ZMP

LOC559632

Ensembl ID:

ENSDARG00000010297

Human Orthologue:

RABGAP1

Human Description:

RAB GTPase activating protein 1 [Source:HGNC Symbol;Acc:17155]

Mouse Orthologue:

Rabgap1

Mouse Description:

RAB GTPase activating protein 1 Gene [Source:MGI Symbol;Acc:MGI:2385139]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44415	Nonsense	Mutation detected in F1 DNA	Not yet available
sa30422	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44415

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000021208	Nonsense	392	1018	10	26

Genomic Location (Zv9):

Chromosome Zv9_NA654 (position 99904)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	8800498
GRCz11	10	9711638

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGCTAGAGACACGGGTTCGAGTGTGTTCACCCAACGAGAGGCTGTTCTG[G/A]CCCTTCAGCAAACGCAGTTACACAGAGACCTTCTATCTCAAACTCAGACA

Long Flanking Sequence:

AAGCTGGACTCACCCACTTTTTCTAATTTATTTTTTAAACTAGAGATGTGAAAACACCCTGCTAAAACTGGGGGGATTTCAAGGTTATGTTTAAAAATATGACCATTTTTCAATTTATTTAAAAAATATTACAGTAGACCTAATAATTTTGTCTTCAACTATACTTTTGTTGTTGACATAATACTACTAATAATGATAAATGACAATATTTATTTAGTTTACTAAGAATTTTTAATAATGGGTTTAATAAAATGTTTGTTATTTTATGACATCACTAACAAGAGTATTAATAAGGTCAATATCACACAAATATGACACATGACATTATGCATTAAGCATTACTAATATGCACATCTGCTTTTCTGTGATTTGTGTCACACAGATAAGTTCATGTACATGACAACGGCGGTTGACTTGGTGATCACTGAGGTCGAGGAGCCTGTGAGGTTCCTGCTAGAGACACGGGTTCGAGTGTGTTCACCCAACGAGAGGCTGTTCTG[G/A]CCCTTCAGCAAACGCAGTTACACAGAGACCTTCTATCTCAAACTCAGACAGGTGAGTTCAGGACTCTAACAGACTGATTTGATACTATACTTAGAAAGACAAAAAAAACTATGTAAACAATGCAGCCAAAAATCAACCTTTTCACTTTTAAAGGGTTCATTGTACTGAGGTCCACATATAATGTTTTCATAAGTGTAACTGTATTATGACTCATAATAAGTATTTATAGGGGCTCCTATCCACAATTAAAAAATATTTACTTTTTTGACAGAACAAAACTTGTTCTTACTACTAATGAGTTTTTGTAACTTTAAGAAAACACCGTTTTAACATTGCAGACTAAGGGCTCTATTTTGACGGTTCATGCGCAGAGCGCAAAACACAGGGCGCAAACGCTTTCAGGGCGTGTCAGAACGCATTTTTGCTAATTTACGGACGGGAAAATGCGCTTTGCGCCAAGGCACATGGGCTAGAAGGGTTGAGTTTATTTTCTTAATGGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30422

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
ENSDART00000021208	Nonsense	609	1018	15	26

Genomic Location (Zv9):

Chromosome Zv9_NA654 (position 39725)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	8740319
GRCz11	10	9771817

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGAAATCGGTTACTGTCAAGGGCAGTCCTTTCTTGCTGCTGTGCTGCTAT[T/G]ACACGTGAGTATCAACGCAGATTAATGCAAAGTTGTTTATAAAAGCTGAC

Long Flanking Sequence:

TGATTATCCTACTTAGTTGTCCATGTATGTCTTTAATGTGCATTTTCAAAATGTATGCAAATCTTGCTATTCACATTAAGCATTTTGTATGTGATATTTCAAAATATCTATAAAATAGGGGGACGGAAACAAAGCTGCTTTGTCAGATTATGCTAGACCTCTAAATTGTTGTTTTGGACACACACATACAGAGACTATACAAGATAAAATAATTAATTTGATACAACATCCTATAAAAGAAAAAAAAAAGACGACACTGTCTGGTGTCCCAAGATCTGTTGTTGTTTACAAAAATCATCAGAAAAAATTCAAATGTTCCAAATTTCATCTAATATTGTGTATTCTGAGCCTGGCATAAGACTGCATGTCTGTTTATTTAGACCATATTTACCCACAATTCCACTAATATTTTGTATTTTCTATCCTCCAGGCGTATTCTGTTTATGATGAAGAAATCGGTTACTGTCAAGGGCAGTCCTTTCTTGCTGCTGTGCTGCTAT[T/G]ACACGTGAGTATCAACGCAGATTAATGCAAAGTTGTTTATAAAAGCTGACATTTAATGTAATGATATACAGTGGGGGAAAAAAGTATTGAACACATCACCATTTTTCTCAGGTAATATATTTATAAAGGTGTTGCTGACTAAAAATGTTGGCTTGGATGTTATTAACAATCAATAGAAATATATATAAGCAAAGAAAACAAAACTGAATAGTTTACAAATTAAGTTATGTGCAATAAAATGAAATGACTCAGTGACAAAGTATTGAAAGGCAGTGAAAGCCCAGACAGCAACTGAAATCTCGCAGTGGTTTTTCAGCAACCTTCTGCCCTTTCTCATTGTAAATTAATATTTTCTGCTTCAGTCCAACATCTGCATTATCAGGATGATAAAGATGAAACTTGGGTGGACAATTTAGTAAAACAATGATTTAAAACAAAGCCAAGGAAATTATCATATGCTATCAGAGAAAGAAAATAAAGCTGTAGAATGGCCCGGCCAA

Associated Phenotype:

Not determined