGTGGCCAACATGATTGAAGTAAGTCAAATCCAGAAAACCAACGTCGTAAACAACACCTCAACTAATACAACAACTGAAGAACAACCTAAATCTCAAGAGGATCCAGACCCAATTTGCACAAAGTCAAACCCACCACAGGAATCGGATGTTTGTAGCACACAAAGTCTGAAAGATCAGCCCACACAGTCTGAGGATGTAGGAAAAGTCGATGCAAATAAAAGCGAACCGGCTAAAGAGAAGCTGGATTTGAGTCGATCTCCTATTCGCACTCAACATGTGCAAACA[C/T]AAGTCAGTCTTGAGGTGATGTACCATTCGGTGGCCACCAGTCCCATGACTCCACCAGAAGCTTCTGGAACTTTCATTTTTCCAAGCACTTTTGGAAAGCTCGCTAATAAATGCAACCAGGAGGACTTAGAGACTAAAAATGTGGAGATGCATTCGGTGGCCACAGCTCCAATGACTCCTTTAGTTCTGAACGCTCCAGAGACGCATTCTGTAGCCACTGCTCCAATGACTCCTTTAGTACTGAATGCTCCAGAGCTGCATTCGATAGGCACAGCTCCAATGACTCCTACAGTACTAAATGCTCCAGAGATGCATTCGACAGGCACAGCTCCAATGACTCCTACAGTACTAAATGCTCCAGAGATGCATTCGACAGGCACAGCTCCAATGACTCCTACAGTACTAAATGCCCCAGAGATGCATTCGATAGGCACAGCTCCAATGACTCCTATAGTTCTGAATGCCCCAGAGATGTGTTCTGTAGCCACAGCTCCAATGACT
Associated Phenotype:
Not determined