Gene (nucleotide) for PMC (Select 4438458) - Gene

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Items: 20

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Name/Gene ID	Description	Location	Aliases	MIM
Select item 106479863 RNU6-670P ID: 106479863	RNA, U6 small nuclear 670, pseudogene [Homo sapiens (human)]	Chromosome 3, NC_000003.12 (10037552..10037655)
Select item 100873541 RNA5SP288 ID: 100873541	RNA, 5S ribosomal pseudogene 288 [Homo sapiens (human)]	Chromosome 9, NC_000009.12 (95142449..95142541, complement)	RN5S288
Select item 100271238 RPS26P37 ID: 100271238	ribosomal protein S26 pseudogene 37 [Homo sapiens (human)]	Chromosome 9, NC_000009.12 (95123501..95123938)	RPS26_12_999
Select item 643342 LOC643342 ID: 643342	ATM interactor pseudogene [Homo sapiens (human)]	Chromosome 9, NC_000009.12 (95292309..95295007)
Select item 360167 CYCSP11 ID: 360167	CYCS pseudogene 11 [Homo sapiens (human)]	Chromosome 3, NC_000003.12 (10057662..10058355, complement)	HCP11
Select item 84464 SLX4 ID: 84464	SLX4 structure-specific endonuclease subunit [Homo sapiens (human)]	Chromosome 16, NC_000016.10 (3581181..3611606, complement)	BTBD12, FANCP, MUS312	613278
Select item 83990 BRIP1 ID: 83990	BRCA1 interacting DNA helicase 1 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (61679139..61863528, complement)	BACH1, FANCJ, OF	605882
Select item 79728 PALB2 ID: 79728	partner and localizer of BRCA2 [Homo sapiens (human)]	Chromosome 16, NC_000016.10 (23603165..23641310, complement)	BROVCA5, FANCN, PNCA3	610355
Select item 57697 FANCM ID: 57697	FA complementation group M [Homo sapiens (human)]	Chromosome 14, NC_000014.9 (45135930..45200890)	FAAP250, KIAA1596, POF15, SPGF28	609644
Select item 55120 FANCL ID: 55120	FA complementation group L [Homo sapiens (human)]	Chromosome 2, NC_000002.12 (58159243..58241380, complement)	FAAP43, PHF9, POG	608111
Select item 8373 IFIT1P1 ID: 8373	interferon induced protein with tetratricopeptide repeats 1 pseudogene 1 [Homo sapiens (human)]	Chromosome 13, NC_000013.11 (32384602..32386641)	G13P1, IFI56P, IFIT1P, II56P
Select item 5889 RAD51C ID: 5889	RAD51 paralog C [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (58692573..58735611)	BROVCA3, FANCO, R51H3, RAD51L2	602774
Select item 2189 FANCG ID: 2189	FA complementation group G [Homo sapiens (human)]	Chromosome 9, NC_000009.12 (35073839..35079942, complement)	FAG, XRCC9	602956
Select item 2188 FANCF ID: 2188	FA complementation group F [Homo sapiens (human)]	Chromosome 11, NC_000011.10 (22622533..22625823, complement)	FAF	613897
Select item 2187 FANCB ID: 2187	FA complementation group B [Homo sapiens (human)]	Chromosome X, NC_000023.11 (14689524..14873069, complement)	FA2, FAAP90, FAAP95, FAB, FACB	300515
Select item 2178 FANCE ID: 2178	FA complementation group E [Homo sapiens (human)]	Chromosome 6, NC_000006.12 (35452338..35467102)	FACE, FAE	613976
Select item 2177 FANCD2 ID: 2177	FA complementation group D2 [Homo sapiens (human)]	Chromosome 3, NC_000003.12 (10026437..10101932)	FA-D2, FA4, FACD, FAD, FAD2, FANCD	613984
Select item 2176 FANCC ID: 2176	FA complementation group C [Homo sapiens (human)]	Chromosome 9, NC_000009.12 (95099054..95317709, complement)	FA3, FAC, FACC	613899
Select item 2175 FANCA ID: 2175	FA complementation group A [Homo sapiens (human)]	Chromosome 16, NC_000016.10 (89737549..89816647, complement)	FA, FA-H, FA1, FAA, FACA, FAH, FANCH	607139
Select item 675 BRCA2 ID: 675	BRCA2 DNA repair associated [Homo sapiens (human)]	Chromosome 13, NC_000013.11 (32315077..32400268)	BRCC2, BROVCA2, FACD, FAD, FAD1, FANCD, FANCD1, GLM3, PNCA2, XRCC11	600185