ZMP

si:dkey-86e23.2

Ensembl ID:

ENSDARG00000076055

ZFIN ID:

ZDB-GENE-091204-132

Human Orthologue:

RPGRIP1

Human Description:

retinitis pigmentosa GTPase regulator interacting protein 1 [Source:HGNC Symbol;Acc:13436]

Mouse Orthologue:

Rpgrip1

Mouse Description:

retinitis pigmentosa GTPase regulator interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1932134]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24443	Nonsense	Available for shipment	Available now
sa44087	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24443

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

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110516	Nonsense	49	981	1	16
ENSDART00000138541	None	None	373	None	13

Genomic Location (Zv9):

Chromosome 24 (position 7879725)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	7737017
GRCz11	24	7766336

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGCTTAAAGAAAGACTGGAGGAAGCAAGGAGTGAAAGGAAAACACTGGAG[C/T]AGGAGAAAGAACAGATGAGGCATGAGATTGATCAAGTTAAAAAGGAGAAG

Long Flanking Sequence:

CTGCAATAACAAGGCAAATAATATAATGAATAATGCAGAGTTTATCAAATATAAGATAAGTTCAAATTCTGCTATAAAGCAGCACTAAACCAGTTCTTTGTTAATAAAGTTTCATATAAATCCTCTGCAAATGTAGCAGATTTGGAAATAGCAGCAGCTATTCTATAAGCTATTCTACATTCTTAACAATTCTATTATCTATAAACAGCTAAACAGCAGGATAGCAGTCTTCTTGAGCCAGATTTGGATGAATCAAGTAACTAATAAACAATGTGTGAACCTGAAAATGGAAAAAATCTAGAGTAAAAGCTATATGCTTTGTAATAATTTATATCAATGGTTTCCACCACAGCACTATGTCCATCCAGAACCATCAAGGAGATAAACATGAAGAAAAAGAGGAAAGAAAGGAAGAGTTAAGAGAGGAAGGATGGAGAGAGGAACTTCAGAGGCTTAAAGAAAGACTGGAGGAAGCAAGGAGTGAAAGGAAAACACTGGAG[C/T]AGGAGAAAGAACAGATGAGGCATGAGATTGATCAAGTTAAAAAGGAGAAGGAGCGAGATAAAGGTACTGTAGTCCAACCTGTAGTGATGTCTTGCAATGCCAGAACATTAAATAGCAACATCAGTTCTGGACCACAAATCTGTTAAAAAAGATCCTGTTTGGATTTCACATACAGTGAGTGACAGTTCAAAATGACTACTACCTCCCTGTGTGACACCGCCATGGGACAAAGTTATTAGTAAACTGTTTAGGTGTAATAGCAGTTTGTGTCAATTCCACCAGGGGGCATAATCTAACCACAAACTTGTCAGCTCAATGCCTTCCTCAGTGCGTAAAAAGTTCTTGAGTTTGTTATTATTTTTTTCAACCAATGAACTATACCTACACTCACCGGCCACTTTATTAGGTACACTTGACCAGTACCGGGTTGGACCCACTTTTGCCTTCAGATCCACCTTAATCCTCCGTGGCATAGATTCAACAAGGTACTGGAAATATTC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44087

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110516	Nonsense	891	981	15	16
ENSDART00000138541	None	None	373	None	13

Genomic Location (Zv9):

Chromosome 24 (position 7862702)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	7719994
GRCz11	24	7749313

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATGAAGGAGCAAGAAGAATGTGAAGATGTCGGCTATGCCTACTTGGATT[T/G]ACGAGAACTTCTGCTGACTGGAAATGATGTTATTGAAAAACAAATCAATG

Long Flanking Sequence:

GGTCTCGGGACTGTTGTGGTCTATGGAGGATGAGGGAGCTCTCTGAATTCATCTAAAATTTATTCTTTTGTGTTCTGAAGATAAATAAAGGTCTTTGAGAATTGGAATATTATTAGGATAAGCAATTAAAAAACAGAACAAACTGAATTTACTTTTTTTGGTGAACCAACCCTACAATTTGGTATGAATATTGTTGAAGAGACACATAATTAACAACTGATGTCCTCTTATCAGTTATCCATGTGGATTCAGTGGGAGCAGCTCCACTGAGACACTACCTCTACACCATGCTGGAAGGCACTGACCCCAACCAGGGCAGGTAAACACAGAGATATTGATGTAATGAAAAGAATTCCATGTTAAAATTAAAATAAATACTTGTATACAAAAAGATATTCAGATTTCTAAGCTTCCTTTATGCAGGCTAAAGTTCACAGTGGTCAGTGAGCCCATGAAGGAGCAAGAAGAATGTGAAGATGTCGGCTATGCCTACTTGGATT[T/G]ACGAGAACTTCTGCTGACTGGAAATGATGTTATTGAAAAACAAATCAATGGTAGGAGAATAAAGTCATTTTAGAAGGAGATGAAAATGTACTTGGAATATACACGCATCATTTAGTGTTTGTTTTTCTCCTTGTCAGTTGTCAGTCCGAATGAAGAGCAGGAAGTGGTGGGAAAGCTGAAAGTCTCTGTAGAAGCTGCTCAGGCTCTGACTGGAATCTATCAGGAATATCATCAGACTGTAAAGAGGAACAGAAGAGATCCTCCAAGCAGCACAGAGGATGAGGAAGAAGAAGGGACAAAGAAAAAGGAGGAGTTGCATGTGCTCGATTTTGAAGTTGACGAAGACAGTGATTTTTATTGAAACTCTCCTCTCAAACCAGGCTAGTCTCAAAAAGAACATCAATTGATTTTTTTTATAGAAAAAAAAATGCTTTTGTGACATTGTAACCATATTCAATACTCATCAAATTGTTTTATGTCGTCGTGCTGAAATGCAAAAT

Associated Phenotype:

Not determined